Final Flashcards

1
Q

Erikson’s 8 stages of social-emotional development

A

Trust vs Mistrust (Birth -12 months)

Autonomy vs Shame and Doubt (12-36 months)

Initiative vs Guilt (preschool 3-5 years)

Industry vs Inferiority (school age)

Identity vs Role Confusion (12-18 years)

Intimacy vs isolation (18–25 years)

Generativity versus self-absorption and stagnation (25–65 years)

Integrity versus despair (65 years–death)

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2
Q

Piaget’s 4 stages of cognitive development

A
  • Sensorimotor (birth to 2 years)
  • Preoperational (2 to 7 years)
  • Concrete operations (7 to 11 years)
  • Formal operations (11 to 15 years)
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3
Q

Expected Findings for child with Autism (5)

A
  • Delays in social interaction and imaginative play before age 3 years (no immitation)
  • Avoidance of eye and physical contact
  • Short attention span
  • Rhythmic movements
  • Attached to routines
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4
Q

Interventions for autism (7)

A
  • Early screening and intervention to maximize their social skills (at 18 and 24 months)
  • Behavior Modification i.e. Limit setting
  • Decreasing environmental stimuli
  • Introduce new situations slowly
  • Involve parents b-c warm up to new people slowly
  • Promote consistency in caregiving
  • Ensure safety (May have poorer safety cues)
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5
Q

Age appropriate toys: infants

A
  • nesting toys
  • teething rings
  • rattles
  • mobile
  • high contrast (0-6m)
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6
Q

Psychosocial Development: Infant

Trust Development (2 )
Mistrust Development (2)
Social behaviors (2)

A

Trust
- Feeding
- Stimulation and Comfort (quality care)

Mistrust
- when gratification of needs is delayed
- when needs met before infant asks (does not learn delayed gratification)

Social modifications
- Grasping (pleasurable tactile)
- Biting (first conflict is biting w/ breastfeeding)

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7
Q

Age-specific difficulties: Infants

2 notes and age ranges

A
  • separation anxiety b/w 4-8 months
    (insecure attachment disorders form here if failure to learn object permanence and discriminate parent from others)
  • stranger fear b/w 6-8 months
    (nurse should be soft, eye-level, stay safe distance and avoid sudden invasive gestures; child may refuse to play with strangers)
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8
Q

Sleep: infants

SIDS prevention (5)

A
  • back to sleep (tummy time in daytime to prevent plagiocephaly)
  • sleep in crib w/ firm mattress in same room as parents
  • no loose objects, crib bumpers, soft toys, and bedding out of baby’s sleep area
  • avoid letting baby overheat at night
  • breastfeed first 6 months
  • use pacifier
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9
Q

5 safety concerns for infants - Preschool (and recommendations)

A

ASPIRATION- check for small objects, feed sitting up, small food bites, avoid pits and bones

SUFFOCATION- “Back to sleep”, avoid extra blankets and pillow, avoid unsafe sleep, crib slats, 6cm apart, no crib bumpers, remove bibs, avoid bags, balloons, and buckets

DROWNING- supervise baths, fence pools, keep bathroom doors closed, keep appliances shut; teach toddlers and up how to swim and not go in water too deep

FALLS-crib rails, car seats, supervise when on furniture, avoid scatter rugs, fence the stairs, keep furniture away from the window.

BODILY DAMAGE-Secure furniture, supervise with animals, keep away sharp items, walk w/ scissors down

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10
Q

Emergency Care for Poisoning (4)

A
  • always assess child (ABCs)- (oxygen, intubate, pulse ox, sodium bicarb for metabolic acidosis)- shock is common
  • call poison control (1-800-222-1222)
  • Terminate exposure to poison (empty mouth, flush w/ water, remove clothes; keep child side-lying
  • identify poison (environmental cues, witnessess, victim)
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11
Q

Poisoning Safety Promotion: Infants - School age (6)

A
  • check paint for furniture and toys- no lead
  • All toxic substances on high shelf
  • Keep plants out of reach
  • Child safe caps and all meds stored out of reach (SAFETY LOCK FOR TODDLERS; do not take meds in front of child)
  • Give medications as a drug, do not call it “candy”
  • Carbon monoxide detector in home
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12
Q

Burns Safety Promotion: Infants- School age (9)

A
  • Smoke detectors
  • Check temperature of all formula and bath waters
  • Water heater set under 120 degrees
  • Avoid cigarettes/ashes near child
  • Flame retardant clothes
  • Store all candles, matches, lighters in high place
  • Caution with sun exposure, use sunscreen
  • Safe cooking (microwave and pot handles turned inward)
  • Do practice fire drills
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13
Q

Psychosocial development: Toddler

6 concepts related to Autonomy vs Shame and Doubt

A
  • Independence (differentiate self from others; accept separation from others, control bodily functions)- risk for injury r/t increased independence and mobility
  • Negativism (negative responses; so reduce opportunities to say no)
  • Ritualism (provides them comfort)
  • Transitional objects
  • Animism
  • Centration- focus on one thing
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14
Q

Age-appropriate activities: toddlers (7)

A
  • Blocks
  • Books
  • Push/pull toys
  • Balls
  • Large piece puzzles
  • Finger paints/thick crayons
  • Imagination (Boxes, kitchen pots/spoons)
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15
Q

What is the purpose of play?

What kind of play do different ages engage in?

A
  • relief of stress, energy, tension (a way to cope)
  • intellectual and social development

Infants- sensory affective and solitary play
Toddlers - parallel play (usually do not share)
Preschool- associative play (group play w/o rigidity)
School age- cooperative and competitive

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16
Q

3 Age-specific Difficulties: Toddlers and preschoolers

What are they? (3 concerns)
How to manage them?

A

Temper Tantrums (kicking, screaming, holding breath)
- manage w/ consistent expectations, ignore noninjurious behavior, time outs
- normal part of development (problem if > 15 mins, > 5x per day, or after 5 yrs

Sibling rivalry (upset by dethronement; preschoolers may act out)
- manage by preparing child before the birth

Regression (during stress or discomfort)
- manage w/ ignoring and praising appropriate behavior

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17
Q

Motor Vehicle Safety Promotion: All ages (9)

A
  • all children in rear seat until 13 yrs
  • rear-facing carseat until 2 yrs
  • front-facing carseat until 4 yrs/ 40 pounds
  • booster seat until 80 pounds or 4 ft 9 in
  • keep trunk closed
  • do not leave child unattended in car
  • seat belt use
  • no phone, alc, or drugs while driving (for adolescents)
  • do not add extra padding to car seats
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18
Q

Psychosocial Development: Preschool (Initiative vs guilt

When does conflict occur?
Tasks (2)

A
  • guilt due to consequences of misbehavior

Tasks
- develop consciousness
- magical thinking (b-c I thought it, it happened)

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19
Q

Typical Age-specific difficulties: Pre-school (2)

A
  • fear of bodily harm (dark, animals, procedure; think broken skin = insides will come out) until 5-6 yrs
  • Aggression due to frustration (thwart self-satisfaction), modeling (parent aggressive), and reinforcement (get attention)– usually normal
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20
Q

Age-appropriate activities: Preschool (6)

A
  • Tricycles, wagons, sports equipment
  • alphabet or number flash cards AND books
  • Electronic games and educational TV for learning
  • Paints, crayons
  • musical toys
  • Imaginative or dramatic play such as dress up clothes, dolls, housekeeping, puppets, Construction sets
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21
Q

Social Development: School age (4)

A
  • self-concept (concious awareness of self and ideals) develops and is influenced by others
  • peer pressure (need to conform and belong; may need to bullying)
  • clubs (groups w/ rigid rules)
  • dyadic relationships w/ same-sex i.e. best friends
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22
Q

Psychosocial Development: School Age

Industry criteria (2)
Inferiority criteria (2)

A

Industry
- sense of accomplishment (competitions, meaningful work)
- extrinsic motivation (rule follower, like to win, rewards)

Inferiority
- fear ridicule by peers
- unable to excel in areas (all children must learn that they can not master everything)

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23
Q

Age-appropriate activities: School Age (5)

A
  • Teams (Clubs and peer groups; organized sports)
  • Hopscotch, jump rope
  • Ride bicycles
  • Quiet activities (Building models, Crafts, board games)
  • Collections (rocks, stamps, cards, coins, stuffed animals)
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24
Q

Bicycle Safety: Preschool-Adolescent (5)

A
  • Wear helmets when riding bike, motorcycle, ATV, skateboards, scooters
  • Learn rules of road (Ride with direction of traffic away from parked cars, use hand signals)
  • Walk bike if busy area
  • Use lights and reflectors, light clothes at night
  • Don’t ride double unless equipped
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25
Q

Bodily harm Safety: School age- adolescent (5)

A
  • protective equipment during sports
  • locked firearms
  • window guards to prevent falls
  • teach address, phone, and stranger safety
  • no trampoline in under 6 yr olds
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26
Q

Cognitive development: Adolescence

Formal Operations Concepts (5)

A
  • Abstract thinking/ imaginative
  • use analytical thinking to make decisions
  • Able to think through more than 2 variables concurrently
  • Evaluate own thinking and others (Able to understand how actions/factors influence others)
  • Idealistic
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27
Q

Psychosocial development: Adolescence

Identities developed (3)
Concepts (1)

A

Identities
- Personal sense of identity (coherent picture of past, present, future; autonomy from parents)
- Group identity with peer group (best friends, rejection of adult group; very important)
- sexual identity (Increased interest in romantic relationships, may experiment, body image))

Concepts
- View themselves as invincible

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28
Q

Age-appropriate activities: Adolescence

A
  • Non-violent video games and music
  • Social Media
  • Sports
  • pets
  • Career training programs
  • Reading
  • Social events- dances, movies, football games
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29
Q

Mental Health Concerns: Adolescence

4 signs

A
  • Poor school performance
  • Lack of interest/ Social isolation
  • Sleep or appetite disturbances (should get 9 hrs)
  • Expression of suicidal thoughts (suicide 3rd leading cause of death; screen ALL)
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30
Q

Body Surface Area

Equation
Units

A

Equation: √((ht (cm) x wt (kg))/3600))

Units: m2

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31
Q

Normal Temperature for children

A

36.7-37.5

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32
Q

Normal Heart Rates for 3mo-2 yrs, 2yrs-10yrs, and 10 yrs+

Resting (awake)
Resting (sleeping)

A

3mo-2 yrs
Resting (awake): 80-150 beats/min
Resting (sleeping): 70-120 beats/min

2yrs-10 yrs
Resting (awake): 70-110 beats/min
Resting (sleeping): 60-90 beats/min

10 yrs+
- 60-100 beats/min

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33
Q

Normal Respiratory rates:

1-11 mo
2-6 yrs
8-10 yrs

A

1-11 mo: 30-60 breaths/min
2-6 yrs: 21-25 breaths/min
8-10 yrs: 19-21 breaths/min

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34
Q

Normal blood pressure:

1-2 yrs
5 yrs
10 yrs
14 yrs

What may discrepancy of lower and upper extremity BP indicate?

A

1-2 yrs: 90/56 mm hg (measured starting at 3 routinely OR for critical care)
5 yrs: 95/56 mm Hg
10 yrs: 102/62 mm Hg
14 yrs: 110/65 mm Hg

Discrepancy: Coarctation of the Aorta

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35
Q

Pediatric Exam

General Tips (7)

A
  • Warm, child-friendly room
  • Include time to play and become acquainted
  • auscultate heart, abdomen lungs early before child disturbed (infants- toddlers)
  • Perform distressing procedures near the end of the exam (ears and mouth; areas of pain; temp and BP)
  • offer choices if they exist
  • be quick and efficient but do not rush
  • record in head to toe but perform in developmentally appropriate sequence
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36
Q

Pediatric Exam: Health history (2)

A
  • able to participate by age 7 yrs
  • most of information is obtained from adult present (dont assume person is mom or dad)
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37
Q

Pediatric Exam: Infant Tips (3)

A
  • perform with child on parent’s lap (or hold confidently
  • assess mouth while crying
  • talk in quiet, unhurried, nonthreatening voice (may need high-pitched voice and smiling)
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38
Q

Pediatric Exam: Toddler tips (6)

A
  • Allow to sit on parent’s lap or stand near parent
  • Use play- count fingers, tickle toes, who can i see in here today (ears)
  • Introduce equipment slowly (let them play with it first; hide scary equipment)
  • Have parent remove outer clothing, leave underwear on until needed to remove
  • Explain things concretely and short sentences
  • Praise for cooperative behavior and use rewards
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39
Q

Pediatric Exam: Pre-schooler tips (5)

A
  • Prefer parent’s closeness (Can be standing and/or sitting)
  • If cooperative (usually like to please), can examine head to toe
  • Request self-undressing. Leave underpants.
  • Demonstrate and let child examine equipment
  • Paper doll technique (demonstrate first on doll then child)
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40
Q

Pediatric Exam: School age and adolescent tips (6)

A
  • Examine head to toe, genitalia last
  • Self-undressing, keep on underwear, provide a gown
  • Explain exam and findings to the child (include long-term benefits for adolescents)
  • Teach about body functions and care (esp sexual development)
  • Respect need for privacy/modesty (May or may not want parent present)
  • encourage them to share feelings and ask questions
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41
Q

Physical Exam: Infant Reflexes

7 and when they disappear
What does it mean if reflexes persist?

A

Stepping-0-4 weeks,
Sucking/rooting, palmar grasp, Moro (startle), tonic neck (fencing), 3-4 months
Plantar grasp-0-8 months
Babinski- 0-1 year (fanning of toes)

If they do not disappear, sign of CNS impairment

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42
Q

Physical Exam: fontanels

How should they feel?
When are they bulging (3)?
When are they sunken

A

Normal: feel soft and flat

Bulging w/ crying, vomiting, increased ICP
sunken w/ dehydration

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43
Q

Physical Exam: Ear

Expected Findings (3)
Unexpected Findings (2)
Procedures (3)

A

Expected Findings
- cerumen in ear
- newborn blinks to sound
- infant turn to sounds

Unexpected Findings
- foreign bodies in ear
- ear infections (more common than in adults b-c close proximity

Procedure
- pinna down and back if under 3 (up and back if older than 3)
- examine hearing in children with speech delays
- use whisper test up until preschool

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44
Q

Physical Exam: Eyes

Expected finding (3)
Procedures (4)

A

Expected
- depth perception around 7-9 months (mature around 2-3 yrs)
- binocularity around 6 wks (esp by 4 months)
- visual acuity 20/40 in toddlers

Procedures
- visual screening for 3 and up (non-letter alternative to snellen for young children)
- corneal light reflex test AND cover-unconver test for strabismus
- check for red reflex
- hold head for H test in young children

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45
Q

Physical Exam: Cardiac

Expected Findings (3)
Unexpected Findings (2)
Tips (3)

A

Expected Findings
- sinus arrhythmia (HR increases w/ inspiration, sleep, waking)
- S2 split on inspiration
- apical pulse at 4th ICS for under 7 yrs, 5th ICS for over 7 yrs

Unexpected Findings
- weak lower pulses (COA)
- murmurs (range from innocent (no problem) to organic (physiological conditions))

Tips
- evaluate while sitting and lying down
- always use apical HR for 60 seconds if < 2 yrs (best while sleep for infants)
- radial pulse okay after 2 yrs

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46
Q

Physical Exam: Respiratory

Expected Findings (5)
Unexpected Findings (2)
Tips (3)

A

Expected Findings
- obligatory nose breathers (up till 4 months)
- diaphragmatic breathing (children under 6-7 yrs)
- irregular rhythm in infants
- 1:2 AP to lateral ratio by 6 yrs (barrel and 1:1 in infancy)
- Hiccups

Unexpected Findings
- s/s of respiratory distress
- allergic salute in allergy season

Tips
- take RR for 60 seconds
- hold feeds if newborn > 60 breaths/min
- take RR at end of each cry if crying b-c takes deep breath

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47
Q

Physical Exam: Abdomen

Expected Findings (2)
Unexpected Findings
Tips (2)

A

Expected Findings
- protuberant abdomen (large liver= fast metabolism/drug usage in toddlers)
- umbilical hernia in infants

Unexpected findings
- sunken abdomen may be dehydration or malnutrition

Tips
- ticklish so place your hand over theres at first
- flex knees to relax abdomen

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48
Q

Physical Exam: Musculoskeletal

Expected Findings (2)
Unexpected Findings (2)
Procedures (2)

A

Expected Findings
- genu varum (bow legged) in infancy till 18 months
- genu valgum (knock kneed) around 2-7 yrs

Unexpected Findings
- scoliosis (screening school age and beyond via leaning forward w/ knees straight)
- hip dysplasia ( seen in infants via ortolani sign and barlow signs)

Procedures
- For leg discrepancy, compare level of malleoli OR child trendelenburg sign (place hands on illiac crest from behind and should be level)
- Romberg test (child close eyes and remains standing straight for 20 sec) for coordination

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49
Q

Physical Exam: Integumentary

Expected Findings (3)
Unexpected Finding (2)
Tips (2)

A

Expected
- bruising on legs when learning to walk
- cyanotic extremities in newborn for first few hrs
- thin skin in young children (use tape w/ caution)

Unexpected
- bruising on padded areas (abdomen)
- diaper rash

Tips
- turgor on above clavicle for school age
- turgor on abdomen for infants-preschool

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50
Q

Respiratory System Variations for children (3)

A
  • smaller and shorter airway
  • short straight eustachian tube
  • increased infections from 3-6 m when maternal antibodies leave and waiting for infant antibodies
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51
Q

Signs of Respiratory Distress (8)

A
  • Retractions
  • Irregular sounds: wheezes (high pitched), stridor
  • Head bopping
  • Nasal flaring (unable to breath w/ an occluded nostril)
  • Mucus-y poops
  • Gargled speech
  • excessive crying
  • nonproductive cough
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52
Q

Asthma: Pathophysiology (3)

A
  • Inflammatory response -> airway remodeling
  • Accumulation of secretions -> hypoxemia
  • Bronchoconstriction (Spasm of bronchi and bronchioles) -> respiratory acidosis
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53
Q

Asthma: Clinical Manifestations (7)

A
  • Hacking, paroxysmal, irritative and nonproductive Cough (especially at night or early morning due to bronchial edema)
  • Frothy, clear, gelatinous sputum (as secretions increase)
  • Coarse and loud breath sounds (sonorous crackles, rhonchi, wheezing)
  • Prodromal itching at front of neck or upper back (seen in some children)
  • absent air movement and air hunger (no breath sounds, chest tightness)- medical emergency b-c sign of ventilatory failure
  • limited speech (unable to say more than 5 words) and anxiety
  • barrel chest (if repeated)
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54
Q

Asthma: Management Priorities (6)

A
  • frequent assessment (esp pulse ox, lung sounds, breathing)
  • give oxygen (nasal cannula, face mask, blow by)
  • Calm environment and reassurance
  • encourage deep breathing (via games like blow out candles or big bad wolf)
  • give medications (bronchodilators then steroids; use spacer for better coordination)
  • suction as needed (mouth then nose)
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55
Q

Asthma: Classifications (4)

A
  • Intermittent <= 2 days a week
  • Mild persistent: > 2 days a week, but not daily
  • Moderate persistent: daily, night-time symptoms 3-4 times a week
  • Severe persistent: several times a day, continual symptoms, night-time symptoms more than once a week less than 5 or nightly greater than 5; Use beta agonist several times a day
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56
Q

Asthma: Diagnostics (4)

A
  • Chest x-ray (may show hyperinflation or infiltrates))
  • Pulmonary Function Test (includes spirometry (5 yrs +), bronchoprovocation (direct exposure to antigens), exercise tolerance)
  • Allergy Testing (skin, Eosinophilia levels, IgE levels)
  • ABG
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57
Q

Peak Flow meters

What is it?
Three levels

A
  • Peak flow meter (used in 5+ to manage asthma by measuring max flow of air forcefully exhaled in 1 second)

Levels
Green– keep doing regular acitivities

Yellow- may need extra treatment

Red- call provider or EMS

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58
Q

Prevention of Asthma exacerbation (7)

A
  • Avoid triggers ( house and outdoor allergens, smoke, temp extremes)
  • Adherence to preventive medications (anti-inflammatories and LABA)
  • Exercise (best is swimming)
  • Hyposensitization/ allergen immunotherapy
  • Breathing exercises
  • Peak Flow Meters
  • use dehumidifiers or air conditioners
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59
Q

Asthma: anti-inflammatories

Important notes for all following:
- Mast cell stabilizer (Cromolyn sodium, necromil) - 1
- Glucocorticoids (Prednisolone, Methylprednisolone)- 3
- Anti-leukotrienes (montelukast sodium) - 1
- Monoclonal antibodies (omalizumab) - 2

A

Cromolyn sodium
- maintenance for 2+

Glucocorticoids (Prednisolone, Methylprednisolone)
- first line for 5 yr +
- usually inhaled for maintenance; systemic for acute exacerbation
- may cause thrush or stunt growth

Anti-leukotrienes (montelukast sodium)
- for moderate persistent asthma in 12m _

Monoclonal antibodies (omalizumab)
- for moderate to severe persistent in 12 yr +
- black box warning for anaphylaxis so monitor for 2 hrs

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60
Q

Asthma: bronchodilators

SABAs (Albuterol, Terbutaline)- 1
LABAs (Salmeterol)- 1
Anticholinergics (ipratropium, atropine)- 2

A

SABAs (Albuterol, Terbutaline)
- for acute relief or prevent EIB

LABAs (Salmeterol)
- never monotherapy, use w/ corticosteroid

Anticholinergics (ipratropium, atropine)
- anticholinergic effects (dry mouth, no secretions, blurry vision)
- for acute relief

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61
Q

Nasopharyngitis/ Common Cold

Causative agent

Key s/s (2)

Treatment
- Do’s (4)
- Don’ts (2)

A

Cause: viral

Key s/s: open mouth breathing (up to 3 yrs), chilling sensations

The Do’s
- supportive care b-c no cure (raise HOB, suctioning, vaporization, acetaminophen)
- reassure family colds are common till age 5
- monitor for complications (fever, dehydration, ear infection)
- rule out strep

The Don’ts
- OTC cough suppressants (dextromethorphan w/ caution in 6 yrs and up)
- Expectorants, antibiotics, antihistamines are not used

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62
Q

Bronchiolitis/RSV

Basic Pathophysiology
Key s/s (3)
Prevention
The Dont’s of treatment (4)

A

Patho: small airways become obstructed -> emphysema and patchy atelectasis at bronchiolar level

Key s/s:
- rhinorrhea
- apnea (first sign in infants under 1 months besides lethargy and irritability)
- low fever

Prevention-palivizumab (monoclonal antibody) once a month IM (given in NICU)

The Dont’s of treatment
- avoid Routine chest percussion and drainage
- Fluids by mouth may be contraindicated
- Bronchodilators rarely beneficial
- no antibiotics b-c viral

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63
Q

Acute Pharyngitis/ strep throat

Causative Agent
Key S/s (3)
Main risks (2)

A

Causative Agent: GABS

S/s
- pharyngitis (inflamed tonsils)
- cervical lymphadenopathy
- scarlet fever (erythematous sandpaper-like rash)

Main risks
- rheumatic fever (inflammatory of heart, CNS, joints)– within 18 days
- acute glomerulonephritis– within 10 days

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64
Q

Tonsillectomy

Contraindications (4)
The Do’s of Post-op care (5)

A

Contraindications: bleeding disorders, cleft palate, acute infection, under 3-4 yrs (b-c hypertrophy of lymphoid tissue possible)

Post-op care
- Pain management-meds (always give PO meds before IV meds run out) and ice collar
- Observe for complications (s/s of hemorrhage)- such as frequent swallowing, tachycardia, pallor, bright red emesis
- position for fluid drainage (prone, side lying)
- expect dark brown emesis (bright red is active bleeding)
- full recovery in 1-2 weeks

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65
Q

Bronchitis

Key S/s
Diagnostic
Treatments (3)

A

Key S/s: coarse, dry, hacking cough worse at night

Diagnostics: previous URI

Treatments
- symptomatic (rest, analgesics, antipyretics, humidity)
- antibiotics if bacterial
- cough suppressants (allow rest at night but interfere w/ secretion clearance)

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66
Q

Cystic Fibrosis

Basic Pathophysiology
Etiology

A

Basic pathophysiology: thick, sticky mucus due to exocrine gland dysfunction

Etiology: autonomic recessive (1 in 4 chance each pregnancy if both parents are carriers)

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67
Q

Cystic Fibrosis: Diagnosis (4)

A
  • newborn screen w/ sweat chloride > 60 mEq/L (normal is 40)
  • absence of pancreatic enzyme
  • stool fat analysis (72 hr)
  • family history
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68
Q

Cystic Fibrosis: Airway clearance Therapy (6)

A
  • usually BID
  • chest physical therapy (percussion, postural drainage, flutter/handheld percussor)
  • Positive expiratory therapy (PEP) - Breathing against resistance to keep airway open and get around mucus so it can be expectorated)
  • High-frequency chest compressions (HFCC)–vibration vest assists mucus breakdown and clearance)
  • Exercises (stimulate mucus excretion, muscle development, pulmonary vital capacity, and sense of well-being)- encourage sports
  • breathing exercises (deep breathing, bubbles)
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69
Q

Cystic Fibrosis: Medication

Things to know

Mucolytics (Dornase alfa) - 2
Antibiotics - 2
Bronchodilators -1
Oxygen -1

A

Mucolytics (Dornase alfa)
- decreases mucus viscosity
- side effects are laryngitis and minor voice alts

Antibiotics
- long course so need PICC or implanted port
- IV vancomycin, inhaled tobramycin

Bronchodilators
- give before Airway clearance therapy

Oxygen
- w/ caution b-c often have CO2 retention

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70
Q

Cystic Fibrosis: Diet (6)

A
  • high-protein, high-caloric diet
  • decreased fat
  • increased sodium
  • needs replacement of fat soluble vitamins
  • may need gastric feedings at night (growth failure despite PN may = deterioration)
  • remain upright post-feed to prevent Gerd
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71
Q

Cystic Fibrosis: Effects in Respiratory system

3 common
3 special concerns

A
  • chronic pneumonia (thick sputum)
  • emphysema (barrel chest, clubbed fingers)
  • recurrent URI due to bronchial obstruction

Severe
- pneumothorax and atelectasis
- hemoptysis (from recurrent infection, emergency if > 250 ml/24 hr)
- nasal polyposis (due to chronic inflammation, may need irrigation or corticosteroids)

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72
Q

Cystic Fibrosis: effects in GI/Endocrine system (7)

A
  • meconium ileus (intestinal obstruction) or constipation – need stool softeners
  • malabsorption syndrome in pancreas (leads to steatorrhea (bulky frothy stools) and azotorrhea (foul smelling stools w/ putrefied protein))
  • Reduced digestive enzymes
  • Cystic-fibrosis Diabetes (common and need insulin)
  • Portal hypertension in bile and liver (due to biliary cirrhosis)
  • rectal prolapse - simple use lubricated finger to put back
  • Chronic GERD - use H2 antagonist and GI motility
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73
Q

Cystic Fibrosis: Effects in

Musculoskeletal (2)
Reproduction (2)

A

Musculoskeletal
- Failure to Thrive due to malnutrition
- bone health concerns due to pancreatic insufficiency and steroid use – may need growth hormones

Reproduction
- most males are sterile
- mucus blocks cervix in females but pregnancy possible (higher risk for complications)

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74
Q

Croup: Epiglottis

Causative Agent
Key S/s (5)
Main risk
Diagnostic

A

Causative Agent: bacterial (abrupt onset)

Key S/s:
- Absence of cough
- Drool (painful swallowing)
- Agitation
- Tripod position (sitting upright and leaning forward w/ mouth open, chin out, and tongue protruding)
- stridor

Main risks: severe respiratory distress

Diagnostics: cherry red epiglottis

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75
Q

Croup: Acute Laryngotracheobronchitis

Causative Agent
Key S/s (4)
Main risk

A

Causative Agent: most common croup, viral

Key S/s
- barky, brassy cough and horseness (worse at night and w/ crying)
- stridor
- prior URI
- Dyspnea (due to narrow airway from inflamed mucosal lining)

Main risks: respiratory acidosis -> respiratory failure

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76
Q

Croup: Acute Spasmodic Laryngitis

Causative Agent
Key S/s (3)
Treatments (2)

A

Causative Agent: viral w/ allergic component

Key S/s
- recurrent paroxysmal nocturnal attacks of laryngeal obstruction (awakes in middle of night w/ barking cough that subsides the next day)
- hoarseness may remain next day
- no fever

Treatments
- humidity or cool night air
- epinephrine for severe

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77
Q

Croup: Bacterial Tracheitis

Causative Agent
Key S/s (4)
Treatments (4)

A

Causative Agent: bacterial of trachea

Key S/s
- large, thick secretions
- stridor in every position
- no response to LTB therapy
- no drooling

Treatments
- intubation
- suctioning (endoscopy w/ HCP)
- antibiotics (erythromycins)
- antipyretics

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78
Q

Speaking Child Language

Words to avoid (5)

A
  • Shot, bee sting — say poke
  • Deaden
  • Take your blood pressure
  • Stool
  • Test
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79
Q

Procedure management

NPO and fluid restriction tips (6)

A
  • have clear liquids >2 hours
  • breast milk >4 hours and infant formula >6 hours before procedure (keep eye out for dehydration)
  • serve liquid in small container to give illusion of a lot
  • keep mouth moist w/ atomizer or ice chips
  • keep close eye on older children who may try to sneak liquids
  • do not leave fluids at bedside
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80
Q

Alternative Feeding: Gavage Feeding (5)

A
  • give by gravity
  • check placement w/ x-ray, pH, measure mark
  • use 5 or 8 french tip
  • do in quiet calm environment
  • use nonnutritive sucking to improve digestion
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81
Q

Medication Administration: 9 rules

A
  1. Do not give a child a choice of the medication.
  2. Allow choices the child can have some control over
  3. Do not lie, saying it won’t hurt or taste bad
  4. Give worst meds last (prednisone = bad taste)
  5. Give brief explanations
  6. Tell the child is ok to be scared.
  7. Always include the child and parent when talking during med administration.
  8. Be confident and positive when approaching the child (Do not use baby talk, you can just change your intonation)
  9. The younger the child the shorter time between explanations and administration.
    Involve the parent.
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82
Q

Medication Administration: Oral

Tips (8)

A
  • orange tips = oral syringe
  • use nipple for infants to suck
  • chewables are good for preschoolers
  • give capsules w/ small amount of food or liquid
  • never mix in bottle b-c may not drink it all or not want to drink if nasty
  • place syringe on side of mouth (spraying at back can cause aspiration)
  • chase bad tasting w/ water, juice, ice pop (nondairy)
  • small puff in face can cause swallow reflex
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83
Q

Medication Administration: IM

What is needle recommended gauge?

What is the needle size (length) AND max amount to administer in the following areas:

  • vastus lateralis and ventrogluteal
  • Deltoid
A

Gauge: 22-25

Vastus lateralis and ventrogluteal
Size: 5/8 - 1 inch
Max volume: 0.5 for infant, 2 ml small child

Deltoid
Size: 1/2 - 1 inch
Max volume: 0.5-1 ml

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84
Q

Medication Administration: IV (7)

A
  • assess site q1-2 hrs
  • use 22-24 gauge for small veins
  • usually by IV pump ( if bolus, 20 ml/kg okay)
  • children 5 and up can use PCA pump (family version available too)
  • Use superficial hand, wrist, forearm, foot, or ankle veins in small infants
  • Avoid foot veins in children learning to walk or walking
  • Use scalp veins in infants up to 9 months after other sites have failed
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85
Q

Medication Administration

  • Enema (4)
  • Intraosseous
A

Enema
- done if NPO due to vomiting or mental status
- contraindicated in immunosuppressed or thrombocytopenia
- max volumes (120-240 for infant, 240-360 small child)
- No soapsuds

Intraosseous
- done in pediatric resuscitation if IV not possible after 3 attempts or 90 seconds

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86
Q

Vital Signs: Temperature

4 tips

A
  • Axillary preferred in infant to 2 years
  • Rectal temps if accuracy needed (age over 1 month)
  • 2-5 years axillary or TM
  • Can take orally when child can hold under tongue (5+)
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87
Q

Pain assessment

Scales (and appropriate ages) - 5

A
  • NIPS- Neonatal Infant Pain Scale-birth -1 month
  • FLACC Pain Scale- 2 month -7 years
    Face Legs Arms/Activitiy Crying Consolability
    For non-verbal child
  • Oucher Scale 0-5 scale; have child place faces in order then choose
  • Faces Pain Scale- 3 years and older
  • Numeric Pain Scale- Children 5 -7 years and older
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88
Q

Pain Assessment

Infants (3)
Toddlers (3)

A

Infants
- Pre-verbal (physiologic response, crying, difficulty sleeping, feeding, relaxing)
- Facial expression most reliable
- Older infant may push or pull away

Toddlers
- loud cry
- words that indicate pain
- stay very still

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89
Q

Pain Assessment

Preschooler (6)

A
  • verbal report as young as 3 yrs for pain, location, and degree
  • Views pain as a punishment for thoughts/behavior
  • Regression to earlier behaviors (bed wetting, thumb sucking, crying, kicking)
  • Denies pain – fear of pain relieving measures “shots”
  • Avoid telling child to be “brave” or good boy or girl after procedure
  • Fears body mutilation (Need all their parts; Band-aids are important, magical thinking)
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90
Q

Pain Assessment

School age (3)
Adolescent (2)

A

School-age
- Describes pain and can quantify intensity (if scale is explained in simple terms)
- Awareness of death
- Bargains or tries to “make a deal” (I’ll let you change my dressing after this tv show)

Adolescent
- understands cause and effect
- quantifies and describes pain

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91
Q

Pain Management: Reducing Needle Stick Pain (8)

A
  • Ice
  • Vapocoolant Sprays (may cause some constriction or may not be liked)
  • TENS units (stimulate nerves above location)
  • EMLA (eutectic mixture of lidocaine) cream- or Lidocaine- apply 60 minutes before poke)
  • Shot Blocker or buzzy (yellow thing which blocks some of the nerves or (distracts nerves)
  • sedation for infants or young children sometimes
  • change needle if pierced rubber stopper
  • apply pressure 10 sec before
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92
Q

Pain Management: Nonpharmacological

Infants (2)
Toddlers and preschoolers
School age and adolescents (2)

A

Infants
- Nonnutritive sucking (pacifier, Sweet ease)
- touch, holding, rocking

Toddlers and preschoolers
- distraction (books, videos, music, bubbles–use child life)

School-age and Adolescents
- guided imagery
- breathing exercises

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93
Q

Informed consent and children

Who can give informed consent?
Who can give assent?

A
  • emancipated minors or parents of children give informed consent
  • assent given by children over 7 which says they permit and understand the procedure but this is not legally binding
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94
Q

7 Tips for immunizations and IM injections

A
  • Use calm and neutral words (here I go vs here comes the sting)
  • Do not give in Dorsogluteal site (potential for nerve damage and less immunity)
  • give multiple immunizations at same time in separate sites or at least 1 inch apart
  • Do not manually stimulate injection site
  • children do not need to restart series after dose missed, just continue where they left off
  • vastus lateralis (preferred) or ventrogluteal (okay for 2m+)
  • wake up sleeping children or may fear going back to sleep
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95
Q

Bright Futures Areas to Assess in Well-Child Visits (5)

A
  • Emotional well-being (coping, mood regulation, mental health, sexuality, Suicidal ideation)
  • Physical growth and development (physical and dental health, body image, healthy nutrition, physical activity)
  • Social and academic competence (relationships with peers and family, school performance, interpersonal relationships)
  • Risk reduction (tobacco, alcohol, other drugs, pregnancy, STIs)– important in adolescence b-c risk taking behavior
  • Violence and injury prevention (safety belt and helmet use, substance abuse and riding in a vehicle, interpersonal violence, bullying)– encourage safe driving
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96
Q

Respiratory Interventions: Ease Respirations at home (6)

A
  • Moisturized air (useful with hoarseness or laryngeal involvement) for 10-15 minutes
  • Steamed vaporizers, kettles, and boiling water are discouraged
  • Steam in shower is good method
  • Use nasal aspiratory or bulb syringe for young infants before feeding and sleeping
  • Saline nose drops (1/2 tsp salt, 1 cup water) useful
  • Topical vapor rub for 2 yrs and older ( never give orally or under the nose)
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97
Q

Tonsillitis

Causative Agent
Key S/s (4)
Treatments (3)

A

Causative Agent: viral or bacterial, often w/ pharyngitis

S/s
- edematous tonsils (difficult breathing, swallowing, hearing (if adenoids))
- snoring and mouth breathing (noctural dyspnea)
- foul mouth odor
- persistent cough

Treatments
- Saline gargles, lozenges, non opioid pain meds
- soft to liquid diet
- If severe and not resolved by other methods, tonsillectomy or adenoidectomy

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98
Q

Acute Pharyngitis/ strep throat

Diagnostics
Treatments (4)

A

Diagnostics: rapid test to screen for strep and do throat culture if screen negative

Treatments
- Warm saline gargles
- Penicillin or macrolide antibiotic (infectious for 24 post initiation of antibiotic; no longer contagious after 24 hrs so can return to school) - unless viral
- cool drinks and foods (ice cream, ice chips)
- chloraseptic or acetaminophen or ibuprofen, for pain (liquid or chewable)

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99
Q

Tonsillectomy

The Dont’s of Post-op care (5)

A

The Dont’s Post-op
- Avoid fluids until child alert and can swallow
- Citrus juice can cause discomfort
- Milk, ice cream and pudding not offered until clear tolerated because can cause child to clear throat
- Avoid gargle, coughing, suctioning, straws, nose blowing
- No red products or red dyes in fluids

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100
Q

Infectious Mononucleosis (Mono)

Causative Agent
Key S/s (3)
Main risk
Severe S/s to report (4)

A

Causative Agent: EBV, viral

Key S/s:
- Sore throat (Exudative pharyngitis w/ petechiae)
- Lymphadenopathy
- Hepatosplenomegaly

Main risks: neurological (meningitis, seizures),

Severe S/s to report to HCP
- severe sore throat (unable to eat or drink)
- severe abdominal pain
- difficulty breathing
- respiratory stridor

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101
Q

Infectious Mononucleosis (Mono)

Diagnostics (3)
Treatments (5)

A

Diagnostics
- heterophil antibody test (positive up to 6m post exposure in 4 yrs and up)
- mono spot test (earlier diagnosis)
- increased WBC (atypical leukocytes)

Treatments
- symptomatic (mild elixir analgesic, gargles, troches, warm drinks)
- corticosteroids
- avoid strenuous activities (contact sports until splenomegaly resolved)
- contagious (just don’t share hygiene products and drinks)
- viral so no antibiotics

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102
Q

Croup: Epiglottis

Treatments (7)
Prevention

A

Treatments
- maintain airway (prep for intubation)
- keep calm (in parent’s lap)
- give IV cephalosporins (Ceftriaxone/cefotaxime or vancomycin )
- do not examine throat if suspected (need provider and resuscitation equipment prior to throat exam)
- Humidified oxygen via mask or blow-by to reduce agitation
- Corticosteroids (can reduce edema early)
- Droplet precautions 24 hrs after initiation of antibiotics

Prevention: Hib vaccine

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103
Q

Croup: Acute Laryngotracheobronchitis

Treatments (6)

A

Treatments
- Cool mist (or cool car ride if no stridor at rest)
- Racemic Epinephrine Tx (short-term relief for moderate or severe croup—rapid onset but short duration)
- Frequent assessment
- Corticosteroids (dexamethasone PO)—standard treatment
- Heliox (helium with oxygen): moderate to severe croup
- Avoid aggravating child b-c can worsen respiratory distress

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104
Q

Bronchiolitis/RSV

The Do’s of treatment (7)

A
  • Contact or droplet Isolation- lives 1 hr on hands
  • Ribavirin-antiviral agent- inhalations (VERY DANGEROUS so limited use)
  • Heated high-flow nasal cannula (HHFNC)- extra humidity with oxygen administration and CPAP
  • CPAP, BiPAP, or intubation required if respiratory acidosis present)
  • Suctioning (Nasal aspiration with aspirator to remove secretions; best treatment)
  • IV fluids for acute phase
  • Nebulized Hypertonic (3%) saline for those hospitalized more than 3 days to help w/ mucociliary clearance
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105
Q

Status Asthmaticus

What is it?
S/s (3)
Treatment (4)

A

Status Asthmatics: an episode of severe asthma that does not respond to normal treatment.

S/s: profuse sweating, sitting upright and refuses to lie down

Treatment
- same as asthma (cardiorespiratory and pulse oximetry monitoring, humidified oxygen, Inhaled SABA, systemic corticosteroid, anticholinergic)

  • IV magnesium sulfate (Muscle relaxant to decrease inflammation and improve pulmonary function)
  • Heliox (helium and oxygen)- decreases airway resistance and work of breathing via nonrebreathing face mask
  • Ketamine (Dissociative anesthetic causes smooth muscle relaxation)
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106
Q

Cystic Fibrosis: Medication

Things to know:
Pancreatic Enzymes (Pancrease) -2
Nebulized hypertonic saline -2
CFTR -2

A

Pancreatic Enzymes (Pancrease)
- enteric-coated given at every meal and snack (powder form in applesauce for infants)
- increase dose if fatty stools

Nebulized hypertonic saline
- only for 6 yrs + and severe b-c may cause bronchospasms
- increases mucus clearance and airway hydration

CFTR Modulator (cystic fibrosis transmembrane conductance regulator)– Ivacaftor
- for 2 yrs and up w/ specific mutation
- reduces likelihood of sticky mucus development

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107
Q

Medication Administration

  • Optic (4)
  • Otic
  • Nasal
A

Optic
- put pressure on lacrimal duct after administration for 1 minute to wash tear duct and prevent medicine from draining into body
- ointment goes inner to outer canthus
- give drops prior to ointment (3 mins apart)
- if eyes clenched, put in nasal corner and it will go in once eyes open

Otic
- warm to room temp to prevent vertigo

Nasal
- hyperextend head to prevent strangling sensation from trickling

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108
Q

Three consequences of impaired intracranial regulation

A

Cerebral edema- increased brain size, fluid accumulation

Increased intracranial pressure- sustained pressures, trauma,

Decreased cerebral perfusion pressure (bleeding r/t hemorrhagic stroke)

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109
Q

Cushing Triad for increased ICP

A

Increased systolic blood pressure (widened pulse pressure)
Decreased pulse rate (bradycardia)
Decreased respirations (irregular)

Note: effects opposite those of shock

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110
Q

ICP Monitoring

Indications (4)
Care (2)

A

Indications
- Glasgow Coma Scale score < 8
- TBI w/ abnormal CT scan
- Deteriorating neurological condition
- Subjective judgment regarding clinical appearance and response

Care
- Do not change dressings daily
- keep drainage bag for direct ventricular pressure measurement at level of ventricles

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111
Q

Types of Head Injuries (6)

A
  • Skull fracture (requires great force)
  • Contusions: visible bruising coup (at impact pt) OR contrecoup (opposite impact pt)– shaken baby syndrome
  • Intracranial hematoma
  • Diffuse injury
  • Laceration (tearing of tissue)
  • Concussion (alteration in neurologic function w/ or w/o loss of consciousness; may have amnesia/confusion but transient)
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112
Q

Complications of Head Trauma (3)

A

Epidural hemorrhage (death likely)
- Bleeding b/w skull and dura lead to tentorial herniation rapidly

Subdural hemorrhage
- Bleeding b/w dura and arachnoid membrane over brain due to vein tearing or direct trauma
- slow development

Cerebral edema
- Associated with TBI
- Increased cytotoxic or vasogenic edema leads to herniation

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113
Q

Types of Skull fractures (6)

A

Basilar: post- Battle sign (bleeding posterior neck, mastoid area), raccoon eyes, leakage of CSF from ears and nose

Diastatic: transverses the sutures and widens sutures.

Comminuted: split into multiple pieces

Linear: does not cross suture lines

Open: leads to rhinorrhea or otorrhea of CSF

Depressed: locally broken into irregular fractures

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114
Q

Diagnostics for Intracranial Regulation (6)

A
  • Neuroimaging (MRI, CT) (Check for allergies if contrast dye to be used; child must be still)
  • Skull radiograph
  • EEG (flat = brain death)
  • Brain biopsy
  • Lumbar puncture (contraindicated w/ increased ICP; lie still)– diagnostic for meningitis
  • Lab tests (hyperglycemia in increased ICP; low HCt, low Platelet, high WBC in head injury)
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115
Q

S/s of Increased ICP in Infant (7)

A

Poor feeding

High-pitched cry, difficult to soothe, irritable

Tense, bulging fontanels

Separated cranial sutures (increased frontooccipital circumference)

Distended Scalp veins

Macewen (cracked-pot) sign (Bones of skull thin and sutures palpably separated to produce cracked-pot sound on percussion of skull

Setting-sun sign (Sclera visible above iris due to eyes being rotated downward)

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116
Q

S/s of Increased ICP in Child (8)

A
  • Headache
  • Forceful NV
  • Seizures
  • Irritability
  • Diminished physical activity (drowsy, lethargy, Inability to follow simple command)
  • Slurred speech
  • Visual changes (diplopia, blurred vision)
  • Inappropriate for age reflexes i.e. primitive and babinski)
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117
Q

Late signs of Increased ICP (9)

A

Bradycardia

Decreased motor response to a command

Decreased sensory response to painful stimuli

Alterations in pupil size and reactivity

Decortication (Rigid flexion w/ arms close to body, flexed elbows and wrists, plantar flexed feet, legs extended & internally rotated)

Decerebrate (rigid extension and pronation of arms and legs, flexed wrists, clenched jaw, extended neck; arched back)

Cushing’s triad-decreased HR. RR. & widening or increased BP (pulse pressure)

Cheyne-Stokes respirations (prolonged apnea, paradoxical chest movement, ataxic breathing, hyperventilation)

Papilledema (optic disc swelling, hemorrhages, tortuosity of vessels, absence of venous pulsations)- develops in 24-48 hrs

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118
Q

8 levels of consciousness

A

Full consciousness

Confusion: impaired decision making

Disorientation: to time and place

Lethargy: sluggish speech

Obtundation: arouses with stimulation; respond to voice or pain

Stupor: responds only to vigorous and repeated stimulation

Coma: no motor or verbal response to noxious stimuli i.e voice nor pain

Persistent vegetative state: permanent loss of function of cerebral cortex

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119
Q

Nursing Care of Unconscious child: Reduce ICP (9)

A
  • ABC (vitals q15 mins)
  • NPO
  • neck stabilization(use jaw thrust vs chin lift for airways)
  • minimize environmental noise, stimulation
  • reduce suctioning
  • position (HOB 30 degrees and avoid neck vein compression)
  • Prevent straining i.e. cough, vomit, defecation, Valsalva maneuver
  • Use vibration instead of cough b-c it does not increase ICP
  • provide thermoregulation (light covering, antipyretics, hypothermia blanket)
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120
Q

Medications to reduce ICP (6)

A
  • Stool softeners
  • Analgesics (pain increases ICP but pain meds decrease LOC so controversial; acetaminophen, NSAIDs, opioids, paralytics (vecuronium)))
  • IV hypertonic NS (no dextrose if on keto; avoid overhydration)
  • manage SIADH (NS and diuretics) or DI (vasopressor or fluid replacement) if present
  • corticosteroids (for inflammation and edema)- watch for hyperglycemia, infection; don’t give if for head trauma
  • osmotic diuretic (Mannitol) - reduce ICP
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121
Q

Acute Care Medications to reduce ICP

4 types

A

Antiepileptics –phenytoin, fosphenytoin, Carbamazepine (Tegretol)
- Look for CBC changes and SJS
- used for seizures

Sedation or amnesic anxiolytics (Propofol, Lorazepam) - agitation can increase ICP

Barbiturates (controversial)- induce coma to decrease metabolic rate and protect brain when reduced cerebral perfusion pressure

Paralytic agents

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122
Q

Hydrocephalus

Patho (3)

A
  • Impaired absorption, production, or flow of CSF within the subarachnoid space
  • Communicating or non-communicating (obstructive)
  • Increased CSF in ventricles leads to dilated ventricles and compresses brain tissue
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123
Q

Management of Hydrocephalus: Shunt

Complications (4)
Nursing Care (6)

A

Complications: infection, malfunction, subdural hematoma, peritonitis

Nursing care
- keep head flat to prevent rapid drainage (flex head prior to shunt placement; place on unoperated side
- shunt is for life and revised when growth
- do not pump shunt
- educate family on name and model of shunt
- no scalp IVs
- test any drainage for glucose (CSF leak)

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124
Q

Shunt Infections

Types of infections (4)
Treatment (3)

A

Infections: Septicemia, Bacterial endocarditis, Wound infection, Meningitis

Treatment
- massive-dose antibiotics
- shunt externalization (at level of auditory meatus, clamp during ambulation)
- shunt removal

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125
Q

Bacterial Meningitis

What is it?
Seasonal Variation
Prevention
Diagnosis
Severe complications (6)

A

Acute inflammation of the meninges and CSF which spreads via vascular dissemination (due to Hib, GBS, Meningococcal)

Seasonal variation: late winter and early spring

Prevention: Hib vaccine; prophylaxis in pregnancy

Diagnosis: Lumbar puncture unless increased ICP then CT scan

Severe complications: seizures, subdural effusions, deafness (from CN VIII damage), sepsis, obstructive hydrocephalus, hemiparesis (r/t thrombi in veins)

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126
Q

S/s of meningitis (7)

A
  • Fever, chills
  • Nuchal rigidity
  • Photophobia
    • Brudzinski’s sign (neck stiffness causes hip and knees to flex when neck flexed)
    • Kernig’s sign (unable to straighten leg >135 degrees w/o pain)
  • Joint problems
  • s/s of increased ICP (poor feeding, vomiting, irritability, seizures, high pitched cry)
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127
Q

Bacterial Meningitis

CSF color
ICP Pressure
Culture

Presence of following in CSF:
WBCs
Protein
Glucose

A

CSF color: cloudy, turbulent, purulent
ICP Pressure: elevated
Culture: positive

Presence of following in CSF:
WBCs: elevated esp. polymorphonuclear leukocytes
Protein: elevated
Glucose: Decreased

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128
Q

Viral Meningitis

CSF color
ICP Pressure
Culture

Presence of following in CSF:
WBCs
Protein
Glucose

A

CSF color: clear or slightly cloudy
ICP Pressure: normal or elevated
Culture: negative

Presence of following in CSF:
WBCs: elevated
Protein: normal or slight elevation
Glucose: normal

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129
Q

Management of Meningitis (6)

A
  • Droplet isolation due to nasopharyngeal secretions
  • 10 day Antibiotic therapy (IV) - not for viral (GIVEN ASAP TO IMPROVE PROGNOSIS)
  • Control fever (hydration, antipyretics)
  • Pain management- meds
  • positioning (sidelying)
  • Reduce ICP (elevate HOB and decreased stimulation)
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130
Q

Encephalitis

Causative organism
Patho
Key S/s (4)

A

Causative organism: virus from vector (mosquitoes and ticks)

Patho: inflammation of CNS by virus

Key S/s: stiff neck, headache, Ataxia, speech difficulties
(also fever, malaise, NV)

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131
Q

Generalized seizures: 4 types

A

Tonic-Clonic seizures (grand mal and most dramatic)
- Tonic (stiffening, eyes roll up)
- Clonic (intense jerking w/ rhythmic contraction and relaxation longer than tonic phase

Absence (petitt mal): Sudden onset of brief loss of consciousness (5-10 sec), blank stare and automatisms; does not fall

Atonic (drop): Sudden, momentary loss of muscle tone

Myoclonic: Sudden brief, shocklike muscle movements

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132
Q

Febrile Seizures (4)

A
  • transient disorder of childhood (rare after 5 yrs of age)
  • fever > 38C (100.4 C)
  • treat w/ antipyretics and PRN benzos at home (alongside seizure precautions)
  • call 911 if > 5 min
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133
Q

Infantile Spasms (4)

A
  • clusters of Jerking of tummy, raising arms, blinks, occur every 3- 5 seconds lasting up to 30 minute
  • abnormal EEG w/ hyperarrhythmia
  • treat w/ ACTH (monitor for immunosuppression, glucose, hypertension) OR prednisolone
  • treat w/ ketogenic diet (monitor ketones and glucose)
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134
Q

Management of Seizures (4)

A

Drug therapy (ideally monotherapy for full control; slow discontinuation)

Ketogenic diet (high fat, to preserve glucose)

Vagus nerve stimulation (palliative, generator in chest sends electrical impulse to Vagus nerve (CN X) at onset of seizure after activation w/ magnet)

Corpus Callosotomy (ligation of area via surgery)

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135
Q

Nursing Care for seizures (5)

A
  • Time and record behavior surrounding Seizure
  • Keep patient safe – ABCs
  • Oxygen
  • Seizure precautions (no restrain, nothing in mouth during, suction equipment at bedside, ease to floor, )
  • aspiration precautions (post seizure NPO and suction; place on side)
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136
Q

Meds for Seizures (what to know?)

  • Diazepam
  • Lorazepam (Ativan)
  • Fosphenytoin
  • phenytoin (DILANTIN)) - 2
  • Levetiracetam
  • Carbamazepine (Tegretol)
  • Phenobarbital or propofol - 2
  • Valproic Acid
A

Diazepam or Lorazepam (Ativan)
-oral, buccal, rectal, IV

Fosphenytoin- (form of phenytoin)

phenytoin (DILANTIN)
- Do not take w/ milk
- can cause gum hyperplasia

Levetiracetam (Keppra)
- rash and mood swings risk

Carbamazepine (Tegretol)
- SJS risk

Phenobarbital
- for status epilepticus
- take adequate vitamin D and folic acid

Valproic Acid
- liver toxicity

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137
Q

Craniosynostosis

What is it?
Treatment
Complications of treatment (3)

A
  • bones join together too early and surgery separates them (posterior fontanel < 8 wks; anterior fontanel < 12-18 months)

Treatment: Surgery

Complications: Edema, Bleeding (black eyes), Infection

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138
Q

Reye’s syndrome

Cause
S/s (2)
Diagnosis
Complications (3)

A

Cause: giving aspirin or Pepto bismol to children with a viral infection

S/s: cerebral edema, liver involvement

Diagnostics: Liver biopsy (fatty liver)

Complications: Coma, Brain herniation, Death

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139
Q

Causes of Cyanosis

Lung vs Heart Issue
- problem?
- response to Oxygen

A

Primary parenchymal lung disease ( Pneumonia, meconium aspiration syndrome)
-Problem is with O2 diffusion
- Responds to increased FiO2

Primary cardiac disease
- combo of decreased pulmonary flow and intracardiac mixing of “blue” and “pink” blood
- Doesn’t respond much to increased FiO2

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140
Q

Cardiac Diagnostics: What are they

ECG
ECHO
Exercise/stress test
Syncope/ Tilt Table Test
Cardiac MRI

A

ECG - electrical activity of heart (assess child, not monitor; takes 15 min)

ECHO -ultrasound of structure, size, blood flow through heart (takes an hr and child be still)

Exercise/Stress test - monitor during exercise

Syncope/ Tilt Table Test- determine cause of fainting (normal: BP stable, HR increases w/ horizontal to vertical position; positive: Pt passes out, hypotension, bradycardia/tachycardia w/ horizontal to vertical position due to heart or BV problem

Cardiac MRI- still and moving pics of heart and major BVs to analyze structure and function (sedation for child < 7; contraindicated w/ metal implants (pacemakers, cochlear)

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141
Q

Cardiac Diagnostics: Cardiac cath Purposes

Diagnostic - 2
Interventional
Electrophysical

A

Diagnostic- prior to surgical repair
– Right and/or Left cath. Right through vein, left through artery to Helps plan for procedures
- Angiogram - visualize the arteries surrounding the heart w/ contrast dye and X-ray images

Interventional – repair or other intervention

Electrophysiology studies – evaluate and destroy (ablate) accessory pathways that cause some tachydysrhythmias

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142
Q

Cardiac Diagnostics: Cardiac cath

Pre-procedure care (6)

A
  • Assess dye allergy (iodine)
  • Age-appropriate teaching (informed consent from parent)
  • NPO at least 4-6 hours (IV fluids for infants)
  • Assessment: VS baseline cardiopulmonary, perfusion, assess and MARK all pulses, height & weight
  • Sedation- oral or IV
  • Assess for infection may be postponed if severe diaper rash
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143
Q

Cardiac Diagnostics: Cardiac cath

Post-procedure care (8)

A
  • Monitor blood glucose (hypoglycemia possible), VS, dressing, I & O, continuous cardiac monitoring
  • Bedrest for 4-6 hr, Strict.
  • Keep affected extremity straight for 2hr, then limited ambulation for 3 days
  • avoid baths and activity for 48-72 hrs
  • HOB flat x 2 hrs, elevate 30˚ 2 hrs after completion of procedure.
  • Check cath site and distal extremity pulses, color and perfusion, q15 min x 4 occurrences, then q 30 min x 4 occurrences , then q1h x 3 h,
  • Pulse - normal to be weaker in affected extremity for a few hours
  • remove dressing in 24 hrs
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144
Q

When to notify HCP post-cardiac cath (5)

A
  • If bleeding, apply pressure at cardiac catheter entry site (2.5 cm above entry site)
  • swelling
  • hematoma
  • arrhythmia (possible and reason for monitoring)
  • fever
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145
Q

4 classifications of CHD

A

↑ Pulmonary blood flow
- Atrial Septal Defect (ASD)*
- Ventricular Septal Defect (VSD)*
- Patent Ductal Arteriosus (PDA)*

Obstruction of blood flow (out of the heart)
- Coarctation of aorta*
- Pulmonic Stenosis *
- Aortic Stenosis

↓ Pulmonary blood flow
- Tetralogy of Fallot (TOF)*

Mixed blood flow
- Transposition of Great Arteries/Vessels (TGA)*
- Hypoplastic Left Heart Syndrome (HLHS)

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146
Q

CHD: Increased Pulmonary Blood Flow (ASD, VSD, PDA)

Characteristics (3)

A
  • Abnormal connection between 2 sides of heart
    increased blood volume on R side
  • Left to Right shunt
  • Decreased systemic blood flow due to increased pulmonary blood flow
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147
Q

CHD: Increased Pulmonary Blood Flow (ASD, VSD, PDA)

Clinical Manifestations (7)

A
  • If small, may be asymptomatic and close spontaneously
  • Fatigue (poor feeding, activity intolerance)
  • Heart Murmur
  • Risk for Endocarditis
  • Risk for pulmonary vascular obstructive disease
  • risk for CHF
  • Growth delay (FTT, poor weight gain)
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148
Q

Atrial Septal Defect

What is it?
S/s (4)
Complications (2)

A

Abnormal opening b/ atria so L-R shunt

Key S/s
- usually asymptomatic
- murmur (systolic w/ fixed split-second sound)
- atrial dysrhythmias (r/t RA and RV enlargement)
- hypertrophy of right side

Complications: HF by 30-40 yrs if untreated; embolism

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149
Q

Atrial Septal Defect

Treatment (2)

A

Surgical- Pericardial/Dacron patch w/ cardiac bypass

Non-surgical- Amplatzer Septal Occluder placed by cardiac cath (need Low dose aspirin x 6 months)

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150
Q

Ventricular Septal Defect

What is it?
S/s (2)
Complication

A

Abnormal opening b/w heart ventricles (most common defect) causing higher systemic resistance and ventricle pressure

Key S/s
- Murmur (loud, harsh)– best heard at left sternal border
- right side hypertrophy

Complications: HF

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151
Q

Ventricular Septal Defect

Treatment (3)

A

Palliative- PA banding to decrease pulmonary blood flow

Surgical- Patch (large defect) or suture w/ cardiac bypass- preferred

Non-surgical- Device closure with catheterization; more risk than ASD for complete AV block

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152
Q

Patent Ductus Arteriosus

What is it?
S/s (3)
Complication

A

failure of fetal ductus arteriosus to close at birth causing shunt from aorta to pulmonary artery

S/s: Murmur (machinery like), widened pulse pressure, pulmonary arterial HTN

Complications: right sided hypertrophy

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153
Q

Patent Ductus Arteriosus: Treatments

Medical (2)
Nonsurgical
Surgery (2)

A

Medical
- prostaglandins to keep PDA if other defects present (side effect = apnea)
- prostaglandin inhibitors (Indomethacin (Indocin) or ibuprofen) in newborns closes PDA

Nonsurgical
- Coiling to occlude in cath lab for > 1 yr if small

Surgery (if large)
- Ligation of PDA with surgery (thoracotomy)
- Thoracoscopic placement of clip

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154
Q

Ductus arteriosus

What keeps it open? (3)
What closes it? (3)

A

What keeps it open:
- Low pO2/ hypoxia
- Prostaglandins
- Nitric oxide

What constricts it?
- O2
- Norepinephrine, acetylcholine, bradykinin
- Indomethacin, ASA

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155
Q

CHD: Coarctation of Aorta

Characteristics (3)

A
  • Localized narrowing near the insertion of the DA
  • Increased pressure proximal to defect (upper extremities); left ventricle and left atrium
  • Decreased pressure distal to the defect (lower extremities)
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156
Q

CHD: Coarctation of Aorta

Clinical manifestations (6)

A
  • bounding pulses in UE’s
  • Weak or absent LE pulses, cool LE’s
  • Heart failure (acidosis and hypotension)
  • HTN in UE shows as dizziness, fainting, headaches, epistaxis in older children
  • Risk for stroke
  • Risk for aortic aneurysm
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157
Q

CHD: Coarctation of Aorta - Treatments

Medical - 1
Nonsurgical - 2
Surgical - 4 notes

A

Medical
- Initially, may need Prostaglandin E to maintain PDA (palliative)

Nonsurgical
- Balloon angioplasty
- stent placement for patency of aorta

Surgical
- end to end anastomosis with prosthetic graft or portion of L subclavian artery
- Cardiac Bypass not required, thoracotomy incision used
- give mechanical ventilation and inotropic support (Digoxin) pre-op
- manage HTN post-op with meds (Nitroprusside or ACE inhibitors)

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158
Q

CHD: Tetralogy of Fallot (TOF)

4 defects

A
  • VSD (pressure equal in right and left ventricles)
  • Overriding aorta (determines blood distribution)
  • Pulmonic stenosis (decreases pulmonary blood flow)
  • Right ventricular hypertrophy
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159
Q

CHD: Tetralogy of Fallot (TOF)

Clinical Manifestations (6)

A
  • Mild to severe cyanosis at birth
  • Murmur
  • Clubbing
  • Polycythemia/clot formation (emboli)
  • Failure to thrive
  • Tet spells (anoxia with crying, feeding – risk for seizures, loss of consciousness, emboli, death)
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160
Q

CHD: Tetralogy of Fallot (TOF) - Treatment

Palliative (2)
Complete Repair (2)

A

Palliative
- during Tet spell, put in knee-to-chest OR squat position
- BT shunt w/ subclavian artery

Complete repair
- Close VSD
- Resect pulmonary stenosis and patch pulmonary valve stenosis to enlarge right ventricle outflow via bypass and median sternotomy

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161
Q

CHD: Transposition of Great Arteries (TGA)

Patho (3)

A
  • PA leaves the LV
  • Aorta leaves the RV
  • Must have other defect to allow for mixing (patent foramen ovale, PDA, or VSD)
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162
Q

CHD: Transposition of Great Arteries (TGA)

Clinical Manifestations (4)

A
  • Severe cyanosis at birth with minimum communication of saturated and desaturated blood unless large VSD or PDA
  • Symptoms of heart failure (pulmonary congestion)
  • Murmur (+/-)
  • Cardiomegaly within a few weeks
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163
Q

CHD: Transposition of Great Arteries (TGA) - Treatment

Medical - 1
Nonsurgical - 1
Surgery - 1

A

Medical
- Prostaglandin E to maintain PDA and O2 sat ≥75% (side effect – apnea (likely need intubation/ventilator)) - IMMEDIATELY

Nonsurgical
- Balloon Atrial Septostomy (BAS; Rashkind) - cath lab

Surgery
- arterial switch in first few weeks of life (transection of great arteries and anastomosing pulmonary artery to aorta to establish normal circulation)

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164
Q

Post-op care after Cardiac Surgery (8)

A
  • Air filters on IV lines to prevent R→L shunt of air bubbles
  • Monitoring (Central/Arterial lines, Cardiac monitor and pulse oximeter, Chest tube (strip only if cardiac), Pacemaker on abdomen))
  • Ventilator usually via nose
  • If murmur expected, you should hear it
  • Strict I and O (UOP > 1 mL/kg/hr; NPO if intubated)
  • Monitoring Labs (K+ (never bolus potassium!), Ca+)
  • do not lift by arms until 6 weeks post-op (scoop instead)
  • maintain thermoregulation (hypothermia possible post- op so use radiant heat warmer for infants
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165
Q

Congestive Heart Failure

What is it?
Causes (3)

A

inability of the heart to pump an adequate amount of blood into the systemic circulation to meet metabolic demands

Causes
- structural abnormalities r/t blood volume and pressure in heart (heart defects)
- Myocardial failure (cardiomyopathy, dysrhythmias, electrolyte imbalance (severe))
- excessive demands on heart muscle (Sepsis, severe Anemia)

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166
Q

CHF: Decrease Cardiac Demands

Nursing Care (4)

A
  • Prevent crying and keep them calm
  • thermoregulation (radiant warmer; shivering increases demand)
  • cluster care to prevent sleep interruption
  • semi-fowler positioning
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167
Q

CHF: Digoxin

Nursing Care (4)

A
  • Monitor apical pulse
  • Hold if HR under 70 bpm in older child or 90-100 in young child/infant OR sig lower than previous reading
  • Do not repeat dose if vomiting, notify health care team if misses more than 2 doses
  • Give water after dosing to prevent tooth decay
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168
Q

CHF: ACE Inhibitors (Captopril, Enalapril, and Lisinopril)

Therapeutic Effect (3)
Side Effects (5)
Care

A

Therapeutic Effect
- Vasodilation decreases PVR and SVR (preload)
- Decreased BP and afterload
- Reduces aldosterone which prevents fluid retention

Side effects: angioedema, Cough, hyperkalemia, hypotension, renal dysfunction

Care: Check BP before and after administration

169
Q

CHF: Diuretics (Furosemide (Lasix), Chlorothiazide (Diurel))

Nursing Care (5)

A
  • Monitor potassium (s/s hypokalemia = muscle weakness, irritability, drowsiness, tachy/bradycardia)
  • Potassium supplements
  • K+ rich foods (bran cereals, potatoes, tomatoes, bananas, oranges, leafy veggies)
  • Daily weights, I & O
  • give early in day
170
Q

CHF: Nutrition

Nursing care (5)

A
  • feed when well rested at first sign of hunger b-c fatigue can decrease feeding
  • increased caloric needs w/ Polycose, corn oil
  • Preemie nipple or enlarge opening
  • Allow at least 30 minutes for feedings (then gavage remaining feeding)
  • stroke jaw to encourage sucking
171
Q

CHF: Improve Tissue Oxygenationand Decrease Oxygen Consumption

Nursing Care (2)

A
  • give oxygen w/ caution b-c can cause vasoconstriction but decreases PVR
  • raise HOB 45 degrees
172
Q

Acute Rheumatic Fever

What is it
Incidence
Complication
Prevention of Recurrence (2)

A

Inflammatory condition impacting joints, heart, brain and skin after untreated Strep infection

Incidence: 2-6 weeks after a group A streptococcal infection

Complications: Rheumatic Heart Disease (mitral valve damage)

Prevention of recurrence: Penicillin or erythromycin BID; or IM penicillin q28 days for 10 yrs if carditis (5 yrs w/o carditis)

173
Q

Acute Rheumatic Fever

Treatment (4)

A
  • Antibiotics (Penicillin)
  • ASA for 2 weeks (aspirin to prevent clots, control inflammation, fever, discomfort) - prednisone if no response to aspirin
  • Bedrest initially followed by quiet activities
  • heart valve repair or replacement for RHD
174
Q

Acute Rheumatic Fever

S/s (8)

A
  • Carditis (New murmur or valve regurgitation; Cardiomegaly; Pericardial friction rub)
  • Polyarthritis (Swollen, hot, red, very painful joint pain); arthralgias
  • Chorea (Sudden aimless, irregular movements of extremities, exacerbated by stress)
  • Nontender SubQ nodules
  • Erythema marginatum (Pink nonpruritic rash)
  • Fever (> 38.5 C)
  • ESR > 60 mm or SRP > 3 mg/dL
  • Prolonged PR
175
Q

Bacterial Endocarditis

What is it?
Transmission
Risk factor
Complications (2)

A

infection of valves and inner lining of heart which can damage or destroy valves, deposit fibrin and platelet thrombi

Transmission: Agents enter blood from any localized infection, brushing teeth, flossing, chewing, invasive procedures (GI, GU, dental, cardiac)

Risk factors: CHD

Complications: heart failure, dysrhythmias

176
Q

Bacterial Endocarditis

Clinical Manifestations (10)

A
  • Heart (HF, dysrhythmias, new/changed murmur)
  • arthralgias
  • headache
  • weight loss
  • Vegetations on ECHO
  • inflammation signs (fever, malaise, +/- blood cultures, increased ESR, leukocytosis)
  • Splinter hemorrhages (thin black lines under the nails)
  • Osler nodes (red, painful intradermal notes on pads of phalanges)
  • Janeway lesions (painless hemorrhagic areas on palms and soles)
  • Petechiae on oral mucous membranes
177
Q

Bacterial Endocarditis

What groups need prophylaxis Amoxicillin before Dental procedures? (5)

A
  • Prosthetic heart valve repair
  • History of endocarditis
  • Heart transplant with history of abnormal valve function
  • Cyanotic CHD not fully repaired (includes shunts or conduits) or for first 6 months after repair
  • Repaired congenital heart disease with residual defects (i.e. persisting leaks or abnormal flow near prosthetic patch or prosthetic device)
178
Q

Kawasaki Disease

Patho/Progression (4)

A
  • Acute stage (inflammation of capillaries, arterioles, venules and pancarditis) esp coronary arteries
  • Progression to muscular arteries (may lead to coronary artery aneurysms or MI)
  • Vessels reach max enlargement in 4-6 weeks from onset of fever
  • disease resolves in 6-8 weeks
179
Q

S/s of Kawasaki Disease (10)

A
  • Fever (>102.2) for 5 days
  • bilateral nonexudative conjunctivitis
  • cervical lymphadenopathy (unilateral)
  • rash esp trunk and perineal
  • mucositis (strawberry tongue, red lips)
  • Swelling or erythema of palms and soles (peripheral edema)
  • desquamation of skin (in 2-3 weeks; painless)
  • IRRITABILITY (last up to 2 months)
  • temporary arthritis, lethargy
  • Inflammation of myocardium (myocarditis, valvulitis, arrhythmias)
180
Q

Kawasaki Disease

Labs and Diagnostics (5)

A

Elevated ESR, CRP
Anemia
Leukocytosis
Do Baseline Echo
Platelet rises in 2nd week

181
Q

Drug Management of Kawasaki Disease

IV Ig
- Purpose
- Nursing Care/Pt education (4)

A

Purpose: high dose to reduce risk of coronary artery abnormalities)

Nursing Care/Pt education
- usually 1 infusion
- same care as blood products (2 nurse check, frequent VS)
- monitor cardiac status and anaphylaxis
- avoid MMRV for 11 months after admin

182
Q

Nursing Care for Kawasaki (5)

A
  • skin (cool compress, lotion, soft cloths)
  • oral care (lip lubrication, soft foods, clear liquids)
  • Monitor VS, I & O, weight, ECG
  • Passive ROM to increase flexibility
  • environment (quiet, respite for parents)
183
Q

Shock

What is it?
Consequences (3)

A

Inadequate tissue perfusion to meet the metabolic needs results in cellular dysfunction and organ failure

Consequences: hypotension, tissue hypoxia, metabolic acidosis

184
Q

Shock

Management (6)

A
  • VS q15 minutes; output hourly
  • Ventilatory support- Early endotracheal intubation
  • IV NS or LRs ( 20 ml/kg push)
  • Albumin (b-c remain in system longer than NS)
  • Catecholamines to improve heart pumping (Dopamine and Epinephrine)
  • legs flat and above heart
185
Q

Sickle Cell Anemia

Patho
Types (3)
Incidence (2)

A

Patho: increased RBC destruction b-c sickled hgb unable to obtain oxygen causing obstruction, inflammation (local hypoxia), adhesion

Types: homozygous HgbSS, heterozygous HgbSC, Beta thalassemia (seen in mediterranean)

Incidence: autosomal recessive seen in AA; manifests after 4-6 months when fetal Hgb disappears

186
Q

Sickle Cell Anemia: Vaso-occlusive crisis

S/s (8)

A

Vaso-occlusive crisis (ischemia and pain) – main
- Painful joints and hands/feet (dactylitis)
- Abdominal pain
- retinal (detachment, blindness or visual changes, icteric sclera)
- renal (Hematuria, dark urine, enuresis)
- Priapism
- AVN (avascular necrosis) of hip or shoulder
- lordosis or kyphosis
- leg ulcers

187
Q

Sickle Cell Crisis: Triggers (6)

A
  • Anything that increases body’s need for oxygen or alters transport of oxygen
  • Hypoxia
  • Fever (notify provider if > 38.5)
  • Infection, trauma
  • dehydration (b-c increases blood viscosity)
  • Physical and emotional stress
188
Q

Sickle Cell Anemia: Prevention of crisis (3)

A
  • Hydration
  • Hydroxyurea- ↑ Hgb F (fetal hemoglobin), lower leukocyte and reticulocyte levels
  • Oxybryta (decreases # of crises in 4yrs +)
189
Q

Hemophilia

What is it?
Incidence
Diagnosis (3)

A

Bleeding disorder r/t congenital deficiency of specific coagulation proteins (Factor VIII or Factor IX)

Incidence: x-linked recessive so usually boys with carrier mother

Diagnosis: Factor VIII and Factor IX assays; PTT, DNA testing

190
Q

Hemophilia

S/s (7)

A
  • excessive Bruising
  • prolonged bleeding (epistaxis)
  • Hemarthrosis (bleeding in joint -> bony changes and deformities) - signs: stiff, tingling, ache, inflammation signs
  • hematuria
  • hemorrhages (brain = fatal, GI = anemia)
  • subQ and IM hemorrhages
  • Hematoma (pain, swell, limited motion)
191
Q

Sickle Cell Anemia

Diagnosis (4)

A
  • Mandatory screening of all newborns
  • Sickledex- detects HgbS but cannot differentiate trait from disease; heel stick
  • Hgb electrophoresis (definitive diagnosis)- separates various forms of Hgb via fingerprint of protein
  • CBC- anemia
192
Q

Sickle Cell Anemia

General manifestations (4)

A
  • Chronic Anemia (hgb 6-9 g/dl)
  • Susceptibility to sepsis (r/t functional asplenia)
  • Growth retardation
  • Delayed sexual maturation
193
Q

Sickle Cell Anemia: Severe Complications

Acute Chest Syndrome (2)
Cerebral Vascular Accident (2)

A

Acute Chest Syndrome (ACS) - r/t pulmonary infiltrates
- Report chest pain, fever of 38.5 C or higher, congested cough, tachycardia, dyspnea, retractions, decreased O2 sat
- Call provider immediately

Cerebral Vascular Accident (CVA) - r/t HgbSS blocking BVs in brain
- Report seizures, abnormal behavior, weakness or inability to move an extremity, slurred speech, visual changes, vomiting, or severe headache
- If hx of CVA or beta thalassemia, child may get monthly chronic transfusions for prevention

194
Q

Sickle Cell Anemia: Sequestration crisis

S/s (3)

A

Sequestration crisis- RBC breaking down quickly
* Hepatomegaly (jaundice)
* Splenomegaly (fibrous or rupture; functional asplenia)– may need spleen removed
* Circulatory collapse/shock (cardiomegaly, systolic murmur, tachycardia, Fatigue)

195
Q

Sickle Cell Anemia: Prevention of complications (3)

A
  • Penicillin prophylaxis – 2m to 5yrs (prevents pneumococcal sepsis)
  • Vaccines (Hib, pneumococcal, meningococcal, influenza)
  • Transcranial Doppler annually for children 2-16 years- Identify blood clots early via measuring intracranial vascular flow
196
Q

Sickle Cell Anemia: Treatment (7)

A
  • Rest
  • Hydration -oral or IV therapy (tell parents specific amount)
  • Electrolyte replacement
  • Blood replacement (phoresis of blood or whole-blood exchange)
  • Antibiotics for infection
  • Monitoring of reticulocyte (baby RBCs) count regularly to evaluate bone marrow function
  • HSCT is only potential for cure (stem cell transplant) – complications (graft rejection, immunosuppression, graft vs host disease, relapse)
197
Q

Hemophilia: Medical Management (5)

A
  • Factor VIII Infusions -replace missing clotting factors; every other day or 3x/week for severe
  • Desmopressin (DDAVP-synthetic vasopressor) (IV or nasal spray)- increases factor VIII activity for mild
  • Aminocaproic acid- prevents clot destruction; give Factor infusion first
  • Corticosteroids- for hematuria, acute hemarthrosis, chronic synovitis
  • Cox-2 inhibitors- for hemophilic arthropathy
198
Q

Sickle Cell Anemia: Patient Education (5)

A
  • Wear medical ID band
  • Frequent rest with physical activity
  • Avoid contact sports with splenomegaly
  • avoid oxygen admin b-c can depress RBC production and worsen anemia
  • refer to crisis as pain episode
199
Q

Sickle Cell Anemia: Pain Management (7)

A
  • PCA preferred
  • Mild: acetaminophen, Ibuprofen, codeine, toradol
  • Severe: opioids, ketorolac
  • avoid meperidine (Demerol) b-c risk for seizures and product breakdown
  • monitor for GI bleeds from NSAIDS
  • Apply heat or massage affected area
  • Avoid cold compresses (we want blood flow to area b-c pain from tissue anoxia)
200
Q

Sickle Cell Anemia: Anemic/aplastic crisis

s/s (2)

A
  • high reticulocyte count (reticulocytosis)
  • reduced RBC production
201
Q

Sickle Cell Anemia: Blood Transfusions

Indication
Risk (4)
Nursing Care (2)

A

Indication: during crisis or monthly if CVA risk or Beta thalassemia

Risk: infection, hyperviscosity, alloimmunization, Hemosiderosis and hemochromatosis (iron deposits with/without tissue damage)

Nursing Care
- Oral chelation agents (deferasirox, deforxamine) to remove excess iron
- oral chelation given IV or subQ over 8-10 hours (during sleep)

202
Q

Hemophilia

Severity (3)

A

Severe (Factor VIII activity <1%)- spontaneous bleeding without trauma

Moderate (Factor VIII activity 1-5%)- bleeding with trauma

Mild (Factor VIII activity 5-40%)- bleeding with severe trauma or surgery

203
Q

Hemophilia: Prevent Bleeding (6)

A
  • Regular exercise and PT may reduce bleeding episodes
  • Noncontact Sports- golf, swimming, jogging, fishing, bowling
  • Oral (Soft bristled toothbrush w/ warm water)
  • Electric shavers vs razors
  • SubQ instead of IM injections
  • Avoid aspirin or ibuprofen (NSAIDs)
204
Q

Hemophilia: Control Bleeding (4)

A
  • factor replacement
  • RICE- rest, ice, compression, elevation
  • Keep cold packs ready
  • Only active ROM (NO PASSIVE) for hemarthrosis
205
Q

Hemophilia: Patient Education (2)

A
  • Medical ID bracelet
  • teach child 8-12 yrs to give injections
206
Q

Management of Hydrocephalus

VA shunt (2)
VP shunt (4)

A

Ventriculoatrial (VA)
- drains fluid from ventricles into atria of the heart usually done when hx of abdominal surgery
- contraindicated with CHD or elevated CSF protein

Ventriculoperitoneal shunt (VP Shunt)
- drains fluid from ventricles into peritoneum
- preferred method b-c longer and allows growth
- observe for abdominal distention (s/s of peritonitis)
- contact sports prohibited

207
Q

CHF: Digoxin

Therapeutic Effect (3)
Toxicity (5)

A

Therapeutic Effect
- Increases force of contraction/contractility (+ inotrope)- prolonged PR
- Decreases HR (- chronotropic) - reduced ventricular rate
- Increases renal perfusion

Toxicity
- bradycardia
- NV
- visual changes (see halos)
- poor feeding, anorexia
- dysrhythmias

208
Q

Drug Management of Kawasaki Disease

Aspirin (4)

A

Aspirin (anti inflammatory and reduce clot formation)
- given 6-8 wks; indefinitely if cardiac abnormalities
- avoid chickenpox and flu to avoid Reye’s
- avoid contact sports b-c low platelets w/ ASA
- Warfarin, Plavix (clopidogrel), lovenox (enoxaparin) if aspirin inadequate)

209
Q

Diagnostics for Mobility concerns- 7

A
  • Assessment (pain, ROM, tenderness, erythema etc.; key for diagnosis)
  • X-rays (Difficult to use for diagnosis because of localized swelling but accesses skeletal trauma
  • CT Scans and MRI (find injuries, areas of infections, and cancer)
  • Ca 2+ (varies w/ bone breakdown from immobility making hydration crucial)
  • CBC, WBC and blood cultures
  • ESR elevation
  • Alkaline phosphatase - increases with growth
210
Q

Mobility: Difference b/w the following

Contusions
Dislocation
Strain
Sprain

A

Contusions: damage to soft tissue, subcutaneous tissue, and muscle causes escape of blood into tissues leading to ecchymosis (black-and-blue discoloration) (s/s. Swelling, pain, disability, crush injuries)

Dislocation - Displacement of normal position of opposing bone ends or of bone ends to socket

Strain - microscopic tear in the muscles and tendons

Sprain - A ligament is torn or partially torn.

211
Q

Difference b/w following fracture:

  • Plastic deformation
  • Buckle
  • Simple or closed
  • Greenstick
  • Open or compound
  • Complicated
  • Comminuted
A
  • Plastic deformation: bone is bent, not broken
  • Buckle: appears raised or bulging due to compression of porous bone
  • Simple or closed: does not produce a break in the skin
  • Greenstick: bone is angulated beyond limits of bending; compressed side bends and tension side fails leading to incomplete fracture
  • Open or compound: fractured bone protrudes through the skin
  • Complicated: bone fragments have damaged other organs or tissues
  • Comminuted: small fragments of bone are broken from fractured shaft and lie in surrounding tissue
212
Q

Epiphyseal Injury

What is It?

Complication

Management (2)

A
  • injury at epiphyseal plate (cartilage growth plate which is weakest point of bone)

Complication: longitudinal or angular growth deformities

Management
- frequent surveillance if type 1 (separation of growth plate)
- Surgery (open reduction and internal fixation) if type 3 (half of bone under plate broken)

213
Q

Management of Fractures - 5

A
  • RICE (no heat)
  • splint (immobilize)- soft splint (pillow or folded towel) or rigid splint (rolled newspaper or magazine)
  • cover wounds w/ sterile or clean dressing
  • surgery (external fixation (rings to bone w/ wires), internal fixation, distraction (separate bones to encourage growth of new bones))
  • calm and reassure family
214
Q

Four goals of management fractures

A
  • regain alignment and length of bony fragments (reduction)
  • Retain alignment (immobilization) - until callus forms
  • Restore function - ROM and weight bearing after site stable
  • Prevent deformity or injury
215
Q

Purposes of Traction (5)

A
  • Relieves fatigue in involved muscles
  • Fatigues muscles to reduce muscle spasms (rare)
  • Position distal and proximal bone ends (Realignment) to promote healing
  • Prevents deformity and contractures
  • Immobilize healing bone and prevent further injury
216
Q

Time frame for Bone healing and remodeling

  • Neonatal period
  • Early childhood
  • Later childhood
  • Adolescence
A

Neonatal period: 2-3 weeks due to thickened periosteum and more blood supply
Early childhood: 4 weeks
Later childhood: 6-8 weeks
Adolescence: 8-12 weeks

217
Q

6 P’s

Which 3 are late signs?

A
  • Pain – unrelieved by pain medication 1 hr after admin, especially w/ passive ROM
  • Pulselessness - no distal pulse palpable
  • Pallor - discoloration OR cyanosis; cool temp; cap refill > 3 sec
  • Paresthesia - tingling or burning
  • Paralysis – inability to move affected part;
  • Pressure - swelling, tenseness or warmth of affected limbs and extremities

Pallor, paralysis, and pulselessness are late

218
Q

Compartment Syndrome

Management - 5

A
  • fasciotomy (cut skin and reduce pressure)
  • do not elevate
  • administer fluids if needed
  • bivalve cast if excessive edema (i.e., cut calf in half a hold w/ elastic bandage)
  • CALL HCP
219
Q

Cast Application (4)

A
  • Plater of Paris dries in 2 to 48 hours
  • Fiberglass dries in a couple of hours
  • handle w/ palms until dry
  • let child know some warmth may be felt but no burning
220
Q

Interventions for Traction (6)

A
  • Diazepam (muscle relaxant for spasms)
  • Provide Skin care (q2h turns, braden scale, hygiene, pressure alt mattress)
  • Pin site Care daily or weekly (cover w/ rubber or padding; antiseptic (chlorhexidine) or topical antibiotic)
  • NURSES DO NOT LIFT OR DISCONTINUE WEIGHTS!!!! LET THEM HANG FREELY
  • prevent constipation (fluids, fiber, stool softener)
  • promote circulation (ROM, bandages not restrictive)
221
Q

Types of traction (3)

A

Manual- applied by hand placed distal to the fracture site during application of a cast or for closed reduction

Skin- Buck’s (leg extended) OR Bryant (legs up 90 degree for DDH)

Skeletal - pins, wire, tongs (ex. 90-90 degree (common at hip and knee) or Halo vest (cervical)

222
Q

Congenital Dislocation of Hip/ Developmental Dysplasia of hip

S/s (7)

A
  • Barlow (thigh adducted, and light pressure applied to femoral head to see if slips out of acetabulum then slips back when pressure is released) - unstable hip
  • Ortolani sign (abduct knees and put forward pressure behind trochanter than backward pressure; audible clunk/thunk if femoral slips forward into acetabulum meaning it is dislocated) - disappears when adduction contractures develop at about 6-10 weeks
  • Galeazzi sign: Limb shortening on affected side
  • Trendelenburg sign: When child stands on one foot and bears weight on affected hip, pelvis tilts downward on normal side instead of upward, as it would with normal stability
  • Asymmetric thigh and gluteal folds seen when prone
  • lordosis
  • waddling gait (bilateral hip dislocation
223
Q

Management of DDH

Birth- 6month - 1
Age 6- 24 months - 3
Older child (4yrs +) - 4

A

Birth to age 6 months
- Pavlik harness for abduction of hip for 6-12 week continuously

Ages 6-24 months
- recognized when child begins to stand and walk
- need closed reduction and spica cast
- may use traction for full abduction of hip

Older child (4yrs +):
- need open reduction w/ preop traction
- tenotomy (lengthen contracted muscles)
- osteotomy ( construct acetabular roof)
- correction and healing is very difficult

224
Q

Slipped Capital Femoral Epiphysis (SCFE)

What is it?
Incidence
Diagnosis (3)
Complications (3)

A
  • Spontaneous movement of femoral neck from femoral head in acetabulum due to increased weight

Incidence: boys before or during rapid growth

Diagnosis: physical exam, hx, Anteroposterior and frog-leg hip x-ray

Complications: avascular necrosis, further slippage, deformity

225
Q

Slipped Capital Femoral Epiphysis (SCFE)

Symptoms (6)

A
  • Obese
  • limp on affected side w/ altered gait
  • internal rotation and loss of abduction of affected leg
  • affected limb shortens
  • groin, hip, and knee pain
  • inability to bear weight
226
Q

Slipped Capital Femoral Epiphysis (SCFE)

Treatment (4)

A
  • strict bedrest and Buck’s traction immediately
  • surgery within 24 hrs w/ pin placement OR surgical hip dislocation
  • post-op no weight bearing to gradual weight- bearing
  • Restriction from certain sports until fusion or closure of proximal femoral physis to prevent further slippage
227
Q

Scoliosis

What is it?
Diagnosis
Three levels

A
  • spinal deformity involving lateral curve, spinal rotation, thoracic hypokyphosis

Diagnosis: x-ray to determine skeletal maturity

Levels
- <10 degrees = postural variation
- 20 or less = may not require intervention; can do exercises or braces
- Greater than 40 = requires surgery

228
Q

Scoliosis screening (5)

A
  • started at School Age (Screening at 10 AND 12 yrs. for girls or at 13 OR 14 yrs. for boys)
  • child in only underpants
  • Child bends at waist, trunk parallel to floor, arms hanging free
  • observe the back for asymmetry of hips, scapula, shoulder height, pelvic obliquity; widened angle between arm and body
  • Hold hips stable and have child turn left / right to assess flexibility of curve
229
Q

Scoliosis: Braces

Types - 3
Notes - 4

A

Types: Boston, TLSO, Milwaukee (usually for kyphosis and has neck ring)

Notes
- Braces are worn for 23 hours per day
- Not curative
- slows or stops the progression of the curvature until child reaches skeletal maturity
- discontinued once growth completed

230
Q

Scoliosis: Surgery

Indication (3)

Types (3)

A
  • depends on degree of curvature (>45-50 degrees), pain, OR if exercise & brace fails

Types
- Spinal fusion is more common and less invasive than rod insertion (via posterior or anterior approach)
- VEPTR (done for younger children with severe scoliosis via lengthening the ribs by using a prosthetic rib to enhance the breathing effort of children with scoliosis and straighten spine)
- instrumentation

231
Q

Scoliosis: Surgery

Post-op care (7)

A
  • Bed rest
  • logrolling
  • PCA / pain control b-c very painful surgery
  • Teds / SCD’s
  • frequent assessment (check for sensation and ileus (stool softeners), retention (foley))
  • early mobility (usually by day 2; PT on 1st day)
  • Brace may or may not be used.
232
Q

Juvenile Idiopathic Arthritis (JIA/JRA)

What is it
Incidence - 2
Classification - 3

A
  • inflammation in joints for > 6 weeks causing pain, swelling, and scar tissue (limited ROM)

Incidence: autoimmune condition in girls < 16; total remission in most by adulthood

Classification: dependent on joints affected, systemic symptoms, and presence of absence of rheumatoid factors

233
Q

Juvenile Idiopathic Arthritis

Joint signs (3)
Systemic Symptoms (5)

A

Joint signs
- limp
- favoring an extremity
- inflammation (pain, swelling, edema, redness)

Systemic signs
- Rash
- fever
- lymphadenopathy
- splenomegaly and hepatomegaly
- uveitis (inflammation in anterior chamber of eye; diagnosed by slit lamp eye exam)

234
Q

Juvenile Idiopathic Arthritis Management

Pharmacology - and side effects (5)

A
  • Ibuprofen (NSAIDs)- GI bleeds
  • Aspirin (NSAIDs)- be wary of viral illness b-c reyes syndrome
  • Methotrexate or Sulfasalazine (DMARD) - teratogenic, hepatotoxic, Bone marrow suppression
  • Corticosteroids (given intra-articular) - risk for infection, adrenal insufficiency, avascular necrosis, cushingoid, osteoporosis, HTN, diabetes
  • Etanercept or Adlimulmab (Biologic DMARDs) - infection risk
235
Q

Juvenile Idiopathic Arthritis

Goal of therapy - 4

A

Goal of therapy - NO CURE
- preserve joint function
- limit abnormalities and deformity
- promote normal growth and development
- decrease the discomfort (relieve symptoms)

236
Q

Muscular Dystrophy

Diagnostics (4)

A
  • DNA analysis (genetic detection of absence of dystrophin (muscle protein product due to muscle fiber degeneration)) - possible at 12 weeks gestation
  • Serum CK (elevated in first 2 yrs of life)
  • EMG (decreased amplitude and duration of motor unit potentials)
  • Muscle Biopsy
237
Q

Muscular Dystrophy

S/S (6)

A
  • waddles (due to weak butt muscles) causes frequent falls
  • lordosis (sway back, awkwardly holds shoulders back; due to weak pelvis
  • Gower’s sign (walking hands up knees and legs to stand up)
  • Mild to moderate mental impairment (Decrease in verbal skills)
  • Higher emotional disturbance
  • fatty muscle hypertrophy (thigh, calf, upper arm)
238
Q

Muscular Dystrophy

Complications (7)

A
  • osteoporosis and fractures
  • contractures
  • scoliosis
  • obesity
  • respiratory infection r/t reduced pulmonary vital capacity from weak respiratory muscles; also difficult clearing secretions via cough b-c weak muscles
  • cardiopulmonary issues due to respiratory, oropharyngeal and facial muscle involvement (heart failure and sleep apnea)
  • disuse atrophy
239
Q

Muscular Dystrophy: Family Education (6)

A
  • encourage normalcy
  • okay to grieve since chronic fatal disease
  • Guilt from passing this to son lies on woman
  • Genetic counseling for female relatives, siblings
  • provide for rest periods ( child can self-regulate activity tolerance)
  • prevent infections ( avoid crowds; get pneumococcal and influenza vacs)
240
Q

Muscular Dystrophy: Nursing Care (4)

A
  • Prevent contractures (passive ROM, soft casts, surgery, braces)
  • Promote pulmonary function ( breathing exercises, incentive spirometer q4h; mechanically assisted coughing)
  • Position changes when in wheelchair (allow for time to lie flat)
  • Keep active as long as possible (don’t wheelchair confine early)
241
Q

Cast Care (7)

A
  • Elevate initially w/ pillow (do not let stay dependent for long)
  • Encourage use of unaffected muscles
  • No coat hangers or straws in cast
  • Use fan or cool air to circulate air if high humidity (no heated air)
  • for spica, use cast petaling (tape edges w/ waterproof tape around perineal)
  • if open cast, cut out window to view wound AND outline any blood
  • Crutches should fit properly w/ soft rubber tip to prevent slipping and well padded (support on hand grips NOT axilla)
242
Q

Cast removal (6)

A
  • reassure muscle atrophy will go away as strength regained
  • avoid cold temps after removal
  • use sunscreen after removal
  • apply mineral oil or lotion to remove
  • Soak in bathtub
  • Do not pull or forcibly remove w/ vigorous scrubbing (may cause excoriation and bleeding)
243
Q

Complications of Casts (3)

A
  • infection (hot spots on dried cast or foul smell)
  • Loose cast (no longer useful and can lead to skin irritation or pressure sores)
  • Compartment syndrome – medical emergency
244
Q

DDH: Management of Pavlik harness (4)

A
  • Avoid lotions and powders because they can cake and irritate the skin.
  • Always place the diaper under the straps
  • Gently massage healthy skin under the straps once a day to stimulate circulation
  • Do not adjust harness
245
Q

Club foot

3 types

A
  • Positional: primarily from IUGR; no bony abnormality; responds to simple passive exercise and casting
  • Congenital (idiopathic): in normal child w/ wide range of rigidity & prognosis; Requires casting w/ surgical intervention (heel-cord tenotomy)
  • Syndromic (teratologic): seen w/ anomalies (such as myelomeningocele or arthrogryposis); requires surgical correction and resistant to treatment
246
Q

Club foot

s/s (5)

A
  • Affected foot or feet smaller
  • shorter, empty heel bed
  • midfoot medial creases
  • If unilateral, affected limb shorter and calf atrophy present
  • Foot pointed down (plantar flexed) and inward
247
Q

Clubfoot: Ponseti method (5)

A
  • Weekly gentle manipulation and stretching of medial side of foot w/ serial long leg casts ideal shortly after birth
  • Casting (6-10 weeks) followed by percutaneous heel-cord tenotomy (corrects equinus deformity)
  • After tenotomy, long leg cast for 3 weeks
  • After casting, Ponseti sandals w/ bar set in abduction to maintain correction and prevent recurrent
  • surgery at 6m-1 yr if casting fails
248
Q

Complications of Spinal Fusion (4)

A
  • Neurologic injury or spinal cord injury
  • hypotension from acute blood loss
  • SIADH
  • Superior mesenteric artery syndrome( due to duodenal compression by aorta and superior mesenteric artery leading to obstruction; causes epigastric pain, copious NV, and eructation(belch); alleviated w/ left lateral or prone position (worsened by supine)
249
Q

Juvenile Idiopathic Arthritis: Diagnostic (5)

A
  • 10% have positive rheumatoid factor
  • ESR/CRP elevated
  • Leukocytosis w/ exacerbations of systemic JIA
  • Antinuclear antibodies common but not specific to JIA (can identify those at risk for uveitis)
  • Radiographs – best to show soft-tissue swelling and joint space widening from increased synovial fluid
250
Q

Muscular Dystrophy: Pharmacology Effects

Corticosteroids - 3
Albuterol - 2

A

Corticosteroids (prednisone, deflazacort)
- Increased muscle strength, bulk, power and decreased progression of weakness (Prolonged ambulation)
- decreased incidence of scoliosis and cardiomyopathy)
- Increased pulmonary function

Oral albuterol
- increase lean body mass and decrease fat mass
- no change in strength

251
Q

Juvenile Idiopathic ARthritis

Interventions (7)

A
  • Physical therapy (strengthen joints and prevent deformities)
  • pain relief (usually avoid opioids unless severe)
  • moist heat ( hot pack, warm bath)
  • exercise
  • promote general health and nutrition (match caloric intake to energy needs)
  • allow child to rest as needed
  • promote independence ( parent only help when necessary)
252
Q

Muscular Dystrophy

What is it?
Incidence - 2

A

Muscle atrophy and fatty infiltrates on extremities leads to progressive degeneration of muscle fibers

Incidence: x-linked; often wheelchair bound by 12 yrs

253
Q

General Symptoms of Cancer (9)

A
  • Unusual mass or swelling
  • Anemia (Pallor and fatigue)
  • thrombocytopenia (Petechiae, Sudden easy tendency to bruise)
  • Persistent, localized pain or limping
  • Prolonged, unexplained fever or illness
  • Frequent headaches, often with vomiting
  • Sudden eye or vision changes (leukocoria in retinoblastoma; squinting, strabismus, swelling if solid eye tumor)
  • Excessive, rapid weight loss
  • enlarged firm lymph nodes
254
Q

Leukemia

Patho
Most affected extramedullary areas (2)

A

Patho: unrestricted proliferation of immature white blood cells (blasts) in the blood-forming tissues of the body

Most affected extramedullary areas: spleen and liver b-c highly vascular

255
Q

Leukemia

Symptoms (5)

A
  • Bone marrow (anemia, thrombocytopenia, leukopenia; bone and joint pain)
  • Physiologic fractures r/t increased pressure in bone
  • Enlarged spleen, liver, lymph nodes r/t infiltration -> can become fibrotic
  • Leukemic meningitis r/t CNS infiltration
  • Cellular Starvation r/t hypermetabolism
256
Q

Leukemia: Diagnostics

  • CBC (2)
  • Biopsy (3)
  • Lumbar puncture
A

CBC
- immature leukocytes (blasts) present
- Low blood counts (WBC, RBC, platelets)

Bone marrow biopsy and/or aspiration
- Definitive diagnosis to differentiate b/w ALL and ALM
- Shows infiltration of blast cells
- Often sedation for pediatrics b-c must remain still

Lumbar Puncture (LP)
- Determination of CNS involvement (metastasis, brain tumors)

257
Q

Leukemia

Treatment (5)

A
  • Surgery (palliative or curative)
  • Chemotherapy (primary)
  • Targeted therapy (tyrosine kinase inhibitors (TKIs), monoclonal antibodies, proteasome inhibitors)
  • Radiotherapy
  • Hematopoietic Stem Cell Transplant (HSCT) or Bone Marrow Transplant (BMT)
258
Q

Chemotherapy Drugs

Notes (2)

A
  • combo drug regimen used b-c optimal cell destruction with minimum toxic effects
  • Not selectively cytotoxic for malignant cells (kills fast growing healthy cells i.e. bone marrow, hair, skin, and GI tract)
259
Q

Monoclonal Antibody drugs

Pros (2)
Cons

A

Pros
- fewer reactions vs chemo (no hair loss or mucositis)
- alters immune system to recognize cancer cells by attaching to proteins

Cons
- anaphylaxis common so premedicate w/ steroids or benadryl

260
Q

Chemotherapy drugs

Nursing Care (6)

A
  • Requires a double check from a second RN
  • PPE (gloves, gowns, masks/face shield if splashes possible)- including gauze when in contact w/ drug
  • Often need central line or infusion port
  • DO NOT crush or alter chemotherapy drugs
  • Stop infusion immediately if s/s of infiltration (pain, stinging, swelling, redness)
  • Observe child for 1 hr after infusion for signs of anaphylaxis (rash, urticaria, hypotension, wheezing, NV)
261
Q

Biologic Response modifiers

  • Action
  • Examples (5)
A

Action: Alters relationship b/w tumor and host by changing the host’s biologic response to tumor cells.

Examples
- Monoclonal antibodies
- Chimeric Antigen Receptor T-cell Inhibitors (CAR-T)
- Angiogenesis inhibitors
- Colony-stimulating factors (CSFs)- G-CSF (filgrastim, pegfilgrastim)
- checkpoint inhibitors (block pathways that allow cancer cells to escape immune system)

262
Q

Radiation

Side effects (9)

A

Side effects (based on area)
- neck (hypothyroidism )
- chest (reduced lung function, heart damage)
- obesity and metabolic syndrome ( hormone-producing organs)
- ovaries and testes (infertility)
- GI (anorexia, mucosal ulceration, NVD)
- Skin (alopecia, dry or moist desquamation, hyperpigmentation)
- Head (NV(stimulation of vomiting center), alopecia, mucositis, parotitis, sore throat, loss of taste, xerostomia, GH deficiency, cognitive deficits, hearing loss)
- bladder (cystitis)
- Bone marrow (myelosuppression)

263
Q

Radiation

Nursing Care (3)
Patient education (5)

A

Nursing Care
- Encourage fluids & nutritional intake (Light, small, frequent meals)
- get I&O and Daily weights
- Do not refer to skin changes as burns b-c implies too much radiation use

Patient Education
- Use mild soap
- Do not remove skin markings
- Avoid creams or lotions
- Loose-fitting clothing over irradiated area to minimize skin irritation
- Protect area from sunlight and sudden temp changes (ice or heating packs)

264
Q

Hematopoietic Stem Cell Transplant (HSCT)

Indication (2)
Risks (3)
Pre-op

A

Indication
- malignancies unable to be cured by other means
- replacement of dysfunctional bone marrow

Risks: infection, relapse, Graft vs Host disease(due to HLA mismatch)

Pre-op: High dose chemo and radiation – to reduce ANC to nadir (0) (irreversible)

265
Q

Effects of Cancer Treatment: Infection

Related to? (2)
Patient education (4)

A

Related to: neutropenia (ANC < 500), altered nutrition (prolongs neutropenia)

Education:
- Avoid crowds and sick individuals
- wear a mask in public
- Low bacterial diet ( no fresh fruits, no soft serve; fully cooked foods, no deli meats)
- Avoid fresh flowers, live plants

266
Q

Effects of Cancer Treatment: Anaphylaxis( tachycardia, tachypnea, flushing, urticaria, hypotension)

Related to?
Nursing Care (6)

A

Related to: chemo, BRMs

Nursing Care
- pre-medicate if ordered
- Monitor patient closely (vital signs, and assessment)
- Assess for hx of anaphylaxis with certain meds
- discontinue drug if happens and maintain patency of IV line w/ NS
- Obtain crash cart give emergency drugs (epinephrine, dopamine)
- administer supplemental O2 (call RRT)

267
Q

Effects of Cancer Treatment: Hemorrhage
(epistaxis, gingival bleeding)

Related to?
Nursing Care (7)

A

Related to: thrombocytopenia (<20K)

Nursing Care
- Administer platelets as ordered (no need for cross matching; peak: 1 hr, Duration:1-3 days)
- Avoid invasive procedures and skin punctures
- Gentle mouth and perineal care (wipes front to back)
- AVOID rectal temperatures and suppositories
- Educate patient to avoid contact sports, bike or skateboard riding if < 100,000
- avoid aspirin products
- Frequent turns and pressure-reducing mattress under bony prominences to prevent pressure sores and decubital ulcers

268
Q

Effects of Cancer Treatment: Anemia

Nursing Care (4)

A
  • Monitor for s/sx of anemia (pallor, fatigue, tachycardia, increased cap refill)
  • Allow for frequent periods of rest (regulated by child
  • Transfuse PRBCs if ordered (to increase Hgb > 10 g/dL)
  • Administer G-CSF (filgrastim, pegfilgrastim)
269
Q

Effects of Cancer Treatment: Pain

Related to?
Nursing Care (3)

A

Related to: bone marrow involvement (acute, chronic, neuropathic)

Nursing Care
- Assess pain frequently w/ age-appropriate pain scale

  • Administer pain meds PRN (IV (morphine or hydromorphone PCA), PO, transdermal patches (Fentanyl, lidocaine), nerve blocks/epidurals_
  • Involve interdisciplinary teams (quality of life team; pain team)
270
Q

Effects of Cancer Treatment: Altered Nutrition
(Anorexia, NV)

Nursing Care (5)

A

Nursing Care (prevention is key)
- administer meds (ondansetron, lorazepam, diphenhydramine, dronabinol, granisetron, hydrocortisone) 30-60 min prior to admin of chemo and for 24 hrs after
- give metoclopramide w/ diphenhydramine if severe b-c metoclopramid has extrapyramidal effects
- Monitor I&O, daily weight, albumin/prealbumin (increased risk of dehydration and electrolyte disturbances)
- Fortify foods with nutritious supplements (High protein, high calorie)
- use NGT and TPN as needed

271
Q

Effects of Cancer Treatment: Mucositis/ Stomatitis (eroded, red, painful areas in mouth, pharynx, rectum)

Nursing Care
- mouth lesions (5)
- rectal lesions (3)

A

Nursing Care for mouth lesions
- Encourage frequent oral care (q2-4 hrs w/ soft sponge toothbrush) and Lubricate lips PRN
- Alkaline saline mouth rinses, viscous lidocaine, chlorhexidine mouth rinse (No lidocaine for under 2 yrs b-c diminishes gag reflex)
- Avoid alcohol rinse, lemon glycerin swabs and hydrogen peroxide b-c drying effects and acidity of lemon is irritating
- Administer nystatin for thrush as indicated
- Encourage a bland, moist, soft diet

Nursing Care for rectal lesions
- AVOID suppositories and rectal temps
- Daily CHG wipes/baths, Sitz bath as needed
- Occlusive ointments

272
Q

Effects of Cancer Treatment: Neurologic problems

Examples w/ nursing care (6)

A
  • Foot drop (Encourage use of foot board or high-top tennis shoes when in bed)
  • severe constipation (use stool softeners, activity, laxatives)
  • Peripheral neuropathy (Give antidepressants (TCAs), AEDs
  • Jaw pain (use repetitive gum chewing or suck hard candy)
  • Developmental delays
  • Post irradiation syndrome (somnolence, anorexia, N/V, fever; 5-8 wks after CNS radiation lasting 4-15 days) (indicator of neurologic sequelae)
273
Q

Effects of Cancer Treatment: Hemorrhagic cystitis (irritation of bladder lining)

Related to?
Nursing Care (5)

A

Related to: urinary stasis r/t radiation and chemo

Nursing Care
- Monitor for hematuria and blood clots in urine
- Ensure adequate oral or parenteral fluid intake (1.5x daily fluid requirement (2L/m2/day))
- Monitor strict I&O and ensure frequent voiding around the clock every 2 hrs until 24 hrs after last dose
- Administer bladder protectant (mesna) after certain chemo
- give chemo early in day to allow adequate flushing and fluids throughout day

274
Q

Effects of Cancer Treatment: Body Image Concerns

Related to? (4)
Nursing Care (2)
Patient education (2)

A

Related to:
- alopecia (all body hair)
- weight changes, steroids (cushingoid)
- body additions (CVAD, IV lines)
- body changes (scars, amputations)

Nursing Care
- Encourage shorter haircuts prior to hair falling out b-c falls out in clumps
- Provide emotional support

Patient education
- Educate on options such as wigs, scarves, and bandanas
- Educate that hair grows back in 3-6 months

275
Q

Effects of Cancer Treatment: Tumor Lysis Syndrome

What is it?
S/s (4)

A

Related to: rapid release of intracellular contents seen in lysis of cells in ALL or burkitt lymphoma

S/s
- hyperkalemia (NV)
- hyperuricemia (flank pain, lethargy, renal failure)
- hyperphosphatemia (muscle cramps, pruritus)
- hypocalcemia (tetany, seizures)

276
Q

Granulocyte Colony stimulating factor (G-CSF)- filgrastim, pegfilgrastim)

Purpose (2)
Care (2)

A

Purpose
- Regulate reproduction, maturation and function of blood cells.
- Decreases duration of neutropenia

Care
- Discontinued when ANC > 10,000
- watch for bone pain, fever, rash, malaise, headache

277
Q

Cancer: Immunizations (4)

A
  • Avoid admin of live, attenuated vaccines (polio, MMR) due to immunosuppression
  • Avoid exposure to childhood diseases such as chickenpox then give antivirals (acyclovir, valgancyclovir) if child develops varicella or is exposed
  • If vaccinated 2 weeks prior to starting chemotherapy or during treatment, consider child unimmunized b-c immune system not strong enough for developing active immunity.
  • Revaccinate or administer live virus vaccines 6 months after treatment is stopped.
278
Q

Non-Hodgkin Lymphoma (NHL)

What is it?
Key s/s
Classifications (3)
Treatment (3)

A

Tumors of the peripheral lymph nodes, thymus, or abdominal organs such as the bowel.

Key s/s: tumors compressing organs (intestinal or airway obstruction, CN palsies, spinal paralysis)

Classifications: Lymphoblastic, Burkitt/Non-Burkitt (mature B-cell), Large Cell/anaplastic

Treatment: chemo, radiation (emergencies), surgery (Burkitt or anaplastic)

279
Q

Hodgkin Lymphoma (HL)

What is it?
Key s/s (5)
Diagnostic
Treatment

A

progressive enlargement of affected lymph nodes and sometimes spread to the spleen, liver, bone marrow, bones, mediastinum, or lungs

Key s/s
- Enlarged, firm, nontender, movable lymph nodes in supraclavicular or cervical areas
- Mediastinal lymphadenopathy – persistent nonproductive cough
- Enlarged retroperitoneal nodes – unexplained abdominal pain
- splenomegaly/hepatomegaly
- Systemic symptoms: low or intermittent fever, anorexia, nausea, weight loss, night sweats, pruritus

Diagnostic: Lymph node biopsy shows Reed Sternberg cells (seen in mono as well)

Treatment: radiation and chemo

280
Q

Neuroblastoma

What is it?
Diagnosis (3)
Treatment (3)

A

originate from embryonic neural crest cells (neuroblasts) which form adrenal medulla and SNS and cause abdomen (arising from adrenal gland) OR head, neck, chest, or pelvis tumor

Diagnosis
- usually after metastasis (silent tumor)- lymph node, bone, liver (lymphadenopathy, bone pain, hepatomegaly)
- Metaiodobenzylguanidine (MIBG) scan – biopsy and aspirate of bone marrow to evaluate metastasis
- CT or MRI to locate primary tumor

Treatment: chemo, radiation, surgery (primary)

281
Q

Wilm’s Tumor

What is it?
Key s/s (3)
Diagnosis (2)
Treatment (4)

A

Solid tumor of the kidneys from immature kidney cells

Key s/s
- UNILATERAL firm, nontender swelling or abdominal mass (does not move w/ respiration)
- hematuria
- HTN (due to excess renin secretion by tumor)

Diagnosis
- Metastasis is rare (Pulmonary metastasis (dyspnea, cough, SOB, pain in chest)
- CBC may show polycythemia if tumor secretes excess erythropoietin

Treatment
- DO NOT PALPATE (appropriate signage in room)
- surgical resection of tumor, adrenal gland, kidney (transplant if stage 5)
- radiation (maybe post-op depending on stage)
- chemo

282
Q

Osteosarcoma

What is it?
Key s/s (4)

A

Arises from bone-forming mesenchyme in osseous tissue of metaphyseal region of long bones

Key S/s
- Pain, swelling, and sometimes decreased joint motion and limp (relieved pain w/ flexion)
- inability to hold heavy items
- occasional fracture at the tumor site if tumor presses on bone
- palpable mass

283
Q

Ewing Sarcoma

What is it?
Key s/s (3)
Diagnosis (3)
Treatment (3)

A
  • small, round cell tumors that arise in marrow spaces of bone or in soft tissues (extraosseous-pelvis, femur, tibia, fibula, humerus, ulna, vertebra, scapula, ribs, and skull

Key s/s
- Localized pain w/ limp
- spinal cord compression (back pain, sensation change, extremity weakness, loss of bowel or bladder function, respiratory insufficiency)
- respiratory distress (metastasis to lungs)

Diagnostic Testing
- X-ray (involvement of diaphysis w/ detachment of periosteum from bone (Codman triangle))
- CT/MRI of primary site and CT chest
- bone marrow aspiration and biopsy

Treatment: Chemotherapy, high dose radiation, surgery (limb salvage more likely)

284
Q

Retinoblastoma

What is it?
Key s/s (4)

A

Intraocular malignancy usually unilateral and nonhereditary

Key s/s
- Leukocoria (whitish pupil glow) esp in flash photo
- Strabismus (due to poor fixation of visually impaired eye esp if tumor in macular (area of sharpest visual acuity)
- Late: blindness, pain, orbital cellulitis, glaucoma
- High risk for secondary malignancy (osteosarcoma)

285
Q

Fluid Requirements

Daily fluid requirements
Measuring Output (4)

A
  • Based on child weight i.e. 100 (first 10 kg)+ 50 (2nd 10kg) + 20 (remaining kg)

Output
- q2h
- subtract weight of dry diaper from wet diaper (unable to distinguish stool from urine)
- minimum 1 mL/kg/hr (30 mL/hr if > 30 kg)
- Bladder capacity (oz) = Age (years) + 2

286
Q

Dehydration: Isotonic

What is it?
Treatment

A
  • balanced loss of electrolytes and water from ECF

Treatment: isotonic fluids (NS, LRs)

287
Q

Dehydration: hypotonic

What is it?
Treatment

A
  • electrolyte deficit (low Na) > water deficit so water goes into ICF

Treatment: hypertonic fluids (D5NS, 3NS)

288
Q

Dehydration: hypertonic

What is it?
Treatment

A
  • water deficit > electrolyte deficit (Na> 150) due to water loss or increased electrolytes; fluid goes from ICF to ECF

Treatment: D5W, 1/2 NS (DO NOT GIVE RAPID b-c risk for water intoxication

289
Q

Dehydration: Mild (3-5% infant, 3-4% child)

Manifestations (4)

A
  • Normal pulse, respiration, blood pressure, behavior, mucus membranes, fontanel
  • Slight thirst
  • Cap refill 2 sec
  • Urine SG ›1.020
290
Q

Dehydration: Moderate (6-9% infant, 6-8% child)

Manifestations (8)

A
  • Slight increased HR, RR, normal to orthostatic BP
  • Irritable
  • Dry mucous membranes
  • Moderate thirst
  • Decreased tears
  • Normal or sunken fontanel
  • Cap refill 2-4 seconds, decreased turgor
  • Oliguria
291
Q

Dehydration: Severe (≥ 9-10%)

Manifestations (8)

A
  • Very tachycardia and hyperpnea
  • decreased BP/shock
  • Lethargic to hyperirritable
  • Parched mucus membranes and intense thirst
  • Absent tears w/ sunken eyes
  • Sunken fontanel
  • Cap refill › 4 seconds, cool skin, mottled, acrocyanotic, tenting
  • Oliguria, anuria
292
Q

Oral Rehydration Therapy (ORT)

Purpose
Choices (6)

A
  • Enhance the reabsorption of Na and water via reducing vomiting, diarrhea, and duration of illness (stomatitis, emesis)

Choices
- Use Centralyte, Pedialyte, Rehydrate w/ 50 mEq/L
- Add unsweetened Kool-Aid to ORS
- Low sugar popsicles
- do not give fruit juice, soft drinks, gelatin (high carb, low electrolyte, high osmolarity)
- do not give chicken or beef broth or gatorade (excess sodium, low carb)
- Avoid BRAT diet (contraindicated b-c little value (low protein, low energy, high carb, low electrolytes)

293
Q

Degrees of Dehydration: Treatment w/ ORT or IV

Mild
Moderate
Severe

Amount Variations (2)

A

Mild dehydration- 50 mL/kg within 4 hours

Moderate dehydration- 100 mL/kg within 4 hours

Severe dehydration- IV fluids 40 mL/kg/hr until HR and LOC normal, then IV or oral rehydration solution

Amount Variations
- Add 10 ml/kg of ORT fluid for every loose stool or episode of vomiting
- If vomiting, ORT frequently in small amounts (5- 10 ml syringe q1-5 min)

294
Q

TPN

Risk
Nursing Care (5)

A

Risk: infection due to hyperglycemia risk or hypoglycemia

Nursing Care
- Administer in central venous catheter
- Filtered tubing to remove particulate matter
- “Ramp up” and “Ramp down” rate of infusion slowly to prevent dysregulation of glucose
- Monitor glucose, electrolytes, liver function tests, triglycerides, albumin, renal function
- Daily weights

295
Q

Diarrhea: Acute vs Chronic

Timing
Cause

A

Acute
- Timing: self-limited under 14 days usually in under 5 yrs old
- Cause: infectious agent (C.diff (antibiotic use), rotavirus (immunization), Giardia lamblia (day cares)) esp. URI, UTI, antibiotics, or laxatives

Chronic
- Timing: over 14 days
- Cause: malabsorption syndromes, IBD, immunodeficiency, food allergy, lactose intolerance, CNSD

296
Q

Spitting up/Regurgitation

Cause
Treatment (5)

A

Cause: due to weakened Sphincter at entry of stomach until 6-12 months of age esp in bottle-fed

Treatment
- Frequent burping before/after feedings
- Minimum handling during/after feedings
- Position child on right side with head slightly elevated after feeding (stomach drains better)
- NEVER overfeed ~ more frequent smaller feedings
- meds (rare but Ondansetron (few side effects) is okay; Avoid promethazine and metoclopramide b-c somnolence, nervousness, irritability, and dystonic reactions)

297
Q

Gastroesophageal Reflux Disease

Cause
Complications (3)

A

Cause: inappropriate relaxation of lower esophageal sphincter causes damage due to variety of conditions (hermia, G-tube, neurological disorders, respiratory disorders, gastric distention)

Complications
- FTT
- respiratory difficulties (dysphagia, pneumonia, laryngitis)
- Barrett’s esophagus (premalignant; esophageal strictures)

298
Q

Gastroesophageal Reflux Disease

S/s in infant (6)

A
  • Passive regurgitation/emesis & vomiting
  • Anorexia/ feeding refusal
  • respiratory problems (e.g., cough, wheeze, stridor, gagging, choking with feedings)
  • Odynophagia (painful swallowing)- Arching of the back
  • Irritability, excessive crying
  • Hematemesis -> anemia
299
Q

Gastroesophageal Reflux Disease

S/s in child (5)

A
  • Intermittent vomiting (preschool)
  • Heartburn
  • Regurgitation and Re-swallowing
  • Hematemesis and melena - > anemia
  • Respiratory problems (Chronic cough, hoarse voice, Dysphagia, Asthma)
300
Q

Gastroesophageal Reflux Disease

Treatment
- Surgery
- Meds (3)
- Feeds (4)

A
  • Surgery (nissan fundoplication) - severe/last resort (post-op: NGT decompression, vent G-tube)

Medications
- PPIs (omeprazole (Prilosec), lansoprazole (Prevacid))
- Histamine antagonists (Famotidine (Pepcid)
- Erythromycin (low dose to help w/ gastric emptying)

Feeds
- Thickened formulas- w/ rice cereal
- Positioning (upright or prone post-feeding unless sleeping)
- Small, frequent feedings
- Avoid caffeine, citrus, tomatoes, alcohol, tobacco, peppermint, spicy or fried foods

301
Q

Pyloric Stenosis

Cause
Labs (4)

A

Cause: hypertrophy of pylorus leads to gastric outlet obstruction and compensatory dilation, hypertrophy, and hyperperistalsis of stomach usually at 3-6 weeks of life

Labs
- Hyperbilirubinemia r/t decreased glucuronyl transferase
- Decreased Na, K, Cl but hemoconcentration may mask
- metabolic alkalosis (elevated HCO3)
- Increased BUN r/t dehydration

302
Q

Pyloric Stenosis

S/s (6)

A
  • Post-prandial emesis (projectile and nonbilious)
  • Hunger
  • weight loss (malnourished or dehydrated)
  • jaundice
  • palpable olive-shaped mass
  • gastric wave
303
Q

Pyloric Stenosis: Pyloromyotomy

  • Pre-op (4)
  • Post-op (2)
A

Pre-op: correct f/e balance
- IV fluids (NS bolus, D51/2 NS at 1.5x maintenance over 24-48 hrs)
- NPO and NGT decompression
- labs: BMP, CBC
- Watch for apnea b-c risk for aspiration w/ vomiting

Post-op
- Feeding (Pedialyte, formula) 4-5 hrs post op (full feeds at 48 hrs)
- Some emesis or spitting up expected- Not projectile

304
Q

Failure to Thrive

Clinical Presentation (8)

A
  • Developmental delay (Non-vocal, Infantile posturing – stiffens and arches back, no stranger anxiety)
  • Poor Hygiene
  • GI and respiratory infections
  • Withdrawn (Dislikes physical contact, No eye contact, unresponsive facial expressions)
  • Self-stimulating behavior: rocking, excessive sucking, head-banging
  • Fussy, irritable
  • Abdominal distention-Constipation
  • Generalized weakness-Decreased muscle mass
305
Q

Failure to Thrive: Treatment (7)

A
  • Increase calories – formula with 24 cal/ounce and lipids
  • Limit juices, water – offer milk and formula
  • Do not force feed (offer for 35 minutes q2-3 hrs)
  • Consistent meal times
  • Feed in quiet environment
  • Establish eye contact
  • If severe, NG tube
306
Q

Cleft Lip

What is it?
Repair
Purpose of repair

A
  • congenital anomaly Involves 1 or more clefts in upper lip w/ varying degrees of nasal distortion

Repair: Surgical by 3-6 months of age; Cosmetic procedures modified later -4-5 years

Early repair promotes bonding and eases feeding

307
Q

Cleft Palate

What is it?
Repair
Purpose of repair

A
  • congenital anomaly from soft palate defect which may include hard palate & portions of maxillary sinus

Repair: multistage surgery at 6-8 months depending on severity (tonsils not removed)

Early repair enables more normal speech pattern development

308
Q

Cleft Lip/Palate: Feeding tips (6)

A
  • Monitor respiratory status while feeding
  • Feed in upright position
  • Feed slowly and burp every 1-2 ounces
  • Rest after each swallow of formula to allow for complete swallowing
  • Remove oral secretions carefully (Milk may come out nose)
  • Encourage bonding: touch-cuddle-hold
309
Q

Cleft lip/palate: Post-op care (7)

A
  • Monitor for respiratory distress
  • Keep objects out of mouth for 7-10 days including tooth brush
  • Arm restraints to prevent touching face
  • Feed child to reduce injury (liquids from a cup, soft foods from side of spoon)
  • Cleanse lip and suture line after feedings and PRN
  • Antimicrobial ointment (Neosporin) to suture line
  • Speech therapy referral
310
Q

Esophageal Atresia/Tracheoesophageal Fistula

Cause

3 C’s of symptoms

A

Cause: failure of esophagus to fully develop leading to abnormal communication b/w trachea and esophagus

3 C’s
- coughing (frothy cough, excessive drooling)
- choking (aspiration pneumonia, inability to pass NG tube)
- cyanosis w/ feeding (Respiratory distress (pneumothorax, atelectasis, laryngeal edema, tracheomalacia(weakness r.t compression by blind pouch)

311
Q

Esophageal Atresia/Tracheoesophageal Fistula: Surgery

Pre-op (4)
Post-op (4)

A

Preoperative care
- Suction: continuous to blind pouch to reduce stomach distention
- Elevate HOB into anti-reflux position (30 degrees)
- O2
- NPO immediately w/ IV I & O

Postoperative (depends on stage of repair)
- G-tube care and feedings (do not clamp or flush; elevate to air)
- Contrast study or esophagram done before oral feedings to determine integrity of esophageal anastomosis
- Monitor: aspiration, respiratory distress, infection
- 4 pre-op care items continue

312
Q

Celiac Disease

Cause

S/s (4)

A

Cause: autoimmune gluten sensitive enteropathy e.g. wheat, oats, rye, barley

S/s
- Bulky, malodorous, fatty, and frothy stools
- General malnutrition (FTT, muscle wasting, fatigue, anemia, anorexia, growth retardation)
- Behavioral changes (irritable, uncooperative, apathy)
- Abdominal distention and pain (aphthous ulcers)

313
Q

Appendicitis

Cause
Diagnostics (5)

A

Cause: inflammation and obstruction of appendiceal lumen due to harden fecal material; swollen lymphoid tissue; or pinworms

Diagnostics
- CBC (> 10000 WBC, elevated % of bands (left shift))
- C-Reactive Protein (elevated > 10)
- CT
- KUB (Kidney, Ureters, Bladder) x-ray
- Ultrasound (enlarged appendiceal diameter, wall thickening, inflammatory changes (fat streaks, phlegmon, fluid collection, and extraluminal gas)

314
Q

Appendicitis

S/s (7)

A
  • Periumbilical pain that migrates to the RLQ
  • pain is colicky constant, not intermittent (child may jump up and down)
  • Fever (typically low-grade)– no sore throat, no headache
  • abdominal distention and palpable mass
  • rebound tenderness at McBurney’s point (b/w anterosuperior iliac spine and umbilicus)
  • No appetite (anorexia, NV)
  • stooped posture
315
Q

Appendicitis

  • Complications (3)
  • Treatment (2)
A

Complications
- sepsis and hypovolemic shock (tachycardia, fever, tachypnea,
- necrosis (perforation or rupture w/ contamination of peritoneal cavity) - s/s: sudden relief then diffuse pain, pallor)-> abscess formation
- peritonitis (rigid abdomen and guarding)

Treatment
- Appendectomy: recommended (Laparoscopic vs Open Appendectomy); delayed 6-8 wks if unable to safely remove or difficulty expected
- Conservative management: antibiotics and IV fluids; avoid palpation unless necessary

316
Q

Intussusception

Cause
S/s (6)

A

Cause: Telescoping or invagination of the distal intestine which leads to obstructive symptoms in the proximal portion (may be r/t viral illness)

S/s
- Colicky abdominal pain
- NV
- Currant jelly stools or sausage-shaped mass
- Lethargy and hypersomnia
- Dance signs (empty RLQ)
- Knees to chest positioning

317
Q

Intussusception: Treatment (3)

A
  • IV Fluids and NGT decompression for stabilization
  • Air contrast enema
  • Surgical reduction with possible bowel resection if failed air reduction enema, Bowel perforation, or Shock/hemodynamic instability
318
Q

GI Red Flags (4)

A
  • Bilious Emesis = pyloric stenosis
  • Twisted Bowel- If it is twisted, you have 6 hours to save it
  • Rigid abdomen = peritonitis
  • Free air visible on x-ray in abdominal cavity = perforation
319
Q

Chronic nonspecific diarrhea (CNSD)

What is it?
Effects (3)

A

irritable colon of childhood and toddlers’ diarrhea which may be r/t sorbitol (artificial sweeteners) or excessive juice for > 14 days

Effects: no blood in stools, no enteric infection, no malnutrition

320
Q

Diarrhea: Stool characteristics and potential problem

  • Watery explosive stools
  • Foul-smelling greasy bulky stools
  • Diarrhea after cow’s milk, fruits, cereal intro (2)
  • Neutrophils or RBCs in stool (2)
  • Eosinophils (2)
  • Gross blood or occult blood (3)
A
  • Watery explosive stools = glucose intolerance
  • Foul-smelling greasy bulky stools = fat malabsorption
  • Diarrhea after cow’s milk, fruits, cereal intro = enzyme deficiency or protein intolerance
  • Neutrophils or RBCs in stool = bacterial gastroenteritis or IBD
  • Eosinophils = protein intolerance or parasitic infection
  • Gross blood or occult blood = shigella, campylobacter, E-coli
321
Q

Gastroesophageal Reflux Disease

Diagnostics (7)

A
  • Modified Barium Swallow (MBS) Study
  • Upper GI series for anatomic abnormalities
  • 24-hr intraesophageal pH monitoring – not helpful for weak acid (4-7 pH seen in kids)
  • Endoscopy w/ biopsy for esophagitis, strictures, Barrett esophagus; excludes Crohn’s
  • Scintigraphy for radioactive substances in esophagus to assess gastric emptying (determine if aspiration from reflux OR poor oropharyngeal muscle coordination)
  • CBC (anemia)
  • hypoproteinemia
322
Q

Celiac Disease

  • Diagnostics (2)
  • Treatment (3)
A

Diagnostic:
- Tissue Transglutaminase IgG or IgA Antibody
- Endoscopy (flattened villi)

Management
- Gluten free diet (No wheat, rye, barley, and oats; cereal, baked goods; READ LABELS)
- Substitute rice, corn, millets for grains
- Avoid high fiber (nuts, raisins, raw veggies, and fruits) while bowel inflamed

323
Q

Retinoblastoma

Diagnosis (2)
Treatment (5)

A

Diagnostic Testing
- ophthalmoscopy
- Blood and tumor samples – test for RB1 gene mutations

Treatment
- eye enucleation (if unilateral)
- chemotherapy
- brachytherapy, radiation
- photocoagulation (laser beam to destroy retinal BVs i.e. nutrition of tumor)
- cryotherapy (freeze tumor and destroys microcirculation of tumor and cells through microcrystal formation

324
Q

Osteosarcoma

Diagnosis (4)
Treatment (3)

A

Diagnostic Testing
- MRI of affected bone
- Plain radiograph - Radial ossification in soft tissue gives sunburst appearance of tumor
- chest CT b-c metastasis to lung usually
- increased alkaline phosphatase.

Treatment:
- Surgery – limb salvage or amputation then Post-op care: continuous passive motion; TCA (amitriptyline) for phantom pain
- Chemotherapy
- Thoracotomy if pulmonary metastasis

325
Q

Neuroblastoma

Key s/s (6)

A
  • firm, nontender abdominal or chest mass that crosses midline
  • Compression of kidney, ureter, bladder (urinary frequency or retention)
  • urine catecholamines (secreted by tumor on adrenal gland)
  • supraorbital ecchymosis
  • periorbital edema (raccoon eyes) or Proptosis (bulging eyes)
  • chest tumor (Dyspnea, stridor, dysphagia, Horner syndrome (ptosis, miosis, anhidrosis))
326
Q

Effects of Cancer Treatment: Tumor Lysis Syndrome

Nursing Care (5)

A

Nursing Care
- monitor frequent serum chemistries and urine pH
- strict I&O
- aggressive IV fluids
- For hyperkalemia, furosemide
- For hyperuricemia, allopurinol (decrease formation) or rasburicase (convert to soluble allantoin)

327
Q

Effects of Cancer Treatment: Altered Nutrition
(Anorexia, NV)

Related to? (3)
Patient Education (4)

A

Related to: chemo, radiation, steroids (increased appetite)

Parental education
- avoid strong smells
- relax pressure placed on eating.
- Allow child to be involved in preparation and selection to make food appealing
- give chemo at night

328
Q

Effects of Cancer Treatment: Infection

Nursing Care (6)

A
  • Handwashing
  • Monitor s/s of infection or sepsis (fever)
  • G-CSF Injections if ANC < 500
  • Cultures and antibiotics as soon as possible for 7-10 days
  • Protective isolation
  • Prophylaxis against Pneumocystis pneumonia (trimethoprim-sulfamethoxazole)
329
Q

Hematopoietic Stem Cell Transplant (HSCT)

Procedure (2)
Post-op (4)

A

Procedure
- Transfuse PRBCs, and platelets as indicated
- Autologous (self-donation) vs Allogeneic (family or volunteer, umbilical cord blood) stem cells

Post transplant
- Give G-CSF if ANC still low
- give calcineurin inhbitor w/ chemo to prevent graft versus host disease
- Minimize pressure in dependent areas (frequent movement, pressure-relieving)
- Promote healing (frequent sitz baths to perianal area and protective skin barriers i.e hydrocolloid dressing or occlusive ointments)

330
Q

General medications for Skin disorders (5)

A
  • Antihistamines- diphenhydramine, hydroxyzine
  • Anti Inflammatory- hydrocortisone creams (topical for allergic dermatitis and pruritus)
  • Antibiotics (topical or parenteral after empiric therapy; or shampoo or lotion)- same for antivirals, antifungals
  • Emollients (lotion, cream, ointment)- retain moisture in skin (gel or powder if too much moisture already); mupirocin (nares)
  • Silver sulfadiazine - antimicrobial to increase healing of burns
331
Q

Contact Dermatitis (Diaper Rash & Candida)

Risk factors (3)
S/s
Treatment (4)

A

Risk factors
- antibiotic use (r/t diarrhea side effect and altering of stool microbials)
- moist areas (urine promote fecal enzyme activity; increased friction, abrasion damage, microbial counts)
- exposure to irritants (urine, feces, soap, wipes, ointments)

S/s: red and bumpy rash (maculopapular) on convex surfaces due to candida

Treatment/Prevention
- observe closely for liquid stools
- Protective ointment (zinc oxide, cornstarch) - no talcum powder; no need to remove completely w/ diaper change
- Keep area dry (superabsorbent diapers
- Apply clotrimazole (Med for Candida Albicans- Yeast)

332
Q

Seborrheic Dermatitis

Cause
Locations (5)
Diagnosis
Treatment (2)

A

Cause: Malassezia yeast due to increased sebum production in early infancy or during puberty

Locations
- Scalp (cradle cap- most common)
- Eyelids (blepharitis)
- External ear canal (otitis externa)
- Nasolabial folds
- Inguinal region

Diagnosis: based on appearance and location or crust or scales (thick, adherent, yellowish, scaly, oily patches w/ or w/o pruritus)

Treatment
- Mild or baby shampoo daily w/ mild soap and brush
- If severe, medicated shampoo (sulfa and salicylic acid)

333
Q

Contact Dermatitis (Poison Ivy)

Cause
S/s
Treatment (6)

A

Cause: sumac from poison oak or poison ivy after two exposures (not spread person-to-person)

S/s: red, raised pinkish-reddish pruritic papules

Treatment
- Cool compress
- Treat pruritus (Antihistamines OR Topical or oral steroids)
- Rinse immediately with cold water to remove irritant b-c penetrates more the longer it stays
- lesions heal w/o treatment in 10-14 days
- DO NOT harshly scrub exposed skin b-c will remove protective skin oil and dilute urushiol and allow spreading
- Do not allow child to scratch lesion b-c can cause secondary infection

334
Q

Atopic Dermatitis: Eczema

Cause (4)
S/s (3)

A

Cause (not contagious)
- stress
- weather (better in humidity; worse in fall and winter)
- autoimmune (esp. IgE elevation)
- fam hx of AD, asthma, allergies (food, rhinitis)

S/s:
- inflammation (red, swelling, pain)
- pruritus
- dry/rough/thick skin

335
Q

Atopic Dermatitis: Eczema

Infantile (2)
Childhood (2)
Adolescent (3)

A

Infantile
- begins at 2-6 months; resolves at any age usually 3 yrs
- Generalized, esp. cheeks, scalp, trunk, and extensor surfaces of extremities

Childhood
-begins around 2-3 yrs., usually seen by 5 years
- Flexural areas (antecubital & popliteal fossa, neck) plus wrists, ankles, & feet

Preadolescent/ Adolescent
- Begins at 12 years and may continue indefinitely
- Mainly face, sides of neck, hands, feet,
- on antecubital and popliteal fossae to lesser extent

336
Q

Impetigo

Cause
S/s (3)
Transmission
Treatment (3)

A

Cause: bacterial (strep or staph) infection of skin r/t scratching

S/s:
- honey-crusted vesicle
- pruritus
- inflammation (red, swelling)

Transmission: contact (from place to place & person to person)

Treatment
- antibiotics (PO penicillin, IV, and occasionally topical mupirocin)
- Avoid scratching b-c can cause spread and is contagious
- For pruritus, use hydroxyzine (Atarax) or diphenhydramine.

337
Q

Dermatophytoses

Treatment (6)

A

Treatment (may take months)
- Topical meds–Monistat, Lotrimin
- Oral – Griseofulvin (take w/ high fat food; watch for leukopenia, liver, photosensitivity, insomnia))
- Itraconazole- (Sporanox- watch liver)
- return to school after treatment has begun
- avoid sharing hygiene products
- Selenium sulfide shampoos, ( decrease infection and fungal shedding)

338
Q

Candidiasis (candida albicans)

S/s (4)
Treatment (2)

A

S/s:
- inflammation (Erythema, edema, and heat)
- pruritus
- White patches in mouth (thrush)
- red, discrete diaper rash (diaper dermatitis)

Treatment
- Nystatin (Mycostatin)-liquid or oral, do not feed after giving)
- Amphotericin B for advanced cases

339
Q

Lyme Disease

Cause
Treatment (5)
Prevention (2)

A

Cause: tick infected with Borrelia burgdorferi bites for 1-2 hrs

Treatment
- antibiotic (2‑ to 3‑week course) for clients who have confirmed disease
- doxycycline (may use erythromycin too) for children older than 8 years
- amoxicillin or cefuroxime for children under 8 years. (cefuroxime for children who have an allergy to penicillin)
- observe for at least 30 days
- remove tick w/ forceps or tissue

Prevention
- use repellents (diethyltoluamide (Deet) and permethrin)
- Vaccine approved for 15-70-year-olds

340
Q

Lyme Disease

Stage 1 (3)
Stage 2 (3)
Stage 3 (3)

A

Stage 1
- 3 to 30 days following bite
- erythema migrans(bulls eye rash) at site
- chills, fever, itching, headache, fainting, stiff neck, muscle weakness

Stage 2
- occurs 3 to 10 weeks following bite
- Systemic involvement begins (neurologic, cardiac and musculoskeletal)
- paralysis or weakness in the face, muscle pain, swelling in large joints (knees), fever, fatigue, splenomegaly

Stage 3
- 2 to 12 months following bite
- Systemic involvement is advanced (musculoskeletal pain that includes the muscles, tendons, bursae and synovial); possible arthritis, abnormal muscle movement and weakness, numbness and tingling
- late neurological problems and cardiac complications (cerebral ataxia, encephalopathy, deafness, speech problems)

341
Q

Rocky Mountain Spotted Fever

Cause
S/s (4)
Major complications (2)
Treatment (2)

A

Cause: tick bite leads to infestation caused by Rickettsia rickettsii

Symptoms
- fever
- Headache
- anorexia
- rash (incubation 2-14 days)

Major complication
- hemorrhagic lesion (if untreated rash)
- risk for thrombus, necrosis, edema, death

Treatment: Chloramphenicol (drug of choice) or tetracycline

342
Q

Prevention of Tick Bites (6)

A
  • Wear long-sleeved shirts, long pants tucked into long socks, and hat when walking in tick-infested areas
  • Wear light-colored clothing to make ticks more visible if they get onto child
  • Check children for the presence of ticks after being in high-risk or tick-infested areas (save tick for later ID)
  • Follow paths vs walking in tall grass and shrub areas
  • Apply insect repellents w/ diethyltoluamide (DEET) and permethrin before possible exposure to areas where ticks are found; also use on pets (use with caution in infants and small children)
  • Keeping yards at home trimmed and free of accumulating leaves and other brush
343
Q

Scabies

Cause
S/s (2)
Treatment (4)

A

Cause: Scabies mites that burrows into the stratum corneum of epidermis and deposits eggs and excrement.

S/s: itching; black dot at end of burrow in intertriginous areas (b/w digits, antecubital, popliteal, inguinal)

Treatment
- anti-scabies med (Elimite (permethrin cream) or Lindane (Kwell))) - lindane is neurotoxic and contraindicated
- Apply over body, head and neck multiple times and overnight
- for pruritus, oral antihistamines or topical corticosteroid creams
- Treat family members and environment b-c spread by contact

344
Q

Anaphylaxis: Epinephrine

Dose (2)
Side effects (4)
Note

A

Dose
- EpiPen Jr (0.15 mg) IM for child 8 to 25 kg (17.5-55 lbs.)
- EpiPen (0.3 mg) IM for child > 25 kg (55 lbs.)

Side effects
- tachycardia
- hypertension and headache
- irritability and tremors
- nausea

Notes
- give ASAP then send to hospital

345
Q

Pediculosis Capitis (lice)

Cause
S/s (3)
Transmission

A

Patho: Infestation on lice and eggs usually in scalp.

S/s
- Scratching (may be only symptom)
- Nits- ¼ - ½ inch from scalp (grayish or whitish)
- red lesions on scalp

Transmission: direct contact (can jump but not fly) via sharing personal items

346
Q

Varicella Zoster (Chicken Pox)

S/s (2)
Transmission (3)

A

S/s
- lesions (macular, papular, vesicles, pustules, crust (MPVPC)) which are red and itchy in clusters
- flu-like symptoms

Transmission
- contact, airborne, droplet
- contagious 1-2 days before onset until lesions are crusted (5-7 days)
- Incubation: 2-3 weeks; 14-21 days

347
Q

Rubeola (Measles)

Complications (4)
Treatment (2)

A

Complications
- Pneumonia,
- Encephalitis,
- Diarrhea
- Obstructive laryngitis (croup)

Treatment
- Stay home and isolate
- supportive w/ vitamin A therapy

348
Q

Rubella (German Measles)

Transmission (2)
Complications (2)
Treatment

A

Transmission
- Incubation 14-21
- Isolation- contact and Droplet (Nasopharyngeal secretions and body fluids)

Complications (less severe than rubeola unless pregnant):
- arthritis or arthralgia
- Congenital Rubella- growth delays, blindness, cardiac problems, deafness, intellectual disabilities (TERATOGENIC)

Treatment: supportive

349
Q

Roseola Infantum (Exanthem Subitum)

Cause
S/s (3)
Transmission (2)
Treatment

A

Cause: Human Herpesvirus 6 in 3-36 month olds

S/s
- abrupt high fever (risk for febrile seizures) for 3-5 days
- maculopapular rash (after fever starting at neck and spreading up and down) disappears after 1-2 days
- Other: lymphadenopathy, cough, coryza

Transmission
- contact and droplet
- Incubation 5-15 days

Treatment: Antipyretics (avoid aspirin b-c viral infection and risk for reyes)

350
Q

Scarlet Fever

Cause
S/s (2)
Treatment
Complications (6)

A

Cause- GABHS carried by direct contact

S/s
- Rash- red, fine located in groin, neck and axillary
- Strawberry tongue

Treatment: complete antibiotics & supportive therapy

Complications (spread of infection)
- Sinusitis
- Abscess
- Meningitis
- Osteomyelitis
- Rheumatic fever
- AGN

351
Q

Erythema Infectiosum (Fifth Disease)

Cause
S/S (3)
Incubation
Complications

A

Cause: parvovirus

S/s:
- slapped cheek appearance
- fever
- runny nose

Incubation: 14-21 days

Complication: aplastic crisis esp in pregnant, sickle cell, or immunocompromised

352
Q

Conjunctivitis

Cause
Transmission
Treatment (5)

A

Cause: bacterial, viral, or allergic

Transmission: direct contact if viral or bacterial

Treatment
- avoid scratching or touching eye
- If viral, clears on its own in 7 to 14 days.
- If bacterial, Starts in one eye, spreads to the other so clear with antibiotics
- If Allergic, clears with allergy medications.
- use warm moist cloth to remove crusted secretions (inner to outer canthus)

353
Q

Otitis Media (acute, chronic, OME)

Cause
Risk Factors (5)

A

Cause: obstruction or partial obstruction of eustachian tube and nose leads to accumulation of secretions in middle ear which impairs ciliary transport in tube and inhibits drainage

Risk factors
- smoking
- bottle propping during feeding (breastfeeding is protective)
- Conditions (down syndrome, cleft palate)
- viral infection esp EBV and influenza
- enlarged adenoids or tonsil tumors

354
Q

Otitis Media (acute, chronic, OME)

Treatment (5)
Prevention (3)

A

Treatment
- Amoxicillin Clavulanate 80-90 mg/kg/day OR Azithromycin
- Cephalosporins (2nd line)
- Myringotomy, Tympanoplasty, pressure equalizing tube (PET)- if chronic (tubes fall out on therir own)
- keep ears dry (sterile alcohol cotton swab)
- For symptoms, corticosteroid or benzocaine drops, pain relievers

Prevention
- avoid lakes and shampoos
- Pneumococcal Vaccine- Prevnar, HIB, strep
- influenza vaccine for > 6 m

355
Q

Sunburns

UVA vs UVB
Prevention (4)

A

UVA: shorter, high frequency cause aging
UVB: r/t tanning and burning

Prevention
- Avoid midday exposure (10am-2pm)
- Use a high SPF
- Wear protective clothing (Wide brimmed hat, cotton with a tight weave clothing)
- avoid sunscreens <6 months (just keep them out of sun)

356
Q

Prognosis of Burn Injury

Factors (8)

A
  • Extent of injury (Life threatening if 10% TBSA; If >30% TBSA, systemic response w/ capillary permeability)
  • Depth of injury
  • Location of wounds
  • Age (poor in tiny baby b-c thin skin esp under 6 months)
  • General health (chronic illness complicate healing)
  • Causative agent
  • Respiratory involvement
  • Concomitant injuries
357
Q

Partial thickness burn: 1st degree

Wound appearance (3)
Wound Sensation
Course of Healing (2)

A

Wound appearance
- epidermis intact w/o blisters
- erythema
- blanches w/ pressure

Wound Sensation: painful w/o systemic effects

Course of Healing
- discomfort for 48-72 hrs
- desquamation in 3-7 days w/o scaring

358
Q

Partial thickness burn: 2nd degree

Wound appearance (3)
Wound Sensation (2)
Course of Healing (2)

A

Wound appearance
- wet, shiny, weeping surface
- blisters
- blanches w/ pressure

Wound Sensation
- very painful and sensitive to touch and air currents
- systemic effects (capillary damage and edema, anemia, SNS activation)

Course of Healing
- superficial heals < 21 days (> 21 for deep)
- various amounts of scarring

359
Q

Full-thickness burn: 3rd degree

Wound appearance (3)
Wound Sensation
Course of Healing

A

Wound appearance
- variable color (deep red, white, black, brown)
- thrombosed vessels visible (nerves, sweat glands, hair follicles destroyed)
- no blanching

Wound Sensation: insensate (decreased pinprick sensation)

Course of Healing: needs autograting

360
Q

Full-thickness burn: 4th degree

Wound appearance (3)
Wound Sensation
Course of Healing (2)

A

Wound appearance
- color variable w/ dull and dry wound
- extremity movement limited
- charring visible in deepest areas (involves bone, muscle, fascia)

Wound Sensation: insensate

Course of Healing
- amputation likely
- autograft for healing

361
Q

Care for Major Burns (6)

A
  • Stop burning (smother flames, place horizontally, roll; remove clothes and jewelry)
  • Airway management (NPO, O2 therapy)
  • Fluid Replacement (lots of diuresis w/ burns; IV fluids of crystalloid then colloid)
  • Prevent infection (Cover wound; high cal/protein diet w/ zinc, vit A and C; topical antimicrobials; tetanus toxoid; debride)
  • Cover the burn with a clean and dry cloth to prevent hypothermia, decrease pain from air contact, and prevent contamination (do not let two burned surfaces touch)
  • Pain management (after other stuff; use IV vs subQ/IM b-c circulatory collapse and edema)
362
Q

Care for Minor Burns (9)

A
  • Stop the burning process AND Remove clothing or jewelry
  • Apply cool water soaks or cool water (no ice b-c can cause burns AND circulatory collapse
  • Flush chemical burns with large amounts of water
  • Clean with mild soap/tepid water (keep wound bed clean and moist and cover w/ clean cloth)
  • Use antimicrobial ointment (silver sulfadiazine, neosporin)
  • No greasy lotions or butter
  • Provide warmth
  • Provide analgesia!!!
  • Immunize for tetanus if > than 5 years since last shot
363
Q

Major complications of burns (4)

A
  • respiratory tract injury (erythema, pulmonary edema, hoarseness, bacterial pneumonia
  • burn shock (fluid loss, reduced cardiac output, hypotension, tachycardia, decreased LOC, hyperthermia to hypothermia)
  • local or systemic sepsis r/t fertile field for bacterial growth
  • increased intra-abdominal pressure r/t larger than calculated number of fluids in resuscitation
364
Q

Otitis Media (acute, chronic, OME)

Complications (6)

A
  • Cholesteatoma (epithelial lining forms scales and erodes middle ear)
  • Tympanosclerosis (eardrum scarring)
  • Adhesive OM (thickening of mucous membranes)
  • Meningitis
  • Mastoiditis
  • hearing loss
365
Q

Otitis Media (acute, chronic, OME)

S/s (4)

A
  • Fever (risk for febrile seizures)
  • otalgia (ear pain)- pulling at ear, turning head side to side
  • Purulent discharge (otorrhea)
  • bulging tympanic membrane seen w/ otoscope (feeling of fullness)
366
Q

Rubella (German Measles)

S/s (6)

A
  • Rash (on face spreads cephalocaudally) for 2-3 days
  • lymphadenopathy)
  • forchheimer spots on soft palate
  • coryza (Nasopharyngeal secretions and body fluids)
  • headache and eye pain
  • Other: fever, nausea, anorexia, sore throat
367
Q

Rubeola (Measles)

Cause
S/s (3)
Transmission (3)

A

Cause: RNA virus

S/s
- 3 C’s: coryza (runny nose), bad cough, conjunctivitis (red eyes)
- white Koplik spots in mouth
- rash at hairline spreads cephalocaudally over 3 days

Transmission
- contact and droplet isolation
- Incubation: 8-12 days incubation
- infectious 3-5 days before and 4 days after rash

368
Q

Varicella Zoster (Chicken Pox)

Complications (3)
Treatment (3)

A

Complications: encephalitis, internal chicken pox, shingles

Treatment:
- avoid scratching to prevent superinfections
- For pruritus, Antihistamine (diphenhydramine or hydroxyzine)
- For Immunocompromised or severe cases, use Acyclovir or immune globulin (VZIG) within first 96 hours

369
Q

Pediculosis Capitis (lice)

Treatment (4)

A
  • wash hair w/ Permethrin (NIX) or Pyrethrum (RID) OTCand leave for a while then comb nits out (malathion Rx for severe)
  • Wash everything in hot water
  • spray down everything except child in insecticide
  • put stuffed animals and non washable items in bags then in heat for 14 days
370
Q

Dermatophytoses

Locations (4)
Transmission

A

Locations (round w/ central clearing)
- Tinea corporis = RINGWORM OF SKIN
- Tinea capitis = SCALP
- Tinea cruris = JOCK ITCH
- Tinea pedis = ATHLETE’S FOOT (maceration and fissuring b/w toes)

Transmission: person-to-person OR animal-to-person

371
Q

Atopic Dermatitis: Eczema

Treatment (5)
Prevention (3)

A

Treatment
- Hydrate skin ~cool or warm tepid baths, mild soap, emollient (Eucerin), humidifier
- Relieve pruritus ~oral antihistamine; avoid scratching
- Reduce flare-ups ~ topical corticosteroids, systemic antibiotics, coal tar
- Cool wet compresses ( soothing and antiseptic protection)
- Avoid heat

Prevent/control infection
- reduced exposure to allergens (i.e wool, rough fabrics, latex)
- topical immunomodulators (i.e., tacrolimus)- give prior to flare up
- avoid scratching

372
Q

General Skin Alterations

Treatment (7)

A

Treatment
- hygiene (hand hygiene, clean wounds, chlorine bath)
- avoid (scratching, squeezing, sun, and other irritants)
- cool compress (or warm)
-treat causative organism- antibiotics, antifungal, antiviral, anti (organism)
- stay hydrated
- Treat Fever (antipyretics, avoid heat)
- Treat pruritus (antihistamine-topical OR oral (do not overdose)- Diphenhydramine, Hydroxyzine); oatmeal baths; steroids)

373
Q

Stress: S/s in Children (7)

A
  • Headache
  • Stomachache
  • Enuresis
  • Encopresis (fecal incontinence)
  • Self-harm
  • Physical Violence
  • Psychosocial- anxiety, depression, anger, irritable
374
Q

Stress: Management (6)

A
  • Play
  • Exercise
  • Breathing exercises
  • Meditation/prayer
  • Talking to adult or peer
  • Journaling or drawing
375
Q

ACEs(Adverse Childhood Events)

What is an ACE? (2)
Impact (3)

A
  • Experiencing or witnessing violence, abuse, or neglect
  • Exposure to mental illness (including suicide), substance abuse, or incarceration.

Impact:
- Mental health (depression, suicidality, stress)
- Physical health (poor self- rated health, heart disease, cancer, chronic pulmonary disease, skeletal fractures, liver disease, obesity)
- Health-related behaviors (alcoholism, illicit drug abuse, smoking, high numbers of sexual partners, adolescent pregnancy)

376
Q

Maslow’ Hierachy of Needs

A

Physiological
Safety
Love/belonging
Esteem
Self-actualization

377
Q

Child Maltreatment: Nursing Care (8)

A
  • mandated reporter (Do not make promises you cannot keep)
  • Remove the child from potential harm (priority)
  • Observe (Bruises of different stages and unusual areas; Glove or stocking like burns; Spiral fractures; head injury)
  • use Clear and objective documentation (pictures)
  • Forensic Interview parents and child separately
  • Be direct, honest, professional, supportive to child and family (avoid asking the child probing questions)
  • Do not express shock or criticism
  • do full head to toe assessment if physical abuse
378
Q

Child Maltreatment: Types (6)

A
  • Physical abuse (abusive head trauma)
  • physical neglect (Deprivation of food, clothing, shelter, supervision, medical care, and education)
  • Emotional neglect (Lack of affection, attention, and emotional nurturance)
  • Emotional abuse or psychological maltreatment (Destruction or impairment of child’s self-esteem )
  • Sexual abuse (s/s: substance use, depression, withdrawn mood, suicidal, somatic complaints)
  • Medical Abuse (Munchausen by proxy)
379
Q

Factors that contribute to child maltreatment (3)

A
  • parental (Negative childhood, social isolation, Low self esteem)
  • environmental (Chronic stress, Unemployment, Divorce, Poverty, Drug Addiction)
  • child (disability, < 1 yrs old, premature)
380
Q

Warning Signs of abuse (8)

A
  • Physical evidence including previous injuries (various stages of healing)
  • Conflicting stories about the “accident” or inconsistent history with injury observed (esp. if does not match developmental level)
  • Cause of injury blamed on sibling or other party
  • chief complaint other than the one associated with signs of abuse (e.g., cold when there is evidence of first- and second-degree burns)
  • Inappropriate response of caregiver (exaggerated or absent emotional response, refusal to sign for additional tests or agree to necessary treatment, excessive delay in seeking treatment, or absence of parents for questioning)
  • Inappropriate response of child (little or no response to pain, fear of being touched, excessive or lack of separation anxiety, indiscriminate friendliness to strangers)
  • Repeated visits to emergency facilities with injuries (or previous reports of abuse)
  • Parent or caregiver report of being gone and finding the child unresponsive, indicating absence during the supposed event that resulted in harm
381
Q

Apparent Life-Threatening Event (ALTE)

S/s (3)
Risk factors (3)
Diagnostics
Nursing Care (2)

A

S/s: apnea, cyanosis, lack of muscle tone or choking

Risk factors: gastric reflux, seizures, infections

Diagnostics: Blood cultures, urine cultures, CBC, glucose, electrolytes, EEG, EKG, sleep study for apnea

Nursing Care
- Prepare for tests
- Monitor for events esp apnea monitor

382
Q

SIDS (Sudden Infant Death Syndrome)

Diagnosis
Risk Factors (7)

A

Diagnosis: exclusion

Risk Factors
- Maternal health (substance abuse, poor prenatal care)
- maternal age less than 20 years
- Twins
- Premature or SGA, LBW
- Respiratory or CNS distress (Persistent apnea, Bronchopulmonary dysplasia (BPD))
- Family history
- Environmental risk factors (unsafe environment)

383
Q

Eye Injuries

Management (3)

A
  • Foreign object- Do not remove penetrating objects
  • Chemical burns- rinse for 20 minutes
  • Hematoma- use flashlight to check for gross hyphema
384
Q

Poisoning: Corrosives

Ex. strong acid or alkaline (bleach, dishwasher liquid, detergent)

S/s (3)
Treatment (3)

A

S/s- burning from mouth and GI tract, drooling, edema of lips

Treatment
- Assess child then call poison control
- Dilute with water or milk
- Do not neutralize or cause emesis

385
Q

Poisoning: Hydrocarbons

Ex. Gasoline, Kerosene, Lighter fluid- Let off fume

S/s (2)
Treatment (3)

A

S/s: respiratory symptoms (gag, cough, choke), chemical pneumonia

Treatment
- Assess child then call Poison control
- Only gavage with cuffed ET tube in place
- Treat symptomatically

386
Q

Poisoning Interventions:

  • ASA/Aspirin (3)
  • Acetaminophen
  • Narcotics
  • Benzodiazepine
  • Iron (2)
  • Lead
A

ASA/Aspirin
- Gastric decontamination/lavage (Ipecac- NO LONGER USED)
- Sodium Bicarbonate for acidosis
- Activated charcoal (airway must be intact)

Acetaminophen
- N-acetylcysteine (mucomyst)

Narcotics
- Naloxone

Benzodiazepine
- Flumazenil

Iron
- Gastric decontamination/lavage
- chelation

Lead
- chelation

387
Q

Lead Poisoning

Cause (3)
Impact (5)

A

Cause:
- lead paint deterioration in old home (ingestion or inhalation)
- ingestion (hot water dissolves lead fast, open cans, more absorbed on empty stomach
- vertical transfer

Impact
- GI (NV, constipation, abdominal pain)
- Renal
- CNS (developmental delay, low IQ, behavioral problems
- Hematologic (iron deficiency anemia b-c interferes w/ iron binding)
- stored in bones and teeth (competition w/ calcium)

388
Q

Lead Poisoning

Four levels and management (4)

A
  • BLL of 10 mcg/dl or greater (level of concern)
  • BLL > 20 mcg/dl (Clinical management – find source)
  • BLL > 45 mcg/dl (Chelation therapy-Ca EDTA and succimer, or BAL; assess urine output and renal function
    *no BAL if peanut allergy or liver problem
  • BLL >70 immediate management in hospital is required
389
Q

Spina Bifida

Types (2)
Prevention (2)

A

Types

  • Meningocele—Hernial protrusion of a saclike cyst of meninges filled with spinal fluid but no neural elements (incomplete paralysis w/ neurogenic bladder(overflow w/ drippling) and bowel dysfunction)
  • Myelomeningocele (meningomyelocele)—Hernial protrusion of a saclike cyst containing meninges, spinal fluid, and a portion of the spinal cord with nerves (Abnormal body function w/ malformations at or below lesion)- more severe

Prevention
- folic acid begin 3 prior to pregnancy and continue in 1st trimester
- detect in utero w/ CVS if elevated AFP

390
Q

Spina Bifida

Nursing Care (8)

A
  • Keep sac free of stool and urine (no infection)
  • keep sac free from drying (Sterile, saline soaked gauze)
  • Position baby on stomach with knees flexed under or elevate foot of bed w/o clothes or diaper (no pressure)
  • Assess neurological function (movement of extremities, skin response, anal reflex, head circumference)
  • Promote parent-infant bonding (caress, stroking)
  • Keep baby NPO for surgery in first 24-72 hrs
  • No rectal temps b-c risk for irritation or prolapse
  • ALWAYS Latex precautions (b-c increased risk for latex allergies; no kiwi, banana, avocado, milk)
391
Q

Spina Bifida: Long-term Collaboration (5)

A
  • realistic goals
  • GU-Clean intermittent catheterization and antispasmodics
  • GI-Bowel training program
  • Neurological: Developmental delays, Increased ICP,epilepsy
  • Musculoskeletal- ambulation, ROM, splints, walking assistance (risk for tethered cord, club foot, scoliosis/kyphosis)
392
Q

Cerebral Palsy

What is it?
Incidence (2)

A

Non-progressive injury to the motor centers of the brain causing neuromuscular problems of spasticity or dyskinesia (ID and seizures risk)

Incidence
- Most common cause of chronic disability
- diagnosed in first 1-2 yrs

393
Q

Risk factors for Cerebral Palsy (6)

A
  • Anoxic injury before, during, after birth (brain malformations, NAT)
  • Maternal infections (perinatal infection (i.e. ToRCH))
  • Kernicterus (high levels of unbound bilirubin- yellow staining of brain cells may result in encephalopathy)
  • Trauma (MVA, abuse, intrauterine insults)
  • Prematurity (most common), LBW
  • Postnatal infections (encephalitis, meningitis)
394
Q

Types of Cerebral Palsy

Spastic (2)
Dyskinetic (3)
Ataxia (2)

A

Spastic (may be Hemiplegia)
- rigidity, hypertonia
- exaggerated DTR, primitive reflexes, contractures and spinal deformities

Dyskinetic
- Athetoid—Chorea (involuntary, irregular, jerking); slow, wormlike, writhing movements; poor voluntary muscle control
- Dystonic—Slow, twisting movements; arched back
- Involvement of the pharyngeal, laryngeal, and oral muscles = drooling and dysarthria (imperfect speech articulation)

Ataxia
- Wide-based gait
- Rapid, repetitive movements performed poorly

395
Q

Cerebral Palsy: General Manifestations (6)

A
  • Persistent neonatal reflexes after 6 months (Moro, palmar plantar, tonic neck)
  • Delayed developmental milestones (may have normal intelligence. Know your patients’ baseline)
  • early preference for one hand
  • Poor suck/ tongue thrust
  • Spasticity w/ scissoring of legs or toe walking: trouble diapering
  • Involuntary &/or asymmetrical movements
396
Q

Cerebral Palsy: Medications (4)

A
  • Baclofen- muscle relaxant for spasticity
  • Diazepam (Valium)- for seizures
  • Botulism toxin A- release tight muscles to allow ambulation w/ orthoses
  • Anti-epileptics (Tagretol, Depakote, gabapentin)- if had seizure in past
397
Q

Cerebral Palsy: Complications (6)

A
  • Musculoskeletal (Contractures, fractures, deformities (upper, spinal, foot), Hip subluxation/dislocation, gait disorders)
  • Neurological (seizures, ADHD)
  • Sensary (Hyper or hypo, visual, hearing)
  • Respiratory (risk for aspiration r/t poor oral musculature)
  • Immobility sequelae (skin breakdown, constipation)
  • Nutrition (FTT r/t dysarthria; may need G-tube)
398
Q

Hearing Impairment

Classifications (2)
Diagnosis (6)

A

Deaf: a person whose hearing disability precludes processing linguistic information with or without hearing aid

Hard of hearing: generally able to hear with hearing aid

Diagnosis
- Profound deafness likely to be diagnosed in infancy (does not follow when someone speaks; no startle or blink reflex to noise)
- FOR CHILDREN 6-19 yrs, diagnosis usually at entry into school
- Failure to localize a source of sound by 6 months old
- Absence of babble or voice inflections by 7 months old
- Absence of well-formed syllables (da, an, yaya) by 11 months
- Failure to develop intelligible speech by 24 months old

399
Q

Sensory Impairment: Prevention

All (3)
Hearing (2)

A

All
- Prenatal preventive measures (prenatal care, avoid infections)
- Early and periodic Screening
- MMR vaccine

Hearing
- treat otitis media
- Avoid exposure to noise pollution (high or continuous noise)

400
Q

Hearing Impairment: Communication Tips (6)

A
  • Lip reading
  • Cued speech (hand signals to help child distinguish b/w words that look alike from lips)
  • Speech language therapy
  • Additional aids (sign language, picture board, flashing lights, dogs, TTD)
  • Supplement with visual and tactile media
  • make sure they can see you before any procedure
401
Q

Visual Impairment

Classifications (2)

A
  • Partially sighted (Acuity of 20/70 to 20/200): education usually in public school system
  • Legal blindness (Acuity of 20/200 or less): legal as well as medical term
402
Q

Types of Visual Impairments (5)

A

Myopia- nearsighted (refraction error where light falls in front of retina)- Tx: glasses

Hyperopia- farsighted (refraction error where light falls beyond retina)- Tx: glasses

Strabismus (may or may not be refractive)- testing important in children, cover uncover, corneal light reflex (Tx- vision occlusion therapy, surgery)

Amblyopia- lazy eye

Astigmatism –unequal curves

403
Q

Visual Impairment: Nursing Care (8)

A
  • Screen all children for visual acuity
  • Suspect in a child whose pupils do not react to light
  • Education (Braille, Audio books and learning materials)
  • Provide reassurance during all treatments
  • Orient child to surroundings
  • consistent Treatment team members
  • provide safe environment (remove clutter, do not rearrange furniture)
  • encourage nonvisual affection in parents
404
Q

Intellectual Disability

Characterized by (3)

A

Characterized by
- significant limitations in both Intellectual functioning (IQ < 70) and Adaptive behavior (conceptual, social, and practical skills)
- Originates before age 22
- Functional impairment in 2 or more areas (Communication/social, Self-care/direction, Home living, Use of community resources , work/academics, leisure, health and safety)

405
Q

Intellectual Disability

Screening Tools (3)
Goal of Care (3)

A

Screening Tools
- Bayley Scales of Infant Development
- Wechsler Intelligence Scale for Children for school-agers
- Environmental Screening in Home esp for tobacco, lead, family assessment

Goal of Care
- To promote optimum social, physical, cognitive, and adaptive development as individuals within a family and community
- provide guidance for establishing acceptable social behavior
- provide guidance for establishing Personal feelings of self-esteem, worth, and security

406
Q

Intellectual Disability: Primary Preventon (5)

A
  • Avoidance of prenatal rubella infection—keep immunizations current
  • Genetic counseling, esp risk of Down or fragile X syndrome or PKU
  • Use of folic acid supplements (neural tube defects)
  • Education (dangers of smoking or alcohol use during pregnancy and ingesting lead during childhood)
  • Reduction of head injuries
407
Q

Intellectual Disability: Secondary Prevention (3)

A
  • Prenatal diagnosis or carrier detection of disorders such as Down syndrome
  • Newborn screening for treatable inborn errors of metabolism (Congenital hypothyroidism, Phenylketonuria (PKU), Galactosemia)
  • monitoring of developmental milestones
408
Q

Intellectual Disability: Tertiary Prevention

A
  • Treatment of coexisting problems to minimize long term consequences
  • Programs for infant stimulation, parent training, preschool education
  • Counseling services to preserve the family unit
408
Q

Intellectual Disability: Early Signs (6)

A
  • No response to contact, voice, movement
  • Irritability
  • Poor/slow feeding
  • Poor eye contact during feeding
  • Diminished spontaneous activity
  • Persistent primitive reflexes (stepping, palmar, plantar, rooting, babinski)
409
Q

Developmental Disability

Characterized by (3)

A
  • severe, chronic mental and/or physical disability which originated at birth or during childhood (before age 22)
  • expected to continue indefinitely
  • Substantially restricts the individual’s functioning in 3 or more of the following major life activities: self-care/direction; receptive and expressive language; learning; mobility; economic self-sufficiency)
410
Q

Developmental Delay

What is it?
Diagnosis
Treatment

A

Any significant lag or delay in physical, cognitive, behavioral, emotional, or social development

Diagnosis
- Routine developmental screening can assist in early identification

Treatment
- Emphasizes abilities, environments, supports, and empowerment b-c underlying assumption: function improves with support

411
Q

Intellectual Disability: Care (5)

A
  • Promote independence in self-care
  • encourage socialization and play
  • provide discipline as needed (Simple, consistent limit setting that is appropriate for child’s mental age)
  • Involve parent and child
  • communicate with child based on developmental level
412
Q

Down Syndrome: Manifestations (8)

A
  • Eyes (Slanted palpebral fissures at eyes, brushfield spots(iris speckles) in eye, Inner epicanthal folds)
  • Mouth and nose (High-arched palate, Small nose w/flat nasal bridge, protruding tongue; periodontal disease)
  • Neck (Excess skin in neck folds)
  • Head (Separated sagittal sutures)
  • Hypotonia and hyperflexible (poor moro reflex)
  • Hand (Hypoplasia of fifth finger (shorter);Simian crease (transverse line on palm))
  • Feet (Plantar crease between big and 2nd toe; Wide space between big and 2nd toe)
  • Development (normal initially then declines; social development > mental age)
413
Q

Down Syndrome:

Types (3)
Prenatal Testing (2)

A

Types
- Nonfamilial trisomy 21 – usual (Increased risk w/ maternal age > 35 yrs)
- Translocation of chromosomes 15 and 21 or 22 due to hereditary causes
- Mosaicism (mixture of normal and abnormal chromosomes)

Prenatal Testing
- Cell free DNA for screening
- Chorionic Villus sampling and amniocentesis for diagnosis

414
Q

Down Syndrome: Comorbidities (9)

A
  • Tracheoesophageal fistula
  • Congenital heart defect: 50%
  • Altered immune function = Early senescence (aging) (risk for URI and otitis media common)
  • Atlantoaxial instability of 1st and 2nd cervical vertebrae
    (no contact sports and no hyperextension of neck if stress on head and neck b-c spinal cord compression (urgent!))- need surgery
  • Sensory: 75% hearing issues and visual issues
  • Growth: weight vs. height
  • Hypothyroidism 10%
  • Small intestinal blockage or Hirschsprung 4%
  • Rare form of leukemia 1%
415
Q

Down syndrome: Care (5)

A
  • Positioning- poor muscle tone so be more careful
  • Nutrition/Feeding- tongue big and thrusts out (refeed feedings)
  • Promote Attachment (family support)
  • Prevent respiratory problems (may be mouth breathers due to underdeveloped nasal bone)- need bulb suctioning, mouth rinses
  • Prevent dry skin (lots of lubricants needed)
416
Q

ADHD

What is it? (2)
Care (3)

A
  • Inattention, impulsiveness, and hyperactivity w/ typical onset before age 7
  • symptoms in more than one setting

Care
- Classroom (Vary learning activities; more test time, reduce assignment, difficult work in morning)
- Behavioral therapy and/or psychotherapy for child
- Environmental manipulation- not too many distractions; control overstimulation; structured

417
Q

ADHD: Medication

Main Med
Side effects (4)

A
  • Stimulant( Dexedrine, Adderall, Ritalin, methylphenidate)

Side effects
- Insomnia (give in morning)
- anorexia/weight loss (give prior to eating)
- hypertension
- long-term use may suppress growth (give drug holiday)