Respiratory Flashcards

1
Q

Anatomical differences in Pedi

A

Narrow and short airway (increased risk of obstruction with mucus and edema)
Alveoli is small in size and number (small surface area for gas exchange)
Infants are nose breathers (until 2-4mo)
Shorter, open, and more horizontal eustachian tubes
Abdominal or diaphragmatic breathers until 6yr/o
Weak muscles that keep the airway open
Bigger tongues than adults (risk for obstruction)

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2
Q

1-11 months respirations

A

30

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3
Q

2 year old respirations

A

25

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4
Q

4 year old respirations

A

23

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5
Q

6 year old respirations

A

21

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6
Q

8 year old respirations

A

20

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7
Q

10 year old respirations

A

19

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8
Q

12 year old respirations

A

19

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9
Q

14 year old respirations

A

18

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10
Q

16 year old respirations

A

17

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11
Q

18 year old respirations

A

16-18

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12
Q

Urgent Respiratory threats

A

Apnea
Apnea of Prematurity (AOP)
Apnea of infancy or ALTE (Apparent life threatening event)
SIDS (Sudden infant death syndrome)

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13
Q

Normal respiration Rates

A

The younger the children are the faster they breathe

Thorax and the lungs are the same size, infants must breathe 2-3x more often than an adult for adequate respirations

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14
Q

Characteristics of Respirations

A

Newborns and infants have episodes of periodic breathing
Normally breathe with an irregular rhythm and may have pauses up to 20 seconds between breaths
Normal unless they show signs of hypoxemia or bradycardia (if they become hypoxic or bradycardic thy have apnea)

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15
Q

Urgent Respiratory threats

A

Apnea
Apnea of Prematurity (AOP)
BRUE
SIDS (Sudden infant death syndrome)

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16
Q

Apnea

A

Cessation of breathing for longer than 20 seconds OR for a shorter period of time when associated with hypoxemia or bradycardia (generally occurs in premature infants and newborns that are classified in different categories depending on the age of onset)

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17
Q

Apnea of Prematurity (AOP)

A

Developmental disorder in premature infants
Occurs as. direct consequence of immature respiratory control
Infants <36wk gestational age: apnea may become evident in the first 2-3 day after birth
Considered clinically significant if the episodes are > 20 seconds in duration or shorter with hypoxia and/or bradycardia
Frequently and severity of symptoms is inversely proportional to gestational age and almost all extremely low birth weight infants (<1000 grams) are effected

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18
Q

Apnea of Prematurity (AOP): Diagnosis of Exclusion

A

Hypoxemia
Anemia
Infection (sepsis)
Metabolic disorders
Unstable thermal environment
Antepartum administration of Magnesium sulfate or opiates to the mother
Neurologic disorders, including intracranial hemorrhage and neonatal encephalopathy
Necrotizing enterocolitis
Congenital abnormalities of the upper airway
Seizures

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19
Q

Apnea of Prematurity (AOP): Nursing Priorities

A

Frequent visual/physical assessment and continuous cardiopulmonary monitoring
Continuously monitor patient for changes in color and tome
Make sure they are pink and active or are they cyanotic and flaccid?
Continuous monitoring VS: especially respirations, HR, SPO2 and have room prepared for emergency

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20
Q

Apnea of Prematurity (AOP): Warning alarms

A

Lower threshold (MD orders specific settings)
Apnea: ≥ 15 or 20 seconds
HR: ≤70 or 80 bpm
SPO2: < 80 or 85%

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21
Q

Apnea of Prematurity (AOP): Treatment

A

Apneic spells are frequent, prolonged, or associated with bradycardia or frequent decreased SPO2
OR the infant requires intervention with ambu bag, or multiple episodes of tactile stimulation
Often needed for several weeks in AOP until the apnea resolves as the respiratory control of infant matures

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22
Q

Apnea of Prematurity (AOP): Non-pharmacological Treatment

A

Provide gentle, tactile stimulation (rubbing their chest, stroking the bottom of their feet) if the child becomes apneic
Continuous cardiopulmonary monitoring with apnea settings
Ambu bag, environmental temp control, head and neck position, maintain nasal patency, O2 supplementation to maintain SPO2 90-95%
NCPAP

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23
Q

Apnea of Prematurity (AOP): Pharmacological Treatment

A

Most commonly used: Methylxanthines (phyllines and Caffeine) stimulates respiratory neural output by inhibiting adenosine receptors
Caffeine is preferred because of its longer half-life, wider margin of safety and lower frequency of A/E
Caffeine A/E: feeding intolerance, tachycardia, tremors, irritability

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24
Q

Apnea of Prematurity (AOP): D/C planning

A

Increased risk for SIDS but will outgrow it
Parents need to become CPR certified
Teach parents: what to do if child shows apnea at home, provide tactile stimulation, how and when to give medication, home monitor use a safety

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25
Q

BRUE

A

Refers to idiopathic or pathologic apnea occuring in infants >37 week gestation
Involves significant intervention such as CPR

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26
Q

BRUE: Infant exhibits

A

Apnea
Change in color
Change in muscle tone
Choking, gagging or coughing

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27
Q

Definition of BRUE

A

May include apnea, but can occur without apnea

Short periods of apnea <15 seconds can be normal at any age

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28
Q

BRUE: Diagnosis

A

May different tests, by exclusion: labs, upper GI, Ph probe, EEG, CT, EKG,CXR, skeletal muscle survey, PCG (pneumocardiogram to monitor respirations, HR, nasal airflow, O2), Polysomnography (sleep study, records brain waves)

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29
Q

BRUE): Treatment

A

If underlying problem is found: treat it

No cause: sent home for monitoring

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30
Q

BRUE: Nursing care

A

Close and continuous monitoring
Provide gentle tactile stimulation
Educate and support the family

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31
Q

BRUE: D/C planning

A

Teach home care: apnea monitoring, med admin, monitoring for A/E, CPR class for family members

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32
Q

SIDS (Sudden infant death syndrome)

A

The sudden death of an infant which remains unexplained after all known and
possible causes have been carefully ruled out through autopsy, death scene investigation, and review of the
medical history. Time of death occurs during sleep.

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33
Q

SIDS (Sudden infant death syndrome): Cause

A

unknown
Problems with the baby’s ability to wake up (sleep arousal)
Inability for the baby’s body to detect a build-up of carbon dioxide in the blood

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34
Q

SIDS (Sudden infant death syndrome): Peak time

A

2-4 months of life

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35
Q

SIDS (Sudden infant death syndrome): Incidence

A

Takes 2250 lives each year, making it the leading cause of death from ages 1 month to 1 year.
Increased incidence in winter. Increased occurrence in lower socio-economical class.

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36
Q

Back to sleep campaign

A

Reinforce with the parents that
evidence based research has shown and proven that infants that are placed on their belly to sleep are at greater risk for SIDS.
Prone sleeping may cause oropharyngeal obstruction or affect the thermal balance or the arousal state. Also rebreathing of CO2 while in the prone position may be a possible cause for SIDS
Sleeping on soft mattresses or bedding may not be able to move their heads from side to side, and this increases their risk for suffocation and lethal rebreathing. Even lying baby on their side isn’t appropriate anymore.

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37
Q

Infants at Risk for SIDS

A
Preterm infants
Multiple births- where mother has been pregnant several times
Low birth weight
Low ABGAR scores
Recent viral illness
Hx of ALTE or AOP
Siblings of SIDS victims
Males
African Americans, Native Americans, Hispanics all have a greater risk for SIDS
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38
Q

Lower Incidence of SIDS in Infants who:

A
are placed in supine position to sleep
sleep in their own crib
sleep on firm mattresses
are breast fed
are put to sleep with pacifier • are immunized
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39
Q

Education for Parents to Reduce Risk for SIDS

A

A (alone), B (back), C (crib), S (smoking)
Healthy infants on back to sleep
No soft bedding, baby crib bumpers, blankets, quilts or pillows anywhere in your baby’s sleep area. Use a firm
sleep surface, such as a mattress in a safety-approved crib, covered by a fitted sheet.
No stuffed animals or towels while sleeping. Keep soft objects, toys, and loose beefing out of baby’s sleep area.
Infant to sleep in same room as caregiver. No co-sleeping though. Baby should NOT sleep in an adult bed, on a
couch, or on a chair alone, with you, or with anyone else. Infant should sleep in own bed/crib
Do not let baby get too hot; dress infant in light clothing. Make sure nothing covers the baby’s head. Dress baby in
sleep clothing, such as a one-piece sleeper, and don’t use a blanket.
Change the position of the baby’s head to prevent flattening of the baby’s skull (called positional plagiocephaly)
Offer pacifier during naps and at bedtime, the research has shown that it decreases the risk for SIDS
Encourage breastfeeding for as long as possible
Schedule and go to all WCC
Have child immunized
Don’t smoke or let anyone smoke around your baby.

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40
Q

SIDS: After Occurance… :(

A

Generally no attempt at resuscitation due to signs of prolonged death: rigor mortis, corneal clouding
Once EMS arrives, they notify coroner of time of death.
Arrival at the ER
Questioned by MD and police officers- must perform an autopsy
Returning home without the child
Provide compassionate care- grieving lasts a year
Support Parents- make sure they get involved in a support group

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41
Q

Acute Nasopharyngitis

A

“common cold”, and like most viruses it usually lasts 7-10 days

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42
Q

Acute Nasopharyngitis: Cause

A
Rhinovirus
RSV
Adenovirus
Influenzavirus
Parainfluenzavirus
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43
Q

Acute Nasopharyngitis: Clinical manifestations in Young children

A
Fever
Irritability
Restlessness
Sneezing
Post nasal drip
Cough
Diarrhea
Runny or dry nose- make sure to keep their nose clean and dry. 
Decreased appetite
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44
Q

Acute Nasopharyngitis: Clinical manifestations in Older children

A
Sneezing 
Chills
Muscular aches
Post nasal drip
Cough
Dry throat
Runny or dry nose
Decreased appetite
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45
Q

Acute Nasopharyngitis: Nursing assessment

A

Eyes- red, puffy
Nose- red, swollen, make sure their not flaring
Mouth- cough
Throat- red, sore
Respiratory effort- make sure breathing effectively, rising and falling appropriately, and not retracting
Lung sounds- check for adventitious sounds
V/S- especially her RR
SPO2: make sure its at least 92% on room air, if not give supplemental O2

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46
Q

Acute Nasopharyngitis: Nursing diagnosis

A

Impaired breathing pattern related to presence of semi- thick nasal discharge
Acute pain related to inflammation of the throat
Ineffective airway clearance related to thick secretions characterized by difficulty in breathing
Imbalance nutrition less than body requirements related to respiratory distress AEB…..
Knowledge deficit related to not familiar with the sources of information

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47
Q

Acute Nasopharyngitis: Nursing interventions

A

Elevate HOB at least 30 degrees
Maintain adequate fluids- because they’re at risk for dehydration
Suction nares PRN, especially before she goes to bed and before she eats
Saline nose drops before feeding and sleep, and before suctioning
Humidification- will help thin secretions
Tylenol/Ibuprofen- if still running a fever
Promote rest- something is very wrong if a child doesn’t want to play

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48
Q

Acute Nasopharyngitis: Goals

A
Decrease work of breathing 
Increase Spo2
Less or no pain
Decrease temperature
Maintain fluid balance 
Increase PO intake
Sleep through the night
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49
Q

Acute Nasopharyngitis: Evaluation

A
Effectiveness?
Did suctioning help?
Nose clear? 
Breathing easier?
Flaring or retracting? 
SPO2?
HOB elevated? 
Were goals achieved?
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50
Q

Acute Nasopharyngitis: Patient teaching

A

Treating symptoms at home (how to use medications)
Importance of hand washing
When to go to the ER
Warm against OTC cough medications for less than 6yr/o (proven to be ineffective and can be harmful; causing heart palpitations, hyperactivity, and even death, and worsen asthma)

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51
Q

Pharyngitis

A

Inflammation of the throat with exudate that can cause pain when swallowing
Can occur at any age. Average age of occurrence 5-10 years
Viral or bacterial (Group AB Hemolytic Streptococcus/GABHS)

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52
Q

Pharyngitis: Clinical manifestations

A
Inflamed throat
Strawberry tongue
Exudate
Pain when swallowing
Headache
Fever
Abdominal pain
Cervical lymphadenopathy
Sandpaper rash: face,trunk, axillary perineal/ Scarlet fever
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53
Q

Pharyngitis: Nursing assessment

A
Throat
Respiratory effort
Lung sounds
V/S: Temp., HR, RR, B/P 
SpO2
Skin
Pain
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54
Q

Pharyngitis: Viral or Bacterial

A

Must do throat swab!!
Quick Strep/Rapid Antigen Test
Throat Culture

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55
Q

Pharyngitis: Treatment plan for GABHS (strep throat)

A

Must be treated with ABX: Penicillin or Amoxicillin
Allergic to penicillin may use a cephalosporin such as cephalexin (Keflex), Clarithromycin (Biaxin),
Azithromycin (Zithromax, Zmax), or Clindamycin

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56
Q

Pharyngitis: Nursing management

A
Monitor V/S
Monitor I & O’s
Monitor Pain
Administer IV ABX as ordered
Cold/warm compress to neck
Warm saline gargles
Encourage fluids
Recommend soothing /soft foods 
Humidification
Encourage low level activities
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57
Q

Pharyngitis: D/C planning, Teaching

A

Disease transmission and prevention
High contagiousness of this condition
Importance of hand washing
Make sure the child does not return to school until they have been on ABX for a full 24 hours
Importance of giving the child ABX until finished
No sharing utensils
No eating or drinking after others
Change out toothbrush after 24 hours of being on ABX

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58
Q

Rheumatic fever

A

Usually occurs 2-6 weeks after pt. infected with GABHS
ASO titers done
Treated with PCN
Prophylactic treatment required and depends on age of child and severity of condition

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59
Q

Acute Glomerulonephritis

A

Most common post-infectious renal diseases in childhood
ASO titers done
Symptomatic treatment

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60
Q

Tonsillitis

A

Inflammation/infection of the tonsils
Occurs most often with pharyngitis
May be viral or bacterial

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61
Q

Tonsillitis: Diagnosis

A

Early rapid strep test/throat culture to determine causative agent

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62
Q

Tonsillitis: Classic S/S

A

Red, inflamed, enlarged, touching tonsils aka “kissing tonsils”, difficulty swallowing and breathing.
Breathe through mouth because the adenoids enlarge and block the space between the posterior nares
making it difficult or impossible for air to pass from the nose to the throat

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63
Q

Tonsillitis: Treatment

A

Depends on causative agent

warm, salt water gargles, throat lozenges, Tylenol if patient in pain

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64
Q

Tonsillitis: Surgical Treatment

A

Severe
Remove the palatine tonsils and it will be nurse’s job to prepare them for surgery and monitor child post-op
Prepare children
Child comes back to surgery: placed on their side or in a prone position with their head to the side to facilitate the drainage of the secretions
Careful suctioning as needed
Avoid coughing and blowing nose
Reddish brown secretions are normal
Bright red blood is not normal and surgeon needs to be be notified immediately
Watch for bleeding for up to 10 days post-operatively
each the family and the patient to avoid red colored liquids and milk based foods (because they increase the production of mucous) initially
Advance from a clear, soft diet to a regular diet. D/C instructions include teaching pt to avoid irritating and spicy foods, avoid gargles and vigorous tooth brushing, avoid coughing or clearing throat, avoid using straws and chewing gum, how to take medication appropriately to control pain/discomfort.

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65
Q

Tonsillitis: Management: Non-pharmacological

A

Humidification
Warm salt water gargles
Throat lozenges

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66
Q

Tonsillitis: Management: Pharmacological

A

Tylenol

Antibiotics if bacterial

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67
Q

Tonsillitis: Management: Surgical

A

Recurrent infections/obstructive sleep apnea

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68
Q

Tonsillectomy/Adenoidectomy: Pre-op Teaching/Consent

A

Room set up

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69
Q

Tonsillectomy/Adenoidectomy: Post-Op Teaching/Care

A

Positioning: abdomen/side lying
Monitor for bleeding
Minimize activities that precipitate bleeding
Monitor I & O’s

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70
Q

Otitis Media

A

Inflammation of the middle ear
Most prevalent diseases of early childhood
Increase incidence between 6 months and 2 years
Breast feed have a lower incidence than those who bottle feed, related to positioning of the baby.
If parents have a history of otitis media, their children will be at greater risk for it. Children who are around passive smoke, in a household with many members, attend day care, cleft lip/palate, have Down’s Syndrome, are at increased risk for it. Most common in winter months

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71
Q

Otitis Media: Risk factors

A

Environmental

Life style factors

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72
Q

Otitis Media: Triggered by

A

Bacterial/ viral infection
Allergies
Enlarged tonsils

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73
Q

Otitis Media: Results from:

A

blocked Eustachian tubes from edema

74
Q

Acute Otitis Media:

A

Bacterial infection that causes inflammation of the middle ear space with rapid onset. It is generally caused by
Streptococcus Pneumonia, H.Influenza, and Marxella Cateralis. Usually follows an upper respiratory infection.

75
Q

Acute Otitis Media: S/S

A
Painful ear
Pulling or rubbing the ears 
Fever
Fussiness or irritability 
Fluid leaking from the ear 
Changes in appetite or sleep 
Trouble hearing
76
Q

Acute Otitis Media: Diagnosis

A

Made by a visual inspection with otoscope of tympanic membrane to check for its mobility. Done by MD or Np

77
Q

Acute Otitis Media: Treatment

A
Tylenol/Ibuprofen
Benzocaine
Cold packs
ABX- usually Amoxicillin 
Surgery
78
Q

Acute Otitis Media: Nursing objectives

A

Relieving pain either with Tylenol or Tylenol with Codeine, ice pack, or Ibuprofen, or Benzocaine
Facilitate drainage when possible, prevent complications of recurrence

79
Q

Acute Otitis Media: Teaching

A

How to hold the baby during feeding, making sure the child is sitting upright, discourage propping of bottle, encourage breastfeeding
Maintain immunization
Decrease exposure to smoke
May need surgical intervention
may also need a tympanostomy, tube placement, and also an adenoidectomy procedure to treat recurrent chronic otitis media.
3 bouts in 6 months, 6 and 12 months, or 6 by 6 years of age.

80
Q

Otitis Media with Effusion

A

Generally caused by middle ear infections, may lead to “glue ear”, which is OME, where sticky fluids build up and affect the child’s hearing.
May also lead to unclear speech and behavioral problems.

81
Q

Otitis Media with Effusion: S/S

A

OME may have no symptoms at all
Most frequent presentation is covert and overt hearing loss, which mostly fluctuates with season and may be affected in changing position
Plugged ear or a stuffy or wooly feeling in the air
Child is talking loudly or not responding to verbal commands
Have their music/tv turned up really loud.
No c/o pain. No fever.
Speech delay.
Sometimes it can be detected on routine audiometry.

82
Q

Otitis Media with Effusion: Diagnosis

A

Visualization of tympanic membrane and use of an otoscope to test for mobility of the tympanic membrane

83
Q

Otitis Media with Effusion: Treatment

A

Bilateral myringotomy/PE (pressure equalizing) tubes, surgical placement of tympanostomy tubes (takes only 15 minutes and usually the tubes come out on their own in 6-12 months)

84
Q

Croup Syndrome

A

General term applied to a symptom complex characterized by hoarseness, a resonant cough, described as “barking” or “brassy” (croupy), varying degrees of inspiratory stridor, and varying degrees of respiratory distress resulting from swelling or obstruction in the region of the larynx and trachea
Affect the larynx, bronchi, and trachea.
Croup syndromes are described according to the primary anatomical area affected

85
Q

Acute epiglottitis or Acute supraglottitis:

A

Serious obstructive inflammatory condition
Predominately in children ages 2 years to 5 years old- but can occur from infancy through adulthood.
H. Influenza B is the main culprit- bacteria
Considered a medical emergency due to fast onset
Epiglottitis looks worse than they sound, there’s a high degree of toxicity, no cough, and dysphagia

86
Q

Acute epiglottitis or Acute supraglottitis: Clinical manifestations

A

Sudden abrupt onset of: heigh fever >39 C, Sore, red, swollen throat, Absence of cough
The 4 D’s
▪ Dysphonia- a muffled, hoarse, or absent voice.
▪ Dysphagia- difficulty swallowing due to the pain
▪ Drooling- also due to the pain
▪ Distressed respiratory effort- inspiratory stridor as the larynx becomes obstructed
Agitation/Irritablity
Tripod position- the child may insist on sitting upright and leaning forward, with the chin thrusted out, mouth
open, and the tongue protruding
Expiratory Stridor

87
Q

Acute epiglottitis or Acute supraglottitis: Diagnosis

A

Clinical manifestations
Radiography- a lateral neck x-ray, which will show a thumb sign from an enlarged epiglottis
Blood cultures- to show what antibiotic to use

88
Q

Acute epiglottitis or Acute supraglottitis: Therapeutic Management

A
Avoid looking in mouth without emergency equipment readily available
Calm environment
Encourage position of comfort
Let caregiver stay with child
Emergency intubation/tracheostomy if child is in severe respiratory distress
Humidified oxygen
Antibiotic therapy
Corticosteroids
89
Q

Acute epiglottitis or Acute supraglottitis: Nursing management

A
Frequent assessments
Continuous cardiopulmonary monitoring
Maintain airway patency
NPO
IV fluid administration as prescribed
ABX
Provide emotional support
Discharge planning- home teaching includes completing a 7-10 day course of antibiotics. 
For children under
the age of 4 years, Rifampin is used for treatment for 4 days.
90
Q

Laryngotracheobronchitis (LTB)

A

Most common of croup syndromes affecting children < 5 years of age
Mostly caused by para-influenza virus types 1 & 2, RSV, influenza A & B*
Usually starts as an upper respiratory tract infection that descends to adjacent structures
Inflammation and swelling of the mucosa lining, the larynx, and trachea causes a narrowing of the airway that result in the onset of the classic symptoms like the croupy, barking cough
They sound worse than they look, have a seal-like cough
*

91
Q

Laryngotracheobronchitis (LTB): Clinical manifestations

A

Gradual onset of low grade-fever- ***
Ill with URI for several days- see a runny nose or cough that’s escalated into a severe cough with hoarseness
(because the inflammation of the trachea and larynx is causing severe swelling)
Inspiratory stridor
Seal like barking cough and hoarseness
Tachypnea

92
Q

Laryngotracheobronchitis (LTB): Diagnostic tests

A

Clinical signs and history
Cardiopulmonary monitoring and SPO2 for hypoxemia
Chest x-ray

93
Q

Laryngotracheobronchitis (LTB): Nursing management of Mild-Moderate symptoms

A

Humidification, Medications- (IV therapy for hydration and steroids for inflammation), O2 therapy
Observation in ER, sent home if showing good
response to treatment.
Encourage fluids if mild symptoms to prevent dehydration
Uncommonly – children will need intubation and be sent to ICU.
Admitted if moderate to severe symptoms.
If LTB is severe, nebulized Epi is often used in children with severe disease, stridor at rest, retractions, or difficulty breathing, administration of Heliox is used to decrease the work of breathing and relieve airway obstruction.

94
Q

Laryngotracheobronchitis (LTB): Nursing management of Severe symptoms

A

Oxygen therapy & Closely monitor pulse oximetry- to monitor O2 status
Nebulized epinephrine- to help with stridor
Corticosteroids
IV therapy
Placing patient on NPO status for RR > 60/ minute, because this puts them at risk for aspiration
ABG/VBG monitoring for acidosis
Accurate & frequent assessments- continuous vigilant observation & accurate assess of respiratory status
because changes in therapy are performed based on your observation as a nurse, child’s response to the therapy, and tolerance of the procedure.
Early signs of airway obstruction include increased pulse, RR, sub-sternal, supra-sternal, and intercostal retractions, nasal flaring, and increased restlessness
Intubation equipment readily available & patient’s code drugs listed on a sheet and readily available

95
Q

Croup syndromes: Nursing care Goals

A

Maintain airway patency, meet fluid & nutritional needs, discharge planning, home care teaching
Home care includes monitoring for worsening of symptoms, continued humidity, adequate nutrition/nourishment

96
Q

Croup syndromes: Nursing Diagnosis

A

Ineffective breathing pattern related to tracheobronchial obstruction, decreased energy and fatigue
Impaired gas exchange related to altered O2 supply
Altered nutrition: less than body requirements related to expenditure of glycogen stores and inadequate food
and fluid intake prior to admission
Fear/anxiety in parents or child related to acute illness, uncertainty of prognosis, unfamiliar surrounds and
procedures
Knowledge deficits in parent- related to diagnosis, prognosis, treatment, and home care needs

97
Q

Bronchitis

A

Inflammation of the large airways
Usually follows an URI in children < 4 years of age
Usually caused from virus
Self-liming, child recovers with symptomatic treatment within 5-10 days

98
Q

Bronchitis: Clinical manifestations

A

Course, hacking, dry/non-productive cough with increased severity at night, may turn productive in 2-3 days
Audible wheezing

99
Q

Bronchitis: Treatment

A

Antipyretics- if they do run a fever
Analgesics- such as Tylenol and Ibuprofen
Humidity- help with inflammation
Hydration
Cough suppressants (caution: can interfere with clearing secretions, don’t used under 6yr)

100
Q

Bronchiolitis

A

An acute viral infection, mostly caused by Respiratory Syncytial Virus (RSV)
Primarily affects the bronchi and bronchioles
Rare in children > 2 years of age
Occurs most often in winter and early spring
Affects boys more than girls

101
Q

Bronchiolitis: Clinical manifestations

A

URI (upper respiratory symptoms such as rhinorrhea, pharyngitis, cough, and fever)
Progress to lower tract, more cough, labored breathing, shallow respiration, nasal flaring, retractions, cyanosis Child acting more ill, may refuse to eat, spits up more
May also have emphysema, increased nasal mucous, wheezing, fever
Apnea may be the first recognized indicator of RSV infection in infants < 1 month of age

102
Q

RSV (Respiratory Syncytial Virus)

A

Most frequent cause of hospitalization in children less than 1 year old
Peak infection season is November – April
Transmitted through direct person-person contact & by droplet inhalation

103
Q

RSV (Respiratory Syncytial Virus): Treatment

A

Primarily supportive, unless high risk give Synagis prophylactically

104
Q

RSV (Respiratory Syncytial Virus): High risk groups

A

Infants born before 35 weeks of gestation, infants with chronic lung disease, and infants born with hemodynamically significant congenital heart disease

105
Q

RSV (Respiratory Syncytial Virus): Synagis

A

Only product available in the US used for the prevention of RSV infection
It’s a monoclonal antibody and is given monthly in an IM injection to prevent hospitalization of patients who are at high risk for developing RSV
It can be given in 3 or 5 doses depending on patient and severity

106
Q

RSV (Respiratory Syncytial Virus): Pathophysiology

A

Edema of bronchioles and thick secretions
Obstruction and hyperinflation
Increased respiratory effort=respiratory distress Respiratory Failure

107
Q

RSV (Respiratory Syncytial Virus): Clinical manifestations

A
Fever
Cough
Tachycardia
Cyanosis
Tachypnea
Retractions
Wheezing
Sepsis like appearance
Apneic episodes (in the very young)
Dehydration
108
Q

RSV (Respiratory Syncytial Virus): Diagnosis

A

Rapid RSV antigen testing done via nasal aspirate or nasal wash or nasopharyngeal swab
Chest X-Ray

109
Q

RSV (Respiratory Syncytial Virus)/ Bronchiolitis: Nursing Diagnosis

A

Ineffective airway clearance related to increased airway secretions, fatigue from coughing, dyspnea, air trapping
Ineffective breathing patterns related to inflamed tracheobronchial tree and progression of bronchiolitis,
increased work of breathing and decreased energy
Fluid volume deficit r/t inability to meet fluid needs and increased metabolic demands
Altered tissue perfusion r/t partially obstructed airways

110
Q

RSV (Respiratory Syncytial Virus): Nursing management

A

Separate rooms or grouped with other RSV infected children
Contact and standard precautions
Maintaining respiratory function
Supporting overall physiologic function
Hydration
Reducing child’s and family’s anxiety
Preparing child and family for home- teaching them about med administration, symptoms of RSV, and when to call doctor

111
Q

Pneumonia

A

Inflammation of the pulmonary parenchyma or infection in one or both lungs is common in childhood but occurs more frequently in early childhood
May occur as a primary disease or as a complication of another illness
Caused from virus, bacteria, fungus or aspiration

112
Q

Pneumonia: Clinical manifestations

A
Fever-Usually high > 39.5 C (103 F) 
Respiratory:
• Cough
• Tachypnea
• Rhonchi
• Crackles
• Chest/abdominal pain
• Retractions
• Flaring
• Pallor
Behavior:
• Irritable
• Restless
• Lethargic
Gastrointestinal:
• Anorexia- doesn’t want to eat
• Vomiting
• Diarrhea
113
Q

Pneumonia: Nursing care

A

Respiratory assessment, and a continuous assessment
Monitoring: VS and pulse oximetry
Administration of supplemental oxygen as ordered
IV fluids- to prevent dehydration
Antibiotics- depending
Pharmacological/non-pharmacological pain relieve measures
Elevate HOB to get good chest expansion
Possible Chest tube placement- to remove fluid or air that’s accumulated in the lung
Daily chest x-rays
Provide calm environment- allow for presence of caregivers as they provide a source of comfort for patient
Teach and support patient/family, prepare for d/c- teach regarding O2 needs, medication needs, positioning

114
Q

Asthma

A

Chronic inflammatory disorder of the airways characterized by:
Recurring symptoms
Airway obstruction
Bronchial hyper-responsiveness

115
Q

Asthma: Causes

A

Exact cause is unknown
Allergies
Frequent viral respiratory infections

116
Q

Asthma: Early warning signs

A

Eczema starting in the early months
Frequent lower respiratory symptoms
Respiratory problems appearing before the first birthday
Having a family history of asthma

117
Q

Asthma: Diagnostics

A

Classic manifestations: Dyspnea, Wheezing, Coughing
History/Physical Exam:
➢History of chronic cough with absence of infection
➢Diffuse expiratory wheezing
PFT
Incentive spirometry
PEFR
Bronchoprovocation testing
Skin prick testing and immunological testing
Laboratory tests
Frontal and lateral view chest X-ray

118
Q

Asthma: Diagnostics: Pulmonary function test

A

Provide an adjective measure of evaluating the presence and degree of lung disease as well as the response to therapy

119
Q

Asthma: Diagnostics: Incentive spirometry

A

Performed reliably on children 5-6 years of age

120
Q

Asthma: Diagnostics: Peak expiratory flow rate

A

Measures maximum flow of air that can be forcefully exhaled/second

121
Q

Asthma: Diagnostics: Skin prick testing and immunological testing

A

For allergen specific IgE, used to ID environmental triggers

122
Q

Asthma: Diagnostics: Lab tests

A

CBC

123
Q

Asthma: Clinical manifestations

A
Cough
Shortness of breath
Audible wheeze
Malar flush, red ears
Cyanosis of nail beds
Circumoral cyanosis
Dyspnea
Nasal flaring
Retractions
Hyperresonance on chest percussion
Coarse and/or crackles and wheezes throughout all the lung fields
Sweating
Posture/ tripod position
Changes in speech
Restlessness 
Anxiety
Fatigue
124
Q

Asthma: Nurse assessment

A

Airway potency, RR, symmetry, effort, and use of accessory muscles, breath sounds in all
lung fields

125
Q

Asthma: Nursing alert!

A

Child who sweats profusely, remains sitting upright, and refuses to lie down is in severe respiratory
distress!!! Pay close attention to this child and have emergency equipment readily available
A child who suddenly becomes agitated or an agitated child who suddenly becomes quiet may have serious
hypoxia and require immediate intervention

126
Q

Asthma: Triggers

A

Allergens: indoor (dust mites, mold, etc.) and outdoor (trees, pollen, pollution, etc.)
Irritants (tobacco or wood burning smoke, odors, sprays)
Exercise
Sudden weather or temperature changes (extreme cold or hot)
Seasonal allergens (grass, trees, weed pollen)
Animal dander
Strong emotions
Food
Medications

127
Q

Asthma: Treatment plan

A

Step 1. Mild intermittent- Symptoms occur < twice a week
Step 2. Mild persistent- Symptoms occur more than twice a week, but not daily
Step 3 or 4: Moderate persistent- Daily symptoms occur in conjunction with exacerbations twice a week
Step 5 or 6: Severe persistent- Symptoms occur continually, along with frequent exacerbations twice a week

128
Q

Asthma: Treatment: Non-Pharmacological

A

Prevention and reduction of exposure to airborne allergens and irritants
Nurses Role: Family and patient teaching on “Allergy proofing the home and community”

129
Q

Asthma: Treatment: Pharmacological Goals

A

Preventing and controlling asthma symptoms
Reducing the frequency and severity of the child’s asthma
Reversing airflow obstruction
Providing long term suppression of inflammation

130
Q

Asthma: Treatment: Short acting meds (Quick action)

A
Bronchodilators used to treat symptoms and exacerbations. 
Include SABA
Prevent exercise induced asthma
Only taken PRN
Albuterol 
Xopenex 
Terbutaline 
Metaproterenol
131
Q

Asthma: Treatment: Long term control

A

Achieve and maintain control of inflammation
Used daily to control and reduce the number of day or night symptoms
Not used for relief
Symptoms more than 2x/week or who wake > 2x/month should be on a controller medication.
Inhaled corticosteroids: QVAR, Pulmicort, Flovent
Long acting bronchodilators (LABA): Salmeterol Leukotriene Receptor Agonists
Methylxanthines: Theophylline

132
Q

Asthma: Treatment: Medications types

A

Metered-dose inhalers, Dry powder inhalers, Liquids that can be used in nebulizers, Pills

133
Q

Asthma: Treatment: Choosing the right medication

A

Severity and frequency of symptoms
Child’s age
Child’s developmental level
Child’s coordination- must be able to push down on inhaler and breathe in at same time

134
Q

Asthma: Treatment: Most common MDIs

A
Corticosteroids
Cromolyn sodium
Nedocromil sodium
Xopenex
Albuterol
Metaproterenol
Terbutaline
Salmeterol (Serevent)
Methylxanthines (theophylline)
135
Q

Asthma: Treatment: Albuterol A/E

A

shakiness, tremors, tachycardia, hyperactivity

136
Q

Asthma: Treatment: Glucocorticoids A/E

A

thrush, modest reduction in height

137
Q

Asthma: Nurses role

A
Observe for signs of trouble breathing 
Teach family on how to avoid allergens 
Take medications appropriately and caution with A/E and dangers of over use of SABA/LABA
Monitor for medication toxicity while in hospital (shakiness, irritability, jitteriness, increased HR) 
Show how to use PEFM in child >5yr
Provide supportive environment
At home action plan 
Have Epipen for severe allergic reaction
138
Q

Asthma: Nurse warning (status asthmaticus)

A

Shortness of breath with air movement in the chest restricted to the point of absent breath sounds accompanied by a sudden rise in respiratory rate is an ominous sign indicating ventilatory failure and imminent respiratory arrest
Not hearing any air movement
Continue to display respiratory distress despite vigorous therapeutic treatment with bronchodilators such as Albuterol and Epinephrine are considered to be in Status Asthmaticus.

139
Q

Status Asthmaticus

A

A life threatening episode of airway obstruction, unresponsive to common treatment
Medical Emergency
Can result in respiratory failure and death if untreated
It may develop gradually or rapidly

140
Q

Status Asthmaticus: Therapy

A
Improving ventilation
Decreasing airway resistance
Relieving bronchospasms
Correcting dehydration and acidosis
Allaying child and parent fears/anxieties by providing a quiet, calm, family-centered environment
141
Q

Status Asthmaticus: Nurses role

A

Maintain patent airway
Administer humidified O2
Administer 3 neb tx of a beta2-agonist, 20-30 apart (usually Albuterol)
Obtain IV access: hydration and to correct acidosis, IV Epi/Magnesium Sulfate
Monitor ABGs and serum electrolytes
Administer corticosteroids, either PO, IV, or IM to help with inflammation
Prepare for emergency intubation if patient goes into respiratory distress
Have crash cart, code sheet and code drugs readily available
Establish calm environment, allowing parent presence at all times

142
Q

Cystic Fibrosis

A

Chronic autosomal recessive disorder of the exocrine glands. It is the most common inherited metabolic disorder
Thick and copious mucous obstructs the small passageways of the affected organs

143
Q

Cystic Fibrosis: Cause

A

Inherited as an autosomal recessive trait
Mutated gene for CF is located on the long arm of chromosome 7.
It codes for a protein of 1480 AA called CF-Transmembrane Regulator

144
Q

Cystic Fibrosis: Areas of abnormal secretions

A

Bronchial – chronic bronchial pneumonia, emphysema
Small intestine – meconium impaction, bowel obstruction
Pancreatic duct – malabsorption syndrome
Bile duct – biliary fibrosis, portal hypertension

145
Q

Cystic Fibrosis: Diagnosis

A

Average age of dx is 14 months
2 Positive sweat chloride tests: a consistent finding of abnormally high NaCl
concentrations in the sweat is a unique characteristic of CF:
Normal < 40 Meq/L
Positive > 60 Meq/L in children
>40 Meq/L in infants
Chest Radiography: patchy atelectasis, obstructive emphysema
Positive family history
72 hour stool sample- steatorrhea (undigested fats), azotorrhea (foul-smelling stools)
Enzyme Analysis- Absence of pancreatic enzymes

146
Q

Cystic Fibrosis: Clinical Manifestations

A
Thick, sticky mucous
Bowel obstruction (newborn)
Intussusception (telescoping bowel)
Impaction in infants and toddlers
Chronic cough
Difficulty in gaining weight 
FTT-failure to thrive
Skin is salty
147
Q

Cystic Fibrosis: Stool characteristics

A

Steatorrhea (fatty), frothy, foul smelling, floats. This is because in the pancreas, the thick
secretions block the ducts, which eventually causes pancreatic fibrosis. This blockage prevents essential pancreatic enzymes from reaching the duodenum, which causes marked impairment in the digestion and impairment of nutrients.

148
Q

Cystic Fibrosis: Goals

A
  1. Prevent or minimize pulmonary complications
  2. Ensure adequate nutrition for growth
  3. Encourage appropriate physical activity
  4. Promote a reasonable quality of life for the child and family, which will require a multi-disciplinary approach
149
Q

Cystic Fibrosis: Management: ABX

A

to treat pulmonary infections

150
Q

Cystic Fibrosis: Management: Physical exercise

A

Very important and is a good adjust to daily ACT. Remember exercise stimulates mucous excretion and provides a sense of well-being and increased sense of self-esteem.

151
Q

Cystic Fibrosis: Management: Bronchodilators

A

Improve ventilation.
These may be given in an aerosolized form to open up the bronchi foreasier expectoration. These are administered before percussion and postural drainage, especially when
patient is exhibiting signs of active airway disease or wheezing.

152
Q

Cystic Fibrosis: Management: Mucolytics

A

Remove mucopurulent secretions. Another aerosolized medication that’s popular is DNase or

153
Q

Cystic Fibrosis: Management: Orkambi

A

New drug
First drug for cystic fibrosis directed at treating the cause of the disease in people who have two copies of a specific mutation
For 12yr/o + who have F508del mutation, which causes the production of an abnormal protein that disrupts thow water and chloride ar transported in the body

154
Q

Cystic Fibrosis: Management: Airway clearance therapies

A

Improve ventilation and remove mucopurulent secretions
Performed 2x a day: upon rising and in the evening, more frequently when they have an infection
Perform at least 30 minutes after meal to prevent N/V
➢Chest Percussion Therapy
➢ Postural drainage- kids like wheel barrow pose, walk on their hands & you hold their feet, works great!
➢ Flutter mucous clearance device
➢ Positive expiratory pressure or PEP devices
➢ Active-cycle-of-breathing techniques
➢ High frequency chest compression

155
Q

Cystic Fibrosis: Management of Gastrointestinal Problems

A

Pancreatic Enzymes- should be taken at the beginning of the meal and should be taken WITH IN 30 minutes
of eating. These can be swallowed whole or sprinkled on food.
Encourage well-balanced, high protein, high calorie diet due to their impaired intestinal absorption
Fat soluble vitamins: A, D, E, K given in water soluble form for easy digestion
Prevent/treat constipation- treat with laxatives or stool softener

156
Q

Cystic Fibrosis: Management of Endocrine Problems

A

Diabetes mellitus (DM) or Cystic fibrosis related diabetes (CFRD) is greater in children with
CF than in general population. CFRD is the most common complication associated with CF.
By age 30 years, approx. 50% of people with CF will develop diabetes
Close monitoring of blood glucose levels is imperative

157
Q

Cystic Fibrosis: Nursing care/goals

A

Main goal also is to prevent respiratory infection
Continuous assessment of Respiratory, GI and Endocrine system
Provide supplemental oxygen as needed
Provide ACT therapy/ but not before meals or immediately after meals, to avoid inducing N/V
Administer pancreatic enzymes with all meals and snacks
Teaching regarding consuming a high calorie, high protein diet, medications, therapy
Encourage compliance with therapeutic medication and diet regimen

158
Q

Cystic Fibrosis: Family support

A

Long disease process
Persistent need for treatment
Child and family activities are built around treatments- so always involve family around treatment plans
Life long medications expensive
Poor prognosis: increased survival rates due to lung, heart, pancreas, and liver transplantation, mean age of life: 38yr, progressive and incurable
Encourage support groups
Anticipatory grieving- it’s a long disease process and life-long medications become very expensive

159
Q

BPD (Bronchopulmonary Dysplasia)

A

BPD can be mild, moderate, or severe. Diagnosis depends on how much extra oxygen a baby needs at the time of his or her original due date. It also depends on how long the baby needs oxygen therapy.

160
Q

BPD (Bronchopulmonary Dysplasia): Effects…

A

Affects infants who are born early- usually more than 10 weeks before their due dates- and still need oxygen therapy by the time they reach their original due dates are diagnosed with broncho-pulmonary dysplasia (BPD).

161
Q

BPD (Bronchopulmonary Dysplasia): Diagnosis

A

Chest x ray- shows: alveolar damage, inflammation lungs, and scarring of lungs
Blood work- to rule out infection
Echocardiogram- to rule out pulmonary HTN

162
Q

BPD (Bronchopulmonary Dysplasia) or Chronic Lung Disease: Description

A

Pathologic process related to alveolar damage from lung disease, prolonged exposure to high peak
inspiratory pressures, antimatter alveoli and respiratory tract.

163
Q

BPD (Bronchopulmonary Dysplasia) or Chronic Lung Disease: Prognosis

A

Mortality is 10-25%

164
Q

BPD (Bronchopulmonary Dysplasia) or Chronic Lung Disease: Clinical manifestations

A
Dyspnea
Barrel chest
Inability to wean from ventilator following a course of respiratory distress syndrome
Wheezing
Cyanosis
Irritability
Nasal flaring
Retractions
165
Q

BPD (Bronchopulmonary Dysplasia) or Chronic Lung Disease: Therapeutic management

A
Administer maternal steroids
Administer exogenous surfactant post-natal ● Use nasal CPAP
Prevent air leaks
Use high frequency ventilation
Maintain adequate oxygenation
Administer bronchodilators
Administer diuretics
Administer immunizations
166
Q

BPD (Bronchopulmonary Dysplasia) or Chronic Lung Disease: Care management

A

Monitor oxygen saturations and VS closely
Avoid hypo/hyperoxemia. So anticipate ABG or VBGs to be done routinely.
Cluster care, provide infant additional time to rest
Observe for signs of fluid overload or pulmonary edema
Assist in preventing upper respiratory infections- includes judicious hand washing and PPE when indicated
Provide increased calorie feedings with human milk fortifiers or protein supplements

167
Q

BPD (Bronchopulmonary Dysplasia) or Chronic Lung Disease: D/C teaching

A

Home ventilatory need
Medications, and their AE
Immunizations- go to all well child check ups
Preventing respiratory infections and frequent hospitalizations

168
Q

Neonatal Respiratory Distress Syndrome (RDS)

A

Almost exclusively in preterm infants.
Most common lung problem in a premature baby.
The name is applied to respiratory dysfunction in the neonate and is primarily a disease related to developmental delay in lung maturation.
Deficiency in pulmonary surfactant in the infants immature lungs.
Surfactant is a substance that keeps the tiny air sacs in the lungs open.
Responsible for more infant deaths than any other disease.
Carries the highest risk in terms of long term respiratory and neurologic complications.

169
Q

Neonatal Respiratory Distress Syndrome (RDS): Diagnosis/Clinical manifestations

A
Tachypnea (> 60 breaths/min)
Dyspnea
Nasal flaring
Retractions
Grunting
Fine inspiratory crackles
Cyanosis and/or pallor
Chest X-ray which shows common characteristics (diffuse granular pattern over both lung fields, resembles ground glass and represents alveolar atelectasis, Dark streaks representing dilated air-filled bronchioles)
170
Q

Neonatal Respiratory Distress Syndrome (RDS): Nursing management

A
Use of warmer
Close monitoring
Pulse oximetry and blood gas monitoring 
O2 therapy with CPAP
Surfactant Administration
Minimize unnecessary physical stimulation 
Positioning to facilitate breathing
Teach parents CPR and home monitoring
171
Q

Neonatal Respiratory Distress Syndrome (RDS): Supportive Measures

A

Maintain adequate ventilation and oxygenation
Maintain acid-base balance
Maintain a neutral thermal environment
Maintain adequate tissue perfusion and oxygenation
Prevent hypotension
Maintain adequate hydration and electrolyte status

172
Q

Neonatal Respiratory Distress Syndrome (RDS): Nursing responsibilities with Surfactant administration

A

Assisting in the delivery of the product
Collecting and monitoring of arterial blood gases
Continuous monitoring of oxygenation with pulse oximetry
Assessment and documentation of the infants tolerance of the procedure

173
Q

Neonatal Respiratory Distress Syndrome (RDS): Surfactant

A

May be administered at birth as a preventative or prophylactic treatment of RDS or later in the course of RDS as a rescue treatment. Studies have shown that early administration of surfactant decreased the overall incidence of BPD, need for mechanical ventilation, and fewer air leaks.

174
Q

Neonatal Respiratory Distress Syndrome (RDS): Nursing responsibilities Before/After Surfactant administration

A

Assisting in the delivery: infant is temporarily intubated, surfactant is administered down the endo-tube, give supportive O2
Turn baby from one side to other for the medication to get farther down into the alveoli, then extubated, then on supplemental O2
Collect ABG, continuous monitoring of O2
Assessment and documentation of infants tolerance of the procedure

175
Q

Foreign body obstruction: Cause

A

Swallowing of small items getting lodged in the bronchi

176
Q

Foreign body obstruction: S/S

A

Sudden, violent coughing, gagging, wheezing, vomiting, brief episode of apnea, cyanosis
Not talking
Can die with in 4 minutes if nothing is done

177
Q

Foreign body obstruction: Diagnosis

A

Good history
Physical Exam
X-ray
Endoscopy can be diagnostic and therapeutic if ever there was a doubt about foreign body obstruction.
Foreign bodies are rarely coughed up and must be removed by endoscopy

178
Q

Foreign body obstruction: Treatment

A

Removal of object via back blows and chest thrusts in infants, abdominal thrusts in children, or endoscopy
Keep environment and child quiet until object removed

179
Q

Aspiration Pneumonia

A

Foods, secretions, or liquids enter the lung and cause inflammation and chemical pneumonitis.
Difficulty swallowing, unable to swallow because of paralysis, weakness, or congenital anomalies, or an absent cough reflex, or in a child who is force fed especially if they’re crying or breathing rapidly, and tracheoesophageal fistula are at high risk for aspiration.

180
Q

Aspiration Pneumonia: Classic S/S

A

Increasing cough, fever, foul-smelling sputum, decrease in oxygenation, and evidence of chest
infiltrates on a chest x-ray.

181
Q

Aspiration Pneumonia: Treatment

A

O2 administration as needed
Elevate HOB at least 30-45. If they are at risk for vomiting or can’t protect their airway, then put them in side lying position
Encourage slow, frequent feeding
Positioning
Antibiotics if infection present
Safety teaching- teach parents how to prevent aspiration pneumonia

182
Q

Asthma: Diagnostics: Bronchoprovocation testing

A

Direct exposure of mucous membranes to a suspected antigen at increasing
concentrations. This helps identify allergens.