exam 2 Flashcards

1
Q

hypoxemia assessment findings

A

Tachypnea
Pallor
cyanosis
Respiratory distress signs
weak peripherial pulses

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2
Q

Resp distress symptoms

A

retractions, nasal flaring, grunting, head bobbing, restlessness, stridor, wheezing, rales

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3
Q

First sign of resp illness?

A

Tachypnea

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4
Q

hypoxemia management

A

-Provide O2 at the lowest liter flow that corrects the hypoxemia
-Less than 91% requires nursing intervention
-Less than 86% is a life-threatening emergency
-Chest physiotherapy–> promotes mucus clearance by mobilizing secretions
-Suctioning–> always suction the mouth before the nose in kids–> do not want to increase risk of aspiration pneumonia

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5
Q

Hypoxemia priorities of care

A

o2 therapy
pulse ox
CPT
suctioning

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6
Q

What is Aerosol therapy?

A
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7
Q

Physical findings of CF (GI)

A

-decrease pancreatic enzymes=abd distention and thick mucous
-meconium ileus at birth –>difficulty passing stool –> vomiting
-steatorrhea
-FTT
-Vitamin A, D, E, K deficiency
-PMH of respiratory infections

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8
Q

diagnostic for CF

A

Sweat chloride test
Sodium higher than 90

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9
Q

SCT indication of CF?

A

> 40 in infants (less than 3mo)
->60 for all ages

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10
Q

CF management (pulmonary)

A

-airway clearance therapy
-CPT
-aersol therapy

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11
Q

How does dornase alfa help alleviate sx of cystic fibrosis?

A

-decreases viscosity of mucus and bronchodilators

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11
Q

What medication is given with cystic fibrosis to treat pulmonary sx?

A

dornase alfa

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12
Q

Croup assessment findings

A

-barking cough
-inspiratory stridor
-tachypnea
-sudden onset at night
-self limiting (resolves on its own)
-lasts 3-5 days

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13
Q

priorities of croup

A

-educate families on sx
hospitalization for significant stridor at rest or severe retractions
-cool mist/steamy bathroom
O2—>ox continuous
-hydration

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14
Q

Racemic epinephrine

A

decrease edema, effects last up to 2 hours and sx may worsen requiring another tx

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15
Q

Chronic Asthma medications

A

Long-acting bronchodilators/B2-adrenergic Agonist (formoterol) Inhalation corticosteroid (Fluticosone) Mast-cell Stabilizer (Cromolyn) Leukotriene Receptor Antagonists (Montelukast

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16
Q

s/s of asthma

A

hacking, nonproductive cough, dyspnea, chest tightness, wheezing or crackles
A SILENT CHEST IS A OMNIOUS SIGN (no airmovement)

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17
Q

Status asthmaticus

A

a prolonged severe asthma attack uncontrolled by typical regimen. LIFE THREATENING

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18
Q

Status asthmaticus symptoms

A

wheezing or lack of air movement in lungs
labored breathing
accessory muscles
hypoxia
diaphoresis

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19
Q

Status asthmaticus Nursing actions/ Priority of care

A

Cardioresp monitoring, O2, ABG’s
-admin bronchodilators and anti-inflammtory meds
-prepare for intubation

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20
Q

Status asthmaticus medication management

A

Theophylline
Mg sulfate Iv
Heliox
Ketamine

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21
Q

Theophylline

A

anti inflammatory and reverses corticosteroid resistance

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22
Q

Theophylline has a risk for toxicity so we have to frequently monitor?

A

Blood levels

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23
Q

Mg sulfate

A

relaxes bronchial muscles, expanding airways

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24
Q

Heliox

A

mix of Helium and O2—> decreases airway resistance

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25
Q

Ketamine

A

smooth muscle relaxant

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26
Q

Epiglottis assessment findings

A

rapid onset (within hours): High fever and toxic appearance
unable to whisper or speak
Lateral neck x-ray +Epiglottis
-Tripod position neck thrust forward.
anxiety
-drooling and dysphagia !!!
NO COUGH

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27
Q

Management of Epiglottis

A

Focuses on airway maintaince, icu admission
iv abx
-100% NRB mask.

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28
Q

Priorties of Epiglottis

A

-Never attempt to visualize the throat
-No supine position
-need HOB elevated.

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29
Q

Foreign Body Aspiration assessment findings

A

sudden onset of cough, wheezing,
stridor: upper airway
Unilateral BS (wheezing & decreased in
R/clear in L)

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30
Q

Foreign Body Aspiration Risk factors

A

common in ages 6 months-3 years, upper and lower resp.

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31
Q

Foreign Body Aspiration parent education

A

keep coins, small batteries, latex balloons out of reach
-no popcorn, peanuts until age 3, chop all foods into pieces

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32
Q

Where are most objects aspirated?

A

right mainstream bronchus because it is at a less acute angle than the left mainstream bronchus.

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33
Q

Dehydration assessment findings

A
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34
Q

Dehydration Management: oral rehydration

A

sunken fontanells
decreased LOC
sunken eyes
no tears
dry mm
sudden weight loss
decreased UOP
delayed cap refill

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35
Q

dehydration findings vitals

A

-electrolyte imbalances
-increased hr
-increased rr
-decreased bp

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36
Q

Rehydration Therapy Oral

A

attempt 1st. Pedialyte
mild: 50ml/kg in 4 hours
moderate: 100ml/kg in 4 hours
Diarrhea losses: 10ml/kg for each stool

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37
Q

Rehydration IV

A

20ml/kg of Ns or LR bolus (in addition to maintenance)

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38
Q

Maintenance fluid

A

100ml/kg–1st
50ml/kg-2nd
20ml/kg for remaining.
24 hours—>24/24

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39
Q

G.E.R.D. managements

A

Conservative: small frequent feedings, thickened feedings,
meds
Surgical: nissan
Meds: PPI/ h2 receptor antagonist

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40
Q

G.E.R.D. pt education

A

sit up after meals

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41
Q

G.E.R.D s/s

A

arching of head an neck during feeding, frequent vomitting, irritability during feeding, wet burps, apnea, ALTE

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42
Q

When should patients with G.E.R.D take their medications?

A

30 minutes before feeding

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43
Q

PPI’s include

A

esomprazole, lansoprazole, omeprazole, pantoprazole

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44
Q

H2-receptor-antagonist include

A

ranitidine, cimetidine, famotidine

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45
Q

What will labs show if patient has GERD?

A

CBC may show anemia
Hemoccult: positive for blood if chronic esophagitis

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46
Q

complications of GERD

A

laryngitis, recurrent PNA, asthma, apnea or ALTE

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47
Q

What is ALTE

A

apparent life threatening event

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48
Q

apparent life threatening event is?

A

a sudden event where the infant exhibits apnea, change in color, change in muscle tone and choking

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49
Q

physical cues in children

A

heartburn, abd pain, diff swallowing, chronic cough, non cardiac Cp
emesis with blood or bile

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50
Q

physical cues in infants

A

arching of head and neck during feeding, irrtiability frequent spitting up or vomitting. Resp issues, FTT, apnea or ALTE

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51
Q

what is HPS and when does it occur?

A

Hypertrophy of the pylorus muscle causing gastric outlet obstruction.
usually in 1st 3-6 weeks of life

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52
Q

s/s of HPS

A

foreceful projectile vomitting
hunger soon after vomitting
weight loss
olive shaped movable mass in RUQ

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53
Q

Labs for HPS

A

Hypochloremia
hypokalemia
metabolic alkalosis

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54
Q

Management for HPS

A

Laproscopic surgery
IVF NGT

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55
Q

Priority care of HPS

A

Iv fluids–> correct electrolyte and dehydration
NGT—? decompression NPO, strict I/O
-Wound care
Resume PO feedings in 1-2 days

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56
Q

Hirschsprung’s expected findings newborn

A

failure to pass meconium, bilious emesis
abd distention

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57
Q

Hirschsprung’s expected findings infant/child

A

FTT, chronic constipation

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58
Q

Treatment of Hirschsprungs

A

4 phase surgery with colostomy

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59
Q

Management of Hirschusprungs

A

high protein high cal diet
accurate I/O
iv fluids and abx
post op teach about stoma care

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60
Q

What should we observe for in Hirschusprungs?

A

entercolitis

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61
Q

S/s of entercolitis

A

fever, vomitting, abd distention, explosive diarrhea or rectal bleeding.
NOTIFY IMMED

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62
Q

tx of entercolitis

A

Broad spectrum abx, IVF resuscitation and rectal washout

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63
Q

Name of surgery for Hirshusprungs

A

resection and re-anastamosis: done in stages depening on degree of colitis/bowel dilation

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64
Q

What is intussusception

A

proximal segment of bowel telescopes into a distal portion of bowel. Results in lymphatic and venous obstruction

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65
Q

s/s Intussusception

A

flare then resolves spontaneous reduction
sudden onset of crampy or severe adb pain, draws knees to chest. v/d

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66
Q

Hallmark sign of Inutssusception

A

sausage shaped mass in upper mid abdomen. Red current jelly stools

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67
Q

Treatment of Intussusception

A

IVF/NGT
air enema to correct or surgery if recurrent

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68
Q

What do stools look like in Intussusception?

A

blood and mucus (red current jelly)

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69
Q

What is important with intussusception?

A

keep patient NPO

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70
Q

Cleft lip and palet pre op

A

priority: nutrition and infant parent bonding
-burp infant to expel excess air
-encourage therapeutic techniques

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71
Q

cleft lip and palet post op

A

Priority: preventing injury to suture line
position on side of supine immediately post op with arm restraints
-avoid straw, spoon anything in mouth
-prevent crying

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72
Q

Risk factors for Cleft

A

smoking
prenatal infection
folate deficiency
antidepressants and steroid use

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73
Q

Complications of Cleft

A

Feeding difficulties
Regurgitation
Altered Dentition
Delayed/altered speech
Otitis media/effusion

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74
Q

What is effusion?

A

fluid build up in the middle ear.

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75
Q
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76
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77
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78
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79
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80
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81
Q
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82
Q

What is heart failure

A

inability of heart to adequately pump blood to meet metabolic and physical demand of the body

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83
Q

L sided heart failure symptoms

A

increased work of breathing, tachypnea, wheezing, rales, cough, DOE, feeding difficulties

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84
Q

Right sided heart failure symptoms

A

hepatomegaly, edema, JVD, periorbital edeam, wt gain

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85
Q

Pathophysiology of coarctation of the aorta (CoA)

A

-narrowing of the aorta that occurs most often near or beyond the PDA (patent ductus arteriosus)

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86
Q

During CoA, pressure increases near the defect and distal to it. What are assessment findings because of this?

A

Increased BP in upper extremities and decreased BP in lower extremities

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87
Q

What is most important to assess when suspecting a patient has CoA

A

all pulses

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88
Q

Key assessment findings for CoA

A

-full bounding pulses in upper extremities
-weak or absent pulses in lower extremities
-soft or moderately loud systolic murmur at base of left axilla
-frequent epistaxis ; leg pain with activity (older child)

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89
Q

Diagnostics for CoA

A

-echo: assess extent of narrowing and collateral circulation
-CXR: left sided cardiomegaly, rib notching
-CT, MRI, ECG: PRN

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90
Q

Treatments for CoA

A

Infants and children: balloon angioplasty
Adolescents: stents
Surgical: repair of defect in children <6 months

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91
Q

What is ventricular septal defect (SVD)

A

-most common congenital heart defect
-Acyanotic heart failure

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92
Q

Pathophysiology of VSD

A

-opening between the ventricles causing left to right shunt
-incrased blood flow to RV –> increased blood flow to lungs –> pulmonary artery HTN, right ventricular hypertrophy

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93
Q

complications of VSD

A

-aortic valve regurgitation and endocarditis

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94
Q

Physical assessment findings for VSD

A

-most children asymptomatic
-palpable thrill in chest
-CHF symptoms
-HOLOSYSTOLIC HARSH MURMUR (big one) heard alone the left sternal border

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95
Q

What type of CHD is Patent Ductus Arteriosus (PDA)

A

cyanotic (increased pulmonary flow)

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96
Q

Assessment findings of PDA?

A

-depends on size of opening
-tachycardia
-diastolic BP typically low due to shunting
-bounding peripheral pulses (from increased CO)
-widened pulse pressure (> 30 mmHg)
-hypoxia/ resp distress (due to pulmonary edema)
-harsh, continuous, machine-like murmur (loudest under left clavicle at 1st/2nd ICS)

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97
Q

Treatment for PDA

A

Non surgical: admin of indomethacin, insertion of coils to occlude the PED, diuretics, extra calories for infants
Surgical: thoracoscopic repair (ligate vessels)

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98
Q

What is the ‘fatal four’ found in Tertralogy of Fallot

A
  1. ventricular septal defect (VSD)
  2. pulmonary stenosis (R to L shunt)
  3. hypertrophy of right ventricle
  4. overriding aorta (hypoxemia)
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99
Q

Clinical features of tetralogy of fallot

A

-fainting, difficulty breathing, easy fatigue, color changes w/ feeding, crying, activity
-loud, harsh systolic murmur
-polycythemia
-TET spells (blue baby) especially in AM

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100
Q

Specific symptoms of TET spells found in Tetralogy of Fallot

A

-cyanosis
-hypoxemia
-dyspnea
-agitation
-all the signs lead to anoxia and unresponsiveness

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101
Q

treatment of tetralogy of fallot

A

-prostaglandins (to keep PDA open to increase pulmonary blood flow)
-surgical repair of R ventricular outflow obstruction and VSD closure

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102
Q

Nursing interventions for tetralogy of fallot

A

-place infant or child in knee-to-chest position or squatting
-supplemental oxygen
-administer morphine sulfate
-supply IV fluids
-administer propranolol

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103
Q

Is Kawasaki’s disease acquired or congenital

A

acquired (caused by unknown infectious organism)

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104
Q

Assessment findings for Kawaski’s disease

A

-High fever 103 F for at least 5 days unresponsive to ABX
-bilateral conjunctivitis (without exudate)
-dry mouth and throat, fissured lips, strawberry tongue, pharyngeal/ oral mucosa edema
-cervical lymphadenopathy
-desquamation (peeling) of fingers, toes and perineal areas; rash over body
-CV: tachycardia, gallop, murmur; note hyperdynamic precordium

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105
Q

Nursing management of Kawaski disease

A

-administer IVF, IVIG, and PO fluids as ordered
-Acetaminophen (fever) , cool cloths
-DW , strict I&O
-rest and quiet, family support
-lip lubricants and mouth care
-clear liquids and soft foods

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106
Q

Medication management for Kawasaki

A

-Immunoglobulin (IVIG)
-high dose IV (2g/kg) over 8-12 h
-High Dose aspirin
-80-100 Mg/Kg/day q 6 h
-follow w/ low dose after fever breaks
-indefinite use if aneurysms develop
-additional anti-coag if large aneurysm

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107
Q

What medications are given for heart failure?

A

Metoprolol
Lasix: used to manage edema
Captopril/ Enalopril
Digoxin

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108
Q

Nursing considerations and side effects of metoprolol

A

-Monitor HR and BP b4 administering
-SE: dizziness, hypotension, HA

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109
Q

Nursing actions and side effects of Lasix

A

-Monitor for hypokalemia, monitor BP, monitor I & O, monitor DW
-SE: hypokalemia, NV, dizziness, ototoxicity

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110
Q

Nursing actions for ace-inhibitors

A

-monitor BP before and after administration

111
Q

Nursing actions for digoxin?

A

-count apical pulse 1 full minute
-HOLD IF: <90 infant, <70 child, <60 adolescent
-monitor digoxin levels (0.8-2)

112
Q

What are signs of digoxin toxicity?

A

-N/V, anorexia, bradycardia, dysrhythmias
-green yellow halos

113
Q

Digoxin antidote

A

-digoxin immune fab

114
Q

Indications of metoprolol

A

-decrease HR and BP and promote vasodilation

115
Q

Indications of Lasix

A

manage excess fluid and sodium

116
Q

Indication for captropril

A

reduce afterload by causing vasodilation –> decreased pulmonary and systemic vascular resistance

117
Q

Indication of digoxin

A

decrease contractility of heart muscle

118
Q

What is the pediatric assessment triangle?

A

addresses Childs appearance, work of breathing, and circulation to skin

119
Q

Examples of appearance the nurse should assess for in the pediatric assessment triangle

A

-abnormal tone
-decreased interactiveness
-decreased consolability
-abnormal look/ gaze
-abnormal speech / cry

120
Q

Examples of work of breathing the nurse should assess for in the pediatric assessment triangle

A

-abnormal sounds
-abnormal position
-retractions
-flaring
-apnea/gasping

121
Q

What is the purpose of Aspirin to treat Kawasaki disease?

A

prevent clots

122
Q

Why are clients wit kawaskis disease at risk for dehydration

A

-painful mouth makes them less likely to drink
-already losing fluids from fever

123
Q

What is acute rheumatic fever?

A

-Group A beta hemolytic strep (GAS) ; strep throat

124
Q

clients with acute rheumatic fever may report a history of?

A

-sore throat and pharyngitis within past 2-3 weeks
-recent URI
-recurrent skin infection
-fever
-joint pain

125
Q

What children are likely to acquire acute rheumatic fever

A

-children who have less access to healthcare

126
Q

Minor manifestations of acute rheumatic fever

A

Fever, arthralgia, increased ESR, prolonged PR interval

127
Q

Major manifestations of acute rheumatic fever

A

-carditis (w/ valvulitis)
-polyarthritis (multiple joints inflamed/ migratory)
-subcutaneous nodules (firm and painless nodules over knees, wrists, elbows)
-chorea (jerking muscle movements in face hands and feet)
-erythema marginatum (rash on trunk and extremities)

128
Q

Diagnostic criteria for acute rheumatic fever includes?

A

-presence of 2 major manifestations
OR
-presence of 1 major and 2 minor

129
Q

Sinus tachycardia characteristics

A

fever, pain, fear, fluid loss or hypoxia.

129
Q

sinus tachycardia in infant characteristics

A

rate is <220(160-220)

130
Q

sinus tachycardia management

A

Focus on underlying cause
-INAPPROPRIATE and dangerous to treat with medications or defib aimed at decreasing heart rate

130
Q

Sinus tachycardia characteristics in children

A

<180 (130-180)bpm with a beat-to beat variability, p wave present and normal
QRS normal

131
Q

SVT characteristics

A

infants: >220bpm
Children >180 with onset of termination, p wave is flattened, and QRS is normal

132
Q

SVT management Compensated

A

Vagal maneuvuers such as ice to face of blowing through a straw that is obstructed
-adeosine if vagal maneuver fails.

133
Q

Sinus bradycardia characteristics

A

No cardiac nodal abnormality
p-wave and qrs remain normal on ecg

133
Q

What causes SVT?

A

re-entry problem in the cardiac conduction system or genetic abnormalities like WOLFF-Parkinson, WHITE syndrome, or with meds like caffeine or theophylline

134
Q

Sinus bradycardia <60

A

life threatening
altered perfusion
hypoxia shock
respiratory compromise

135
Q

Sustained bradycardia is commonly associated with ___ and is a ___

A

arrest, ominous sign

135
Q

SVT management uncompensated

A

adenosine or synchronized cardioversion

136
Q

post-streptococcal glomerulonephritis
history

A

current or past history of recent pharyngitis/strep throat or skin infection

136
Q

Compensated SVT s/s

A

tachycardia, Heart rate >220
Abnormal p waves
alert well perfused child
ha, dizzy in older child

137
Q

post-streptococcal glomerulonephritis physical findings

A

fever, lethargy, HA, decreased urine output, abd pain, vomitting, and anorexia
Htn edema, urine for gross hematuria

137
Q

Uncompensated SVT s/s

A

Tachy, hr>220
abnormal p-waves
signs of shock: aloc, poor perfusion, weak pulse.

138
Q

post-streptococcal glomerulonephritis
labs and dx

A

urine dip stick: hematuria and proteinuria
Bun/ Creatinine: increase
ESR: increased
ASO Titer: increased

139
Q

post-streptococcal glomerulonephritis priority of care

A

-Monitoring fluid status and managing hypertension
-Maintain sodium and fluid restriction during acute phase
-Daily weights
-Urine output improvement of color
-skin break down
-bed rest

140
Q

meds for post-streptococcal glomerulonephritis

A

antihypertensives: nifedipine, labetalol
diuretics

141
Q

What should we educate our clients and family to do for post-streptococcal glomerulonephritis?

A

monitor OPand BP and follow diet restrictions

141
Q

What is post-streptococcal glomerulonephritis?

A

inflammation resulting in altered GF function (decreased GFR )

142
Q

Hemolytic uremic syndrome history

A

Recent episode of acute gastroenteritis watery diarrhea accompanied by cramping that becomes bloody over several days. Possible vomitting

143
Q

Hemolytic uremic syndrome assessment findings

A

pallor and toxic appearance
edema and oliguria or anuria
Neuro: irritability, altered LOC, seizures, posturing or coma.

144
Q

UA of post-streptococcal glomerulonephritis

A

proteinuria, hematuria, leukocytes, casts

144
Q

What does the urine look like in post-streptococcal glomerulonephritis?

A

tea color, cola color or dirty green color

145
Q

CBC of HUS

A

CBC: mod-sev anemia
mild-sev thrombocytopenia,

145
Q

What kind of edema do they have in post-streptococcal glomerulonephritis?

A

general or periorbital, signs of fluid overload or CHF.

146
Q

Chem panel of HUS

A

decreased sodium, increased potassium, increased PO4
Hyponatremia/ Hyperkalemia

147
Q

ABG of HUS

A

metabolic acidosis

148
Q

Patient education of hus

A

prevention measures: handwashing after everything bahahha
cook to 155

149
Q

Priority of care HUS

A

maintaining fluid balance, managing hypertension, acidosis, electrolyte abnormalities

150
Q

Continued priorities of care for HUS

A

PRBC and platelets (only for active bleeding or severe thrombocytopenia. IVIG may be considered
REPORT all abnormal findings

150
Q

What are the three features of hemolytic uremic syndrome?

A

hemolytic anemia, thrombocytopenia, acute renal failure

151
Q

Hydrocele

A

fluid in scrotal sac: usually resolves by 12 months of age: transilluminate

152
Q

Varicocele

A

venous varicosity along the spermatic cord

152
Q

What are other assessments from the history we should pay attention to for HUS?

A

ingestion of ground beef
visits to water park
public pool
petting zoo
all prior to developing diarrhea

153
Q

What does the scrotal look like with varicocele?

154
Q

What can varicocele cause?

A

low sperm count and infertility

155
Q

Management for Compensated SVT

A

-vagal maneuvers: ice on face / blow through obstructed straw
-Adenosine if maneuvers fail

156
Q

Uncompensated SVT management

A

-adenosine or synchronized cardioversion

157
Q

If we notice our client has sudden weight gain, what is our priority nursing action?

A

-assess height and weight and compare
-take daily weights

158
Q

If our client has difficulty eating, what questions should we ask the parent?

A

Onset of sx, how much they eat, if they tire easily, if there are color changes present

159
Q

Nursing actions with difficulty feeding?

A
  1. limit feedings to 20 min –> remainder via OG / NG
  2. cut cross in nipple
  3. semi-upright position
160
Q

Interventions if our client has a decreased activity level?

A

-cluster care, frequent rest periods, bathe PRN

161
Q

If our client has decreased # of wet diapers, what nursing assessments should we perform?

A
  1. I and O
  2. edema
  3. pulses
  4. organomegaly
162
Q

Nursing actions for decreased number of wet diapers

A

I and o’s, medications

163
Q

What current/ past Hx will be seen with glomerulonephritis?

A

-recent pharyngitis/ strep throat or skin infection

164
Q

What are physical assessment findings of glomerulonephritis

A

-fever, lethargy, HA, decreased UOP, abd pain, vomiting, anorexia

165
Q

Will blood pressure be high or low in glomerulonephritis

A

High –> have HTN

165
Q

Treatment of hydrocele and varicocele?

A

surgery to correct spontaneous resolution

166
Q

Glomerulonephritis causes what kind of edema?

A

-general or periorbital
-other sx of fluid overload or CHF

166
Q

Management of hydrocele?

A

watchful waiting, to observe for spontaneous resolution

167
Q

What color is urine in glomerulonephritis

A

-tea color
-cola color
-dirty green color

167
Q

Management of Varicocele

A

if no resolution or decreased testicular volume, urologist referral for possible surger

168
Q

What will be seen on a urine dipstick that indicate glomerulonephritis

A

-hematuria, proteinuria

168
Q

Important teaching for Hydrocele and Varicocele

A

Hydrocele does not interfere with fertility but VARICOCELE can if left untreated.

169
Q

BUN, creatinine, and ESR will be elevated or decreased in glomerulonephritis?

169
Q

Hydrocele physical cues

A

enlarged painless scrotum decreases in size when lying down. Transilluminate with light source. Fluid renders testes impalpable

170
Q

What is the priority of care for glomerulonephritis?

A

-monitoring fluid status and managing HTN

170
Q

Varicocele physical cues

A

mass on one or both sides, blueish in color, worm-like spermatic veins and pain with palpitation

171
Q

What should be restricted in glomerulonephritis during the acute phase

A

sodium and fluids

171
Q

What is nephrotic syndrome?

A

kidney filtration disorder where too much protein (albumin) is filtered out of the blood due to damaged basement membrane of the renal glomerulus

172
Q

Nursing interventions during glomerulonephritis also include?

A

-DW
-monitor urine output and color
-monitor skin breakdown
-monitor for renal/ neuropathy changes
-maintain bed rest and cluster care

172
Q

Nephrotic syndrome most common in?

A

children (minimal change nephrotic syndrome with onset of age by 6.

173
Q

What precautions should children with glomerulonephritis be placed on

A

seizure precautions

173
Q

Nephrotic syndrome history

A

Periorbital edema upon waking that progresses to generalized edema throughout the day
FROTHY URINE

174
Q

What medications are used to treat glomerulonephritis

A

-ABX for strep
-nifedipine and labetalol
-diuretics

174
Q

Nephrotic syndrome physical cues

A

irritability or fussiness
skin stretched, tight appearance, pallor or breakdown
heart and lung sounds related to fluid overload
abd distention and note ascities

175
Q

What are the three features of hemolytic uremic syndrome (HUS)

A

-hemolytic anemia, thrombocytopenia, acute renal failure

175
Q

Nephrotic syndrome nursing management

A

I/O daily weights, urine protein, sodium restriction when edematous.
Prevent infection: can cause relapse.

176
Q

What bacteria causes hemolytic uremic syndrome?

176
Q

Nephrotic syndrome labs

A

Proteinuria
hyperlipidemia
edema

177
Q

what happens in the kidneys causing hemolytic uremic syndrome?

A

RBC are destroyed and fibrin clots are formed clogging the kidneys

177
Q

Medications for Nephrotic syndrome

A

Diuretics (furosemide), may require K replacement
Corticosteroids (prednisone) take with meals for 4-6 weeks then taper over 2-5 months

178
Q

What may our clients say in their recent hx that will pinpoint hemolytic uremic syndrome?

A

-recent acute gastroenteritis
-watery diarrhea
-cramping
-becomes bloody
-possible vomiting
-ingestion of ground beef, visits to water park/public pool/ petting zoo prior to developing bacteria

178
Q

Side effects of Prednisone

A

increased appetitie, weight gain, cushings features, mood swings.

179
Q

Physical assessment findings of hemolytic uremic syndrome?

A

-pallor and toxic appearance
-edema, HTN, oliguria, anuria
-jaundice and weakness
-dark colored urine
-petechiae, ecchymoses, hematuria, hematoemesis, splenomegaly

180
Q

Neuro status with hemolytic uremic syndrome will be

A

-irritable
-altered LOC
-seizures
-posturing and coma

180
Q

What is Enuresis ?

A

Bedwetting: continued incontience beyond the age of toilet training

181
Q

What is hydrocele?

A

-fluid in scrotal sac
-benign, common in newborns
-usually resolves by 12 months

181
Q

Primary enuresis

A

never achieved extended dry periods

182
Q

What is varicocele?

A

-venous varicosity along the spermatic cord
-most common in adolescence
-can cause low sperm count or reduced motility –> infertility

182
Q

Secondary enuresis

A

Onset after a period of urinary continence

183
Q

Physical cues of hydrocele?

A

-enlarged painless scrotum
-size decreases when lying down
-testes impalpable
-transilluminate with light source

183
Q

Enuresis nursing assessment

A

daytime or nighttime incontience
urine holding behaviors (squatting dancing staring, rushing to bathroom)

184
Q

Physical cues of varicocele?

A

-mass on one or both sides
-blueish in color
-worm like veins
-pain with palpation

184
Q

Enuresis history

A

note history of constipation
toilet training history
family disruption and stress and excessive family demands regarding TT.
Large amounts of fluid before HS, caffiene?
night time routine

185
Q

Management of hydrocele

A

-‘watchful waiting’ to observe for spontaneous resolution
-surgical correction if no resolving on own

185
Q

Enuresis interventions

A

Assist in management of incontinence and promote wellness and prevent complications

186
Q

Management of varicocele?

A

-if no resolution or decreased testicular volume urologist referral
-possible varicocelectomy

186
Q

Enuresis parent education

A

restrict fluids 2 hours before bedtime
void before going to bed
include child in bed linen changes.
avoid pull ups.

187
Q

What is nephrotic syndrome?

A

too much protein (mainly albumin) is filtered out of the blood due to damaged membrane of glomerulus

187
Q

Medications for Enuresis

A

Antiduretic (desmopressin)

188
Q

Nephrotic syndrome is usually idiopathic which means?

A

it occurs on its own ; usually occurs by age 6

188
Q

Desmopressin for Enuresis

A

pill or melt away at bedtime
hold for diarrhea or vomiting
adverse: HA nausea

189
Q

Children with nephrotic syndrome will show a history of

A

periorbital edema upon waking that progresses to generalized edema thorughout the day

189
Q

Phimosis

A

Foreskin can not be retracted, normal in newborn, pathological if persists

190
Q

Physical cues of nephrotic syndrome include

A

-recent, sudden weight gain
-frothy urine
-N/V
-pallor and skin breakdown
-stretched skin
-irritability
-sx of fluid overload (have severe edema)

190
Q

Paraphimosis

A

restrictive band behind the glans penis—->incarceration and necrosis
pain or swollen penis
BOTH: irritation, erythmea, edema, or discharge

191
Q

Do children with nephrotic syndrome have edema, proteinuria, and hyperlipidemia?

191
Q

Phimosis s/s

A

uti, irritation, balantis (inflammation of the foreskin)
bleeding in the prepuce on dysuria

192
Q

Serum albumin will be ___ with nephrotic syndrome, but urine albumin will be ?

A

deceased ; increased (have proteinuria)

192
Q

Tx of Phimosis

A

topical steroid cream BID x1

193
Q

will cholesterol and lipids be elevated in nephrotic syndrome?

193
Q

Treatment of Paraphimosis

A

surgical reduction

194
Q

will BUN and creatinine be elevated in nephrotic syndrome?

A

yes IF renal failure is occurring

194
Q

Priorities of care for Phimosis and paraphimosis

A

Apply topical steroid medications as prescribed for phimosis with genital retraction of foreskin.

195
Q

Priority nursing care for nephrotic syndrome include?

A

-monitoring I and O’s
-monitoring urine protein
-DW
-sodium restrictions
-prevent infection – can cause relapse ; vaccination status

195
Q

Priority care of paraphimosis

A

Routine post-op care and pain management of surgical site
teach families appropriate hygiene

196
Q

What medications are given with nephrotic syndrome>

A

Prednisone (60 mg/m2/day for 4-6 wks then tapered over next 2-5 months)
Furosemide (diuretics)

196
Q

Hypospadias

A

an abnormal urethral opening on ventral surface of penis (below glans penis)

197
Q

Epispadias

A

an opening on the dorsal penile surface (above glans penis)

197
Q

Nursing considerations with prednisone

A

-take with meals
-can cause increased appetite, weight gain, Cushing’s features, and mood swings

198
Q

Hypospadias physical findings

A

urethral opening off center/ not a tip of penis
presence or absence of testicles in scrotal sac (cryptorchidism) or hydrocele or inguinal hernia.

198
Q

Nursing consideration with diuretics

A

may require K+ replacement

199
Q

Hypospadias/ Epispadias main s/s

A

cannot direct urine stream in standing position
Circumcision should be delayed until repaired.

199
Q

Children with nephrotic syndrome taking corticosteroids may experience

A

altered body image

200
Q

hypospadias treatment

A

surgically repaired

200
Q

What education is important to tell families with children that have nephrotic syndrome

A

-may return to school but avoid sick children
-monitor temp and urine dipsticks to prevent relapse
-how to properly use urine dipstick to monitor for protein

201
Q

Post op Hypospadias/ Epispadias care

A

secure urethral stent/drainage tubing. Compression dressing, Double diapering.

201
Q

What is enuresis?

A

continued incontinence beyond the age of toilet training

202
Q

What is primary and secondary enuresis

A

primary: never achieved extended dry periods
Secondary: onset after a period of urinary continence

203
Q

Fluid requirements and children with enuresis?

A

encourage fluids during the day, restrict at least 2 h before bed

204
Q

Caffeine and chocolate with enuresis

A

-limit caffeine and chocolate after dinner

205
Q

What type of toileting schedule should be used for children with enuresis?

A

ensure child voids before bedtime ; wake up at scheduled intervals to void

206
Q

Should pull-ups be used in enuresis?

A

no pull-ups, use a reward system

207
Q

Children with enuresis that wet the bed should be included in?

A

bed linen changes in a non-punitive manner

208
Q

Nursing interventions for enuresis?

A

-conditioning therapy - alarm sensor
-Kegal/pelvic exercises

209
Q

What medication is given for enuresis?

A

antidiuretic (desmopressin)

210
Q

Nursing considerations for giving desmopressin to treat enuresis?

A

-give at bedtime
-hold for diarrhea and vomiting
-restrict fluid intake after dinner
-only allow sips of water 1 h b4 taking and 8 h after

211
Q

Adverse effects of desmopressin?

A

headache and nausea

212
Q

What is phimosis?

A

when the foreskin cannot be retracted, which is normal in the newborn, but pathological later

213
Q

What is paraphimosis?

A

serious medical condition causing a restrictive band behind the glans penis, which can cause an incarceration and necrosis of the penile head

214
Q

What should be applied BID for one month to treat phimosis?

A

topical steroid cream

215
Q

If urine is retained in foreskin after voiding during phimosis, what can occur?

A

irritation, UTI, and balanitis

216
Q

What is required to correct paraphimosis?

A

surgical reduction

217
Q

What can be done to cure both phimosis and paraphimosis?

A

circumcision

218
Q

Physical cues for phimosis?

A

-irritation or bleeding in the prepuce
-dysuria

219
Q

Physical cures for paraphimosis?

A

-pain and swollen penis

220
Q

Irritation, erythema, edema, or discharge from penis are physical cues for both

A

phimosis and paraphimosis

221
Q

What is hypospadias?

A

-when urethra opens on ventral surface of penis

222
Q

What may happen if hypospadias is left uncorrected

A

-may cause erectile dysfunction

223
Q

Physical findings of hypospadias?

A

-hx of unusual urine stream
-urethral opening off center/ not at tip of penis
-chordee (fibrous band that causes penis to bend downward)
-presence of absence of testicles in scrotal sac (cryptorchidism)
-hydrocele
-inguinal hernia

224
Q

What is the treatment for hypospasias

225
Q

What should be delayed in infants to help treatment for hypospadias

A

circumcision

226
Q

Management of GI sx in cystic fibrosis include

A

-pancreatic enzymes
-high protein and calorie diet
-fluids
-fat-soluble vitamins