Test #4 Flashcards

1
Q

results from the failure of a fetal duct in the intestine to fuse normally in utero

A

Meckel’s diverticulum

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1
Q

baseline tests to get before scoliosis surgery

A

x-rays, PFTs, ABGs

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2
Q

complications of chronic vaso-occlusive crisis

A

increased r/f URI osteomyelitis retinal detachment liver and renal failure

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2
Q

Duchenne MD

A

mutation in gene for dystrophin protein that maintains muscle fibers; muscle wasting that begins in pelvis and hips

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2
Q

antidote for iron OD

A

Deferoxamine

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3
Q

Failure to Thrive diagnosed when weight is

A

below the 3rd percentile

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3
Q

first 24-48h after a burn injury

A

Emergent (Resuscitative) Phase Fast fluid resus

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4
Q

s/s Vaso-occlusive crisis

A

**pain; swollen joints; hematuria; fever

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5
Q

complications of infant GER

A

can injure esophageal mucosa, lead to FTT, bleeding, dysphagia; can trigger RAD; stricures; aspiration PNA; esophagitis

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6
Q

Post op care for Hirschprung’s correction

A

ng tube, NPO to decompress ostomy care monitor abd girth

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7
Q

aplastic crisis

A

worsening of baseline anemia in SCA; viral trigger

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7
Q

s/s child abuse

A

inconsistency between injuries and story; chip/spiral Fx; child withdraws or is fearful of parents; behavior changes, sleep disturbances

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8
Q

s/s TEF

A

excessive drooling; 3Cs after feeding: coughing, choking, and cyanosis

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9
Q

Meckel’s diverticulum s/s

A

Painless bloody stools with bright red mucus

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9
Q

tylenol antidote

A

large dose Mucomyst

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10
Q

congenital aganglionic megacolon

A

Hirschprung’s disease–missing nerves at the end of the colon, obstruction results from inadequate motility

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11
Q

treatment for imperforate anus or fistula

A

surgical reconstruction and temporary colostomy

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11
Q

complications of Hirschprung’s disease

A

Enterocolitis (fever and explosive diarrhea) that can lead to sepsis, peritonitis, or shock of bowel perfs; anal stricture/incontinence; fussy eating/manipulation with meals

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12
Q

Meckel’s diverticulum Dx

A

radionucleotide scan

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13
Q

surgery to fix pyloric stenosis

A

pyloromyotomy

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14
Q

non-surgical treatment for intussusception

A

enema or air inflation; successful if brown stool passes but can often recur

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15
Q

noninvasive, keeps hips abducted and in socket in a child with DDH

A

Pavlik harness (6 mos)

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16
Q

with hemophilia its important to monitor for

A

brain bleed: HA, slurred speech, decreased LOC

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16
Q

Pre op most babies with TEF have

A

aspiration pneumonia

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17
cleft palate repair
palatoplasty; performed between 12-18 mos; only cup liquids and soft foods 4-6 weeks postop
17
three zones of burns
Zone of Coagulation (non-viable); Zone of Stasis (tissue can be salvaged by fluid resus and reducing edema); Zone of Hyperemia (usually heals spontaneously)
18
severe GER causing FTT or tracheomalacia treat with
Nissan fundoplication: stomach wrapped around esophagus to increase LES tone
19
sickle cell anemia s/s
pain; SOB/fatigue/tachycardia; pallor or jaundice; nail bed deformities; Hand Foot syndrome=symmetric painful swelling; low fever; FTT
20
sickle cell pts need this test yearly to monitor for CVA from ages 2-16
transcranial doppler
21
screening tool for sickle cell anemia
SickleDex
22
RFs for sickle cell crisis
hypoxemia; infection; dehydration; fever
23
s/s hemophilia
bleeding episodes; joint pain and stiffness (hemoarthrosis), can lead to deformities; activity intolerance, prolonged PTT
23
inheritance pattern of Duchenne MD
X-linked recessive
25
Complications of cleft lip/palate
Aspiration, sinus infections; ear infections, hearing loss; speech delay; dental delay; feeding aversions
26
pinworm dx
Tape test
28
TEF diagnosis
X-ray with ng/og tube and air injection to show pouch
29
s/s tylenol OD
n/v; jaundice; RUQ pain; bleeding; coma
31
Leukemia Dx
Bone marrow biopsy showing immature leukemic blast cells
32
s/s tracheomalacia
barky cough and intermittent stridor; may outgrow or need trach temporarily
32
post op for scoliosis surgery
ICU; ng tube, foley, blood transfusions (autologous if possible), log rolling
33
s/s narcotic OD
decreased LOC, pinpoint pupils
35
risk factors for leukemia
family history; Down's syndrome; chemical exposure; maternal smoking
36
often first sign of Duchenne MD
difficulty climbing stairs, riding a bike
37
RFs for DDH
Family history; uterine position, especially breech presentation
38
position to avoid GER
feed upright; prone HOB elevated 30 deg after feeding; thicken feeding, avoid overfeeding
39
s/s Hirschprung's disease
bilious vomiting, refusal to feed; no meconium 48h after birth, abd distention; Child: ribbon-like stool, visible peristalsis
40
group of genetic diseases with progressive weakness and degeneration of skeletal muscles.
Muscular Dystrophy
42
best way to prevent sickle cell crisis
adequate hydration
44
most common childhood cancer
leukemia; 60% ALL, 38% AML
45
s/s intussusception
sudden colicky abd pain, knees to chest; currant jelly-like stools; palpable sausage-shape in RUQ; vomiting, abd distention
46
s/s rotavirus
mild/mod fever and vomiting for 2 days, followed by frequent watery foul-smelling stools for 5-7 days
47
frostbite treatment (white waxy areas)
water bath 38-41 deg; pain meds, Td
48
leukemia: Early s/s
low grade fever; recurrent infections; pallor; bruising; enlarged lymph nodes; joint pain
49
RFs for cleft lip/palate
heredity; maternal intake of dilantin, alcohol, smoking; maternal infection; Vitamin B/folate deficiency
50
cyanide antidote
amyl nitrate or IV sodium nitrate
51
goal of fluid admin in emergent phase of burn
good urine output (30-50 mL/hr)
52
an infant may have an imperforate anus or fistula if they haven't passed stool in the first
24 hours of birth
53
MD Dx
muscle biopsy
54
purpose of traction in DDH treatment
stretch soft tissues to allow femoral head to return to socket
56
inheritance pattern of sickle cell anemia
autosomal recessive (both parents must be carriers)
57
this applied after closed reduction for DDH
spica cast for 3-6 mos, then a brace
58
s/s infant GER
excessive non-bilious vomiting; wt loss, FTT; chronic cough;
60
post op position for pyloromyotomy
head up and on side to aid stomach emptying
61
sickle cell anemia usually dosn't present until 4-6 months of age because
before that babies have fetal hemoglobin from mother
62
after leukemia there is high risk for
secondary malignancy
62
thickened pyloric sphincter; surgical emergency
Pyloric stenosis
64
s/s DDH
"click" in hips; asymmetrical gluteal/thigh folds; shorter leg on affected side, turned outward
65
hypothermia s/s
67
pinworm treatment
Vermox or Pyrantel; treat family; stool precautions--wash linen in hot water, T/L hygeine
69
abnormal, uncontrolled and destructive proliferation of one type of white blood cell and its precursors.
Leukemia
70
hemophilia severity depends on
% of clotting factor missing
71
inheritance pattern of hemophilia
X-linked recessive
73
definitive diagnosis for sickle cell anemia
Hgb electrophoresis
74
complications to watch for after TEF repair
Pleural effusion, pneumothorax; Feeding aversions (may need Gtube); Strictures (may need future eso dilations)
75
Hirschprung's Dx
rectal biopsy to see aganglionic cells
75
burn extends into dermis, painful scalds, blisters can form; edema, pain, and moistness
second degree: superficial or deep partial thickness
76
acute painful splenomegaly due to trapped sickled rbcs; decreased Hgb, can lead to shock; medical emergency
splenic sequestration
77
cleft lip repair
cheiloplasty; performed at 6-12 weeks, use staggered sutures to prevent scar
78
s/s acute chest syndrome
pulmonary infiltrates, dyspnea, tachypnea, congested cough
79
palmar surface rule for burn estimation
the patient's palmar surface is equal to 1% of their BSA
80
RFs for esophageal atresia/ TEF
maternal: Vit A, riboflavin deficiency, polyhydramnios
81
treatment for ethylene glycol poisoning
activated charcoal and gastric lavage
83
MD complications
contractures; disuse atrophy; infections; obesity; CP problems
84
Dx of infant GER
esophagus pH monitoring
85
s/s pyloric stenosis
Projectile vomiting, especially 30-60 min after eating, non-bilious; constant hunger with FTT and dehydration; Olive-shaped mass in epigastric area
86
pre op for intussusception monitor for this complication
peritonitis
87
rotavirus transmission
fecal-oral
87
edema in a burn can convert partial thickness burns into full thickness burns because of
decreased perfusion to the area--therefore, decrease edema and admin fluids quickly
89
s/s smoke inhalation damage
singed nasal hairs and brows, sooty sputum, hoarseness, wheezing and increased secretions; can be delayed 24-48h
90
third degree burn=full thickness burn
dry, non-edematous, and painless; no residual epidermal cells so no healing possible; tissue is called eschar; may be waxy white or black; elasticity is lost so escharotomy may be necessary to restore blood flow
91
s/s Heat Stroke
HoTN, tachypnea, tachycardia, anxiety and confusion/AMS, weakness, thirst, leading to seizures and coma
92
painful burn, pink to red skin; only epidermis affected, skin function intact; no systemic response
superficial (first degree)
93
leukemia: Late s/s
Pain; hematuria; mouth ulcerations; enlarged kidneys and testicles; IICP
94
eye disorder associated with DM
cataracts
95
Rett disorder
mostly in females; initially normal development, then around 18 mos: deceleration of head growth, loss of speech and hand control, eventual dementia
96
97
very rare dev. disorder, regression in multiple areas on function after 2 years of normal development
Child Disintegrative Disorder
98
social disorder with increased verbal and cognitive ability and social interaction compared with other forms of social disorder, especially concerning the child's current obsessive preoccupation
Aperger's disorder
99
to diagnose autism, s/s must present by
3 years of age
100
hallmark of autism
impaired social interaction--nonverbals, attention, and social reciprocity. Impairments in socialization, communication, and behavior
101
102
loss of lens elasticity with age
presbyopia
103
light rays focus on two differrnt points on retina due to vurvature abnormality of cornea or lens
astigmatism
104
blunt trauma causes bloor in anterior chamber of eye; red color on lower iris as blood pools
hyphema
105
Tx for chemicals in eye
rinse with cool tap water 20 minutes
106
with eye impalement, cover both eyes initially to
stop movement of the affected eye--eyes move together
107
treatment for corneal abrasion or tearing
steriod eye drops`
108
RFs for retinal tear/detachment
Age; Cataract surgery; DM
109
s/s retinal tear/detachment
light flashes, floaters; ring in field of vision
110
edema of optic disc
papilledema; can be caused by severe HTN
111
normal IOP
10-21 mmHg
112
Increased pressure in eye causes atrophy of optic disc and retinal cells, with loss of peripheral vision first, then central if untreated; also visual halos and blurred vision
glaucoma
113
normally aqueous humor flows
from posterior chamber to anterior chamber and is absorbed by the veins of the trabecular network
114
aqueous humor cannot drain well from anterior chamber through trabecular meshwork; insidious development
open angle glaucoma; chronic glaucoma ;IOP 22-32
115
iris bows forward and completely blocks fluid access to trabecular meshwork, causing pressure buildup, leading to more bowing and pressure; emergency with severe eye pain and fast vision loss
closed angle glaucoma; acute glaucoma; IOP\>50
116
treatment for open angle glaucoma
laser trabeculoplasty--holes made in meshwork to accomodate fluid movement; meds: BBs, cholinergics, miotics to decreased IOP
117
clouding of eye lens resulting in nighttime glare, reduced color perception, and image distortion
cataracts
118
most common cause of vision loss \>55 yrs
age related macular degeneration
119
Tx for closed angle glaucoma
laser iridectomy
120
eye drops to treat cataracts before surgery
mydriatics-cycloplegic agents to temporarily paralyze IO muscles
121
light sensing cells are damaged in the macula--area in the retina specialized for high acuity vision
macular degeneration
122
RFs for macular degeneration
aging; smoking; alcohol; UV exposure; heredity
123
macular degeneration is diagnosed when this is observed with the opthalmoscope
drusen: yellow exudate of extracellular debris
124
two forms of macular degeneration
Dry (atrophic)--drused accumulates between choroid and retina, can cause detachment; gradual vision loss; Wet (exudative)--rapid progression, BVs grow between choroid and retina; distinctly darkened or blurred vision
125
sensorineural hearing loss involves
cranial nerve 8--vestibulocochlear nerve
126
vertigo and nystagmus caused by calcium carbonate accumulation
benign paroxysmal positional vertigo (BPPV)
127
endolymph buildup in inner ear causes fullness, tinnitus, and vertigo that can last 30-60 minutes and be accompanied by nystagmus
Meniere's disease
128
Meniere's disease
Head trauma, URI, chronic aspirin use, smoking and alcohol use
129
meniere's disease lifestyle treatment
los sodium diet to prevent fluid retention; diuretics, avoid caffeine and nicotine