NICU Baby Nelson Flashcards

(65 cards)

1
Q

IUGR

A

< placental abruption

vs. SGA
<10th percentile or 2SD below

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2
Q

Problems associated with babies who are IUGR or SGA

A

(table pg 189)

  1. intrauterine fetal demise
  2. temperature instability
  3. perinatal asphyxia
  4. hypoglycemia
  5. polycythemia (from fetal hypoxia with increased epo)
  6. dysmorphology associated
  7. pulmonary hemorrhage
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3
Q

What are the hormones abnormalities that suggest chromosome anomalies

A
  1. low estriols
  2. low AFP
  3. elevated chorionic gonadotropin levels (placental)
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4
Q

What are the main differences between fetal and adult hemoglobin?

A

fetal hemoglobin (2 alpha and 2 gamma) has higher affinity for O2 than adult Hg (this is why the baby steals all the O2) , the curve is shifted to the left - fetal hemoglobin is saturated with lots of O2, but harder to unload O2 to the tissue, but in the placenta, easier to unload the O2

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5
Q

when does the body start to make more adult Hg?

A

in the third trimester , body begins to decrease making fetal Hg and makes more adult (usually full adult by 3-6 months of life as per baby nelson) and at this point have adult Hg O2 dissociation curves

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6
Q

What are the effects of fever, acidosis, high PCO2 and 2,3 diphosphoglycerate on the Hg dissociation curve?

A

shifts the O2 dissociation curve to the right
because this means the body can unload O2 to the tissues more easily
and in these stressed states the tissues need more O2

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7
Q

which is the dominant ventricle in utero?

A

right ventricle

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8
Q

Why do we give babies silver nitrate? To prevent

a) chlamydia
b) gonorrhea
c) both

A

to prevent gonorrhoea - can cause panophthalmitis and blindness
not effective against C trachoma tis

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9
Q

Why do we give erythromycin drops? To prevent

a) chlamydia
b) gonorrhea
c) both

A

both

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10
Q

what comes back first after resuscitation of neonate who has arrested?

A

first get your heart rate, then cyanosis and perfusion improves
also remember that newborns respond to hypoxia with apnea rather than tachypnea

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11
Q

does of epi for neonatal resuscitation

A

1:10000 0.1-0.3 ml/kg

if giving endotracheal (less predictable, can try higher ode)

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12
Q

Large fontanelle, name 3 conditions to think of

A

hydrocephalus
hypothyroid
rickets

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13
Q

What are congenital melanocytic nevi

A

pigemented lesions

in 1% of neonates

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14
Q

true or false - giant pigmented nevi have malignant potential

A

true but they are rare (also the pics are intense)

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15
Q

leukocoria in newborn, differential

A

cataracts, chorioretinitis, ROP, ocular tumor, persistent hyperplastic primary vitreous

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16
Q

What does the TM look like in first 1-4 weeks?

A

dull, gray opaque adn imobile int eh first 1-4 weeks

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17
Q

supernumerary nipples, what organn should you look at?

A

renal anomalies

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18
Q

when do most term babies have their first pee

A

within first day of life in 95% of normal term babies

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19
Q

Abdominal mass in the neonate, most common 2 causes? other causes?

A

most common: hydronephrosis, muticystic dysplastic kidney disease
less common: ovarian cysts, intestinal duplication, neuroblastoma, mesoblastic nephroma
should do an U/S for masses asap

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20
Q

when do 99% of term babies pass their med

A

within 48 hours of birth in 99%

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21
Q

Differential of scrotal swelling in the neonate

A

(pg 200 baby Nelson)

  1. hernia
  2. hydrocele - eaily illuminate and clear
  3. in utero torsion of testicle - painless dark swelling
  4. meconium from meconium ileum and peritonitis
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22
Q

what is epispadias? what is hypospadias?should you worry about pseudohermaphroditism when these are present?

A
  1. epispadias: opening at top of penis
  2. hypospadias: opening at bottom of penis **don’t circumcize, may need foreskin

don’t need to worry if only this finding on own, however if can’t palpate testes, then worry about DSD

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23
Q

bloody discharge from baby girl’s newborn vagina, worry or not?

A

not worry, can be normal either blood streaked or clear (from withdrawal of maternal hormones)

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24
Q

do newborns shiver?

A

no

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25
difference between central facial nerve injury, peripheral facial nerve injury (i.e. from compression ) and from absence of depressor anguli
1. central facial nerve - forehead NOT involved, lower 2/3 involved 2. facial nerve peripheral - whole face (including forehead, eye, nasolabial fold, mouth etc) 3) depressor anguli - nasolabial fold and upwards should all be normal, just the mouth moves funny, can be associated with cardiac (double check this)
26
What is hemorrhagic stroke encephalopathy syndrome?
rare condition | with excessive temperatures
27
Type of neonatal hypocalcemia
1. early : within first 3 days of life, often no symptoms; Groups affected (special ones, all babies do have a transient decrease 24-48 hours or so) a) . prems b). IDMa - from transient hypoparathyroidism and reduced parathyroid response (for prems and IDMs) (early in prem and IDM often resolves on its own) c) DiGeorge (absence of parathyroid **can also get hypoMg - risk in IDM especially d) associated with asphyxia 2. late : a) from drinking high phosphate milk, or inability to excrete phosphate ; usually will get hyperphosphatemia after first week of life in these infants b) vitamin D deficiency states and malabsorption **all infants have decrease in Ca at 24-48 hours or so
28
Clinical features of hypocalcemia
apnea, muscle twitching, seizures, laryngospasm Chvostek sign - facial muscle spasm when 7th nerve tapped Trousseau sign - (no usually in newborn) To prevent in high risk - gee Ca
29
symptomatic hypocalcemia, treatment
2-4 ml/kg 10% calcium gluconate also give mg if both for late hypoCa, same as above, but should also do low phosphate feedings subcutaneous infiltration of IV calcium can cause tissue necrosis oral can irritate the intestinal mucosa
30
When will a baby born to a heroin using mom withdraw
1-5 days
31
methadone mom, when withdraw
1-4 weeks
32
name symptoms of withdrawal from opiate
jittery, sneezing, irritable, diarrhea, poor feeding (but starving) , poor sleep, cry lots (high pitched), tachypnea **often methadone withdrawal is worse
33
Treatment of withdrawing baby
``` start with swaddling, no light if significant (i.e. constant hyperactive, irritability doesn't allow sleeping and feeding, or when diarrhea/seizures present, treatment with meds 1. seizures - treat with phenobarb 2. other symptoms - with opiod weaning can take 1-2 months ```
34
Effects of cocaine use during pregnancy
``` preterm labor placental abruption decreased attentiveness irritable newborn SGA small heads usually no treatment needed ```
35
What type of antibody can cross placenta
IgG (which is usually the type that autoantibodies are)
36
Treatment of neonate with ITP with hemorrhage (and mom has ITP also
``` (table 205) can give platelets if hemorrhage can try IVIG usually resolves in 4-6 weeks risk is intracranial hemorrhage ```
37
Problems of Diabetic Pregnancy (pg 206) for baby
1. LGA 2. hypoglycemia 3. hypocalcemia 4. hypomagnesemia 5. birth asphyxia/shoulder dystocia 6. congenital heart defects - hypertrophy of septum 7. tachypnea (RDS or TTN) 8. small left colon 9. renal disorders 10. polycythemia others also include lubosacral dysgenesis, neural tube defects
38
contrindications to indomethacin for PDA
thrombocytopenia bleeding creatinine >1.8 oliguria
39
how much blood do babies have?
70-90 ml/kg for term | 90-100ml/kg for preterm
40
Delayed cord clamping advantages and disadvantages?
1. can increase blood volume transiently for first few days, improves glomerular filtration 2. disadvantage: can increase jaundice early: can lead to anemia, murmur, poor perfusion, less tachypneas **should hold the baby below the placenta (otherwise the baby will give too much blood back to the placenta)
41
Causes of anemia in the newborn period
1. decreased production (low retics 0-2%) Ddx: bone marrow failure (Diamond-Blackfan anemia), infection (congenital viral infections, i.e. parvo/rubella, sepsis), nutritional deficiencies (protein, iron, folate, vitamin B12), congenital leukemia 2. increased Destruction of RBC (normal or elevated retics (>5-10%) Immune mediated: (Coombs positive) - hemolytic disease of the newborn (anemia and hyperbili mainly) ABO incompatibility (less severe than Rh disease, doesn't get worse in subsequent pregnancies ) - Erythroblastosis fetalis (Rh incompatibility) make anti-D antibody (which is the antibody which is most likely to be present) Non Immune mediated (Coombs negative) 1. RBC enzyme deficiencies - ie pyruvate kinase or G6PD 2. RBC membrane disorders - ie hereditary spherocytosis (autosomal recessive is severe, less severe autosomal dominant form) 3. hemoglobinopathies - ie thalassemias **see chart pg 217
42
Clinical manifestations of erythroblastosis fettles
anemia, hyperbili in first pregnancy, then worse because will start hemolysing in utero fetal anemia, heart failure, portal vein obstruction, hypoalbuminemia- i.e. fetal hydrous - ascites, pleural and pericardial effusions, anasarca
43
How to tell difference between acute and chronic blood loss at birth
1. Acute blood loss - after fetal maternal hemorrhage, rupture of the umbilical cord, placenta pre via or internal hemorrhage - pallor, diminished peripheral pulses, shock - no signs of extra medullary hematopoesis, no HSM - ininitial Hg can be normal but then decline over 24 hours 2. Chronic blood loss: i.e. chronic fetal-maternal hemorrhage, twin twin transfusion: marked pallor, heart failure, HSM with or without hydrous, a low hemoglobin level at birth fetal-maternal bleedin is very common - 50-75% , blood losses range from 1-50 ml
44
What is the Kleihauer-Betke acid test
look at the mom's blood smear - will see fetal pink pRBCs and counted (because fetal Hg is resistant to acid and adult hemoglobin is eluted) false positive Kleihauer Betke: sickle cell or hereditary persistence of fetal hemoglobin false negative - ABO incompatibility (since all will be negative)
45
What is Crigler-Najjar syndrome
serius, rare autosomal REcessive, permanent deficiency of glucoronosyltransferase that results in severe indirect hyperbilirubinemia Type 2 - responds to phenobarbital (so randome) Type 1 - persistent indirect hyperbili - can lead to kernicterus
46
What is Gilbert disease
mutation of glucoronosyltransferase and results in a mild indirect hyperbilirubinemia
47
How high is the bill in typically breast milk jaundice
shouldn't be more than 20 mg/dL (which equals 20 x 17 = 340) I think interupt fo 1-2 days will result in rapid decline
48
At what levels of bill is jaundice observed?
5-10 mg/dL
49
Work up to do for direct (conjugated hyperbili)
``` conjugated hyperbili is >20% of total bill do liver enzymes - AST/ALT ALP GGT bacterial and viral cultures metabolic screening hepatic U/S sweat chloride occasionally liver biopsy ```
50
Causes of conjugated hyperbili
``` Common 1. hyperalimentation cholestasis 2. CMV infection and other TORCH infections 3. Inspissated bile from prolonged hemolysis 4. neonatal hepatitis 5. sepsis Uncommon: 1. hepatic infarcation 2. IEMs - galactosemia, tyrosinemia 3. CF 4. biliary atresia 5. choledochal cyst 6. alpha 1 -antitrypsin deficiency 7. neonatal iron storage disease 8. alagille syndrome 9. Byler disease ```
51
early sign of kernicterus vs late
early : lethargy, hypotonia, irritability, poor moro ad feeding later signs: bulging fontanelle, opisthotonus, pulmonary hemorrhage, fever, hypertonicity, paralysis of upward gaze and seizures
52
Complications of exchange transfusion
related to glood: transfusion reaction, metabolic instability, infection catheter - vessel perforation hemorrhage procdure: hypotension or NEC - unusual: thrombocytopenia, GVHD
53
Polycythemia in neonate (pg 221)
``` Hematocrit >65% People at risk: SGA IDM delayed cord clamping hyperthyroidism adrenogenital syndrome T13, T18, T21 Twin twin (recipient) Beckwith - Wiedemann ```
54
Symptoms of polycythemia
1. plethoric/ruddy may have acrocyanosis Symptoms are from vascular stasis, hypo perfusion and schema seizures, lethargy, irritability hyperbili - poor hepatic circulation of Hg broken down into bill Resp distress PPHN NEC, hypoglycemia, thrombocytopenia, pripism, testicular infarction, stroke, feeding intolerance
55
Long term sequelae of polycythemia
neurodevelopment abnomalities | partial exchange transfusion how to calculate the volume:
56
how to calculate amount of blood for partial exchange transfusion pg 222 nelson baby
volume to exchange (mL) = [blood volume x (observed hematocrit - desired hematocrit)/ observed hematocrit desired hematocrit is 50%, blood volume is 85 ml/kg pg 222 baby nelson need to use central venous hematocrit (peripheral might be falsely elevated)
57
eye discharge at day 1 of life, initially clear then purulent, also have chemises and hyperaemia, more likely gonorrhoea or chlamydia
gonorrhea gonorrhea presents in first 5 days of life, chlamydia is ted 5-14 days of life chlaydia can last 1-2 weeks gonorhea auses your eye to perforate and go blind
58
staccato cough, which infection
chlamydia pneumonia CXR - hyperinflation with diffuse infiltrates prophylaxis does not treat the chlamydia when you have pneumonia +/- pneumonia with chlamyda, need to treat systemically with erythromycin
59
drugs which can impair vitamin K metabolism
warfarin, antibiotic
60
baby with late hemorrhagic disease of newborn, things to think of
breastfed also might have vitamin K problems ie CF, biliary atreisia, hepatitis, antibiotic suppression of colonic bacteria that make vitamin K
61
Treatment of bleeding from vitamin K deficiency
IV 1mg vitamin K | if severe, also can do FFP
62
Differential of bleeding in the newborn
1. sick newborn: DIC< hepatic failure, thrombocytopenia (including consumption i.e. Kasabach-Merritt) 2. Well child: hemophilia (cutaneous or mucosa bleeding and no systemic illness) , thrombocytopenia from syndromes (i.e. Fanconi anemia with no thumbs, radial aplasia-thrombocytopenia syndrome (thumbs present0 or Wiskott-Aldrich syndrome , maternal drugs can reduce platelet count (i.e. sulfonamids, quinidin, quinine, thiazide) most common thrombocytopenia; isoimmune thrombocytopenia (mom has anti platelet but her platelets are find) treat with transfusion and/or IVIG , sometimes need to do C/S and transient neonatal thrombocytopenia neonatal thrombocytopenia in babies of mom's with ITP
63
Lab findings in baby with DIC
prolonged PTT and PT (minutes rather than seconds ), thrombocytopenia and bood smear suggesting MAHA (burr or fragmented blood cells) low fibrinogen elevated levels of fibrin degradation products
64
labs in vitamin K deficiecy
PT most prolonged - X, VII, V, II, I
65
in hemophilia - factors XII, IX, VIII, X , V, II, and I
PTT most prolonged