Peds Exam 1 - NEED TO KNOWS

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119 Terms

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Preterm

Born on or before the last day in the 36th week

(Before 37 weeks)

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Early term

37 weeks to 38 weeks and 6 days

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Full term

39 weeks to 40 weeks and 6 days

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Late term

41 weeks to 41 weeks and 6 days

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Post term

>42 weeks

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small for gestational age (SGA) and causes

<10th percentile

Causes: genetic disorder, placental abnormalities, drug/etoh during pregnancy, infection

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Large for gestational age (LGA)

>90th percentile

Causes: maternal gestational diabetes

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low, very low, extremely low birth weight

Low: <2500 g

Very low: <1500 g

Extremely low: <1000g

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When is BW doubled? Tripled?

Doubled at 6 months

Tripled at 1 year

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When do babies gain back the weight they lost post birth?

Lose 10% in first few days

Regain in 10-14 days

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Umbilical cord competent

2 arteries: carry deoxygenated blood from fetus to placenta

1 veins carries oxygenated blood from placenta to fetus

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Complications associated with infants of diabetic mothers

-hypoglycemia

-hypocalcemia

-hyperbilurubinemia

-macrosomnia (overweight)

-RDS

-HOCM

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What does APGAR stand for? What is it used for

Quick assessment of infants immediate adaption to life

Appearance

Pulse

Grimace

Activity

Respiration

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How is APGAR graded?

>5 @ 1 min: smooth transition

<4 @ 1 min: severe depression, need resuscitation

<7 @ 5 min: high ris of CNS dysfunction/cardiac problems

Score again @ 10 min if infant cyanotic at 5 min

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What does the new Ballard score assess?

Gestational age

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Routine newborn protocol

-Eye prophylaxis: silver nitrate & erythro

-Vit K

-Hep B

-Labs

-hearing screenings

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Newborn labs

-state newborn screening

-hematocrit

-glucose

-bili

-blood type

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Cause of RDS

surfactant deficiency

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Risk factors for RDS

-males

-preterm

-maternal DM

-monozygotic twins

-C section

-fam Hx

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How to diagnose RDS

CXR: air bronchograms and ground glass appearance

PE: dec breath sounds, nasal flaring, tachypnea

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Cause of transient tachypnea of the newborn

Fetal lung fluid not expelled in delivery, & retained in lung

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Most common cause of respiratory distress in TERM infants

Transient tachypnea of the newborn

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How to diagnose tachypnea of the newborn

CXR: inc lung volume w/ flat diaphragm, no air bronchogram/ground glass

PE: tachypnea (>60) nasal flaring

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Presentation of necrotizing enterocolitis

Gastric residuals after feeding

Hematochezia

Abd wall tenderness

Apnea, bradycardia

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How to diagnose necrotizing enterocolitis

KUB: pneumatosis intestinalis

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Most common hernia on the left side

Bochdalek

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When are pregnant women tested for strep?

35-37 weeks

If postive: treat w PCN or amoxicillin

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Cause of jaundice @ day 1, 2-3 days, 1 week, and 3 weeks

Day 1: always pathological

Day 2-3: physiologic/sepsis

1st week: breast fed

3rd week: biliary atresia

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What is a Bhutani nomogram used for?

Assess risk of developing severe hyperbilirubinemia based on age and total bili

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Normal bili levels in term vs preterm

Term: <12

Preterm: <15

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Complications of jaundice in the newborn

kernicterus

-lethargy

-vomiting

-irritability

-poor feeding

-crying

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Prevention of SIDS

-regular prenatal care

-avoiding tobacco

-supine sleep position

-avoid blankets, bumpers, pillows

-avoid co sleeping

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caput succedaneum

Superficial edema that crosses suture line

Reconfigure in 1 week

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Absent red reflex is indicative of

Retinoblastoma

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cause of retinopathy of prematurity

-hypoxia, hypotension that disrupts normal angiogenesis

-incomplete retinal vascularization

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Turner's syndrome presentation

-wide set nipples

-excessive nuchal skin

-lymphedema

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Weak pulses could mean

-possible coarctation

-left ventricular flow obstruction

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When should you be worried about a sacral tuft/sinus tract

If sinus tract or tuft of hair present

(If not: benign)

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Sacral tuft/sinus tract can be indicative of

-spina bifida

-meningocele

-myelomeningocele

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Abnormal develop of acetabulum and femur w/ mechanical instability of the hip

Hip dysplasia

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Barlow vs Ortolani Maneuver

Barlow: dislocates by adducting and pulling down

Ortalani: reduces the joint but ABducting w/ anterior pressure

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Galaezzi sign

knowt flashcard image
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What do you evaluate during a neuro exam

Movement and reflexes

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Open vs closed spina bifida

Open: myelomeningocele

Closed: spina bifida occulta

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Waiters tip sign

Erb's palsy

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Erb duchenne palsy

-Adduction and internal rotation of the shoulde

-elbow extension and pronation of forearm

-intact grasp reflex

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PHACE syndrome

Posterior fossa malformation

Hemangioma

Arterial abnormalities

Cardiac abnormalities

Eye abnormality's

Sternal cleft

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Most common vascular tumor of infancy

Hemangioma

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When are screening tests done?

At physicals:

-9 mo

-18 mo

-24 mo

-30 mo

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Screenings for autism

M-CHAT

CARS

CHAT

@ 18 mo and 24 mo physicals

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Involuntary muscle reaction to a stimulus

Reflex

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Absense of Moro reflex suggests?

Absent: UMN lesion

Incomplete: brachial plexus injury

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Asymmetric Tonic Neck Reflex (ATNR)

Childs head is turned to the side and assumes the fencer position

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parachute reflex

extension of extremities when thrust downward in the prone position

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I would personally know all of the reflexes cuz he could switch em up

:)

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What age does an infant grasp objects and brings to mouth

4 months

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What age does an infant have mature pincer grasp

12 mo

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What age does an infant have early pincer grasp

9 mo

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What age does an infant transfer objects from hand to hand

6 mo

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Language development rule of 4s

2 years: 50% intelligible to strangers

3 years: 75% intelligible

4 years: 100% intelligible

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normal dysfluency stuttering occurs when

2.5 - 5 yrs and is not distressing to child

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How to manage stuttering

-reassurance

-if >5 yr : speech therapy

-SSRIs

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Trisomy 21

Down syndrome

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Features of Down syndrome

-intellectual disability

-dementia

-atlantoaxial instability

-inc cardiovascular risk (VSD, CHD)

-hypotonia

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Most common sex chromosome abnormality in females

Turner syndrome

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Cause of turner syndrome

Absence of an X chromosome

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Turner syndrome presentation

-short stature

-sexual infantilism

-primary hypogonadism

-ovarian dysgenesis

-nipple hypertelorism

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Cause of Klinefelter syndrome

Extra X chromosome in males

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Klinefelter syndrome presentation

-micropenis

-hypospadias

-small testes

-cryptorchidism

-infertility

-gynecomastia

-incomplete virilization

-hypergonadotropic

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Treatment of Klinefelter syndrome

-testosterone therapy

-ref to endocrine/genetics

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Cause of fragile X syndrome

Religion of a single trinucleotide gene sequence (CGG) on the X chromosome

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Developmental features of fragile X syndrome

-delayed milestones

-speech delay

-impaired short term memory

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Prader-Willi Syndrome cause

Paternal deletion of chromosome 15q11

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Features of Prader-Willi Syndrome

Infant: neonatal hypotonia, poor weight gain

Early childhood: weight gain, speech delay

Adolescence: behavioral issues, CV probs d/t obesity, OSA

(Short, obese, fish mouth, hypogonadism)

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Genetic condition that increases connective tissue growth

Marfans

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MC cardiopulmonary disorders with marfans

1. Aortic root dissection

2. MVP

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Cause of marfans syndrome

Mutation in fibrillin 1 gene

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Autosomal recessive disorder of cholesterol biosynthesis

Smith-lemli-opitz syndrome

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Fetal alcohol syndrome features

-Thin vermillion border of upper lip

-smooth philitrum

-short palpebral fissure

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Catch 22

Deletion of 22q

Cardiac defect

T cell defect

Cleft palate

Hypocalcemia

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Treacher Collin's syndrome definition and cause

Def: autosomal dominant disorder of craniofacial development

Cause: mutation on chromosome 5

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Features of Treacher Collin's

-malar hypoplasia

-hearing loss

-G tube feedings d/t swallowing prob

-Coloboma lower lid

-beak like nose

-micrognathia

-cleft palate

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PKU

Phenylalanine hydroxylase deficiency

Autosomal recessive

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PKU features

-seizures

-hyperactivity

-aggressive behavior

-intellectual disability

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Most common breath holding spell

Cyanotic: related to tantrums

Crying: breath holding: cyanotic: LOC

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ADHD diagnostic criteria

Inattentive: 6+ sx

Hyperactivity: 6+ sx

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Associations with ADHD

-learning disabilities

-mood disorders (depression)

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Pattern of hostile and defiant behavior that is excessive

Oppositional defiant disorder

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Persistent pattern of behavior that violates rules/norms and the basic rights of others

Conduct disorder

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Night terrors vs nightmares

Terrors: occur in stage 3 of sleep, no recollection of event, 18 months-6 yrs

Nightmares: occurs during REM, may remember

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Night terrors are are precipitated by

Stress, illness, sleep deprivation

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Night terror presentation

Child awakened from deep sleep seemingly confused, dilated pupils, and sweating

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Most common congenital heart defect

VSD

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What CHD is common in Down's syndrome

ASD

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Features of CoA

-murmur loudest @ ULSB, left interscapular

-bounding radial pulses

-diminished femoral pulses

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tetrad of tetralogy of fallot

PROV

Pulmonary stenosis

RVH

Overriding aorta

VSD

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Ebstein Anomaly

Tricuspid vale is displaces towards the apex of the right ventricle

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Ebstein anomaly is commonly associated with

Maternal lithium ingestion

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Marfan syndrome genetics

75% inherited

25% new mutation

50% chance of passing it only offspring

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Venous hum is caused by

Turbulence in SVC

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