Peds Flashcards

1
Q

Define the two parts of the prenatal period

When do the most critical stages of development occur

What are TORCH infections

A

Embryonic: through 8wks EGA
Fetal: 9wks EGA +

First trimester

Toxoplasmosis Rubella CMV HSV

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2
Q

Rh incompatibility can lead to ? OB complication

Define APGAR

Why are the timings of this score different

A

Hydrops fetalis

Appearance Pulse Grimace Activity Respiration:
0-10pts w/ 5 features, done at 1min and 5min-
Rpt q5min if score <8

1min: tolerance of birthing process
5min: tolerance to life

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3
Q

What are the APGAR scores made

A

Appearance:
0- cyanotic 1- Acrocyanosis/blue extremities 2- all pink

Pulse:
0- none 1- <100bpm 2- >100bpm

Grimace w/ bulb suction to nares:
0- none 1- grimace/cry w/ stimulation 2- sneeze/cough/withdrawal w/ stimulation

Activity:
0- limp/none 1- some flexion 2- active

Respiration:
0- none 1- weak/slow/irregular 2- strong cry

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4
Q

Newborn respiratory rate

Newborn HR

What are the next steps taken for abnormal HR ranges

A

30-60/min w/ inc number if premature

120-160

> 100: routine care
60-99: ventilation support
<60: ventilation w/ compressions

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5
Q

Neonatal Resuscitation Protocol flow chart

A

Compressions at 120bpm w/ two thumbs > two fingers
3 compression : 1 respiration

BVM sniffing position (neck w/ slight extension) w/ 40-60 bpm

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6
Q

How do premature/neonates respond to hypoxia

What fluids are used during NRP

What is the next step for asystole/bradycardia unresponsive to O2

A

Apnea rather than tachypnea

10mL/kg NS for hypo-volemia/tension

IV Epinephrine

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7
Q

Rules for Narcan usage in newborns

? care is routine for all infants and w/ ? goal

What are the two categories of this care and what is done during each

A

Yes- opiates used during labor
No- maternal addict/methadone d/t withdrawal seizures

Nursing- prevent illness/complications w/ high level of morbidity/mortality

A) Shortly after:
Erythromycin ointment- prevent G/C conjunctivitis
Vit K injection- prevents Hemorrhagic Dz of Newborn
HBV- only vaccine given at birth

B) 24hr Routine Care:
Bilirubin screen
Congenital heart screening
Genetic/Metabolic screen (AKA- newborn screen)
Hearing
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8
Q

Infants receive Vit K injections into their thigh at birth to prevent HDzoN which is more common in ? population and will present as ?

? genetic/metabolic tests are included in the Newborn Screen

Infant length is done in ? position until ? time frame and when are inaccurate measurements most likely to occur

A

MC in breast fed infants in first few weeks of life;
Generalized ecchymosis
GI bleeds
Umbilical/Circumcision bleeding

CF CAH PKU Sickle TSH

Laying down until 2yrs old;
First week d/t positioning

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9
Q

Congenital heart dz screening is done at 24hrs of life/before d/c and is interpreted how

A

Spo2 95% or higher w/ 3% or less difference between right hand/foot= negative screening, plan for d/c

SpO2 90-94% in right hand/foot or 3% difference= repeat in one hour; same results- repeat again in one hour; 3 readings in same range= echo

SpO2 <90% in right hand/foot= +screen- order Echo

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10
Q

? is the number one cause of LBW

Criteria for Low/Very Low birth weights

What are the RFs for LBW

A

Prematurity

Low: <2500gm; Very: <1500gm

Previous LBW baby
Age <16, >35
Socioeconomic status
Tobacco/ETOH/Drugs
Poor weight gain during pregnancy
Education
Antenatal care
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11
Q

Normal sutures and two abnormal findings possibly seen in newborn HEENT exam

Define Caput Seccedaneum

Define Cephalohematoma

A

Normal: open/flat sutures
Anterior suture >5cm suggests hypothyroidism
Closed sutures: craniosynostosis

Boggy, edematous swelling crossing lines, self resolves

RBC breakdown/jaundice causing swelling w/out crossing suture lines

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12
Q

? head malformation is associated w/ vacuum deliveries and how is it Tx

Define Hydrocephalus, the two types, and Tx

A

Subgleal hemorrhage- swelling crosses suture lines pushing ears anteriorly;
Tx: Compression w/ resuscitation PRN

Inc CSF volume- macrocephaly, bulging fontanelle, ‘setting sun’ gaze;
Communicating w/ subarachnoid
Non-Communicating= obstructed
Tx: ventriculoperitoneal shunt

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13
Q

What can cause an abnormal red reflex on newborn eye exam

What optic abnormality can be normal until 4mon old

How is normal ear positioning verified

A

Leukocoria: cataract, tumor, retinopathy of prematurity

Disconjugate gaze: eyes fail to move in same direction; alignment achieved at 4mon old

1/3 of ear above canthus/occipital protuberance line
20* from anterior of lobe to superior helix

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14
Q

Define Epstein Pearls and Bohn Nodules

What parent education goes w/ Dx

When conducting new born exams, how do neck bulge locations hint at Dx

A

EP: Keratin cysts on gums/palate
BN: Keratin cysts on salivary tissues

Harmless, resolve in first week of life

Anterior midline: thyroid d/o
Anterior to SCM: brachial cleft cyst
Posterior to SCM: cystic hygroma

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15
Q

What do each of the following suggest for cardiac d/o/dz

Weak pulse

Bounding pulse

Single second sound

Holosystolic, continuous, harsh

Grade 3/>

Diastolic murmur

Hempatomegaly

A

Weak: poor CO/AS

Bounding: high CO, PDA

Second sound: cyanotic dz- truncus/hypoplastic heart

Holosystolic, continuous, harsh- pathologic

Grade 3/>: pathologic

Diastolic: pathologic

Hempatomegaly: left sided HF

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16
Q

How are lower extremity pulses assessed during newborn exam

? abdomen shape suggests diaphragmatic hernia

? umbilical finding suggests need for detailed exam

A

Brachial and femoral together:
Pulse pressure >40mm= r/o PDA
LE < UE pulse= r/o coarctation

Scaphoid

Two vessels: 1 artery, 1 vein instead of normal 2A/1V

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17
Q

Umbilical cord stump remaining longer than ? needs further work up

? DDxs need to be r/o

A

1mon

Umbilical polp: sticky surface
Patent Urachas: urinary d/c
Meckels: proximal end of vitelline duct
Vitelline duct: odorous d/c

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18
Q

What is the main concern w/ hip exam

Since all infants are born w/ limited laxity, what are the three concerns if this persists

RFs for Congenital Hip Dysplasia

A

Congenital Hip Dysplasia- spontaneous dislocation and reduction of femoral heads; L > R

Flat acetabulum
Muscle contraction limiting ROM
Capsule tightening

Female First FamHx
Breech
Oligohydramnios
Postnatal swaddling position

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19
Q

What are the two maneuvers done for hip stability during newborn exam

If ‘clunk’ is heard, ? is the next step

What populations should received this next step

A

Barlow
Ortolani- clunk from hip relocating anteriorly

Hip US at 4-6wks to avoid confusion w/ normal laxity

Clunk or persistant click x 2wks of age
+ RFs- US after 4-6wks old

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20
Q

Congenital Hip Dysplasia referred to Peds Ortho will be placed in ? device for ? age groups

? is the MC foot d/o in infants

Infants w/ this MC are at risk for developing ? later in life

A

Pavlik harness- up to 6mon old

Metatarsus adductus- medial deviation of mid and forefoot

Developmental hip dysplasia

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21
Q

How is Metatarsus Adductus Dx

How are these Tx

Define Talipes Equinovarus

What is the next step after Dx Talipes Equinovarus

A

Mid-heel bisector line- should go between toes 2-3
V-finger- should not gap at base of 5th MT (styloid)

Most self-resolve
If not w/in 2yrs= Ortho referral cast/brace/surgery

Clubfoot- entire leg involved d/t hypoplastic tarsals and limb muscles
MC affected- talus, causes foot shortening/calf atrophy

Refer to Ortho: casting/tenotomy to correct deformity, preserve mobility

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22
Q

? testi/female genitalia abnormalities can be seen on newborn exam

Define Spina Bifida

When/How is this normally identified during pregnancy

A

Testi: retractile
Female: hypertrophy d/t maternal estrogen

Cleft Spine; Lumbosacral tube defect d/t incomplete brain/cord/meninge development

2nd-Tri Quad screen- maternal A-fetoprotein/US

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23
Q

Define Rachischisis and ? risk needs to be r/o

A

Spina Bifida Occulta- hair tuft/minor defect w/out neuro S/Sxs; r/o connecting sinus d/t inc risk for meningitis

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24
Q

What are the categories of Spina Bifida

How is this Tx and avoided

A

Meningocele- meninges herniates through neural arch

Meningomyelocele- meninges and cord herniate through neural arch

Myeloschisis- open skin w/ cord exposed

Neurosurgery;
Folate prior to tube closure at 4-6wks EGA

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25
Q

What are the primitive reflexes tested for on newborn exam

What do these reflexes evaluate

When do these normally disappear

What could cause an asymmetric/persistent response

A

Suck Moro Grasp

Brain stem, Basal ganglia

4-6mon d/t increased cerebral inhibition of

Focal brain/peripheral nerve lesion

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26
Q

Only reflex not present at birth and never disappears

What reflexes disappear at 3, 4, 6 or 12mon

A

Parachute- appears at 8-10mon; suspended face down, move towards table causes arm extension for protection

3: Asymmetric tonic neck
4: Rooting, Gallant, Placing
6: Moro, Grasp
12: Babinski

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27
Q

Facial palsy in newborn is associated w/ ?

Define the MC brachial plexus lesion

What reflex is present/absent in this MC

A

Forcep delivery

Erb-Duchenne palsy- C5/6 lesion, association w/ phrenic nerve lesion d/t shoulder dystocia

+ grasp
- bicep

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28
Q

Define Klumpke Palsy

What syndrome is this associated w/ if a cervical sympathetic nerve root was injured

Define Vernix Caseosa

A

C8-T1 lesion: - grasp +bicep w/ claw hand

Ipsilateral Horner’s Syndrome

Chalky white mixture of shed epithelials cells, sebum, keratin and hair; common in preterms for suspected fetal protection

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29
Q

When is term infant desquamation typically seen

Define Milia

Define Milia Rubra

A

24-48hrs of life

Smooth, white papules on face/scalp d/t trapped keratin; self limited/resolves 1-4wks

Heat rash d/t overheated/febrile infant w/ erythematous papules; Tx/correct overheating

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30
Q

Define Cutis Marmorata

Define Slate Gray Nevi

Define Cafe Au Lait macules and when are further work ups indicated

A

Mottling- cold response; persistent suggests hypothyroidism/vascular malformation

Transient dark macule on lower back/buttocks that fade w/ time

Sharply defined, pigmented macules;
6 or more/ 5cm or bigger to r/o NF-1, TB, McCune Albright Syndrome

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31
Q

Nevus Simplexes are AKA ?

Define Nevus Flameus

? syndrome needs to be r/o depending on location

A

Salmon patches
Stork bite- nape of neck
Angel kiss- forehead/eyelids

Port Wine Stain; d/t capillary bed malformation

Sturge Weber Syndrome if trigeminal nerve distribution

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32
Q

Define Erythema Toxicum Neonatorum

Wat would be seen on microscopy results

What causes neonatal acne

A

Pustules w/ erythematous base on back/trunk appearing 1-2 days after birth, resolves in 14days

Eosinophils

Maternal estrogen

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33
Q

Primitive reflexes are usually gone by ? age

RFs for neonatal sepsis

A

4-6mon

Prematurity
PROM
Fetal tachy
Amnionitis
Maternal fever
GBS
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34
Q

Neonatal sepsis etiologies w/ early onsets

Neonatal sepsis etiologies w/ late onsets

A
Mycoplasma
GBS- MC/#1
E coli
Klebsiella
Listeria
Salmonella
Hflu
Neisseria meningitidis
CMV
HSV
Enterovirus
Strep pneumo
Staph
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35
Q

Early onset neonatal sepsis begins on ? day and presents w/ ?

Late onset neonatal sepsis begins on ? day and is more likely associated w/ ?

What orders are needed

A

0-7d old;
Fast onset, Hypo-thermia/tone/tension

8-28d old;
Insidious onset, Dec feeding/tone, Bulging fontanelle; associated w/ meningitis

CBC 
CXR if + resp Sxs
Blood culture x2
UA w/ culture
Blood glucose
LP
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36
Q

How is Neonatal Sepsis Tx

Why would Vanc be added to Tx regiment

Three steps for GBS mother

A

Draw labs then:
IV Ampicillin+Gentamicin
IV Amp+Cefotaxime if >3wks d/t liver function

Late onset, + meningitis, MRSA coverage

1: infant have S/Sxs?
Yes: eval w/ empiric Tx
No: step 2

2: infant <35wks EGS?
yes; limited eval w/ 48hr observation
no: step 3

3: Two maternal ABX doses prior to delivery?
Yes: no eval/therapy, observe x48hrs
No: limited eval w/ 48hr observation

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37
Q

? PE finding is a sign of neonatal respiratory distress

What Dzs make this finding MC found

Respiratory Distress Syndrome is AKA ? and caused by ?

A

Grunting (can sound like meowing)

Dec functional residual capacity:
Pneumonia
Pulmonary edema
Peripheral airway obstruction

Hyaline Membrane Dz: dec surfactant from Type 2 pneumatocytes in <34wks EGA

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38
Q

RDS results in ? and looks like ? on CXR

How is RDS Tx prior to birth

How is RDS Tx after birth

A

End expiration atelectasis; Ground glass

Maternal steroids 32-34wks EGA

Intubation w/ surfactant/support via ET tube

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39
Q

What complications can arise from RDS

Which one appears on day 2-4 of life and what does this look like

How is this Tx

A

PDA PTX
Bronchopulmonary dysplasia
Retinopathy of prematurity

PDA: L to R shunt (systemic to pulm) as pulmonary edema/hepatomegaly

Fluid restriction w/ diuretic
Indomethacin/Ibuprofen

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40
Q

How is RDS induced PTX Tx

What causes the Bronchopulmonary Dysplasia after RDS

What are the 3 RFs for this dysplasia

A

Sxs= chest tube

O2 toxicity/barotrauma

O2 dependence at 36wks old
RDS persists >14days
Prolong mechanical ventilation

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41
Q

How does RDS cause Retinopathy of Prematurity

Criteria for Apnea of Prematurity

What are the two types and causes

A

O2 toxicity causes vasoconstriction in developing vessels= obliteration/blindness (term infant eyes fully vascularized- no risk)

10-20sec w/out pulmonary airflow

Central: medulla/pons don’t stimulate phrenic nerve (more common in premature infants)
Obstructive: malformation/positional

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42
Q

How is Apnea of Prematurity Tx

When does this usually correct itself by?

? is the MC congenital tracheal abnormality

A

O2, Stimulants: caffeine/theophylline

36-40wks post-conceptual age

Tracheomalacia- weak/floppy tracheal wall worse during expiration (harsh, monophonic wheeze/normal voice/inspiration)

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43
Q

Four possible outcomes from Meconium Aspiration Syndrome

How are non-vigorous babies w/ aspiration managed

How does aspiration appear on CXRs

A

Respiratory distress
Pneumo-nia/nitis/thorax

Suction mouth/trachia
Unsuccessful: BVM w/ PPV

Coarse, irregular infiltrates

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44
Q

What causes Transient Tachypnea of the Newborn

How would this appear on CXR

When is this type of issue more commonly seen

A

Retained amniotic fluid causes hypoxia that resolves <24hrs

Fluid in fissures

C-section, LGA d/t no ‘squeeze’ during birth

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45
Q

How does P-HTN in term infant present

MCC of Hemolytic Dz of newborn

What are the three reasons all newborn have an elevated bili

A

Primary: Hypoxia w/out cardiac/pulm dz and normal CXR
Non-Primary: induced L to R shunt

ABO incompatibility

Inc RBC turnover
Dec hepatic clearance/gut motility

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46
Q

Neontal hyperbilirubinemia is ? levels

? is the MCC of neonatal jaundice

Define Kernicterus

A

Total Bili >5mg/dL

Hemolytic Dz of the newborn- ABO incompatability is MCC

Bilirubin Encephalopathy- indirect bili deposits in brain, disrupts neuron metabolism/function

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47
Q

Early signs of Kernicterus

Late signs of Kernicterus

A
Day 4 of life w/:
Lethargy
Emesis
Hypotonia
High pitch cry
Irritable
Poor Moro/feeding
Fever
Hypertone
Bulging fontanelle
Opisthotonic posture
Pulmonary hemorrhage
Paralysis of upward gaze
Seizures
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48
Q

What are the two classifications of hyperbilirubinemia

What is a common cause of jaundice in first time mothers

What causes Adequate Intake Breast Milk Jaundice

A

Unconjugated: estimated w/ indirect (MC)
Conjugated: direct; rare but more serious

Breastfeeding jaundice- lack of adequate feeds causes dec gut motility on day 2-3 of life

Defected milk w/ conjugation inhibitor, increased hepatic recirculation d/t glucuronidase; seen on day 7-10 w/ bili rarely above 20mg

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49
Q

What is seen on lab results to aid w/ Dx of Breast milk Jaundice

Jaundice seen at ? point in time is always pathologic

Un/Conjugated DDxs

A

Unconjugated hyperbilirubinemia w/out hemolysis

1st day of life

Indirect: Hemolysis, Insufficient conjugation
Direct: Biliary atresia, Unresponsive to phototherapy or transfusions

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50
Q

Characteristic clues of Physiological Jaundice

Characteristic clues of Pathological Jaundice

When evaluating jaundice, ? is the first location that needs to be assessed

A

Evidence starts w/ bili at 5-6 or,
Preterm w/ bili <15 on day 5 of life:
Yellow skin started on face, moves down

Very early, very fast:
Peak bili w/in 24hrs of life in term infant
Bili rises 0.5/hr or 5mg/dl/day
Jaundice w/in 24hrs of life
Hepatosplenomegaly and anemia

Under tongue THEN sclera

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51
Q

? is first line test ordered for evaluation of neonatal jaundice

How are these Tx if Mild, Mod or Severe

What are the short and long term adverse effects of neonatal phototherapy

A

Transcutaneous then serum bili

Mild: lifestyle, breast feed, sunlight
Mod: phototherapy
Sev: exchange transfusion if levels >20

Short:
Diarrhea, Dec bonding, GI hypermotility
Temp instability

Long:
Inc risk for asthma and DMT1

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52
Q

What is included in a standard well visit

Define Neonate

Define Infant

A

Growth Development Imms Guidance Screenings

0-28d old

29d-1y/o

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53
Q

Define Toddler

Define Pre-Schooler

Define Child

A

1-3y/o

2-5y/o

1-12y/o

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54
Q

Define Adolescent

Define Growth

Define Development

A

13-18y/o

Increase in body size

Increase in function/process

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55
Q

Developmental Scales are AKA ? and use ? as more more detailed screening

Define Developmental Milestones

What is the MCC of abnormal growth chart results

A

Ages and Stages;
Denver Developmental Screening Test 2

Observable traits/actions that present/fade at predictable ages

Operator error

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56
Q

Weight loss expected during first few days of life

Time frame to return to birth weight, double and triple their weight

What is considered normal daily weight gain

A

5-10% of birth weight

Return by day 14
Double 4-5mon
Tripled birth weight by 12mon

20-30g x first 3-4mon
15-20g x remainder of first year

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57
Q

Average length at birth is ?

By 4y/o, average child length has increased by ? much

Average head circumference at birth is ? and increases by ? much

A

20” at birth
30” at first year

Double birth length or, 40”

35cm at birth
Inc 1cm/mon x first 12mon (2cm/mon first 3mon)

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58
Q

How long are head circumferences taken at child appointments

Pediatric weight percentiles/categories

How are heights predicted for fe/males

A

Until 2y/o

<5th: underweight
5-85th: normal
85-95th: over weight
>95th: obese

M: Paternal + Maternal/2 + 2.5
W: Paternal + Maternal/2 - 2.5

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59
Q

What is the 2 Year x 2 Method for predicting height

What is the most accurate method for predicting height

MC factor affecting growth

A

Height inches at 2y/o x 2

Bone age w/ hand x-ray

Hereditary factors

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60
Q

Babies born small/premature can be expected to go through ‘catch up’ growth during ? frame

When is medical interventions indicated for deficient growth patterns

When is it normal to see a decline in growth rate

A

First 6mon

<5% w/out cause
Crosses two percentile lines w/out cause
Discrepancy between Circumference/Weight/Length

After 2y/o

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61
Q

Nutrition/growth during ? pat of life predict adult stature and health outcomes

When is the biggest risk for stunted growth

It is recommended breast milk as sole nutrition source for premature infants d/t ? benefits

A

First 3yrs

4-24mon

6mon;
Lower readmission rates
Long term IQ development

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62
Q

What can be used for Vit D/Fe supplementation for breast feeding mothers

Absolute c/is to breast feeding

Mothers should limit alcohol consumption to ? much

A

Polyvisol

HIV
Active TB
Varicella
H1N1
HSV on breast

<0.5mg/kg

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63
Q

What are the three categories of formula

A

Cow milk based:
Fortified w/ Fe, no sterilization needed

Soy based:
Lactose free alternative w/ possible isoflavone effect

Casein hydrolysate:
Used when absorption/digestion problem exists, $$

64
Q

Do not feed infants honey/canned goods until ? age

Begin solid foods at ? age

Avoid cows milk until ? age

Avoid whole milk until ? age

A

12mon

6mon

12mon d/t risk for GI bleed/anemia

24mon

65
Q

Do not substitute formula w/ soy milk for infants under ? age d/t ? risks

Toddlers 1-12y/o need to avoid ingesting more than ? muck cows milk/day

Over weight children don’t need to be on diets before ? age

A

<12mon; Scurvy Anemia Malnutrition

> 24oz

3y/o

66
Q

What age groups should WHO growth charts be used

? age should CDC growth charts be used

When/How is autism screened for

A

Birth - 2y/o

2y/o - 20y/o

M-CHAT-R at 18, 24mon
>2 predictive or >3 total behavior= further work up

67
Q

What is the ASQ

How is it adjusted for pre-mature born infatns

What 5 areas are surveyed

A

21 age specific surveys about developmental skills

3wks premature for up to 2y/o

Problem solving
Communication
Motor
Personal/Social

68
Q

What are the red flags for Gross Motor

What are the red flags for Language

A

Rolling <3mon old= inc tone
Poor head control at 5mon= dec tone
Lack of sitting at 7mon= dec tone
Hand dominance <18mon= contralateral motor abnormality

Vary pitch by 4mon
Lack of babble by 6mon
No word/gesture by 15mon
No pointing by 18mon
Less than 50% intelligible speech at 24mon
69
Q

All children w/ speech delay need ? tests

When do Well Child Exams take place

BP is not a standard part of VS until ? age and how is it calculated

A

Ear exam
Hearing eval w/ tympanometry and audiometry
Auditory Brain Stem Response- r/o peripheral loss

Day 3-5
Week 2
Mon 2 4 6 9 12 15 18 24 30, then annual

After 3y/o
SBP= 80 + Age x 2
DBP= 2/3 of SBP

70
Q

How is newborn metabolic screening conducted

? metabolic issue is screened for at every visit

Guidelines for newborn exams when 0-6mon, 6-36mon and >36mon old

A

Hgb electrophresis

Obesity

0-6: no fear, easily comforted/distracted
6-36: fear of stranger/doctor, harder to restrain; moody
>36mon: less fear, more interaction

71
Q

When are anemia screenings conducted

How much lead accumulation can cause irreversible developmental/behavior abnormalities

When does cholesterol screening begin

A

12mon if healthy
4mon if high risk

5-10ug/dL; screen at 12mon

Non fasting 9-11y/o and 17-21y/o
Overweight/Obese- fasting
Parent cholesterol >240= high risk, start at 2y/o

72
Q

What are the accepted cholesterol limits in kids

? populations are considered high risk for TB and when do screenings begin

A

Borderline: <170
High: >200
Acceptable LDL: <110; Border: 110-129; High: >130
HDL should be >40

12mon/>:
Close contact; w/ high risk adults
Health care workers
Foreign born in high TB areas

73
Q

Define Active Immunity

Define Passive Immunity

Define Primary Prophylaxis

Define Secondary Prophylaxis

A

Immunity from vaccine/toxoid

Maternal Ab transfer/administration of Abs

Prevent infection before first occurrence

Prevent recurrence after first infective episode

74
Q

How are premature infants immunized

What is the exception to this schedule

When is DTaP given

A

Regardless of birth weight, same chronological age/schedule

Hep B vaccine if <2000g w/ HBsAg negative mother- give first dose at 1mon

5 doses at 2, 4, 6, 15, 48mon
One adult dose at 12

75
Q

When is Hep B vaccine given

Why his HIB vaccine given

When is MCV4 Meningococcal given

A

First of three at <24hrs old if healthy term

Protection from meningitis/epiglottitis

11-12y/o or prior to college

76
Q

When is Hep A given

When can influenza be given

Prevnar vaccine is given to protect from ?

A

Two doses: 1-2y/o

6mon

Pneumococcal

77
Q

When is HPV vaccine given

Describe the Rotavirus vaccine and when it’s given

How long should rear facing car seats be used and how long should kids ride in back seat

A

Early as 9
Target of 11
Two doses if completed by 15y/o

Live attenuated cow virus;
First dose- 15wks old, final dose NLT 8mon

2y/o;
Back seat until 13y/o

78
Q

Risks of tobacco smoke

Sequence of teeth eruptions at ? ages

What labs are ordered if delayed tooth eruption is present

A

LBW
SIDS
Respiratory illness- asthma
Otitis media

Deciduous: lower central incisors to upper central incisors to lateral incisors;
Permanent 6-12y/o w/ 3rd molars by 18y/o

TSH, Ca for Hypothyroid/Hypopituitary, Rickets

79
Q

Sequence of deciduous teeth eruptions

Sequence of permanent teeth eruprtions

A
Lower central incisor 
Upper central incisor
Lower lateral incisor
Upper lateral incisor
Lower first molar
Upper first molar
Lower second molar
Upper second molar
L central incisor
First molars
U central incisor
L lateral incisor
U lateral incisor 
L cuspid
U cuspid
U second cuspid
L second cuspid
L second molars
U second molars
Third molars
80
Q

Avoid fluoride tooth past until ?

When do dental visits/cleanings begin

What is the ultimate goal of discipline

A

24mon

12mon w/ cleanings q6mon

Child’s self control

81
Q

Define SIDS

What stats belong to this Dx of exclusion

What therapy may be beneficial in prevention during the first year

A

Unexpected death <1y/o unexplained by autopsy/CSI and review of clinical history

Third leading cause of US infant mortality
MCC of death 1mon-12mon old

Pacifiers

82
Q

What is the risk of Back-To-Sleep position

When does this Dx require no further eval

When is further eval warranted

A

Pagiocephaly

Normal then Dx develops w/ improvement in 2-3mon

No improvement in 4-6mons- craniofacial specialist

83
Q

Gross Motor Skills at 4mon old

Gross Motor Skills at 9mon old

Minimum age for child to be forward facing in car seat

A

Rolls front to back, no head lag w/ pull from supine

Pulls to stand, gets into seated position

2y/o that outgrew rear facing weight/height limits

84
Q

Criteria for FTT Dx

What are the three classifications of FTT

What are the two patterns and their meaning

A

Weight <3rd percentile
Weight decreases by two major percentile lines
Weight <80% of median weight for heigt

Type 1: Wasting; deficient weight gain d/t malnutrition

Type 2: Shunting; deficient linear growth w/ head circumference spared d/t malnutrition x months

Type 3: Symmetric; proportional loss weight, height and circumference d/t long standing malnutrition, chromosome abnormalities or infection/exposures

Dec weight after certain age: infection, endocrine, environment
Body asymmetry: epiphyseal, chromosomal

85
Q

Basically FTT is d/t ? and 1/3 of organic causes are ?

How is FTT corrected

Why is Refeeding Syndrome deadly

A

Insufficient nutrition at cellular level;
GI causes

Inc calories/protein <>1.5x

During starvation- dec metabolism to force storage for homeostasis
Rapid feeding- loss of fluid/E+; fluid retention, Hypo-Phos/Mg/K/Ca

86
Q

Autosomal dominant congenital malformations

Autosomal recessive congenital malformations

X-linked congenital malformations

A
Achondroplasia
Neurofibromatosis
Huntingtons
Marfans
Polycystic kidney

CF PKU CAH SS

Fragile X- excessive gene base repeats
Muscular dystrophy
Hemophilia A
G6PD deficiency
Color blindness
87
Q

RFs for Downs Syndrome

What do all Pts w/ Downs need to have ordered

What are the three forms of Trisomy 21

A

Inc maternal age, Parental genetics

Chromsomal analysis, + translocation= parental analysis

MC- maternal non-disjunction
Translocation- part of #21 is stuck on another chromosome prior to replication
Mosaicism- rarest; pehnotypical normal Pt

88
Q

What will be seen on PE of Down Syndrome

What are the face characteristics

What are the extremity characteristics

A

Generalized hypotonia- dec Moro reflex
Small head

Flat bridge d/t midface hypoplasia
Up slanting fissures
Macroglossia
Epicanthal folds
Dysplastic pinna

Single palmar crease
Shortened mid-5th phalanx
Wide first toe interspace

89
Q

All Down Syndrome Pts will have ?, two-thirds have ? and half will have ?

What type of hearing loss will majority have

What eye defects will they have

A

All- developmental delay
2/3: polycythemia
Half- cardiac anomalies

SNHL

Cataracts
Refractive error
Ectopic lens
Brushfield spots
Strabismus
90
Q

? x-ray finding in Down Syndrome needs immediate surgical Tx

What is the routine health care check list for all Down Syndrome Pts

A

Duodenal atresia; seen as “double-bubble” sign

Hearing screening q3mon until 3y/o, then annual
Cards for Echo
Optho by 6mon then annual
Annual TSH/CBC, Celiac screen

91
Q

? is the most preventable cause of developmental delay/intellectual disability

What are the classic facial features

What hand feature is seen

A

Fetal Alcohol Spectrum D/o

Short palpebral fissures
Smooth philtrum
Thin upper lip

Clinodactyly- hockey stick crease

92
Q

What developmental abnormalities are seen in FASD

How much ingestion puts fetus at risk for developing this

What multidisciplinary team is assigned to these Pts

A

Fine motor delay
ADHD
Retardation

> 7/wk or >3 drinks per period

ADHD
Anxiety therapy
Speech
SpEd

93
Q

Developmental/Neuro problems seen win Fragile X Syndrome

What physical attributes will be seen

How is this definitively Dx

A

Hyperarousal Anxiety Mood lability Epilepsy Sterotypy

Joint laxity
Oblong face
Hypotonia
Macro-orchidism

DNA amplification w/ direct analysis

94
Q

Define 45XO

Majority of defects arise from ? side

What may be seen shortly after birth if infant survives to delivery

A

Turner Syndrome d/t no/abnormal X

2/3 of X are maternal

Extremity edema

95
Q

What type of mental development is seen w/ Turner Syndrome

What CV issues are usually seen

What endocrine d/os are seen

A

Poor visual-spacial skills
Superior verbal skills

Coarctation
Early onset HTN
Bicuspid aorta

Hypothyroidism
Osteoporosis
DMT1

96
Q

How is Turner’s Dx

What Dx method is not recommended

How are these Pts Tx/managed

A

Direct karytotyping

Barr body analysis

Annual TSH, Chem-7, UA
Cards- Echo, MRI, EKG
Endo- GH initiation

97
Q

Define Klinefelter Syndrome

What issue can present

How is this screened, Dx and what would be seen on lab results

How are these Pts Tx and what are they at risk for

A

47XXY: phenotypically normal prior to puberty

Result of testosterone deficiency:
Irregular features
Violent tendencies
Severe MR

Screen: Barr body
Dx: direct karytopying
Inc LH/FSH w/ low T

T replacement
16-30x inc risk for breast Ca

98
Q

What type of genetic defect leads to Marfans

What three systems are affected

Crying from an infant can signal ? possible issues

A

Fibrillin 1 gene on Chrom #15

Ortho: arachnodactyly
CV: AV insufficiency/dissection
Ocular: dislocation

Pain Distress Fatigue Hunger
Pain > Hunger= higher pitch/intensity

99
Q

What is the correlation to crying if infant is preterm

When is the diurnal variation more common

How loud can these reach

A

Little before 40wks old
More than term infant at corrected 6wks

Late afternoon/evening

80dB

100
Q

What findings suggest a crying infant has colic

What is the Wessel’s Rule of 3 for Colic

When does the Dx of exclusion begin to risk maternal health

A

Paroxysmal crying w/ grimace, leg flexion and flatus

Starting at 3wks:
Crying >3hrs/day
Crying 3d/wk
Crying longer than 3wks
Resolves around 3mon old

Inc PPD risk if crying episodes >20min

101
Q

? is the MC reported behavior problem in kids 2-3y/o

When does this MC become an abnormal

How can these be prevented

A

Temper tantrum

Past 4y/o
Injury to self/others
Lasting >15min
>5/day
Negative mood swings w/ tantrum

Parental education at 12-18mon

102
Q

Define Intellectual Disability

What type of testing results aids w/ Dx

DSM-5 requires impaired behavior across ? areas

A

D/o w/ common deficits of adaptive/intellectual function and an onset before maturity is reached

<2SD, IQ <70

Practical/conceptual/social behavior

103
Q

Define Global Developmental Delay

Possible environmental RFs for Autism

What screening form is used for this Dx and when

A

Children <5y/o w/ >2SD delay in multiple milestones

Infections- Rubella, CMV
Maternal obesity
Advanced parent age
Premature
Short interval from prior pregnancy

M-CHAT-R at 18-24mon
Two predictive- hearing concern, finger movement near eye, noise sensitivity or,
Three total

104
Q

Define Cerebral Palsy

What are 3 potential RFs

Two PE findings suggestive of Dx

A

Non-progressive motor impairment syndromes; static encephalopathy

Intrauterine infection
Multiple pregnancies
Infertility Tx

Athetosis, Chorea

105
Q

What are the 6 classifications of Cerebral Palsy

A

Mixed- catch all for Pts that don’t fit other patterns

Ataxic- cerebellar injury causing abnormal posture/coordination

Dyskinetic- involuntary, repetitive movements

Dystonic- rare; stiff/dec movements

Spastic- MAJORITY; pyramidal tract injury to upper neurons w/ two: abnormal movement, inc tone, pathologic reflexes

Choreoathetotic- hyperkinesia, hypotonia; rare now that bilirubin is Tx

106
Q

How is ADHD Dx if Pt is 16y/o or <

How is ADHD Dx if PT is 17y/o or older

What genetic d/os are associated w/ this condition

A

16y/o or :
5 Sxs of inattention or hyperactive impulsitivity
x 6mon in two environments

Fragile X
22a11.2 deletion syndrome
NF-1

107
Q

What is at the core of all ADHD Tx

What meds are used first line

What SNRI can be used

What A-agonists can be used

A

Behavior management

Methylphenidate
Amphetamine

Atomoxetine

Clinidine, Guanfacine

108
Q

Define Oppositional Defiant D/o

Define Conduct D/o

What screening tool is used for OCD

A

Moody, defiant, vindictive behavior

Pattern of behavior where basic rights/norms are violated:
Aggression Destruction Deceit Violation

Vanderbilt

109
Q

What is the mnemonic for interviewing adolescent Pts

A
HEADDSS:
Home/Friends
Education
Alcohol
Drugs
Diet
Sex
Suicide/Depression
110
Q

Average age for female puberty is ? but preccocious puberty is defined as ?

Tanner stages associated w/ TAPuPMe

Completion of Tanner stages takes ? amount of time for male and female

A

11y/o;
6y/o in AfAm; 7 y/o in Caucasian

Thelarche: Tanner 2
Ad/Pub: Tanner 2
Peak: one year after thelarche, tanner 3-4

Female: 4-5yrs
Male: 2.5-5yrs

111
Q

Once female starts menarche, ? much expected height growth is expected remaining

Tanner Stages Mnemonics from OBGYN

Sexual Maturity Rating for female for pubic hair/breast

A

2-5cm

Deck

1: preadolescent/preadolescent
2: sparse/elevations
3: darker curls/enlargement w/out contour separation
4: abundant and coarse/secondary mound
5: adult triangle/adult contours

112
Q

When do boys going through puberty pass through Tanner 1 to 2

How does onset of adrenarche present

Both male and female Pts going through puberty will have ? elevated lab result and ? previous issue may worsen

A

9-11y/o

Pubic, axillary <12mon later

inc ALP d/t rapid bone turnover;
Scoliosis worsens

113
Q

Male tanner stages

A

1: childhood
2: testicle enlargement w/ scrotal reddening
3: all 3 grow in size; length
4: all 3 grow; width
5: adult

2: sparse hair at base
3: dark/coarse/curled hair
4: adult hair not on thighs
5: adult hair including thighs

114
Q

Male Sexual Maturity Ratings

Normal male puberty growth sequence

A

Table

Testicular growth SMR 2
Pubarche
Penile growth SMR 3
Peak height velocity SMR 4

115
Q

Breast mass in adolescent females are usually ? type and evaluated by ?

What is a normal variant of puberty seen in peripubertal females and

What causes this variant

How is is evaluated

A

Fibroadenoma, cyst; eval w/ US

Physiologic leukorrhea- clear vaginal d/c w/out odor/pruritus;

Estrogen from ovary stimulating uterus/vagina

Vaginal culture w/out speculum

116
Q

Menarche usually presents ? long after thelarche

How long are these classified as irregular after onset

How do Pts know when ovulation has set in

A

2-3yrs after

1-2yrs

Cycle length 21-45 days

117
Q

Define Premature Thelarche

What can cause this

What labs/rads need to be ordered

A

Isolated breast development in 6-7y/o female

Estrogen exposure to phytoestrogens in soy, legumes, flax seed, tofu

Estradiol, LH, FSH, bone age
Head MRI, Pelvic US, GNRH stimulation test

118
Q

Define Premature Adrenarche

What are two etiologies for this variant

What labs/rads need to be ordered

A

Body odor, pubic/axillary hair, acne in females <8y/o/males <9y/o

Obesity, CNS injury

DHEAS, Androstenedione, Testosterone, 17-OH, Bone age
ACTH stimulation test, Adrenal/Pelvic imaging

119
Q

Define Premature Testelarche

What is the next step

Why is this next step so important

A

Enlarged testis >3cc/2.5cm in male <9y/o

Endocrine emergency

50% have brain tumor

120
Q

How is Male Gynecomastia evaluated

When is further work up needed

What medication may be used

A

Round, freely mobile, tender mass under areola in Tanner Stage 3

Large, Hard, Fixed or w/ d/c

Bromocriptine

121
Q

When does irregular bleeding suggest organic abnormality may exist

When is further evaluation needed for irregular menses

Define Primary Amenorrhea and the MCC

A

1yr of regular cycles followed by irregular bleeds

Two or more cycles that are not 21-35d, 7d/

122
Q

Menses frequency

Menses regularity

Menses duration

Menses flow

A

Frequent: <21d/cycle
Infrequent: >35d/cycle

Amenorrhea: absent x 6mon/>
Irregular: >20 day variation in cycle length

Prolonged: >8 days
Shortened: <2 days

Heavy: >80cc loss
Light: <5cc loss

123
Q

Define Secondary Amenorrhea

Criteria to Dx PCOS

MCC of abnormal uterine bleeding in adolescents

A

Menses that have stopped x 3mon after menarche

Two of:
Hyperandrogenism
Infrequent bleed/Secondary amenorrhea
Polycystic morphology on ovary US

Anovulation

124
Q

How is AUB Tx

What is the mainstay of Tx for Pts w/ bleeding d/o such as Von Willebrand Dz

Define Primary Dysmenorrhea

A

Fe therapy
Combo E/P to regulate cycle and allow HPO axis to mature

Combo E/P

Pelvic pain DURING menstruation w/out pelvic pathology;
Feature of ovulation developing 1-3yrs after menarche

125
Q

What causes the pain associated w/ dysmenorrhea

MCC of Secondary Dysmenorrhea

What is the initial screening study for Dysmenorrhea Evaluation

A

Prostaglandins and leukotrienes from degenerating endometrium after progesterone declines causing increased uterine tone; inc pain fiber sensitivity to bradykinin

Endometriosis or PID

Outlet obstruction w/ US

126
Q

How is Dysmenorrhea Tx

When is referral/second opinion warranted

What is the most important part of a Sports Physical

A

NSAIDs- first line therapy
Failure= hormones

Combo OCPs >4mon w/ persistence

Hx

127
Q

What is an example of a disqualifying and non-disqualifying finding on sports physical

How long are Peds disqualified from sports for Mono

How many calories do boys/girls 14-18y/o need per day

A

MedHx of seizures that are controlled- not
Stage 2 HTN/poorly controlled- dq’d

28d d/t risk for spleen injury

B: 2000-3200
G: 1800-2400

128
Q

How much Ca/day do teens need

When is a teen considered Obese and Morbidly Obese

How is Obesity managed in Pts <7y/o and >7y/o

A

1300mg/day

> 120% ideal body weight
200% ideal body weight

<7y/o: goal of weight maintenance to let linear height catch up
>7y/o: goal is 1lb/mon until BMI is <85%

129
Q

What are the SMART Goals when managing Peds w/ obesity

One in five adolescents are depressed and are at risk for developing ?

? has a higher rate of adolescent death than MVCs

A

Specific Measurable Attainable Realistic Timely

Bipolar d/o

Suicide

130
Q

What are the only two meds approved for depression Tx in children

How often are Pts f/u w/ after starting meds

? is the MC psychiatric d/o of childhood

A

Fluoxetine, Escitalopram

Weekly x 2mon

Anxiety

131
Q

Substance abuse screening acronym

Done w/

A
CRAFFT:
Car- driving under influence
Relax- using drugs to relax/fit in
Alone- alcohol/drug use while alone
Forget- d/t consumption
Fam/Friend- tell teen to stop/cut down
Trouble- d/t substance abuse

Slide deck 7

132
Q

How does Post-Strep Glomerulonephritis present

How are these Pts managed

A

Hematuria, Periorbital edema, and HTN two weeks after strep pharyngitis or 3-6wks after strep skin infection Dx/Tx

ABX if active infection
Volume overload w/ Furosemide/fluid restriction
Dialysis if severe renal impairment

133
Q

How does Henoch Schnelein Purpura/IgA Vasculitis present

What will lab results show

A

Purpuric rash, Abdominal pain, Arthralgia, Arthritis 1-3wks after URI

Normal platelet counts
Heme-pos stool
Proteinuria w/ elevated BUN/Cr

134
Q

? is the MC solid renal tumor in kids <15y/o

? is the imaging method of choice

What medication can be used to help reduce the cosmetic effect of Acanthosis Nigricans

A

Wilms tumor

US then CT w/ contrast

Topical retinoids

135
Q

Name of microbe causing pinworms

How is this Tx

A

E. vermicularis

Me/Al-bendazole and w/ repeat dose at 2wks
Pyrantel pamoate

136
Q

How does acute urticaria present

What is first line therapy

A

Raised, erythematous plaques w/ central pallor w/ intense pruritus

Second generation H1 antihistamine:
Levo-Cetirizine- citrus magazine
Des-Loratadine- low-riding jeans
Fexofenadine- fox fencing

137
Q

? is the MC abnormality of male GU tract

What is the MC location of this MC abnormality

When is surgical intervention indicated

A

Cryptorchidism

High scrotal > Inguinal canal > abdominal

Undescended at 6mon= orchopexy

138
Q

Define Rumpel Leede phenomenon seen w/ RMSF

Name of tick carrier

How is it Tx

A

Petechiae formation after BP cuff

Dermacentor

Doxy
Chloramphenicol if preg/allergic to tetracyclines

139
Q

Criteria for Kawasaki Dz Dx

What will lab results show

What inflammatory markers will be elevated or normal

How is this Tx

What unique GI finding is associated w/ this Dx

A
Fever 5d or more w/ 4 of the following:
Bilateral conjunctival injections
Oral mucus membrane changes
Peripheral extremity erythema/edema/desquamation
Polymorphous rash
Cervical lymphadenopathy

Thrombocytosis
Leukocytosis
Normocytic anemia

+: CRP, ESR, A-1 antitrypsin
-: ANA, RF

High dose ASA and IVIG w/ f/u at Cards for Echo

Hydrops of Gallbladder: pain, jaundice, boggy on US

140
Q

Testicular torsion is corrected w/ in ? time frame and w/ ? procedure

How is pain described

Stopped on

A

<6hrs w/ bilateral orchiopexy

Radiating towards abdomen

Rosh #10

141
Q

? is most frequently reported as perpetrator of child abuse

Who is more likely to inflict serious head/abdominal trauma

? is the MC type of abuse that is also ?

A

Mother

Father/Maternal boyfriend

Neglect- failure to provide for child’s needs; also hardest to document/prove

142
Q

? is the 2nd MC type of abuse

? is the MC type of emotional abuse

? are six complications that can arise from abuse

A

Physical, non-accidental trauma; MC perp is primary care giver

Verbal

Aggression Relationships Language Depression Substance abuse Sleep/Anxiety d/os

143
Q

What would be seen on PE if child was experiencing neglect

? types of Fxs have high abuse suspicion

Abdominal injuries are more common in ? populations

A

Type 1 growth deficiency: normal head/length, low weight

Metaphyseal Scapula Rib Spiral Vertebral

Infant/Toddler

144
Q

? type of abuse is the leading cause of morbidity/mortality

How does the color of a bruise correlate to age

A

Head injuries- shaking or blunt/force trauma

Red: 0-2d
Blue/Purple: 2-5d
Green: 5-7d
Yellow: 7-10d
Brown: 10-14d
Hbg to Biliverdin to Bilirubin
145
Q

What image is done for suspected abuse in kids <3y/o

Sequence of events for Fxs to heal

A

Skeletal surveys

7-14d: new bone/callus
14-21d: loss of Fx line, callus matures
3-6wks: dense callus
>6wks: sclerotic thickening

146
Q

? is the Shaken Baby Triad

Sexual assault kits can be collected w/in ? time frame

Diabetes is characterized by ? and ?

A

Retinal hemorrhage
Brain swelling
Subdural hematoma

<72hrs from attack

Hyperglycemia and glycosuria

147
Q

What are the two type of DM in Peds

Criteria for Pre-Diabetic and Diabetic

A

DMT1: MC type in childhood d/t autoimmune destruction of B-islet cells leading to permanent insulin deficiency

DMT2: MC in adulthood d/t insulin resistance and obesity

Pre: A1c 5.7-6.4
DM: Fasting 126 or higher
2hr OGTT 200 or higher
A1c 6.5% or higher

148
Q

? is first line medical therapy for DMT2 Tx

What are the 4 phases of DMT1

What are the 3 Ps of DMT1 presentation

A

Metformin

Pre-clinical B-cell destruction
Clinical onset
Transient remission w/ honeymoon
Established diabetes

Poly-dipsia/uria/phagia

149
Q

Potential fatal outcome from undetected/poorly acknowledged DMT1

What are the 3 classifications of this outcome

A

DKA: glucose >300, pH <7.3, BiCarb <15

Mild: Co2 16-20, pH 7.25-7.35
Mod: Co2 10-15, pH 7.15-7.25
Sev: Co2 <10, pH <7.15

150
Q

How is DKA Tx

What is the most serious complication from this Dx and how is it Tx

What RF places Pt highest risk for developing this outcome

A

Admit for insulin/fluid w/ E+ therapy
Switch D5W when glucose 250-300
10% once glucose <200

Cerebral edema; IV Mannitol w/ HOB raised

Dec in glucose >100mg/hr

151
Q

How is DKA Tx

What is the most serious complication from this Dx and how is it Tx

What RF places Pt highest risk for developing this outcome

A

Admit for insulin/fluid w/ E+ therapy
Switch D5W when glucose 250-300
10% once glucose <200

Cerebral edema; IV Mannitol w/ HOB raised

Dec in glucose >100mg/hr

152
Q

What should DM diet compose of

What are the A1c goals for Peds

What are the blood glucose goals

A

55% carbs
15% protein
<30% fat
<300mg/24hrs cholesterol

<6y/o: 7.5-8.5%
6-13y/o: <8%
13-18y/o: <7.5%

<5y/o: 80-180
School aged: 80-150
Adolescent: 70-130

153
Q

Define Honeymoon Period seen in DMT1

Define Dawn Phenomenon

Define Somogyi Phenomenon

A

Residual B-cell function, measured w/ C-peptide

Inc morning glucose d/t GH release and fading insulin levels; Tx w/ inc bedtime insulin

Hypoglycemic level at 0300 d/t counter regulatory effect; Tx w/ lower bedtime insulin

154
Q

MC complication of DMT1 and when is it most likely to occur

How are Mild or Sev complications Tx

What f/u do these Pts need

A

Hypoglycemia; after hypoglycemic episode d/t reduce autonomic responses

Mild: PO glucose
Sev w/ seizure/LOC: glucagon

Annual Ophth for Pts w/ dx >3yrs
Annual UA for microalbuminuria
Annual cholesterol/BP checks
Annual thyroid

155
Q

Sick Day Rules for DMT1

What is the rule used for insulin insensitivity and establishing sliding scale

A

BG >240= check for ketones w/ fluid/insulin management
Insulin pump- change site, give correction dose via injection
Re-check BG/mental status q3hrs
Re-check ketones qVoid
Min 8oz sugar free fluid/hr
15g carbs/hr

Rule of 1500:
1500/total insulin= amount 1unit of insulin will lower glucose

156
Q

? is the most sensitive test of thyroid function in Peds

? is the MC cause for this most sensitive to be elevated if on corrective meds

Only indication to US thyroid in Peds

A

TSH

Non-compliance

Nodular; No if symmetrical