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Angel Solomon, MS PA‐C
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Infant & Childhood DevelopmentGross Motor3 month – head control4 month – roll over6 month – sit independently9 month – crawl12 month – walk18 month – climbs stairs, run24 month – kick ball
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Infant & Childhood DevelopmentLanguage2 month – coos6 month – babbles12 month – mama, dada18 month – 4‐20 words24 month – combining words, 50% comprehensible
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Infant & Childhood DevelopmentLanguage cont…3 year – 75% comprehensible4 year – 100% comprehensibleAge 7 or 8 – speech, language, articulations close to adult
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Infant & Childhood Development
Social/Fine motor3 month – laugh6 th h f d lf6 month – reaches, feeds self9 month – indicates wants, pincer grasp12 month – imitates, follow 1 step commands
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Infant & Childhood DevelopmentSocial/Fine motor cont…18 month – scribbles, feeds self w/spoon, potty training, stacks 3‐4 blocks h f ll d h/d h d24 month – follow 2 step commands, wash/dry hands
3 yr – dresses with supervision
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Newborn & Infant GrowthNewborns may lose up to 10% of their birth weight in the first week of lifeMost regain birth weight in about 10 daysFirst 6 months: gain about 1oz/dayFirst 6 months: gain about 1oz/dayAt 6 months: weigh 2x birth weightAt 12 months: weigh 3x birth weight, height 1.5x birth length
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Childhood Growth
After 2 years of age: 2‐3 kg and 5‐7cm/yearAverage 30 month child weighs 30 pounds and is 30 inches tallA ld i h d d i i h Average 4 year‐old weighs 40 pounds and is 40 inches tallWeight LOSS in a child is always suspicious
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Abnormal GrowthFailure to ThriveShort Stature
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FTTDefinition: Weight that decreases to below the 3rd/5thpercentile or weight loss that crosses 2 major percentilesCauses:Nonorganic: Environmental/Social is #1 (poverty, poor feeding technique, neglect/abuse, parental mental health)
Organic – Affects every system, 1st 3 months MC due to infection, Metabolic Disease, Congenital Heart Disease, GERD, Milk Protein intolerance, Cystic Fibrosis
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FTT‐continuedInitial Eval:History – Identifies cause of in majority of cases (feeding patterns, vomiting, bowel habits, social/emotional/financial stability, development)
Physical focus on signs of organic disease evidence Physical – focus on signs of organic disease, evidence of abuse/neglect, dysmorphic features, skin lesions, heart murmur, abdominal masses, neuro exam
Labs – Cbc, Bun, Cre, Electrolytes, UA C&STreatment – R/O organic cause, Hi calorie diet, Education, Frequent monitoring, If severe require hospitalization, social services
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GROWTH DISTURBANCESDistinguish between normal and abnormal conditions
Tools for Evaluation:1. Growth Curves – critical factor in evaluation
2. Target Height – helpful to evaluate growth potentialBoys ‐ [(Mothers Ht in cm + 13) + Father’s Ht in cm] / 2Girls – [Mothers Ht in cm + (Father’s Ht in cm – 13)] / 2
3. Bone Age – measure of skeletal maturation
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SHORT STATURE1. Familial Short Stature2. Constitutional Growth Delay3. Chronic Conditions
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SHORT STATURENormal Variants
Familial Short Stature – Normal birth size, deceleration on growth curve first 2 years of life, Normal bone age and puberty, target height is short
Constitutional Growth Delay – Normal birth size, growth pattern similar to familial short stature, Delayed bone age and puberty, “Late bloomers” Target height normal
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SHORT STATURE
Chronic conditions
Endocrine – GH Deficiency, Hypothyroidism, Cushing syndrome/diseaseNutritionalSystemic Disease – GI, Renal, Cardiac, Pulmonary, ImmunologyGenetic Syndromes – Turner, Prader‐Willi, Down
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HEENTURIAcute Otitis MediaChronic Otitis Media
AmblyopiaENT Foreign Bodies
Otitis ExternaCroup
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VIRAL URICommon in any age group; especially infants and toddlersLasts 7‐10 daysMCC: RhinovirusSymptoms:Symptoms:
Runny nose, nasal congestion, coryza, sneezing, mild conjunctivitis, sore throat, hoarseness, cough. Fever often presents for first 2‐3days
Tx: Cough and cold medications. No antibiotics!!!
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OTITIS MEDIAAcute Otitis Media
Suppurative infection of the middle ear cavityMost prevalent in children between 6 and 24 mo
BacterialSt t P i ( t ) Streptococcus Pneumoniae (most common) Haemophilus influenzaMoraxella Catarrhalis
Viral Respiratory Syncytial VirusRhinovirus Influenza virus
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Otitis MediaRisk Factors
Day Care AttendanceFormula Fed Infants (feeding position)Second hand cigarette smoke
Presentation & DiagnosisOften follows an upper respiratory tract infection(URI) by 1‐7 daysUsually presents with fever, poor feeding, pain and/or irritability, vomiting, ear pulling
TM : bulging, red, landmarks not visualized, immobile (Pneumatic Otoscopy with evaluation of movement of TM)
AntibioticsDOC: Amoxicillin 80‐90 mg/kg/d (erythromycin if allergic) If tx failure after 48 hours: amoxicillin/clavulanate, cefuroxime, cefdinir, ceftriaxoneComplications: mastoiditis Rutgers PANCE/PANRE Review Course
Chronic Otitis MediaDefinition – recurring or persistent infection or inflammation for several months
Risk Factors ‐multiple ear infections, allergies, trauma, swelling of the adenoids
Sx h i l t h hSx – hearing loss, otorrhea, pressure, ear achePE: infxn, air‐fluid levels. discharge, perforationTx: Abx, Surgery (Myringotomy/Repair/Adenoids)Complications: Mastoiditis, Deafness
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OTITIS EXTERNAInflammation of the skin in the outer ear canalCommonly caused by water trapped in the canal from swimming in lakes or poolsPathogens:
Staphylococcus aureusp yPseudomonas aeruginosa
Symptoms:Pain, purulent discharge, pain elicited with traction on pinna or tragus
Treatment:Topical Antibiotic/Corticosteroid drops(Acetic Acid/Polymyxin B/Neomycin/Quinolone)
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Viral Croup
Viral Croup – Laryngotracheobronchitis
Most common cause of stridor in children
Peak ages : 6 months to 3 years. Fall/WinterPeak ages : 6 months to 3 years. Fall/Winter• Sx: Barking cough, URI symptoms, hoarseness, fever, inspiratory stridorPathogen: parainfluenza virus commonDiagnosis: H & P, season helpful (Fall/Winter)
<50% “steeple sign on ant neck X‐rayTreatment: Hydration, Humidity! Steroids, Racemic Epinephrine
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AMBLYOPIA
Definition: decreases or loss of vision in one or both eyes in the absence of ocular or CNS pathologyInitiated by any condition that results in abnormal/unequal visual input between the “critical period” of birth to 8‐9 years of age
Dx: Visual Acuity, RF ie.. Strabismus, congenital cataracts, FHxTx: Patching, essential within the critical period; otherwise loss may be permanent
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Courtesy of WikepediaRutgers PANCE/PANRE Review Course
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AMBLYOPIA
Definition: decreases or loss of vision in one or both eyes in the absence of ocular or CNS pathologyInitiated by any condition that results in abnormal/unequal visual input between the “critical period” of birth to 8‐9 years of age
Dx: Visual Acuity, RF ie.. Strabismus, congenital cataracts, FHxTx: Patching, essential within the critical period; otherwise loss may be permanent
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ENT FOREIGN BODIES
Commonly seen: Buttons, beads, marbles, nuts, toy parts, Bugs tooEar: Ear pain, drainage, hearing lossNose: Unilateral purulent rhinitis, persistent sinusitis blocked nasal passage on examsinusitis, blocked nasal passage on examRemoval: Do not blindly probe! If visible, forceps, curette, Foley (inflated past foreign body), etc Restraint is essential to prevent further injury
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When treating clinical croup, you could reasonably include all of the following except:
1. IV steroids2. Intubation
R i
84%
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3. Racemic epinephrine
4. Oxygen and cool mist
5. IV Ceftriaxone IV steroids
Intubation
Racemic epinephrine
Oxygen and cool mist
IV Ceftriaxone
0%
16%
0%0%
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A 15 month old male presents with a 2 day history of upper respiratory infection type symptoms followed by a barky cough and low grade fever. Which of the following is the most appropriate management of this patient?
1. Albuterol2. Racemic L‐
33%
42%
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epinephrine3. Intubation for
ventilatory support4. IV Antibiotics5. Dexamethasone IV,
IM or PO Albuterol
Racemic L‐epinephrine
Intubation for ventilator...
IV Antibiotics
Dexamethasone IV, IM
..
20%
4%0%
An 18 month old male is brought to the emergency department because he has had a fever and cough for the past 3 days. PE shows an ill appearing but well hydrated child with a bright red tympanic membrane and green discharge from the nose. Temp is 103F. CXR is negative. Which of the following is the most likely dx?
1. Serous otitis media2 Acute otitis media
93%
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2. Acute otitis media3. Chronic otitis media4. External otitis media5. Cholesteatoma
Serous otitis m
edia
Acute otitis media
Chronic otitis m
edia
External otitis media
Cholesteatoma
2% 0%0%5%
LungsBronchiolitisPneumonia
Virall
Hyaline Membrane DiseaseCystic FibrosisForeign bodies
BacterialAtypical
Pertussis
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BRONCHIOLITIS
The most common lower respiratory illness in infants and young children less than 2 years old.Pathogen: Respiratory Syncytial Virus(RSV) in 50‐90% of casesSymptoms: Cough, mild fever, tachypnea, and wheezing.
Thick nasal congestiongDiagnosis: RSV antigen nasal wash. CXR ‐ Hyperinflation
WBC ‐ Increases lymphocytesTreatment: Controversial
Nebulized albuterol commonly usedOral steroids if sx severeRibavirin has been used in hospitalized casesSynagis now used to prevent RSV in preemies
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PNEUMONIA ‐ VIRALCommon in all age groups; follows URIEtiology:
MCC of pneumonia in children. RSV (MC), parainfluenza, & influenza viruses
Symptoms:URI precedes onset of cough Wheezing, grunting, nasal flaring common
Labs:WBC may be low, normal, or slightly elevated. A high WBC makes viral etiology unlikely
Imaging:CXR may show perihilar streaking, increased interstitial markings, peribronchial cuffing
Treatment:It is rarely possible to reliably differentiate viral from bacterial pneumonia based upon history, exam, labs or radiographsTherefore it is common for appropriate concomitant antibiotic coverage to be used for viral pneumonia in children Rutgers PANCE/PANRE Review Course
PNEUMONIA ‐ BACTERIALInflammation of the lung classified according to the infecting organism and siteOccurs in all age groups, but more commonly in children < 2 years oldCommon pathogens:
S. pneumoniae, Group A strepG B t ( t )Group B strep (neonates)
Symptoms:URI precedes abrupt onset of fever, chills, SOB, anorexia, cough, dyspneaN/V, abdominal/chest/shoulder pain typical, malaise
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Pneumonia ‐ BacterialSigns:
tachypnea: reliable sign of pneumonia in kids!Cough, grunting, nasal flaring, Exam usually shows decreased breath sounds, rales, dullness to percussion, but can be normalWheezing unusual in bacterial pneumonia unless pt has baseline reactive airway disease
Labs:WBC >15,000 or greaterBlood cultures positive in 10‐15% of cases
Imaging:Lobar consolidation, patchy infiltrates commonMay see effusionsAtelectasis vs infiltrate ‐ often hard to tell
Treatment:Neonates: IV ampicillin/gentamycinOthers: penicillin. Amoxicillin, 2nd or 3rd generation cephalosporin
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PNEUMONIA ‐ ATYPICALChlamydia pneumonia
Occurs between 2 weeks to 6 months of age. Peak incidence (>90%) by 8 weeksMost common cause of pneumonia in children under 6 months of age (25‐45% of cases)Pathogen: C trachomatis (maternal STD)Pathogen: C. trachomatis (maternal STD)URI prodrome; nearly 100% afebrileStaccato cough, tachypnea, rales, conjunctivitisDx: Nasal wash, eosinophilia commonTx: Erythromycin. Hospitalization for those with paroxysmal cough, apnea, resp distress
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Pneumonia ‐ AtypicalMycoplasma pneumonia:
Common over the age of 5 years, esp teensPathogen: Mycoplasma pneumoniaLong incubation: 2‐3 weeks
Symptoms: Gradual onset, Dry cough, progressing to productive. Fever, HA, malaise, Signs: Rales, bullous myringitisCXR: Middle and lower lobe infiltratesTx: Macrolides usually shorten course and may lessen severity of symptoms
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PERTUSSIS“Whooping Cough”
Infants/toddlers; un‐/partially immunizedPathogen: Bordetella pertussis
Spread by teens/adults who are no longer immune
Sx: 3 stages3 gCattarhal: URI (1‐2 weeks)Paroxysmal: Staccato cough and ‘whoop’ on inspiration(1‐2 weeks)Convalescent: Dry cough (1‐2 weeks)
Dx: Hx, characteristic paroxysmal coughGold standard‐Nasopharyngeal culture, PCR
Tx: ErythromycinRutgers PANCE/PANRE Review Course
Hyaline Membrane DiseaseCause: Deficiency of surfactantS&S: increased RR, cyanosis, expiratory gruntingD CXR h h i B/L t l t iDx: CXR shows hypoexpansion, B/L atelectasis
“Ground glass” “Air bronchograms”
Tx: Oxygen, early intubation, ventilationSurfactant replacement
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CYSTIC FIBROSISMost common severe inherited disease in the Caucasian population ‐ 1:2500Resp symptoms: chronic cough or sinusitis, recurrent pneumonia, nasal polyps, clubbingGI symptoms: meconium ileus (20%), pancreatic insufficiency (85%) failure to thriveinsufficiency (85%), failure to thriveDx: Sweat chloride is the “gold standard” >60meq/L is abnormal. Genetic testingTx: ATB, pancreatic enzymes, bronchodilators, postural drainage. Mean survival age is increasing!
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RESPIRATORY FOREIGN BODIES
Throat: Stridor, choking, cyanosis. (Can also occur if foreign body is in esophagus)Ball‐valve effect may cause hyperinflationHeimlich if suspected upper airway FB and respiratory distressRi id b h if i l iRigid bronchoscopy if in lower airway.
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End of Pediatrics OneEnd of Pediatrics OnePlease go on to Pediatrics Two
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CardiologyAcquired Heart Disease
Rheumatic FeverFunctional murmurs
Still’s MurmurVenous Hum
Congenital Heart DiseaseAcyanotic LesionsCyanotic Lesions
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RHEUMATIC FEVERInflammatory disease triggered by Group A strep and can cause permanent damage to heart muscle and valvesAffects ages 5‐15 yearsJones criteria: Major ‐ carditis, polyarthritis, chorea,
erythema marginatum, subcutaneous nodules Minor ‐ fever, arthralgia, elevated ESR and/or , g , /C‐reactive protein,, prolonged PR interval on ECG
Dx: 2 major criteria OR 1 major and 2 minorTx: Bed rest, salicylates, steroids for severe carditis, chlorpromazine or Haloperidol for choreaPrevention: Recurrences ‐ Benzathine penicillin q month
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FUNCTIONAL MURMURS
Still’s murmurMost common innocent murmur of childhoodUsually age 2 years to adolescenceLoudest apex to LSB. Musical or vibratory, high pitched, I‐III early systolicdiminishes with sitting/standing/Valsalvadiminishes with sitting/standing/Valsalva
Venous HumVery common after age 3 yearsProduced by turbulence in subclavian and jugular veinsContinuous, musical, I‐II at upper R, LS, & lower neckDisappears if supine or jugular vein compression
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Cardiology Acyanotic lesions
Atrial Septal Defect (ASD)Ventricular Septal Defect (VSD)
Most common form of congenital heart diseaseOccurs in about 2 per 1000 live birthsOccurs in about 2 per 1000 live birthsLoud, holosystolic murmur along LSB
Atrioventricular Septal Defect (AVSD)Patent Ductus Arteriosus (PDA)Coarctation of the Aorta
BP in upper extremity 20mmHg or greater than lower extremity
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Atrial Septal DefectCommunication between right and left atriachildren asymptomaticS2 widely split and fixedT i l iTx: surgical repair
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Ventricular Septal DefectMost common congenital heart diseaseCommunication between left and right ventriclesSmall VSD ‐ asymptomaticL VSD t t 6 k i ti h t f ilLarge VSD ‐ present at 4‐6 weeks in congestive heart failureloud, harsh, holosystolic murmur along the lower left sternal borderTx: control CHF, surgery if unresponsive to meds
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Patent Ductus ArteriosusPresence in fetal life allows blood from the pulmonary artery to flow to the aorta, bypassing the nonaerated fetal lungsusually closes spontaneously by 3‐5 days of lifeRF: prematurity, female, maternal rubellaS M iSx: Most are asymptomaticMachinery murmur that is continuous and maximal at 2nd intercostal space, bounding peripheral pulses, wide pulse pressureTx: Medical management ie Indomethacin in preemies, cardiac cath in full term infants, may require surgical correction
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Coarctation of the AortaNarrowing of the aortic lumenMore common in malesSx: CHF, HTNDx: 1 pulses greater in upper extremitiesDx: 1. pulses greater in upper extremities
2. BP of upper extremity is > than lower extremity by 20 mm Hg
3. blowing systolic murmur in left axillaX‐ray: notching of the ribs in older kidsTx: Surgical correction
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Cyanotic Lesions
Tetralogy of FallotVSDPulmonary stenosisOverriding AortaRVH
Tricuspid AtresiaTransposition of the Great VesselsTotal Anomalouus Pulmonary Venous ReturnTruncus Arteriosus
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Tetralogy of FallotMost common type of cyanotic heart lesion4 components: VSD, pulmonary stenosis, overriding aorta, right ventricular hypertrophysudden cyanosis dyspnea on exertion hypoxemic spells sudden cyanosis, dyspnea on exertion ‐ hypoxemic spells aka “tet spells”rough, systolic ejection murmur 3rd intercostal spaceX‐ray: Boot shaped heartTx: Medical then surgical by 18 months
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Courtesy of Wikipedia Rutgers PANCE/PANRE Review Course
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Tetralogy of FallotMost common type of cyanotic heart lesion4 components: VSD, pulmonary stenosis, overriding aorta, right ventricular hypertrophysudden cyanosis dyspnea on exertion hypoxemic spells sudden cyanosis, dyspnea on exertion ‐ hypoxemic spells aka “tet spells”rough, systolic ejection murmur 3rd intercostal spaceX‐ray: Boot shaped heartTx: Medical then surgical by 18 months
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A 2 year old is brought to the ED by his mother w/ sudden onset of choking, gagging, coughing and wheezing. Vital signs are: Temp: 37C(98.6F) Pulse: 120/min, Resp: 28/min The physical exam reveals decreased breath sounds over the right lower lobe w/ inspiratory rhonchi and localized exp wheezing. CXR reveals nlinspiratory views, but exp views show localized hyperinflation, with mediastinal shift to the left. Which of the following is the most likely diagnosis?
A h
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1. Asthma2. Epiglottitis3. Foreign body
aspiration4. Pulmonary embolism5. Viral pneumnia As
thma
Epiglottitis
Foreign body aspiration
Pulmonary em
bolism
Viral pneumnia
0% 0% 0%2%
A 6 month old comes to your office during the winter looking mildly ill with a fever of 100.7 and a RR of 72. He has wheezing throughout his chest and scattered rales and rhonchi. Your working dx is:
1. Heart failure2 Bronchiolitis
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2. Bronchiolitis3. Croup4. Epiglottitis5. Pneumonia
Heart failure
Bronchiolitis
Croup
Epiglottitis
Pneumonia
0%7%
0%0%
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An 18 month old documented as less than tenth percentile on your growth chart is having trouble breathing. He has a history of intermittent dyspnea and a chronic cough since birth. Post delivery, the patient did not defecate for quite some time. Which of the following diagnostic tests will be most useful in this child’s evaluation?
1. Rectal biopsy2. Chest X‐ray
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3. Urine glucose assessment
4. Urine protein assessment
5. Sweat test Rectal biopsy
Chest X‐ray
Urine glucose assessm
ent
Urine protein assessm
ent
Sweat test
0% 0% 0%0%
Which of the following congenital heart defects is associated with cyanosis?
1. Patent ductus arteriosus
2. Atrial septal defect3 Ventricular septal
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3. Ventricular septal defect
4. Coarctation of the aorta
5. Tetralogy of Fallot
Patent ductus arteriosus
Atrial septal defect
Ventricular septal defect
Coarctation of the aorta
Tetralogy of Fallot
0% 0% 0%2%
Gastrointestinal/Nutrition Pyloric StenosisIntussusceptionPKUGI foreign bodies
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PYLORIC STENOSIS
Hypertrophy of muscular layers of pylorus leading to obstruction, B i b t k R t bi th Begins between ages 2‐4 weeks. Rare at birth or over the age of 6 monthsMuch more common in malesClassic presentation “Projectile, non‐bilious vomiting and palpable pyloric mass or “olive”.Well, hungry childDx: Physical exam, ultrasound. Tx: Surgery
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INTUSSUSCEPTIONInvagination of part of the bowel into an adjacent part of the bowelMost cases idiopathic; males>femalesMost common from 6 12 months of ageMost common from 6‐12 months of ageSx: Paroxysmal abdominal pain is main symptom, followed by vomiting and diarrhea“Currant‐jelly” stool in 50% of casesExam: Sausage‐shaped massTx: Reduction (Barium enema) and/or open surgery
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PKUCause: Dec activity of phenylalanine hydroxylase (enzyme that converts phenylalanine to tyrosine)S&S: severe mental retardation, hyperactivity, seizures, light complexion, urine w/mouse‐like odorD I d h l l i D d iDx: Increased phenylalanine, Decreased tyrosineTx: Limit dietary phenylalanine
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GI FOREIGN BODIESCoins, toys, and batteries are most commonUpper esophagus ‐ remove to lower risk of aspiration (Foley catheters often used)Lower esophagus remove if > 24 hoursLower esophagus ‐ remove if > 24 hoursStomach ‐ < 3‐5 cm usually pass GI tractIf object is sharp or caustic (open safety pin, camera batteries) ‐ endoscopy.If toxic (medication tablets) ‐ lavage
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A 12 year old accidentally swallowed a broken tab from an aluminum soft drink more than 6 hours ago. She can swallow liquids but solids cause discomfort. On X‐ray, a flat metallic object is located at the level of the aortic arch. Which of the following is the most appropriate course of action:
1. Admission for surgical extraction
2. Removal of tab by endoscopy
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endoscopy3. Extract with Fogarty
catheter4. Gastrogafin swallow to
r/o esophageal injury5. Observation of the
patient’s stool for passage of tab
Admission for surgical ex...
Removal of tab by endo...
Extract with Fogarty cat...
Gastrogafin swallow to r..
Observation of the patie...
2%11%
0%4%
Which of the following findings is most suggestive of a diagnosis of pyloric stenosis in an infant?
1. Epigastric mass2. Failure to thrive3 Projectile vomiting
43%
57%
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3. Projectile vomiting4. Abdominal
distention
Epigastric mass
Failure to thrive
Projectile vomiting
Abdominal distention
0%0%
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OrthopedicsClassification of fracturesCongenital Hip DysplasiaSCFEOsgood‐SchlatterNursemaid’s Elbow
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Salter‐Harris ClassificationType I ‐ Epiphyseal separation through the physisType II ‐ Fracture through a portion of the physis but exiting across the metaphysisType III Fracture through the physis but exiting across the Type III ‐ Fracture through the physis but exiting across the epiphysis into the jointType IV ‐ Fracture through metaphysis, physis, and epiphysisCrush injury to the physis
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S A
Reproduced with permission of author, Dr Frank Gaillard L T R
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CONGENITAL HIP DYSPLASIA(Developmental Dislocation of the Hip)
Increased risk in first‐born females, breech birth, or family history of DDHDx: Screening exam essential at each visitOrtolani (Out) test ‐ Abduct/external rotation Palpable click as dislocation reducedBarlow test: Adduct/Internal rotation Palpable click as hip dislocatesPhysical Exam: Assymetric thigh foldsUltrasound under 3 months. X‐rays if olderTx: Harness. SurgeryComplications: (untreated) Limp, pain, degenerative disease of hip Above image courtesy of wikipediaRutgers PANCE/PANRE Review Course
SCFE: Slipped Capital Femoral Epiphysis
F l h d “ li ” i h i d i Femoral head “slips” ‐ exposing the anterior and superior aspects of the femoral neckMales (14‐16 yrs) > Females (11‐13 yrs)Associated with obesity, increased height, genital underdevelopment, pituitary tumorsSx: Acute or chronic hip or knee painX‐ray pearl: Ice cream falling off the coneTx: Surgery
Above image courtesy of www.expertconsult.com Rutgers PANCE/PANRE Review Course
OSGOOD‐SCHLATTER SYNDROMEFibrocartilage microfracture of the patellar ligamentMost common in adolescent malesActivity related pain lasts 12‐24 hrsTenderness, thickening at tibial tubercletubercleX‐rays: Prominent, irregular. Fx?Tx: Rest, ice, compression, NSAIDS
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NURSEMAID’S ELBOWSubluxation of the Radial Head
Occurs after forearm or wrist is jerked with longitudinal/pronational forces (“airplane”)C t ti Child h ld i Common presentation: Child holds arm in pronated and flexed position and resists extension
Dx: History, exam. Radiographs are normalTx: Reduction by supinating/extending arm. Splint if recurrent. Prevention
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SkinMeaslesMumpsRubellaVaricellaRoseolaRoseolaErythema infectiosumHand‐foot‐mouth diseaseKawasaki syndromeReview Immunization schedule
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Measles: Rubeola
Morbillivirus in the Paramyxovirus familyRare at any ageIncubation: 8‐12 days for sx, 14 days for rashProdrome: fever (101+), cough, coryza, conjunctivitis Koplik spots Rash: Neck & Abdomen first ‐maculopapularTx: Primarily supportive
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Courtesy of Centers for Disease Control and Prevention
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“Mumps: “Parotitis”ParamyxovirusIncubation 12‐25 daysLate winter & springPain & swelling in front of and below earOften testicular pain within 1 weekComplete recovery with supportive care in 1‐2 weeks is the rule
Image above courtesy of Centers for Disease Control and Prevention
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Rubella: “German measles
Rubella virus is a togavirus; RubivirusRare at any ageCongenital rubella is deadly, especially in the first trimester, TRIAD: deafness, cataracts, cardiac defectsDescription: Blueberry muffin babyA i d E th t h i f h d Acquired: Erythematous rash progressing from head to toesPREVENTION!
Courtesy of wikepedia
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Varicella: “Chicken Pox”
Varicella‐zoster virus Usually 5 to 9 yrs oldLate winter/early springIncubation: 10‐21 daysVesicular, erythematous rash on torso, then face and extremitiesDescription: “Dew drops on a rose petal”Tx is supportive
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Courtesy of Centers for Disease Control and Prevention
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Rutgers PANCE/PANRE Review CourseCourtesy of Centers for Disease Control and Prevention
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Roseola: “Roseola infantum”HHV‐6Ages 3 months ‐ 4 yearsIncubation 5‐15 daysMaculopapular rashHigh fever (102‐105) for 3‐5 daysFever starts resolving, THEN rash appearsTx is supportive
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Erythema infectiosum:“Fifth Disease” or“Slapped Cheek Syndrome
ParvovirusSchool aged childrenIncubation 4‐14 daysRed facial rash and lacy, pink macular rash on torso & extremitiesPregnant woman at risk: hydrops fetalisTx is supportive
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Courtesy of WikepediaRutgers PANCE/PANRE Review Course
4/29/2015
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Hand‐Foot‐and‐Mouth DiseaseCoxsackie A16 virus (most common)Under 5 yearsIncubation 3 ‐ 7 daysLate summer & fallPainful oral ulcers, low grade fever, gray‐red vesicles on hands and feetTx is supportive
DDx: Herpangina/Gingivostomatitis
Rutgers PANCE/PANRE Review Course
Courtesy of Dr. William Sears, www.askdrsears.com Rutgers PANCE/PANRE Review Course
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Courtesy of Dr. William Sears, www.askdrsears.com
Rutgers PANCE/PANRE Review Course
Courtesy of Dr. William Sears, www.askdrsears.comRutgers PANCE/PANRE Review Course
Kawasaki Syndrome/Disease“Mucocutaneous Lymph Node Syndrome
Etiology unknown ‐ infectious agent likelyUnder 5 years oldFever > 5 days AND four of the following: conjunctivitis, rash, mucosal changes, edema of hands/feet, cervical adenopathy > 1.5 cmComplications: anuerysmsTx: IVIG, Aspirin
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4/29/2015
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Recommended Childhood Immunization Schedule, United States
RotavirusHepatitis ApVaricellaPertussisMeningococcalHuman papilloma virus
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Six days ago, a 2‐year‐old boy had a temperature of 40.0°C (104.0°F). No specific cause was found. His fever has persisted and he now has injected conjunctivae, strawberry tongue, dry fissured lips, erythema and desquamation of his hands and feet, and bilateral cervical adenopathy. Which of the following is the most likely complication of this condition?
1. Chorea2. Congestive heart
91%
gfailure
3. Coronary artery aneurysm
4. Mesenteric arteritis5. Valvular heart disease
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Chorea
Congestive hea...
Coronary arter...
Mesenteric art...
Valvular heart...
5%0%
5%0%
An 18‐month‐old boy is brought to the emergency department because he has had fever and cough for the past three days. While in the waiting room, he has a generalized tonic‐clonic seizure that lasts five minutes. He has no history of a seizure disorder. Physical examination shows a postictal child with a bright red tympanic membrane and green discharge from the nose. Temperature is 40.6°C (105.0°F). Which of the following is the most appropriate initial diagnostic study?
1. CT scan
59%
2. Electroencephalography3. Lumbar puncture4. MRI scan5. Myelography
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CT scan
Electroencepha...
Lumbar punctur...
MRI scan
Myelography
30%
9%
0%2%
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A previously healthy 15‐month‐old boy becomes anxious and begins crying and drooling copiously. A few minutes earlier he had been calmly playing with his toys. Temperature is 36.7°C (98.1°F), pulse rate is 84/min, and respirations are 18/min. On physical examination, the posterior pharynx is mildly injected but otherwise clear. The lungs are clear to auscultation and percussion. Findings on chest x‐ray study are normal. Within an hour he is calmer, but he continues to drool heavily. Which of the following is the most appropriate next step?
1. Administration of syrup of ipecac
68%
ipecac2. Barium swallow x‐ray study3. Chest physical therapy4. Esophagogastroduodenoscopy5. Insertion of a nasogastric tube
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Administration
of syrup ..
Barium
swallow x‐ray study
Chest physical therapy
Esophagogastroduoden...
Insertion of a nasogastri...
5%
20%
8%0%
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