Develop a pediatric case on Atrial septal defect on a 20 months old chlid with the chief complaints of cough since 3days, fever since 1day , shortness of breath for 6 hours accordingly provided case sheet format

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PEDIATRIC CLINICAL CASE SHEET

Standard OSCE / Clinical Case Format


PATIENT IDENTIFICATION

FieldDetails
NameBaby Arjun Kumar (fictitious)
Age20 months
SexMale
Weight8.5 kg (below 3rd centile for age)
Height78 cm (below 5th centile for age)
Date of Admission14-July-2026
Ward / UnitPediatric Medical Ward, Bed 4
InformantMother (reliable)
MRD No.XXXX

CHIEF COMPLAINTS

S. No.ComplaintDuration
1.Cough3 days
2.Fever1 day
3.Shortness of breath6 hours

HISTORY OF PRESENT ILLNESS

Baby Arjun, a 20-month-old male child, was apparently well until 3 days ago when he developed a cough - initially dry, progressing to productive with whitish sputum. The cough is continuous, non-paroxysmal, and aggravated on lying down. There is no history of barking character or whooping. Fever started 1 day ago, low grade initially (recorded at home as 99.5-100.4°F), becoming high grade (101.8°F) at presentation. The fever is continuous, not associated with chills or rigors. Shortness of breath started 6 hours before admission, progressively worsening, associated with fast breathing and visible use of neck muscles during breathing. The child was unable to feed well since the onset of dyspnea.
The child has a documented history of a cardiac murmur noted incidentally at 4 months of age during a routine well-child visit. Echocardiography done at 6 months confirmed a secundum atrial septal defect (ASD) of 8 mm with significant left-to-right shunt. The child was under cardiology follow-up but no intervention had been performed.
The mother reports 4 similar episodes of lower respiratory tract infections (LRTIs) in the past 10 months, each requiring hospitalization, consistent with recurrent pulmonary infections in a child with a large left-to-right shunt. The child tires easily during feeding (takes >30 minutes per feed), frequently stops to breathe, and sweats profusely during feeds.

HISTORY OF PAST ILLNESS

  • 4 previous hospitalizations for pneumonia / bronchiolitis (at 10, 13, 16, and 18 months of age)
  • No surgeries or cardiac interventions to date
  • No known drug allergies
  • No history of rheumatic fever or tuberculosis

BIRTH HISTORY

ParameterDetail
Type of deliveryFull-term normal vaginal delivery
Birth weight2.8 kg
Birth cryImmediate
NICU admissionNo
Antenatal historyNo maternal illness, no teratogenic drug exposure; rubella serology not done
Perinatal complicationsNone

DEVELOPMENTAL HISTORY

MilestoneAge of AttainmentExpected AgeStatus
Social smile2 months2 monthsNormal
Head holding4 months3-4 monthsSlightly delayed
Sitting with support8 months6 monthsDelayed
Sitting without support10 months8 monthsDelayed
Standing with support14 months9 monthsDelayed
Walking independently18 months12-13 monthsDelayed
Meaningful words (2-3)15 months12 monthsMildly delayed
Pincer grasp12 months9-10 monthsMildly delayed
Impression: Global developmental delay, predominantly motor - likely related to chronic cardiopulmonary compromise and poor weight gain.

DIETARY HISTORY

  • Breastfed exclusively for 5 months; supplementary feeds started at 5 months
  • Currently on semi-solid diet + cow's milk
  • Poor appetite, tires during feeds, takes small frequent feeds
  • No diet diversification; micronutrient supplementation not consistent

IMMUNIZATION HISTORY

VaccineStatus
BCGGiven at birth
OPV 0, 1, 2, 3Complete
Pentavalent 1, 2, 3Complete
IPVGiven
RotavirusGiven
PCV2 doses given (3rd pending)
Measles/MRGiven at 9 months
Booster doses (DPT/OPV)Not yet due
Immunization status: Complete for age as per National Immunization Schedule (India).

FAMILY HISTORY

  • Father: 28 years, healthy
  • Mother: 25 years, healthy, one prior normal pregnancy
  • No family history of congenital heart disease or other hereditary conditions
  • No consanguinity

SOCIOECONOMIC HISTORY

  • Lower-middle socioeconomic class (Kuppuswamy scale)
  • Nuclear family, lives in a 2-room house
  • Father is a daily wage laborer
  • Immunization from government health center
  • No tobacco or biomass smoke exposure in the household

SYSTEMIC REVIEW

  • Respiratory: Recurrent LRTIs (as above); no history of wheeze in between episodes
  • CVS: Known ASD; no cyanosis at rest; no syncope; no palpitations; feeding difficulties as described
  • GI: Anorexia; no vomiting, diarrhea, or abdominal distension; no jaundice
  • CNS: No seizures; developmental delay as above
  • Renal: Normal urine output; no puffiness of face
  • Musculoskeletal: No joint swelling or pain

GENERAL PHYSICAL EXAMINATION

ParameterFinding
General appearanceIrritable, not in severe respiratory distress at rest; sitting propped up
AnthropometryWeight 8.5 kg (< 3rd centile); Height 78 cm (< 5th centile) - Grade II Protein Energy Malnutrition (IAP classification)
Temperature101.8°F (38.8°C)
Heart Rate148 beats/min, regular
Respiratory Rate58 breaths/min (tachypnea)
SpO291% on room air (improved to 96% on 2 L/min O2 via nasal prongs)
Blood Pressure88/54 mmHg (upper limb, right)
Capillary Refill Time3 seconds
PallorMild pallor present
IcterusAbsent
CyanosisNo cyanosis at rest; no peripheral or central cyanosis; no clubbing
LymphadenopathyNo significant cervical lymphadenopathy
EdemaAbsent
SkinNo rashes; mild subcutaneous fat loss

SYSTEMIC EXAMINATION

A. Respiratory System

FindingDetail
InspectionTachypnea (RR 58/min); subcostal and intercostal retractions present; nasal flaring; no chest deformity
Chest shapeSlight precordial bulge on left (consistent with cardiomegaly)
PalpationTrachea central; tactile fremitus increased on right infra-axillary and right infrascapular region
PercussionDull note in right lower zone posteriorly
AuscultationDecreased breath sounds with coarse crepitations in right lower lobe; fine crepitations bilateral; no wheeze
Impression: Right lower lobe consolidation (pneumonia) superimposed on a background of pulmonary plethora from left-to-right shunt.

B. Cardiovascular System

FindingDetail
InspectionPrecordial bulge present; visible cardiac impulse at left 4th intercostal space
PalpationApex beat at left 5th intercostal space, lateral to midclavicular line - displaced (left ventricular enlargement); left parasternal heave present (RV volume overload); no thrill
PercussionCardiac dullness slightly enlarged to left
Auscultation
- S1Normal
- S2Wide and fixed splitting of S2 - hallmark of ASD; P2 slightly accentuated
- MurmurGrade 2/6 ejection systolic murmur heard best at left upper sternal border (pulmonary area) - due to increased flow across pulmonary valve (relative pulmonary stenosis from large left-to-right shunt)
- AdditionalMid-diastolic murmur at tricuspid area (Carey Coombs equivalent - increased tricuspid flow in large ASD)
Femoral pulsesNormal volume bilaterally
JVPNot assessable in infant; anterior fontanelle: flat
Cardiovascular impression: Features consistent with large secundum ASD with significant left-to-right shunt and right ventricular volume overload.

C. Abdomen

FindingDetail
InspectionSlightly distended
PalpationLiver palpable 3 cm below right costal margin, firm, non-tender - hepatomegaly (early right heart failure / increased venous return)
SpleenNot palpable
KidneysNot palpable
PercussionShifting dullness absent
AuscultationBowel sounds present

D. Central Nervous System

  • Conscious, irritable
  • Anterior fontanelle flat and normotensive
  • Tone: normal for age
  • Reflexes: normal
  • No meningeal signs

INVESTIGATIONS

Bedside / Immediate

InvestigationResultInterpretation
SpO2 (room air)91%Low - hypoxia due to pneumonia
Blood glucose (rapid)80 mg/dLNormal
CRT3 secondsBorderline prolonged

Haematology

TestResultNormal (20 months)Interpretation
Hb9.2 g/dL11.0-14.0 g/dLMild anemia
TLC17,400 cells/mm³6,000-17,000Mild leukocytosis
Neutrophils74%25-70%Neutrophilia
Lymphocytes22%--
Platelets3.4 lakhs/mm³1.5-4.0 lakhsNormal
ESR38 mm/hr< 20Elevated
CRP28 mg/L< 6 mg/LElevated (acute infection)

Biochemistry

TestResultInterpretation
Serum Na134 mEq/LMild hyponatremia
Serum K3.8 mEq/LNormal
Serum Ca8.6 mg/dLNormal
Blood urea28 mg/dLNormal
Serum creatinine0.4 mg/dLNormal
Serum albumin2.9 g/dLLow (malnutrition)
LFTMildly elevated ALT 38 U/LHepatic congestion
Blood cultureSent; pending-

Radiology

Chest X-Ray (PA view):
  • Cardiomegaly: Cardiothoracic ratio = 0.58 (> 0.55 abnormal in infants)
  • Plethoric lung fields (increased pulmonary vascular markings bilaterally)
  • Right lower lobe consolidation (homogenous opacity with air bronchograms)
  • Prominent pulmonary artery segment
  • No pleural effusion

ECG

FeatureFinding
Rate148/min
RhythmSinus tachycardia
AxisRight axis deviation (+110°)
P waveNormal
QRSrSR' pattern (incomplete RBBB) in V1 - classic for ASD
ST-T changesNone
ECG impression: Sinus tachycardia with right axis deviation and incomplete right bundle branch block - consistent with ASD-related right ventricular volume overload.

Echocardiography (previous report at 6 months; repeat ordered)

FindingDetail
ASD typeSecundum
Defect size8 mm (significant)
Shunt directionLeft-to-right
Qp:Qs ratio2.4:1 (at 6 months)
RVDilated
PA pressureMildly elevated (35 mmHg estimated)
LVNormal function, EF 62%
Mitral valveNormal
No other defects-
Current echo ordered to reassess shunt, RV function, and PA pressure in context of clinical deterioration.

DIAGNOSIS

Working Diagnosis (Primary)

Community-Acquired Pneumonia (right lower lobe) with respiratory failure in a known case of Secundum Atrial Septal Defect (large, 8 mm) with significant left-to-right shunt

Background Diagnoses

  1. Secundum ASD - large, unrepaired
  2. Right ventricular volume overload with mild pulmonary arterial hypertension
  3. Recurrent lower respiratory tract infections (4th episode in 10 months) - related to pulmonary plethora from large shunt
  4. Grade II Protein Energy Malnutrition - related to high metabolic demand and feeding difficulties
  5. Global developmental delay - secondary to chronic cardiopulmonary compromise

Differential Diagnosis

ConditionForAgainst
VSD with LRTISystolic murmur, recurrent LRTI, cardiomegalyMurmur at LUSB, fixed split S2, rSR' pattern - all favor ASD over VSD
PDA with LRTIPulmonary plethora, recurrent LRTINo continuous murmur, no bounding pulses
Simple community-acquired pneumoniaFever, cough, consolidationBackground cardiac disease, recurrent pattern, cardiomegaly
Heart failure (primary)Hepatomegaly, tachycardia, failure to thriveTriggered by current infection, underlying structural defect

MANAGEMENT PLAN

Immediate Stabilization (A-B-C-D-E)

  1. Airway: Clear, patent - maintain positioning (semi-recumbent)
  2. Breathing: O2 supplementation 2 L/min via nasal prongs; target SpO2 > 95%; monitor for worsening respiratory failure (may need escalation to high-flow oxygen or CPAP)
  3. Circulation: IV access established; fluid restrict at 80% maintenance (due to cardiac compromise)
  4. IV fluids: DNS + KCl @75 mL/hr (80% maintenance for 8.5 kg child); monitor for fluid overload
  5. IV antibiotics:
    • Injection Ampicillin-Sulbactam 200 mg/kg/day IV q6h (first-line CAP with cardiac background)
    • Injection Azithromycin 10 mg/kg OD IV (atypical coverage)
    • Review culture sensitivity at 48-72 hours
  6. Antipyretics: Syrup Paracetamol 15 mg/kg/dose q6h PRN (oral/nasogastric)
  7. Diuretics: Injection Furosemide 1 mg/kg IV stat, then 0.5 mg/kg q12h (to reduce pulmonary congestion; monitor serum electrolytes)
  8. Positioning: Head-end elevated 30°; prone positioning avoided acutely
  9. NBM / NG feeds: NPO during acute distress; start NG feeds once RR < 50/min

Cardiac-Specific Management

  1. Digoxin: Syrup Digoxin 0.01 mg/kg/day (5 mcg/kg/day) OD - for rate control and mild inotropic support (if signs of CHF persist after diuresis); check serum levels
  2. Repeat Echocardiography: Reassess shunt fraction, RV function, PA pressures after acute illness
  3. Pediatric Cardiology referral: For definitive management planning - timing of ASD closure
  4. ASD closure indications in this child:
    • Recurrent LRTIs (4 episodes in 10 months)
    • Failure to thrive / PEM Grade II
    • Large defect (8 mm) with Qp:Qs > 2:1
    • Elective device closure (Amplatzer Septal Occluder) or surgical closure advised after resolution of acute illness - typically recommended before school age, but brought forward here due to recurrent complications

Supportive Management

InterventionDetail
Nutritional rehabilitationHigh-calorie feeds (100-150 kcal/kg/day) via NG tube during acute phase; dietitian consultation
Vitamin and micronutrientsIron supplementation (3 mg/kg/day elemental iron) for anemia; Zinc 10 mg OD x 14 days (pneumonia)
PhysiotherapyChest physiotherapy after acute fever settles (postural drainage, percussion)
Nebulization3% hypertonic saline / salbutamol 0.15 mg/kg q4h if significant wheeze or atelectasis
Developmental assessmentFormal neurodevelopmental assessment after discharge; early intervention program

Monitoring

ParameterFrequency
SpO2, HR, RRContinuous monitoring
Temperature4-hourly
WeightDaily (assess fluid status)
Urine outputHourly (catheter if needed)
Serum electrolytes12-hourly while on diuretics
Blood culture sensitivityAt 48 hours
ABGIf SpO2 < 90% despite O2 therapy
Chest X-RayRepeat at 48-72 hours
EchoAfter recovery from acute illness

Criteria for ICU Transfer

  • SpO2 < 88% despite high-flow O2
  • RR > 70/min with worsening retractions
  • Altered sensorium / apnea
  • Shock (CRT > 4 sec, BP falling)
  • Need for mechanical ventilation

PROGNOSIS

AspectComment
Immediate (acute pneumonia)Favorable with appropriate antibiotic and supportive therapy
Medium-term (cardiac)Good if ASD closure performed soon; risk of progressive pulmonary hypertension, Eisenmenger syndrome if left unrepaired beyond childhood
Long-term (post-closure)Near-normal life expectancy; pulmonary hypertension partially reversible at this stage
Nutritional / developmentalSignificant improvement expected post-cardiac repair with adequate nutritional support

COUNSELLING POINTS (For Parents)

  1. The child has a hole between the upper chambers of the heart (ASD) that is causing extra blood flow to the lungs - this weakens the lungs and causes repeated chest infections.
  2. The current infection is being treated with IV antibiotics and oxygen.
  3. The hole in the heart needs to be closed by a minimally invasive procedure (catheter-based device closure) once this infection is treated - this will prevent future pneumonias and improve the child's growth.
  4. Regular follow-up with the pediatric cardiologist is essential.
  5. Ensure all vaccines are up to date, including Influenza and PCV booster.
  6. Nutritional counselling: high-calorie small frequent feeds; follow up with a dietitian.
  7. Signs of worsening to watch for at home: fast breathing, bluish discoloration of lips, poor feeding, excessive sweating - report immediately.

SIGNATURE / DESIGNATION

Attending Pediatrician: Dr. _______________________
Resident / Intern: Dr. _______________________
Date: 14-July-2026 | Time: 19:47 hrs

References: Harrison's Principles of Internal Medicine 22E (2025) - ASD pathophysiology and clinical features; Sabiston Textbook of Surgery - ASD surgical management; The Harriet Lane Handbook 23rd ed. - Pediatric cardiac murmur classification and management; Nelson Textbook of Pediatrics - standard pediatric assessment framework.
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