2. HISTORY
โข 25 Yrs. Old
โข 7 Months Amenorrhoea
โข Swelling of Feet 1 month
โข Headache 3 days
OBST. HISTORY
โข G5 P4 L1 A0
โข First 3 Preterm deliveries all died.
โข 4th
FTND 3 year old female live KAY
3. GENERAL EXAMINATION
โข GC Moderate, afebrile, pulse 96 /min.,
BP โ 150/110 mm.Hg.
โข Pallor +, Edema +
โข CVS, RS wnl
โข Per abdomen
โข Ut over distended, tense, fetal parts
not felt, FHS CNL
โข Per Vaginum Cx 1 Fl, 60 % Effaced,
Membranes + breech at โ 2 St.
โข Pelvis adequate
โข Provisional Diagnosis G5 P4 L1 A0,
Sev. PIH, ? Twins ? Hydramnios
โข Ultrasonography KAY
9. INVESTIGATIONS
โข Bld gr Orh+ve
โข Hemogram Normal
โข LFTs, KFTs Wnl
โข BSL Normal
โข Urine Exam. Normal
โข Findings of neonatal autopsy :
โข Macerated baby, distension of abd, edema all over body,
peeling of skin.
โข Pericardial effusion, fluid in peritoneal cavity 200 cc.
โข Congested liver, lungs, spleen, kidneys
โข diagnosis โ non immunize hydrops fetalis
KAY
10. INTRODUCTION
Potter in 1943 described clinical entity, that
affected non-Rh sensitised pregnancies,
NIH โ
1) Fetal ansarca.
2) Placental oedema
3) Fetal serous effusions
NIH does not represent a specific
disease. โLate manifestation of many
severe diseasesโ. KAY
13. DIAGNOSIS
โข Ultrasound evaluation.
โข Skin thickness more than 5 mm.
โข Placental thickness more than 4 cm
โข Ascitis, pericardial effusion, pleural
effusion.
โข Polyhydramnios. KAY
14. MANAGEMENT
All NIH should be referred to a unit where
facilities exist for detailed anomaly scans
including - echocardiography, fetal blood
sampling and tertiary neonatal care.
Principles of Management
โข If detected at <20 wks option for
termination of pregnancy given.
โข Establish underlying cause
โข Determine appropriate therapy & optimal
timing of therapy.
Prognosis :Overall mortality ranges 50% - 90% .
15. CONCLUSION
โข USG has a pivotal role in diagnosis.
โข Generalised lymphoedema has a poor
prognosis
โข Cardiovascular anomalies is the most
identifiable cause. Arrhythmias are
amenable to therapy.
โข Knowledge of etiology and fetal karyotype
will determine whether aggressive
management is warranted.
โข Parentโs of affected child, need counselling
regarding accurate diagnosis and prognosis.