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NON IMMUINE HYDROPS
FETALIS UNIT IV
DR VARSHA DESHMUKH
KAY
HISTORY
โ€ข 25 Yrs. Old
โ€ข 7 Months Amenorrhoea
โ€ข Swelling of Feet 1 month
โ€ข Headache 3 days
OBST. HISTORY
โ€ข G5 P4 L1 A0
โ€ข First 3 Preterm deliveries all died.
โ€ข 4th
FTND 3 year old female live KAY
GENERAL EXAMINATION
โ€ข GC Moderate, afebrile, pulse 96 /min.,
BP โ€“ 150/110 mm.Hg.
โ€ข Pallor +, Edema +
โ€ข CVS, RS wnl
โ€ข Per abdomen
โ€ข Ut over distended, tense, fetal parts
not felt, FHS CNL
โ€ข Per Vaginum Cx 1 Fl, 60 % Effaced,
Membranes + breech at โ€“ 2 St.
โ€ข Pelvis adequate
โ€ข Provisional Diagnosis G5 P4 L1 A0,
Sev. PIH, ? Twins ? Hydramnios
โ€ข Ultrasonography KAY
Ultrasonography
KAY1. Placental Oedema 2. Scalp Oedema
Ultrasonography
KAY1. Ascitic Fluid 2. Liver 3. Peri. Effusion
LABOUR NOTES
โ€ข Preterm Vaginal Delivery
on 11/7/2003 (within 7 hrs.of active
labour)
โ€ข Female child 2200 gm., MSB,
e/o Hydrops Fetalis +
โ€ข Hyperplacentosis +, WT 1500 gm
KAY
KAY
KAY
INVESTIGATIONS
โ€ข Bld gr Orh+ve
โ€ข Hemogram Normal
โ€ข LFTs, KFTs Wnl
โ€ข BSL Normal
โ€ข Urine Exam. Normal
โ€ข Findings of neonatal autopsy :
โ€ข Macerated baby, distension of abd, edema all over body,
peeling of skin.
โ€ข Pericardial effusion, fluid in peritoneal cavity 200 cc.
โ€ข Congested liver, lungs, spleen, kidneys
โ€ข diagnosis โ€“ non immunize hydrops fetalis
KAY
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. โ€œLate manifestation of many
severe diseasesโ€. KAY
ETIOLOGY
โ€ข Cardiovascular anomalies -
tachyarrhythmia, Anatomic defects
โ€ข Chromosomal - Down syndrome, Turner
Syndrome.
โ€ข Malformation syndrome
โ€ข Twin pregnancy- Twin transfusion
syndrome
โ€ข Hematologic - Arteriovenous shunt
โ€ข Genitourinary - Congenital nephrosis
KAY
ETIOLOGY
โ€ข Respiratory - Pulmonary hypoplasia
โ€ข Gastrointestinal
โ€ข Liver
โ€ข Maternal - Severe diabetes mellitus,
severe anemia, Hypoproteinemia
โ€ข Placenta-umbilical cord - Chorionic vein
thrombosis
โ€ข Medications - Antepartum indomethacin
โ€ข Infectious - Parvovirus B 19, TORCH
โ€ข Miscellaneous KAY
DIAGNOSIS
โ€ข Ultrasound evaluation.
โ€ข Skin thickness more than 5 mm.
โ€ข Placental thickness more than 4 cm
โ€ข Ascitis, pericardial effusion, pleural
effusion.
โ€ข Polyhydramnios. KAY
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
โ€ข If detected at <20 wks option for
termination of pregnancy given.
โ€ข Establish underlying cause
โ€ข Determine appropriate therapy & optimal
timing of therapy.
Prognosis :Overall mortality ranges 50% - 90% .
CONCLUSION
โ€ข USG has a pivotal role in diagnosis.
โ€ข Generalised lymphoedema has a poor
prognosis
โ€ข Cardiovascular anomalies is the most
identifiable cause. Arrhythmias are
amenable to therapy.
โ€ข Knowledge of etiology and fetal karyotype
will determine whether aggressive
management is warranted.
โ€ข Parentโ€™s of affected child, need counselling
regarding accurate diagnosis and prognosis.
Non immuine hydrops fetalis

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Non immuine hydrops fetalis

  • 1. NON IMMUINE HYDROPS FETALIS UNIT IV DR VARSHA DESHMUKH KAY
  • 2. HISTORY โ€ข 25 Yrs. Old โ€ข 7 Months Amenorrhoea โ€ข Swelling of Feet 1 month โ€ข Headache 3 days OBST. HISTORY โ€ข G5 P4 L1 A0 โ€ข First 3 Preterm deliveries all died. โ€ข 4th FTND 3 year old female live KAY
  • 3. GENERAL EXAMINATION โ€ข GC Moderate, afebrile, pulse 96 /min., BP โ€“ 150/110 mm.Hg. โ€ข Pallor +, Edema + โ€ข CVS, RS wnl โ€ข Per abdomen โ€ข Ut over distended, tense, fetal parts not felt, FHS CNL โ€ข Per Vaginum Cx 1 Fl, 60 % Effaced, Membranes + breech at โ€“ 2 St. โ€ข Pelvis adequate โ€ข Provisional Diagnosis G5 P4 L1 A0, Sev. PIH, ? Twins ? Hydramnios โ€ข Ultrasonography KAY
  • 5. Ultrasonography KAY1. Ascitic Fluid 2. Liver 3. Peri. Effusion
  • 6. LABOUR NOTES โ€ข Preterm Vaginal Delivery on 11/7/2003 (within 7 hrs.of active labour) โ€ข Female child 2200 gm., MSB, e/o Hydrops Fetalis + โ€ข Hyperplacentosis +, WT 1500 gm KAY
  • 7. KAY
  • 8. KAY
  • 9. INVESTIGATIONS โ€ข Bld gr Orh+ve โ€ข Hemogram Normal โ€ข LFTs, KFTs Wnl โ€ข BSL Normal โ€ข Urine Exam. Normal โ€ข Findings of neonatal autopsy : โ€ข Macerated baby, distension of abd, edema all over body, peeling of skin. โ€ข Pericardial effusion, fluid in peritoneal cavity 200 cc. โ€ข Congested liver, lungs, spleen, kidneys โ€ข 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. โ€œLate manifestation of many severe diseasesโ€. KAY
  • 11. ETIOLOGY โ€ข Cardiovascular anomalies - tachyarrhythmia, Anatomic defects โ€ข Chromosomal - Down syndrome, Turner Syndrome. โ€ข Malformation syndrome โ€ข Twin pregnancy- Twin transfusion syndrome โ€ข Hematologic - Arteriovenous shunt โ€ข Genitourinary - Congenital nephrosis KAY
  • 12. ETIOLOGY โ€ข Respiratory - Pulmonary hypoplasia โ€ข Gastrointestinal โ€ข Liver โ€ข Maternal - Severe diabetes mellitus, severe anemia, Hypoproteinemia โ€ข Placenta-umbilical cord - Chorionic vein thrombosis โ€ข Medications - Antepartum indomethacin โ€ข Infectious - Parvovirus B 19, TORCH โ€ข Miscellaneous KAY
  • 13. DIAGNOSIS โ€ข Ultrasound evaluation. โ€ข Skin thickness more than 5 mm. โ€ข Placental thickness more than 4 cm โ€ข Ascitis, pericardial effusion, pleural effusion. โ€ข 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 โ€ข If detected at <20 wks option for termination of pregnancy given. โ€ข Establish underlying cause โ€ข Determine appropriate therapy & optimal timing of therapy. Prognosis :Overall mortality ranges 50% - 90% .
  • 15. CONCLUSION โ€ข USG has a pivotal role in diagnosis. โ€ข Generalised lymphoedema has a poor prognosis โ€ข Cardiovascular anomalies is the most identifiable cause. Arrhythmias are amenable to therapy. โ€ข Knowledge of etiology and fetal karyotype will determine whether aggressive management is warranted. โ€ข Parentโ€™s of affected child, need counselling regarding accurate diagnosis and prognosis.