Слайд 2Immunologic disorder that occurs in pregnant Rh negative lady carrying
Rh positive fetus
Слайд 3Pathophysiology
The rhesus system which comprises number of antigens C, D,
E, c, e.
A person who lacks D antigen is called
Rh negative.
15% of Caucasians, 5% African Americans and 2 % of Asians are Rh negative.
Rh isoimmunisation is due to D antigen in more than 90% of cases.
Occasionally hemolytic disease of the newborn is a result of maternal immunization to Irregular RBC antigens other than Rh group like anti- Kell and anti- Duffy
Слайд 4Pathophysiology
Initial response is forming IgM antibodies for short period followed
by production of IgG which crosses placenta
IgG antibodies adhere to
the antigen site on the surface of erythrocytes causing hemolysis.
The excessive removal of circulatory RBCs leads to severe anemia and hypoxia.
Erythropoiesis results in hepatosplenomegaly.
Tissue hypoxia and hypoproteinemia results in cardiac and circulatory failure, with generalized odema and hydrops
Слайд 5Pathophysiology
Maternal immune system becomes sensitized when there is fetal blood
leak into the maternal circulation.
Although leaks are common only 8%
are sensitized within 6 months after first del of ABO compatible preg.
16% are sensitized after second full term pregnancy of Rh positive ABO compatible pregnancy.
The risk of sensitization after ABO incompatible pregnancy is only 2%
Risk after spontaneous miscarriage is 3.5%
Risk after induce abortion is 5.5%
Risk after ectopic pregnancy is about 1%
Слайд 6Natural History
50% of affected infants have no or mild
anemia, requiring either phototherapy or no treatment.
25% have some degree
of hepatosplenomegaly and moderate anemia and progressive jundice culminating in kernicterus, neonatal death or severe handicap.
25% are hydropic and usually die in utero or in the neonatal period ( half of these the hydrops develops before 34 weeks gestation ).
Слайд 7The aim of antenatal management
To predict which pregnancy is at
risk
To predict whether or not the fetus is severely affected.
To
correct anemia and reverse hydrops by intrauterine transfusion.
To deliver the baby at the appropriate time, weighing the risks of prematurity against these of intrauterine transfusion.
Слайд 8Recognition of pregnancy at risk
First ante-natal visit check blood group,
antibody screening.
If indirect coombs test is positive, the father’s Rh
should be tested.
Serial maternal Anti D titers should be done every 2- 4 weeks.
If titer is less than 1/16 the fetus is not at risk.
If titer is more than 1/16 then severity of condition should be evaluated.
Слайд 9Prediction of the severity of fetal hemolysis
History of previous
affected pregnancies
The levels of maternal hemolytic antibodies
Amniocentesis
Biophysical surveillance
Fetal
blood sampling
Слайд 10Amniocentesis
There is an excellent correlation between the amount of bilirubin
in amniotic fluid and fetal hematocrit.
The optical density deviation
at 450 nm measures the amniotic fluid unconjugated bilirubin.
Слайд 12Ultrasound detection of Rh Sensitization
Serial U/S examination for fetal well
being.
Placental size and thickness and hepatic size.
Fetal hydrops is easy
to diagnose when finding one or more of the following: Ascites, pleural effusion, pericardial effusion, or skin edema.
Doppler assessment of peak velocity of fetal middle cerebral artery proved to valuable in predicting fetal anemia
Слайд 13Biophysical surveillance
Middle cerebral artery peak velocity
Слайд 14Biophysical surveillance
Middle Cerebral Artery peak systolic velocity
C
Median
80
70
60
50
40
30
20
20 25 30
35
A 1.5 MOM
B 1.29 MOM
Gestational Age (wks)
MCA peak velocity cm/sec
from Mari et al, NEJM 2000; 342:9-14
A = moderate-severe anaemia
B = mild anaemia
C = no anaemia
Слайд 15Fetal Blood Sampling FBS
Percutaneous Umbilical Blood Sampling BUBS
Allows measurement
of fetal Hb, Hct, pH, reticulocytes and nucleated RBCs.
Risk fetal
exanguination and fetal death 1%.
Слайд 17Confirmation of fetal blood
Visualizing the needle tip within the cord
vessel
Turbulance when injecting a small amount of saline into the
vessel.
Fetal blood has a higher mean corpuscular volume ( MCV usually 100 fL
An alkali elusion method can be used
Acid elution Betke-Kleihauer test
Слайд 20Intrauterine Transfusion
Radiologically guided intraperitoneal transfusion by Liley in 1963.
Adoption
of ultrasound guided IPT resulted in dramatic improvement in survival
rates.
Fetoscopic intravascular route was renewed by Rodeck in 1981.
Percutaneous transfusion into the intrahepatic umbilical vein, Bang 1982.
Cordocentesis, Daffos 1983.
The use of cordocentesis for fetal top up transfusion by Berkowitz.
Слайд 21Intravascular transfusion IVT has superseded intraperitoneal transfusion in most centres.
It has superior results, regarding survival rates, quality of survivors,
prolongation of gestation and the higher rate of vaginal delivery.
Access to the fetal circulation is extremely essential to avoid the lethal mistake of transfusing the Rh negative fetus or the nonanemic Rh positive fetus.
Decisions regarding transfusion and delivery are made on the basis of fetal blood group, Hb estimation and other hematologic parameters
. IVT results are better in the compromised hydropic fetus.
Слайд 23Donor Blood
Washed, filtered or irradiated with 2500 rad
Gamma ray packed red blood cells with Hct 75%
Group O negative heterologous blood
Maternal blood
Слайд 24 Transfusion volume (ml)
=(Gestation in weeks - 20) X 10
Слайд 25Timing of transfusions
Subsequent transfusions are timed on
the basis of the fetal Hct achieved at the end
of the previous transfusion and the rate of fall in fetal Hct. The latter has been reported to be on average equal to 1% of Hct/day
Слайд 26Complications of cordocentesis and intravascular transfuaion
Hemorrhage.
Hematomas..
Bradycardias.
Fetomaternal hemorrhage.
Infection.
Abruptio placetae.
Preterm labor.
Слайд 27Timing of Delivery
Weighing the risk of fetal loss including that
related to intrauterine transfusion against the risk of prematurity.
Слайд 28Prevention
The widespread use of anti D prophylaxis in the late
1960s has led to a great reduction in isoimmunisation.
Following
delivery and caesarean section
Routine anti D administration at 28 weeks.
Following spontaneous and induced abortion.
Vaginal bleeding and threatened miscarriage.
Performing amniocentesis, CVS,
Abdomenal trauma and external cephalic version.
Слайд 29Prevention
The usual dose is 300 µg within 72 hours following
delivery.
This covers 30 ml of fetal blood leak into maternal
circulation.
If greater transplacental hemorrhage is suspected the dose should be tailored after Kleihauer- Betke test to determine the volume of hemorrhage.
Слайд 30Kleihauer- Betke test
The adult hemoglobin is more readily acid eluted
through the cell membrane than fetal hemoglobin.
Maternal blood is
fixed on a slide with ethanol 80%, treated with citrate phosphate buffer.
After staining with hematoxylin and eosin the fetal cells will be stained while the adult cells appear like ghost cells.
No. of fetal cells/ No. of adult cells is equal to
fetal blood volume/ maternal blood volume.