Js. Morris et al., HEMATOLOGICAL RISK-FACTORS FOR PREGNANCY OUTCOME IN JAMAICAN WOMEN WITH HOMOZYGOUS SICKLE-CELL DISEASE, British journal of obstetrics and gynaecology, 101(9), 1994, pp. 770-773
Objective To examine the association between fetal outcome and the ste
ady state haematology of mothers with homozygous sickle cell disease.
Design A retrospective observational study. The data were taken from d
ockets kept at the Sickle Cell Clinic and verified by interview with 4
5 % of the patients. Setting The Sickle Cell Clinic at the University
Hospital of the West Indies or two peripheral clinics operated by the
staff of the MRC Laboratories. Subjects All women aged 14 years or old
er with homozygous sickle cell disease who had experienced at least on
e pregnancy in the period 1977 to 1986. Main outcome measures Three fe
tal outcomes including miscarriages, perinatal deaths, and birthweight
. Results There were 270 singleton pregnancies in 175 women with an ov
erall fetal wastage of 32.2 %. There was a significant increased risk
of perinatal death with low maternal fetal haemoglobin level, but ther
e were no haematological associations with miscarriages or birthweight
. Conclusions These data suggest that maternal steady-state haematolog
y has little influence on fetal outcome, with the exception that mothe
rs with high HbF levels are less prone to perinatal deaths. Further st
udy is required to investigate acute haematological changes associated
with pregnancy.