PROPHYLACTIC TRANSFUSIONS IN PREGNANT PATIENTS WITH SICKLE HEMOGLOBINOPATHIES - BENEFIT VERSUS RISK
- 1 January 1980
- journal article
- research article
- Vol. 56 (3) , 274-280
Abstract
Pregnancy in patients with sickle cell disease was a significant threat to maternal survival and good reproductive outcome. In the past several years, statistics for maternal and perinatal outcome have improved. There is controversy, however, as to whether this improvement has resulted from the use of maternal transfusions or the aggressive and intense medical management afforded these patients in recent years. This study details the reproductive experience of 80 pregnant patients with significant hemoglobinopathies, 75 of whom were treated with partial prophylactic exchange transfusions during gestation. Each of the 75 patients who completed the protocol received 2 transfusions using buffy coat-poor washed packed red cells. The results show that there was no maternal mortality and a significant improvement in maternal morbidity compared to previous studies. There was also a significant improvement in fetal salvage, with a perinatal mortality rate of 26/1000. There were few premature and low birth weight infants as compared to other studies in the literature. Although these results were favorable, only a randomized multicentered study in the future will detail advantages and disadvantages of such therapy in the gravid sickle cell patient compared to intensive medical treatment without transfusion.This publication has 7 references indexed in Scilit:
- Transfusion Therapy in Pregnant Patients with Sickle-Cell Disease: A National Institutes of Health Consensus Development ConferenceAnnals of Internal Medicine, 1979
- Fluctuation of fetal hemoglobin in sickle-cell anemiaAmerican Journal of Obstetrics and Gynecology, 1976
- The effect of maternal partial exchange transfusion on the infants of patients with sickle cell anemiaThe Journal of Pediatrics, 1976
- USE OF PROPHYLACTIC PARTIAL EXCHANGE TRANSFUSION IN PREGNANCIES ASSOCIATED WITH SICKLE-CELL HEMOGLOBINOPATHIES1976
- Some Experiences in Managing Sickle-cell Anaemia in Children and Young Adults, Using Alkalis and MagnesiumBMJ, 1964
- Effect of Normal Cells on Viscosity of Sickle-Cell BloodArchives of internal medicine (1960), 1963
- PREGNANCY AND SICKLE CELL DISEASE1953