Idiopathic thrombocytopenic purpura in pregnancy

被引:30
作者
Sainio, S
Joutsi, L
Jarvenpaa, AL
Kekomaki, R
Koistinen, E
Riikonen, S
Teramo, K
机构
[1] Univ Helsinki, Cent Hosp, Dept Obstet & Gynecol, FIN-00290 Helsinki, Finland
[2] Finnish Red Cross & Blood Transfus Serv, SF-00310 Helsinki, Finland
[3] Helsinki City Matern Hosp, Joensuu, Finland
[4] N Carelian Cent Hosp, Joensuu, Finland
关键词
idiopathic thrombocytopenic purpura (ITP); platelet autoantibodies; platelet immunofluorescence test (PIFT); pregnancy; thrombocytopenia;
D O I
10.1034/j.1600-0412.1998.770303.x
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective. The aim of this study was to evaluate retrospectively our strategies in monitoring and treating pregnant women with idiopathic thrombocytopenic purpura (ITP). Methods. Medical records were reviewed for diagnosis, clinical course, treatment, and neonatal outcome in 35 Finnish women with ITP giving birth to 55 neonates during 53 pregnancies. The outcome of the first (i.e. index) pregnancy was used in the statistical analyses. The platelet immunofluorescence test (PIFT) was used for detection of platelet autoantibodies. The correlation between neonatal platelet counts and results of PIFT was calculated with the Pearson's correlation coefficient and the Fisher's exact test. Results. There were no serious bleeding complications although five of 35 women had platelet counts of less than 50x10(9)/l in the third trimester of the index pregnancy. Prophylactic platelet transfusions were given to six of lj women delivered by cesarean section. Five of 35 (14.3%; 95% confidence interval, 2.6 to 25.8%) neonates had platelet counts of less than 50x10(9)/l median 3 days after delivery versus only one of 28 (3.6%; 95% confidence interval, 0.1 to 10.5%) at birth. No infant showed any clinical signs of intracranial hemorrhage. No significant correlation was encountered between neonatal thrombocytopenia and maternal platelet autoantibodies. The history of a previous infant with thrombocytopenia was the only important information in estimating the risk of fetal thrombocytopenia. Conclusions. To avoid unnecessary and possibly harmful monitoring and treatment, we need further tests for predicting the perinatal risks in pregnant women with ITP.
引用
收藏
页码:272 / 277
页数:6
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