Rimer B A
Am J Obstet Gynecol. 1975 Sep 1;123(1):6-11. doi: 10.1016/0002-9378(75)90933-3.
The obstetric experiences of 128 gravidas delivered at Charlotte Memorial Hospital in 1973 who, on hemoglobin electrophoresis, exhibited an SA pattern of hemoglobin are reviewed. In addition to previously reported complications of increased rates of pyelonephritis and refractory anemia, this group of patients exhibited a marked increase in premature rupture of membranes and prematurity. It is suggested that the routine screening procedures be used for discovering sickle-cell trait individuals and that they be categorized as "high-risk" obstetric patients because of the increased complication rates described here and by previous authors.
对1973年在夏洛特纪念医院分娩的128名孕妇的产科经历进行了回顾，这些孕妇经血红蛋白电泳显示为血红蛋白SA模式。除了先前报道的肾盂肾炎发病率增加和难治性贫血等并发症外，这组患者的胎膜早破和早产明显增加。建议采用常规筛查程序来发现镰状细胞性状个体，并由于此处及先前作者所述的并发症发生率增加，将他们归类为“高危”产科患者。
