目的探讨与分析妊娠合并全血细胞减少孕妇不良围产结局的危险因素。
方法收集2014年9月—2005年1月北京大学人民医院收治的106例妊娠合并全血细胞减少孕妇的临床资料,回顾性分析其妊娠结局及围产儿不良结局的危险因素。
结果(1)病因诊断:106例孕妇中,84例为孕前发现全血细胞减少,22例为孕期发现;64例诊断为再生障碍性贫血,30例为骨髓增生异常综合征,2例为阵发性睡眠性血红蛋白尿,4例为脾功能亢进,1例为抗磷脂综合征,另外5例未明确诊断。(2)孕期治疗:106例孕妇中,69例孕妇孕期接受1次以上的输血治疗,37例未予输血治疗。(3)孕期并发症及妊娠结局:106例孕妇中,9例并发妊娠期糖尿病,22例并发重度子痫前期,2例并发贫血性心脏病,3例并发呼吸道感染。产后出血量为50~3 800 ml,中位数为400 ml,其中6例产后出血量>1 000 ml。终止妊娠孕周为24~40周,中位数为37.0周。(4)围产儿结局及多因素分析:106例孕妇中,31例出现不良围产儿结局,其中,3例胎死宫内、4例治疗性中期引产、6例孕34周前早产、2例新生儿颅内出血、2例新生儿呼吸窘迫综合征、3例缺血缺氧性脑病、2例新生儿重度窒息并死亡、14例小于胎龄儿。有不良围产儿结局的31例孕妇中,26例孕期接受输血治疗,17例并发重度子痫前期;孕期白细胞计数最高值(4.9± 1.4)×10 9/L,最低值(2.9±0.8)×10 9/L;血红蛋白(Hb)最高值(88.6±14.9)g/L,最低值(57.9±14.5)g/L;血小板计数最高值(47.7±27.4)×10 9/L,最低值(11.9±12.3)×10 9/L。围产儿无不良结局的75例孕妇中,43例孕期接受输血治疗,5例并发重度子痫前期;白细胞计数最高值(5.2±1.5)×10 9/L,最低值(3.2±0.9)×10 9/L;血红蛋白最高值(101.4±16.2)g/L,最低值(71.9±14.5)g/L;血小板计数最高值(52.3±24.0)×10 9/L,最低值(19.0±12.1)×10 9/L。多因素分析显示,孕期并发重度子痫前期( OR=20.1, P<0.01),Hb<70 g/L( OR= 4.8, P<0.01)及血小板计数<20×10 9/L( OR=6.7, P<0.05)是合并全血细胞减少孕妇发生不良围产儿结局的独立危险因素。
结论合并全血细胞减少孕妇的妊娠并发症显著增加;孕期并发重度子痫前期、Hb<70 g/L及血小板计数<20×10 9/L是围产儿不良结局的独立危险因素。
ObjectiveTo explore the pregnancy outcomes of women with pancytopenia and the risk factors for the adverse perinatal outcomes.
MethodsA total of 106 pregnant women with pancytopenia were admitted to Peking University People 's Hospital from Jan. 2005 to Sep. 2014. The clinical data and the pregnancy outcomes were reviewed retrospectively to investigate the risk factors for the adverse perinatal outcomes.
Results(1 )Eighty-four patients were found pancytopenia before pregnancy while 22 were found for the first time during pregnancy. Sixty-four patients were diagnosed as aplastic anemia; 30 as myelodysplastic syndrome; 2 as paroxysmal nocturnal hemoglobinuria; 4 as hypersplenism, and 1 as anti-phospholipid syndrome. Diagnoses of the remaining 5 patients were uncertain. (2) Sixty-nine patients received at least one time blood transfusion before delivery. (3) As for the complications, nine women developed gestational diabetes; twenty-two suffered severe preeclampsia (SPE); two were diagnosed as anemic heart disease and three experienced respiratory tract infection. The postpartum blood loss ranged from 50 ml to 3 800 ml, with the median of 400 ml. And six women had the blood loss more than 1 000 ml. The gestational age at delivery ranged from 24 weeks to 40 weeks, with the median of 37.0 weeks. (4)Thirty-one patients suffered adverse perinatal outcomes, including 3 cases of intrauterine death, 4 therapeutic labor induction before 28 gestational weeks, 6 premature delivery before 34 weeks. There were 2 neonates complicated with intracranial hemorrhage, 2 with neonatal respiratory distress syndrome, 3 with hypoxic-ischemic encephalopathy, 2 with severe asphyxia and death, and 14 with small for gestational age. Among the patients with adverse perinatal outcomes, 26 women received blood transfusion during pregnancy and 17 developed SPE. The maximum and the minimum value of their white cell count (WBC), hemoglobin concentration (Hb) and blood platelet count (BPC) were (4.9±1.4)×10 9/L, (2.9±0.8)×10 9/L, (88.6±14.9) g/L, (57.9±14.5) g/L, (47.7±27.4)×10 9/L and (11.9±12.3)×10 9/L, respectively. For those patients without adverse perinatal outcomes, 43 received blood transfusion during pregnancy and 5 developed SPE. The maximum and the minimum value of their WBC, Hb and BPC were (5.2±1.5)×10 9/L, (3.2±0.9)×10 9/L, (101.4±16.2) g/L, (71.9 ± 14.5) g/L, (52.3 ± 24.0) × 10 9/L and (19.0±12.1) × 10 9/L, respectively. The multivariate regression analyses indicated that SPE, Hb less than 70 g/L and BPC less than 20×10 9/L were the independent risk factors for the poor perinatal outcomes in pregnant women with pancytopenia ( P<0.05).
ConclusionsThe incidence of adverse perinatal complications increased dramatically in pregnant women with pancytopenia. Concurrent SPE, minimum Hb less than 70 g/L and minimum BPC less than 20 × 10 9/L may be the independent risk factors for the adverse perinatal outcomes.
王雪燕,张超,梁梅英,等. 妊娠合并全血细胞减少孕妇不良围产结局的危险因素分析[J]. 中华妇产科杂志,2015,50(12):931-936.
DOI:10.3760/cma.j.issn.0529-567X.2015.12.010版权归中华医学会所有。
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