Beiner Mario E, Simchen Michal J, Sivan Eyal, Chetrit Angela, Kuint Jacob, Schiff Eyal
Department of Obstetrics and Gynecology, The Chaim Sheba Medical Center, Tel-Hashomer, Tel-Aviv University, Israel.
Am J Perinatol. 2003 Jan;20(1):49-54. doi: 10.1055/s-2003-37948.
The objective of this study is to identify the risk factors for neonatal thrombocytopenia among preterm infants. During a 4-year study period all consecutive, singleton preterm deliveries (between 27 and 35 weeks of gestation) were evaluated, and separate cohorts were compared-growth restricted (small-for-gestational-age; SGA) and appropriately grown (appropriate-for-gestational-age; AGA) infants. An initial comparison was done for the presence of thrombocytopenia (platelet count below 150,000/mL) and marked thrombocytopenia (below 100,000/mL). Following that, a comparison was made between the groups as determined by platelet count for various possible risk factors. Three hundred and five preterm infants were included in the study. Mean platelet count was significantly lower in the SGA group (p = 0.0009). Ninety-three neonates (31%) were thrombocytopenic and 212 infants with a normal platelet count served as controls. In the thrombocytopenic group, the rate of preeclampsia was significantly higher (p = 0.002). Thrombocytopenic infants had a significantly lower average gestational age at delivery (p = 0.002), lower birth weight (p = 0.0001), and low 5-minute Apgar score (p = 0.0002). They were more likely to suffer from intraventricular hemorrhage (IVH) ( p = 0.04) and sepsis (p = 0.002). Growth restriction, lower gestational age and low 5-minute Apgar score (<7) were found to be significantly independent risk factors for marked thrombocytopenia, when analyzed separately. Growth restriction, lower gestational age at delivery, and low 5-minutes Apgar score are significantly associated with neonatal thrombocytopenia in preterm infants, which may lead to significant morbidity. Screening these high-risk groups for thrombocytopenia might be beneficial in terms of early diagnosis and management.
本研究的目的是确定早产儿发生新生儿血小板减少症的危险因素。在为期4年的研究期间,对所有连续的单胎早产(妊娠27至35周)进行了评估,并对不同队列进行了比较——生长受限(小于胎龄儿;SGA)和生长正常(适于胎龄儿;AGA)的婴儿。首先比较了血小板减少症(血小板计数低于150,000/mL)和显著血小板减少症(低于100,000/mL)的情况。随后,根据血小板计数对各组的各种可能危险因素进行了比较。305名早产儿纳入了本研究。SGA组的平均血小板计数显著较低(p = 0.0009)。93名新生儿(31%)血小板减少,212名血小板计数正常的婴儿作为对照。在血小板减少组中,先兆子痫的发生率显著较高(p = 0.002)。血小板减少的婴儿出生时平均孕周显著较低(p = 0.002)、出生体重较低(p = 0.0001),5分钟Apgar评分较低(p = 0.0002)。他们更易发生脑室内出血(IVH)(p = 0.04)和败血症(p = 0.002)。单独分析时,生长受限、较低孕周和5分钟Apgar评分低(<7)被发现是显著血小板减少症的显著独立危险因素。生长受限、较低的出生孕周和5分钟Apgar评分低与早产儿的新生儿血小板减少症显著相关,并可能导致显著的发病率。对这些高危组进行血小板减少症筛查可能在早期诊断和管理方面有益。