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Antenatal Calcium Channel Blocker Exposure and Subsequent Patent Ductus Arteriosus in Extremely Low-Birth-Weight Infants

机译:极低出生体重婴儿的产前钙通道阻滞剂暴露及随后的动脉导管未闭

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摘要

This study aimed to assess whether tocolytic fetal exposure to antenatal calcium channel blockers (aCCB) increases the risk for hemodynamically significant patent ductus arterioses (hsPDA) in extremely low-birth-weight (ELBW) infants. This case-control study investigated ELBW infants (1,000 g) without cardiac defects in a level 3 neonatal intensive care unit who had survived at least 7 days. Nifedipine was the only aCCB used for this study population. The measurements included the history of aCCB exposure, selected maternal data, hsPDA diagnosis, gestational age at birth, birth weight, mode of delivery, sex, maternal race, location of birth, Apgar scores, and selected neonatal morbidities. The end point of the study was hsPDA, defined as an echocardiographically confirmed PDA with clinical symptoms. A total of 180 infants met the study criteria. The diagnosis was hsPDA for 56% of these patients, 20% of whom had aCCB exposure. Of the infants without hsPDA, 11% had aCCB exposure (p = 0.09). No statistically significant associations were found between aCCB exposure and hsPDA after adjustment for gestational age (odds ratio [OR], 1.5; 95% confidence interval [CI], 0.6–3.7) or for gestational age and cumulative aCCB exposure of 100 mg or more (OR, 2.0; 95% CI, 0.6–6.5). A history of aCCB exposure does not appear to increase hsPDA risk in ELBW infants. Studies using neonatal serum nifedipine concentrations after antenatal exposure should be performed to confirm this conclusion.
机译:这项研究的目的是评估超低出生体重儿(ELBW)的胎儿溶解性胎儿暴露于产前钙通道阻滞剂(aCCB)是否会增加血液动力学上显着的动脉导管未闭动脉(hsPDA)的风险。这项病例对照研究调查了在3级新生儿重症监护病房中存活至少7天的无心脏缺陷的ELBW婴儿(<1,000 g)。硝苯地平是该研究人群唯一使用的aCCB。这些测量包括aCCB暴露史,选定的母体数据,hsPDA诊断,出生时的胎龄,出生体重,分娩方式,性别,母体种族,出生地点,Apgar评分和选定的新生儿发病率。研究的终点是hsPDA,定义为具有临床症状的超声心动图确认的PDA。共有180名婴儿符合研究标准。其中56%的患者诊断为hsPDA,其中20%的aCCB暴露。在没有hsPDA的婴儿中,有11%的人暴露于aCCB(p = 0.09)。调整胎龄(优势比[OR],1.5; 95%置信区间[CI],0.6-3.7)或胎龄和累积的aCCB暴露量为100 mg或更高后,aCCB暴露量与hsPDA之间无统计学意义的关联(OR,2.0; 95%CI,0.6-6.5)。暴露于aCCB的病史似乎并未增加ELBW婴儿的hsPDA风险。产前暴露后应使用新生儿血清硝苯地平浓度进行研究以证实这一结论。

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