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布洛芬治疗动脉导管未闭相关的胃肠道并发症。

Gastrointestinal complications associated with ibuprofen therapy for patent ductus arteriosus.

机构信息

Division of Newborn Medicine, Washington University in St Louis, St Louis, MO 63110, USA.

出版信息

J Perinatol. 2011 Jul;31(7):465-70. doi: 10.1038/jp.2010.199. Epub 2011 Jan 20.

Abstract

OBJECTIVE

To review intestinal complications associated with ibuprofen treatment of patent ductus arteriosus (PDA).

STUDY DESIGN

Data from preterm infants treated with ibuprofen were retrospectively reviewed. χ(2) test and Fischer's exact test were used for univariate analyses. Multivariate analyses with logistic regression modeling were used to identify risk factors.

RESULT

One hundred and two infants were treated with ibuprofen for PDA. Nine (9/102, 8.8%) infants developed spontaneous intestinal perforation (SIP), whereas 93/102 (91.2%) did not. The mean (± s.d.) gestational age (GA) at birth in infants with and without SIP was 25.2 (± 1.3) vs 27.6 (± 2.4) weeks (P=0.02) and the median (interquartile) length of stay (LOS) was 109.5 (91.0 to 116.5) vs 75.0 (53.0 to 94.5) days (P=0.002), respectively. The mean (± s.d.) age at starting ibuprofen was 3.3 (± 1.3) vs 5.8 (± 3.5) days in infants with and without SIP, respectively (P=0.03). In logistic regression analyses, increasing GA and later initiation of ibuprofen treatment were protective against risk of SIP; odds ratio, 95% confidence interval (OR, 95% CI)=0.26 (0.09 to 0.75), P=0.01 and 0.63 (0.41 to 0.95), P=0.03, respectively.

CONCLUSION

Infants at lower GA are at risk of SIP when treated early with ibuprofen for symptomatic PDA.

摘要

目的

回顾布洛芬治疗动脉导管未闭(PDA)相关的肠道并发症。

研究设计

回顾性分析接受布洛芬治疗的早产儿数据。采用卡方检验和 Fisher 确切概率法进行单因素分析。采用 logistic 回归模型进行多因素分析,以确定危险因素。

结果

102 例婴儿接受布洛芬治疗 PDA。9 例(9/102,8.8%)婴儿发生自发性肠穿孔(SIP),93 例(91.2%)未发生。SIP 组和非 SIP 组婴儿的出生时平均(±标准差)胎龄(GA)分别为 25.2(±1.3)周和 27.6(±2.4)周(P=0.02),中位(四分位间距)住院时间(LOS)分别为 109.5(91.0 至 116.5)天和 75.0(53.0 至 94.5)天(P=0.002)。SIP 组和非 SIP 组婴儿开始使用布洛芬的平均(±标准差)年龄分别为 3.3(±1.3)天和 5.8(±3.5)天(P=0.03)。在 logistic 回归分析中,GA 增加和延迟开始使用布洛芬治疗可降低 SIP 风险;比值比(OR),95%置信区间(95%CI)=0.26(0.09 至 0.75),P=0.01 和 0.63(0.41 至 0.95),P=0.03。

结论

对于症状性 PDA ,GA 较低的婴儿在早期接受布洛芬治疗时,SIP 风险较高。

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