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用于预测呼吸窘迫综合征发生的稳定微泡试验。

Stable microbubble test for predicting the occurrence of respiratory distress syndrome.

作者信息

Wu T J, Teng R J, Yau K I

机构信息

Department of Pediatrics, Provincial Taoyuan Hospital, Taipei Taiwan, R.O.C.

出版信息

Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1995 Mar-Apr;36(2):101-3.

PMID:7793273
Abstract

To predict the development of respiratory distress syndrome (RDS) in premature neonates who might benefit from early administration of surfactant, the clinical applicability of stable microbubble (SM) test was prospectively evaluated. Fifty-nine preterm neonates with the gestational ages of less than 37 weeks were studied. SM test was performed on gastric aspirates obtained within 30 minutes after birth. The number of microbubbles was correlated with later development of RDS. With a cut-off value of less than 10 microbubbles/mm2, the SM test showed a positive predictive value of 76.0% (19/25) and a negative predictive value of 97.1% (33/34), while sensitivity and specificity were 95.0% (19/20) and 84.6% (33/39), respectively. The overall accuracy was 88.1% (52/59). It was concluded that use of the SM test on gastric aspirates immediately after birth is a rapid, simple and reliable procedure for identifying those neonates with surfactant deficiency who may benefit from prophylactic surfactant therapy.

摘要

为预测可能从早期给予表面活性剂中获益的早产儿呼吸窘迫综合征(RDS)的发生情况,前瞻性评估了稳定微泡(SM)试验的临床适用性。研究了59例孕周小于37周的早产儿。在出生后30分钟内获取的胃吸出物上进行SM试验。微泡数量与RDS的后续发生情况相关。以小于10个微泡/平方毫米为临界值时,SM试验的阳性预测值为76.0%(19/25),阴性预测值为97.1%(33/34),而敏感性和特异性分别为95.0%(19/20)和84.6%(33/39)。总体准确率为88.1%(52/59)。得出结论,出生后立即对胃吸出物进行SM试验是一种快速、简单且可靠的方法,可用于识别那些可能从预防性表面活性剂治疗中获益的表面活性剂缺乏新生儿。

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