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外科新生儿的新生儿多系统器官衰竭的特征

Characterization of neonatal multisystem organ failure in the surgical newborn.

作者信息

Smith S D, Tagge E P, Hannakan C, Rowe M I

机构信息

University of Pittsburgh School of Medicine, PA.

出版信息

J Pediatr Surg. 1991 Apr;26(4):494-7; discussion 497-9. doi: 10.1016/0022-3468(91)91002-g.

Abstract

With advances in critical care, multisystem organ failure (MSOF) has replaced single organ failure as the major cause of death in adult patients. The purpose of this report is to characterize neonatal MSOF (NMSOF) in the surgical newborn. The records of 84 infants who died during a 5-year period in the surgical neonatal intensive care unit were reviewed. There was sufficient information available in 10 newborns to characterize the NMSOF syndrome. Criteria for renal, hepatic, microvascular, pulmonary, cardiac, and hematologic failure were developed. The sequence of organ failure was determined by calculating the number of days prior to death when these criteria were first noted. Systemic infections were recorded. The sequence of organ failure was as follows: microvascular (edema) 17 +/- 10 days, renal 14 +/- 7 days, hepatic 13 +/- 5 days, hematologic 8 +/- 4 days, pulmonary 5 +/- 2 days, and cardiac 3 +/- 2 days. Adult respiratory distress syndrome (ARDS) was absent. The 10 infants showed both culture-positive sepsis (8) and culture-negative sepsis (2). This is the first report to characterize NMSOF in newborn surgical patients. The earliest findings were edema, followed by renal and hepatic failure. In contrast to adult MSOF, anasarca is a prominent early finding, pulmonary failure develops late, and classic ARDS is absent.

摘要

随着重症监护技术的进步,多系统器官衰竭(MSOF)已取代单器官衰竭,成为成年患者死亡的主要原因。本报告旨在描述外科新生儿中的新生儿多系统器官衰竭(NMSOF)。回顾了外科新生儿重症监护病房5年内死亡的84例婴儿的记录。10例新生儿有足够的信息来描述NMSOF综合征。制定了肾、肝、微血管、肺、心脏和血液系统衰竭的标准。通过计算首次发现这些标准时至死亡前的天数来确定器官衰竭的顺序。记录全身感染情况。器官衰竭的顺序如下:微血管(水肿)17±10天,肾14±7天,肝13±5天,血液系统8±4天,肺5±2天,心脏3±2天。无成人呼吸窘迫综合征(ARDS)。这10例婴儿中8例血培养阳性败血症,2例血培养阴性败血症。这是第一份描述外科新生儿患者NMSOF的报告。最早的表现是水肿,随后是肾和肝功能衰竭。与成人MSOF不同,全身性水肿是一个突出的早期表现,肺衰竭出现较晚,且无典型的ARDS。

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