Safavi Arash, Skarsgard Erik, Butterworth Sonia
BC Children's Hospital, Vancouver, BC, Canada.
Pediatr Surg Int. 2012 May;28(5):495-500. doi: 10.1007/s00383-012-3055-0. Epub 2012 Feb 14.
BACKGROUND/PURPOSE: Validated outcome prediction for gastroschisis (GS) permits early risk stratification. The aim of our study was to determine whether the need for GS defect extension: (a) correlates with bowel injury severity at birth, and (b) predicts outcome.
A national dataset was used to study GS babies born between 2005 and 2010. The primary outcome was days of parenteral nutrition (PN). Outcomes were analyzed according to the need for fascial extension to facilitate closure or silo placement as follows: Group 1, no extension; Group 2A, extension <2 cm; Group 2B, extension >2 cm. Univariate and where appropriate, multivariate analyses were used.
Of 507 cases, 402 had complete defect extension data: Group 1, 297 (73%); Group 2A, 67 (17%); Group 2B, 42 (10%). Group 2B patients had higher rates of atresia, perforation and severe matting (P = 0.001) and required more days on PN compared to Group 1 (63.0 ± 100.4 vs. 39.7 ± 44.5 days: CI 1.2-45.1; P = 0.03). Multivariate analysis revealed that the presence of atresia (P = 0.01) and surgical site (P = 0.001) or bloodstream (P = 0.001) infections were predictive of prolonged PN; however, the need for fascial extension was not.
GS newborns who require fascial extension are more likely to have complicated GS and are at greater risk for adverse outcome, although it is not an independent predictor of the latter.
背景/目的:对腹裂(GS)进行有效的预后预测有助于早期风险分层。本研究的目的是确定GS缺损延长的必要性:(a)是否与出生时肠损伤的严重程度相关,以及(b)是否能预测预后。
使用一个全国性数据集来研究2005年至2010年期间出生的GS婴儿。主要结局指标是肠外营养(PN)的天数。根据是否需要筋膜延长以利于关闭或放置肠袋,将结局分析如下:第1组,无需延长;第2A组,延长<2 cm;第2B组,延长>2 cm。采用单因素分析,并在适当情况下进行多因素分析。
在507例病例中,402例有完整的缺损延长数据:第1组,297例(73%);第2A组,67例(17%);第2B组,42例(10%)。与第1组相比,第2B组患者闭锁、穿孔和严重粘连的发生率更高(P = 0.001),且需要的PN天数更多(63.0±100.4天对39.7±44.5天:CI 1.2 - 45.1;P = 0.03)。多因素分析显示,闭锁的存在(P = 0.01)、手术部位(P = 0.001)或血流(P = 0.001)感染可预测PN时间延长;然而,筋膜延长的必要性并非如此。
需要筋膜延长的GS新生儿更有可能患有复杂的GS,且不良结局风险更高,尽管它并非后者的独立预测因素。