Arnold Meghan A, Chang David C, Nabaweesi Rosemary, Colombani Paul M, Bathurst Melinda A, Mon Kyaw S, Hosmane Soneil, Abdullah Fizan
Division of Pediatric Surgery, Center for Pediatric Surgery Outcomes Research & Clinical Trials, Johns Hopkins University School of Medicine, Baltimore, MD 21287-0005, USA.
J Pediatr Surg. 2007 Sep;42(9):1520-5. doi: 10.1016/j.jpedsurg.2007.04.032.
Gastroschisis is a congenital full-thickness abdominal wall defect characterized by the protrusion of intraabdominal organs outside the abdominal domain that requires surgical management in the early neonatal period. The goal of this study was to validate a previous risk stratification classification of infants born with this defect.
A retrospective analysis of a nonoverlapping combination of the databases National Inpatient Sample and Kids' Inpatient Database (1988-2003) was performed. These combined databases contain information from nearly 93 million discharges in the United States. Infants with gastroschisis were identified by an International Classification of Diseases, Ninth Revision procedure code of 54.71 (repair of gastroschisis) and an age at admission of less than 8 days. Infants were divided into simple and complex categories based on the absence or presence of intestinal atresia, stenosis, perforation, necrosis, or volvulus. Variables of sex, race, geographic region, coexisting diagnoses, hospital type and charges adjusted to 2005 dollars, length of stay, inpatient mortality, and complications were collected. Comparison between the 2 groups was performed using Pearson chi2 for categorical outcomes and the Kruskal-Wallis test for non-normally distributed continuous variables.
A total of 4344 infants with gastroschisis were identified and divided into simple and complex categories. Simple gastroschisis represented 89.1% (n = 3870) of the group, whereas 10.9% (n = 474) had complex disease. Simple and complex patients differed in coexisting cardiac disease (8.3% vs 11.8%, P = .01), hospital type (78.7% vs 84.1% treated at urban teaching centers, P < .01), median length of stay (28 vs 67 days, P < .01), median inflation-adjusted hospital charges ($90,788 vs $197,871; P < .01), and inpatient mortality (2.9% vs 8.7%, P < .01). Gastrointestinal (14.4% vs 83.5%, P < .01), respiratory (2.6% vs 4.6%, P = .01), and infectious disease complications (24.3% vs 45.4%, P < .01) also differed between the groups.
These data use the largest data set to date to validate the risk stratification of infants with gastroschisis. This analysis improves the characterization and understanding of clinical subsets of infants in whom this congenital condition is diagnosed.
腹裂是一种先天性全层腹壁缺损,其特征是腹腔内器官突出到腹腔外,需要在新生儿早期进行手术治疗。本研究的目的是验证先前对患有这种缺损的婴儿的风险分层分类。
对国家住院样本数据库和儿童住院数据库(1988 - 2003年)的非重叠组合进行回顾性分析。这些合并后的数据库包含了美国近9300万份出院记录的信息。通过国际疾病分类第九版手术编码54.71(腹裂修补术)和入院年龄小于8天来确定腹裂婴儿。根据是否存在肠道闭锁、狭窄、穿孔、坏死或肠扭转,将婴儿分为简单型和复杂型。收集性别、种族、地理区域、并存诊断、医院类型和调整为2005年美元的费用、住院时间、住院死亡率和并发症等变量。使用Pearson卡方检验对分类结果进行两组间比较,对非正态分布的连续变量使用Kruskal - Wallis检验。
共识别出4344例腹裂婴儿,并分为简单型和复杂型。简单型腹裂占该组的89.1%(n = 3870),而10.9%(n = 474)患有复杂疾病。简单型和复杂型患者在并存心脏病(8.3%对11.8%,P = 0.01)、医院类型(78.7%对84.1%在城市教学中心治疗,P < 0.01)、中位住院时间(28天对67天,P < 0.01)、中位经通胀调整后的医院费用(90,788美元对197,871美元;P < 0.01)和住院死亡率(2.9%对8.7%,P < 0.01)方面存在差异。两组在胃肠道(14.4%对83.5%)、呼吸道(2.6%对4.6%,P = 0.01)和传染病并发症(24.3%对45.4%,P < 0.01)方面也存在差异。
这些数据使用了迄今为止最大的数据集来验证腹裂婴儿的风险分层。该分析改进了对诊断出这种先天性疾病的婴儿临床亚组的特征描述和理解。