Department of Paediatric Surgery, Emma Children's Hospital, Amsterdam University Medical Centre, University of Amsterdam and Vrije Universiteit Amsterdam, Meibergdreef 9, 1005 AZ, Amsterdam, The Netherlands.
Tytgat Institute for Liver and Intestinal Research, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
Sci Rep. 2020 Dec 3;10(1):21170. doi: 10.1038/s41598-020-77976-1.
Incisional hernia (IH) in children could result in life-threatening complications, including incarceration and bowel strangulation. The incidence and risk factors of IH in infants are scarcely reported. Since IH-correction may require extensive surgery and a long recovery program, identifying infants and birth defects at risk, may lead to a different approach during the primary surgery. Therefore, the aim of this review is to systematically review the available data on the incidence of IH following surgery for congenital anomalies in infants. All studies describing IH were considered eligible. PubMed and Embase were searched and risk of bias was assessed. Primary outcome was the incidence of IH, secondary outcomes were difference in IH occurrence between disease severity (complex vs simple) and closure method (SILO vs primary closure) in gastroschisis patients. A meta-analysis was performed to pool the reported incidences in total and per congenital anomaly separately. Subgroup analysis within gastroschisis articles was performed. The 50 included studies represent 3140 patients. The pooled proportion of IH was 0.03 (95% CI 0.02-0.05; I = 79%, p ≤ 0.01) all anomalies combined. Gastroschisis (GS) reported highest pooled proportion 0.10 (95% CI 0.06-0.17; n = 142/1273; I = 86%; p ≤ 0.01). SILO closure (OR 3.09) and simple gastroschisis, i.e. without additional anomalies, (OR 0.18) were of significant influence. This review reports the incidence of IH in infants with different congenital abdominal anomalies, of which gastroschisis reported the highest risk. In GS patients, complex GS and SILO closure are risk factors for IH development.
切口疝(IH)可导致儿童出现危及生命的并发症,包括嵌顿和肠绞窄。婴儿 IH 的发生率和危险因素很少有报道。由于 IH 矫正可能需要广泛的手术和长期的康复计划,因此识别有风险的婴儿和出生缺陷可能会导致在初次手术中采取不同的方法。因此,本综述的目的是系统地回顾婴儿先天性畸形手术后 IH 的发生率。所有描述 IH 的研究都被认为是合格的。检索了 PubMed 和 Embase,并评估了偏倚风险。主要结局是 IH 的发生率,次要结局是复杂性与简单性(复杂性与简单性)和复杂性与简单性(SILO 与直接缝合)之间 IH 发生率的差异在先天性腹壁畸形患者中的差异。对报告的发病率进行了荟萃分析,总发病率和每种先天性异常的发病率分别进行了荟萃分析。对先天性腹壁畸形文章进行了亚组分析。纳入的 50 项研究代表了 3140 名患者。IH 的汇总发生率为 0.03(95%CI 0.02-0.05;I=79%,p≤0.01),所有异常均合并。先天性腹壁裂(GS)报道的 IH 发生率最高,为 0.10(95%CI 0.06-0.17;n=142/1273;I=86%;p≤0.01)。SILO 闭合(OR 3.09)和简单性先天性腹壁裂,即无其他异常(OR 0.18)有显著影响。本综述报告了不同先天性腹部畸形婴儿 IH 的发生率,其中先天性腹壁裂报告的风险最高。在 GS 患者中,复杂性 GS 和 SILO 闭合是 IH 发展的危险因素。