Pravisani Riccardo, Baccarani Umberto, Toso Francesco, Adani Gian Luigi, Lorenzin Dario, Cherchi Vittorio, Calandra Sergio, Scarpa Edoardo, Crestale Sara, Avellini Claudio, Terrosu Giovanni, Sponza Massimo, Risaliti Andrea
Liver-Kidney Transplant Unit - Department of Medicine, University of Udine, Udine, Italy.
Liver-Kidney Transplant Unit - Department of Medicine, University of Udine, Udine, Italy.
Transplant Proc. 2019 Nov;51(9):2974-2976. doi: 10.1016/j.transproceed.2019.02.068. Epub 2019 Oct 10.
Gastrointestinal perforation (GIP) is a rare complication after adult liver transplant (LT) associated with high morbidity and mortality. Limited data are available about clinical risk factors and underlying pathogenic mechanisms.
The retrospective study included all GIP cases from a consecutive cohort of 361 LT recipients during the period 2005-2017. Clinical variables were investigated as potential risk factors for GIP, and radiologic and histopathologic evaluations were undertaken to identify any causative mechanism.
A total of 22 patients developed at least 1 episode of GIP (prevalence 6.1%) at a median time of 18.5 [interquartile range, 12.5-28.5] days after LT. The perforations occurred in the small bowel (63.6%), transverse colon (27.3%), right colon (22.7%), left colon (9.1%), and stomach (9.1%). A total of 27.3% of patients developed multiple sites of GIP, and in 31% GIP recurred after curative surgery. The 30-day mortality rate after relaparotomy was 40%. A history of previous abdominal surgery (odds ratio, 2.5) and early post-LT relaparotomy due to other complications (odds ratio, 2.6) were significant risk factors for GIP. No thromboembolic or steno-occlusive complications of any splanchnic vessel were detected at computed tomography scan, while histopathology examination on perforated gastrointestinal segments excluded cytomegalovirus infection, graft-vs-host disease, and inflammatory bowel disease. In all the cases, ischemic necrosis with aspecific microangiopathy and microembolization were the pathologic features detected.
GIP is a severe complication after LT with frequent multiple gastrointestinal involvement and recurrence after curative surgery. The pathologic underlying mechanism is usually microvascular ischemia. Clinical risk factors are history of previous abdominal surgery and early post-LT relaparotomy.
胃肠道穿孔(GIP)是成人肝移植(LT)后一种罕见的并发症,其发病率和死亡率均较高。关于临床风险因素和潜在致病机制的数据有限。
这项回顾性研究纳入了2005年至2017年期间连续361例LT受者队列中的所有GIP病例。对临床变量进行调查,以确定其作为GIP潜在风险因素的可能性,并进行影像学和组织病理学评估,以确定任何致病机制。
共有22例患者在LT术后中位时间18.5天[四分位间距,12.5 - 28.5天]出现至少1次GIP发作(患病率6.1%)。穿孔发生在小肠(63.6%)、横结肠(27.3%)、右结肠(22.7%)、左结肠(9.1%)和胃(9.1%)。共有27.3%的患者出现多处GIP,31%的患者在根治性手术后GIP复发。再次剖腹手术后30天死亡率为40%。既往腹部手术史(比值比,2.5)和LT术后因其他并发症早期再次剖腹手术(比值比,2.6)是GIP发病的显著风险因素。计算机断层扫描未检测到任何内脏血管的血栓栓塞或狭窄闭塞性并发症,而对穿孔胃肠道节段的组织病理学检查排除了巨细胞病毒感染、移植物抗宿主病和炎症性肠病。在所有病例中,缺血性坏死伴非特异性微血管病和微栓塞是检测到的病理特征。
GIP是LT术后一种严重并发症,常累及多处胃肠道,根治性手术后易复发。其病理潜在机制通常是微血管缺血。临床风险因素为既往腹部手术史和LT术后早期再次剖腹手术。