From the Department of Pediatrics, Päijät-Häme Central Hospital, Lahti, Finland.
the Section of Pediatric Surgery, New Children's Hospital, Helsinki University Hospital, Helsinki, Finland.
J Pediatr Gastroenterol Nutr. 2023 May 1;76(5):553-559. doi: 10.1097/MPG.0000000000003729. Epub 2023 Feb 7.
Autologous intestinal reconstructive (AIR) surgery is frequently utilized in the management of pediatric short bowel syndrome (SBS). However, little is known about the long-term sequela of these procedures.
We undertook a retrospective follow-up study addressing parenteral nutrition (PN) dependence, nutritional status, intestinal morbidity, and related complications in SBS patients having undergone AIR surgery (SBS-AIR, n = 19). We compared results with conservatively treated control SBS patients (SBS-C, n = 45). Eligible patients were identified from our institutional intestinal failure registry during 1985-2019.
After median 11.4 follow-up years, 42% of SBS-AIR patients received PN in relation to 36% in SBS-C group ( P = 0.6210), and overall PN duration was significantly longer (35.4 vs 10 months, P = 0.0004) in SBS-AIR group. Although symptoms of intestinal dysfunction improved in majority (62%) of patients after AIR surgery, their symptoms remained more frequent and severe at latest follow-up compared to SBS-C group (39% vs 5%, P = 0.0015). Although bacterial overgrowth was more frequent in SBS-AIR group (53% vs 24%, P = 0.0416), latest endoscopy findings and fecal calprotectin levels as well as occurrence of anastomotic/staple line ulcerations were comparable between groups. Histological liver steatosis (50% vs 18%, P = 0.042) and impaired bone health (26% vs 6.7%, P = 0.042) were more frequent in SBS-AIR patients.
While AIR surgery improved gastrointestinal symptoms and transition to enteral autonomy in majority of patients, a noteworthy proportion of them continued to suffer from clinically significant intestinal dysfunction and related complications. Close long-term follow-up of pediatric AIR surgery patients is mandatory.
自体肠重建(AIR)手术常用于小儿短肠综合征(SBS)的治疗。然而,对于这些手术的长期后果知之甚少。
我们进行了一项回顾性随访研究,调查接受 AIR 手术的 SBS 患者(SBS-AIR,n=19)的肠外营养(PN)依赖、营养状况、肠道发病率和相关并发症,并与保守治疗的 SBS 患者(SBS-C,n=45)进行比较。合格的患者是从我们机构的肠衰竭登记处于 1985 年至 2019 年期间确定的。
中位随访 11.4 年后,42%的 SBS-AIR 患者与 SBS-C 组的 36%患者(P=0.6210)需要接受 PN,并且 SBS-AIR 组的总体 PN 持续时间明显更长(35.4 与 10 个月,P=0.0004)。尽管 AIR 手术后大多数(62%)患者的肠道功能障碍症状有所改善,但与 SBS-C 组相比,他们的症状在最新随访时仍更为频繁和严重(39%与 5%,P=0.0015)。尽管 SBS-AIR 组的细菌过度生长更为常见(53%与 24%,P=0.0416),但两组的最新内镜检查结果、粪便钙卫蛋白水平以及吻合口/吻合钉溃疡的发生情况相当。SBS-AIR 患者的肝脂肪变性(50%与 18%,P=0.042)和骨健康受损(26%与 6.7%,P=0.042)更为常见。
尽管 AIR 手术改善了大多数患者的胃肠道症状并使他们过渡到肠内自主,但仍有相当一部分患者继续遭受临床显著的肠道功能障碍和相关并发症。对小儿 AIR 手术患者进行密切的长期随访是强制性的。