Kakkadasam Ramaswamy Pradeep
Department of Digestive Health, Gold Coast University Hospital, Gold Coast, Queensland, Australia.
Department of Nutrition and Food Services, Gold Coast University Hospital, Gold Coast, Queensland, Australia.
JPEN J Parenter Enteral Nutr. 2022 Feb;46(2):423-432. doi: 10.1002/jpen.2273. Epub 2021 Dec 17.
Exclusive enteral nutrition (EEN) is not routinely used as induction therapy for adults with active Crohn's disease (CD). The aim of this study was to assess the effectiveness of EEN with oral polymeric formula as an adjunct for inducing clinical and biochemical remission in adults with active CD.
We performed a retrospective analysis of data from January 2018 to September 2019 on all patients with active CD who commenced EEN. The primary end point (PE) was clinical remission (Crohn's Disease Activity Index [CDAI] ≤150) or response (100-point decrease in CDAI) at 8 weeks. The secondary end point (SE) was biochemical remission (C-reactive protein level ≤5 mg/L or feces calprotectin level ≤150 mcg/g) at 8 weeks in those whose baseline values were elevated. We also aimed to identify predictors of response to EEN therapy.
Sixty-six patients commenced EEN; 53 (of 66; 80.3%) completed the prescribed EEN course. At 8 weeks, 42 (of 66; 63.6%) patients achieved the PE, and 30 (of 53; 56.6%) patients achieved the SE. Patients receiving EEN for ≥6 weeks achieved the PE (72% vs 47.8%; odds ratio [OR], 2.8; P = 0.047; CI, 0.97-8.16) and SE (67.6% vs 36.8%; OR, 3.58; P = 0.035; CI, 1.1-11.63) more frequently compared with patients who received EEN for <6 weeks. Nine patients reported adverse effects.
Polymeric EEN is well tolerated, safe, and effective in inducing clinical and biochemical remission in adults with active CD. EEN duration of ≥6 weeks has better outcomes.
对于成年活动期克罗恩病(CD)患者,肠内营养(EEN)未被常规用作诱导治疗。本研究旨在评估以口服聚合物配方进行EEN作为辅助手段诱导成年活动期CD患者实现临床和生化缓解的有效性。
我们对2018年1月至2019年9月期间所有开始接受EEN治疗的成年活动期CD患者的数据进行了回顾性分析。主要终点(PE)为8周时的临床缓解(克罗恩病活动指数[CDAI]≤150)或缓解(CDAI下降100分)。次要终点(SE)为基线值升高的患者在8周时的生化缓解(C反应蛋白水平≤5mg/L或粪便钙卫蛋白水平≤150mcg/g)。我们还旨在确定EEN治疗反应的预测因素。
66例患者开始接受EEN治疗;其中53例(66例中的;80.3%)完成了规定的EEN疗程。8周时,66例患者中有42例(63.6%)达到主要终点,53例患者中有30例(56.6%)达到次要终点。接受EEN治疗≥6周的患者比接受EEN治疗<6周的患者更频繁地达到主要终点(72%对47.8%;优势比[OR],2.8;P=0.047;可信区间[CI],0.97-8.16)和次要终点(67.6%对36.8%;OR,3.58;P=0.035;CI,1.1-11.63)。9例患者报告了不良反应。
聚合物EEN耐受性良好、安全,且能有效诱导成年活动期CD患者实现临床和生化缓解。EEN持续时间≥6周有更好的治疗效果。