Pancreatic Enzyme Replacement Therapy Improves Exclusive Enteral Nutrition Related Diarrhea in Crohn's Disease: A Prospective Randomized Trial.

IF 5.8 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Jian Kang, Jing Wang, Juan Su, Wei Wang, Yueyue Lu, Zhishun Tang, Liping Zou, Anning Yin, Jiao Li, Haixia Ren, Qian Zhou, Huipeng Wan, Ping An
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引用次数: 0

Abstract

Background & aims: Previous results showed that combined treatment of biologics and exclusive enteral nutrition (EEN) brought moderate-to-severe Crohn's disease patients significant improvements in clinical and endoscopic outcomes. Despite its essential role and favorable safety profile, EEN in the treatment of adult Crohn's disease is frequently underestimated because of lower compliance and several side effects, including EEN-related diarrhea (EEND).

Methods: In this prospective, single-center randomized clinical trial, 147 eligible patients with actively moderate-to-severe Crohn's disease treated with biologics and concomitant 16-week EEN were included. Sixty-one patients without EEND were enrolled in the ND group (without EEN-related diarrhea), and other patients with EEND who received pancreatic enzyme replacement therapy (PERT) (43 patients) or not (43 patients) were recruited in PERT and NPERT groups, respectively. The clinical outcomes, biologic outcomes, and endoscopic outcomes were evaluated. Quality of life (QoL) and psychological status were also assessed at baseline and endpoints (week 16).

Results: Bowel movements (daily frequency decreased by 5.3 times) and stool consistency (reduced watery and loose stool) were greatly improved in PERT group at week 16. At week 16, patients in the ND and PERT groups achieved similar clinical responses (93% in ND group and 94.7% in PERT group, p = 0.731) and clinical remission (86.0% in ND group and 86.8% in PERT group, p = 0.90) while patients in the NPERT group had significantly lower proportions of these clinical outcomes (67.9% clinical response and 57.1% clinical remission). No significant difference was observed in endoscopic outcomes between each group (p = 0.904). QoL and mental status including anxiety and depression in PERT group had great improvement compared with the NPERT group.

Conclusions: Our prospective results provided invaluable evidence that PERT supplementation efficiently improved EEND in Crohn's disease patients with combined treatment of biologics and 16-week EEN, which had a promising effect in active Crohn's disease induction.

Trial registration: ChiCTR2200058343.

胰酶替代疗法改善克罗恩病独家肠内营养相关腹泻:一项前瞻性随机试验
背景与目的:以往的研究结果表明,生物制剂和单独肠内营养(EEN)联合治疗可显著改善中重度克罗恩病患者的临床和内镜预后。尽管EEN具有重要的作用和良好的安全性,但由于其较低的依从性和一些副作用,包括EEN相关的腹泻(EEND), EEN在成人克罗恩病的治疗中经常被低估。方法:在这项前瞻性、单中心随机临床试验中,纳入147例接受生物制剂治疗并伴有16周EEN的中重度活动性克罗恩病患者。61例无EEND患者被纳入ND组(无een相关性腹泻),其他接受胰酶替代治疗(PERT)的EEND患者(43例)和未接受胰酶替代治疗的EEND患者(43例)分别被纳入PERT组和NPERT组。评估临床结果、生物学结果和内窥镜结果。生活质量(QoL)和心理状态也在基线和终点(第16周)进行评估。结果:在第16周,PERT组的排便(每日次数减少5.3次)和大便一致性(减少水样和稀便)显著改善。在第16周,ND组和PERT组患者获得相似的临床反应(ND组为93%,PERT组为94.7%,p = 0.731)和临床缓解(ND组为86.0%,PERT组为86.8%,p = 0.90),而NPERT组患者的这些临床结果比例明显较低(67.9%的临床反应和57.1%的临床缓解)。两组间内镜检查结果无显著差异(p = 0.904)。与NPERT组相比,PERT组患者的生活质量和焦虑、抑郁等精神状态均有显著改善。结论:我们的前瞻性结果提供了宝贵的证据,证明补充PERT可有效改善克罗恩病患者在生物制剂和16周EEN联合治疗下的EEND,这对活动性克罗恩病诱导有很好的效果。试验注册:ChiCTR2200058343。
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来源期刊
United European Gastroenterology Journal
United European Gastroenterology Journal GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
10.50
自引率
13.30%
发文量
147
期刊介绍: United European Gastroenterology Journal (UEG Journal) is the official Journal of the United European Gastroenterology (UEG), a professional non-profit organisation combining all the leading European societies concerned with digestive disease. UEG’s member societies represent over 22,000 specialists working across medicine, surgery, paediatrics, GI oncology and endoscopy, which makes UEG a unique platform for collaboration and the exchange of knowledge.
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