Azathioprine Plus Exclusive Enteral Nutrition Versus Azathioprine Monotherapy for the Prevention of Postoperative Recurrence in Patients with Crohn’s Disease: An Open-Label, Single-Centre, Randomized Controlled Trial

Author:

Duan Ming1,Lu Mengjie2,Diao Yanqing1,Cao Lei1,Wu Qiong3,Liu Yuxiu45,Gong Jianfeng1,Zhu Weiming6,Li Yi1ORCID

Affiliation:

1. Department of General Surgery, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University , Nanjing 210002 , China

2. School of Public Health, Shanghai Jiao Tong University School of Medicine , Shanghai 200025 , China

3. Department of Scientific Research and Training, Jinling Hospital, Affiliated Hospital of Medical School , Nanjing 210002 , China

4. Data and Statistics Division, Department of Critical Care Medicine, Jinling Hospital, Nanjing Medical University , Nanjing 210002 , China

5. Department of Biostatistics, School of Public Health, Southern Medical University , Guangzhou, Guangdong 510515 , China

6. Department of Colorectal and Proctology, Affiliated Hospital of Nanjing University of Chinese Medicine , Nanjing 210023 , China

Abstract

Abstract Background Azathioprine [AZA] effectively prevents postoperative endoscopic recurrence [ER] in Crohn’s disease [CD]. However, the efficacy of AZA emerges after 3 months. Exclusive enteral nutrition [EEN] can maintain remission in CD. The present trial investigates whether AZA plus postoperative 3-month EEN is superior to AZA alone in preventing ER of CD. Methods In total, 84 high-risk CD patients undergoing intestinal resection received AZA alone or AZA plus 3 months of EEN [AZA + EEN] postoperatively. The primary endpoint was the rate of ER at 12 months. Secondary endpoints included the rate of ER at 3 months, clinical recurrence [CR], CD activity index [CDAI] scores, faecal calprotectin [FC], and C-reactive protein [CRP]. Quality of life was assessed using Short Form-36 [SF-36] and the Inflammatory Bowel Disease Questionnaire [IBDQ]. Results Patients in the AZA + EEN group exhibited significantly lower rates of ER compared to the AZA group at both 12 months (33.3% [13/39] vs 63.2% [24/38], P = 0.009) and 3 months (8.6% [3/35] vs 28.1% [9/32], P = 0.037) post-surgery. The rates of CR between the two groups at 3 and 12 months were similar. CDAI scores, FC, albumin level, and CRP were all comparable between the two groups. Quality of life was significantly higher in the AZA group than in the AZA + EEN group at 3 months but became comparable from 5 to 12 months postoperatively. Conclusion In high-risk CD patients, combining AZA with postoperative 3-month EEN reduces 1-year ER but may temporarily impact quality of life. Further large-scale, long-term studies are warranted. Trial Number NCT05214430.

Funder

National Natural Science Foundation of China

Project of Jinling Hospital

Publisher

Oxford University Press (OUP)

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