Long‐term safety and effectiveness of azathioprine in the management of inflammatory bowel disease: A real‐world experience

Author:

Yewale Rohan V1,Ramakrishna Balakrishnan S1ORCID,Doraisamy Babu Vinish1,Basumani Pandurangan2,Venkataraman Jayanthi3,Jayaraman Kayalvizhi1,Murali Ananthavadivelu4,Premkumar Karunakaran5,Kumar Akkim Sathish6

Affiliation:

1. Institute of Gastroenterology, SRM Institutes for Medical Science Chennai Tamil Nadu India

2. Department of Gastroenterology Apollo Hospitals Greams Road Chennai Tamil Nadu India

3. Department of Hepatology Sri Ramachandra Institute of Higher Education and Research Chennai Tamil Nadu India

4. Department of Gastroenterology MIOT Hospital Chennai Tamil Nadu India

5. Institute of Gastroenterology, Madras Medical College Chennai Tamil Nadu India

6. Satish Gastro Hospital Tirupati Andhra Pradesh India

Abstract

AbstractBackground and AimAzathioprine (AZA) forms the cornerstone for maintenance of sustained remission in inflammatory bowel disease (IBD). There is apprehension regarding the long‐term effectiveness and safety of AZA in IBD. We present our experience with AZA use and outcomes in a cohort of IBD patients followed up over a long period of time.MethodsRecords of 507 IBD patients under treatment at a single, tertiary care center in south India between 2013 and 2022 were evaluated retrospectively. Long‐term compliance, tolerance, clinical outcome at the point of last follow‐up, type and duration to the onset of adverse events, and subsequent amendment to treatment with regard to AZA were analyzed.ResultsOf 507 patients with IBD, 320 patients (207 Crohn's disease [CD], 113 ulcerative colitis [UC]) who received AZA were included. The median follow‐up was 41 months (interquartile range 15.5–77.5). Total duration of exposure was 1359 patient‐years with median usage of 33 months. Of the patients, 26.9% received AZA for >5 years. Mean initiation and maximum doses of AZA were 0.97 and 1.72 mg/kg/day. Among the participants, 20.6% experienced side effects, including myelotoxicity (7.2%) and gastrointestinal intolerance (5.6%). Six patients developed malignancy. Among the side effects, 39.4% of side effects were dose‐dependent. Among the patients, 38.1% had relapses requiring pulse corticosteroid therapy, and 16.2% had more than one relapse after commencement of AZA. AZA was continued till the last follow‐up in 76.5%. Among the patients, 49.7% (UC 51.3, CD 48.8) attained durable remission without biologics, and 5.3% continued to have active disease.ConclusionAZA is safe and effective in the long‐term in IBD. Effectiveness, tolerance, and compliance with AZA are well sustained beyond 5 years of usage and comparable between UC and CD.

Publisher

Wiley

Subject

Gastroenterology,Hepatology

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