5‐aminosalicylate maintenance is not superior to no maintenance in patients with newly diagnosed Crohn's disease—A nationwide cohort study

Author:

Atia Ohad1ORCID,Goren Idan23ORCID,Fischler Tali Sharar2,Weisband Yisca Loewenberg4,Greenfeld Shira5,Kariv Revital5,Ledderman Natan6,Matz Eran7,Rimon Ramit Magen8,Dotan Iris2,Turner Dan1,Yanai Henit2ORCID

Affiliation:

1. Juliet Keidan Institute of Pediatric Gastroenterology Hepatology and Nutrition, Shaare Zedek Medical Center The Hebrew University of Jerusalem Jerusalem Israel

2. Division of Gastroenterology, Rabin Medical Center, Petah Tikva, Israel and The Sackler Faculty of Medicine Tel Aviv University Tel‐Aviv Israel

3. Department of Inflammation and Immunity Lerner Research Institute, Cleveland Clinic Cleveland Ohio USA

4. Clalit Research Institute, Chief's Office, Clalit Health Services Tel Aviv Israel

5. Maccabi Healthcare Services Tel Aviv Israel

6. Meuhedet Health Services Tel Aviv Israel

7. Leumit Health Services Tel Aviv Israel

8. Rambam Medical Center, Faculty of Medicine Pediatric Gastroenterology & Nutrition Institute, Ruth Rappaport Children's Hospital, Technion Haifa Israel

Abstract

SummaryBackground5‐aminosalicylates (5‐ASA) are widely used in Crohn's disease (CD) despite guidelines advising otherwise. We aimed to assess in nationwide study the outcomes of first‐line 5‐ASA maintenance therapy (5‐ASA‐MT) compared with no maintenance treatment (no‐MT) in patients with newly diagnosed CD.MethodsWe utilised data from the epi‐IIRN cohort, including all patients with CD diagnosed in Israel between 2005 and 2020. Propensity score (PS) matching was utilised to compare outcomes in the 5‐ASA‐MT versus no‐MT groups.ResultsOf the 19,264 patients diagnosed with CD, 8610 (45%) fulfilled the eligibility criteria (3027 [16%] received 5‐ASA‐MT and 5583 [29%] received no‐MT). Both strategies declined over the years; 5‐ASA‐MT from 21% of CD patients diagnosed in 2005 to 11% in 2019 (p < 0.001) and no‐MT from 36% to 23% (p < 0.001). The probability of maintaining therapy at 1, 3 and 5 years from diagnosis: 5‐ASA‐MT—78%, 57% and 47% and no‐MT—76%, 49% and 38% respectively (p < 0.001). PS analysis successfully matched 1993 pairs of treated and untreated patients and demonstrated comparable outcomes of time to: biologic (p = 0.2), steroid dependency (p = 0.9), hospitalisation (p = 0.5) and CD‐related surgery (p = 0.1). Rates of acute kidney injury (5.2% vs. 3.3%; p < 0.001) and pancreatitis (2.4% vs. 1.8%; p = 0.03) were higher in the 5‐ASA‐MT group compared with the no‐MT group but after PS matching the rates of adverse events were similar.ConclusionFirst‐line 5‐ASA monotherapy was not superior to no‐MT but associated with a slightly higher rates of adverse events, while both strategies have declined over the years. These findings suggest that a subset of patients with mild CD may be offered a watchful waiting approach.

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

Reference36 articles.

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