Abstract

Factors Associated With Biologic Therapy After Ileal Pouch-Anal Anastomosis in Patients With Ulcerative Colitis

Inflamm Bowel Dis.2024 Nov 14:izae272. doi: 10.1093/ibd/izae272. Online ahead of print.

Maya Fischman 1Lihi Godny 2 3Adi Friedenberg 2 3Revital Barkan 2 3Ian White 3 4Nir Wasserberg 3 4Keren Rabinowitz 5Irit Avni-Biron 2Hagar Banai 2Yifat Snir 2Yelena Broitman 2Henit Yanai 2 3Iris Dotan 2 3Jacob E Ollech 2 3

 
     

Author information

1Department of Military Medicine, Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

2Division of Gastroenterology, Rabin Medical Center, Petah Tikva, Israel.

3Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.

4Division of Surgery, Rabin Medical Center, Petah-Tikva, Israel.

5Felsenstein Medical Research Center, Rabin Medical Center, Tel Aviv University, Petah-Tikva, Israel.

Abstract

Background: Patients with ulcerative colitis (UC) undergoing proctocolectomy and ileal pouch-anal anastomosis (IPAA) may eventually require biologic therapy. Factors associated with biologic therapy after IPAA have not been previously studied.

Methods: All patients with UC after total proctocolectomy and IPAA who were followed at Rabin Medical Center comprehensive pouch clinic and who consented to prospective observational follow-up were included. The primary outcome was the initiation of biologic therapy after IPAA. Cox proportional hazard models were used to evaluate potential associations.

Results: Out of 400 patients receiving their care at the pouch clinic, 148 patients consented to prospective observational follow-up and constituted the study cohort. The median age at diagnosis was 21 years and the age at IPAA was 30 years. Median time-to-biologic therapy initiation post-IPAA was 9.2 years, with 34 patients (23%) initiating biologic therapy: Associated factors for initiating biologic therapy post-IPAA were preoperative treatment with biologic therapy and immunomodulatory therapy (hazard ratio [HR] 6.1 and 3.6, respectively, P < .001); Arab descent (HR 5.3, P < .001); heterozygosity of NOD2 variant rs2066845 (HR 5.1, P = .03); past smoking status (HR 2.3, P = .03); 3-stage IPAA (HR 2.3, P = .02); immediate postoperative complications (HR 2.1, P = .033); and pediatric-onset UC (HR 2.1, P = .03). None of the patients undergoing IPAA due to dysplasia (n = 27) required biologic therapy.

Conclusions: Several demographic, disease-related, surgery-related, and genetic factors associated with post-IPAA biologic therapy were identified. Physicians treating patients with UC undergoing colectomy should incorporate these factors into their decision-making process. These patients may benefit from closer postoperative follow-up, and earlier initiation of biologic therapy should be considered.

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