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Gastroesophageal and bile reflux after one-anastomosis gastric bypass: long-term outcomes in a functionally evaluated cohort

A. Delcarro, G. Cesana, F. Ciccarese, M. Uccelli, A. Zanoni, R. Giorgi, A. Oldani, C. Rubicondo et al.

Surgery for Obesity and Related Diseases, 2026

150 participants

Abstract

BACKGROUND

One-anastomosis gastric bypass (OAGB) is increasingly performed worldwide, but concerns persist regarding postoperative gastroesophageal reflux disease (GERD), bile reflux, and related complications.

OBJECTIVES

To evaluate the incidence and clinical relevance of GERD and bile reflux after OAGB and to investigate whether preoperative esophageal functional parameters predict postoperative reflux-related complications.

SETTING

Department of General Surgery, Policlinico San Marco, Bergamo, Italy.

METHODS

This retrospective cohort study included 150 consecutive patients undergoing laparoscopic OAGB between 2016 and 2023. All patients underwent preoperative esophagogastroduodenoscopy and esophageal manometry, with selective pH-impedance monitoring when indicated. Postoperative GERD, esophagitis, bile reflux, anastomotic ulcers, and revisional surgery were assessed during a follow-up of 24-84 months. At last follow-up, 142 patients were available for evaluation, while 8 patients (5.3%) were lost to follow-up.

RESULTS

The mean preoperative body mass index was 48 kg/m2, decreasing to 27 kg/m2 at last follow-up. Postoperative GERD developed in 26 patients (17.3%), all of whom had a preoperative hypotensive lower esophageal sphincter (LES) (<16 mmHg). Bile reflux was diagnosed in 30 patients (20%) by pH-impedance monitoring and was refractory to medical therapy in all cases, leading to conversion to Roux-en-Y gastric bypass (RYGB) with complete symptom resolution.…

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 150 participants or records.

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