Efficacy and safety of EUS-directed transgastric ERCP (EDGE) versus laparoscopic-assisted ERCP: A systematic review and meta-analysis

Author:

Gangwani Manesh Kumar1,Haghbin Hossein2,Priyanka Fnu3,Hadi Yousaf4,Dahiya Dushyant Singh5,Kamal Faisal6,Lee-Smith Wade7,Nawras Ali8,Aziz Muhammad8,Adler Douglas G.9

Affiliation:

1. Department of Medicine, The University of Toledo Medical Center, Toledo, OH 43614, USA

2. Department of Gastroenterology and Hepatology, Ascension Providence Hospital, Southfield, MI 43614, USA

3. Department of Medicine, Shaheed Mohtarma Benazir Bhutto University, Larkana, Pakistan

4. Department of Gastroenterology and Hepatology, West Virginia University, Morgantown, WV 26506, USA

5. Department of Internal Medicine, Central Michigan University College of Medicine, Saginaw, MI 48859, USA

6. Division of Gastroenterology, University of San Francisco, SF 94413, USA

7. University of Toledo Libraries, University of Toledo, Toledo, OH 43614, USA

8. Department of Gastroenterology and Hepatology, University of Toledo Medical Center, Toledo, OH 43614, USA

9. Center for Advanced Therapeutic Endoscopy, Porter Adventist Hospital, Center Health, Denver, CO 80210, USA.

Abstract

ABSTRACT The altered anatomy in Roux-en-Y gastric bypass (RYGB) makes conventional endoscopic retrograde cholangiopancreatography (ERCP) a technically challenging procedure. EUS–directed transgastric ERCP (EDGE) and laparoscopic-assisted ERCP (LA-ERCP) are alternative modalities used with comparable efficacy and adverse events in such patients. We conducted a meta-analysis comparing EDGE and LA-ERCP to assess the efficacy and safety in patients with RYGB. We conducted a comprehensive literature search from inception to July 7, 2022, on MEDLINE, EMBASE, Cochrane Register of Controlled Trials, and Web of Science databases using the core concepts of EDGE and LA-ERCP. We excluded case reports, case series (<10 patients), and review articles. Relative risk (RR) was calculated when comparing dichotomous variables, whereas mean difference was calculated for continuous outcomes. A 95% confidence interval (CI) and P values (<0.05 considered significant) were also generated. The search strategy yielded a total of 55 articles. We finalized 4 studies with total 192 patients (75 EDGE and 117 LA-ERCP). The rates of technical success were not significantly different for LA-ERCP and EDGE (RR, 0.994; 95% CI, 0.939–1.051; P = 0.830, I 2 = 0%) Similarly, no difference in adverse events was noted between the 2 groups (RR, 1.216; 95% CI, 0.561–2.634; P = 0.620, I 2 = 10.67%). Shorter procedure time was noted for EDGE compared with the LA-ERCP group (mean difference, 91.53 minutes; 95% CI, 69.911–113.157 minutes; P < 0.001 I 2 = 8.32%). EDGE and LA-ERCP are comparable in terms of efficacy and safety. In addition, EDGE has overall lower procedural time. Our study suggests that EDGE should be considered as a first-line therapy if expertise available.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Radiology, Nuclear Medicine and imaging,Hepatology,Gastroenterology,Radiology, Nuclear Medicine and imaging,Hepatology

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