We evaluated evidence related to the use of a rod (bridge) to prevent stoma retraction during loop ostomyconstruction.
METHODS:
We completed a systematic review of the literature. We searched MEDLINE, EMBASE, and COCHRANE databases up to December 4, 2019. We posed the following question based on a PICO format. Do adultpatients undergoing ostomysurgery experience less stomal retraction when compared to patients managed without placement of a stoma rod?
FINDINGS:
Our initial search returned 182 articles; after reading studies in full, 5 articles were identified that collectively enrolled 1058 participants. Four studies were randomized controlled trials and one was a prospective cohort study. Meta-analysis could not be performed because of the small number of studies and the heterogeneity of outcomes measurements. The incidence of stoma retraction ranged between 0%-8% in patients managed with a rod and 0.78%-8.2% in patients with no rod. The number of reported adverse events was low. Placement of a stoma rod was associated with more adverse outcomes than in patients managed without a rod. Adverse events included local edema, stoma necrosis, skinnecrosis, peristomal moisture-associated skin damage (irritant dermatitis), peristomal abscess, bleeding, and mucocutaneous separation.
CONCLUSIONS:
Stoma rod does not seem to reduce the risk of stoma retraction and might result in other adverse events. IMPLICATIONS We recommend avoidance of stoma rod/bridge placement during ostomysurgery.