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Anti-reflux versus conventional self-expanding metal stents in the palliation of esophageal cancer: A systematic review and meta-analysis. | LitMetric

AI Article Synopsis

  • Self-expanding metal stents (SEMS) are used to relieve swallowing difficulties in esophageal cancer patients, with valved SEMS (SEMS-V) developed to potentially reduce gastroesophageal reflux disease (GERD) symptoms compared to non-valved SEMS (SEMS-NV).
  • A systematic review and meta-analysis of 10 randomized clinical trials involving 467 patients showed no significant differences in GERD symptoms, dysphagia relief, technical success, or adverse events between the two types of stents.
  • Both SEMS-V and SEMS-NV are deemed safe and effective for palliation in esophageal cancer, with comparable outcomes regarding GERD, dysphagia improvement, and quality of life.

Article Abstract

Self-expanding metal stents (SEMS) are an effective palliative endoscopic therapy to reduce dysphagia in esophageal cancer. Gastroesophageal reflux disease (GERD) is a relatively common complaint after non-valved conventional SEMS placement. Therefore, valved self-expanding metal stents (SEMS-V) were designed to reduce the rate of GERD symptoms. We aimed to perform a systematic review and meta-analysis comparing the two stents. This was a systematic review and meta-analysis including only randomized clinical trials (RCT) comparing the outcomes between SEMS-V and non-valved self-expanding metal stents (SEMS-NV) following the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines. The risk of bias was assessed using the Cochrane Risk of Bias 2 tool. Data were analyzed with Review Manager Software. Quality of evidence was evaluated using Grading of Recommendations Assessment, Development, and Evaluation guidelines. Ten randomized clinical trials including a total of 467 patients, 234 in the SEMS-V group and 233 in the SEMS-NV group, were included. There were no statistically significant differences regarding GERD qualitative analysis (RD -0.17; 95 % CI -0.67, 0.33;  = 0.5) and quantitative analysis (SMD -0.22; 95 % CI -0.53, 0.08;  = 0.15) technical success (RD -0.03; 95 % CI -0.07, 0.01;  = 0.16), dysphagia improvement (RD -0.07; 95 % CI -0.19, 0.06;  = 0.30), and adverse events (RD 0.07; 95 % CI -0.07, 0.20;  = 0.32). Both SEMS-V and SEMS-NV are safe and effective in the palliation of esophageal cancer with similar rates of GERD, dysphagia relief, technical success, adverse events, stent migration, stent obstruction, bleeding, and improvement of the quality of life.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576338PMC
http://dx.doi.org/10.1055/a-1894-0914DOI Listing

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