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Percutaneous or Endoscopic Treatment of Peripheral Bile Duct Leaks: Initial Experience with an Innovative Approach of Microcatheter-Delivered Argon Plasma Coagulation. | LitMetric

AI Article Synopsis

  • * Materials and Methods: The procedure was tested on three patients of varying ages (7-year-old, 14-year-old, and 81-year-old) who had persistent bile leaks after surgery or trauma, involving either percutaneous or endoscopic approaches.
  • * Results and Conclusion: All procedures were successful, achieving complete closure of bile leaks without complications. The findings suggest potential effectiveness of APC for such injuries, warranting further research for safety and clinical application.

Article Abstract

Purpose: Biliary ductal injuries are challenging to treat, and often lead to severe morbidity and mortality. The first-line approach involves endoscopic retrograde cholangiopancreatography with sphincterotomy and, in case of refractory leakage, long-lasting percutaneous transhepatic biliary drainage, endoscopic or percutaneous injection of sclerosing agents and/or coiling can be used. We describe a treatment procedure using microcatheter-mediated percutaneous or endoscopic argon plasma coagulation (APC).

Materials And Methods: Three patients (7-year-old male, 14-year-old male, 81-year-old female) with refractory postsurgical and/or post-traumatic bile leaks underwent percutaneous (n = 2) or endoscopic (n = 1) APC through a detachable microcatheter.

Results: The procedure was technically feasible in all patients. Postoperative imaging showed complete occlusion of biliary leakage. The technique was uneventful intraoperatively with no adverse events occurring during recovery or follow-up.

Conclusion: Our initial experience demonstrates that refractory bile duct leaks may be successfully treated with microcatheter-mediated APC endoscopically or percutaneously. Further research is needed to confirm the safety, efficacy, and clinical indications for this innovative technique.

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Source
http://dx.doi.org/10.1007/s00270-021-03016-8DOI Listing

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