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Minimal-access video-assisted retroperitoneal and/or transperitoneal debridement (VARTD) in the management of infected walled-off pancreatic necrosis with deep extension: initial experience from a prospective single-arm study

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BMC
DOI: 10.1186/s40001-023-01030-9

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Necrotizing pancreatitis; Walled-off pancreatic necrosis; Extensive necrosis; Minimal-access debridement

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This study assessed the effectiveness and safety of a minimal-access video-assisted retroperitoneal and/or transperitoneal debridement (VARTD) in managing infected walled-off pancreatic necrosis with deep extension (iWONde). The majority of participants (14/21, 67%) achieved the primary efficacy endpoint, and there was no need for repeated interventions. The primary safety endpoint occurred in six patients (29%), with one in-hospital death attributed to repeated intra-abdominal hemorrhage.
BackgroundThe currently preferred minimally invasive approaches have substantially improved outcomes of infected walled-off pancreatic necrosis (iWON). However, iWON with deep extension (iWONde) still poses a tricky challenge for sufficient necrosis evacuation by one stand-alone approach, often requiring repeated interventions. The aim of this study was to assess the effectiveness and safety of a minimal-access video-assisted retroperitoneal and/or transperitoneal debridement (hereafter called VARTD) in the management of iWONde.MethodsPatients who had developed an iWONde were recruited to receive the VARTD in this prospective single-arm study. The primary efficacy endpoint was clinical improvement up to day 28 after the VARTD, defined as a >= 75% reduction in size of necrotic collection (in any axis) on CT and clinical resolution of sepsis or organ dysfunction. The primary safety endpoint was a composite of major complications or death during follow-up. Six-month postdischarge follow-up was available.ResultsBetween July 18, 2018, and November 12, 2020, we screened 95 patients with necrotizing pancreatitis; of these, 21 iWONde patients (mean [SD] age, 42.9 [11.7] years; 10 [48%] women) were finally enrolled. The primary efficacy endpoint was achieved by most participants (14/21, 67%). No participants required repeated interventions. The primary safety endpoint occurred in six patients (29%). Except one in-hospital death attributable to repeated intra-abdominal hemorrhage, others were discharged without any major complication.ConclusionsThe VARTD approach appears to have a reasonable efficacy with acceptable complication rates and thus might be an option for improving clinical management of iWONde.

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