Publications by authors named "Madeleine Poirier"

Article Synopsis
  • The study aimed to assess how deep neuromuscular blockade (NMB) affects pain and opioid use during laparoscopic colorectal surgery compared to moderate NMB.
  • 100 patients were randomly divided into deep and moderate NMB groups, with the deep group requiring significantly less remifentanil (an opioid) during surgery.
  • Results indicated that deep NMB improved surgical conditions, evidenced by a better Leiden Surgical Rating Scale and lower intra-abdominal pressure, while postoperative pain and analgesic use were similar to the moderate group.
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A cholecystoenteric fistula (CEF) is a rare complication of cholelithiasis with cholecystitis. Cholecystocolonic fistulas (CCFs) account for 8-26.5% of all CEFs.

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Background: The NOL index is based on multiparametric analysis of heart rate (HR), skin conductance, wave plethysmography, and their time derivative. The aim of this study was to evaluate the NOL to detect standardized nociceptive stimuli with various remifentanil dosages under general anesthesia.

Methods: A prospective, observational study at a single center (NCT02602379) included 40 ASA I to III patients undergoing laparotomy under remifentanil-desflurane anesthesia with epidural analgesia.

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The subclass of cysteine proteases termed lysosomal cathepsins has long been thought to be primarily involved in end-stage protein breakdown within lysosomal compartments. Furthermore, few specific protein substrates for these proteases have been identified. We show here that cathepsin L functions in the regulation of cell cycle progression through proteolytic processing of the CDP/Cux transcription factor.

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Two isoforms of the CCAAT-displacement protein/cut homeobox (CDP/Cux) transcription factor have been characterized thus far. The full length protein, p200, which contains four DNA binding domains, transiently binds to DNA and carries the CCAAT-displacement activity. The p110 isoform is generated by proteolytic processing at the G1-S transition and is capable of stable interaction with DNA.

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