Department of Gastroenterology and Hepatology, Cairns Hospital, Cairns, Queensland, Australia.
J Gastroenterol Hepatol. 2021 Feb;36(2):490-497. doi: 10.1111/jgh.15204. Epub 2020 Aug 21.
Endoscopist directed nurse administered propofol sedation (EDNAPS) is widely considered to be safe and efficient, but there are limited data from the Australian health-care setting, and Australian sedation guidelines do not support the practice. Thus, we report data from a prospective audit of EDNAPS over a 6.5-year period in an Australian referral hospital.
Consecutive endoscopic procedures performed between January 2013 and June 2019. Sedation protocol was an initial dose of midazolam 1-3 mg intravenously (i.v.) and propofol 10-50 mg i.v.. Further aliquots of propofol 10-30 mg i.v. were given as required. ProvationMD® endoscopic reporting system was used to prospectively record patient demographics, medication and dose, American Society of Anesthesiologist's (ASA) class, and sedation-related complications.
During the 78-month period, 28 051 eligible procedures were performed; 3093 procedures performed with anesthetic support or without EDNAPS were excluded. In total, 24 958 procedures with EDNAPS were analyzed including 7563 gastroscopies, 12 941 colonoscopies, 2932 gastroscopy and colonoscopy, 1440 flexible sigmoidoscopies, and 82 combined gastroscopy and flexible sigmoidoscopy. Of these, 9539 were ASA 1 (38.2%), 13 680 were ASA 2 (54.8%), 1733 were ASA 3 (6.9%), and 4 were ASA 4 (0.02%). Sedation-related complications occurred in 66 patients (0.26%), predominantly transient hypoxic episodes. No patient required intubation for an airway emergency, and there was no sedation-related mortality. Sedation-related complications increased with ASA class and were significantly more common with gastroscopy.
Endoscopist directed nurse administered propofol sedation is a safe way of performing endoscopic sedation in low-risk patients in the hospital setting.
内镜医师指导下由护士进行的异丙酚镇静(EDNAPS)被广泛认为是安全有效的,但在澳大利亚医疗保健环境中数据有限,且澳大利亚镇静指南不支持这种做法。因此,我们报告了在澳大利亚转诊医院进行的为期 6.5 年的 EDNAPS 前瞻性审核数据。
连续进行的内镜检查程序在 2013 年 1 月至 2019 年 6 月之间进行。镇静方案为初始剂量为 1-3 毫克咪达唑仑静脉内(i.v.)和 10-50 毫克异丙酚 i.v.。根据需要给予进一步的 10-30 毫克异丙酚 i.v.等分剂量。使用 ProvationMD®内镜报告系统前瞻性记录患者人口统计学信息、药物和剂量、美国麻醉医师协会(ASA)分级以及镇静相关并发症。
在 78 个月期间,进行了 28051 次合格的检查程序;排除了 3093 次有麻醉支持或无 EDNAPS 的检查程序。总共分析了 24958 次 EDNAPS 检查程序,包括 7563 次胃镜检查、12941 次结肠镜检查、2932 次胃镜和结肠镜检查、1440 次乙状结肠镜检查和 82 次胃镜和乙状结肠镜联合检查。其中,9539 例为 ASA 1(38.2%),13680 例为 ASA 2(54.8%),1733 例为 ASA 3(6.9%),4 例为 ASA 4(0.02%)。66 例患者发生镇静相关并发症(0.26%),主要为短暂缺氧发作。无患者需要气管插管治疗气道紧急情况,也没有与镇静相关的死亡。镇静相关并发症随 ASA 分级增加而增加,且在胃镜检查中更为常见。
内镜医师指导下由护士进行的异丙酚镇静是在医院环境中对低风险患者进行内镜镇静的一种安全方法。