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Impact of Adoption of Smart Pump System With Continuous Capnography Monitoring on Opioid-Related Adverse Event Rates: Experience From a Tertiary Care Hospital

机译:智能泵系统采用与持续的CAPNography监测采用对阿片类药物相关的不良事件率的影响:来自第三级护理医院的经验

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Objectives The use of opioid analgesics for pain management in hospitalized patients is associated with a high risk of adverse events, including respiratory depression which may lead to respiratory arrest and death. Patients who experience opioid-related adverse drug reactions (ADRs) have been shown to experience longer and more costly hospital stays and have a higher risk of requiring a readmission after discharge. In this study, we report on the impact of the introduction of Wesley Medical Center's Safe Medication Practice Protocol on opioid-related ADRs. Methods A retrospective, pre-post cohort study using electronic health records combined with manual chart review was undertaken at the Wesley Medical Center, a 760-bed tertiary care facility. The Safe Medication Practice Protocol incorporating a smart infusion pump system with capnography monitoring was implemented in May 2010 hospital-wide. The number and severity of ADRs and the duration of opioid treatment were compared between the pre (2007-April 2010) and post (May 2010-2014) periods. Results A total of 139,734 (pre-period) versus 267,573 (post-period) patients received opioid treatment during the hospital stay. Compared with the pre-period, the post-period resulted in a 79.2% reduction in the number of severe adverse reactions (3.08 vs 0.64 per 10,000 patients treated with opioid,P< 0.0001) as well as a shorter duration of opioid treatment (average 2.05 vs 1.37 days,P< 0.0001). Conclusions Implementing education, revisions to patient-controlled analgesia policies and procedures, and capnography monitoring with patient-controlled analgesia pause is associated with significantly lower rates of severe ADRs and shorter opioid treatment duration.
机译:目的在住院患者中使用阿片类药物镇痛药与患者疼痛管理有关的不良事件风险很大,包括呼吸抑郁症,可能导致呼吸系统逮捕和死亡。经历与阿片类药物相关的不良药物反应(ADRS)的患者已被证明经历更长,更昂贵的医院住院,并且在放电后需要更高的风险。在这项研究中,我们报告了韦斯利医疗中心安全药物实践议定书的引入对阿片类药物相关ADR的影响。方法采用电子健康记录的回顾性,使用电子健康记录与手动图表审查相结合,在Wesley Medical Center,A 760床第三级护理设施进行了手动图表。含有CAPNography Montroly的安全药物练习协议,在2010年5月期间实施。在Pre(2007年4月)和职位(2010-2014年5月)期间比较ADR的数量和严重程度和阿片类药物治疗持续时间。结果总共139,734名(前期)与267,573名(后期)患者在住院期间接受了阿片类药物治疗。与前期前期相比,后期的严重不良反应的数量减少了79.2%(每10,000名患者,每10,000名患者,每10,000名患有阿片类药物,P <0.0001)以及较短的阿片类药物治疗持续时间(平均值2.05 vs 1.37天,p <0.0001)。结论实施教育,对患者控制镇痛政策和程序的修订,以及患者受控镇痛暂停的CAPNography监测与严重ADRs的显着较低率和较短的阿片类药物治疗持续时间相关。

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