降低社区获得性肺炎住院患者不符合指南的治疗率

Kellie Arensman Hannan, Paul Frykman, Eric Mathiowetz, Jill Sathre, Nou Cheng Yang, Kelsey Jensen
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引用次数: 0

摘要

背景:尽管指南建议缩短治疗时间,并仅对具有某些危险因素的患者使用铜绿假单胞菌和耐甲氧西林金黄色葡萄球菌(MRSA),但优化社区获得性肺炎(CAP)的治疗仍然是抗菌药物管理(AMS)团队面临的一个挑战。我们调查了多模式AMS倡议对CAP经验抗生素选择与指南不一致率和总治疗时间的影响。方法:2022年在9家社区医院实施了质量改进倡议,以优化CAP治疗。向药剂师和提供者提供教育。在电子病历中实施警报,以提示AMS团队审查为CAP订购的氟喹诺酮类药物、抗假单胞菌β-内酰胺类药物和抗mrsa药物。临床药剂师在出院时审查CAP的抗生素订单,并鼓励提供者开出总抗生素持续时间为5-7天的处方。在干预前(2021年7月至9月)和干预后(2022年7月至9月),通过图表回顾对随机抽样的320例CAP抗生素订单患者进行回顾性评估。排除非CAP指征的患者。主要终点是总治疗时间为7天的患者比例。次要结局包括平均治疗时间、指南不一致的经验治疗率和指南不一致的类型。结果:共纳入317例患者。总治疗时间为7天的患者比例从29%降至14% (P <. 01)。平均治疗时间和与指南不一致的经验治疗时间也显著减少(表1)。结论:这种多方面的AMS倡议与减少指南不一致的经验治疗和减少CAP的总治疗时间有关。披露:无
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Reducing the rate of guideline-discordant therapy for inpatients with community-acquired pneumonia
Background: Despite guidelines recommending shorter durations of therapy and empiric coverage of Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus (MRSA) only for patients with certain risk factors, optimizing therapy for community-acquired pneumonia (CAP) remains a challenge for antimicrobial stewardship (AMS) teams. We investigated the impact of a multimodal AMS initiative on the rate of guideline-discordant empiric antibiotic selection and total duration of therapy for CAP. Methods: A quality improvement initiative was implemented at 9 community hospitals in 2022 to optimize CAP therapy. Education was provided to pharmacists and providers. Alerts were implemented within the electronic medical record to prompt the AMS team to review fluoroquinolones, antipseudomonal β-lactams, and anti-MRSA agents ordered for CAP. Clinical pharmacists reviewed antibiotic orders for CAP at hospital discharge and encouraged providers to prescribe a total antibiotic duration of 5–7 days. For the preintervention period (July– September 2021) and the postintervention period (July to September 2022), a random sample of 320 patients with an antibiotic order for CAP were evaluated retrospectively via chart review. Patients treated for an indication other than CAP were excluded. The primary outcome was the proportion of patients with a total duration of therapy >7 days. Secondary outcomes included average duration of therapy, rate of guideline-discordant empiric therapy, and type of guideline discordance. Results: In total, 317 patients were included. The proportion of patients with a total duration of therapy >7 days decreased from 29% to 14% ( P < .01). Average duration of therapy and guideline-discordant empiric therapy also decreased significantly (Table 1). Conclusions: This multifaceted AMS initiative was associated with decreased guideline-discordant empiric therapy and decreased total duration of therapy for CAP. Disclosures: None
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