Service of Infectious Diseases, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Infection Prevention and Control Unit, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Antimicrob Resist Infect Control. 2022 Dec 30;11(1):165. doi: 10.1186/s13756-022-01203-x.
We previously reported an increase in meropenem prescriptions for Pseudomonas aeruginosa infections in our hospital after the implementation of the 10th version of the EUCAST breakpoints table for P. aeruginosa in January 2020. As a consequence, antibiotic susceptibility testing results were adapted by masking meropenem for P. aeruginosa isolates susceptible to either ceftazidime, cefepime or piperacillin-tazobactam. We aimed to assess the changes in meropenem prescriptions after the implementation of the selective reporting.
In this retrospective single-centre observational study, we analysed antimicrobial therapies prescribed for P. aeruginosa infections after the susceptibility testing results have been made available over three periods: "before EUCAST update", "after EUCAST update without selective reporting" and "after EUCAST update with selective reporting", at Lausanne University Hospital, Switzerland. We collected epidemiological, microbiological and clinical data. The primary outcome was the prescription of meropenem to treat P. aeruginosa infections after the release of susceptibility testing results. Secondary outcomes were the use of increased dosage of non-meropenem anti-pseudomonal drugs, and IDs' consultations rates after the release of susceptibility testing results.
Among the 457 patients included, 65 (14.2%) received meropenem: 5/148 (3.4%) before EUCAST update, 51/202 (25.3%) after EUCAST update without selective reporting, and 9/107 (8.4%) after EUCAST update with selective reporting. Supervision and counselling from IDs as well as the use of increased dosages of non-carbapenem antibiotics increased in both periods after EUCAST update, compared to the first period, respectively: 40.5% (60/148) versus 61.4% (124/202) versus 51.4% (55/107) (P < 0.001), and 57.9% (84/148) versus 91.1% (183/202) versus 90.7% (97/107) (P < 0.001).
Selective reporting of antibiotic susceptibility testing results might decrease unnecessary meropenem prescriptions for the treatment of P. aeruginosa infections and could be part of multimodal antibiotic stewardship interventions.
我们之前报道过,在 2020 年 1 月实施第 10 版欧盟药敏折点表后,我院治疗铜绿假单胞菌感染的美罗培南处方有所增加。因此,当铜绿假单胞菌分离株对头孢他啶、头孢吡肟或哌拉西林他唑巴坦敏感时,我们通过掩盖美罗培南来调整抗生素药敏试验结果。我们旨在评估选择性报告实施后的美罗培南处方变化。
在这项回顾性单中心观察性研究中,我们分析了瑞士洛桑大学医院在三个时期内铜绿假单胞菌感染的抗菌治疗方案:“欧盟药敏更新前”、“欧盟药敏更新后但无选择性报告”和“欧盟药敏更新后且有选择性报告”。我们收集了流行病学、微生物学和临床数据。主要结局是在药敏试验结果发布后,治疗铜绿假单胞菌感染的美罗培南处方。次要结局为非美罗培南抗假单胞菌药物的增加剂量使用,以及药敏试验结果发布后的 ID 咨询率。
在纳入的 457 名患者中,65 名(14.2%)接受了美罗培南治疗:“欧盟药敏更新前”为 5/148(3.4%),“欧盟药敏更新后但无选择性报告”为 51/202(25.3%),“欧盟药敏更新后且有选择性报告”为 9/107(8.4%)。与第一个时期相比,在“欧盟药敏更新后”的两个时期中,ID 的监督和咨询以及非碳青霉烯类抗生素的增加剂量使用均有所增加,分别为:40.5%(60/148)与 61.4%(124/202)与 51.4%(55/107)(P<0.001),和 57.9%(84/148)与 91.1%(183/202)与 90.7%(97/107)(P<0.001)。
选择性报告抗生素药敏试验结果可能会减少不必要的美罗培南治疗铜绿假单胞菌感染的处方,并且可能成为多模式抗生素管理干预措施的一部分。