Department of Infectious Diseases, Bellvitge University Hospital, L'Hospitalet de LLobregat, Barcelona, Spain.
Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Nat Commun. 2024 Aug 17;15(1):7098. doi: 10.1038/s41467-024-51547-8.
We assessed whether multiplex real-time PCR plus conventional microbiological testing is safe and more effective than conventional microbiological testing alone for reducing antibiotic use in community-acquired pneumonia (CAP). In this randomised trial, we recruited adults hospitalised with CAP at four Spanish hospitals. Patients were randomly assigned (1:1) to undergo either multiplex real-time PCR in non-invasive respiratory samples plus conventional microbiological testing or conventional microbiological testing alone. The primary endpoint was antibiotic use measured by days of antibiotic therapy (DOT). Between February 20, 2020, and April 24, 2023, 242 patients were enrolled; 119 were randomly assigned to multiplex real-time PCR plus conventional microbiological testing and 123 to conventional microbiological testing alone. All but one of the patients allocated to multiplex real-time PCR plus conventional microbiological testing underwent PCR, which was performed in sputum samples in 77 patients (65.2%) and in nasopharyngeal swabs in 41 (34.7%). The median DOT was 10.04 (IQR 7.98, 12.94) in the multiplex PCR plus conventional microbiological testing group and 11.33 (IQR 8.15, 16.16) in the conventional microbiological testing alone group (difference -1.04; 95% CI, -2.42 to 0.17; p = 0.093). No differences were observed in adverse events and 30-day mortality. Our findings do not support the routine implementation of multiplex real-time PCR in the initial microbiological testing in hospitalised patients with CAP. Clinicaltrials.gov registration: NCT04158492.
我们评估了多重实时 PCR 加常规微生物检测是否比单独进行常规微生物检测更安全、更能减少社区获得性肺炎 (CAP) 的抗生素使用。在这项随机试验中,我们招募了四家西班牙医院因 CAP 住院的成年人。患者被随机分配(1:1)接受非侵入性呼吸样本的多重实时 PCR 加常规微生物检测或单独进行常规微生物检测。主要终点是通过抗生素治疗天数(DOT)测量的抗生素使用。2020 年 2 月 20 日至 2023 年 4 月 24 日,共纳入 242 名患者;119 名患者被随机分配至多重实时 PCR 加常规微生物检测组,123 名患者被分配至单独进行常规微生物检测组。除 1 名患者外,所有分配至多重实时 PCR 加常规微生物检测组的患者均接受了 PCR 检测,其中 77 名患者(65.2%)的痰液样本和 41 名患者(34.7%)的鼻咽拭子进行了 PCR 检测。多重 PCR 加常规微生物检测组的中位 DOT 为 10.04(IQR 7.98,12.94),单独进行常规微生物检测组为 11.33(IQR 8.15,16.16)(差值-1.04;95%CI,-2.42 至 0.17;p=0.093)。两组不良事件和 30 天死亡率无差异。我们的研究结果不支持在 CAP 住院患者的初始微生物检测中常规实施多重实时 PCR。Clinicaltrials.gov 注册号:NCT04158492。