Clarithromycin For Improved Clinical Outcomes in Community-Acquired Pneumonia: A Subgroup Analysis of the ACCESS Study

克拉霉素 子群分析 社区获得性肺炎 医学 肺炎 内科学 重症监护医学 幽门螺杆菌 荟萃分析
作者
Karolina Akinosoglou,Konstantinos Leventogiannis,Elisavet Tasouli,Nikolaos Kakavoulis,Georgios Niotis,Sarantia Doulou,Lamprini Skorda,Konstantina Iliopoulou,Anna Papailiou,Paraskevi Κatsaounou,Vassiliki Rapti,George Chrysos,Theodoros Seferlis,Styliani Gerakari,Konstantina Dakou,Ιlias Papanikolaou,Haralampos J. Milionis,Stefanie Kewitz,Sara Georgiadou,Theano Kontopoulou
出处
期刊:International Journal of Antimicrobial Agents [Elsevier BV]
卷期号:65 (2): 107406-107406
标识
DOI:10.1016/j.ijantimicag.2024.107406
摘要

In the ACCESS trial, the addition of clarithromycin to standard-of-care antibiotics (SoC) enhanced early clinical response and attenuated the inflammatory burden in adults with community-acquired pneumonia (CAP) requiring hospitalisation. A post-hoc analysis was performed to investigate the benefit in specific subgroups. The primary endpoint comprised two conditions to be met during the first 72 h: ≥50% decrease in respiratory symptom severity score; and any of ≥30% decrease in sequential organ failure assessment score and favourable change in the kinetics of procalcitonin (PCT, defined as ≥80% PCT decrease or PCT <0.25 ng/mL). In this exploratory post-hoc analysis, achievement of the study composite primary endpoint was compared between the two treatment groups within subsets differentiated by demographic characteristics, comorbidities, CAP severity, baseline laboratory findings and corticosteroid co-administration. The impact of clarithromycin treatment on the need for mechanical ventilation (MV) in all subgroups was also analysed. The addition of clarithromycin significantly increased the proportion of patients achieving the primary endpoint across all subgroups and decreased the need for MV in 19 out of the 37 subgroups studied. For instance, the primary endpoint was attained in 32.7% of placebo-treated patients and in 67% of clarithromycin-treated patients with CURB-65 score ≥2 (P<0.0001), whereas MV was required in 18.8% and 7.4% of patients, respectively (P=0.022). The addition of corticosteroids alone was not as clinically advantageous as the use of clarithromycin alone, when added to SoC. Adding clarithromycin to SoC in the ACCESS trial achieved early clinical anti-inflammatory responses and decreased the need for MV in subgroups of hospitalised patients with CAP.
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