| Literature DB >> 27338144 |
Nobuyuki Horita1, Tatsuya Otsuka2, Shusaku Haranaga3, Ho Namkoong4, Makoto Miki5, Naoyuki Miyashita6, Futoshi Higa7, Hiroshi Takahashi8, Masahiro Yoshida9, Shigeru Kohno10, Takeshi Kaneko11.
Abstract
It is unclear whether in the treatment of community-acquired pneumonia (CAP) beta-lactam plus macrolide antibiotics lead to better survival than beta-lactam alone. We report a systematic review and meta-analysis. Trials and observational studies published in English were included, if they provided sufficient data on odds ratio for all-cause mortality for a beta-lactam plus macrolide regimen compared with beta-lactam alone. Two investigators independently searched for eligible articles. Of 514 articles screened, 14 were included: two open-label randomized controlled trials (RCTs) comprising 1975 patients, one non-RCT interventional study comprising 1011 patients and 11 observational studies comprising 33 332 patients. Random-model meta-analysis yielded an odds ratio for all-cause death for beta-lactam plus macrolide compared with beta-lactam alone of 0.80 (95% CI 0.69-0.92, P = 0.002) with substantial heterogeneity (I(2) = 59%, P for heterogeneity = 0.002). Severity-based subgroup analysis and meta-regression revealed that adding macrolide had a favourable effect on mortality only for severe CAP. Of the two RCTs, one suggested that macrolide plus beta-lactam lead to better outcome compared with beta-lactam alone, while the other did not. Subgrouping based on study design, that is, RCT versus non-RCT, which was almost identical to subgrouping based on severity, revealed substantial inter-subgroup heterogeneity. Compared with beta-lactam alone, beta-lactam plus macrolide may decrease all-cause death only for severe CAP. However, this conclusion is tentative because this was based mainly on observational studies.Entities:
Keywords: anti-inflammatory effect; antibiotics; infectious disease; meta-regression; mortality
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Year: 2016 PMID: 27338144 DOI: 10.1111/resp.12835
Source DB: PubMed Journal: Respirology ISSN: 1323-7799 Impact factor: 6.424