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Efficacy of tetracyclines and fluoroquinolones for the treatment of macrolide-refractory Mycoplasma pneumoniae pneumonia in children: a systematic review and meta-analysis
DC Field | Value | Language |
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dc.contributor.author | Ahn, Jong Gyun | - |
dc.contributor.author | Cho, Hye-Kyung | - |
dc.contributor.author | Li, Donghe | - |
dc.contributor.author | Choi, Miyoung | - |
dc.contributor.author | Lee, Jina | - |
dc.contributor.author | Eun, Byung-Wook | - |
dc.contributor.author | Jo, Dae Sun | - |
dc.contributor.author | Park, Su Eun | - |
dc.contributor.author | Choi, Eun Hwa | - |
dc.contributor.author | Yang, Hyeon-Jong | - |
dc.contributor.author | Kim, Ki Hwan | - |
dc.date.accessioned | 2022-01-14T06:56:26Z | - |
dc.date.available | 2022-03-21T13:50:37Z | - |
dc.date.issued | 2021-09-25 | - |
dc.identifier.citation | BMC Infectious Diseases, 21(1):1003 | ko_KR |
dc.identifier.issn | 1471-2334 | - |
dc.identifier.uri | https://hdl.handle.net/10371/176913 | - |
dc.description.abstract | Abstract
Background Mycoplasma pneumoniae is a common pathogen that causes community-acquired pneumonia in school-age children. Macrolides are considered a first-line treatment for M. pneumoniae infection in children, but macrolide-refractory M. pneumoniae (MRMP) strains have become more common. In this study, we assessed the efficacy of tetracyclines and fluoroquinolones in MRMP treatment in children through a systematic review and meta-analysis. Methods Two reviewers individually searched 10 electronic databases (Medline/Pubmed, Embase, the Cochrane Library, and core Korean, Chinese, and Japanese journals) for papers published from January 1, 1990 to March 8, 2018. The following data for each treatment group were extracted from the selected studies: intervention (tetracyclines and fluoroquinolones/comparator), patient characteristics (age and sex), and outcomes (fever duration, hospital stay length, treatment success rate, and defervescence rates 24, 48, and 72h after starting treatment). Results Eight studies involving 537 participants were included. Fever duration and hospital stay length were shorter in the tetracycline group than in the macrolide group (weighted mean difference [WMD] = −1.45, 95% confidence interval [CI]: −2.55 to −0.36, P = 0.009; and WMD = −3.33, 95% CI: −4.32 to −2.35, P < 0.00001, respectively). The therapeutic efficacy was significantly higher in the tetracycline group than in the macrolide group (odds ratio [OR]: 8.80, 95% CI: 3.12–24.82). With regard to defervescence rate, patients in the tetracycline group showed significant improvement compared to those in the macrolide group (defervescence rate after 24h, OR: 5.34, 95% CI: 1.81–15.75; after 48h, OR 18.37, 95% CI: 8.87–38.03; and after 72h, OR: 40.77, 95% CI: 6.15–270.12). There were no differences in fever improvement within 24h in patients in the fluoroquinolone group compared to those in the macrolide group (OR: 1.11, 95% CI: 0.25–5.00), although the defervescence rate was higher after 48h in the fluoroquinolone group (OR: 2.78, 95% CI: 1.41–5.51). Conclusion Tetracyclines may shorten fever duration and hospital stay length in patients with MRMP infection. Fluoroquinolones may achieve defervescence within 48h in patients with MRMP infection. However, these results should be carefully interpreted as only a small number of studies were included, and they were heterogeneous. | ko_KR |
dc.description.sponsorship | This study was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) funded by the Ministry of Health & Welfare, Republic of Korea (Grant number: HI16C2300). | ko_KR |
dc.language.iso | en | ko_KR |
dc.publisher | BMC | ko_KR |
dc.subject | Mycoplasma pneumoniae | - |
dc.subject | Macrolide-resistant | - |
dc.subject | Tetracycline | - |
dc.subject | Fluoroquinolone | - |
dc.subject | Child | - |
dc.title | Efficacy of tetracyclines and fluoroquinolones for the treatment of macrolide-refractory Mycoplasma pneumoniae pneumonia in children: a systematic review and meta-analysis | ko_KR |
dc.type | Article | ko_KR |
dc.contributor.AlternativeAuthor | 안종균 | - |
dc.contributor.AlternativeAuthor | 조혜경 | - |
dc.contributor.AlternativeAuthor | 이동해 | - |
dc.contributor.AlternativeAuthor | 최미영 | - |
dc.contributor.AlternativeAuthor | 이지나 | - |
dc.contributor.AlternativeAuthor | 은병욱 | - |
dc.contributor.AlternativeAuthor | 조대선 | - |
dc.contributor.AlternativeAuthor | 박수은 | - |
dc.contributor.AlternativeAuthor | 최은화 | - |
dc.contributor.AlternativeAuthor | 양현종 | - |
dc.contributor.AlternativeAuthor | 김기환 | - |
dc.identifier.doi | https://doi.org/10.1186/s12879-021-06508-7 | - |
dc.citation.journaltitle | BMC Infectious Diseases | ko_KR |
dc.language.rfc3066 | en | - |
dc.rights.holder | The Author(s) | - |
dc.date.updated | 2021-09-26T03:11:22Z | - |
dc.citation.number | 1 | ko_KR |
dc.citation.startpage | 1003 | ko_KR |
dc.citation.volume | 21 | ko_KR |
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