Evidence map›Paper›PMID 42559097›Full record

ArticleFrontiers in cellular and infection microbiology2026

Efficacy and short-term safety of intravenous omadacycline as second-line therapy for macrolide- unresponsive Mycoplasma pneumoniae pneumonia in children: a retrospective cohort study.

Yang Yu, Tingting Zhang, Yu Xia, Yao Sun

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Article in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yang YuDepartment of Pediatrics, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, China.
Tingting ZhangDepartment of Pediatrics, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, China.
Yu XiaDepartment of Pediatrics, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, China.
Yao SunDepartment of Pediatrics, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate the efficacy and short-term safety of omadacycline as second-line therapy for macrolide-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP) in children aged 8-16 years. Methods: A total of 64 hospitalized children with MUMPP admitted between September 2023 and December 2024 were enrolled. Children with persistent fever (>38.0 °C) after 72 hours of azithromycin monotherapy were assigned to receive intravenous omadacycline (n=18) or continued azithromycin (n=46). Omadacycline was dosed according to body surface area (BSA)-based scaling from the approved adult regimen (loading dose on day 1; maintenance dose once daily for 7 days). Primary outcome: time to defervescence (TTD). Secondary outcomes: 72-hour defervescence rate, radiological improvement, corticosteroid use, and adverse events. Three-month follow-up included dental examinations. Results: Omadacycline achieved shorter TTD than continued macrolides (50.78 ± 20.71 vs. 72.46 ± 25.61 hours; P = 0.002) and higher 72-hour defervescence rate (55.6% vs. 26.1%; P = 0.026). On multivariate linear regression, continued macrolide therapy (B = 13.43 h, 95% CI: 2.02-24.84, P = 0.022), positive 23S rRNA mutation status (B = 20.85 h, 95% CI: 10.94-30.77, P<0.001), and systemic corticosteroid use (B = 21.21 h, 95% CI: 10.79-31.62, P<0.001) were independently associated with prolonged TTD. No significant difference was observed in radiological improvement (P = 0.668). Corticosteroid requirement was significantly lower in the omadacycline group than in the macrolide group (27.8% vs. 67.4%; P = 0.004). Adverse events were comparable (5.6% vs. 8.7%; P = 0.645). At 3-month follow-up, no clinically significant changes were observed in hematological indices, hepatic or renal function, or cardiac enzyme profiles, and dental examination revealed no discoloration or enamel hypoplasia in any patient. Conclusion: In this retrospective cohort, omadacycline as second-line therapy was associated with significantly faster fever resolution than continued macrolide treatment, with acceptable short-term safety profiles over a 3-month follow-up. Prospective randomized trials are needed to confirm these findings.

Indexed as

Anti-Bacterial AgentsMacrolidesMycoplasma pneumoniaePneumonia, MycoplasmaTetracyclinesAdministration, IntravenousAdolescentAzithromycinChildDrug Resistance, BacterialFemaleHumansMaleRetrospective StudiesTreatment OutcomeAnti-Bacterial AgentsAzithromycinMacrolidesomadacyclineTetracyclinescommunity-acquired pneumoniamacrolide resistancemacrolide-unresponsive pneumoniaMycoplasma pneumoniaeomadacyclinepediatric pneumoniatetracyclines

Identifiers

PMID42559097
PMCPMC13439457

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.