<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">JMDS</journal-id><journal-title-group><journal-title>Journal of Medicines Development Sciences</journal-title></journal-title-group><issn>2382-6363</issn><eissn>2382-6371</eissn><publisher><publisher-name>WHIOCE PUBLISHING PTE. LTD.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18063/JMDS.v11i2.2005</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Comparison of the Efficacy of Two Initial Treatment Regimens for Macrolide-Unresponsive Mycoplasma Pneumoniae Pneumonia in Children</title><url>https://artdesignp.com/journal/JMDS/11/2/10.18063/JMDS.v11i2.2005</url><author>LiuShan,WanLinfang</author><pub-date pub-type="publication-year"><year>2026</year></pub-date><volume>11</volume><issue>2</issue><history><date date-type="pub"><published-time>2026-06-23</published-time></date></history><abstract>Objective: To compare the clinical efficacy of two first-line regimens&amp;mdash;azithromycin combined with methylprednisolone versus doxycycline monotherapy&amp;mdash;in the treatment of macrolide-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP) in children.&amp;nbsp;Methods: A retrospective study design was adopted. Children with MUMPP hospitalized in our institution from January 2023 to December 2023 were enrolled and divided according to their initial treatment regimen into Group A (azithromycin + methylprednisolone) and Group B (doxycycline monotherapy). Only cases that achieved clinical cure following the initial regimen were included in the between-group comparative analysis. The adjusted length of hospital stay required for clinical cure, time to effective defervescence, and pulmonary imaging resolution were compared between the two groups. Between-group comparisons were performed using the chi-squared test and the Mann&amp;ndash;Whitney U test.&amp;nbsp;Results: A total of 79 children with MUMPP who responded to treatment and met the discharge criteria for clinical cure were included, comprising 39 in Group A and 40 in Group B. No statistically significant difference in pulmonary imaging findings at discharge was observed between the two groups (P&amp;gt;0.05). The adjusted length of hospital stay was significantly shorter in Group B than in Group A (5 (IQR, 4&amp;ndash;6)&amp;nbsp;days vs.&amp;nbsp;7 (IQR, 6&amp;ndash;9)&amp;nbsp;days,&amp;nbsp;p = 0.005).&amp;nbsp;The time to effective defervescence did not differ significantly between the two groups. No serious adverse events occurred in either group.&amp;nbsp;Conclusion:&amp;nbsp;In children with MUMPP who respond to initial treatment, azithromycin combined with methylprednisolone and doxycycline monotherapy demonstrate comparable efficacy in terms of time to defervescence and final pulmonary imaging resolution; however, doxycycline significantly shortens the length of hospital stay required to achieve clinical cure.</abstract><keywords>Children,Macrolide-unresponsive Mycoplasma pneumoniae pneumonia,Doxycycline,Azithromycin,Methylprednisolone</keywords></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>[1] Diaz MH, Hersh AL, Olson J, et al., 2025, Mycoplasma pneumoniae Infections in Hospitalized Children - United States, 2018-2024. MMWR Morb Mortal Wkly Rep, 74(23): 394-400. DOI:10.15585/mmwr.mm7423a1.
[2] Wang X, Li M, Luo M, et al., 2022, Mycoplasma pneumoniae triggers pneumonia epidemic in autumn and winter in Beijing: a multicentre, population-based epidemiological study between 2015 and 2020. Emerg Microbes Infect, 11(1): 1508-1517. DOI:10.1080/22221751.2022.2078228.
[3] Waites KB, Xiao L, Liu Y, et al., 2017, Mycoplasma pneumoniae from the Respiratory Tract and Beyond. Clin Microbiol Rev, 30(3): 747-809. DOI:10.1128/CMR.00114-16.
[4] Li ZJ, Zhang HY, Ren LL, et al., 2021, Etiological and epidemiological features of acute respiratory infections in China. Nat Commun, 12(1): 5026. DOI:10.1038/s41467-021-25120-6.
[5] Fu C, Mo L, Feng Y,&amp;nbsp;et al., 2025, Detection of Mycoplasma pneumoniae in hospitalized pediatric patients presenting with acute lower respiratory tract infections utilizing targeted next-generation sequencing. Infection, 53(4):1437-1447. DOI:10.1007/s15010-024-02467-8.
[6] Wang J, Wu M, Liu M, et al., 2025, Panoramic quantitative and visualization-based bibliometric analysis of Mycoplasma pneumoniae. Infection. 53: 1699&amp;ndash;1713. DOI:10.1007/s15010-025-02482-3.
[7] Wang YS, Zhou YL, Bai GN, et al., 2024, Expert consensus on the diagnosis and treatment of macrolide-resistant Mycoplasma pneumoniae pneumonia in children. World J Pediatr, 20(9): 901-914. DOI:10.1007/s12519-024-00831-0.
[8] National Health Commission of the People's Republic of China, 2023, Guidelines for the diagnosis and treatment of Mycoplasma pneumoniae pneumonia in children (2023 edition). Int J Epidemiol Infect Dis, 50(2): 79-85.
[9] Prebble K, Marefat L, 2025, Impact of Comprehensive Education on Antibiotic Duration of Therapy for Community-Acquired Pneumonia in a Community Hospital. Hosp Pharm, 61(2): 00185787251390774. DOI:10.1177/00185787251390774.
[10] Nguyen DD, Ho NT, Dover LG, et al., 2024, Novel Variant and Known Mutation in 23S rRNA Gene of Mycoplasma pneumoniae, Northern Vietnam, 2023. Emerg Infect Dis, 30(5): 1034-1036. DOI:10.3201/eid3005.231632.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
