TY - JOUR
T1 - The epidemiology, clinical characteristics, and macrolide susceptibility of Mycoplasma pneumoniae pneumonia in children in Southern Taiwan, 2019–2020
AU - Taiwan Pediatric Infectious Disease Alliance (TPIDA)
AU - Kuo, Cheng Yen
AU - Tsai, Wei Chun
AU - Lee, Hui Feng
AU - Ho, Tzong Shiann
AU - Huang, Li Min
AU - Shen, Ching Fen
AU - Liu, Ching Chuan
N1 - Funding Information:
This study was supported by grants from the Ministry of Science and Technology, Taiwan. (MOST107-2314-B-002-168) and National Health Research Institutes, Taiwan (10A1-PDSP01-014). The funder had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
This study was supported by grants from the Ministry of Science and Technology, Taiwan . ( MOST107-2314-B-002-168 ) and National Health Research Institutes, Taiwan ( 10A1-PDSP01-014 ). The funder had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2021
PY - 2022/8
Y1 - 2022/8
N2 - Background: Since the global use of the pneumococcal conjugate vaccine, Mycoplasma pneumoniae (MP) has become the most common bacterial cause of lower respiratory tract infections among children. Monitoring the changing epidemiology and antimicrobial resistance rates of this organism is important for MP clinical management. Methods: This study characterizes key features of MP during the 2019–2020 epidemic in children in Taiwan. The cohort included all hospitalized children under 18 years of age with polymerase chain reaction (PCR)-confirmed community-acquired mycoplasma pneumonia (CAMP) in southern Taiwan. Macrolide resistance was identified by mutations in domain V of MP 23S rRNA. Severe disease referred to symptoms warranting oxygen therapy, septic shock, or intensive care unit admission. Results: Among 495 LRTI patients, 195 (39.4%) had CAMP, of which 106 (54.4%) had concurrent serological evidence of MP infection. The diagnostic sensitivity of IgM in the acute phase was 65.6%. CAMP case numbers were highest from July 2019 to January 2020. The most common clinical presentations of CAMP were fever (99.0%), cough (99.0%), and coryza (31.8%). Despite a high rate of macrolide resistance (88.1%), macrolide-resistant MP (MRMP) did not differ from macrolide-sensitive MP (MSMP) in clinical course or severity. Delayed administration of effective antimicrobial treatment was also associated with severe disease (p < 0.05). Conclusion: Early diagnosis and determination of MRMP are needed for effective management of MP infection.
AB - Background: Since the global use of the pneumococcal conjugate vaccine, Mycoplasma pneumoniae (MP) has become the most common bacterial cause of lower respiratory tract infections among children. Monitoring the changing epidemiology and antimicrobial resistance rates of this organism is important for MP clinical management. Methods: This study characterizes key features of MP during the 2019–2020 epidemic in children in Taiwan. The cohort included all hospitalized children under 18 years of age with polymerase chain reaction (PCR)-confirmed community-acquired mycoplasma pneumonia (CAMP) in southern Taiwan. Macrolide resistance was identified by mutations in domain V of MP 23S rRNA. Severe disease referred to symptoms warranting oxygen therapy, septic shock, or intensive care unit admission. Results: Among 495 LRTI patients, 195 (39.4%) had CAMP, of which 106 (54.4%) had concurrent serological evidence of MP infection. The diagnostic sensitivity of IgM in the acute phase was 65.6%. CAMP case numbers were highest from July 2019 to January 2020. The most common clinical presentations of CAMP were fever (99.0%), cough (99.0%), and coryza (31.8%). Despite a high rate of macrolide resistance (88.1%), macrolide-resistant MP (MRMP) did not differ from macrolide-sensitive MP (MSMP) in clinical course or severity. Delayed administration of effective antimicrobial treatment was also associated with severe disease (p < 0.05). Conclusion: Early diagnosis and determination of MRMP are needed for effective management of MP infection.
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U2 - 10.1016/j.jmii.2021.09.010
DO - 10.1016/j.jmii.2021.09.010
M3 - Article
C2 - 34688576
AN - SCOPUS:85118320451
SN - 1684-1182
VL - 55
SP - 611
EP - 619
JO - Journal of Microbiology, Immunology and Infection
JF - Journal of Microbiology, Immunology and Infection
IS - 4
ER -