Authors
Zihao Ouyang, Yamin Lu, Lei Chen, Yanrong Lai, Pingsen Zhao
Published in
Frontiers in microbiology. Volume 17. Pages 1866146. Epub Jul 15, 2026.
Abstract
Infection remains a leading cause of morbidity and mortality in burn patients, particularly in those with extensive injuries. However, comprehensive analyses integrating pathogen distribution, antimicrobial resistance, and advanced molecular diagnostics across burn severity remain limited.
We retrospectively analyzed 814 burn patients with infections admitted to two tertiary burn centers in southern China between 2020 and 2024, stratified by total body surface area (TBSA). Pathogen distribution, antimicrobial resistance patterns, complications, hospitalization costs, and length of stay were evaluated. In addition, 40 clinical specimens were prospectively analyzed using both conventional culture and targeted next-generation sequencing (t-NGS).
Among 814 infected burn patients stratified by TBSA (<10%, n = 358; 10-49%, n = 292; ≥50%, n = 164), polymicrobial infections rose from 25.7 to 64.4% (p < 0.001), Gram-negative bacteria from 27.1 to 56.6% (p < 0.001; e.g., Acinetobacter baumannii 14.2%, Klebsiella pneumoniae 18.9%), and fungi from 9.0 to 20.6% (p < 0.001; e.g., Candida albicans 5.2%). MDR organisms increased, with A. baumannii >85% resistant to cephalosporins/carbapenems. Severe burns were associated with higher complication rates (shock 70.7%, MODS 29.3%; p < 0.001), 58-day median LOS, and hospitalization costs of 554,246 CNY (p < 0.001). In the 40-specimen pilot diagnostic comparison, t-NGS showed 77.5% positivity and culture showed 55.0% positivity (p = 0.012), with a shorter turnaround time for t-NGS than culture (1.7 vs. 3.9 days; p < 0.001). In blood specimens, t-NGS positivity was 55.6% compared with 16.7% for conventional culture (p = 0.039).
Burn severity is strongly associated with pathogen spectrum and antimicrobial resistance, underscoring the need for severity-stratified management strategies in burn care. In this pilot comparison, t-NGS showed a higher positivity rate than conventional culture and may serve as an adjunct diagnostic method. However, its clinical interpretation must be integrated with phenotypic data given the potential for colonization or genotypic-phenotypic discordance.
PMID:
42528821
Bibliographic data and abstract were imported from PubMed on 30 Jul 2026.
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