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Peer-reviewedCC BYAntibiotics (Basel, Switzerland)

Divergent Organism-Specific Trajectories of Multidrug Resistance Across the COVID-19 Pandemic: An Interrupted Time-Series Study in a Mexican Tertiary Hospital, 2017-Early 2026.

9 affiliations
  1. 1División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS), Sierra Mojada 800, Colonia Independencia, Guadalajara 44340, Jalisco, Mexico.
  2. 2Programa de Doctorado en Ciencias en Biomédicas, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara 44340, Jalisco, Mexico.
  3. 3División de Medicina, Antiguo Hospital Civil de Guadalajara "Fray Antonio Alcalde", Calle Hospital 278, Centro Barranquitas, Guadalajara 44280, Jalisco, Mexico.
  4. 4Urgencias Adultos, Hospital Civil de Guadalajara "Fray Antonio Alcalde", Calle Hospital 278, Centro Barranquitas, Guadalajara 44340, Jalisco, Mexico.
  5. 5Unidad de Investigación Epidemiológica y en Servicios de Salud, Instituto Mexicano del Seguro Social (IMSS), Guadalajara 44340, Jalisco, Mexico.
  6. 6Laboratorio de Microbiología, Antiguo Hospital Civil de Guadalajara "Fray Antonio Alcalde", Calle Hospital 278, Centro Barranquitas, Guadalajara 44280, Jalisco, Mexico.
  7. 7Departamento de Disciplinas Filosófico, Metodológicas e Instrumentales, Instituto de Investigación de Recursos Humanos en Salud, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara 44340, Jalisco, Mexico.
  8. 8Departamento de Disciplinas Especializadas I, Decanato de Ciencias de la Salud, Universidad Autónoma de Guadalajara, Av. Patria 1201, Guadalajara 45129, Jalisco, Mexico.
  9. 9Unidad de Vigilancia Epidemiológica y Medicina Preventiva, Antiguo Hospital Civil de Guadalajara "Fray Antonio Alcalde", Calle Hospital 278, Centro Barranquitas, Guadalajara 44280, Jalisco, Mexico.

Abstract

Background/Objectives: Whether the COVID-19 pandemic uniformly increased antimicrobial resistance (AMR) is contested, and aggregate analyses may mask organism-specific patterns. The objective of the study was to characterize changes in the level and slope of monthly multidrug-resistant (MDR), possible extensively drug-resistant (pXDR), possible pandrug-resistant (pPDR), vancomycin-resistant enterococci (VRE), and methicillin-resistant Staphylococcus aureus (MRSA) positivity at a Mexican tertiary-care hospital, and to assess heterogeneity by organism, antimicrobial class, specimen type, and hospital service. Methods: Retrospective interrupted time-series of deduplicated bacterial isolates (October 2017 to January 2026), analyzed by segmented regression across pre-pandemic, pandemic, and post-peak phases. Results: Cohort-wide MDR positivity had been declining before 2020 and rose abruptly at pandemic onset (level shift +6.81 percentage points, p = 0.0092) with a simultaneous slope reversal, reaching 24.27 percentage points above the extrapolated pre-pandemic trend by February 2022 (95% CI 14.26-34.28, p < 0.0001). The decline resumed after the pandemic peak, but the two slope changes did not offset one another (joint p = 0.0064). pXDR and pPDR moved in the same direction (+8.93, p = 0.0233; +15.40, p = 0.0113). VRE showed no significant departure, whereas MRSA declined in every phase yet departed significantly from its extrapolated trajectory (+23.68, p = 0.0040). Among species, Escherichia coli showed the largest departure from its counterfactual (+48.82 percentage points, p < 0.0001) and Klebsiella pneumoniae had the largest abrupt level rise (+14.46 percentage points, p = 0.0055), while S. aureus declined in every phase despite an abrupt rise in level at pandemic onset. At the class level, carbapenem and third-/fourth-generation cephalosporin non-susceptibility rose at pandemic onset and returned to baseline afterwards (19.1% to 28.0% to 18.7%, and 51.7% to 59.4% to 52.5%; all q < 0.001), whereas fluoroquinolone non-susceptibility rose and did not revert, climbing further in E. coli (61.5% to 65.2% to 72.7%, q = 0.0012) and plateauing at an elevated level in K. pneumoniae (37.6% to 46.5% to 49.3%, q = 0.1919 post-peak). Conclusions: Resistance trajectories across pandemic-related phases were divergent and, for the Gram-negative organisms, incompletely reversed, with the highest burden of advanced resistance in high-intensity settings. Organism-resolved surveillance and sustained stewardship are needed.

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BibTeX
@article{garciagomez2026divergent,
  title = {{Divergent Organism-Specific Trajectories of Multidrug Resistance Across the COVID-19 Pandemic: An Interrupted Time-Series Study in a Mexican Tertiary Hospital, 2017-Early 2026.}},
  author = {Jesús García-Gómez and Mauricio Alfredo Ambriz-Alarcón and Brian Rafael Rubio-Mora and Luis Felipe Jave-Suárez and Adriana Aguilar-Lemarroy and María Martha Villaseñor-García and Georgina Hernández-Flores and María Concepción Rodríguez-Lora and Teresita De Jesús Hernández-Flores and Liliana Iñiguez-Gutiérrez and Luis Eduardo Del Moral-Trinidad and Anibal Samael Méndez-Clemente},
  journal = {Antibiotics (Basel, Switzerland)},
  year = {2026},
  month = oct,
  doi = {10.3390/antibiotics15101005},
  url = {https://europepmc.org/article/MED/42938746},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Divergent Organism-Specific Trajectories of Multidrug Resistance Across the COVID-19 Pandemic: An Interrupted Time-Series Study in a Mexican Tertiary Hospital, 2017-Early 2026.
AU  - Jesús García-Gómez
AU  - Mauricio Alfredo Ambriz-Alarcón
AU  - Brian Rafael Rubio-Mora
AU  - Luis Felipe Jave-Suárez
AU  - Adriana Aguilar-Lemarroy
AU  - María Martha Villaseñor-García
AU  - Georgina Hernández-Flores
AU  - María Concepción Rodríguez-Lora
AU  - Teresita De Jesús Hernández-Flores
AU  - Liliana Iñiguez-Gutiérrez
AU  - Luis Eduardo Del Moral-Trinidad
AU  - Anibal Samael Méndez-Clemente
PY  - 2026
DA  - 2026/10/10
JO  - Antibiotics (Basel, Switzerland)
DO  - 10.3390/antibiotics15101005
UR  - https://europepmc.org/article/MED/42938746
AB  - Background/Objectives: Whether the COVID-19 pandemic uniformly increased antimicrobial resistance (AMR) is contested, and aggregate analyses may mask organism-specific patterns. The objective of the study was to characterize changes in the level and slope of monthly multidrug-resistant (MDR), possible extensively drug-resistant (pXDR), possible pandrug-resistant (pPDR), vancomycin-resistant enterococci (VRE), and methicillin-resistant Staphylococcus aureus (MRSA) positivity at a Mexican tertiary-care hospital, and to assess heterogeneity by organism, antimicrobial class, specimen type, and hospital service. Methods: Retrospective interrupted time-series of deduplicated bacterial isolates (October 2017 to January 2026), analyzed by segmented regression across pre-pandemic, pandemic, and post-peak phases. Results: Cohort-wide MDR positivity had been declining before 2020 and rose abruptly at pandemic onset (level shift +6.81 percentage points, p = 0.0092) with a simultaneous slope reversal, reaching 24.27 percentage points above the extrapolated pre-pandemic trend by February 2022 (95% CI 14.26-34.28, p < 0.0001). The decline resumed after the pandemic peak, but the two slope changes did not offset one another (joint p = 0.0064). pXDR and pPDR moved in the same direction (+8.93, p = 0.0233; +15.40, p = 0.0113). VRE showed no significant departure, whereas MRSA declined in every phase yet departed significantly from its extrapolated trajectory (+23.68, p = 0.0040). Among species, Escherichia coli showed the largest departure from its counterfactual (+48.82 percentage points, p < 0.0001) and Klebsiella pneumoniae had the largest abrupt level rise (+14.46 percentage points, p = 0.0055), while S. aureus declined in every phase despite an abrupt rise in level at pandemic onset. At the class level, carbapenem and third-/fourth-generation cephalosporin non-susceptibility rose at pandemic onset and returned to baseline afterwards (19.1% to 28.0% to 18.7%, and 51.7% to 59.4% to 52.5%; all q < 0.001), whereas fluoroquinolone non-susceptibility rose and did not revert, climbing further in E. coli (61.5% to 65.2% to 72.7%, q = 0.0012) and plateauing at an elevated level in K. pneumoniae (37.6% to 46.5% to 49.3%, q = 0.1919 post-peak). Conclusions: Resistance trajectories across pandemic-related phases were divergent and, for the Gram-negative organisms, incompletely reversed, with the highest burden of advanced resistance in high-intensity settings. Organism-resolved surveillance and sustained stewardship are needed.
SN  - 2079-6382
ER  -