Association of antimicrobial use and incidence of hospital-acquired pneumonia in critically ill trauma patients with pulmonary contusion: an observational study
Associação do uso de antimicrobianos e incidência de pneumonia hospitalar em pacientes graves traumatizados com contusão pulmonar: um estudo observacional☆
Estevão Bassi, Camila Trevizani Merighi, Carlos Issamu Tomizuka, Thais Guimarães, Fernando da Costa Ferreira Novo, Sergio Henrique Bastos Damous, Edivaldo Massazo Utiyama, Luiz Marcelo Sá Malbouisson
Abstract
Background
Pneumonia occurs in about 20% of trauma patients with pulmonary contusions. This study aims to evaluate the association between empirical antibiotic therapy and nosocomial pneumonia in this population.
Methods
Retrospective cohort of adult patients admitted to a trauma-surgical ICU. The Antibiotic Therapy Group (ATG) was defined by intravenous antibiotic use for more than 48 h starting on hospital admission, while the Conservative Group (CG) was determined by antibiotic use no longer than 48 h. Primary outcome was microbiologically documented nosocomial pneumonia within 14 days after hospital admission. Logistic regression was used to estimate the association between group allocation and primary outcome. Exploratory analyses evaluating the association between resistant strains in pneumonia and antibiotic use were performed.
Results
The study included 177 patients with chest trauma and pulmonary contusion on CT scan. ATG were more severely ill than CG, as shown by higher Injury Severity Score, SAPS3, SOFA score, higher rates, and longer duration of mechanical ventilation. In the multivariate analysis, ATG was associated with a lower incidence of primary outcome (OR = 0.25, 95% CI 0.09–0.64; p < 0.01). Similar results were found in the sensitivity analysis with another set of variables. However, each day of antibiotic use was associated with an increased risk of pneumonia by resistant bacteria (OR = 1.18 per day, 95% CI 1.05–1.36; p < 0.01).
Conclusions
Empiric antibiotic therapy was independently associated with lower incidence of nosocomial pneumonia in critically ill patients with pulmonary contusion. However, each day of antibiotic use was associated with increased resistant strains in infected patients.
Keywords
Resumo
Introdução
A pneumonia ocorre em cerca de 20% dos pacientes traumatizados com contusões pulmonares. Este estudo tem como objetivo avaliar a associação entre antibioticoterapia empírica e pneumonia nosocomial nesta população.
Métodos
Coorte retrospectiva de pacientes adultos internados em UTI traumato-cirúrgica. O Grupo Antibiótico (GAT) foi definido pelo uso de antibiótico intravenoso por mais de 48 horas a partir da admissão hospitalar, enquanto o Grupo Conservador (GC) foi determinado pelo uso de antibióticos por período não superior a 48 horas. O desfecho primário foi pneumonia nosocomial documentada microbiologicamente dentro de 14 dias após a admissão hospitalar. A regressão logística foi utilizada para estimar a associação entre a alocação do grupo e o desfecho primário. Foram realizadas análises exploratórias avaliando a associação entre cepas resistentes na pneumonia e uso de antibióticos.
Resultados
O estudo incluiu 177 pacientes com trauma torácico e contusão pulmonar na tomografia computadorizada. O GAT estava mais gravemente doente do que o GC, conforme demonstrado pelo maior Injury Severity Score, SAPS3, pontuação SOFA, taxas mais altas e maior duração da ventilação mecânica. Na análise multivariada, o GAT foi associado a uma menor incidência de desfecho primário (OR = 0,25, IC 95% 0,09–0,64; p < 0,01). Resultados semelhantes foram encontrados na análise de sensibilidade com outro conjunto de variáveis. No entanto, cada dia de uso de antibióticos foi associado a um risco aumentado de pneumonia por bactérias resistentes (OR = 1,18 por dia, IC 95% 1,05–1,36; p < 0,01).
Conclusão
A antibioticoterapia empírica foi independentemente associada à menor incidência de pneumonia nosocomial em pacientes críticos com contusão pulmonar. No entanto, cada dia de uso de antibióticos foi associado ao aumento de cepas resistentes em pacientes infectados.
Palavras-chave
References
1. Cook A, Norwwod S, Berne J. Ventilator-associated pneumonia is more common and of less consequence in trauma patients compared with other critically Ill patients. J Trauma. 2010;69 (5):1083−91.
2. Landeen C, Smith HL. Examination of pneumonia risks and risk levels in trauma patients with pulmonary contusion. J Trauma Nurs. 2014;21:41−9.
3. Kesinger MR, Kumar RG, Wagner AK, et al. Hospital-acquired pneumonia is an independent predictor of poor global outcome in severe traumatic brain injury up to 5 years after discharge. J Trauma Acute Care Surg. 2015;78:396−402.
4. Mangram AJ, Sohn J, Zhou N, et al. Trauma-associated pneumonia: time to redefine ventilator-associated pneumonia in trauma patients. Am J Surg. 2015;210:1056−62. 5. Poole D, Chieregato A, Langer M, et al. Systematic review of the literature and evidence-based recommendations for antibiotic prophylaxis in trauma: results from an Italian Consensus of Experts. PLoS ONE. 2014;9:e113676.
6. Hoth JJ, Franklin GA, Stassen NA, Girard SM, Rodriguez RJ, Rodriguez JL. Prophylactic antibiotics adversely affect nosocomial pneumonia in trauma patients. J Trauma. 2003;55:249−54.
7. Rendeki S, Molnar TF. Pulmonary contusion. J Thorac Dis. 2019;11:S141−51.
8. Hoover L, Bochicchio GV, Napolitano LM, et al. Systemic inflammatory response syndrome and nosocomial infection in trauma. J Trauma. 2006;61:310−7.
9. Kalil AC, Metersky ML, Klompas M, et al. Management of adults with hospital-acquired and ventilator-associated pneumonia: 2016 Clinical Practice Guidelines by the Infectious Diseases Society of America and the American Thoracic Society. Clin Infect Dis. 2016;63:e61−111.
10. Lederer DJ, Bell SC, Branson RD, et al. Control of confounding and reporting of results in causal inference studies. guidance for authors from editors of respiratory, sleep, and critical care journals. Ann Am Thorac Soc. 2019;16:22−8.
11. Wutzler S, Blasius FM, St € ormann P, et al. Pneumonia in severely € injured patients with thoracic trauma: results of a retrospective observational multi-centre study. Scand J Trauma Resusc Emerg Med. 2019;27:31.
12. Ayoub F, Quirke M, Frith D. Use of prophylactic antibiotic in preventing complications for blunt and penetrating chest trauma requiring chest drain insertion: a systematic review and metaanalysis. Trauma Surg Acute Care Open. 2019;4:e000246. 13. R Core Team. R: The R Project for Statistical Computing [Internet]. https://www.R-project.org/. 2022. Available from: http://www.R-project.org.
14. Tejada Artigas A, Bello Dronda S, Chacon Vall es E, et al. Risk factors for nosocomial pneumonia in critically ill trauma patients. Crit Care Med. 2001;29:304−9.
15. Salomao MC, Guimar ~ aes T, Duailibi DF, et al. Carbapenem-resis- ~ tant Enterobacteriaceae in patients admitted to the emergency department: prevalence, risk factors, and acquisition rate. J Hosp Infect. 2017;97:241−6. 16. Skjøt-Arkil H, Mogensen CB, Lassen AT, et al. Carrier prevalence and risk factors for colonisation of multiresistant bacteria in Danish emergency departments: a cross-sectional survey. BMJ Open. 2019;9:e029000.
17. Baggs J, Jernigan JA, Halpin AL, Epstein L, Hatfield KM, McDonald LC. Risk of Subsequent Sepsis Within 90 Days After a Hospital Stay by Type of Antibiotic Exposure. Clin Infect Dis. 2017;66:1004−12.
18. Chastre J, Trouillet J, Combes A, Luyt C. Diagnostic techniques and procedures for establishing the microbial etiology of ventilator-associated pneumonia for clinical trials: the pros for quantitative cultures. Clin Infect Dis. 2010;51:S88−92.
19. Loftus TJ, Brakenridge SC, Moore FA, et al. Intubated trauma patients receiving prolonged antibiotics for pneumonia despite negative cultures: predictors and outcomes. Surg Infect (Larchmt). 2016;17:766−72.
20. Haverkate MR, Weiner S, Lolans K, et al. Duration of colonization with klebsiella pneumoniae carbapenemase-producing bacteria at long-term acute care hospitals in Chicago, Illinois. Open Forum Infect Dis. 2016;3:ofw178.
Submitted date:
12/01/2022
Accepted date:
07/21/2023