Effect of antibiotic therapy on the prognosis of ventilator-associated pneumonia caused by Stenotrophomonas maltophilia.

Antibiotic therapy Outcome Stenotrophomonas maltophilia Ventilator-associated pneumonia

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
26 Nov 2021
Historique:
received: 04 06 2021
accepted: 12 11 2021
entrez: 26 11 2021
pubmed: 27 11 2021
medline: 27 11 2021
Statut: epublish

Résumé

Ventilator-associated pneumonia (VAP) caused by Stenotrophomonas maltophilia is poorly described in the literature. However, it has been shown to be associated with increased morbidity and mortality. Probabilistic antibiotic therapy against S. maltophilia is often ineffective as this pathogen is resistant to many antibiotics. There is no consensus at present on the best therapeutic strategy to adopt (class of antibiotics, antibiotic combination, dosage, treatment duration). The aim of this study was to evaluate the effect of antibiotic therapy strategy on the prognosis of patients with VAP caused by S. maltophilia. This retrospective study evaluated all consecutive patients who developed VAP caused by S. maltophilia between 2010 and 2018 while hospitalized in the intensive care unit (ICU) of a French university hospital in Reunion Island, in the Indian Ocean region. A total of 130 patients with a median Simplified Acute Physiology Score II of 58 [43-73] had VAP caused by S. maltophilia after a median duration of mechanical ventilation of 12 [5-18] days. Ventilator-associated pneumonia was polymicrobial in 44.6% of cases, and ICU mortality was 50.0%. After multivariate Cox regression analysis, the factors associated with increased ICU mortality were older age (hazard ratio (HR): 1.03; 95% CI 1.01-1.04, p = 0.001) and high Sequential Organ Failure Assessment score on the day of VAP onset (HR: 1.08; 95% CI 1.03-1.14, p = 0.002). Appropriate antibiotic therapy, and in particular trimethoprim-sulfamethoxazole, was associated with decreased ICU mortality (HR: 0.42; 95% CI 0.24-0.74, p = 0.003) and decreased hospital mortality (HR: 0.47; 95% CI 0.28-0.79, p = 0.04). Time to start of appropriate antibiotic therapy, combination therapy, and duration of appropriate antibiotic therapy had no effect on ICU mortality (p > 0.5). In our study, appropriate antibiotic therapy, and in particular trimethoprim-sulfamethoxazole, was associated with decreased ICU and hospital mortality in patients with VAP caused by S. maltophilia.

Sections du résumé

BACKGROUND BACKGROUND
Ventilator-associated pneumonia (VAP) caused by Stenotrophomonas maltophilia is poorly described in the literature. However, it has been shown to be associated with increased morbidity and mortality. Probabilistic antibiotic therapy against S. maltophilia is often ineffective as this pathogen is resistant to many antibiotics. There is no consensus at present on the best therapeutic strategy to adopt (class of antibiotics, antibiotic combination, dosage, treatment duration). The aim of this study was to evaluate the effect of antibiotic therapy strategy on the prognosis of patients with VAP caused by S. maltophilia.
RESULTS RESULTS
This retrospective study evaluated all consecutive patients who developed VAP caused by S. maltophilia between 2010 and 2018 while hospitalized in the intensive care unit (ICU) of a French university hospital in Reunion Island, in the Indian Ocean region. A total of 130 patients with a median Simplified Acute Physiology Score II of 58 [43-73] had VAP caused by S. maltophilia after a median duration of mechanical ventilation of 12 [5-18] days. Ventilator-associated pneumonia was polymicrobial in 44.6% of cases, and ICU mortality was 50.0%. After multivariate Cox regression analysis, the factors associated with increased ICU mortality were older age (hazard ratio (HR): 1.03; 95% CI 1.01-1.04, p = 0.001) and high Sequential Organ Failure Assessment score on the day of VAP onset (HR: 1.08; 95% CI 1.03-1.14, p = 0.002). Appropriate antibiotic therapy, and in particular trimethoprim-sulfamethoxazole, was associated with decreased ICU mortality (HR: 0.42; 95% CI 0.24-0.74, p = 0.003) and decreased hospital mortality (HR: 0.47; 95% CI 0.28-0.79, p = 0.04). Time to start of appropriate antibiotic therapy, combination therapy, and duration of appropriate antibiotic therapy had no effect on ICU mortality (p > 0.5).
CONCLUSION CONCLUSIONS
In our study, appropriate antibiotic therapy, and in particular trimethoprim-sulfamethoxazole, was associated with decreased ICU and hospital mortality in patients with VAP caused by S. maltophilia.

Identifiants

pubmed: 34825962
doi: 10.1186/s13613-021-00950-1
pii: 10.1186/s13613-021-00950-1
pmc: PMC8626555
doi:

Types de publication

Journal Article

Langues

eng

Pagination

160

Informations de copyright

© 2021. The Author(s).

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Auteurs

Bérénice Puech (B)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France. berenice.puech@gmail.com.

Clémence Canivet (C)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Laura Teysseyre (L)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Guillaume Miltgen (G)

Service de Microbiologie, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.
UMR Processus Infectieux en Milieu Insulaire Tropical (PIMIT), CNRS 9192, INSERM U1187, IRD 249, Université de La Réunion, Saint-Denis, France.

Thomas Aujoulat (T)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Margot Caron (M)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Chloé Combe (C)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Julien Jabot (J)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Olivier Martinet (O)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Jerome Allyn (J)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.
Département d'Informatique Clinique, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Cyril Ferdynus (C)

Département d'Informatique Clinique, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Nicolas Allou (N)

Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.
Département d'Informatique Clinique, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.

Classifications MeSH