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Treatment of severe hospital-acquired and ventilator-associated pneumonia: a systematic review of inclusion and judgment criteria used in randomized controlled trials.
Weiss, Emmanuel; Essaied, Wafa; Adrie, Christophe; Zahar, Jean-Ralph; Timsit, Jean-François.
Afiliação
  • Weiss E; Department of Anesthesiology and Critical Care, HUPNVS, Hôpital Beaujon, APHP, 92110, Clichy, France. emmanuel.weiss@aphp.fr.
  • Essaied W; Paris Diderot University, Paris, France. emmanuel.weiss@aphp.fr.
  • Adrie C; Inserm UMR_S 1149 Center for Research On Inflammation Inserm/University Paris Diderot, Sorbonne Paris Cité, F-75018, Paris, France. emmanuel.weiss@aphp.fr.
  • Zahar JR; UMR 1137 - IAME Team 5 - DeSCID: Decision SCiences in Infectious Diseases, control and care Inserm/University Paris Diderot, Sorbonne Paris Cité, F-75018, Paris, France.
  • Timsit JF; Physiology Department, APHP, Hôpital Cochin, Paris, France.
Crit Care ; 21(1): 162, 2017 Jun 27.
Article em En | MEDLINE | ID: mdl-28655326
ABSTRACT

BACKGROUND:

Hospital-acquired and ventilator-associated pneumonia (HAP/VAP) are often selected for randomized clinical trials (RCTs) aiming at new drug approval. Guidelines for the design of such RCTs have been repeatedly updated by regulatory agencies. We hypothesized that large variability in the enrolled populations, the endpoints assessed and the HAP/VAP definition criteria may impact the results of these studies, and addressed this through a systematic review of HAP/VAP RCTs.

METHODS:

A search (Pubmed-Embase-ICAAC-ECCMID) of all RCTs published between 1994 and 2016 comparing antimicrobial treatment for HAP/VAP in the intensive care unit was conducted. The populations enrolled, inclusion/exclusion criteria, statistical design and endpoints assessed were recorded. All unpublished RCTs recorded on the ClinicalTrials.gov registry were also screened.

RESULTS:

From the 93 abstracts reviewed, 39 potentially relevant studies were inspected, leading to 27 studies being included. As expected, illness severity or the proportion with VAP (27-100%) differed greatly among the enrolled populations. The HAP/VAP definition used various clinical and biological criteria, and only 55% of studies required a microbiological sample. The mandatory duration of prior hospital stay was variable; the mechanical ventilation duration was an inclusion criterion in only 41% of VAP studies. Nine studies had non-inferiority design, but nine studies (33%) did not have a pre-specified statistical hypothesis. Clinical cure was the primary endpoint in 24 studies, but was recorded in several populations or as the co-primary endpoint in 13 studies. The definition of clinical cure and the timing of its assessment greatly differed. This variability slightly improved over time but remained significant in the 13 registered but currently unpublished RCTs that we screened.

CONCLUSION:

Our study provides a description of populations and endpoints of RCTs evaluating antimicrobials for treatment of HAP/VAP in the ICU. There was significant heterogeneity in enrollment criteria, endpoints and statistical design, which may influence the ability of studies to demonstrate differences between studied drugs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Infecção Hospitalar / Pneumonia Associada à Ventilação Mecânica Tipo de estudo: Clinical_trials / Guideline / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Crit Care Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Controlados Aleatórios como Assunto / Infecção Hospitalar / Pneumonia Associada à Ventilação Mecânica Tipo de estudo: Clinical_trials / Guideline / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Crit Care Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França