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Factors Associated With Treatment Failure in Moderately Severe Community-Acquired Pneumonia: A Secondary Analysis of a Randomized Clinical Trial.
Dinh, Aurélien; Duran, Clara; Ropers, Jacques; Bouchand, Frédérique; Davido, Benjamin; Deconinck, Laurène; Matt, Morgan; Senard, Olivia; Lagrange, Aurore; Mellon, Guillaume; Calin, Ruxandra; Makhloufi, Sabrina; de Lastours, Victoire; Mathieu, Emmanuel; Kahn, Jean-Emmanuel; Rouveix, Elisabeth; Grenet, Julie; Dumoulin, Jennifer; Chinet, Thierry; Pépin, Marion; Delcey, Véronique; Diamantis, Sylvain; Benhamou, Daniel; Vitrat, Virginie; Dombret, Marie-Christine; Guillemot, Didier; Renaud, Bertrand; Claessens, Yann-Erick; Labarère, José; Aegerter, Philippe; Bedos, Jean-Pierre; Crémieux, Anne-Claude.
Afiliação
  • Dinh A; Infectious Diseases Unit, Raymond-Poincaré University Hospital, Assistance Publique-Hôpitaux de Paris (APHP) Paris Saclay University, Garches, France.
  • Duran C; Epidemiology and Modeling of Bacterial Evasion to Antibacterials Unit, Institut Pasteur, Paris, France.
  • Ropers J; Infectious Diseases Unit, Raymond-Poincaré University Hospital, Assistance Publique-Hôpitaux de Paris (APHP) Paris Saclay University, Garches, France.
  • Bouchand F; Clinical Research Unit, Pitié-Salpétrière University Hospital, APHP, Paris, France.
  • Davido B; Pharmacy Department, Raymond-Poincaré University Hospital, APHP Paris Saclay, Garches, France.
  • Deconinck L; Infectious Diseases Unit, Raymond-Poincaré University Hospital, Assistance Publique-Hôpitaux de Paris (APHP) Paris Saclay University, Garches, France.
  • Matt M; Infectious Disease Department, Bichat University Hospital, APHP, University of Paris, Paris, France.
  • Senard O; Infectious Diseases Unit, Raymond-Poincaré University Hospital, Assistance Publique-Hôpitaux de Paris (APHP) Paris Saclay University, Garches, France.
  • Lagrange A; Infectious Disease Department, Marne La Vallée Hospital, Grand Hôpital de l'Est Francilien, Marne La Vallée, France.
  • Mellon G; Pneumology Department, Pontoise Hospital, Pontoise, France.
  • Calin R; Infectious Diseases Unit, Raymond-Poincaré University Hospital, Assistance Publique-Hôpitaux de Paris (APHP) Paris Saclay University, Garches, France.
  • Makhloufi S; Infectious Diseases Unit, Raymond-Poincaré University Hospital, Assistance Publique-Hôpitaux de Paris (APHP) Paris Saclay University, Garches, France.
  • de Lastours V; Infectious Diseases Unit, Raymond-Poincaré University Hospital, Assistance Publique-Hôpitaux de Paris (APHP) Paris Saclay University, Garches, France.
  • Mathieu E; Internal Medicine, Beaujon University Hospital, APHP, Clichy, France.
  • Kahn JE; Emergency Medicine, Foch Hospital, Suresnes, France.
  • Rouveix E; Internal Medicine, Ambroise-Paré University Hospital, APHP Paris Saclay, Boulogne-Billancourt, France.
  • Grenet J; Internal Medicine, Ambroise-Paré University Hospital, APHP Paris Saclay, Boulogne-Billancourt, France.
  • Dumoulin J; Emergency Medicine, Ambroise-Paré University Hospital, APHP Paris Saclay, Boulogne-Billancourt, France.
  • Chinet T; Pneumology Department, Ambroise-Paré University Hospital, APHP Paris Saclay, Boulogne-Billancourt, France.
  • Pépin M; Pneumology Department, Ambroise-Paré University Hospital, APHP Paris Saclay, Boulogne-Billancourt, France.
  • Delcey V; Geriatric Department, Ambroise-Paré University Hospital, APHP Paris Saclay, Boulogne-Billancourt, France.
  • Diamantis S; Internal Medicine, Lariboisière University Hospital, APHP, Paris, France.
  • Benhamou D; Infectious Disease Department, Melun Hospital, Melun, France.
  • Vitrat V; Pneumology Department, Rouen University Hospital, Rouen, France.
  • Dombret MC; Infectious Disease, Annecy Hospital, Annecy, France.
  • Guillemot D; Pneumology Department, Bichat University Hospital, APHP, Paris, France.
  • Renaud B; Epidemiology and Modeling of Bacterial Evasion to Antibacterials Unit, Institut Pasteur, Paris, France.
  • Claessens YE; Emergency Department, Cochin University Hospital, APHP, Paris, France.
  • Labarère J; Emergency Department, Princesse Grace University Hospital, Monaco, France.
  • Aegerter P; Quality of Care Unit, Grenoble University Hospital, Grenoble Alpes University, Grenoble, France.
  • Bedos JP; UMRS 1168 VIMA, INSERM, Versailles Saint-Quentin University, Versailles, France.
  • Crémieux AC; Intensive Care Unit, Le Chesnay Hospital, Versailles, France.
JAMA Netw Open ; 4(10): e2129566, 2021 10 01.
Article em En | MEDLINE | ID: mdl-34652445
Importance: Failure of treatment is the most serious complication in community-acquired pneumonia (CAP). Objective: To assess the potential risk factors for treatment failure in clinically stable patients with CAP. Design, Setting, and Participants: This secondary analysis assesses data from a randomized clinical trial on CAP (Pneumonia Short Treatment [PTC] trial) conducted from December 19, 2013, to February 1, 2018. Data analysis was performed from July 18, 2019, to February 15, 2020. Patients hospitalized at 1 of 16 centers in France for moderately severe CAP who were clinically stable at day 3 of antibiotic treatment were included in the PTC trial and analyzed in the per-protocol trial population. Interventions: Patients were randomly assigned (1:1) on day 3 of antibiotic treatment to receive ß-lactam (amoxicillin-clavulanate [1 g/125 mg] 3 times daily) or placebo for 5 extra days. Main Outcomes and Measures: The main outcome was failure at 15 days after first antibiotic intake, defined as a temperature greater than 37.9 °C and/or absence of resolution or improvement of respiratory symptoms and/or additional antibiotic treatment for any cause. The association among demographic characteristics, baseline clinical and biological variables available (ie, at the first day of ß-lactam treatment), and treatment failure at day 15 among the per-protocol trial population was assessed by univariate and multivariable logistic regressions. Results: Overall, 310 patients were included in the study; this secondary analysis comprised 291 patients (174 [59.8%] male; mean [SD] age, 69.6 [18.5] years). The failure rate was 26.8%. Male sex (odds ratio [OR], 1.74; 95% CI, 1.01-3.07), age per year (OR, 1.03; 95% CI, 1.01-1.05), Pneumonia Severe Index score (OR, 1.01; 95% CI, 1.00-1.02), the presence of chronic lung disease (OR, 1.85; 95% CI, 1.03-3.30), and creatinine clearance (OR, 0.99; 95% CI, 0.98-1.00) were significantly associated with failure in the univariate analysis. When the Pneumonia Severe Index score was excluded to avoid collinearity with age and sex in the regression model, only male sex (OR, 1.92; 95% CI, 1.08-3.49) and age (OR, 1.02; 95% CI, 1.00-1.05) were associated with failure in the multivariable analysis. Conclusions and Relevance: In this secondary analysis of a randomized clinical trial, among patients with CAP who reached clinical stability after 3 days of antibiotic treatment, only male sex and age were associated with higher risk of failure, independent of antibiotic treatment duration and biomarker levels. Another randomized clinical trial is needed to evaluate the impact of treatment duration in populations at higher risk for treatment failure.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Falha de Tratamento Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Falha de Tratamento Tipo de estudo: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article