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Description, clinical impact and early outcome of S. maltophilia respiratory tract infections after lung transplantation, A retrospective observational study.
Pilmis, Benoît; Rouzaud, Claire; To-Puzenat, Deborah; Gigandon, Anne; Dauriat, Gaelle; Feuillet, Séverine; Mitilian, Delphine; Issard, Justin; Monnier, Alban Le; Lortholary, Olivier; Fadel, Elie; Le Pavec, Jérôme.
Afiliação
  • Pilmis B; Equipe Mobile de Microbiologie Clinique, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France; Institut Micalis UMR 1319, Université Paris-Saclay, INRAe Châtenay Malabry, AgroParisTech, Domaine de Vilvert 75352 Jouy-en-Josas, France. Electronic a
  • Rouzaud C; Equipe Mobile de Microbiologie Clinique, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France; Service de Maladies infectieuses et Tropicales, Hôpital Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Université de Pari
  • To-Puzenat D; Equipe Mobile de Microbiologie Clinique, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France.
  • Gigandon A; Service de Microbiologie Clinique, Plateforme de dosage des anti-infectieux, Hôpitaux Saint-Joseph et Marie-Lannelongue, 185 rue Raymond Losserand, 75014, Paris, France.
  • Dauriat G; Service de Pneumologie et Transplantation Pulmonaire, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France.
  • Feuillet S; Service de Pneumologie et Transplantation Pulmonaire, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France.
  • Mitilian D; Service de chirurgie thoracique et Transplantation Pulmonaire, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France.
  • Issard J; Service de chirurgie thoracique et Transplantation Pulmonaire, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France.
  • Monnier AL; Institut Micalis UMR 1319, Université Paris-Saclay, INRAe Châtenay Malabry, AgroParisTech, Domaine de Vilvert 75352 Jouy-en-Josas, France; Service de Microbiologie Clinique, Plateforme de dosage des anti-infectieux, Hôpitaux Saint-Joseph et Marie-Lannelongue, 185 rue Raymond Losserand, 75014, Paris,
  • Lortholary O; Service de Maladies infectieuses et Tropicales, Hôpital Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Université de Paris, 149 rue de Sèvre, 75015 Paris, France.
  • Fadel E; Service de chirurgie thoracique et Transplantation Pulmonaire, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France; Université Paris-Saclay, Faculté de Médecine, 63 rue Gabriel Péri, 94270 Le Kremlin Bicêtre, France; INSERM UMR_S 999, Hôpital Ma
  • Le Pavec J; Service de Pneumologie et Transplantation Pulmonaire, Hôpitaux Saint-Joseph et Marie-Lannelongue, 133 avenue de la Résistance, 92350 Le Plessis-Robinson, France; Université Paris-Saclay, Faculté de Médecine, 63 rue Gabriel Péri, 94270 Le Kremlin Bicêtre, France; INSERM UMR_S 999, Hôpital Marie Lanne
Respir Med Res ; 86: 101130, 2024 Aug 19.
Article em En | MEDLINE | ID: mdl-39260187
ABSTRACT
BACKGROUND AND RESEARCH QUESTION S. maltophilia infections are associated with significant morbidity and mortality. Little is known regarding its presentation, management, and outcome in lung transplant recipients. STUDY DESIGN AND

METHODS:

This retrospective case control study reviewed S. maltophilia respiratory tract infection in lung transplant recipients (01/01/2011-31/01/2020) and described the clinical, microbiological and outcome characteristics matched with lung transplant recipients without respiratory tract infection. RESULTS AND

INTERPRETATION:

We identified 63 S. maltophilia infections in lung transplant recipients. Among them none were colonized before transplantation. Infections occurred a median of 177 (IQR 45- 681) days post transplantation. Fifty-four (85.7 %) patients received trimethoprim-sulfamethoxazole (400/80 mg three times a week) to prevent Pneumocystis jirovecii pneumonia (PJP). S. maltophilia strains were susceptible to trimethoprim-sulfamethoxazole, levofloxacin, minocycline and ceftazidime in respectively 85.7 %, 82.5 %, 96.8 % and 34.9 % of cases. Median duration of treatment was 9 days (IQR 7-11.5). Clinical and microbiological recurrence were observed in respectively 25.3 % and 39.7 % of cases. Combination therapy was not associated with a decrease in the risk of recurrence and did not prevent the emergence of resistance. S. maltophilia respiratory tract infection was associated with a decline in FEV-1 at one year.

CONCLUSION:

S. maltophilia is an important cause of lower respiratory tract infection in lung transplant recipients. Trimethoprim-sulfamethoxazole use as prophylaxis for PJP doesn't prevent S. maltophilia infection among lung transplant recipients. Levofloxacin and trimethoprim-sulfamethoxazole appear to be the two molecules of choice for the treatment of these infections and new antibiotic strategies (cefiderocol, aztreonam/avibactam) are currently being evaluated for multi-resistant S. maltophilia infections.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article