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The ICU-Diary study: prospective, multicenter comparative study of the impact of an ICU diary on the wellbeing of patients and families in French ICUs.
Garrouste-Orgeas, Maïté; Flahault, Cécile; Fasse, Léonor; Ruckly, Stéphane; Amdjar-Badidi, Nora; Argaud, Laurent; Badie, Julio; Bazire, Amélie; Bige, Naike; Boulet, Eric; Bouadma, Lila; Bretonnière, Cédric; Floccard, Bernard; Gaffinel, Alain; de Forceville, Xavier; Grand, Hubert; Halidfar, Rebecca; Hamzaoui, Olfa; Jourdain, Mercé; Jost, Paul-Henri; Kipnis, Eric; Large, Audrey; Lautrette, Alexandre; Lesieur, Olivier; Maxime, Virginie; Mercier, Emmanuelle; Mira, Jean Paul; Monseau, Yannick; Parmentier-Decrucq, Erika; Rigaud, Jean-Philippe; Rouget, Antoine; Santoli, François; Simon, Georges; Tamion, Fabienne; Thieulot-Rolin, Nathalie; Thirion, Marina; Valade, Sandrine; Vinatier, Isabelle; Vioulac, Christel; Bailly, Sebastien; Timsit, Jean-François.
Afiliação
  • Garrouste-Orgeas M; Infection, Antimicrobials, Modelling, Evolution (IAME), UMR 1137, INSERM and Paris Diderot University, Department of Biostatistics - HUPNVS - AP-HP, UFR de Médecine - Bichat University Hospital, Paris, France. maite.garrouste@ihfb.org.
  • Flahault C; Department of Biostatistics, Outcomerea, Paris, France. maite.garrouste@ihfb.org.
  • Fasse L; Medical unit, French British Hospital Institute, Levallois-Perret, France. maite.garrouste@ihfb.org.
  • Ruckly S; Psychology laboratory and work process, Paris Descartes University, Paris, France.
  • Amdjar-Badidi N; Laboratoire Psy-DREPI EA-7458, Bourgogne Franche Comté University, Dijon, France.
  • Argaud L; Infection, Antimicrobials, Modelling, Evolution (IAME), UMR 1137, INSERM and Paris Diderot University, Department of Biostatistics - HUPNVS - AP-HP, UFR de Médecine - Bichat University Hospital, Paris, France.
  • Badie J; Department of Biostatistics, Outcomerea, Paris, France.
  • Bazire A; Medical-Surgical ICU, General Hospital René Dubos, Pontoise, France.
  • Bige N; Medical ICU, Edouard Herriot University Hospital, Lyon, France.
  • Boulet E; Medical-Surgical ICU, General Hospital Belfort-Montbeliard, Belfort, France.
  • Bouadma L; Medical ICU, La Cavale Blanche University Hospital, Brest, France.
  • Bretonnière C; Medical ICU, Saint Antoine University Hospital, Paris, France.
  • Floccard B; Medical ICU, Beaumont General Hospital, Beaumont, France.
  • Gaffinel A; Infection, Antimicrobials, Modelling, Evolution (IAME), UMR 1137, INSERM and Paris Diderot University, Department of Biostatistics - HUPNVS - AP-HP, UFR de Médecine - Bichat University Hospital, Paris, France.
  • de Forceville X; Medical ICU, Bichat University Hospital, Paris, France.
  • Grand H; Medical ICU, Nantes University Hospital, Nantes, France.
  • Halidfar R; EA3826, Laboratory of clinical and experimental therapeutics of infections, University of Nantes, Nantes, France.
  • Hamzaoui O; Medical ICU, Hospices Civils de Lyon, Edouard Herriot University Hospital, Lyon, France.
  • Jourdain M; Medical-Surgical ICU, Gustave Roussy Cancer Campus, Villejuif, France.
  • Jost PH; Medical-Surgical ICU, Est Francilien Hospital network, Meaux, France.
  • Kipnis E; Medical-Surgical ICU, Hospital Robert Boulin, Libourne, France.
  • Large A; Medical ICU, Albert Michallon University Hospital, Grenoble, France.
  • Lautrette A; Medical ICU, University Hospital Paris-Sud, Beclère University Hospital, Clamart, France.
  • Lesieur O; Lille University, Inserm U1190, Lille, France.
  • Maxime V; Group of medical ICUs, Lille University Hospital, Lille, France.
  • Mercier E; Surgical ICU, Henri Mondor University Hospital, Créteil, France.
  • Mira JP; Surgical ICU, Lille University Hospital, Lille, France.
  • Monseau Y; Medical ICU, François Mitterrand University Hospital, Dijon, France.
  • Parmentier-Decrucq E; Medical ICU, Gabriel-Montpied University Hospital, Clermont Ferrand, France.
  • Rigaud JP; LMGE UMR CNRS 6023, University of Clermont-Ferrand, Clermont Ferrand, France.
  • Rouget A; Medical-Surgical ICU, General Hospital, La Rochelle, France.
  • Santoli F; EA 4569, University Paris Descartes, Paris, France.
  • Simon G; Medical ICU, Raymond Poincaré University Hospital, Garches, France.
  • Tamion F; CRICS group, Medical-Surgical ICU, Tours University Hospital, Tours, France.
  • Thieulot-Rolin N; Medical ICU, Cochin University Hospital, Paris, France.
  • Thirion M; Medical-Surgical ICU, General Hospital, Périgueux, France.
  • Valade S; Group of medical ICUs, Lille University Hospital, Lille, France.
  • Vinatier I; Department of Intensive Care, Dieppe General Hôpital, Dieppe, France.
  • Vioulac C; Medical-Surgical ICU, Rangueil University Hospital, Toulouse, France.
  • Bailly S; Medical ICU, General Hospital Robert Ballanger, Aulnay-Sous-Bois, France.
  • Timsit JF; Medical-Surgical ICU, General Hospital, Troyes, France.
Trials ; 18(1): 542, 2017 Nov 15.
Article em En | MEDLINE | ID: mdl-29141694
ABSTRACT

BACKGROUND:

Post-intensive care syndrome includes the multiple consequences of an intensive care unit (ICU) stay for patients and families. It has become a new challenge for intensivists. Prevention programs have been disappointing, except for ICU diaries, which report the patient's story in the ICU. However, the effectiveness of ICU diaries for patients and families is still controversial, as the interpretation of the results of previous studies was open to criticism hampering an expanded use of the diary. The primary objective of the study is to evaluate the post-traumatic stress syndrome in patients. The secondary objectives are to evaluate the post-traumatic stress syndrome in families, anxiety and depression symptoms in patients and families, and the recollected memories of patients. Endpoints will be evaluated 3 months after ICU discharge or death.

METHODS:

A prospective, multicenter, randomized, assessor-blind comparative study of the effect of an ICU diary on patients and families. We will compare two groups one group with an ICU diary written by staff and family and given to the patient at ICU discharge or to the family in case of death, and a control group without any ICU diary. Each of the 35 participating centers will include 20 patients having at least one family member who will likely visit the patient during their ICU stay. Patients must be ventilated within 48 h after ICU admission and not have any previous chronic neurologic or acute condition responsible for cognitive impairments that would hamper their participation in a phone interview. Three months after ICU discharge or death of the patient, a psychologist will contact the patient and family by phone. Post-traumatic stress syndrome will be evaluated using the Impact of Events Scale-Revised questionnaire, anxiety and depression symptoms using the Hospital Anxiety and Depression Scale questionnaire, both in patients and families, and memory recollection using the ICU Memory Tool Questionnaire in patients. The content of a randomized sample of diaries of each center will be analyzed using a grid. An interview of the patients in the intervention arm will be conducted 6 months after ICU discharge to analyze in depth how they use the diary.

DISCUSSION:

This study will provide new insights on the impact of ICU diaries on post-traumatic stress disorders in patients and families after an ICU stay. TRIAL REGISTRATION ClinicalTrial.gov, ID NCT02519725 . Registered on 13 July 2015.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ansiedade / Pacientes / Qualidade de Vida / Transtornos de Estresse Pós-Traumáticos / Prontuários Médicos / Cuidados Críticos / Depressão / Relações Familiares / Unidades de Terapia Intensiva Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Qualitative_research Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ansiedade / Pacientes / Qualidade de Vida / Transtornos de Estresse Pós-Traumáticos / Prontuários Médicos / Cuidados Críticos / Depressão / Relações Familiares / Unidades de Terapia Intensiva Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Qualitative_research Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article