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A three-step support strategy for relatives of patients dying in the intensive care unit: a cluster randomised trial.
Kentish-Barnes, Nancy; Chevret, Sylvie; Valade, Sandrine; Jaber, Samir; Kerhuel, Lionel; Guisset, Olivier; Martin, Maëlle; Mazaud, Amélie; Papazian, Laurent; Argaud, Laurent; Demoule, Alexandre; Schnell, David; Lebas, Eddy; Ethuin, Frédéric; Hammad, Emmanuelle; Merceron, Sybille; Audibert, Juliette; Blayau, Clarisse; Delannoy, Pierre-Yves; Lautrette, Alexandre; Lesieur, Olivier; Renault, Anne; Reuter, Danielle; Terzi, Nicolas; Philippon-Jouve, Bénédicte; Fiancette, Maud; Ramakers, Michel; Rigaud, Jean-Philippe; Souppart, Virginie; Asehnoune, Karim; Champigneulle, Benoît; Goldgran-Toledano, Dany; Dubost, Jean-Louis; Bollaert, Pierre-Edouard; Chouquer, Renaud; Pochard, Frédéric; Cariou, Alain; Azoulay, Elie.
Afiliación
  • Kentish-Barnes N; AP-HP Nord, Saint Louis Hospital, Medical Intensive Care, Famiréa Research Group, Paris, France. Electronic address: nancy.kentish@aphp.fr.
  • Chevret S; Department of Biostatistics and Medical Information, UMR 1153, ECSTRRA Team, INSERM, Paris University, Saint Louis Hospital, AP-HP, Paris, France.
  • Valade S; AP-HP Nord, Saint Louis Hospital, Medical Intensive Care, Famiréa Research Group, Paris, France; AP-HP Centre, Cochin Hospital, Medical Intensive Care, Paris, France.
  • Jaber S; Saint Eloi University Hospital, Department of Anesthesia and Critical Care Medicine, Montpellier and PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
  • Kerhuel L; AP-HP Nord, Saint Louis Hospital, Medical Intensive Care, Famiréa Research Group, Paris, France.
  • Guisset O; Saint André University Hospital, Medical Intensive Care, Bordeaux, France.
  • Martin M; Hôtel Dieu University Hospital, Medical Intensive Care, Nantes, France.
  • Mazaud A; Hospices Civils de Lyon, Edouard Herriot University Hospital, Surgical Intensive Care, Lyon, France.
  • Papazian L; AP-HM, Hôpital Nord, Medical Intensive Care and Aix-Marseille University, Faculté des Sciences Médicales et Paramédicales, Centre d'Etudes et de Recherches sur les Services de Santé et qualité de vie EA 3279, Marseille, France.
  • Argaud L; Hospices Civils de Lyon, Edouard Herriot Hospital, Medical Intensive Care, and Université de Lyon, Lyon, France.
  • Demoule A; AP-HP Sorbonne Université, La Pitié-Salpêtrière University Hospital, Medical Intensive Care Unit and Sorbonne Université, INSERM, UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Paris, France.
  • Schnell D; Angoulême Hospital, Medical and Surgical Intensive Care, Angoulême, France.
  • Lebas E; Bretagne Atlantique Hospital, Medical and Surgical Intensive Care, Vannes, France.
  • Ethuin F; Côte de Nacre University Hospital, Surgical Intensive Care, Caen, France.
  • Hammad E; AP-HM, Hospital Nord, Anaesthesia and Intensive Care, Marseille, France.
  • Merceron S; André Mignot Hospital, Medical Intensive Care, Le Chesnay, France.
  • Audibert J; Louis Pasteur Hospital, Medical and Surgical Intensive Care, Chartres, France.
  • Blayau C; AP-HP Sorbonne University, Tenon Hospital, Medical Intensive Care, Paris, France.
  • Delannoy PY; Chatilliez Hospital, Medical and Surgical Intensive Care, Tourcoing, France.
  • Lautrette A; Gabriel Montpied University Hospital, Medical Intensive Care, Clermont Ferrand, France.
  • Lesieur O; La Rochelle Hospital, Medical and Surgical Intensive Care, La Rochelle, France.
  • Renault A; Cavale Blanche University Hospital, Medical Intensive Care, Brest, France.
  • Reuter D; Sud Francilien Hospital, Medical and Surgical Intensive Care, Evry, France.
  • Terzi N; Grenoble Alpes University Hospital, Medical Intensive Care, Grenoble, France.
  • Philippon-Jouve B; Roanne Hospital, Medical and Surgical Intensive Care, Roanne, France.
  • Fiancette M; Les Oudairies Hospital, Medical and Surgical Intensive Care, La Roche-sur-Yon, France.
  • Ramakers M; Saint Lô Hospital, Medical and Surgical Intensive Care, Saint Lô, France.
  • Rigaud JP; Dieppe Hospital, Medical and Surgical Intensive Care, Dieppe, Paris.
  • Souppart V; AP-HP Nord, Saint Louis Hospital, Medical Intensive Care, Famiréa Research Group, Paris, France.
  • Asehnoune K; Hôtel Dieu University Hospital, Department of Anesthesia and Critical Care, Nantes, France.
  • Champigneulle B; AP-HP Centre, Hôpital Européen Georges Pompidou, Department of Aaesthesia and Critical Care, Paris, France.
  • Goldgran-Toledano D; Montfermeil Hospital, Medical and Surgical Intensive Care, Montfermeil, France.
  • Dubost JL; René Dubos Hospital, Medical and Surgical Intensive Care, Pontoise, France.
  • Bollaert PE; University Hospital Central, Medical Intensive Care, Nancy, France.
  • Chouquer R; Annecy Hospital, Medical and Surgical Intensive Care, Annecy, France.
  • Pochard F; AP-HP Nord, Saint Louis Hospital, Medical Intensive Care, Famiréa Research Group, Paris, France; AP-HP Nord, Fernand Widal Hospital, DMU Neurosciences, Département de Psychiatrie et de Médecine Addictologique, Paris, France.
  • Cariou A; AP-HP Centre, Cochin Hospital, Medical Intensive Care, Paris, France; Paris University, Paris, France.
  • Azoulay E; AP-HP Nord, Saint Louis Hospital, Medical Intensive Care, Famiréa Research Group, Paris, France; Department of Biostatistics and Medical Information, UMR 1153, ECSTRRA Team, INSERM, Paris University, Saint Louis Hospital, AP-HP, Paris, France.
Lancet ; 399(10325): 656-664, 2022 02 12.
Article en En | MEDLINE | ID: mdl-35065008
ABSTRACT

BACKGROUND:

In relatives of patients dying in intensive care units (ICUs), inadequate team support can increase the prevalence of prolonged grief and other psychological harm. We aimed to evaluate whether a proactive communication and support intervention would improve relatives' outcomes.

METHODS:

We undertook a prospective, multicentre, cluster randomised controlled trial in 34 ICUs in France, to compare standard care with a physician-driven, nurse-aided, three-step support strategy for families throughout the dying process, following a decision to withdraw or withhold life support. Inclusion criteria were relatives of patients older than 18 years with an ICU length of stay 2 days or longer. Participating ICUs were randomly assigned (11 ratio) into an intervention cluster and a control cluster. The randomisation scheme was generated centrally by a statistician not otherwise involved in the study, using permutation blocks of non-released size. In the intervention group, three meetings were held with relatives a family conference to prepare the relatives for the imminent death, an ICU-room visit to provide active support, and a meeting after the patient's death to offer condolences and closure. ICUs randomly assigned to the control group applied their best standard of care in terms of support and communication with relatives of dying patients. The primary endpoint was the proportion of relatives with prolonged grief (measured with PG-13, score ≥30) 6 months after the death. Analysis was by intention to treat, with the bereaved relatives as the unit of observation. The study is registered with ClinicalTrials.gov, NCT02955992.

FINDINGS:

Between Feb 23, 2017, and Oct 8, 2019, we enrolled 484 relatives of ICU patients to the intervention group and 391 to the control group. 379 (78%) relatives in the intervention group and 309 (79%) in the control group completed the 6-month interview to measure the primary endpoint. The intervention significantly reduced the number of relatives with prolonged grief symptoms (66 [21%] vs 57 [15%]; p=0·035) and the median PG-13 score was significantly lower in the intervention group than in the control group (19 [IQR 14-26] vs 21 [15-29], mean difference 2·5, 95% CI 1·04-3·95).

INTERPRETATION:

Among relatives of patients dying in the ICU, a physician-driven, nurse-aided, three-step support strategy significantly reduced prolonged grief symptoms.

FUNDING:

French Ministry of Health.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Grupo de Atención al Paciente / Cuidado Terminal / Aflicción / Pesar / Actitud Frente a la Muerte / Familia / Comunicación Tipo de estudio: Clinical_trials / Prognostic_studies / Qualitative_research / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Grupo de Atención al Paciente / Cuidado Terminal / Aflicción / Pesar / Actitud Frente a la Muerte / Familia / Comunicación Tipo de estudio: Clinical_trials / Prognostic_studies / Qualitative_research / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Año: 2022 Tipo del documento: Article