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Influence of socioeconomic status on functional recovery after ARDS caused by SARS-CoV-2: a multicentre, observational study.
Declercq, Pierre-Louis; Fournel, Isabelle; Demeyere, Matthieu; Ksiazek, Eléa; Meunier-Beillard, Nicolas; Rivière, Antoine; Clarot, Caroline; Maizel, Julien; Schnell, David; Plantefeve, Gaetan; Ampere, Alexandre; Daubin, Cédric; Sauneuf, Bertrand; Kalfon, Pierre; Federici, Laura; Redureau, Élise; Bousta, Mehdi; Lagache, Laurie; Vanderlinden, Thierry; Nseir, Saad; La Combe, Béatrice; Bourdin, Gaël; Monchi, Mehran; Nyunga, Martine; Ramakers, Michel; Oulehri, Walid; Georges, Hugues; Salmon Gandonniere, Charlotte; Badie, Julio; Delbove, Agathe; Monnet, Xavier; Beduneau, Gaetan; Artaud-Macari, Élise; Abraham, Paul; Delberghe, Nicolas; Le Bouar, Gurvan; Miailhe, Arnaud-Felix; Hraiech, Sami; Bironneau, Vanessa; Sedillot, Nicholas; Hoppe, Marie-Anne; Barbar, Saber Davide; Calcaianu, George-Daniel; Dellamonica, Jean; Terzi, Nicolas; Delpierre, Cyrille; Gélinotte, Stéphanie; Rigaud, Jean-Philippe; Labruyère, Marie; Georges, Marjolaine.
  • Declercq PL; Service de Médecine Intensive-Réanimation, Hospital Centre Dieppe, Dieppe, France.
  • Fournel I; Centre d'Investigation Clinique INSERM 1432, Centre Hospitalier Universitaire de Dijon, Dijon, France.
  • Demeyere M; Department of Radiology, University Hospital Centre Rouen, Rouen, France.
  • Ksiazek E; Centre d'Investigation Clinique, Épidémiologie Clinique/Essais Cliniques, University Hospital Centre Dijon, Dijon, France.
  • Meunier-Beillard N; Module Epidémiologie Clinique, INSERM CIC 1432, Dijon, France.
  • Rivière A; Centre d'Investigation Clinique, Épidémiologie Clinique/Essais Cliniques, University Hospital Centre Dijon, Dijon, France.
  • Clarot C; Service de Médecine Intensive-Réanimation, Abbeville Hospital Centre, Abbeville, France.
  • Maizel J; Service de Pneumologie, Abbeville Hospital Centre, Abbeville, France.
  • Schnell D; Service de Médecine Intensive-Réanimation, University Hospital Centre Amiens-Picardie, Amiens, France.
  • Plantefeve G; Service de Médecine Intensive-Réanimation, Hospital Centre Angouleme, Angouleme, France.
  • Ampere A; Service de Médecine-Intensive Réanimation, Centre Hospitalier d'Argenteuil, Argenteuil, France.
  • Daubin C; Service de Pneumologie, Hospital Centre Bethune, Bethune, France.
  • Sauneuf B; Department of Medical Intensive Care, CHRU de Caen, Caen, France.
  • Kalfon P; Service de Médecine Intensive-Réanimation, Cotentin Public Hospital Centre, Cherbourg-Octeville, France.
  • Federici L; Service de Médecine Intensive-Réanimation, Hospital Centre Chartres, Chartres, France.
  • Redureau É; Service de Médecine Intensive-Réanimation, Hôpital Louis-Mourier, Colombes, France.
  • Bousta M; Service de Médecine Intensive-Réanimation, Departmental Hospital Centre La Roche-sur-Yon, La Roche-sur-Yon, France.
  • Lagache L; Service de Réanimation Médico-Chirurgicale, Hospital Group Le Havre, Le Havre, France.
  • Vanderlinden T; Service de Réanimation Médico-Chirurgicale, Hospital Group Le Havre, Le Havre, France.
  • Nseir S; Service de Médecine Intensive-Réanimation, Hospital Group of Lille Catholic University, Lille, France.
  • La Combe B; Médecine Intensive-Réanimation, Regional and University Hospital Centre Lille, Lille, France.
  • Bourdin G; Service de Réanimation Polyvalente, Groupe Hospitalier Bretagne Sud, Lorient, France.
  • Monchi M; Service de Médecine Intensive-Réanimation, Centre Hospitalier Saint Joseph Saint Luc, Lyon, France.
  • Nyunga M; Service de Médecine Intensive-Réanimation, Melun Hospital Centre, Melun, France.
  • Ramakers M; Service de Médecine Intensive-Réanimation, Roubaix Hospital Center, Roubaix, France.
  • Oulehri W; Service de Médecine Intensive-Réanimation, Centre Hospitalier Mémorial de Saint-Lô, Saint-Lo, France.
  • Georges H; Service de Réanimation Chirurgicale, University Hospitals Strasbourg, Strasbourg, France.
  • Salmon Gandonniere C; Service de Médecine Intensive-Réanimation, Hospital Centre Gustave Dron de Tourcoing, Tourcoing, France.
  • Badie J; Service de Médecine Intensive-Réanimation, Regional University Hospital Centre Tours, Tours, France.
  • Delbove A; Service de Médecine Intensive-Réanimation, Hopital Nord Franche-Comte, Montbeliard, France.
  • Monnet X; Réanimation Polyvalente, Centre Hospitalier Bretagne Atlantique, Vannes, France.
  • Beduneau G; Service de Médecine Intensive-Réanimation, University Hospitals Southern Paris, Le Kremlin-Bicetre, France.
  • Artaud-Macari É; Département de Réanimation Médicale, Centre Hospitalier Universitaire de Rouen, Rouen, France.
  • Abraham P; Service de Pneumologie, University Hospital Centre Rouen, Rouen, France.
  • Delberghe N; Service d'Anesthésie-Réanimation, Groupement Hospitalier Edouard Herriot, Lyon, France.
  • Le Bouar G; Service de Pneumologie, Hospital Centre Eure-Seine, Evreux, France.
  • Miailhe AF; Service de Médecine Intensive-Réanimation, University Hospital Centre Rouen, Rouen, France.
  • Hraiech S; Service de Médecine Intensive-Réanimation, University Hospital Centre Nantes, Nantes, France.
  • Bironneau V; Service de Médecine Intensive-Réanimation, Hôpital Nord, Marseille, France.
  • Sedillot N; Service de Pneumologie, University Hospital Centre Poitiers, Poitiers, France.
  • Hoppe MA; Réanimation Polyvalente, Hôpital Fleyriat, Centre Hospitalier de Bourg-en-Bresse, Bourg-en-Bresse, France.
  • Barbar SD; Service de Médecine Intensive-Réanimation, Hospital Centre La Rochelle, La Rochelle, France.
  • Calcaianu GD; Intensive Care Unit, Centre Hospitalier Universitaire de Nimes, Nimes, France.
  • Dellamonica J; Service de Pneumologie, Mulhouse and South Alsace Region Hospital Group, Mulhouse, France.
  • Terzi N; Medical ICU, University Hospital Centre Nice, Nice, France.
  • Delpierre C; Service de Médecine Intensive-Réanimation, University Hospital Centre Grenoble Alpes, Grenoble, France.
  • Gélinotte S; Centre d'Epidémiologie et de Recherche en santé des POPulations (CERPOP), University of Toulouse, Toulouse, France.
  • Rigaud JP; Service de Médecine Intensive-Réanimation, Hospital Centre Dieppe, Dieppe, France.
  • Labruyère M; Service de Médecine Intensive-Réanimation, Hospital Centre Dieppe, Dieppe, France.
  • Georges M; Service de Médecine Intensive-Réanimation, University Hospital Centre Dijon, Dijon, France.
BMJ Open ; 12(4): e057368, 2022 04 22.
Article in English | MEDLINE | ID: covidwho-1807412
ABSTRACT

INTRODUCTION:

Prognosis of patients with COVID-19 depends on the severity of the pulmonary affection. The most severe cases may progress to acute respiratory distress syndrome (ARDS), which is associated with a risk of long-term repercussions on respiratory function and neuromuscular outcomes. The functional repercussions of severe forms of COVID-19 may have a major impact on quality of life, and impair the ability to return to work or exercise. Social inequalities in healthcare may influence prognosis, with socially vulnerable individuals more likely to develop severe forms of disease. We describe here the protocol for a prospective, multicentre study that aims to investigate the influence of social vulnerability on functional recovery in patients who were hospitalised in intensive care for ARDS caused by COVID-19. This study will also include an embedded qualitative study that aims to describe facilitators and barriers to compliance with rehabilitation, describe patients' health practices and identify social representations of health, disease and care. METHODS AND

ANALYSIS:

The "Functional Recovery From Acute Respiratory Distress Syndrome (ARDS) Due to COVID-19 Influence of Socio-Economic Status" (RECOVIDS) study is a mixed-methods, observational, multicentre cohort study performed during the routine follow-up of post-intensive care unit (ICU) functional recovery after ARDS. All patients admitted to a participating ICU for PCR-proven SARS-CoV-2 infection and who underwent chest CT scan at the initial phase AND who received respiratory support (mechanical or not) or high-flow nasal oxygen, AND had ARDS diagnosed by the Berlin criteria will be eligible. The primary outcome is the presence of lung sequelae at 6 months after ICU discharge, defined either by alterations on pulmonary function tests, oxygen desaturation during a standardised 6 min walk test or fibrosis-like pulmonary findings on chest CT. Patients will be considered to be socially disadvantaged if they have an "Evaluation de la Précarité et des Inégalités de santé dans les Centres d'Examen de Santé" (EPICES) score ≥30.17 at inclusion. ETHICS AND DISSEMINATION The study protocol and the informed consent form were approved by an independent ethics committee (Comité de Protection des Personnes Sud Méditerranée II) on 10 July 2020 (2020-A02014-35). All patients will provide informed consent before participation. Findings will be published in peer-reviewed journals and presented at national and international congresses. TRIAL REGISTRATION NUMBER NCT04556513.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Long Covid Limits: Humans Language: English Journal: BMJ Open Year: 2022 Document Type: Article Affiliation country: Bmjopen-2021-057368

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Long Covid Limits: Humans Language: English Journal: BMJ Open Year: 2022 Document Type: Article Affiliation country: Bmjopen-2021-057368