Continuous prolonged prone positioning in COVID-19-related ARDS: a multicenter cohort study from Chile.

Acute respiratory distress syndrome Coronavirus disease 2019 Mechanical ventilation Prone positioning

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
28 Nov 2022
Historique:
received: 18 08 2022
accepted: 06 11 2022
entrez: 28 11 2022
pubmed: 29 11 2022
medline: 29 11 2022
Statut: epublish

Résumé

Prone positioning is currently applied in time-limited daily sessions up to 24 h which determines that most patients require several sessions. Although longer prone sessions have been reported, there is scarce evidence about the feasibility and safety of such approach. We analyzed feasibility and safety of a continuous prolonged prone positioning strategy implemented nationwide, in a large cohort of COVID-19 patients in Chile. Retrospective cohort study of mechanically ventilated COVID-19 patients with moderate-to-severe acute respiratory distress syndrome (ARDS), conducted in 15 Intensive Care Units, which adhered to a national protocol of continuous prone sessions  ≥ 48 h and until PaO We included 417 patients who required a first prone session of 4 (3-5) days, of whom 318 (76.3%) received only one session. During the first prone session the main adverse event was grade 1-2 pressure sores in 97 (23.9%) patients; severe adverse events were infrequent with 17 non-scheduled extubations (4.2%). 90-day mortality was 36.2%. Ninety-eight patients (24%) were classified as group C; they exhibited a more severe ARDS at baseline, as reflected by lower PaO Nationwide implementation of a continuous prolonged prone positioning strategy for COVID-19 ARDS patients was feasible. Minor pressure sores were frequent but within the ranges previously described, while severe adverse events were infrequent. The duration of prone session did not have an adverse effect on safety.

Sections du résumé

BACKGROUND BACKGROUND
Prone positioning is currently applied in time-limited daily sessions up to 24 h which determines that most patients require several sessions. Although longer prone sessions have been reported, there is scarce evidence about the feasibility and safety of such approach. We analyzed feasibility and safety of a continuous prolonged prone positioning strategy implemented nationwide, in a large cohort of COVID-19 patients in Chile.
METHODS METHODS
Retrospective cohort study of mechanically ventilated COVID-19 patients with moderate-to-severe acute respiratory distress syndrome (ARDS), conducted in 15 Intensive Care Units, which adhered to a national protocol of continuous prone sessions  ≥ 48 h and until PaO
RESULTS RESULTS
We included 417 patients who required a first prone session of 4 (3-5) days, of whom 318 (76.3%) received only one session. During the first prone session the main adverse event was grade 1-2 pressure sores in 97 (23.9%) patients; severe adverse events were infrequent with 17 non-scheduled extubations (4.2%). 90-day mortality was 36.2%. Ninety-eight patients (24%) were classified as group C; they exhibited a more severe ARDS at baseline, as reflected by lower PaO
CONCLUSIONS CONCLUSIONS
Nationwide implementation of a continuous prolonged prone positioning strategy for COVID-19 ARDS patients was feasible. Minor pressure sores were frequent but within the ranges previously described, while severe adverse events were infrequent. The duration of prone session did not have an adverse effect on safety.

Identifiants

pubmed: 36441352
doi: 10.1186/s13613-022-01082-w
pii: 10.1186/s13613-022-01082-w
pmc: PMC9702866
doi:

Types de publication

Journal Article

Langues

eng

Pagination

109

Investigateurs

Nicole Rossel (N)
María José Martin (MJ)
Juan Nicolás Medel (JN)
Vanessa Oviedo (V)
Magdalena Vera (M)
Vicente Torres (V)
José Miguel Montes (JM)
Álvaro Salazar (Á)
Carla Muñoz (C)
Francisca Tala (F)
Mariana Migueles (M)
Claudia Ortiz (C)
Felipe Gómez (F)
Luis Contreras (L)
Itzia Daviu (I)
Yurimar Rodriguez (Y)
Carol Ortiz (C)
Andrés Aquevedo (A)
Rodrigo Parada (R)
Cristián Vargas (C)
Miguel Gatica (M)
Dalia Guerrero (D)
Araceli Valenzuela (A)
Diego Torrejón (D)

Informations de copyright

© 2022. The Author(s).

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Auteurs

Rodrigo A Cornejo (RA)

Unidad de Pacientes Críticos, Departamento de Medicina, Hospital Clínico Universidad de Chile, Dr. Carlos Lorca Tobar 999, 2º Piso, Independencia, Santiago, Chile. racornej@gmail.com.
Center of Acute Respiratory Critical Illness (ARCI), Santiago, Chile. racornej@gmail.com.

Jorge Montoya (J)

Unidad de Pacientes Críticos, Departamento de Medicina, Hospital Clínico Universidad de Chile, Dr. Carlos Lorca Tobar 999, 2º Piso, Independencia, Santiago, Chile.

Abraham I J Gajardo (AIJ)

Unidad de Pacientes Críticos, Departamento de Medicina, Hospital Clínico Universidad de Chile, Dr. Carlos Lorca Tobar 999, 2º Piso, Independencia, Santiago, Chile.

Jerónimo Graf (J)

Departamento de Paciente Crítico, Clínica Alemana de Santiago, Santiago, Chile.
Facultad de Medicina, Clínica Alemana-Universidad de Desarrollo, Santiago, Chile.

Leyla Alegría (L)

Departamento de Medicina Intensiva, Facultad de Medicina, Edificio Académico Escuela de Medicina, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, 6º Piso, Santiago, Chile.

Romyna Baghetti (R)

Unidad de Pacientes Críticos Adultos, Hospital Carlos Van Buren, Valparaíso, Chile.

Anita Irarrázaval (A)

Unidad de Paciente Crítico, Hospital La Serena, Coquimbo, Chile.

César Santis (C)

Unidad de Pacientes Críticos, Hospital Barros Luco Trudeau, Santiago, Chile.
Departamento de Medicina Interna Campus Sur, Universidad de Chile, Santiago, Chile.

Nicolás Pavez (N)

Unidad de Pacientes Críticos, Hospital Regional de Concepción, Concepción, Chile.
Departamento de Medicina Interna, Facultad de Medicina, Universidad de Concepción, Concepción, Chile.

Sofía Leighton (S)

Unidad de Pacientes Críticos, Hospital Padre Hurtado, Santiago, Chile.

Vinko Tomicic (V)

Unidad de Paciente Crítico, Hospital Clinico Regional de Antofagasta, Antofagasta, Chile.
Facultad de Medicina y Odontología, Universidad de Antofagasta, Antofagasta, Chile.

Daniel Morales (D)

Unidad de Pacientes Críticos, Hospital Clínico Dra. Eloisa Diaz I-La Florida, Santiago, Chile.

Carolina Ruiz (C)

Departamento de Medicina Intensiva, Facultad de Medicina, Edificio Académico Escuela de Medicina, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, 6º Piso, Santiago, Chile.
Unidad de Paciente Crítico, Complejo Asistencial Dr. Sótero del Río, Santiago, Chile.

Pablo Navarrete (P)

Unidad de Pacientes Críticos, Hospital Clínico Herminda Martín, Chillán, Chile.

Patricio Vargas (P)

Unidad de Paciente Crítico, Hospital de Urgencia Asistencia Pública, Santiago, Chile.
Facultad de Medicina, Universidad Finis Terrae, Santiago, Chile.

Roberto Gálvez (R)

Unidad de Pacientes Críticos, Hospital Regional de Iquique, Iquique, Chile.

Victoria Espinosa (V)

Unidad de Paciente Crítico, Clínica Alemana de Temuco, Temuco, Chile.
Facultad de Medicina, Universidad de La Frontera, Temuco, Chile.

Marioli Lazo (M)

Unidad de Pacientes Críticos, Departamento de Medicina, Hospital Clínico Universidad de Chile, Dr. Carlos Lorca Tobar 999, 2º Piso, Independencia, Santiago, Chile.

Rodrigo A Pérez-Araos (RA)

Departamento de Paciente Crítico, Clínica Alemana de Santiago, Santiago, Chile.
Facultad de Medicina, Clínica Alemana-Universidad de Desarrollo, Santiago, Chile.

Osvaldo Garay (O)

Unidad de Pacientes Críticos Adultos, Hospital Carlos Van Buren, Valparaíso, Chile.

Patrick Sepúlveda (P)

Unidad de Paciente Crítico, Hospital La Serena, Coquimbo, Chile.

Edgardo Martinez (E)

Unidad de Pacientes Críticos, Hospital Padre Hurtado, Santiago, Chile.

Alejandro Bruhn (A)

Departamento de Medicina Intensiva, Facultad de Medicina, Edificio Académico Escuela de Medicina, Pontificia Universidad Católica de Chile, Diagonal Paraguay 362, 6º Piso, Santiago, Chile. alejandrobruhn@gmail.com.
Center of Acute Respiratory Critical Illness (ARCI), Santiago, Chile. alejandrobruhn@gmail.com.

Classifications MeSH