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Abstract
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
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 PaO2:FiO2 increased above 200 mm Hg. The number and extension of prone sessions were registered, along with relevant physiologic data and adverse events related to prone positioning. The cohort was stratified according to the first prone session duration: Group A, 2–3 days; Group B, 4–5 days; and Group C, > 5 days. Multivariable regression analyses were performed to assess whether the duration of prone sessions could impact safety.
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 PaO2:FiO2 ratio and higher ventilatory ratio, and had a higher rate of pressure sores (44%) and higher 90-day mortality (48%). However, after adjustment for severity and several relevant confounders, prone session duration was not associated with mortality or pressure sores.
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.
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1 Hospital Clínico Universidad de Chile, Unidad de Pacientes Críticos, Departamento de Medicina, Santiago, Chile (GRID:grid.412248.9) (ISNI:0000 0004 0412 9717); Center of Acute Respiratory Critical Illness (ARCI), Santiago, Chile (GRID:grid.412248.9)
2 Hospital Clínico Universidad de Chile, Unidad de Pacientes Críticos, Departamento de Medicina, Santiago, Chile (GRID:grid.412248.9) (ISNI:0000 0004 0412 9717)
3 Clínica Alemana de Santiago, Departamento de Paciente Crítico, Santiago, Chile (GRID:grid.418642.d) (ISNI:0000 0004 0627 8214); Clínica Alemana-Universidad de Desarrollo, Facultad de Medicina, Santiago, Chile (GRID:grid.412187.9) (ISNI:0000 0000 9631 4901)
4 Pontificia Universidad Católica de Chile, Departamento de Medicina Intensiva, Facultad de Medicina, Edificio Académico Escuela de Medicina, Santiago, Chile (GRID:grid.7870.8) (ISNI:0000 0001 2157 0406)
5 Hospital Carlos Van Buren, Unidad de Pacientes Críticos Adultos, Valparaíso, Chile (GRID:grid.460660.2) (ISNI:0000 0004 0628 4710)
6 Hospital La Serena, Unidad de Paciente Crítico, Coquimbo, Chile (GRID:grid.479669.3)
7 Hospital Barros Luco Trudeau, Unidad de Pacientes Críticos, Santiago, Chile (GRID:grid.414372.7) (ISNI:0000 0004 0465 882X); Universidad de Chile, Departamento de Medicina Interna Campus Sur, Santiago, Chile (GRID:grid.443909.3) (ISNI:0000 0004 0385 4466)
8 Hospital Regional de Concepción, Unidad de Pacientes Críticos, Concepción, Chile (GRID:grid.490152.b); Universidad de Concepción, Departamento de Medicina Interna, Facultad de Medicina, Concepción, Chile (GRID:grid.5380.e) (ISNI:0000 0001 2298 9663)
9 Hospital Padre Hurtado, Unidad de Pacientes Críticos, Santiago, Chile (GRID:grid.413125.0)
10 Hospital Clinico Regional de Antofagasta, Unidad de Paciente Crítico, Antofagasta, Chile (GRID:grid.413125.0); Universidad de Antofagasta, Facultad de Medicina y Odontología, Antofagasta, Chile (GRID:grid.412882.5) (ISNI:0000 0001 0494 535X)
11 Hospital Clínico Dra. Eloisa Diaz I-La Florida, Unidad de Pacientes Críticos, Santiago, Chile (GRID:grid.412882.5)
12 Pontificia Universidad Católica de Chile, Departamento de Medicina Intensiva, Facultad de Medicina, Edificio Académico Escuela de Medicina, Santiago, Chile (GRID:grid.7870.8) (ISNI:0000 0001 2157 0406); Complejo Asistencial Dr. Sótero del Río, Unidad de Paciente Crítico, Santiago, Chile (GRID:grid.7870.8)
13 Hospital Clínico Herminda Martín, Unidad de Pacientes Críticos, Chillán, Chile (GRID:grid.7870.8)
14 Hospital de Urgencia Asistencia Pública, Unidad de Paciente Crítico, Santiago, Chile (GRID:grid.513879.1); Universidad Finis Terrae, Facultad de Medicina, Santiago, Chile (GRID:grid.440629.d) (ISNI:0000 0004 5934 6911)
15 Hospital Regional de Iquique, Unidad de Pacientes Críticos, Iquique, Chile (GRID:grid.440629.d)
16 Clínica Alemana de Temuco, Unidad de Paciente Crítico, Temuco, Chile (GRID:grid.440629.d); Universidad de La Frontera, Facultad de Medicina, Temuco, Chile (GRID:grid.412163.3) (ISNI:0000 0001 2287 9552)
17 Pontificia Universidad Católica de Chile, Departamento de Medicina Intensiva, Facultad de Medicina, Edificio Académico Escuela de Medicina, Santiago, Chile (GRID:grid.7870.8) (ISNI:0000 0001 2157 0406); Center of Acute Respiratory Critical Illness (ARCI), Santiago, Chile (GRID:grid.7870.8)