| Literature DB >> 32928787 |
Rob J Hallifax1,2, Benedict Ml Porter3, Patrick Jd Elder3, Sarah B Evans3, Chris D Turnbull3,2, Gareth Hynes3, Rachel Lardner3,4, Kirsty Archer4, Henry V Bettinson3, Annabel H Nickol3, William G Flight3, Stephen J Chapman3, Maxine Hardinge3, Rachel K Hoyles3, Peter Saunders3, Anny Sykes3, John M Wrightson3, Alastair Moore3, Ling-Pei Ho3,5, Emily Fraser3, Ian D Pavord5, Nicholas P Talbot3,5, Mona Bafadhel3,2, Nayia Petousi3,5, Najib M Rahman3,5.
Abstract
The SARS-CoV-2 can lead to severe illness with COVID-19. Outcomes of patients requiring mechanical ventilation are poor. Awake proning in COVID-19 improves oxygenation, but on data clinical outcomes is limited. This single-centre retrospective study aimed to assess whether successful awake proning of patients with COVID-19, requiring respiratory support (continuous positive airways pressure (CPAP) or high-flow nasal oxygen (HFNO)) on a respiratory high-dependency unit (HDU), is associated with improved outcomes. HDU care included awake proning by respiratory physiotherapists. Of 565 patients admitted with COVID-19, 71 (12.6%) were managed on the respiratory HDU, with 48 of these (67.6%) requiring respiratory support. Patients managed with CPAP alone 22/48 (45.8%) were significantly less likely to die than patients who required transfer onto HFNO 26/48 (54.2%): CPAP mortality 36.4%; HFNO mortality 69.2%, (p=0.023); however, multivariate analysis demonstrated that increasing age and the inability to awake prone were the only independent predictors of COVID-19 mortality. The mortality of patients with COVID-19 requiring respiratory support is considerable. Data from our cohort managed on HDU show that CPAP and awake proning are possible in a selected population of COVID-19, and may be useful. Further prospective studies are required. © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: non invasive ventilation; respiratory infection; viral infection
Mesh:
Year: 2020 PMID: 32928787 PMCID: PMC7490910 DOI: 10.1136/bmjresp-2020-000678
Source DB: PubMed Journal: BMJ Open Respir Res ISSN: 2052-4439
Figure 1Flow chart of COVID-19 admitted to Oxford University Hospitals NHS Foundation Trust (OUHNFT. CPAP, continuous positive airways pressure; HDU, high-dependency unit; HFNO, high-flow nasal oxygen; ICU, transferred to intensive care unit for intubation and ventilation; NIV, (bilevel) non-invasive ventilation.
Demographics of 48 patients requiring respiratory support on respiratory high-dependency unit managed by continuous positive airways pressure (CPAP) initially
| CPAP only | CPAP to HFNO | Overall | |
| Number of patients | 22 (45.8%) | 26 (54.2%) | 48 (100%) |
| Age (years; median, IQR) | 63 (54–77) | 73 (57–83) | 69 (54–80) |
| Male | 17 (77.3%) | 15 (57.7%) | 32 (66.7%) |
| Female | 5 (22.7%) | 11 (42.3%) | 16 (33.3%) |
| BMI (kg/m2) | 29.9 (25.5–33.3) | 28.3 (26.2–31.8) | 29.5 (25.6–33.4) |
| Comorbidities | |||
| Hypertension | 11 (50%) | 12 (46.2%) | 23 (47.9%) |
| Diabetes | 10 (45.5%) | 7 (26.9%) | 17 (35.4%) |
| Chronic lung disease: | 10 (45.5%) | 5 (19.2%) | 15 (31.3%) |
| - Asthma | 3 (13.6%) | 3 (11.5%) | 6 (12.5%) |
| - COPD | 5 (22.7%) | 1 (3.8%) | 6 (12.5%) |
| - ILD | 2 (9.1%) | 1 (3.8%) | 3 (6.3%) |
| CKD | 3 (13.6%) | 6 (23.1%) | 9 (18.8%) |
| Cardiovascular | 4 (18.2%) | 4 (15.4%) | 8 (16.7%) |
| Anticoagulated | 5 (22.7%) | 2 (7.7%) | 7 (14.6%) |
| Immunosuppressed | 0 (0%) | 6 (23.1%) | 6 (12.5%) |
| Stroke | 2 (9.1%) | 2 (7.7%) | 4 (8.3%) |
| Autoimmune | 0 (0%) | 2 (7.7%) | 2 (4.2%) |
| Other | 4 (18.2%) | 1 (3.8%) | 5 (10.4%) |
| Number of comorbidities median (IQR) | 2.5 (1.25–4) | 2 (1–3) | 2 (1–3) |
| Clinical Frailty Score median (IQR) | 3 (2–3) | 4 (3–5) | 3 (3–4) |
| Laboratory findings | |||
| Lymphocytes (109/L)* | 0.7 (0.5–1.1) | 0.7 (0.5–0.9) | 0.7 (0.5–0.9) |
| CRP (mg/L) | 163.0 | 182.5 | 172.5 |
| D dimer (µg/L) | 1272.0 (818.3–2132.8) | 1377.5 (805.3–2808.0) | 1291.5 (793.3–2220.3) |
Data presented as number (%) unless otherwise stated.
*Excluding one patient with chronic lymphocytic leukaemia.
BMI, body mass index; CKD, chronic kidney disease; COPD, chronic obstructive pulmonary disease; CRP, C-reactive protein; HFNO, high-flow nasal oxygen; ILD, interstitial lung disease.
Outcomes of 48 patients requiring respiratory support on respiratory high-dependency unit managed by continuous positive airways pressure (CPAP) initially
| CPAP only (n=22) | CPAP to HFNO (n=26) | Overall (n=48) | |
| Outcome | |||
| Discharged | 7 (31.8%) | 4 (15.4%) | 11 (22.9%) |
| ICU | 7 (31.8%) | 4 (15.4%) | 11 (22.9%) |
| Died | 8 (36.4%) | 18 (69.2%) | 26 (54.2%) |
HFNO, high flow nasal oxygen; ICU, transferred to intensive care unit for intubation and ventilation.
Figure 2Sankey plot of 48 patients requiring continuous positive airways pressure (CPAP): patient management and outcomes. HDU, high-dependency unit; HFNO, high-flow nasal oxygen.
OR for mortality
| OR | 95% CI | χ2 | P value | |
| Age | 1.08 | 1.02 to 1.15 | 7.22 | 0.007* |
| Clinical frailty score | ||||
| CFS 1–4 | 0.617 | |||
| CFS 5–9 | 1.56 | 0.27 to 11.09 | 0.25 | |
| Oxygen therapy prior to respiratory support | ||||
| Moderate | 0.088 | |||
| High | 4.18 | 0.81 to 29.70 | 2.91 | |
| Full proning | ||||
| Unsuccessful | 0.031* | |||
| Successful | 0.06 | 0.00 to 0.80 | 4.68 | |
| CPAP | ||||
| Required transfer onto HFNO | 0.761 | |||
| Required CPAP only | 0.76 | 0.13 to 4.88 | 0.09 |
Multivariate logistic regression (Firth bias reduced).
*p<0.05
CFS, clinical frailty score; CPAP, continuous positive airway pressure; HFNO, high flow nasal oxygen.