| Literature DB >> 33042547 |
Sally L Wootton1, Meredith King1, Jennifer A Alison2,3, Sri Mahadev4,5, Andrew S L Chan4,5.
Abstract
International statements have suggested the pulmonary rehabilitation (PR) model as an appropriate rehabilitation option for people recovering from coronavirus disease 2019 (COVID-19). In this case series, we present our COVID-19 telehealth rehabilitation programme, delivered within a PR setting, and discuss the management of our first three cases. All patients were male, with a median age of 73 years. Following hospital discharge, the patients presented with persistent limitations and/or symptoms (e.g. breathlessness, fatigue, and reduced exercise capacity) which warranted community-based rehabilitation. Patients were assessed and provided with an initial six-week rehabilitation programme supported via telehealth using a treatable traits approach. Patients demonstrated improvements in exercise capacity and breathlessness; however, fatigue levels worsened in two cases and this was attributed to the difficulties of managing returning to work and/or carer responsibilities whilst trying to recover from a severe illness. We found that PR clinicians were well prepared and able to provide an individualized rehabilitation programme for people recovering from COVID-19.Entities:
Keywords: COVID‐19; exercise; pulmonary rehabilitation; rehabilitation; telehealth
Year: 2020 PMID: 33042547 PMCID: PMC7541010 DOI: 10.1002/rcr2.669
Source DB: PubMed Journal: Respirol Case Rep ISSN: 2051-3380
Outcome measures from hospital discharge and PR assessments.
| Case 1 | Case 2 | Case 3 | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Baseline PR | After six weeks of PR | Change after PR | D/C from hospital | Baseline PR | After six weeks of PR | Change after PR | D/C from hospital | Baseline PR | After six weeks of PR | Change after PR | |
| 5STS (sec) | 10.66 | 5.04 | −5.62 | 14.82 | 11.48 | 8.45 | −3.03 | 22 | 18 | 13.18 | −4.82 |
| 1minSTS (reps) | 26 | 46 | 26 | 23 | 27 | 32 | 5 | 14 | 18 | 22 | 4 |
| Dyspnoea, (rest/exertion) | 0/2 | 0/2 | 0/1 | 0/1 | 0/3 | N/A | 0/2 | 0/4 | |||
| HR, bpm, (rest/exertion) | 82/103 | 71/105 | 78/102 | 85/110 | 80/129 | N/A | 75/83 | 72/85 | |||
| SpO2, % (rest/exertion) | 96/96 | 98/99 | 97/96 | 97/96 | 99/99 | N/A | 97/97 | 98/98 | |||
| FSS | 9 | 9 | 0 | N/A | 20 | 33 | 13 | N/A | 13 | 29 | 16 |
| mMRC | 0 | 0 | 0 | N/A | 2 | 1 | −1 | N/A | 2 | 2 | 0 |
1minSTS, 1‐min sit‐to‐stand test (higher reps indicate better capacity); 5STS, five‐repetition sit‐to‐stand test (lower time indicates better capacity); bpm, beats per minute; D/C, discharge; FSS, Fatigue Severity Scale (lower score indicates less symptoms); HR, heart rate (from 1minSTS test); mMRC, modified Medical Research Council dyspnoea scale (lower score indicates less symptoms); N/A, not available; PR, pulmonary rehabilitation; reps, repetitions; SpO2, oxygen saturation (from 1minSTS test).
Clinical characteristics of cases and hospital admission details.
| Case 1 | Case 2 | Case 3 | |
|---|---|---|---|
| Age (years) | 73 | 59 | 80 |
| Gender | Male | Male | Male |
| Height (m) | 1.70 | 1.84 | 1.80 |
| Weight (kg) | 68 | 87 | 97 |
| BMI (kg/m2) | 24 | 26 | 29 |
| Diagnostic features on hospital admission | Onset of non‐productive cough and fatigue. Home quarantine initially. Worsening dyspnoea and productive cough by Day 11 | One‐week history of fever, non‐productive cough, dyspnoea, pleuritic chest pain, and diarrhoea. Respiratory distress | Dyspnoea for five days. Dry cough especially nocturnal. Night sweats |
| Blood | Elevated CRP, | Elevated CRP and | Elevated CRP, procalcitonin, |
| Chest X‐Ray/CT | Bilateral peripheral pulmonary infiltrates | Bilateral GGO | Bilateral peripheral pulmonary GGO infiltrates |
| SpO2 on room air (%) | 88 | 93 | 91 |
| Respiratory rate/min | 36 | 28 | 28 |
| Heart rate (bpm) | 79 | 78 | 99 |
| Temperature (degrees) | 38.0 | 39.8 | 38.0 |
| PCR | COVID‐19 +ve | COVID‐19 +ve | COVID‐19 +ve |
| Acute admission, management |
Admitted to ICU Augmentin and azithromycin Hydroxychloroquine VTE prophylaxis Supplemental oxygen. Nasal high flow |
Managed on a general medical ward (no ICU on site) Augmentin and azithromycin Hydroxychloroquine VTE prophylaxis Supplemental oxygen |
Admitted to ICU Augmentin and doxycycline Diuretics and fluid restriction VTE prophylaxis Supplemental oxygen. Nasal high flow |
| ICU length of stay (days) | 3 | 0 | 1 |
| Hospital length of stay (days) | 9 | 12 | 15 |
| Comorbidities |
Diabetes Hypertension | Nil | Nil |
| Social history/pre‐morbid function/activity level/work status |
Lives with wife High physical activity Daily strenuous walk/hike 30 min Intermittent work |
Lives with wife and dependent child High physical activity Nil structured exercise Full‐time work |
Full‐time carer for wife Moderate physical activity Structured exercise twice/week—5 km walk Retired |
| Impairments identified at PR assessment |
Fatigue Dyspnoea on moderate exertion Reduced exercise capacity Weight loss Altered taste Gait dysfunction |
Fatigue Dyspnoea on minimal exertion Reduced endurance with ADLs Cognitive fatigue Weight loss Altered taste Chest tightness Muscle weakness Poor sleep |
Fatigue Dyspnoea on minimal exertion Reduced exercise capacity Reduced endurance with ADLs Cognitive fatigue Weight loss Altered taste Chest tightness Muscle weakness Poor sleep |
+ve, Positive; ADLs, activities of daily living; BMI, body mass index; bpm, beats per minute; COVID‐19, coronavirus disease 2019; CRP, C‐reactive protein; CT, computed tomography; GGO, ground‐glass opacity; ICU, intensive care unit; PCR, polymerase chain reaction; PR, pulmonary rehabilitation; SpO2, oxygen saturation; VTE, venous thromboembolism.