Keywords
Key points
- •Post-acute sequelae of SARS-COV-2 or post-COVID conditions are a poorly defined syndrome, possibly with long-lasting effects.
- •Respiratory failure is one of the most serious complications of COVID-19 infection and contributes to major morbidity and mortality.
- •Several studies have demonstrated abnormal lung function tests and radiological findings in patients who recovered from COVID-19 infection.
- •Evidence on post-COVID pulmonary fibrosis is evolving.
Introduction
Post-COVID lung disease
Abnormal Pulmonary Function Tests
Study | N | Timing | Obstructive Pattern (FEV1/FVC < 70 or < LLN) | Restrictive Pattern (FVC < LLN or 80% TLC < LLN or 80%) | DLCO < 80% |
---|---|---|---|---|---|
Van Gassel et al, 10 2021 | 43 | 3 mo after discharge | 0 | 16 (37.2%) 23 (53.5%) | 36 (87.8%) |
Van den Borst et al, 7 2021 | 124 | 10 wk after discharge | 12 (10%) | 15 (13%) | 41 (34%) |
Gonzalez et al, 8 2021 | 62 | 3 mo after discharge | 1 (2%) | 23 (37.1%) | 50 (82%) |
Liang et al, 9 2020 | 76 | 3 mo after discharge | 5 (6.6%) | 0 | 15 (19.7%) |
Lerum et al, 6 2021 | 103 | 3 mo after admission | NA | 7 (7%) | 24 (24%) |
You et al, 97 2020 | 18 | 40 ± 11.6 d in cases with nonsevere illness, and 34.7 ± 16.5 d in cases with severe illness | 3 (33%) | 3 (33%) | NA |
Huang et al, 70 2021 | 349 | 6 mo after symptom onset | 22 (6.3%) | 56 (16%) | 114 (32.7%) |
Huang et al, 98 2020 | 57 | 30 d after discharge | 1 (1.8%) | 6 (10.5%) | 30 (52.6%) |
Bellan et al, 5 2021 | 224 | 3–4 mo after discharge | NA | NA | 113 (50.4%) |
Smet et al, 99 2021 | 220 | 74 ± 12 d after diagnosis | NA | 84 (38%) | 48 (22%) |
Shah et al, 100 2021 | 60 | 3 mo after symptom onset | 11.7% (7) | 23.3% (14) | 51.7% (31) |
Zhao et al, 12 2020 | 55 | 3 mo after discharge | NA | 4 (7.25%) | 9 (16.4%) |
Mo et al, 101 2020 | 110 | On discharge | 5 (4.5%) | 27 (25%) | 51 (47.2%) |
Chen et al, 4 2021 | 41 | 1 y after discharge | 3 (7.3%) | 5 (12.2%) | 3 (7.3%) |
Timing | Dyspnea mMRC N (%) | 6 MW Test (Distance in Mean or Median) | 6 MWD <80% or < LLN | Significant Desaturation | |
---|---|---|---|---|---|
Van Gassel et al, 10 2021 | 3 mo after discharge | 16 (37.2%) with score ≥ 1 | 482 m (82% p) | NA | 2 (4.7%) |
Van der Borst et al, 7 2021 | 10 wk after discharge | Median 1 | Normal | 25 (22%) | 20 (16%) |
Gonzalez et al, 8 2021 | 3 mo after discharge | NA | 400 m | NA | NA |
Lerum et al, 6 2021 | 3 mo after admission | 37 (54%) with score ≥ 1 | 580 m | NA | NA |
Huang et al, 70 2021 | 6 mo after symptom onset | 419/1615 (26%) | 495 m (87.7% p) | 392 (23%) | NA |
Shah et al, 100 2021 | 3 mo after symptom onset | NA | NA | NA | 4 (7%) |
Huang et al, 98 2020 | 30 d after discharge | NA | 561 m (94% p) | NA | NA |
Guler et al, 11 2021 | 4 mo after discharge | NA | 456 m (severe/critical disease) 576 (mild/moderate disease) | NA | NA |
Radiological Sequelae
Fibrotic Lung Disease: The Proof Is in the Pudding
Role of Steroids and Antifibrotics in Post-COVID Lung Disease
ClinicalTrials.gov Identifier | Study | Status |
---|---|---|
NCT04657484 | Comparison of Two Corticosteroid Regimens for Post-COVID-19 Diffuse Lung Disease (COLDSTER) | Completed |
NCT04551781 | Short-Term Low-Dose Corticosteroids for Management of Post-COVID-19 Pulmonary Fibrosis | Completed |
NCT04988282 | Systemic Corticosteroids in Treatment of Post-COVID-19 Interstitial Lung Disease (STERCOV-ILD) | Recruiting |
NCT04534478 | Oral Prednisone Regimens to Optimize the Therapeutic Strategy in Patients With Organizing Pneumonia Post-COVID-19 (NORCOVID) | Not yet recruiting |
NCT04541680 | Nintedanib for the Treatment of SARS-Cov-2 Induced Pulmonary Fibrosis (NINTECOR) | Recruiting |
NCT04338802 | Efficacy and Safety of Nintedanib in the Treatment of Pulmonary Fibrosis in Patients With Moderate to Severe COVID-19 | Unknown |
NCT04619680 | The Study of the Use of Nintedanib in Slowing Lung Disease in Patients With Fibrotic or Non-Fibrotic Interstitial Lung Disease Related to COVID-19 (ENDCOV-I) | Recruiting |
NCT04856111 | Pirfenidone vs Nintedanib for Fibrotic Lung Disease After Coronavirus Disease-19 Pneumonia (PINCER) | Recruiting |
NCT04653831 | Treatment With Pirfenidone for COVID-19-Related Severe ARDS | Recruiting |
NCT04607928 | Pirfenidone Compared to Placebo in Post-COVID19 Pulmonary Fibrosis COVID-19 (FIBRO-COVID) | Recruiting |
Post-Acute Sequelae of SARS-CoV-2
Assaf G.D.H., McCorkell L., Louise T., et al., What does COVID-19 recovery actually look like? An analysis of the prolonged COVID-19 symptoms survey by patient-led research team. Available at: https://patientresearchcovid19.com/research/report-1/ Accessed May 15, 2022 2020.

Post-Viral Syndromes
- Diagnosis requires that the patient has the following three symptoms:
- 1.A substantial reduction or impairment in the ability to engage in pre-illness levels of occupational, education, social, or personal activities that persist for more than 6 months and are accompanied by fatigue, which is often profound, is of new or definite onset (not lifelong), is not the result of ongoing excessive exertion, and is not substantially alleviated by rest
- 2.Post-exertional malaise
- 3.Unrefreshing sleep
- 1.
- At least one of the following manifestations is also required:
- 1.Cognitive impairment or
- 2.Orthostatic intolerance
- 1.
Incidence
Hospitalized Patients
Nonhospitalized Patients
Risk Factors
Post-Acute Sequelae of SARS-CoV-2 Phenotypes
Type 1 | Type 2 | Type 3 | Type 4 | Type 5 | |||
---|---|---|---|---|---|---|---|
Initial symptoms | Variable | Mild | A | B | A | B | None |
Mild | Mild | None | None | ||||
Duration of symptoms | Variable | >6 wk | 3–6 mo | >6 mo | Variable | Variable | N/A |
Period of quiescence | No | No | Yes | Yes | No | No | N/A |
Delayed onset of symptoms | No | No | No | Yes | Yes | Yes |
Subtype | Proposed Diagnostic Guide | Main Pathophysiology |
---|---|---|
NSC-MOS | Multi-organ symptoms lasting for ≥ 3 mo after acute COVID-19 (regardless of disease severity), especially fatigue, dyspnea, and cognitive impairment. | Tissue damage across multiple organs or system-wide dysregulation |
PFS | Pulmonary fibrosis and other pulmonary sequelae (ie, impaired lung function or respiratory symptoms) lasting for ≥ 3 mo after acute COVID-19, especially severe COVID-19. | Extensive tissue damage, especially in the lungs |
ME/CFS | Disabling fatigue, unrefreshing sleep, PEM, and either cognitive impairment or orthostatic intolerance lasting for ≥ 6 mo after acute COVID-19. | Dysfunction of the immune and nervous systems |
POTS | Increased heart rate of >30 beats per minute within 5–10 min of standing or upright tilt without orthostatic hypotension. May occur with dizziness, palpitations, blurred vision, headache, generalized weakness, exercise intolerance, and fatigue. | Dysfunction of the autonomic nervous system |
PICS | Physical (eg, muscular weakness, weakened handgrip, poor mobility), cognitive (eg, memory and concentration) and mental (eg, anxiety, depression and PTSD) sequelae lasting for ≥ 3 mo after acute COVID-19 of ICU level of severity. | Severe-to-critical illnesses in need of ICU level of care, from which full recovery is difficult |
MCS | Acute or chronic diseases or other clinical sequelae that require medical care. Examples include respiratory, cardiovascular, gastrointestinal, kidney, liver and neurologic diseases, diabetes, infectious diseases, and mental health disorders. | Health deterioration or unmasking of chronic diseases |
Mechanism(s) of Post-Acute Sequelae of SARS-CoV-2
Triage, Workup, and Treatment
Summary
Clinics care points
- •Post-acute sequelae of SARS-CoV-2 (PASC) are a syndrome of nonspecific “head-to-toe” symptoms of unclear cause, mechanism, and duration. Supportive and holistic care is paramount.
- •Abnormalities in lung function testing and chest imaging are fairly common in patients recovering from COVID-19. These abnormalities are heterogenous, often improve with time (though may not always normalize), and may not correlate with symptoms.
- •Reduced diffusion capacity is the most common abnormality in pulmonary function testing.
- •Patients who recover from COVID-19 may develop interstitial lung disease/pulmonary fibrosis. So far, data do not suggest that this represents a progressive fibrotic phenotype. The role of antifibrotic agents in the treatment of post-COVID fibrosis is being studied.
Disclosure
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