1. Introduction
After the first wave of the global coronavirus disease 2019 (COVID-19) pandemic, it became increasingly clear that the pulmonary sequelae often persist far beyond the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Apart from the diverse cluster of symptoms collectively coined “long COVID” [
1] (breathlessness, chest pain, and fatigue), several studies have documented various degrees of reduced pulmonary diffusing capacity of carbon monoxide (DLco) in previously hospitalised patients up to 12-months post-discharge [
2,
3,
4,
5,
6,
7,
8,
9]. In many cases, concomitant residual radiological abnormalities are present on high-resolution chest CT, (HRCT) most typically ground-glass opacities (GGO), interlobular septal thickening, and reticulations [
4,
8].
The mechanisms of post-COVID-19 DLco reduction and the associated symptoms are currently unknown. While previous studies have reported relatively few patients with signs of overt pulmonary fibrosis (PF) on HRCT post-COVID-19 [
10], it is still not known if changes on HRCT such as GGO, interlobular septal thickening, and reticulations will remain and for how long. Given that both in situ pulmonary thrombosis and thromboembolism, triggered by aberrations in the coagulation system and pulmonary endothelialitis [
11], are considered cardinal in the conspicuous and “silent” hypoxaemia often observed in COVID-19 [
12], this may also contribute to late stage changes in lung function. Thus, apart from post-viral PF, persistent pulmonary thromboembolic disease may contribute to persistent DLco reduction and associated symptoms after COVID-19 [
6,
13].
This paper is the first report from the Danish SECURe (Sequelae of COVID-19, Copenhagen University Hospital, Rigshospitalet) to present a prospective cohort study monitoring the severity and duration of post-COVID complications by the use of extensive clinical, physiological, and radiologic assessments, both in previously hospitalised and non-hospitalised COVID-19 patients.
The aim of the current study was to investigate the association between initial COVID-19 severity and haemoglobin-corrected diffusion capacity to carbon monoxide (DLco) reduction at follow-up. Furthermore, the aim was also to analyse if DLco reduction could be linked to pulmonary fibrosis (PF) and/or thromboembolic disease within the first months after the illness.
2. Materials and Methods
2.1. Study Design and Setting
The SECURe study is an ongoing prospective cohort study of individuals with polymerase chain reaction (PCR) confirmed SARS-CoV-2 infection conducted at Copenhagen University Hospital, Rigshospitalet, a tertiary health care centre, aimed to assess long-term sequalae of COVID-19.
The protocol was developed based on early reports from China [
14,
15] and on follow-up data from the first SARS outbreak in Hong Kong in 2002–2003 [
16]. In Denmark, as elsewhere, the COVID-19 treatment strategies have been modified during the study period along with the availability of scientific data. Thus, steroids were first implemented from June 2020 [
17,
18]. Likewise, some patients admitted during the early epidemic were included in the remdesivir trial, the usage of which increased from May 2020 and became widely available from August 2020 [
17,
19].
Inclusion was closed ultimo March 2021 due to the significant decline in SARS-CoV-2 transmission rates in Denmark and closure of our dedicated COVID-19 ward. We enrolled 190 participants.
2.2. Study Participants
All COVID-19 patients admitted to Rigshospitalet, March 2020–March 2021 were invited to participate. Additionally, non-hospitalised SARS-CoV-2 infected patients were offered inclusion with the aim of including 200 patients, ≥2/3 hereof being hospitalised.
Exclusion criteria included dementia, living at an old age facility and being unable to come for follow-up visits.
The initial SECURe study visit was planned to be conducted 3–4 months after SARS-CoV-2 positive testing/post-discharge for non-hospitalised and hospitalised study participants, respectively. Due to a high workload at the participating departments, it was not always possible to adhere fully to this time-plan (see below).
Here, we report on all participants (n = 67) who had completed their first follow-up by 31 December 2020.
2.3. Recruitment
Patients were invited to participate in the study at discharge and/or at a post-discharge telephone consultation. Non-admitted patients were identified through the affiliated testing site and by word of mouth among health care personnel.
2.4. Data Sources
Age, sex, Charlson co-morbidity index [
20], date of testing SARS-CoV-2 positive, initial COVID-19 symptoms and duration thereof prior to admission, treatment during hospitalisation including maximal oxygen demand, ICU admission, mechanical ventilation and/or extra-corporal membrane oxygenation (ECMO) and duration thereof, as well as total duration of hospitalisation were extracted from the participant’s electronic health record. Even though there is now consensus regarding a more advanced disease severity classification system [
21,
22], this had not yet been established at the time of this study, and we therefore pragmatically used a trinary system to classify the patients according to the clinical severity of the initial COVID-19 disease, similar to previous studies patients not requiring hospitalization (Group I), patients requiring hospitalization but not ICU admission (Group II), and patients requiring both hospitalisation and ICU admission (Group III) [
23,
24,
25,
26,
27,
28,
29,
30].
At the follow-up visit, participants were questioned about post-COVID-19 symptoms and respiratory complaints according to the chronic obstructive pulmonary disease assessment test (CAT) [
31]. Furthermore, participants completed the health-related quality of life SF-36 questionnaire [
32], had an extended assessment of physical performance including Hand Grip strength (HGS) and 30-s Sit-To-Stand Test (STS) muscle strength tests and the Six-Minutes’ Walk Test (6MWT) [
33,
34,
35] (
Supplemental File S1), lung function testing [
36,
37,
38], HRCT with subsequent scoring [
39] and ventilation-perfusion (VQ) scintigraphy [
40,
41] (
Supplemental Files S2–S4, and described briefly below).
Participants with signs of post-COVID-19 sequelae were offered re-assessment at 12 months.
2.5. Lung Function Testing
Dynamic spirometry, body plethysmography and single breath measurement of DLco were performed in accordance with the ERS/ATS guidelines [
36,
37,
38]. Forced expiratory volume in the first second (FEV1), forced expiratory volume (FVC), FEV1/FVC-ratio, total lung capacity (TLC), residual volume (RV), RV/TLC-ratio, Hb corrected DLco and diffusion coefficient for CO (Kco) were measured. A FEV1/FVC-ratio and a TLC below the lower limit of normal was classified as an obstructive and restrictive ventilation defect, respectively [
42,
43].
2.6. HRCT Chest Scan
HRCT was obtained both after a breath-hold at deep inspiration and deep expiration. The scans were divided into six zones (three on each side), and evaluated for GGO, PF, and honeycombing (HC). PF was indicated by reticulation, traction and bronchiectasi, in combination or separate. For each of these findings, the extent in every zone was scored from 0 to 4 (
Supplemental File S3) [
39]. All scans were scored by two experienced readers (AK (radiologist) and TKL (pulmonologist)). The readings were carried out as a multidisciplinary reading with consensus. The two readers were blinded to the clinical and functional data.
At the starting point of the SECURe study, there were no validated CT scoring systems in the context of COVID alterations, so we had to choose a system. The scoring system chosen here was based on the system developed in the “Scleroderma Lung Study” [
39]. A proportion of scleroderma patients have lung involvement with both GGO of PF and the scoring system was transferable to this population. There is no consensus regarding which scoring system to use, and various methods have historically been used.
2.7. VQ Scintigraphy
VQ scintigraphy was conducted as single photon emission computed tomography (SPECT) with a low dose CT used for attenuation correction. The European Association of Nuclear Medicine interpretation criteria were applied [
41]. Perfusion and ventilation defects were visually identified, localised, and classified as mismatched (only defect in perfusion), matched (both perfusion and ventilation defects) or inversely mismatched (only defect in ventilation), and sized as subsegmental or segmental. A matched or inversely mismatched ventilation defect was classified as a ventilatory abnormality, regardless of concomitant HRCT findings, while a mismatched perfusion defect without any concomitant signs of fibrosis in the same area on HRCT, including reticulation with or without GGO, was classified as a vascular abnormality, most likely pulmonary embolism. However, if the HRCT showed signs of fibrosis precisely corresponding to a perfusion defect, it was interpreted as a ventilatory abnormality. Various studies have shown that interstitial lung fibrosis may cause mismatched perfusion defects that may incorrectly be interpreted as pulmonary embolism if not correlated to concomitant CT findings [
44,
45,
46]. All scans were read independently by two experienced pulmonary nuclear medicine specialists (JM & RB) and discrepancies were resolved in consensus. The readers were blinded to the clinical and functional data.
2.8. Statistical Analyses
All data were entered into REDCap (10.6.18 ©2021 Vanderbilt University, Nashville, TN, USA). Clinical characteristics, lung function, HRCT, VQ scintigraphy, and physical performance were summarised as percentage (n), mean with standard deviation (SD) for normally distributed variables or median [interquartile range, IQR] for non-normally distributed variables. The differences between clinical severity groups were assessed using Fisher’s exact test for dichotomous and categorical data, Kruskal-Wallis H test for non-normally distributed data, or one-way ANOVA for normally distributed data. If a difference was found, bivariate comparisons with Bonferroni correction for multiple comparisons were made. Wilcoxon rank-sum test was used to assess the difference in groups for time from discharge to follow-up. Fisher’s exact test was used to assess the association between VQ defects and HRCT chest findings of GGO and signs of PF. Univariate linear regression models were used to assess the association between CAT score, VQ defects or HRCT findings with DLco. Multivariable logistic regression models were used to assess the association between VQ defects, HRCT findings or DLco with admission to ICU, age and sex.
Data for physical performance were presented as raw scores and presented as % of age and sex adjusted reference norms.
For all data, a two-sided p < 0.05 was considered statistically significant. Statistical analyses were performed using STATA 12 (StataCorp., Stata Statistical Software: College Station, TX, USA: StataCorp LLC).
4. Discussion
In this Danish cohort of patients with mild to severe COVID-19 the majority had subjective health complaints 5 months after testing SARS CoV-2 positive, irrespective of disease severity. The most common lung function abnormality was reduced DLco. Indeed, both the frequency and severity of reduced DLco differed between clinical severity groups, as did HRCT findings of GGO and fibrosis, and the number of matched defects on VQ SPECT. In contrast, the frequency and extent of mismatched perfusion defects and other signs or pulmonary vascular disease were neither related to reduced DLco nor to clinical severity group.
DLco has been reported at various follow-up times after COVID-19. As in the present study, a reduced DLco is typically noted as part of a restrictive lung disease pattern with a reduced TLC, while signs of obstructive lung disease with a concomitantly low FEV1/FVC is rare [
2,
4,
7,
47,
48,
49,
50]. We found that the prevalence of reduced DLco was 17% in Group I. Previous studies have likewise found that a reduced DLco is common in this group within the first months after COVID-19 and vary markedly from 6 to 43%. In our study, the prevalence of reduced DLco was 40% and 70% in Group II and III, respectively. This is consistent with previous findings from Germany and USA, where reduced DLco was reported in 1/3 of Group II patients and >90% among Group III patients [
24,
25,
26]. In contrast, one study, reported lower prevalence of reduced DLco in Group III compared to Group II patients [
23], perhaps reflecting selection bias in the former group due to a high mortality rate in patients admitted to the ICU in this population. Thus, in the current and other studies, indices of severity, such as ICU admission, high-flow nasal cannula oxygen therapy, mechanical ventilation and duration thereof have been found to predict the prevalence and extent of DLco reduction [
8,
23]. Of note, DLco has been reported to gradually increase with time in most Group II patients, but it remains pathologically low at 12-month follow-up in more than half of the patients with a reduced DLco at 3-month follow-up [
8]. While the exact prevalence estimates are difficult to compare between countries, due to the differences in the extend of the COVID-19 epidemic, healthcare capacity, as well as, preventive, diagnostic, and therapeutic strategies including hospital/ICU admission thresholds, it can be inferred that a pathologically reduced DLco is exceedingly common after COVID-19, and the prevalence increases with the acute phase clinical severity.
GGO was the most common finding in HRCT, which agrees well with other studies conducted at various follow-up times within the first year after infection (1–12 months) [
4,
6,
8,
9,
25]. In accordance with previous studies [
23,
24], we found a gradient across the severity groups with a GGO prevalence of 8, 66 and 100% in Groups I, II and III, respectively. GGO indicate localised infection, inflammation, or fluid in the interstitial or alveolar space, none of which are mutually exclusive. They occur from the onset of COVID-19, and GGO may reflect residual changes from the acute infection [
8,
9]. The extent of GGO after COVID-19 has previously been associated with peak HRCT pneumonia scores during hospitalisation, and the GGO scores gradually decrease over the first 12 months. Moreover, in accordance with previous studies [
4,
6,
8,
9,
25], GGO provide a mechanistic link to reduced DLco. The same pathological changes within the lung parenchyma that cause GGO may thus also adversely affect DLco.
Fibrosis was another key HRCT finding, in most cases in the form of reticulation. This was not observed in Group I, but was present in 37% of Group II patients, and all Group III patients. We identified a broad spectrum from very little to substantial fibrosis, but without HC, which would have indicated end-stage pulmonary fibrosis. At follow-up five months after testing SARS CoV-2 infected (and four months after discharge (for those admitted)), fibrosis was notably seen in Group III patients, while some studies [
6,
9,
23,
24,
49], but not all [
8], have also found fibrosis in Group II patients. Though group III included individuals with asthma and or current/past tobacco usage, none of them were registered in the electronic patient file system with a chronic lung disease diagnosis, nor was this disclosed at the initial encounter due to COVID-19 (data not shown). It is therefore unlikely that the difference in CT-scan findings between the groups was (fully) due to pre-existing signs of fibrosis among the SECURe patients requiring treatment at the ICU unit.
The presence of pulmonary fibrosis was associated with both the presence of GGO and reduced DLco. We speculate that the presence of GGO and pulmonary fibrosis reflect a spectrum of underlying interstitial lung changes that may lead to varying degrees of restrictive lung disease with reduced DLco in a severity-dependent fashion. Accordingly, it is well established that long-standing pulmonary inflammation may facilitate pulmonary fibrosis [
51,
52], and, recently, several elevated plasma biomarkers of pulmonary fibrosis have been reported in COVID-19 patients across severity groups in a manner that is associated with the concurrent decline in DLco [
26]. However, further evaluation of this link is needed.
Though there is an overlap in the CT features found in conjunction with and at follow-up after various viral infections, including influenza- and coronaviruses, differences also exist [
53]. Models have been developed to differentiate between COVID-19 vs. Influenza A (H1N1) pneumonia based on clinical and radiologic features [
54]. With the availability of effective and easily accessible microbiological tests, the differentiation based on radiological findings, including CT features, is not necessary. However, identification of the various patterns and understanding the reasons behind it might be helpful for evaluating treatment response.
To the best of our knowledge, this is the first study to report on systematic VQ SPECT/CT in the follow-up of COVID-19 patients. We found that 95 % had V/Q defects, which was slightly more prevalent in Group II and III (though also highly prevalent in Group I). Sixty-six percent had mismatched defects, all of which were small subsegmental and 40 % had matched defects, the majority segmental and larger. In addition, reverse ventilatory mismatched defects were very prevalent (75%). The high frequency of ventilatory defects (matched and reverse matched) might have made it difficult to identify possible associations between mismatched defects and DLco (
Table 4). It is well-documented that pulmonary vascular disease may complicate COVID-19 in the acute stage and contribute to hypoxaemia and respiratory failure [
55,
56,
57], but it is unknown whether this also contributes to the post-COVID decline in DLco observed in many patients. In the present study, more than 20% showed evidence of vascular disease, notably mismatched perfusion defects. Apart from in situ thrombosis and/or pulmonary embolism, this may also reflect the long-term effects of the remarkable COVID-19-associated loss of pulmonary microvasculature recently reported and is also consistent with fibrosis-like inflammatory processes in the lung parenchyma [
58]. However, this was neither related to the clinical severity group nor to DLco. Rather, reduced DLco was associated with the number of matched VQ defects, indicating ventilatory disturbance, although the association with clinical severity groups was less clear than for HRCT. This provides a functional correlate of the structural lung parenchymal changes seen on HRCT associated with reduced DLco.
There are several study limitations, which may limit the generalisability. Firstly, although all patients discharged from Rigshospitalet were invited to participate, several patient groups were not included in the current analysis, including patients with dementia and patients living at old age facilities. These patients have a higher risk of developing severe COVID-19 and possibly, consequently hereof, more marked long-term sequelae. Conversely, patients with symptoms believed to be related to their COVID-19 might be more inclined to participate. Furthermore, many patients chose not to participate in the study. Among the patients without the need for hospitalisation, there was an overrepresentation of health care workers.
Due to the epidemic and the ensuing strain on the health care system, the follow-up exams could not always be performed at 3–4 months post infection/discharge; however, the divergence from this timing was limited.