key: cord-0829068-btteneni
authors: Komici, Klara; Bianco, Antonio; Perrotta, Fabio; Dello Iacono, Antonio; Bencivenga, Leonardo; D’Agnano, Vito; Rocca, Aldo; Bianco, Andrea; Rengo, Giuseppe; Guerra, Germano
title: Clinical Characteristics, Exercise Capacity and Pulmonary Function in Post-COVID-19 Competitive Athletes
date: 2021-07-09
journal: J Clin Med
DOI: 10.3390/jcm10143053
sha: 762e6b35f9fe6203504ef7e779559b0d0c6cd81b
doc_id: 829068
cord_uid: btteneni

Background: Limited evidence exists regarding adverse modifications affecting cardiovascular and pulmonary function in physical active adults affected by COVID-19, especially in athletic populations. We aimed to describe the clinical presentation of COVID-19 in a cohort of competitive athletes, as well as spirometry and echocardiography findings and cardio-respiratory performance during exercise. Methods: Twenty-four competitive athletes with COVID-19 were recruited for this study after ending self-isolation and confirmation of negative laboratory results. All athletes underwent clinical evaluation, spirometry, echocardiography and cardiopulmonary exercise testing (CPET). These data were compared to a group of healthy control athletes. Results: Anosmia was the most frequent symptom present in 70.83% patients, followed by myalgia, fatigue and ageusia. The most frequent persisting symptoms were anosmia 11 (45.83%) and ageusia 8 (33.33%). Compared to controls, COVID-19 patients presented lower FEV1%: 97.5 (91.5–108) vs. 109 (106–116) p = 0.007. Peak Oxygen Uptake (VO(2)) in COVID-19 patients was 50.1 (47.7–51.65) vs. 49 (44.2–52.6) in controls (p = 0.618). Conclusions: Reduced exercise capacity was not identified and pulmonary and cardiovascular function are not impaired during early recovery phase in a population of physical active adults except FEV1 reduction.

The Coronavirus disease 2019 , caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has affected millions of people globally [1] . The most commonly described symptoms are fever, cough, shortness of breath, anosmia, ageusia, fatigue, myalgia, and nausea/vomiting or diarrhea [2] . Complications of COVID-19 in hospitalized patients include respiratory failure, thromboembolic events, myocarditis, arrhythmias and hemodynamic instability. Young and fit individuals with COVID-19 seem to generally suffer from mild to moderate symptoms [3] , which are limited to the upper respiratory tract, without requiring hospitalization or additional laboratory, chest X-ray or lung computer tomography (CT) examination. Importantly, a recent study performed on athletes with previous asymptomatic to mild COVID-19 did not reveal significant 2 of 13 anomalies in laboratory tests, echocardiography and exercise test monitoring [4] . However, several reports have described prolonged impairment in lung function in post-COVID-19 patients [5, 6] , with a significant percentage of patients after rehabilitation programs, which still present exertional dyspnea. The altered lung function, observed in some post-COVID-19 patients [6] and persistent ground glass opacity together with a lack of improvement in respiratory function for up to 12 months [7] , raise concerns regarding long-term impairment of respiratory system and physical performance. At present, several information regarding myocarditis in young athletes after COVID-19 disease has been described with heterogeneous prevalence, ranging from 0-15% [8] , indicating the necessity of further data and standardized screening protocols before a safe return to play. In addition, post-viral myocarditis has been documented as a cause of sudden cardiac death in young competitive athletes [9] , and experimental animal models of myocarditis have shown that physical exertion may have fatal consequences [10] . However, the evidence on the impact of COVID-19 in athletes remain poor, and actually no accurate definition is available regarding clinical presentation and impact of the disease on physical performance. Therefore, in the present study we aimed to: (a) Describe COVID-19 clinical presentation in a cohort of competitive athletes; (b) evaluate in competitive athletes the impact of SARS-CoV-2 infection on cardio-respiratory performance at rest and during exercise.

Competitive athletes affected by COVID-19 were considered for enrollment in this study. Inclusion criteria were: (a) Age ≥ 18 years and ≤35; (b) positive testing to SARS-CoV-2 by reverse transcription polymerase chain reaction-based (rt-PCR) SARS-CoV-2 RNA from nasopharynx swab; (c) negative rt-PCR SARS-CoV-2 RNA performed 10 days after the first positive nasopharynx, and end of self-isolation period, as indicated by National Government Recommendations (Italian Ministry of Health 12 October 2020 Normative); (d) willingness to participate in this study. Physical examination, weight, height, Body Mass Index (BMI), resting electrocardiogram (ECG), resting systolic and diastolic blood pressure (SBP, DBP) were registered for all patients. Individual records regarding symptoms presentation, their duration in days and persistence if at the time of the study commencement any were also collected. In addition, previous medical conditions, such as asthma, allergy, hypertension, diabetes, dyslipidemia, arrhythmia, heart valve diseases, familiarity for sudden cardiac death and cardiovascular risk factors were collected. A group of competitive athletes following previous physical capacity evaluation after summer holidays and before starting training program tested negative for COVID-19 was recruited as a matched control group. Post-Covid-19 athletes and controls were soccer players. Patients with positive nasopharynx swabs, non-competitive athletes and recovered patients from more than 30 days were excluded from the study.

This study was approved by the Institutional Review Board of Department of Medicine and Health Sciences, University of Molise protocol number 07/2021, and conducted in compliance with the Declaration of Helsinki. All participants gave written informed consent.

Spirometry was performed in accordance to recommended standards [11] with the subjects seated, on the same day immediately before the exercise test. Forced Vital Capacity (FVC), Forced Expiratory Volume in one second (FEV1), FEV1/FVC ratio and Forced Expiratory Flow at rates 25-75% were measured using a clinical spirometer (Sensormedics Viasys Carefusion Vmax Encore 22). The spirometry measurements were also expressed as percentages of theoretical values using reference values normative scores determined through prediction equations, as described elsewhere [12, 13] .

A standard trans-thoracic echocardiography was performed using a Philips iU22 ultrasound system with cardiac sector transducer sampling at 1-5 MHz. All measurements were performed according to the European Society of Cardiology Recommendations for Chamber Quantification [14] . Left Ventricular (LV) size end-diastolic and end-systolic diameter, volume and wall thickness were measured. Global and regional LV functions were evaluated and LV Ejection Fraction (LVEF) was calculated from apical four-and two-chamber views using Simpson's biplane method. Right ventricle size kinetics and function, such as the tricuspid annular plane systolic excursion (TAPSE); fractional area of contraction (FAC), and; presence of pericardial effusion were evaluated. Peak flow velocity during the early diastolic filling phase (E) and during the atrial contraction (A), as well as the deceleration time (DT) were measured. For each Doppler-based measurement, estimates were obtained from 3 cardiac cycles and averaged.

Ventilation and gas exchange variables were measured continuously using a breathby-breath gas analysis system Omnia Quark CPET Cosmed 2019, which was calibrated according to the instructions of the manufacturer. Participants were fitted and familiarized to a two-way breathing Hans Rudolph 7450 series V2mask and headgear before stepping on a motorized treadmill Cosmed T150med and starting the test. A 12 lead ECG recording system Quark T12X wireless12-lead ECG was used continually. Arterial blood pressure was measured at the end of each stage of the test. Non-invasive saturation of peripheral oxygen at rest (SpO 2 %), peak effort and at the end of recovery were assessed. To evaluate significant desaturation during exercise test the difference between rest and peak effort oxygen saturation was calculated. All patients performed an incremental exercise test beginning with 8 km/h speed with stepwise increases of 1 km/h every minute. After reaching a speed of 14 km/h, the inclination was increased by 1% every minute. Patients were encouraged to continue the exercise test until a maximal effort attainment indicated by: (a) Failure of oxygen uptake or heart rate (HR) increase with further increase in work rate; (b) peak respiratory exchange ratio (RER) ≥ 1.10; (c)) rating of perceived exertion ≥ 8 (on the 10-point Borg scale) [15, 16] . Peak VO 2 was recorded as the highest averaged value across 10-30 s during exercise phase. The first ventilatory threshold (1st VT) estimated by the V-slope or respiratory equivalents methods, Ventilation (VE)/Volume of exhaled carbon dioxide (VCO 2 ) slope were evaluated as determined by Wasserman et al. [17] and Clinical Recommendations for Cardiopulmonary Exercise Testing Data Assessment in Specific Patient Populations [18] .

Data are expressed as median and interquartile range (IQR) for continue variables and as absolute frequencies and percentage for categorical variables. Since the normality distribution of different variables could not be assumed as evaluated by Shapiro-Wilk test, univariate analysis Wilcoxon rank-sum (Mann-Whitney) test was performed for continuous variables. The association between categorical variables was assessed by Chi square test. Statistical significance was at p ≤ 0.05. Statistical analyses were performed with STATA SE 16.1 software.

Twenty-four post-COVID-19 athletes represented the final study population. Two patients with negative nasopharynx swabs, performed one month previously, were excluded. Detailed descriptions of COVID-19 clinical presentation, medical history, duration of main symptoms, persistence of symptoms, clinical and instrumental evaluations are shown in Table 1 . The most frequent symptoms reported were anosmia presented by 17 (70.83%) subjects followed by myalgia, fatigue and ageusia, observed in 16 (66.67%), 15 (62.5%) and 15 (62.5%) patients, respectively. Less common symptoms were: fever and rhinitis (n = 12; 50%), cough (n = 11; 45.83%), pharyngodynia (n = 9; 37.5%) shortness of breath (n = 5; 20.83%) and headache (n = 3; 12.5%). Diarrhea was present in 4 patients (16.67%), while only 1 patient (4.17%) suffered from nausea. The mean symptom duration ranged from 2 to 5 days, while only two patients were completely asymptomatic. Figure 1 depicts frequency distribution of symptoms and their persistence at the time of the study enrollment. Shortness of breath, fever, headache or gastro-intestinal disorders were not persisting symptoms in the study population. The most frequent persisting symptoms were anosmia (n = 11; 45.83%) and ageusia (n = 8; 33.33%). Sporadic cough was present in 4 patients (16.67%), rhinitis in 5 patients (20.83%) and myalgia in 2 patients (8.33%). Five patients (20.83%) did not present symptoms' persistence. Spirometry parameters revealed a reduction in FEF 25-75% in 6 (25%) patients without significant alternation in other parameters. Clinical examination, EKG and echocardiography did not show any significant abnormality, with the exception of physical activity-induced modification in cardiac function and structure. EKG monitoring, during CPET, reported isolated Premature Ventricular Beats (PVB) and Premature Supraventricular Beats (PSVB) in two patients and T wave inversion without chest pain or other symptoms in one patient. These alterations were already described in previous tests, and were performed before the COVID-19 pandemic. Cardiac magnetic resonance imaging (CMR) together with CT coronary-angiography did not report any pathological finding. Predicted Peak VO 2 % was more than 100% in all patients except for one patient. However, none of these patients showed ventilatory inefficiency or significant desaturation, but only muscles discomfort. In all patients, the VE/VCO 2 slope was less than 30 and no significant reduction of SpO 2 during exercise was registered. None of the patient presented Ventilatory Oscillations (VO) during exercise. Table 2 reports the main CPET data in COVID-19 patients.

patients with negative nasopharynx swabs, performed one month previously, were excluded. Detailed descriptions of COVID-19 clinical presentation, medical history, duration of main symptoms, persistence of symptoms, clinical and instrumental evaluations are shown in Table 1 . The most frequent symptoms reported were anosmia presented by 17 (70.83%) subjects followed by myalgia, fatigue and ageusia, observed in 16 (66.67%), 15 (62.5%) and 15 (62.5%) patients, respectively. Less common symptoms were: fever and rhinitis (n = 12; 50%), cough (n = 11; 45.83%), pharyngodynia (n = 9; 37.5%) shortness of breath (n = 5; 20.83%) and headache (n = 3; 12.5%). Diarrhea was present in 4 patients (16.67%), while only 1 patient (4.17%) suffered from nausea. The mean symptom duration ranged from 2 to 5 days, while only two patients were completely asymptomatic. Figure  1 depicts frequency distribution of symptoms and their persistence at the time of the study enrollment. Shortness of breath, fever, headache or gastro-intestinal disorders were not persisting symptoms in the study population. The most frequent persisting symptoms were anosmia (n = 11; 45.83%) and ageusia (n = 8; 33.33%). Sporadic cough was present in 4 patients (16.67%), rhinitis in 5 patients (20.83%) and myalgia in 2 patients (8.33%). Five patients (20.83%) did not present symptoms' persistence. Spirometry parameters revealed a reduction in FEF 25-75% in 6 (25%) patients without significant alternation in other parameters. Clinical examination, EKG and echocardiography did not show any significant abnormality, with the exception of physical activity-induced modification in cardiac function and structure. EKG monitoring, during CPET, reported isolated Premature Ventricular Beats (PVB) and Premature Supraventricular Beats (PSVB) in two patients and T wave inversion without chest pain or other symptoms in one patient. These alterations were already described in previous tests, and were performed before the COVID-19 pandemic. Cardiac magnetic resonance imaging (CMR) together with CT coronary-angiography did not report any pathological finding. Predicted Peak VO2% was more than 100% in all patients except for one patient. However, none of these patients showed ventilatory inefficiency or significant desaturation, but only muscles discomfort. In all patients, the VE/VCO2 slope was less than 30 and no significant reduction of SpO2 during exercise was registered. None of the patient presented Ventilatory Oscillations (VO) during exercise. Table 2 reports the main CPET data in COVID-19 patients. 

No statistically significant differences between post-COVID-19 athletes and SARS-CoV-2-negative players were found for age, BMI, previous medical conditions and ECG. Echocardiography data did not show differences in LV systolic or diastolic function and structure. Pulmonary artery pressure (PAP) was higher in post-COVID-19 patients compared to controls ( No statistical difference was found in resting and peak exercise HR, BP and VE. Furthermore, peak VCO 2 , peak Oxygen pulse, peak RER, VE/VCO2 slope and lowest VE/VCO2 were not different between post-COVID-19 athletes and controls. A trend to reduction in VO 2 at 1st VT expressed as % of peak VO 2 was observed in the post-COVID-19 group compared to controls (74.07% {71.6-78.6}vs. 79.04% {76.04-80.01}; p = 0.082. Echocardiographic, spirometry and CPET data are reported in Table 3 . 

The main findings of the present study, included; (a) the clinical presentation of SARS-CoV-2 infection in competitive athletes is mainly characterized by anosmia, ageusia, myalgia and fatigue with a frequency around 60-70%. Fever and upper respiratory tract symptoms were present in 40-50% of the subjects. Other symptoms as shortness of breath or gastro-intestinal symptoms were less common; (b) cardio-respiratory function was not significantly altered in post-COVID-19 athletes both, at rest and during exercise; (c) post-COVID-19 athletes showed a reduction in FEV1% of theoretical value compared to SARS-CoV-2-negative competitive players, despite that ventilatory efficiency and overall performance were not impaired.

The most frequent COVID-19 symptoms, described in non-hospitalized adult patients, include fever, fatigue and cough [19] . Anosmia and ageusia are reported more often than in other viral infections [20] . However, in adult competitive athletes, we found that anosmia and myalgia are most frequently reported. Fever and dry cough are present in up to 90% of hospitalized patients [2] . Whereas, anosmia, fever and myalgia were the only symptoms associated with SARS-CoV-2 positivity among healthcare workers [21] .

Physical fitness and frequent aerobic training have been demonstrated to reduce the frequency, severity and symptomatology of upper respiratory tract infections [22] . Although the role of exercise in specific immune mechanism is not well-established, it has been reported that exercise modifies the number of circulating lymphocytes and the release of stress hormones, and in particular, cortisol, which may influence the activity of anti-inflammatory cytokines [23] . In addition, experimental models report that lung macrophages mediates the beneficial effects of exercise regarding response to infections [24] . From the other side, SARS-CoV-2 infection impairs lymphopoiesis, and the thickening of alveolar wall with macrophages and mononuclear cells have been found in lungs of COVID-19 patients [25] . Furthermore, obesity has emerged as a risk factor for COVID-19 severity and negative outcome [26] , and the protective role of exercise in weight control in COVID-19 presentation and consequences should be further investigated.

In our cohort of competitive athletes' spirometry, the findings did not reveal modifications related to SARS-CoV-2 infection with the only exception of reduced FEV1%. It has been reported that 11% of patients with severe COVID-19, had reduced FVC [7] , while FEV1% was significantly lower in patients after severe or critical COVID-19 compared to patients presenting mild to moderate disease [27] . In a recent study, Gervasi and colleagues [4] found a reduction of PEF in professional athletes recovering from previous mild-to-moderate symptomatic SARS-CoV-19 infection. However, the authors could not clarify whether the observed clinical outcomes resulted from the disease condition or as a consequence of the forced detraining period. Conversely, we did not found any difference in FEF25-75%. Although FEF25-75% measurements could theoretically have higher sensitivity in detecting small airway disease. To date, there has been no reported evidence of changes in subjects suffering from SARS-CoV-2 infection [28] . A study performed on patients with suspected or known lung disease concluded that the contributive role of FEF25-75% measurements, in addition to FEV1, FVC and FEV1/FVC ratio for effective clinical decision making is trivial. [29] . However, it has been reported that in the asthmatic population, changes in FEV1 of more than 20% in short-term trials are confident to a clinically significant change [30] . In our study, we did not observe any difference in FEF among post-COVID-19 and SARS-CoV-2 negative athletes. Whereas, COVID-19 was associated with a reduction in FEV1%. Data regarding minimal clinically important difference regarding pulmonary parameters in post-Covid-19 are lacking and future studies are needed to explore whether these variations have a clinical significance.

We underline that none of the patients presented sinus tachycardia however an implication of autonomic nervous system imbalance has been suggested in "long COVID" [31] . The effects of SARS-CoV-2 infection on cardiac function in competitive athletes are not fully clarified. A previous report investigating cardiac function through cardiac magnetic resonance (CMR) has reported results that are suggestive of myocarditis [32] . However this finding remains debated. In a cohort of 145 subjects, Starekova and colleagues [3] observed that only 2 athletes (1.4%) showed CMR evidence of acute inflammation. Furthermore, in a cohort performed on 1597 after COVID-19 infection, CMR screening detected 37 subjects (2.3%) with clinical and subclinical myocarditis [33] , and recent data from a multi-centered prospective study reported that the prevalence of myocarditis following SARS-CoV-2 infection is about 0-5-3% and no adverse cardiac events were registered during a median follow-up of 113 days in young competitive athletes with RMN signs of myocarditis [34] . Other studies evaluating symptom persistence in adults with mild COVID-19 disease reported that, during three-to-six month follow-up palpitations, chest pain and dyspnea were present, respectively in 9, 5 and 30% of adults [35] . Another study with 1946 patients who suffered out-of-hospital cardiac arrest and 1080 in hospital cardiac arrest had a 2.3 to 3.4-fold risk of dying within one month, and COVID-19 was involved in at least 10% of out of hospital cardiac arrest [36] . Post-mortem studies of athletes who died from sudden cardiac death myocarditis was diagnosed in up to 8% [37] . Moreover, only in 21.6% of sudden cardiac deaths related to myocarditis among young athletes was characterized by typical symptoms as chest pain, dyspnea and palpitations [38] . Therefore, short-and long-term outcome data are strongly required to clarify the implications of COVID-19 disease on cardiac events. Compared to HC, a higher PAP level in COVID-19 patients was found. It should be mentioned that none of the patients presented pathologically elevated PAP and other data regarding RV function as TAPSE, TAPSE/PAP ratio, F.A.C or even pulmonary acceleration time were not different. However, in hospitalized non-intensive care unit patients the prevalence of pulmonary hypertension was 12%, a finding that warrants further investigations to establish its causal-relationships with the COVID-19 disease [39] . CPET examination did not reveal significant modifications regarding exercise limitation, ventilatory efficiency, respiratory reserve and oxygen pulse, indicating no impairments were present in pulmonary or cardiac function, at least in adult competitive athletes at early post COVID-19 recovery. This is not surprising, given that exercise-induced ventilatory limitation was not detected, even in post-SARS patients requiring hospitalization [40] . Despite limited evidence regarding COVID-19 sequelae on respiratory and physical function, few reports suggest impairment during short-term follow-up. Moreover, a recent study described that patients who experienced severe-to-critical COVID-19 disease are characterized by a reduction in pulmonary function as measured by diffusing capacity of the lung for carbon monoxide (DLCO), radiological findings of ground glass opacities with mosaic attenuation, seen up-to-four months during follow-up, which can lead to ventilation/perfusion mismatching and contribute to physical impairment and hypoxemia during exercise [27] . Of interest, we noticed that the first VT expressed as percentage of peakVO 2 was lower than in HC. Modification of first VT has been described in detrained subjects [17] . Although, the underpinning molecular mechanisms triggered by SARS-CoV-19 infection and the consequences on modifying the ventilatory drive response to excessive lactate accumulation is unknown yet.

This study presents a few limitation worthy of consideration. First, it was performed in a single center on a relatively small number of patients, which limits the possibility of generalizing the observed findings to other populations. Second, while the main symptoms were self-reported during interviews performed briefly after patients' recovery, no indication of their severity was obtained. Finally, no instrumental examinations were administered for the recruited patients before they contracted COVID-19, which precludes any causal relationships assumption about the effects SARS-CoV-19 infection on the cardiorespiratory and functional outcomes. However, the main anthropometric, clinical history and athletic characteristics (e.g., age, BMI, comorbidities, training background) were homogenous between the COVID-19 group and the healthy control group. Moreover, the control group was tested immediately prior to the start of the competitive season, whereby it can be assumed that this cohort is representative of competitive athletes and used for comparative analysis. Finally, in this study, we did not provide follow-up data regarding cardio-respiratory consequences of SARS-CoV-19 infection in competitive athletes, and long-term implications could not be excluded. However, baseline examinations and CPET monitoring excluded the presence of complex arrythmias or other conditions of clinical significance.

The COVID-19 disease seems to affect competitive athletes mainly with clinical symptoms, such as anosmia, ageusia myalgia and fatigue. Persisting symptoms, such as anosmia, ageusia, sporadic cough and myalgia may also present in these athletes. Reduced exercise capacity was not identified, and pulmonary and cardiovascular function were not found to be impaired during the early recovery phase in a population of physically active adults, except FEV1 reduction. Data Availability Statement: Data that underlie the results reported in this article, after deidentification, protocol and statistical analysis will be available on request. Researchers should provide a methodologically sound proposal.

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We thank Maria Filangeri for her great work, technical support and collaboration in this study. Leonardo Bencivenga has been supported by a research grant provided by the Cardiopath PhD program.

The authors declare no conflict of interest.