Impact of impaired pulmonary function on clinical outcomes in survivors of severe COVID-19 without pre-existing respiratory disease

ABSTRACT

Objective:

To investigate the impact of impaired pulmonary function on patient-centered outcomes after hospital discharge due to severe COVID-19 in patients without preexisting respiratory disease.

Methods:

This is an ongoing prospective cohort study evaluating patients (> 18 years of age) 2-6 months after hospital discharge due to severe COVID-19. Respiratory symptoms, health-related quality of life, lung function, and the six-minute walk test were assessed. A restrictive ventilatory defect was defined as TLC below the lower limit of normal, as assessed by plethysmography. Chest CT scans performed during hospitalization were scored for the presence and extent of parenchymal abnormalities.

Results:

At a mean follow-up of 17.2 ± 5.9 weeks after the diagnosis of COVID-19, 120 patients were assessed. Of those, 23 (19.2%) reported preexisting chronic respiratory diseases and presented with worse lung function and exertional dyspnea at the follow-up visit in comparison with their counterparts. When we excluded the 23 patients with preexisting respiratory disease plus another 2 patients without lung volume measurements, a restrictive ventilatory defect was observed in 42/95 patients (44%). This subgroup of patients (52.4% of whom were male; mean age, 53.9 ± 11.3 years) showed reduced resting gas exchange efficiency (DL_CO), increased daily-life dyspnea, increased exertional dyspnea and oxygen desaturation, and reduced health-related quality of life in comparison with those without reduced TLC (50.9% of whom were male; mean age, 58.4 ± 11.3 years). Intensive care need and higher chest CT scores were associated with a subsequent restrictive ventilatory defect.

Conclusions:

The presence of a restrictive ventilatory defect approximately 4 months after severe COVID-19 in patients without prior respiratory comorbidities implies worse clinical outcomes.

Keywords:
Post-acute COVID-19 syndrome; Respiratory function tests; Exercise test; Quality of life; Follow-up studies

RESUMO

Objetivo:

Investigar o impacto do comprometimento da função pulmonar nos desfechos centrados no paciente após a alta hospitalar em pacientes sem doenças respiratórias preexistentes que foram hospitalizados em virtude de COVID-19 grave.

Métodos:

Trata-se de um estudo prospectivo de coorte em andamento, no qual pacientes com COVID-19 grave (com idade > 18 anos) são avaliados 2-6 meses depois da alta hospitalar. Avaliamos os sintomas respiratórios, a qualidade de vida relacionada à saúde, a função pulmonar e a distância percorrida no teste de caminhada de seis minutos. A definição de distúrbio ventilatório restritivo foi CPT abaixo do limite inferior da normalidade na pletismografia. As imagens de TC de tórax realizadas durante a hospitalização foram avaliadas quanto à presença e extensão de alterações parenquimatosas.

Resultados:

Em média 17,2 ± 5,9 semanas depois do diagnóstico de COVID-19, foram avaliados 120 pacientes. Destes, 23 (19,2%) relataram doenças respiratórias crônicas preexistentes e apresentaram pior função pulmonar e maior dispneia aos esforços na consulta de acompanhamento quando comparados aos outros participantes. Quando excluímos os 23 pacientes com doenças respiratórias preexistentes e mais 2 pacientes (sem medidas de volumes pulmonares), observamos distúrbio ventilatório restritivo em 42/95 pacientes (44%). Esse subgrupo de pacientes (52,4% dos quais eram do sexo masculino, com média de idade de 53,9 ± 11,3 anos) apresentou menor eficiência das trocas gasosas (DL_CO), maior dispneia na vida diária e dessaturação de oxigênio ao exercício e redução da qualidade de vida relacionada à saúde em comparação com aqueles sem redução da CPT (50,9% dos quais eram do sexo masculino, com média de idade de 58,4 ± 11,3 anos). A necessidade de terapia intensiva e pontuações mais altas no escore de alterações parenquimatosas na TC de tórax apresentaram relação com distúrbio ventilatório restritivo subsequente.

Conclusões:

A presença de distúrbio ventilatório restritivo aproximadamente 4 meses depois da COVID-19 grave em pacientes sem comorbidades respiratórias prévias implica piores desfechos clínicos.

Descritores:
Síndrome pós-COVID-19 aguda; Testes de função respiratória; Teste de esforço; Qualidade de vida; Seguimentos

INTRODUCTION

Long-lasting respiratory symptoms and impaired pulmonary function have been increasingly recognized as post-COVID-19 sequelae.¹ Although the respiratory system is subject to major involvement during SARS, a substantial burden of health loss that spans several extrapulmonary systems has also been reported.² Perceived poor health status after COVID-19 was not related to respiratory sequelae (persistent chest imaging abnormalities) or disease severity in the acute phase in one study with a median follow-up of 75 days after diagnosis.² Conversely, impaired pulmonary function parameters have shown significant correlations with worse dyspnea, as assessed by the modified Medical Research Council (mMRC) dyspnea scale, and worse Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) physical functioning domain scores 45 days after hospital discharge.³

The impact of prior respiratory comorbidities on pulmonary function and its relationship with enduring respiratory complaints and health-related quality of life (HRQoL) was also less explored in previous studies. It is conceivable that patients with prior respiratory comorbidities should ideally be excluded for an unbiased analysis of the effects that pulmonary function sequelae of acute COVID-19 have on clinical outcomes.⁴ Furthermore, the international standard recommendation to define lung function impairment (values below the lower limit of normal, i.e., the 5th percentile of a healthy population)⁵ has not been consistently followed^1,6,7 or reported.⁸

We hypothesized that persistent pulmonary dysfunction after severe COVID-19 would further impair clinical outcomes in patients recovering from the disease. Therefore, our primary objective was to assess the impact of resting ventilatory impairment (i.e., values below the lower limit of normal) on general HRQoL, respiratory symptoms, and exercise performance after hospitalization for severe COVID-19 in patients without chronic respiratory disease. Secondary objectives were to compare these clinical outcomes between patients with and without chronic respiratory disease, and identify predictors during hospitalization on the subsequent presence of ventilatory impairment in the latter group of patients.

METHODS

This is an ongoing single-center prospective cohort study including adult patients hospitalized for severe COVID-19 pneumonia between March 31, 2020 and November 23, 2021. The burden of comorbidities was assessed by calculating the Charlson Comorbidity Index.⁹ All procedures were performed during a single study visit, which occurred 2-6 months after laboratory confirmation of SARS-CoV-2 infection. During the visit, the study participants underwent full pulmonary function testing and a six-minute walk test (6MWT). Subsequently, they completed questionnaires to evaluate HRQoL and respiratory symptoms, as well as symptoms of anxiety, depression, and posttraumatic stress disorder (PTSD). The main outcome measures were obtained from cross-sectional analysis of the aforementioned data. The clinical, laboratory, and chest imaging data obtained during hospitalization were collected from patient medical records. A semiquantitative scoring system¹⁰ was used in order to assess lung involvement on the first chest CT scan performed during hospitalization. Each of the five lung lobes was visually scored on a scale of 0 to 5, with 0 indicating no involvement, 1 indicating an involvement of < 5%, 2 indicating an involvement of 5-25%, 3 indicating an involvement of 26-49%, 4 indicating an involvement of 50-75%, and 5 indicating an involvement > 75%. The total CT score was the sum of the individual lobar scores and ranged from 0 (no involvement) to 25 (maximum involvement). Two thoracic radiologists evaluated the chest CT images in a digital database system (IMPAX, version 8.1.2.SP&.1; Agfa HealthCare, Mortsel, Belgium), and final scores were determined by consensus.

The study was approved by the local research ethics committee (Protocol no. 2020-0169) and was performed in accordance with the Declaration of Helsinki. All participating patients gave written informed consent. The study protocol was registered at ClinicalTrials.gov (Identifier: NCT04410107).

Patients ≥ 18 years of age with laboratory-confirmed severe COVID-19 seen in the respiratory department just before discharge were invited to participate, constituting a convenience sample. Laboratory confirmation of SARS-CoV-2 infection was defined as a positive RT-PCR result from a nasal swab. Severe COVID-19 was defined as fever or suspected lower respiratory tract infection plus one of the following criteria: 1) respiratory rate > 30 breaths/min; 2) severe respiratory distress or SpO₂ of ≤ 93% on room air; or 3) pulmonary infiltrates > 50% on chest imaging within 24-48 h of hospital admission.¹¹ Patients who were clinically unstable 2 months before enrollment, those who had active respiratory tract infection, and those who had any clinical condition precluding the performance of the study procedures were excluded.

Procedures

Spirometry, body plethysmography, single-breath DL_CO measurement, and impulse oscillometry were performed in accordance with the American Thoracic Society/European Respiratory Society standards, with the use of an automated system (MasterScreen™ PFT; CareFusion, Yorba Linda, CA, USA). The last hemoglobin value measured during hospitalization was used for DL_CO correction. Spirometry, lung volumes, and DL_CO parameters were expressed as absolute and percent predicted values, in accordance with the Global Lung Function Initiative reference values.^12-14 Impulse oscillometry measurements were also expressed as absolute and percent predicted values.¹⁵ Obstructive ventilatory defect (a reduction in the FEV₁/FVC ratio after bronchodilator administration), restrictive ventilatory defect (reduced TLC), and reduced DL_CO were characterized by measurements below the lower limit of normal (i.e., below the −1.645 z-score).⁵

The 6MWT was performed indoors in a flat, 25-m corridor, in accordance with the latest European Respiratory Society/American Thoracic Society technical standards. All 6MWTs were performed at least 30 min after the pulmonary function tests. Continuous monitoring of SpO₂ was performed with a pulse oximetry sensor (PureLight^® 8000AA; Nonin Medical, Inc., Plymouth, MN, USA) connected to an oximeter. The six-minute walk distance was expressed as a percentage of the predicted value,¹⁶ and values below the lower limit of normal defined reduced exercise capacity.

The mMRC dyspnea scale was used in order to grade dyspnea during activities of daily living, the levels of dyspnea being graded from 0 (absence of dyspnea during strenuous exercise) to 4 (too breathless to leave the house or breathless while dressing or undressing).¹⁷ Cough and sputum production were assessed through an adapted translation of the American Thoracic Society respiratory symptoms questionnaire.¹⁸

General HRQoL was assessed with the SF-36. The SF-36 is a 36-item questionnaire divided into eight domains that measure social, physical, and mental health aspects. Each domain score ranges from 0 to 100, with higher scores reflecting better quality of life.¹⁹ Reference values for the Brazilian population²⁰ were used for comparison with the values obtained in the present study.

Depression and anxiety symptoms were assessed by the Beck Depression Inventory (BDI) and the Beck Anxiety Inventory (BAI), respectively. The BDI and the BAI consist of 21 sets of statements about depression and anxiety symptoms in the last 7 days, rated on a 0-to-3 ordinal Likert scale.^21,22 A BDI > 14 and a BAI > 8 indicate some level of depression²³ and anxiety,²² respectively.

PTSD was evaluated through the self-report PTSD Checklist, Civilian Version,²⁴ which comprises 17 items that assess three symptom groups during the previous month, on a scale of 1 to 5 (not at all to very much): reexperiences, avoidance behavior/emotional numbness, and increased arousal.²³ A score ≥ 3 (average) for any of the 17 items is considered clinically significant.²⁵

Statistical analysis

Data were analyzed with the Predictive Analytics Software package, version 18.0 (SPSS Inc., Chicago, IL, USA). The level of significance was set at p < 0.05. Normality was assessed by the Kolmogorov-Smirnov test. Continuous data were presented as mean ± SD or median (25^th-75^thpercentiles), depending on the data distribution. Categorical variables were reported as frequencies and proportions. Comparisons between groups were performed with the independent Student’s t-test, Pearson’s chi-square test, or Fisher’s exact test. Stepwise logistic regression analysis was used in order to identify hospitalization variables related to abnormal lung function in individuals without prior respiratory comorbidities.

RESULTS

A total of 152 patients were evaluated for inclusion in the study. Of those, 120 (88.1%) were enrolled within a mean of 17.2 weeks of a positive RT-PCR test for SARS-CoV-2 infection (95% CI, 16.1-18.3; Figure 1). Twenty-three participants (19.2%) reported having chronic respiratory disease before COVID-19 (asthma, in 11; COPD, in 9; pulmonary tuberculosis, in 2; and bronchiectasis, in 1). Other comorbidities, daily-life dyspnea before COVID-19, duration of COVID-19 symptoms before admission, and hospitalization characteristics were similar between those with and without preexisting respiratory disease (data not shown). During the follow-up study visit, however, despite similar HRQoL and psychological symptoms, those with preexisting respiratory disease presented with worse lung function, exertional dyspnea, and oxygen saturation. Accordingly, the prevalences of obstructive ventilatory defect and abnormally reduced DL_CO were higher (p < 0.001 and p = 0.10, respectively; Table 1), as were the prevalences of clinically relevant cough (4-6 times a day, ≥ 4 days a week; 31.8% vs. 11.0%; p = 0.01) and phlegm from the chest (> twice a day; 23.8% vs. 8.8%; p = 0.06).

Table 1
Comparison between patients with and without preexisting respiratory disease in terms of lung function, exercise performance, and health-related quality of life at the follow-up visit.^a

Demographic/anthropometric data	Patients with preexisting respiratory disease	Patients without preexisting respiratory disease	p
	n = 23	n = 97
Age, years	53.9 ± 17.1	56.7 ± 11.6	0.462
Weight, kg	87.4 ± 19.6	87.8 ± 17.4	0.926
Height, m	1.66 ± 0.05	1.66 ± 0.12	0.954
BMI, kg/m2	31.6 ± 6.7	31.7 ± 5.5	0.918
mMRC dyspnea scale score	2 (0-4)	1 (0-3)	0.210
Spirometry	n = 23	n = 97
Number of weeks after COVID-19 diagnosis	15.9 ± 8.0	17.2 ± 5.8	0.484
FVC, % predicted	78.9 ± 16.5	87.6 (72.7-98.8)	0.661
FEV1, % predicted	76.7 ± 19.2	93.6 (83.6-106.6)	0.194
FEV1/FVC	0.77 ± 0.11	0.87 ± 0.05*	< 0.001
FEV1/FVC < LLN, n (%)	5 (21.7)	0*	< 0.001
Plethysmography	n = 23	n = 95
TLC, % predicted	85.7 ± 18.4	83.8 (74.5-92.7)	0.959
TLC < LLN, n (%)	11 (47.8)	42 (44.2)	0.754
FRC, % predicted	98.8 (71.2-109.5)	81.7 (69.2-91.6)	0.255
RV, % predicted	126.4 ± 59.9	94.7 (78.7-110.2)*	0.019
Diffusing capacity of the lung	n = 23	n = 95
DLCO, % predicted	68.3 ± 22.3	83.3 (67.6-93.9)	0.149
DLCO < LLN, n (%)	13 (59.1)	38 (40.0)	0.104
Impulse oscillometry	n = 14	n = 62
Resistance at 5 Hz, % predicted	187.5 ± 60.8	127.5 (105.4-170.1)*	< 0.001
Resistance at 20 Hz, % predicted	138.8 ± 43.2	123.2 ± 34.9	0.153
R5-R20, Kpa/L/s	0.24 ± 0.14	0.08 (0.06-0.13) *	0.004
Reactance at 5 Hz, Kpa/L/s	−0.25 ± 0.15	−0.11 (−0.15 to −0.08)*	0.008
Resonance frequency, 1/s	22.4 ± 7.0	16.3 ± 4.3*	0.008
Area of resonance, Kpa/L	2.13 ± 1.52	0.53 (0.3-1.0)*	0.011
6MWT	n = 23	n = 95
6MWD, m	377.4 ± 117.8	410.0 ± 104.0	0.201
6MWD, % predicted	69.0 ± 20.5	74.7 ± 25.1	0.329
6MWD < LLN, n (%)	14 (60.9)	37 (38.9)	0.057
Resting SpO2, %	94.5 ± 1.9	96 (94-97)	0.568
Final SpO2, %	91.1 ± 4.7	94 (92-96)*	0.033
Final Borg dyspnea scale score	3.0 ± 2.4	0 (0-3.2)	0.071
Final Borg leg fatigue scale score	2 (0-4)	0 (0-3)	0.698
Final Borg dyspnea score/6MWD, n/km	8.1 (0.0-12.6)	0.0 (0.0-0.9)*	0.014
SF-36	n = 16	n = 70
Physical functioning	46.2 ± 27.6	42.5 (30-61)	0.541
Role-physical	12 (0-81)	0 (0-75)	0.637
Bodily pain	56.9 ± 25.3	51.0 (31-74)	0.689
General health	56.6 ± 22.8	62.0 (45-82)	0.411
Vitality	58.7 ± 25.0	55 (43-70)	0.542
Social functioning	53.1 ± 30.7	62 (25-87)	0.489
Role-emotional	66 (0-100)	33.3 (0-75)	0.116
Mental health	68.5 ± 24.4	58.4 ± 24.2	0.139
Psychological symptoms	n = 16	n = 70
Beck Anxiety Inventory	18.3 ± 16.6	11.5 (4-24.2)	0.584
Beck Depression Inventory	8.5 (6.5-15.5)	9.0 (5.2-17.4)	0.934
PCL-C	25.0 (23-31)	28.0 (22.5-40)	0.328

• mMRC: modified Medical Research Council; LLN: lower limit of normal (i.e., below the 5th percentile); FRC: functional residual capacity; R₅-R₂₀: resistance at 5 Hz-resistance at 20 Hz; 6MWT: six-minute walk test; 6MWD: six-minute walk distance; SF-36: Medical Outcomes Study 36-Item Short-Form Health Survey; and PCL-C: Posttraumatic Stress Disorder Checklist, Civilian Version. ^aData presented as mean ± SD, median (IQR), or n (%). *Values of p < 0.05.

Figure 1
Flow chart of the patient inclusion process.

When we excluded patients with preexisting respiratory disease (n = 23) and those without lung volume measurements (n = 2), we observed a prevalence of 42/95 patients (44.2%) with restrictive disorder and a prevalence of 37/95 patients (38.9%) with abnormally reduced DL_CO. Of the 42 patients with restrictive ventilatory impairment, 14 (33.3%) did not show reduced DL_CO. None was found to have an obstructive ventilatory defect (with the use of the lower limit of normal or a fixed ratio below 0.7). Patients with a restrictive ventilatory defect had a shorter duration of symptoms before hospitalization and higher proportions of ICU admission and invasive mechanical ventilation, as well as longer length of hospital stay, longer duration of invasive mechanical ventilation, and higher chest CT scores. During the follow-up study visit, these patients presented with worse daily-life dyspnea and DL_CO, as well as higher prevalences of reduced exercise capacity, exertional dyspnea, and oxygen desaturation (Table 2). General HRQoL was worse in almost all domains, the exceptions being bodily pain, role-emotional, and mental health (Figure 2). Although the prevalence of significant dyspnea (i.e., an mMRC dyspnea scale score ≥ 2) was higher in those with a restrictive ventilatory defect, there were no differences between those with and those without a restrictive ventilatory defect in terms of clinically relevant cough and sputum production (Figure 3). Regarding psychological symptoms, only anxiety-related complaints were higher in the former group of patients (Table 2).

Table 2
Comparison between patients without preexisting respiratory disease presenting with a restrictive ventilatory defect at the follow-up visit and those not presenting with a restrictive ventilatory defect at the follow-up visit.^a

Variable	RVD	No RVD	p
	n = 42	n = 53
Age, years	53.9 ± 11.3	58.4 ± 11.3	0.061
Male sex, n (%)	22 (52.4)	27 (50.9)	0.527
Weight, kg	93.6 ± 17.9	84.0 ± 15.7*	0.007
Height, m	1.68 ± 0.1	1.64 ± 0.1	0.084
BMI, kg/m2	33.0 ± 5.8	30.9 ± 5.0	0.067
Current or former smoker, n (%)	10 (24.4)	24 (45.3)*	0.037
Comorbidities
Hypertension	24 (57.1)	24 (45.3)	0.251
Diabetes	13 (31)	12 (22.6)	0.361
Obesity	24 (57.1)	17 (32.1)*	0.014
Cardiovascular disease	4 (9.5)	3 (5.7)	0.371
Cerebrovascular disease	3 (7.1)	2 (3.8)	0.390
Chronic liver disease	0 (0.0)	1 (1.9)	0.558
Chronic kidney disease	2 (4.8)	1 (1.9)	0.413
Cancer	3 (7.1)	3 (5.7)	0.545
Charlson Comorbidity Index	1 (0-3)	2 (1-3)	0.784
mMRC dyspnea scale score before COVID-19	0 (0-1)	0 (0-0)	0.070
Symptoms before admission, days	6 (4-10)	8 (6-10)*	0.028
Data during hospitalization
Length of stay, days	24 (15-45)	10 (9-15)*	< 0.001
ICU admission, n (%)	31 (73.8)	17 (32.1)*	< 0.001
NIV, n (%)	11 (26.2)	19 (35.8)	0.315
IMV, n (%)	19 (45.2)	4 (7.5)*	< 0.001
Duration of IMV, days	0 (0-20)	0 (0-0)*	0.002
Chest CT score	21 (16-24)	13 (11-18)*	< 0.001
Follow-up study visit
Number of weeks after COVID-19 diagnosis	17.7 ± 5.9	16.8 ± 5.6	0.489
mMRC dyspnea scale score	2 (0-3)	1 (0-2)*	0.008
mMRC dyspnea scale score ≥ 2, n (%)	24 (57.1)	13 (24.5)*	0.001
Spirometry
FVC, % predicted	72.3 ± 15.9	100.9 ± 60.0*	0.006
FEV1, % predicted	80.0 ± 17.7	103.4 (93.2-111.5)*	0.007
FEV1/FVC	0.87 ± 0.00	0.85 ± 0.00	0.061
FEV1/FVC, % predicted	110.2 ± 7.2	107.5 (104-11.5)	0.569
FEV1/FVC < LLN, n (%)	0	0
Plethysmography
TLC, % predicted	72.7 (61.6-77.6)	91.7 (87.8-96.1)*	< 0.001
FRC, % predicted	71.41 ± 13.10	88.7 (80.7-99.8)	0.071
RV, % predicted	84.4 ± 18.9	101.6 (92.2-119.1)*	0.009
Diffusing capacity of the lung	n = 40	n = 53
DLCO, % predicted	70.73 ± 18.40	90.6 (79.2-98.4)*	0.001
DLCO < LLN, n (%)	28 (66.7)	9 (17.3)*	< 0.001
Impulse oscillometry	n = 24	n = 38
Resistance at 5 Hz, % predicted	140.8 ± 41.7	134.9 ± 41.2	0.587
Resistance at 20 Hz, % predicted	110.5 (94.2-143.2)	125 ± 35.6	0.601
R5-R20, Kpa/L/s	0.12 ± 0.00	0.07 (0.0-0.1)*	0.027
Reactance at 5 Hz, Kpa/L/s	−0.13 ± 0.00	−0.10 (−0.10 to 0.00)	0.116
Resonance frequency, 1/s	17.4 ± 4.4	15.6 ± 4.2	0.108
Area of resonance, Kpa/L	0.67 (0.4-1.6)	0.48 (0.2-0.8)	0.124
6MWT	n = 38	n = 52
6MWD, m	385.7 ± 94.6	430.2 ± 109.1	0.051
6MWD, % predicted	72.2 ± 15.7	77.9 ± 28.5	0.275
6MWD < LLN, n (%)	20 (52.6)	15 (28.8)*	0.020
Resting SpO2, %	95 (2)	96 (3)*	0.030
Final SpO2, %	93 (6)	95 (3)*	0006
Final Borg dyspnea scale score	2 (0-5)	0 (0-2)*	0.014
Final Borg leg fatigue scale score	2 (0-4)	0 (0-2)	0.164
Final Borg dyspnea score/6MWD, n/km	6.06 (0-13)	0 (0-5.3)*	0.011
Psychological symptoms	n = 29	n = 40
Beck Anxiety Inventory	22.0 ± 17.4	8 (3-21)*	0.008
Beck Depression Inventory	11 (6-17)	8 (3-16)	0.128
PCL-C	29 (23-42)	28 (22-39)	0.952

• RVD: restrictive ventilatory defect; mMRC: modified Medical Research Council; NIV: noninvasive ventilation; IMV: invasive mechanical ventilation; LLN: lower limit of normal (i.e., below the 5th percentile); FRC: functional residual capacity; R₅-R₂₀: resistance at 5 Hz-resistance at 20 Hz; 6MWT: six-minute walk test; 6MWD: six-minute walk distance; and PCL-C: Posttraumatic Stress Disorder Checklist, Civilian Version. ^aData presented as mean ± SD, median (IQR), or n (%). *p < 0.05.

Figure 2
Comparison of general health-related quality of life (as assessed by Medical Outcomes Study 36-Item Short-Form Health Survey [SF-36^ domain scores) between patients with and without a restrictive ventilatory defect (RVD) at the follow-up visit, after exclusion of those with prior respiratory comorbidities. The red dotted lines represent the mean reference values for each SF-36 domain, derived from randomly selected Brazilian men and women who were in the same age bracket as were the patients included in the present study (i.e., the 55- to 64-year age bracket).²⁰

Figure 3
Comparison of respiratory symptoms between patients without prior respiratory comorbidities presenting with a restrictive ventilatory defect (RVD) at the follow-up visit and those not presenting with an RVD at the follow-up visit. mMRC: modified Medical Research Council.

Stepwise multivariate logistic regression analysis including age, sex, and the Charlson Comorbidity Index revealed that intensive care need and the magnitude of pulmonary involvement (as assessed by chest CT scores) predicted the presence of a restrictive ventilatory defect at the follow-up visit (Table 3).

Table 3
Multivariate logistic regression model to predict a restrictive ventilatory defect at the follow-up visit in patients without preexisting chronic respiratory comorbidities.^a

	Exp (b)	95% CI		p
		Lower	Upper
Intensive care (reference: no)	5.522	1.997	15.273	0.001
Chest CT score	1.135	1.033	1.247	0.008

• ^a
  Other variables included in the first step of the backward stepwise logistic regression model were age, sex, and the Charlson Comorbidity Index.

DISCUSSION

Persistent respiratory symptoms and impaired pulmonary function have been increasingly recognized as post-acute COVID-19 sequelae.¹ The extent to which preexisting respiratory conditions and impaired lung function after COVID-19 affect clinical outcomes is less clearly established. The present study showed that prior respiratory disease implied lower lung function and worse respiratory symptoms. By excluding these patients, we demonstrated that a restrictive ventilatory defect was a common finding (in 44%), usually associated with impaired gas exchange (¯DL_CO) a few months (≈ 4 months) after hospitalization for severe COVID-19. A restrictive ventilatory defect was associated with negative effects on patient-centered outcomes, including exertional and daily-life dyspnea (an mMRC dyspnea scale score ≥ 2), as well as exercise capacity and general HRQoL.

Fatigue, dyspnea, and cough are among the most common complaints in studies examining symptoms after hospitalization or disease onset.²⁶ Interestingly, the aforementioned symptoms are also highly prevalent among patients not hospitalized during the acute phase. One recent study showed that persistent dyspnea after COVID-19 (13% of the sample had been hospitalized) was not associated with overt cardiopulmonary impairment or exercise intolerance.²⁷ Conversely, persistent dyspnea, fatigue, and exercise intolerance have been associated with peripheral oxygen delivery/utilization mismatch, respiratory limitation, or dysfunctional breathing in samples with hospital admission rates ranging from 10% to 96% during the acute phase of COVID-19.²⁸ In a study including only noncritically ill patients (27% of whom had no hypoxemia and were treated on an outpatient basis), those with persistent dyspnea were found to have lower FVC, lower DL_CO, lower six-minute walk distance, and increased exertional desaturation,²⁹ findings that are consistent with ours. However, the authors of the aforementioned study²⁹ did not quantify the severity of persistent dyspnea or measure TLC in order to diagnose a restrictive ventilatory defect. A reduced FVC and/or FEV₁ with normal FEV₁/FVC are suggestive of a restrictive pattern, and lung volume measurements are usually needed in order to confirm that. Restriction is a potential dysfunction following severe lung injury (and related medical care) caused by parenchymal abnormalities (interstitial lung disease) or extraparenchymal abnormalities (respiratory muscle wasting resulting in atrophy and weakness).⁵ A low DL_CO in the presence of reduced TLC (and alveolar volume) may result from any one of the aforementioned mechanisms. Meanwhile, reduced DL_CO in patients without restriction (or obstruction) indicates impaired gas exchange efficiency, which, in the present context, indicates either interstitial lung disease (alveolar destruction, alveolar thickening, or ventilation/perfusion mismatch) without mechanical abnormalities, or it indicates pulmonary vascular disease.³⁰ Finally, the presence of reduced TLC with preserved DL_CO indicates extraparenchymal restriction.⁵ The complexity of interpreting DL_CO, lung volume (or rather, alveolar volume), and the relationship between the two, however, makes it difficult to determine the underlying abnormality (or abnormalities) on the basis of the available data.³¹ Respiratory muscle evaluation and more specific measures of the alveolar-capillary membrane (e.g., combined DL_CO and diffusing capacity of the lung for nitric oxide measurements or advanced chest imaging techniques) might be useful to assess the contribution of interstitial lung abnormalities, pulmonary vascular injury, and/or extraparenchymal abnormalities to reduced DL_CO in individual cases.³¹

The roles that acute disease severity and the extent of pneumonia on chest CT scans play in the development of impaired lung function and respiratory symptoms are also contradictory. A significant relationship between disease severity and abnormal lung function has been reported in some studies,^6,29 but not in others.³² In agreement with the findings of a study assessing risk factors for post-COVID-19 pulmonary fibrosis,³³ our findings show that the need for intensive care and a greater extent of acute pulmonary inflammation (i.e., a higher chest CT score) independently predicted restrictive lung disease at the follow-up visit.

Psychological stress is highly prevalent after COVID-19.³⁴ It is associated with breathlessness and poorer functional status in the general population.³⁵ In the present study, self-report questionnaires were used in order to assess the modulation of PTSD, depression, and anxiety symptoms in the relationship between impaired respiratory function and worse clinical outcomes. Mean BDI scores indicated mild to no depression. Although PTSD symptoms were clinically significant, there were no differences between patients with and without a restrictive ventilatory defect. Anxiety symptoms were significantly higher in the former group of patients, raising the question of the contribution of anxiety symptoms to worsening clinical outcomes. Regardless of the direction of this relationship (cause or consequence), it seems valuable to assess and manage anxiety symptoms, and further research is needed in order to explore the impact of anxiety management on post-COVID-19 symptom relief.

The prevalences of asthma and COPD before COVID-19 have been reported to range from 5% to 15% and from 1% to 9%, respectively.²⁶ Of the patients in our sample, 19% reported baseline respiratory comorbidities and were excluded from later analyses. Significant dyspnea (an mMRC dyspnea scale score ≥ 2) was more common in patients with restrictive lung disease than in those without it (57% vs. 24%). The overall proportion of patients presenting with clinically significant cough and sputum production was not negligible for patients without preexisting respiratory conditions (i.e., 8-12%). However, this rate was not worse in the presence of a restrictive ventilatory defect. Cough and expectoration are typical symptoms of airway inflammation secondary to tracheobronchitis or pneumonia. Viral respiratory tract infections can be associated with acute bronchiolitis in adults, and constrictive bronchiolitis can be seen as a late sequela of viral lower respiratory tract infections.³⁶ The prevalence of an obstructive ventilatory pattern after COVID-19 was reported to be 7% in a previous systematic review.¹ However, differences across studies regarding the criteria to define obstruction and the presence of prior chronic respiratory disease justify caution in considering persistent expiratory airflow obstruction to be a late sequela of COVID-19. For example, of the studies included in the aforementioned systematic review,¹ only one³² used the recommended lower limit of normal to define obstruction, and none of the patients in that study had an obstructive ventilatory pattern. In another study using impulse oscillometry measurements, mean values of the respiratory system resistance at an oscillation frequency of 5 Hz and of 20 Hz were reported to be normal 30 days after hospital discharge (127 ± 29% of predicted and 133 ± 31% of predicted, respectively).³⁷ As expected, the prevalence of obstructive lung disease was higher in our patients with preexisting respiratory disease (i.e., 21.7%), and they had worse impulse oscillometry measurements than did those without preexisting respiratory disease. Although mean values of respiratory system resistance at an oscillation frequency of 5 Hz and of 20 Hz were within the normal range in our patients without preexisting respiratory disease, the mean resonance frequency and area of resonance were altered. These findings suggest the involvement of peripheral lung parenchyma without airway disease.³⁸

From a clinical perspective, we demonstrated that persistent lung function impairment implies worse dyspnea and physical functioning after COVID-19, mainly represented by a restrictive ventilatory defect associated with abnormal gas exchange. Therefore, pulmonary function testing might be useful to uncover factors contributing to such complaints; to monitor changes over time; and to guide future studies aimed at evaluating potential interventions for their relief.

One of the limitations of the present study is the lack of assessment of other potential mechanisms for respiratory symptoms and impaired HRQoL after COVID-19. Cardiac dysfunction, musculoskeletal dysfunction, immune response to SARS-CoV-2,³⁴ and impaired oxidative metabolism³⁹ have been suggested to explain dyspnea, fatigue, and exercise intolerance beyond alterations in pulmonary function. Another limitation is the relatively short-term follow-up. Although data from long-term follow-up of previous coronavirus outbreaks⁴⁰ and 12-month follow-up of the current COVID-19 pandemic⁶ suggest that some patients will have long-term respiratory complications, improvement in pulmonary function is commonly observed over time.⁶ Nevertheless, this is an ongoing prospective cohort study that will provide long-term (> 12-month) follow-up of pulmonary function, exercise capacity, HRQoL, and their interplay. Finally, we do not know whether our findings apply to cases of milder disease, because only patients hospitalized for severe COVID-19 pneumonia were included in the present study.

In this prospective cohort of patients followed for approximately 4 months after a confirmed diagnosis of severe COVID-19, those with preexisting chronic respiratory comorbidities showed worse lung function and respiratory symptoms. When those patients were excluded, poor resting gas exchange (reduced DL_CO), increased dyspnea, reduced HRQoL, and reduced exercise performance were observed in those with a restrictive ventilatory defect. Intensive care need and a greater extent of pulmonary involvement during the acute phase were associated with the presence of a restrictive ventilatory defect at the follow-up visit.

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• Financial support:

  This study received financial support from the Fundo de Incentivo à Pesquisa do Hospital de Clínicas de Porto Alegre (FIPE-HCPA, Research Incentive Fund of the Porto Alegre Hospital de Clínicas; Grant no. 2020-0169). DCB is the recipient of a research fellowship grant from the Brazilian Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, National Council for Scientific and Technological Development; Grant no. 304061/2019-0). The funding sources had no involvement in the study design, analysis of data, or decision to submit the article for publication.
• 2
  Sudy carried out at the Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre, Porto Alegre (RS) Brasil.
• 3
  (ClinicalTrials.gov identifier: NCT04410107 [http://www.clinicaltrials.gov/^)

Publication Dates

• Publication in this collection
  26 May 2023
• Date of issue
  2023

History

• Received
  12 Dec 2022
• Accepted
  04 Feb 2023