High 24-Hour Respiratory Symptoms and Low Physical Activity in the Stable COPD Romanian Cohort of SPACE Study.

OBJECTIVE: This study assessed the characteristics and the relationship between symptoms in any part of the 24-hour (24-h) day, physical activity level (PAL), and other clinical and functional outcomes in stable COPD patients. PATIENTS AND METHODS: Out of the 2162 patients enrolled in the SPACE study (The Symptoms and Physical Activity in COPD patients in Europe, clinicaltrials.gov NCT03031769), 406 (18.8%) were recruited from Romania. Here, we present the Romanian cohort results. Eligible patients were adults with age at least 40 years, confirmed diagnosis of stable COPD, current or former smokers with a smoking history of minimum 10 pack-years. The 24-h respiratory symptoms were assessed using Early Morning Symptoms of COPD Instrument (EMSCI), Evaluating Respiratory Symptoms in COPD (E-RS™: COPD) and Nighttime Symptoms of COPD Instrument (NiSCI). During clinical interview, patients self-evaluated PAL through Exercise as Vital Sign (EVS) and Yale Physical Activity Survey (YPAS). Physicians assessed PAL through their clinical judgment.
RESULTS: For each combination of 2 between the early morning (EM), daytime (DT) and night-time (NT) symptoms of the 24-h day, there was a significant association (p < 0.001 for each). All symptoms significantly correlated with exacerbation history (p < 0.001 for EM and NT, p=0.002 for DT), and number of severe exacerbations (p < 0.001 for DT, p=0.001 for EM and p=0.026 for NT, respectively). The 24-h symptoms correlated negatively and significantly with PAL (p < 0.001), irrespective of the assessment used. Self-reported PAL negatively correlated with dyspnea, symptom burden, severity of disease and number of exacerbations (p < 0.001). Patients spent an average (standard deviation) of 25.8 (21.0) hours/week performing physical activity. Physicians overestimated their patients' daily PAL.
CONCLUSION: A negative and significant correlation between the 24-h day symptoms and PAL was identified in stable COPD patients. Physicians need to routinely assess PAL using adequate tools and start educating inactive COPD patients to optimize their disease outcomes.

Introduction

With significant morbidity and mortality, Chronic Obstructive Pulmonary Disease (COPD) is an important public health burden worldwide, despite being considered preventable and treatable.1 The Global Initiative for Obstructive Lung Disease (GOLD) launched the combined assessment in 2011, when symptom burden was added to the previous spirometric grading system of pulmonary function and history of exacerbations.2 Through this multidimensional GOLD assessment, the clinicians could classify patients into four quadrants (ABCD), which allowed making more individualized treatment decisions. GOLD ABCD classification system was further simplified in 2017, when spirometric measures were removed from the combined assessment, leaving only the respiratory symptoms and exacerbation history.3

The negative impact of COPD symptom burden on patients’ routine activities, health-related and overall quality of life has been previously demonstrated.4–11 The perceived symptoms vary throughout the 24-hour (24-h) day4,5,7–11 and do not correlate with the level of airflow limitation.6 Frequently, COPD patients need to reduce their level of physical activity and tend to underestimate the symptom burden.1 Moreover, a downward spiral of inactivity induced by symptoms characterizes COPD.12 Previous studies have shown that physical inactivity leads to a higher risk of hospitalizations, exacerbations and mortality and a reduced health-related quality of life in COPD patients, although the exact relationship between various clinical and functional indicators and physical activity is not yet elucidated.13–15 In consequence, increasing physical activity has the potential of being one key non-pharmacological interventions in COPD patients, irrespective of the specific ABCD group.1

In Romania, the respiratory symptoms (RS) were explored in several national COPD awareness campaigns that showed an increasing prevalence of lung function impairment.16,17 However, the daily variability and the impact of symptoms in stable COPD were not assessed so far in depth. Several local studies showed a low physical activity level (PAL) of patients with COPD,18–20 a finding in line with data reported in the literature,21–24 but less is known about the RS burden, patterns of physical activity and their relationship in stable COPD patients from Romania.

Objectives

The overarching primary objective of this study was to describe the prevalence and severity of early morning (EM), daytime (DT) and night-time (NT) symptoms of the 24-h day, and the patterns of physical activity in COPD stable patients. The secondary objectives of the study were to explore the relationship between the 24-h day symptoms and PAL and other COPD clinical and functional dimensions including, without being limited to, level of dyspnea, health status, comorbidities, severity of disease, and exacerbation history.

Materials and Methods

Study Design

The multinational, multicenter, observational, cross-sectional study of Symptoms and Physical Activity in COPD patients in Europe (SPACE, NCT03031769) was performed in 10 European countries and Israel and enrolment lasted for 9 months (from December 2016 to August 2017). From Romania, 17 pulmonary centers participated to this study. This paper presents the results of the Romanian cohort of patients with stable COPD enrolled in SPACE study.

Details on the study design have been already reported,25 but this is the first evaluation of the Romanian COPD cohort of patients. This study had a single visit to collect data (eg, socio-demographic data, smoking history, comorbidities, year of COPD diagnosis, current COPD treatment, spirometry information, number, type and number of exacerbations and COPD-related healthcare resource use in the previous 12 months) from medical charts or during clinical interview with COPD patients. The definition of exacerbation used in the study was: an acute worsening of respiratory symptoms that resulted in additional therapy, eg, bronchodilators only (mild exacerbation), bronchodilators plus antibiotics and/or oral corticosteroids (moderate exacerbation) or required hospitalization or emergency room visits (severe exacerbation).

Based on all data collected in the study, several parameters were determined (COPD specific comorbidities test [COTE] index,26 combined index of body mass index, spirometry assessment of the presence and severity of air flow obstruction, dyspnea and exacerbations [BODEx]).27 Patients were divided into ABCD groups according to GOLD 201328 and 20173 recommendations, the latter guide being in use at the time of the study.

The Romanian National Bioethics Committee of Medicines and Medical Devices approved the study at central level (approval number 29SNI/21.11.2016). This study was conducted in accordance with the Declaration of Helsinki. All COPD patients expressed their written informed consent before enrollment.

Patients

The study population consisted of COPD patients aged ≥40 years, with ≥1 year since diagnosis and stable disease defined by no exacerbation history or any change in current COPD maintenance treatment in the last two months before enrolment. Other inclusion criteria referred to smoking history of at least 10 pack-years and documented post-bronchodilator forced expiratory volume in 1 second/forced vital capacity (FEV1/FVC) ratio of <0.7 in the year before enrolment. Other chronic respiratory disorders besides COPD or sleep apnea syndrome, any acute or chronic disease that would have altered the ability to complete the questionnaires, and concomitant inclusion in a clinical trial that would have influenced participation in the SPACE study represented exclusion criteria. Patients previously diagnosed with asthma or non-idiopathic pulmonary fibrosis could participate in SPACE study only if COPD was the primary documented diagnosis.

Assessments

The patients participating to SPACE study completed several interviewer- and patient-administered questionnaires Dyspnea assessment was performed using the modified Medical Research Council (mMRC) scale.29 The COPD Assessment Test (CAT) was utilized to determine the health status and symptomatic impact of COPD.30 The thresholds for separating the low- and high-symptom burden groups in the GOLD ABCD assessment were ≥2 for mMRC and ≥10 points for CAT.2,3

COPD symptoms were assessed using specific, validated questionnaires for early morning, daytime and night-time periods: Early Morning Symptoms of COPD Instrument (EMSCI),31 Evaluating Respiratory Symptoms in COPD (E-RS™:COPD),32 and Nighttime and Symptoms of COPD Instrument (NiSCI).33 For EMSCI and NiSCI questionnaires, responses were coded from 0 to 4, using 0 for “no symptoms” and 4 for “very severe symptoms”. The overall severity score and 6-item severity scores were calculated. For the E-RS™: COPD questionnaire, the RS were quantified using total score (RS-Total score), with values from 0 to 40, higher scores meaning more severe symptoms.

For the PAL assessment, physicians used their clinical judgment to estimate the level of physical activity for their patients and classify them as active (performing ≥150 minutes/week of moderate to vigorous exercise such as brisk walk), insufficiently active (1–149 minutes/week of moderate to vigorous exercise) or inactive (0 minutes/week of moderate to vigorous activity).34 At study visit, patients were asked to self-evaluate their PAL. Within this scope, two questions originating in the Exercise as Vital Sign (EVS) program35 () and the Investigator-administered Yale Physical Activity Survey (YPAS)36 were included in the clinical interview.

Statistical Analysis

The database included all eligible patients enrolled in the study. Descriptive statistics were performed using version 3.3.3 of the R package ()l The analysis included Student’s t and Wilcoxon signed rank tests for the exploration of the differences in means and distributions between independent groups. The relationships of symptoms or physical activity levels with COPD clinical and functional indicators (level of dyspnea, disease severity, and COPD exacerbations), comorbidities, and impact on physical activities were evaluated using the Pearson correlation coefficient for continuous variables or Spearman correlation coefficient for ordinal variables. All statistical tests were two-sided and used a 5% significance level.

Results

Patients’ Characteristics

The Romanian cohort of patients enrolled in SPACE consisted in 406 cases (18.8%), with a mean age of 65.9 years, and predominantly males (85%) (Table 1). Most patients reported dyspnea of grade ≥2 on mMRC scale (72.4%) and a CAT score ≥10 (86.7%). The most frequently reported non-respiratory comorbidities were of cardio-vascular nature: hypertension (63.3%), coronary heart disease (33.5%), and chronic heart failure (19.5%). Respiratory comorbidities included non-idiopathic pulmonary fibrosis (7.1%), while a previous diagnosis of asthma was noticed in 6.7% of cases. One third of patients (32.8%) reported influenza flu vaccine performed in the last year and just a minority (2.7%) received the pneumococcal vaccine ().

Table 1

Socio-Demographic and Clinical Characteristics of Patients

Characteristic	N=406
Males, n (%)	339 (83.5)
Age, mean (SD), years	65.9 (8.5)
Educational level, n (%)
Primary school	42 (10.3)
Secondary school	141 (34.7)
High-school	172 (42.4)
University and post-university education	51 (12.6)
Employment status, n (%)
Retired	309 (76.1)
Employed	28 (6.9)
Unemployed	3 (0.7)
Other	7 (1.7)
Smoking history
Active smokers, n (%)	96 (23.6)
Former smokers, n (%)	310 (76.4)
Pack-years, mean (SD)	38.1 (23.8)
% predicted FEV1, mean (SD)	47.82 (16.2)
Post-BD FEV1/FVC, mean (SD)	0.55 (0.1)
COPD severity, n (%)
GOLD group I (mild)	11 (2.7)
GOLD group II (moderate)	176 (43.3)
GOLD group III (severe)	164 (40.4)
GOLD group IV (very severe)	55 (13.5)
mMRC
mMRC 0–1, n (%)	112 (27.6)
mMRC ≥2, n (%)	294 (72.4)
CAT
CAT score, mean (SD)	18.97 (8.2)
CAT <10	54 (13.3)
CAT ≥10	362 (86.7)
COTE index, mean (SD)	1.41 (1.9)
BODEx index, mean (SD)	3.04 (1.8)
Mean number of comorbidities per patient, mean (SD)	1.33 (1.0)
Exacerbations in previous 12 months
History of exacerbations, n (%)	282 (69.5)
Number of COPD exacerbations/patient, mean (SD)	1.97 (2.7)
History of severe exacerbations in last year, n (%)	75 (18.5)
Number of mild exacerbations/patient, mean (SD)	0.29 (0.7)

Abbreviations: BD, bronchodilator; BODEx, body mass index, obstruction, dyspnea and exacerbations; CAT, COPD Assessment Test; COPD, Chronic Obstructive Pulmonary Disease; COTE, COPD specific comorbidities test; FEV1, Forced Expiratory Volume in 1 second; FVC, Forced Vital Capacity; GOLD, Global Initiative for Chronic Obstructive Lung Disease; mMRC, modified Medical Research Council; SD, standard deviation.

The proportion of patients classified in ABCD groups differed by edition (GOLD 2013 or GOLD 2017) and within each edition according to the cut-off point of mMRC grade ≥2 or CAT score ≥10 (Figure 1A and B). The percentage of patients in group B increased from 16.0% by GOLD 2013 edition to 32.0% by GOLD 2017 edition when using mMRC, and from 19.5% to 40.9% when using CAT, respectively. The proportion of patients having high symptom burden (B+D) remained constant between editions when the same ABCD assessment tool was used but differed between tools: 72.4% patients classified by mMRC in B+D groups in contrast to 86.7% by CAT.

Figure 1

Distribution of patients in ABCD groups using the 2013 (A) and 2017 (B) GOLD edition.

Respiratory Symptoms

In total, 87.7% of patients presented at least one EM symptom, 71.4% at least one NT symptom and 92.6% at least one DT symptom. During night-time, 36.0% of patients were awakened by their RS. Most of individual RS were mild or moderate (Figure 2). The mean RS-total score (standard deviation) was 12.6 (8.1), overall NiSCI symptom summary score 0.9 (1.0) and overall EMSCI symptom summary score 1.4 (0.9).

Figure 2

Prevalence of individual respiratory symptoms assessed by questionnaires corresponding for each part of the 24-h day EMSCI, NiSCI and E-RS™:COPD.

Physical Activity Level

The Investigators’ assessment (clinical judgment) and patients’ self-assessment (EVS questions) of PAL showed discrepant results: 37.2% of patients considered themselves inactive and 23.9% active, while physicians considered inactive <10% of patients and active 54.4% (Figure 3).

Figure 3

The physical activity level assessed by Investigators (clinical judgment) and self-assessed by patients (EVS questions).

The analysis of the YPAS checklist of activities showed that patients spent an average (SD) of 25.8 (21.0) hours/week performing physical activity, with a total mean energy expenditure (SD) of 5685.0 (4841.1) kcal/week and mean summary index of 45.3 (24.6) (Table 2).

Table 2

Physical Activity Results – YPAS Dimensions

Characteristic	N=406
YPAS checklist total time (min/week), mean (SD)	1549.3 (1258.7)
Energy expenditure summary index (kcal/week), mean (SD)	5685.0 (4841.1)
Vigorous activity index score, mean (SD)	10.2 (12.5)
Leisurely walking index score, mean (SD)	18.6 (14.3)
Moving index score, mean (SD)	7.2 (3.3)
Standing index score, mean (SD)	6.7 (3.4)
Sitting index score, mean (SD)	2.6 (1.1)
Summary index, mean (SD)	45.3 (24.6)
Seasonal adjustment score, mean (SD)	1.0 (0.1)

Abbreviations: SD, standard deviation; YPAS, Yale Physical Activity Survey.

Relationship Between Respiratory Symptoms and Physical Activity or Other Outcomes

A significant correlation was found between EM, DT and NT RS and physical activity (p < 0.001), irrespective of the assessment tool used (eg, Investigator’s assessment, EVS or YPAS total score); however, the correlations were weak (the maximum value of the coefficient of determination was 0.114 for the correlation between DT RS and Investigator’s assessment of PAL). A significant association between EM, DT and NT RS was described for each combination of symptoms (p < 0.001). Each type of symptom correlated significantly with CAT, mMRC, BODEx index and number of exacerbations (p < 0.001). All RS correlated significantly with history of prior exacerbations (p < 0.001 for EM and NT symptoms, and p=0.002 for DT symptoms), and with the number of severe exacerbations (p < 0.001 for DT, p=0.001 for EM symptoms, and p=0.026 for NT symptoms, respectively) (Table 3). Self-reported physical activity either using EVS or YPAS total score correlated negatively with CAT, mMRC, BODEx index and number of exacerbations (p < 0.001) (Table 4).

Table 3

Relationship Between 24-h Respiratory Symptoms Severity Score and Patients’ Outcomes

	Early Morning Symptoms			Daytime Symptoms			Night-Time Symptoms
	Correlation Coefficient R	Coefficient of Determination R2	P-value	Correlation Coefficient R	Coefficient of Determination R2	P-value	Correlation Coefficient R		Coefficient of Determination R2	P-value
PAL
Investigator’s assessment	−0.272	0.074	<0.001	−0.338	0.114	<0.001	−0.251		0.063	<0.001
EVS	−0.303	0.092	<0.001	−0.324	0.105	<0.001	−0.304		0.092	<0.001
YPAS checklist total time	−0.081	0.006	0.110	−0.115	0.013	0.023	−0.130		0.017	0.009
Energy expenditure summary index	−0.095	0.009	0.061	−0.140	0.020	0.005	−0.142		0.020	0.004
YPAS total score	−0.173	0.030	0.001	−0.293	0.086	<0.001	−0.200		0.040	<0.001
Other outcomes
CAT	0.702	0.493	<0.001	0.748	0.560	<0.001	0.614		0.377	<0.001
Comorbidities (COTE)	0.017	0.000	0.739	0.040	0.002	0.431	0.089		0.008	0.075
Number of comorbidities	0.008	0.000	0.878	0.038	0.001	0.455	0.028		0.001	0.571
BODEx	0.389	0.151	<0.001	0.462	0.213	<0.001	0.339		0.115	<0.001
mMRC	0.424	0.180	<0.001	0.526	0.277	<0.001	0.392		0.154	<0.001
Post-BD FEV1 predicted	−0.192	0.037	<0.001	−0.229	0.052	<0.001	−0.146		0.021	0.003
Post-BD FEV1/FVC %	−0.134	0.018	0.008	−0.171	0.029	0.001	−0.080		0.006	0.110
Number of severe exacerbations	0.166	0.028	0.001	0.178	0.032	<0.001	0.111		0.012	0.026
Number of exacerbations	0.264	0.070	<0.001	0.272	0.074	<0.001	0.216		0.047	<0.001
Exacerbation history	0.175	0.031	<0.001	0.159	0.025	0.002	0.185		0.034	<0.001

Note: The Pearson’s correlation coefficient was used.

Abbreviations: BD, bronchodilator; BODEx, body mass index, obstruction, dyspnea and exacerbations; CAT, COPD Assessment Test; COPD, Chronic Obstructive Pulmonary Disease; COTE, COPD specific comorbidities test; EVS, Exercise Vital Sign; FEV1, Forced Expiratory Volume in 1 second; FVC, Forced Vital Capacity; GOLD, Global Initiative for Chronic Obstructive Lung Disease; mMRC, modified Medical Research Council; PAL, physical activity level; YPAS, Yale Physical Activity Survey.

Table 4

Relationship Between Physical Activity and Patients’ Outcomes

	EVS			YPAS Total Score
	Correlation Coefficient R	Coefficient of Determination R2	P-value	Correlation Coefficient R	Coefficient of Determination R2	P-value
CAT	−0.291	0.085	<0.001	−0.353	0.125	<0.001
Comorbidities (COTE)	0.034	0.001	0.496	−0.140	0.020	0.005
Number of comorbidities	0.101	0.010	0.042	−0.057	0.003	0.251
BODEx	−0.353	0.124	<0.001	−0.425	0.181	<0.001
mMRC	−0.432	0.186	<0.001	−0.475	0.225	<0.001
Post-BD FEV1 predicted	0.200	0.040	<0.001	0.242	0.059	<0.001
Post-BD FEV1/FVC %	0.152	0.023	0.002	0.187	0.035	<0.001
Number of severe exacerbations	−0.074	0.005	0.137	−0.197	0.039	<0.001
Number of exacerbations	−0.147	0.021	0.003	−0.226	0.051	<0.001
Exacerbation history	−0.073	0.005	0.143	−0.201	0.040	<0.001

Note: The Pearson’s correlation coefficient was used.

Abbreviations: BD, bronchodilator; BODEx, body mass index, obstruction, dyspnea and exacerbations; CAT, COPD Assessment Test; COPD, Chronic Obstructive Pulmonary Disease; COTE, COPD specific comorbidities test; EVS, Exercise Vital Sign; FEV1, Forced Expiratory Volume in 1 second; FVC, Forced Vital Capacity; GOLD, Global Initiative for Chronic Obstructive Lung Disease; mMRC, modified Medical Research Council; PAL, physical activity level; YPAS, Yale Physical Activity Survey.

Discussion

To our knowledge, this is the first detailed analysis of respiratory symptoms throughout the 24-h day in a Romanian cohort of stable COPD patients. Despite being under treatment, patients reported symptoms in any part of the 24-h day.

Considered for a long time mostly a feature of asthma, the variability of RS in COPD was in depth explored in the last decade. The symptoms perceived by patients may vary in number and intensity over the course of a week or a day.5,7 Previous studies showed that nocturnal symptoms are usually under-reported and less taken into consideration in the general management of COPD, although they affect the patients’ sleep quality, daily activities and overall health status, and are additionally correlating with a higher risk of cardiovascular adverse outcomes.10,37 Increased variability of COPD symptoms (mainly dyspnea) is associated with their severity, it indicates respiratory impairment and leads to exercise limitation.5 In our group of patients, the presence of early-morning, diurnal and nocturnal symptoms correlated significantly with the reported low level of physical activity, irrespective of the assessment used. Consistent to other reports,5,7 in the Romanian and overall SPACE study cohorts,25 the 24-h day symptoms impacted the patients’ ability to perform their routine activities involving effort, from walking up and down stairs to doing sport or hobbies or performing intense housework chores. This negative relationship is hard to break, because dyspnea is the major key limitation of physical activity in advanced COPD disease and many patients have to reduce their effort just to avoid breathlessness.38 Dyspnea is a predictor factor for a low physical activity level, which was recently shown to fluctuate annually.39,40 Additionally, cough and fatigue influence the level of physical activity.41,42 However, a study investigating PAL in COPD patients prior to hospitalization reported that patients who performed regularly physical activity had less respiratory and extra-respiratory symptoms during an exacerbation.43 Such findings underline the importance of periodic evaluations of RS and physical activity in COPD patients to early understand any changes and act in a timely fashion. A more intensive multifactorial approach that considers burden of symptoms, pre-existent level of physical activity, but also patients’ goals, needs and living conditions is required for sustainable changes in patients’ life with COPD.

In SPACE study, the physical activity was evaluated in a non-interventional manner through patients’ perspective and physicians’ evaluation.25 Patients were asked to answer to a questionnaire administered by their physician: YPAS,36 a validated tool for elderly patients covering a broad range of work, recreation and other physical activities. Romanian COPD stable patients spent less than 4 hours/day in any kind of activity, whereas healthy subjects or older patients usually spend between 4 to 9 hours/day.36,44 A score <51 in the YPAS summary index was proposed to help identifying the COPD patients at risk for sedentarism.45 The mean value of the summary index across our cohort is suggestive for a predominantly sedentary group, although the true percentage of patients with summary index <51 was not calculated in the country cohort. The results of YPAS are indicative of longer standing and sitting times and less time or effort spent in vigorous activities (in average 3–6 hours daily vs <1 hour a few times a week). A longer sitting time is correlated with a higher risk of mortality, independently of leisure time physical activity.46 In light of these findings, clinicians need to actively discuss with COPD patients about their daily routine and what type of activities they usually perform. This will help identifying sedentary behavior and inactivity patterns. Previous research has shown that interrupting long sitting times and replacing their sedentary behavior with low-intensity activities is beneficial for COPD patients.47–49 Yet, in real-life practice clinicians lack clear guidance on the most appropriate type, intensity and duration of physical activity for various categories of COPD patients and no strategies to promote effective physical activity interventions are available.50,51

The SPACE study superposed the perception of COPD patients about their level of physical activity with the physicians’ evaluation of every patient’s PAL at the time of the visit. For the patient’s self-assessment of PAL, EVS35 was used. To not influence physicians’ evaluation, the EVS category derived (active/insufficiently active/inactive) was not displayed to Investigators in the electronic case report form at the time of study data entry. For the assessment of patients’ PAL, Investigators were asked to use their clinical judgment without any instruction on how to explore the level of activity. The results in the Romanian set of data found that physicians overestimated the PAL of their patients, while stable COPD patients seemed to underestimate it. The discrepancy found indicates a different perception and perhaps relevance of physical activity for patients and physicians, which warrant further research from various angles. This finding also underlines the unmet need for simple and standardized instruments to help practitioners identifying the COPD patients at risk for inactivity as a preliminary step before using more objective measures for the PAL evaluation. A recent qualitative study from Australia52 showed that clinicians recognized the value of physical activity in COPD, but the evaluation of PAL in their patients was problematic. Additionally, they did not assess PAL, nor promoted activity at every consultation with COPD patients. Such insights from local practice are not available, but they would prove useful in understanding the constraints and goals of both parties. Initiating conversations about physical activity with patients would be a first step into this direction. Adapting best practices of existing, successful PR programs53,54 and other movement initiatives55 might be a preliminary phase together with assembling multidisciplinary task forces to further build, implement, and monitor relevant strategies, which are urgently needed at national level.

In addition, with the current Coronavirus Disease 2019 (COVID-19) pandemic and measures such as social distancing and quarantine taken to limit the spread of the disease, the COPD patients are at even higher risk for physical inactivity and sedentary behavior.56 All changes experienced at society level across the world brought additional challenges, calling for a different behavioral approach to foster patients’ motivation to maintain a healthy, active lifestyle.57 Even though maintenance pulmonary rehabilitation can be safely delivered by means of communication technology, as shown by a recent Cochrane review,58 this is challenging to implement in Romania due to lack of resources and limited access to and/or proficiency in using new technology. Additionally, home exercises for patients with mild or moderate COPD proved to be difficult to implement and associated with a reduced patient’s satisfaction even long before COVID-19 outbreak, as shown by a small observational study.59

Due to the observational nature of this study and its cross-sectional design, there are some inherent limitations. For example, in this set of data, no additional matched or stratified analyses were conducted to address confounding factors. Despite the significant relationships found between symptoms and physical activity and other outcomes, no causality can be proven. Another drawback of the study is the use of subjective measures only for the evaluation of the patients’ PAL. Self-reported questionnaires are known as imprecise and subjective to recall bias. Additionally, they tend to be incongruent with objectively measured PAL and overestimate it.4,60 Wearing sensitive motion detectors for a pre-specified period would have influenced considerably the design of the study (prospective, interventional). Preliminary feasibility discussions indicated that in real-life practice, not all offices/clinics afford motion detectors, while for the 6-minutes walking test space may be problematic in small practices. Nevertheless, the results provided by the self-reported questionnaires emphasized that clinicians lack unsophisticated, standard instruments to assess and track COPD patients’ PAL and/or inactivity patterns in real-life practice. Lastly, our paper characterizes the Romanian cohort of patients participating in a large international project and may be less generalizable. However, the main findings followed the trend of the entire study cohort with persistent 24-h RS, low level activity of physical activity and Investigators’ overestimation of PAL in their patients.

Conclusion

Romanian stable COPD patients, despite being under treatment, are experiencing respiratory symptoms during day and night. These high 24-h day symptoms negatively correlate with a low level of physical activity. Despite the overall low physical activity level reported by patients, physicians considered their patients to be more active. The main clinical explanation is that practitioners may misjudge the true extent and effects of the patients’ sedentary behavior. Simple tools to assess the physical activity in routine care are needed to allow the timely identification of inactivity patterns in all COPD patients, followed by more objective measures and tailored interventions within a comprehensive disease management program.