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Association between patient-reported outcomes and exercise test outcomes in patients with COPD before and after pulmonary rehabilitation

Health and Quality of Life Outcomes volume 18, Article number: 300 (2020) Cite this article

Abstract

Background

Over the years, the scope of outcomes assessment in chronic obstructive pulmonary disease (COPD) has broadened, allowing for the evaluation of various patient-reported outcomes (PROs). As it still remains unclear whether and to what extent PROs mirror the exercise performance of patients with COPD, the current study aimed to assess the association between different exercise test outcomes and PROs, before and after pulmonary rehabilitation (PR).

Methods

Correlations between PROs used to describe health-related quality of life (HRQoL), mood status, level of care dependency and dyspnea in patients with COPD and commonly used laboratory- and field-based exercise test outcomes were evaluated in 518 individuals with COPD attending PR.

Results

Overall, correlations between PROs and exercise test outcomes at baseline were statistically significant. The correlation between modified Medical Research Council (mMRC) dyspnea score and 6-min walking distance (6MWD) was strongest (ρ:-0.65; p<0.001). HRQoL related PROs showed weak correlations with exercise outcomes at baseline. Moderate correlations were found between St George’s Respiratory Questionnaire total score and 6MWD (r:-0.53; p<0.001) and maximal workload achieved during cardiopulmonary exercise testing (ρ:-0.48; p<0.001); and between Clinical COPD Questionnaire (CCQ) total score and 6MWD (r:-0.48; p<0.001) and maximal workload (ρ:-0.43; p<0.001). When significant, correlations between changes in exercise test outcomes and changes in PROs after PR were generally very weak or weak. The highest correlation was found between changes in CCQ total score and changes in 6MWD (ρ: − 0.36; p<0.001).

Conclusions

PROs and exercise test outcomes, although significantly correlated with each other, assess different disease features in patients with COPD. Individual PROs need to be supported by additional functional measurements whenever possible, in order to get a more detailed insight in the effectiveness of a PR program.

Trial registration

Netherlands Trial Register (NL3263/NTR3416). Registered 2 May 2012.

Background

Patients with chronic obstructive pulmonary disease (COPD), a highly-prevalent chronic lung disease, frequently suffer from symptoms of dyspnea, exercise intolerance, an impaired mood status and a reduced health status [1,2,3]. These features are typically weakly related to the degree of lung function impairment [4]. Therefore, the use of additional assessments such as exercise tests and patient-reported outcomes (PROs) has been advocated [3, 5, 6]. Appraisal of these extra-pulmonary features is necessary to better understand the patients’ daily needs or problems, to identify possible treatable traits for integrated COPD care programs, and to evaluate its efficacy [7].

Several laboratory- and field-based exercise tests can be performed to measure exercise performance, which is typically affected in patients with COPD [3, 8], due to a downward spiral of dyspnea, disability and physical inactivity [9]. Important aspects from the patient’s perspective like health-related quality of life (HRQoL), dyspnea, anxiety, depression, and the level of care dependency, all of which have a direct impact on daily life [10], are measured using PROs.

Punekar and colleagues systematically reviewed the strength of the available evidence supporting correlations between the outcomes of different exercise tests and PROs most commonly used to assess HRQoL and dyspnea [11]. They concluded that only a limited amount of studies have focused on the correlations between exercise test outcomes and PROs in patients with COPD. The available evidence indicates a very weak to moderate negative correlation between 6-min walking distance (6MWD) and HRQoL, measured with the St. George’s Respiratory Questionnaire (SGRQ). The relationship between PROs for dyspnea and 6MWD showed contrasting results, with both moderate to strong positive and negative correlations being reported [11]. So, it still remains unclear whether and to what extent PROs mirror the exercise performance of patients with COPD. It seems reasonable to hypothesize that other exercise test outcomes than 6MWD may be stronger correlated with different PROs. For example, disease-specific questionnaires like the Clinical COPD Questionnaire (CCQ) and the COPD Assessment Test (CAT) focus more on functional impairments and symptoms related to COPD and may therefore be more closely associated with exercise test outcomes in patients with COPD.

Pulmonary rehabilitation (PR) reduces dyspnea, increases exercise capacity, and improves HRQoL in individuals with COPD [6]. Exercise training is a major component of PR and therefore exercise test outcomes are consistently used to assess the individual patient’s response to PR [12,13,14,15,16,17]. Nevertheless, improvements in exercise performance after PR do not necessarily lead to a concurrent decrease in symptoms in patients with COPD and vice versa [18]. Therefore, the question remains whether changes in exercise test outcomes after PR translate into changes in disease-specific PROs.

In this observational study, we aimed to assess the association between different exercise test outcomes and PROs most commonly used to describe HRQoL, anxiety, depression and disease-specific symptoms, such as dyspnea, in patients with COPD before and after PR. A priori, we hypothesized that the correlation between PROs for dyspnea and HRQoL and exercise test outcomes would be statistically significant, but that there would be no strong or very strong association. Furthermore, it was expected that improvements in exercise test outcomes after PR showed weak correlations with changes in PROs in patients with COPD.

Methods

Study design and participants

The current study is a retrospective analysis of the ‘COPD, Health status and Comorbidities’ (Chance) study, Netherlands Trial Register NTR3416 [19]. The Medical Ethical Committee of the Maastricht University Medical Centre+ (MEC 11–3-070) approved this trial, which conformed to the ‘Declaration of Helsinki’ as amended most recently by the 64th WMA General Assembly, Fortaleza, Brazil, October 2013 [20]. The Medical Research Involving Human Subjects Act (WMO) does not apply for the secondary analysis of the Chance study. Therefore, an additional official approval of this secondary analysis by the Medical Ethical Committee is not required (MEC letter 2019–0987).

Patients with mild to very severe COPD were recruited before the start of a comprehensive PR program at CIRO in Horn, The Netherlands [21]. Patients between the age of 40 and 85 years with a diagnosis of COPD according to GOLD guidelines [22] were eligible. The protocol and part of the results of the Chance-study have been published before [1, 4, 10, 15, 19, 23,24,25,26]. All patients gave written informed consent prior to inclusion in the study.

PR program

PR took place inpatient (8 weeks, 5 sessions per week; total of 40 sessions) or outpatient (8 weeks, 3 sessions per week, followed by 8 weeks, 2 sessions per week; total of 40 sessions), in line with the 2013 American Thoracic Society & European Respiratory Society Statement [4]. Extensive pre- and post-PR assessments were performed, as described before [19].

Measurements

Demographics, body mass index (BMI), body composition (fat-free mass index) [27], smoking history were assessed, as part of standard care. Lung function was determined with standardized spirometry equipment of Masterlab (CareFusion, Hoechberg, Germany) [28].

To evaluate HRQoL, three disease-specific PROs, the CAT (range 0–40 points) [29], the CCQ (range 0–6 points) [30] and the COPD-specific version of the SGRQ (range 0–100 points) [31] were assessed in all participants. Mood status was measured with the Hospital Anxiety and Depression scale (HADS; range 0–21 points) [32]. Higher scores are equivalent to a decreased HRQoL and/or increase in symptoms of anxiety or depression, respectively. The mMRC dyspnea scale was used to establish functional impairment due to dyspnea [33]. The level of care dependency was determined at baseline with the Care Dependency Scale (CDS; range 15–75 points) with a lower score representing a higher level of care dependency [34].

The 6-min walking test (6MWT) [35], cardiopulmonary exercise test (CPET; only at baseline) [36] were used to assess exercise capacity. Exercise tolerance was determined as cycle endurance time (CET) during the constant work rate cycle test (CWRT) [37]. Functional mobility was measured with the Timed ‘Up and Go’ (TUG) test [15, 17]. Isokinetic quadriceps muscle function (i.e. strength and endurance/total work) was determined using a Biodex System 4 Pro (Biodex Medical Systems Inc., New York, USA) [38].

Statistical analyses

Analyses were performed using SPSS software (statistical package for the social sciences) for Windows (version 25.0). Results are presented as mean and standard deviation (SD), median and interquartile range (IQR), and/or proportions, as appropriate. Continuous variables were tested for normality. Differences at baseline between completers and non-completers were analyzed using independent samples T-tests or Mann-Whitney U tests. Correlations between PROs and exercise test outcomes were analyzed using Scatter plots and Pearson’s or Spearman’s correlations, as appropriate. The strength of correlations has been classified according to British Medical Journal guidelines, which regard significant correlation coefficients of 0–0.19 as very weak, 0.2–0.39 as weak, 0.4–0.59 as moderate, 0.6–0.79 as strong, and 0.8–1 as very strong [39]. A priori, the level of significance was set at ≤0.01.

Results

A total of 518 patients (55.6% male, age 64.1 ± 9.1 years) volunteered to participate and attended the pre-PR assessment. The mean baseline 6MWD was 424 ± 124 m and 25.1% of the patients had a 6MWD below 350 m [40] and in 74.7% of the patients, quadriceps muscle strength was less than 80% of the predicted value [41]. The PROs showed a high degree of dyspnea (80.7% with mMRC dyspnea grade of two or higher) [22], anxiety (34.8% with ≥10 points) [32], depression (33.4% with ≥10 points) [32], care dependency (28.5% with CDS total score of ≤68 points) [25], and an impaired HRQoL (81.9% with a SGRQ total score of ≥44 points; 75.0% with a CAT total score of ≥18 points; 76.7% CCQ total score of ≥1.9 points) [22]. Baseline characteristics, exercise test outcomes and PROs at baseline are presented in Table 1.

Table 1 Patient characteristics, patient-reported outcomes and exercise test outcomes at baseline
Full size table

Correlations between exercise test outcomes and PROs at baseline

Overall, correlations between PROs and exercise test outcomes at baseline were statistically significant (Table 2). Of these, the correlation between mMRC score and 6MWD was the strongest (ρ: −0.65; p<0.001), which is visually presented in Fig. 1. A moderate correlation was found between mMRC score and CPET maximum workload (Wmax; ρ: −0.54; p<0.001), CPET peak oxygen uptake (VO2peak; ρ: −0.40; p<0.001), TUG time (ρ: 0.49; p<0.001), quadriceps total work (ρ: −0.43; p<0.001), respectively.

Table 2 Correlations between exercise test outcomes and PROs at baseline
Full size table
Fig. 1
figure 1

Association between the mMRC score and 6MWD at baseline (a) and between changes in mMRC score and changes in 6MWD after PR (b)

Full size image

HRQoL PROs showed weak correlations with exercise outcomes at baseline. Moderate correlations were only found between SGRQ-C and 6MWD (r: −0.53; p<0.001) and CPET maximum workload (ρ: −0.48; p<0.001) and between CCQ and 6MWD (r: −0.48; p<0.001) and CPET maximum workload (ρ: −0.43; p<0.001). See Fig. 2 for a scatter plot illustrating the relationship between HRQoL PROs and 6MWD. CDS score was significantly correlated with all exercise test outcomes, with correlations ranging from 0.24 (CWRT cycle endurance time) to 0.50 (6MWD). Both HADS-D and HADS-A showed non-significant or very weak to weak correlations with all exercise test outcomes.

Fig. 2
figure 2

Left: Association between the SGRQ-C score (a), CAT score (b), CCQ score (c), and the 6MWD. Right: association between the change in SGRQ-C score (d), CAT score (e), CCQ score (f), and the change in 6MWD after PR. On the X-axis the MCID of 30 m for the 6MWT [42] is marked, on the Y-axis the MCIDs for SGRQ-C (−4.0), CAT (−2.0) and CCQ score (−0.4) are marked [10, 43]. MCID, minimal clinically important difference

Full size image

Correlations between changes in exercise test outcomes and changes in PROs after PR

Four hundred nineteen patients completed the PR program. Completers and non-completers were comparable with respect to baseline characteristics (Table 1). Only the amount of current smokers was significantly higher in the non-completer group (p<0.001). All PROs and exercise test outcomes changed significantly after PR (Table S1). When significant, correlations between changes in exercise test outcomes and changes in PROs were generally very weak or weak. The highest correlation, being classified as weak, was found between ΔCCQ and Δ6MWD (ρ: −0.36; p<0.001; Fig. 2). Changes in other HRQoL PROs demonstrated similar association with changes in exercise test outcomes (Table 3). Changes in quadriceps peak muscle strength were not correlated with changes in any of the PROs.

Table 3 Correlations between changes in exercise test outcomes and changes in PROs (pre vs. post PR)
Full size table

Discussion

This study demonstrates that PROs and exercise test outcomes are associated to some extent in patients with mild to very severe COPD, but, in general, these correlations are weak to moderate. A strong relationship was merely found between the severity of dyspnea (mMRC) and distance covered in the 6MWT at baseline. In the current study, dyspnea tended to indicate at least moderate negative correlations with exercise test outcomes at baseline, suggesting that exercise performance decreases as dyspnea scores increase. However, these associations attenuated considerably or even became non-significant once the changes in dyspnea were correlated with changes in exercise test outcomes following PR, indicating that an improvement in exercise performance after PR does not necessarily imply that self-reported breathlessness decreases concurrently, like shown before [18]. As a side remark, it is important to note that correlations between changes in parameters are always lower than cross-sectional correlations. After all, the measurement error is included twice (pre vs. post) in the analysis, which always results in a weaker signal [44].

While the mMRC-scale is a unidimensional method to quantify only dyspnea, there are several multidimensional disease-specific PROs, which assess not only dyspnea but also other symptoms and perceived HRQoL in COPD [1]. Of these HRQoL PROs (CAT, CCQ, SGRQ), their association with exercise test outcomes was weak to moderate, indicating that no single exercise test accurately reflects HRQoL (or the other way around), proving that HRQoL is indeed a multi-dimensional concept that includes domains related to physical, mental, emotional, and social functioning. Overall, these results support the findings by Punekar et al. [11] who showed that generally there was a very weak to moderate negative correlation between the 6MWD and the SGRQ.

While guidelines on the diagnosis and treatment of COPD have intensively stated that the assessment of disease severity is substantially improved by using functional criteria [22], such as exercise capacity, the current study demonstrates that the variance in PROs can only be partially explained by attributes related to exercise performance. So, despite the fact that PROs for HRQoL, dyspnea, anxiety, depression and the level of care dependency are crucial when evaluating the disease severity and effectiveness of a treatment in COPD, it is justified to conclude that these PROs assess features not measured by exercise tests. Consequently, if we solely use a few outcome measures (for example, walking distance or HRQoL) to evaluate performance after PR, the clinical complexity and multidimensional aspect of PR in patients with COPD appears to be ignored [18].

In our study, the 6MWD showed the strongest relationship with important clinical PROs, underlining the fact that the 6MWT indeed seems to play a key role in evaluating functional exercise capacity [14]. Since the 6MWT is self-paced, test outcomes are likely to be affected by a patient’s mental and emotional status [3].

Limitations

Patients were solely recruited in a specialized PR centre, resulting in a selected group of COPD patients. This should be considered when applying results to other COPD samples. Furthermore, by quantifying the associated exercise limitation, a mMRC-score of 4 reflects the most disabled COPD patients who are not always able to perform a symptom-limited CPET, as a result of their dyspnea. In the current study, patients unable to perform a CPET and, concurrently, a CWRT were automatically excluded from the correlation analysis, since they did not present any values for both exercise tests, possibly affecting the correlation coefficients.

Conclusions

In conclusion, we have found that patient-reported outcomes and exercise test outcomes, although significantly correlated with each other, assess different disease features in patients with COPD. Therefore, it can be stated that relevant features from the patient’s perspective like HRQoL, anxiety, depression, and the level of care dependency are not an accurate reflection of a patient’s exercise capacity. The only exception to this seems to be dyspnea, the only PRO that tended to imply at least moderate association with exercise test outcomes. We would like to highlight the complexity of evaluating the effectiveness of a personalized PR program, in which we note that changes in PROs and changes in exercise test outcomes correlate poorly. Indeed, improvements in exercise capacity obtained after PR do not necessarily result in alterations in PROs in patients with COPD. Individual PROs need to be supported by additional functional measurements whenever possible, in order to get a more detailed insight in the effectiveness of a PR program.

Availability of data and materials

The datasets generated during and/or analyzed during the current study are available from the Board of Directors of CIRO on reasonable request and following the CIRO’s data request policy.

Abbreviations

6MWD:

Six-minute Walking Distance

6MWT:

Six-minute Walking Test

BMI:

Body Mass Index

CAT:

COPD Assessment Test

CCQ:

Clinical COPD Questionnaire

CDS:

Care Dependency Scale

COPD:

Chronic Obstructive Pulmonary Disease

CPET:

Cardiopulmonary Exercise Test

CWRT :

Constant Work Rate (cycle) Test

FEV1 :

Forced Expiratory Volume in One Second

HADS:

Hospital Anxiety and Depression Scale

HRQoL:

Health-Related Quality of Life

IQR :

Interquartile Range

mMRC:

modified Medical Research Council

MEC:

Medical Ethics Committee

PR:

Pulmonary Rehabilitation

PRO:

Patient-reported Outcome

SD:

Standard Deviation

SGRQ-C :

St George’s Respiratory Questionnaire (COPD-specific version)

TUG :

Timed Up and Go

VO2peak :

Peak Oxygen Uptake

Wmax :

Maximal Workload

WMO:

Medical Research Involving Human Subjects Act

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Acknowledgements

The authors would like to thank Professor W. Derave (Ghent University) and Dr. P. Klijn (Merem Hilversum) for their input and collaboration within the BASES-consortium, in the context of which the current manuscript was written.

Funding

The BASES project is supported by the Lung Foundation Netherlands (#5.1.18.232). The Chance project was supported by the Lung Foundation Netherlands (#3.4.10.015) and GlaxoSmithKline (SCO115406).

Author information

Authors and Affiliations

  1. Department of Research and Development, CIRO, Hornerheide 1, 6085NM, Horn, the Netherlands

    Roy Meys, Anouk A. F. Stoffels, Sarah Houben-Wilke, Daisy J. A. Janssen, Frits M. E. Franssen, Emiel F. M. Wouters & Martijn A. Spruit

  2. Department of Respiratory Medicine, Maastricht University Medical Centre, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht, The Netherlands

    Roy Meys, Anouk A. F. Stoffels, Frits M. E. Franssen, Emiel F. M. Wouters & Martijn A. Spruit

  3. Department of Pulmonary Diseases, Radboud UMC Dekkerswald, Nijmegen, the Netherlands

    Anouk A. F. Stoffels, Hieronymus W. H. van Hees & Bram van den Borst

  4. Department of Health Services Research, Care and Public Health Research Institute, Faculty of Health Medicine and Life Sciences, Maastricht University, Maastricht, the Netherlands

    Daisy J. A. Janssen

  5. Reval Rehabilitation Research, Biomedical Research Institute, Faculty of Rehabilitation Sciences, Hasselt University, Diepenbeek, Belgium

    Chris Burtin & Martijn A. Spruit

Authors
  1. Roy Meys
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  2. Anouk A. F. Stoffels
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  3. Sarah Houben-Wilke
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  4. Daisy J. A. Janssen
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  5. Chris Burtin
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  6. Hieronymus W. H. van Hees
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  7. Frits M. E. Franssen
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  8. Bram van den Borst
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  9. Emiel F. M. Wouters
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  10. Martijn A. Spruit
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Consortia

on behalf of the BASES-consortium

Contributions

Drafting of the manuscript, RM, FMEF, MAS. Conception and design of the original study, SH-W, DJAJ, MAS. Acquisition and analysis of data, SH-W, DJAJ, MAS. Analysis and interpretation of data, RM, FMEF, MAS. Editing manuscript, AAFS, SH-W, DJAJ, CB, HWHH, BB, EFMW. All authors critically revised the article and gave final approval of this version to be submitted.

Corresponding author

Correspondence to Roy Meys.

Ethics declarations

Ethics approval and consent to participate

The COPD, health status and co-morbidities (Chance) study was approved by the local ethics committee of Maastricht University Medical Centre+, The Netherlands (MEC 11–3-070). All patients gave written informed consent.

Consent for publication

Not applicable.

Competing interests

DJAJ reports personal fees from Boehringer Ingelheim, personal fees from Novartis, personal fees from Astra Zeneca, outside the submitted work; FMEF reports grants and personal fees from AstraZeneca, personal fees from Boehringer Ingelheim, personal fees from Chiesi, personal fees from GlaxoSmithKline, grants and personal fees from Novartis, personal fees from TEVA, outside the submitted work; BB reports personal fees from AstraZeneca, personal fees from Boehringer Ingelheim bv, outside the submitted work; EFMW reports personal fees from Nycomed, personal fees from Boehringer Ingelheim BV, grants and personal fees from AstraZeneca, grants and personal fees from GlaxoSmithKline, personal fees from Novartis, personal fees from Chiesi, outside the submitted work; MAS reports grants from Lung Foundation Netherlands, grants from GlaxoSmithKline Netherlands, during the conduct of the study. RM, AAFS, SH-W, CB and HWHH have nothing to disclose.

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Supplementary information

Additional file 1: Table S1.

Changes in PROs and exercise test outcomes after PR.

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Meys, R., Stoffels, A.A.F., Houben-Wilke, S. et al. Association between patient-reported outcomes and exercise test outcomes in patients with COPD before and after pulmonary rehabilitation. Health Qual Life Outcomes 18, 300 (2020). https://doi.org/10.1186/s12955-020-01505-x

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Keywords

Health and Quality of Life Outcomes

ISSN: 1477-7525

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