Background
Chronic obstructive pulmonary disease (COPD) is a prevalent and debilitating respiratory condition characterized by irreversible airflow limitation, primarily resulting from chronic bronchitis and emphysema. It significantly impairs patients’ quality of life and is a leading cause of morbidity and mortality worldwide, contributing to a substantial burden on healthcare systems. Despite advancements in pharmacological management and rehabilitation approaches, there remains a critical need for comprehensive strategies that address the multifaceted nature of COPD, including its exercise-induced symptoms and associated comorbidities.1,2
In particular, exercise-induced desaturation (EID) during physical activity is a common phenomenon among COPD patients, with studies indicating that approximately 20% or more of this patient population experiences significant oxygen desaturation during exertion.3–5 Current literature highlights the importance of assessing EID as an indicator of disease severity and a predictor of adverse outcomes, such as increased hospitalization and mortality rates.6 Nonetheless, the criteria for diagnosing EID are inconsistent across studies,7 often relying on single assessments of resting SpO2 or subjective evaluations of exercise tolerance. This inconsistency underlines a significant gap in our understanding of how EID manifests in different COPD phenotypes and its implications for patient management.8 Furthermore, dynamic monitoring of SpO2 during standardized exercise tests, particularly the six-minute walk test (6MWT), is essential for accurately capturing EID and its physiological correlates.9 The 6MWT has emerged as a widely accepted tool for evaluating exercise capacity in COPD patients, providing valuable insights into their functional status and prognosis.10 It is not only straightforward to administer but also sensitive to changes in patient condition, making it a pivotal component of routine clinical assessments. Previous studies have demonstrated that a decline in SpO2 during the 6MWT is associated with a higher risk of COPD exacerbations and mortality, reinforcing the need for continuous monitoring of oxygen levels during exertion.9,11–13 However, the relationship between EID severity and health-related quality of life remains underexplored, with limited research investigating how varying degrees of desaturation impact patients’ daily functioning and overall well-being. In summary, while the multifactorial nature of COPD necessitates a nuanced understanding of its clinical manifestations, existing literature provides a foundation for investigating the prevalence and implications of exercise-induced desaturation. This study endeavors to fill the current research void regarding EID characteristics and health-related quality of life among COPD patients, thereby advancing the knowledge base in this critical area of respiratory medicine. The present study adopts a retrospective design to address these gaps by analyzing data from 116 COPD patients who underwent the 6MWT. It aims to classify the severity of EID and evaluate its association with various physiological parameters, including forced expiratory volume (FEV1) and the distance walked during the test. Additionally, the research will assess the impact of EID on health-related quality of life, utilizing standardized measures such as the EQ-5D, to identify potential predictors of EID severity and their clinical implications. By elucidating these relationships, this study seeks to contribute to the development of targeted interventions for COPD patients, ultimately enhancing their management and quality of life.14–17
Materials and Methods
Data Collection
The study ethical approval was obtained from the China–Japan Friendship Hospital (2022-KY-141; clinical trial registration number: NCT04318912). Informed consent was obtained from all participants prior to their inclusion in the study. Patient data confidentiality was strictly maintained, and all procedures were in compliance with the Declaration of Helsinki. This study included 116 COPD patients diagnosed between May 1, 2023, and June 30, 2024, at the China–Japan Friendship Hospital. The cohort consisted of 97 males and 20 females. Inclusion criteria were based on the 2020 GOLD guidelines for stable COPD. Exclusion criteria included:
1. Resting SpO2 ≤ 92%, HR > 120 bpm.
2. Systolic BP > 180 mmHg or diastolic BP > 100 mmHg.
3. Malignant arrhythmias.
4. Severe valvular disease.
5. Walking limitations due to neurological or musculoskeletal disorders.
6. Concurrent malignancy. Demographic data such as gender, age, baseline heart rate, and SpO2 were extracted from electronic medical records.
Pulmonary Function Testing
Pulmonary function tests were performed using the MasterScreen™ PFT system (CareFusion Germany GmbH, Höchberg, Germany) following ATS/ERS guidelines. Parameters measured included forced expiratory volume in the first second (FEV1), forced vital capacity (FVC), FEV1/FVC ratio, peak expiratory flow (PEF), and their respective predicted values.
Six-minute Walk Test (6MWT) and SpO2 Monitoring
The 6MWT was performed in a 30-meter indoor hallway following ATS guidelines as described previously,18,19 supervised by two trained assessors. Continuous SpO2 was monitored using a Multidimensional assessment system for 6-minute walk test with integrated wearable cardiopulmonary exercise test (Yiliankang Medical Technology Co., Zhejiang, China), with Bluetooth-enabled data acquisition at 3-second intervals from 1 minute pre-test to 4 minutes post-test. Subjective dyspnea and fatigue were assessed using the Borg scale post-test. EID was classified as follows: Mild EID: SpO2 decrease ≥4% with nadir SpO2 ≥90%. Severe EID: SpO2 decrease ≥4% with nadir SpO2 ≤90%. Non EID: SpO2 decrease <4% with nadir SpO2 ≥90%.16
The COPD Assessment Test (CAT)
The validated questionnaire was administered to evaluate symptom burden.20 The CAT consists of 8 items (cough, cough sputum, chest tightness, shortness of breath climbing/walking up stairs, limitation of daily activities, confidence to go out, sleep quality, energy level), each using a 0–5 point Likert scale (0 = no effect, 5 = extremely severe).
Hand Grip Strength
Measured using a Jamar Hydraulic Hand Dynamometer (KDG Grip Strength Tester, Bolingbrook, USA), with participants seated and elbow flexed at 90°.
Quadriceps Strength
Assessed with an isokinetic dynamometer (MicroFET 2; Hoggan, West Jordan, UT), with participants positioned in 90° hip flexion and 60° knee flexion.
Follow-Up
Patients were followed up six months post-clinic visit via telephone to record survival status, adverse events (acute exacerbations, complications, rehospitalizations), and quality of life using the Chinese EQ-5D-5L questionnaire.
The EQ-5D-5L
EQ-5D-5L questionnaire includes five dimensions graded into five levels and a visual analog scale (EQ-VAS) for overall health evaluation.21 Five dimensions of health included mobility, self-care, activities of daily living, pain/discomfort, anxiety/depression with 5 severity levels for each dimension. Health Status Codes: 5-digit codes (eg, “12345” for no difficulty with mobility, minor difficulty with self-care, etc), detailed information regarding the scoring system of the EQ-5D-5L questionnaire has been added to the Table S1. Indicator conversion was based on country/region-specific utility weights (eg, China). Conversion of 5-digit code to a single health utility index based on country/region-specific utility weights.
Statistical Analysis
Statistical analysis was performed using IBM SPSS Statistics (version 26.0; IBM Corporation, Armonk, New York, USA). Measurement data following a normal distribution were expressed as mean ± standard deviation (xˉ±s). ANOVA was used to compare means across ≥3 groups, justified by confirmed normality (Shapiro–Wilk test) and equal variance (Levene’s test). Post hoc Bonferroni tests identified specific group differences if ANOVA was significant (*p < 0.05*). Count data were expressed as numbers or percentages and analyzed using the chi-square test. Significance testing of regression coefficients was performed at a significance level of 0.05. Multivariate logistic regression was used to analyze factors influencing severe EID in COPD patients. ROC curves were plotted to evaluate the predictive ability of influencing factors for the severity of EID.
Results
General Characteristics of Patients
A total of 116 COPD patients were included in the study, with an average age of 63.32 ± 7.99 years. Among them, 44.8% patients had no EID, 36.2% had mild EID, and 19.0% had severe EID. There were no statistically significant differences in gender, age, BMI, grip strength, knee extension strength, or rest heart rate among the three groups (p > 0.05). Compared to patients with no or mild EID, those with severe EID had significantly lower levels of rest SPO2 (%), PEF (L/s), PEF (%), FEV1 (L), and FEV1 (%) (SPO2: p = 0.002; PEF: p < 0.001; PEF (%): p < 0.001; FEV1: p = 0.026; FEV1 (%): p = 0.001). Severe EID patients also had shorter 6MWD (P < 0.001) and experienced more severe dyspnea and fatigue (Borg dyspnea: p = 0.040; Borg fatigue: p = 0.015). (See Table 1).
Table 1 Basic Characteristic Information of Patients with Different Degrees of EID in Chronic Obstructive Pulmonary Disease
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Multivariate Logistic Regression Analysis of Factors Influencing Severe EID in COPD Patients
Taking the severity of EID in COPD patients as the dependent variable (1 = severe EID, 0 = non-severe EID), variables with p <0.05 from Table 1 were included as independent variables in the logistic regression analysis. Results showed that low FEV1(%), low 6MWD, and low blood SpO2 were risk factors for severe EID in COPD patients (FEV1(%): p = 0.002; 6MWD: p = 0.008; blood oxygen: p = 0.018). (See Table 2).
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Table 2 Identifies the Factors Influencing Severe EID Through Logistic Regression and Establishes a Regression Model
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Analysis of FEV1(%), 6MWD, and Resting SpO2 in Relation to EID Severity
The optimal cut-off values for predicting EID severity were as follows: FEV1(%): 54.45, with an AUC of 0.716. 6MWD (m): 450.5 m, with an AUC of 0.761. SpO2 (%) at rest: 94.5%, with an AUC of 0.737. FEV1(%), 6MWD, and resting SpO2 effectively distinguished patients with severe EID from those with non-severe EID. (See Figure 1 and Table 3).
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Table 3 Comparison of FEV1(%), 6MWD, and Resting SpO2 Between Severe and Non-Severe EID Patients
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Figure 1 ROC curve with FEV1, 6MWD, and resting blood oxygen can distinguish between severe EID patients and non-severe EID patients.
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Health-Related Quality of Life in Patients with Different EID Severity
No deaths were reported during the follow-up period. Severe EID patients had significantly lower EQ-5D index and EQ VAS scores (EQ-5D index: p = 0.002; EQ VAS: p = 0.005). Among the five dimensions of the EQ-5D-5L scale, there were no significant differences in self-care, pain/discomfort, or anxiety/depression scores among groups (p > 0.05). However, patients with severe EID had significantly lower scores in mobility and usual activities compared to those with no or mild EID (mobility: p = 0.001; usual activities: p = 0.038). (Figure 2 and Table 4). Besides, there is no statistically significant difference in the frequency of acute exacerbations, emergency department visit or hospitalization rates, and Respiratory tract infection incidence rates among the different EID groups (p > 0.05) (Table 5).
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Table 4 Follow-Up EQ-5D Data of COPD Patients with Different Degrees of EID at 6 Months
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Table 5 Follow-Up Data of COPD Patients with Different Degrees of EID During 6 Months
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Figure 2 The violin plot used to display the distribution of EQ-5D index across three groups, including statistical information such as density distribution, median, and quartiles. P-value * < 0.05, ***< 0.001, ns >0.05.
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Discussion
The study highlights actionable thresholds (FEV1%, 6MWD, SpO2) and symptom metrics (Borg scores) that are clinically practical for EID management. By translating these findings into care pathways, clinicians can improve early diagnosis, tailor interventions, and optimize patient-centered outcomes.
Effective management strategies are critical, yet they often fall short of comprehensively addressing the multifaceted nature of the disease, particularly as COPD progresses and leads to exacerbations and comorbidities that further complicate patient care.4 This study aims to investigate the characteristics of EID in COPD patients, identify predictive factors for varying degrees of EID, and evaluate the impact of EID on health-related quality of life (HRQoL). By analysis of clinical data from 116 COPD patients undergoing the six-minute walk test (6MWT), we aim to elucidate the relationship between physiological parameters and EID severity. In this study, approximately 55% of COPD patients exhibited EID. Research has shown that the severity of airflow limitation is associated with EID, with patients experiencing reduced FEV1 having a higher risk of EID.3 Another study indicated that the decline in SpO2 was significantly associated with reduced FEV.19 This study demonstrated that pulmonary function parameters such as FEV1, and FEV1%value were associated with EID, suggesting that worsening EID is related to deteriorating pulmonary function, consistent with previous studies. However, some studies have indicated that pulmonary function alone may not sufficiently predict a reduction in 6MWD. The relationship between obesity and EID remains unclear. Some studies have identified obesity as a positive predictor of EID, possibly because obese patients are more prone to dyspnea.3,12 Waatevik et al13 found a significant association between obesity and EID before incorporating the modified Medical Research Council dyspnea score into their model. However, other studies reported a negative correlation, with moderate obesity potentially mitigating hyperinflation and improving dyspnea in COPD patients.4 Kim et al6 found that patients with EID had lower average BMI, with BMI reduction linked to increased mortality risk. In this study, obesity was not associated with EID, possibly due to the small sample size. The relationship and underlying mechanisms between obesity and EID require further exploration. Furthermore, some studies have indicated that advanced age and female sex are associated with an increased risk of EID.5 However, in this study, neither age nor sex was related to EID, which may be attributed to selection bias in the sample.
The prediction of EID can provide valuable guidance for clinical practice and prognostic management. Perez et al4 reported that an abnormal reduction in resting SpO2 could serve as a predictor of EID. Andrianopoulos et al7 identified the 6MWT as the preferred exercise test due to its simplicity and sensitivity to arterial oxygen desaturation. This study showed that FEV1%, 6MWD, and resting SpO2 could effectively predict the degree of EID, consistent with previous research. Additionally, some studies have suggested that diffusion capacity of the lung for carbon monoxide (DLCO) could predict the extent of oxygen desaturation. CT-defined emphysema has been found to outperform19 and resting SpO2 in specific predictive contexts.13 The current limitations of single-factor EID prediction emphasize the need for further research into multifactorial predictive models to more accurately predict EID and guide clinical and prognostic interventions.
Furthermore, this study found that severe EID reduces HRQoL, primarily by impairing mobility and causing inconvenience in daily life. Patients with EID face a higher risk of dyspnea or fatigue during routine activities. Salant et al14 reported that the mean utility value for assessing COPD patients using EQ-5D-5L in a meta-analysis was 0.676, compared to 0.780 for EQ-5D-3L. Moreover, longer timeframes in the EQ-5D scale can reduce ceiling effects and enhance reliability.17 In this study, the timeframe for the EQ-5D scale was set as “today”. Using a longer timeframe, such as “1 week” or “4 weeks”, might better reflect the overall HRQoL of patients.
The findings will enhance our understanding of the predictors of EID and provide insights into how EID correlates with patients’ functional status and overall quality of life, thereby guiding clinical management approaches tailored to individual patient needs. The innovation of this study lies in its comprehensive evaluation of EID in COPD patients through the lens of the 6MWT. Unlike previous research which primarily focused on static measurements of lung function,4,9,10,22 our study highlights the dynamic nature of SpO2 during exertion, filling a significant gap in the literature. While earlier studies, such as those by Chang et al,5 indicated correlations between static pulmonary function metrics and EID, our findings suggest that factors such as the 6MWD and resting SpO2 levels serve as critical predictive markers for EID severity. This research not only corroborates existing knowledge but also provides novel insights into the prognostic implications of EID for COPD patients, particularly in predicting long-term outcomes and guiding therapeutic interventions. The implications of our findings extend to clinical practice and policy-making. By identifying specific risk factors associated with EID, such as low FEV1% and diminished 6MWD, clinicians can implement targeted interventions for high-risk patients. This could include more personalized rehabilitation programs and the potential use of supplemental oxygen during physical activity to enhance exercise tolerance. Moreover, the identification of EID as a significant predictor of adverse outcomes highlights the necessity for routine monitoring of SpO2 during physical exertion in COPD management protocols. These insights could influence health policy by advocating for integrated care approaches that prioritize exercise assessments alongside traditional pulmonary function tests, ultimately aiming to improve patient quality of life and reduce healthcare costs associated with COPD exacerbations.
Importantly, our previous study did examine the relationship between cardiovascular function and EID, despite evidence suggesting that conditions such as atrial fibrillation may increase the risk of EID during six-minute walk tests.16 Chang et al5 had found that atrial fibrillation was associated with EID, with COPD patients exhibiting higher risks of oxygen desaturation during the 6MWT. Mesquita et al23 had reported that COPD patients with impaired left ventricular ejection fraction had significantly reduced 6MWD. But, the impact of left ventricular ejection fraction on six-minute walk distance was not investigated, despite existing literature indicating that compromised cardiac function could affect exercise capacity in COPD patients. In the future, the relationship between cardiovascular function and EID should be analyzed.
However, this study is not without limitations. The relatively small sample size may hinder the generalizability of the findings. Future research should aim to include larger, multicentric cohorts to validate our results further. Additionally, the proportion of patients who experienced exacerbations during the 6-month follow-up was relatively low, which may have reduced the statistical power to detect the association between EID and the risk of exacerbations. This limitation is partly due to the characteristics of the study cohort, which included stable COPD patients with good adherence to treatment and regular health management. Therefore, caution is needed when interpreting the relationship between EID and exacerbation risk based on our findings, and future studies involving cohorts with higher exacerbation rates are warranted to validate these results.
In summary, this study elucidates the clinical characteristics and predictive factors associated with EID in COPD patients, revealing a significant impact on their quality of life. The findings underscore the importance of early identification and management of EID to improve patient outcomes. By establishing the relationship between various physiological parameters and EID severity, this research provides a foundation for developing targeted interventions aimed at enhancing the quality of life for individuals with COPD. Future studies should focus on validating these predictive factors in larger, diverse populations and exploring the interplay between cardiovascular and pulmonary functions to further refine management strategies.
Conclusion
This study highlights the necessity of a multifactorial approach to EID management, considering pulmonary function parameters, mobility, baseline oxygen saturation, and subjective patient experiences. These factors not only aid in identifying high-risk patients but also provide a basis for personalized treatment. Moreover, the relationship between EID and HRQoL underscores the importance of considering patient quality of life in COPD management. Monitoring parameters such as FEV1%, 6MWD, and resting SpO2 can facilitate the effective assessment of EID in COPD patients, enabling earlier interventions to enhance patient outcomes and quality of life.
Data Sharing Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Acknowledgments
We thank the staff of the Department of Rehabilitation Medicine and Department of Clinical Research and Data Management for participating in this research.
Author Contributions
All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.
Funding
This work was supported by 1.National High Level Hospital Clinical Research Funding, 2.Elite Medical Professionals Initiative of China-Japan Friendship Hospital (NO.ZRJY2025-GG04), 3.the National Natural Science Foundation of China (82102654), 4.the Beijing Natural Science Foundation (2024BZR-7242126), 5.Medical and health technology innovation project of Chinese Academy of Medical Sciences (2021-12M-1-049), 6. the Capital’s Funds for Health Improvement and Research (2024-2-4069). The funding body had no role in the design of the study or collection, analysis, or interpretation of data, nor in writing the manuscript.
Disclosure
The authors report no conflicts of interest in this work.
References
1. Agustí A, Br C, Gj C, et al. Global initiative for chronic obstructive lung disease 2023 report: GOLD executive summary. Arch De Bronconeumol. 2023;59:232–248. doi:10.1016/j.arbres.2023.02.009
2. Wang C, Xu J, Yang L, et al. Prevalence and risk factors of chronic obstructive pulmonary disease in China (the China pulmonary health [CPH] study): a national cross-sectional study. Lancet. 2018;391:1706–1717. doi:10.1016/S0140-6736(18)30841-9
3. Andrianopoulos V, Br C, Fm F, et al. Determinants of exercise-induced oxygen desaturation including pulmonary emphysema in COPD: results from the ECLIPSE study. Respir Med. 2016;119:87–95. doi:10.1016/j.rmed.2016.08.023
4. Perez T, Deslée G, Burgel PR, et al. Predictors in routine practice of 6-min walking distance and oxygen desaturation in patients with COPD: impact of comorbidities. Int J Chronic Obstr. 2019:1399–1410. doi:10.2147/COPD.S188412
5. Chang C-H, Lin H-C, Yang C-H, et al. Factors associated with exercise-induced desaturation in patients with chronic obstructive pulmonary disease. Int J Chronic Obstr. 2020;Volume 15:2643–2652. doi:10.2147/COPD.S272511
6. Kim C, Ko Y, Lee JS, et al. Predicting long-term mortality with two different criteria of exercise-induced desaturation in COPD. Respir Med. 2021;182:106393. doi:10.1016/j.rmed.2021.106393
7. Andrianopoulos V, Franssen FME, Peeters JPI, et al. Exercise-induced oxygen desaturation in COPD patients without resting hypoxemia. Respir Physiol Neurobiol. 2014;190:40–46. doi:10.1016/j.resp.2013.10.002
8. Lulu Y, Minghui S, Xuanming S, et al. Prediction of exercise-induced desaturation in COPD patients without resting hypoxemia: a retrospective study. BMC Pulm Med. 2022;22:405. doi:10.1186/s12890-022-02174-w
9. Marie W, Ane J, Francisco GR, et al. Oxygen desaturation in 6-min walk test is a risk factor for adverse outcomes in COPD. Europ Resp J. 2016;48:82–91. doi:10.1183/13993003.00975-2015
10. Gupta R, Ruppel GL, Espiritu JRD; Pulmonary Do, Critical Care Medicine DHS, Evansville, IN 47747, USA. Indiana University School of Medicine E, IN 47710, USA. Exercise-induced oxygen desaturation during the 6-minute walk test. Med Sci. 2020;8:8. doi:10.3390/medsci8010008
11. Pinto-Plata VM, Cote C, Cabral H, Taylor J, Celli BR. The 6-min walk distance: change over time and value as a predictor of survival in severe COPD. Europ Resp J. 2004;23(1):28–33. doi:10.1183/09031936.03.00034603
12. García-Talavera I, Figueira-Gonçalves JM, Gurbani N, et al. Clinical characteristics of COPD patients with early-onset desaturation in the 6-minute walk test. Pulmonology. 2018;24(5):275–279. doi:10.1016/j.pulmoe.2018.04.007
13. Marie W, Bente F, Gómez RF, et al. CT-defined emphysema in COPD patients and risk for change in desaturation status in 6-min walk test. Respir Med. 2021;187:106542. doi:10.1016/j.rmed.2021.106542
14. Salant N, Mohiuddin S, Zhang Y, et al. EQ-5D based utility values for adults with chronic obstructive pulmonary disease: a systematic review, meta-analysis, and meta-regression. COPD. 2024;21:2385358. doi:10.1080/15412555.2024.2385358
15. Shirisha P, Bagepally BS, Kumar SS, Raghu B. Quality of life among obstructive sleep apnoea patients: a systematic review and meta-analysis of EQ-5D studies. Qual Life Res. 2024;2024:1–11.
16. Wang S, Gao B, Shi M, et al. Exercise-induced oxygen desaturation increases arterial stiffness in patients with COPD during the 6WMT. Int J Chronic Obstr. 2024;2024:1479–1489.
17. Chua AP, Janssen MF, Cheng LJ, et al. An exploratory study of alternative timeframes and descriptors for EQ-5D-5L in obstructive airway diseases using mixed methods. Value Health. 2024;27:1564–1572. doi:10.1016/j.jval.2024.07.004
18. Fujimoto Y, Oki Y, Kaneko M, et al. Usefulness of the desaturation-distance ratio from the six-minute walk test for patients with COPD. Int J Chron Obstruct Pulmon Dis. 2017;12:2669–2675. doi:10.2147/COPD.S143477
19. Dogra AC, Gupta U, Sarkar M, Padam A. Exercise-induced desaturation in patients with chronic obstructive pulmonary disease on six-minute walk test. Lung India. 2015;32:320–325. doi:10.4103/0970-2113.159550
20. Garcia-Sidro P, Naval E, Martinez Rivera C, et al. The CAT (COPD assessment test) questionnaire as a predictor of the evolution of severe COPD exacerbations. Respir Med. 2015;109:1546–1552. doi:10.1016/j.rmed.2015.10.011
21. Zanini A, Aiello M, Adamo D, et al. Estimation of minimal clinically important difference in EQ-5D visual analog scale score after pulmonary rehabilitation in subjects with COPD. Respir Care. 2015;60:88–95. doi:10.4187/respcare.03272
22. Cen J, Ma H, Chen Z, Weng L, Deng Z; Department of Respiratory Medicine TAHoMSoNU, Ningbo, Zhejiang, China, Department of Respiratory Medicine NNH, Ningbo, Zhejiang, China. Department of Respiratory Medicine TAHoMSoNU, Ningbo, Zhejiang, China. Monitoring peak expiratory flow could predict COPD exacerbations: a prospective observational study. Respir Med. 2019;148:43–48. doi:10.1016/j.rmed.2019.01.010
23. Mesquita R, Franssen FME, Houben-Wilke S, et al. What is the impact of impaired left ventricular ejection fraction in COPD after adjusting for confounders? Int J Cardiol. 2016;225:365–370. doi:10.1016/j.ijcard.2016.10.016