Clinically important changes and adverse events with centre-based or home-based pulmonary rehabilitation in chronic respiratory disease: A systematic review and meta-analysis

Abstract

Objectives: To determine the proportion of people who achieve minimal clinically important differences (MCID) with centre-based or home-based pulmonary rehabilitation and to synthesise data on adverse events.

Methods: Cochrane reviews and electronic databases were searched to identify randomised trials comparing centre-based to home-based pulmonary rehabilitation, or either model to usual care, in people with chronic respiratory disease. Primary outcomes were the proportion of participants achieving MCIDs in exercise capacity and disease-specific quality of life. Secondary outcomes were symptoms and adverse events. Cochrane Risk of Bias 1.0 and GRADE were used to assess the risk of bias and certainty of evidence respectively.

Results: Forty-nine trials were eligible. Compared to usual care, a higher proportion of pulmonary rehabilitation participants achieved the MCID for exercise capacity (6MWT: 47% vs 20%, p = 0.11), dyspnoea (43% vs 29%, p = 0.0001), fatigue (48% vs 27%, p = 0.0002) and emotional function (37% vs 25%, p = 0.02), with all of these between group differences statistically significant except for exercise capacity. There were no differences between centre-based and home-based pulmonary rehabilitation in the proportion of participants who achieved MCIDs (34%- 58% across studies). Ninety percent of trials reported no adverse events. Certainty of evidence was low-to- moderate with all outcomes except for CRQ-mastery (centre-based vs home-based pulmonary rehabilitation, or pulmonary rehabilitation vs usual care in COPD), ESWT (pulmonary rehabilitation vs usual care in COPD) and 6MWT (pulmonary rehabilitation vs usual care in bronchiectasis) where evidence was very uncertain.

Discussion: Clinically meaningful outcomes are achieved by similar proportions of participants in centre-based and home-based pulmonary rehabilitation, with few adverse events. Reporting of trial outcomes according to MCIDs is necessary for informed decision making regarding pulmonary rehabilitation models.

Keywords

Chronic obstructive pulmonary disease bronchiectasis interstitial lung disease exercise training rehabilitation

Introduction

Chronic respiratory diseases including bronchiectasis, chronic obstructive pulmonary disease (COPD) and interstitial lung diseases (ILD) are leading causes of morbidity and mortality^1,2 and frequently present with increased dyspnoea, fatigue, reduced exercise tolerance and health-related quality of life.^3–5

Pulmonary rehabilitation is a cornerstone of treatment for people with chronic respiratory disease⁶ and has traditionally consisted of supervised exercise training, self-management strategies, and support delivered to groups of people in-person by a multidisciplinary team.⁷ There is level one evidence supporting the effectiveness of pulmonary rehabilitation for people with COPD,^8,9 and increasing evidence in bronchiectasis and ILD.^10,11

Despite compelling evidence for the benefits of pulmonary rehabilitation, access to this treatment remains limited worldwide and barriers are multifactorial.^12–18 Referrals by health care professionals are influenced by their knowledge and perceptions regarding the benefits and harms of the program, and referral uptake by patients is influenced by their beliefs, expectations, and the physical challenges of attendance.¹⁹ International policy statements²⁰ have called for novel pulmonary rehabilitation program models that are accessible and acceptable to people with chronic respiratory disease. Alternative models, such as telerehabilitation; home-based models; and web-enabled pulmonary rehabilitation are reported to provide comparable outcomes to traditional centre-based pulmonary rehabilitation.^21–23

Offering a range of pulmonary rehabilitation models is aligned with contemporary principles of person-centred care in which treatment choices are informed by an individual’s characteristics, preferences, and the likelihood of personal success.⁷ With multiple effective models of pulmonary rehabilitation available, it is important to measure what patients perceive as a valuable change. The minimal clinically important difference (MCID) is defined as the “smallest difference in score in the domain of interest which patients perceive as beneficial”.²⁴ National COPD audit programs (UK) have reported on the number of people who achieve the MCID in exercise capacity, health-related quality of life and symptoms with pulmonary rehabilitation.¹⁶ Previous systematic reviews of clinical trials have only reported the absolute mean changes in these continuous outcome measures.^8–11 To our knowledge, no systematic review has attempted to collate all the available evidence on the number of patients achieving MCID in key outcomes with pulmonary rehabilitation, including head-to-head comparisons of different pulmonary rehabilitation models or comparisons to usual care. Although the incidence of adverse events has been reported in some systematic reviews, an up-to-date synthesis of studies in a wider range of settings and comparisons of novel program models is necessary. A full understanding of the benefits and safety of different models will help health professionals and patients make informed decisions on pulmonary rehabilitation.²⁵

The aims of this systematic review were to compare the proportion of people with chronic respiratory disease who achieve clinically significant changes in exercise capacity, health-related quality of life and symptoms with pulmonary rehabilitation versus usual care, and centre-based versus home-based pulmonary rehabilitation; and collate all the available evidence on the number and type of adverse events during pulmonary rehabilitation.

Methods

The protocol for this study was pre-specified (International Prospective Register of Systematic Reviews, PROSPERO: CRD42020185841).

Participants/population

Studies were included where more than 90% of adult participants had a diagnosis of bronchiectasis, COPD or ILD. Studies with participants who were stable and post-acute exacerbation (except where mechanically ventilated) were included.

Intervention

Eligible interventions were any centre-based or home-based rehabilitation program of at least 4 weeks’ duration that included exercise training (that was aerobically demanding) with or without any form of education and/or psychological support. Centre-based pulmonary rehabilitation was defined as any in-patient, out-patient, or community-based program. Home-based rehabilitation was defined as any program where the majority (>75%) of the program took place in the home or primary residential setting (nursing home/supported accommodation), including tele-rehabilitation.

Comparator

Eligible comparisons were pulmonary rehabilitation versus usual care, and centre-based versus home-based pulmonary rehabilitation. Usual care was defined as conventional care. This may have included verbal advice about physical activity, education, and self-management, but no supervised exercise or self-management training.

Outcomes

Primary outcomes were the proportion of patients achieving the MCID for exercise capacity (e.g. 6-min walk test (6MWT), incremental shuttle walk test (ISWT), endurance shuttle walk test (ESWT), cycle endurance test (CET), incremental cycle ergometry) and disease-specific health-related quality of life (e.g. chronic respiratory disease questionnaire (CRQ); St Georges Respiratory Questionnaire (SGRQ)).

Secondary outcome measures were symptom control (modified Medical Research Council dyspnoea scale (mMRC), COPD Assessment Test (CAT)) and adverse events categorised as mild or serious, and documented as the number of participants experiencing one or more event.

Studies were only included for exercise capacity, health-related quality of life and symptom control if they reported data according to the MCID of outcome measures.

Study design

Studies were eligible if they adopted a trial design with allocation of participants by individual or cluster randomisation, or via a quasi-randomised method.

Search strategy

Firstly, we searched for existing Cochrane systematic reviews of exercise training and/or pulmonary rehabilitation in Bronchiectasis, COPD or ILD in the Cochrane Database of Systematic Reviews that had evaluated eligible comparisons. The following bibliographic databases were searched from the last search date of the final Cochrane review to August 2023: MEDLINE, CINAHL, EMBASE, Cochrane Central Register of Controlled Trials (CENTRAL), Physiotherapy Evidence Database (PEDro). No limits were set on publication or language. Search strategies for all bibliographic databases are presented in Table S1-5. Search results were imported into Covidence (Veritas Health Innovation, Melbourne, Australia). Following removal of duplicate citations, titles and abstracts were screened independently by two reviewers. For studies that were not excluded based on title/abstract, full text papers were retrieved and independently assessed by two reviewers for eligibility. Any discrepancies in decisions of study eligibility were resolved through discussion.

Data extraction and quality appraisal

Data extraction was completed within Covidence using a form based on the Cochrane data extraction template for randomised controlled trials. Study characteristics were extracted in accordance with the pre-specified protocol. The number of participants achieving the MCID for exercise capacity, health-related quality of life and symptoms and total number per group were extracted from the studies and entered into Review Manager 5.4. Data on adverse events were compiled in Microsoft Excel. One reviewer undertook data extraction for each study, with the accuracy of this extraction cross-checked by a second reviewer.

Risk of bias (quality) assessment

Two reviewers independently assessed the risk of bias of included studies using the Cochrane Tool for Risk of Bias 1.0. The protocol was registered prior to publication of Risk of Bias 2.0. The domains evaluated were random sequence generation, allocation concealment, blinding of outcome assessment, incomplete outcome data, selective outcome reporting and other bias. Due to the nature of the intervention, blinding of participants and personnel to treatment allocation was not expected, and hence this was not considered during the assessments. Each of the domains were categorised as having high, low or unclear risk of bias, with the overall risk of bias for each study then determined as high (more than two ‘unclear’ or more than one ‘high’ risk domain), moderate (two ‘unclear’ or one ‘high’ risk domain), or low (no ‘unclear’ or ‘high’ risk domains). Any disagreements in risk of bias assessments were resolved through discussion.

Strategy for data synthesis

All meta-analyses were performed using Review Manager version 5.4. For exercise capacity, health-related quality of life and symptoms, the measure of effect was the number and proportion of people with chronic respiratory disease who achieved the MCID (relative risk). Where possible the following MCID thresholds were used: 30 m on 6MWD,²⁶ 36 m on ISWT,²⁷ between 174 and 279 s on ESWT,²⁸ 100 s on cycle endurance time,²⁹ 4 W on peak cycle exercise capacity,³⁰ 4 points on SGRQ,³¹ 0.5 points on CRQ,³² 1 grade on mMRC dyspnoea scale,³³ 2 points on CAT.³⁴ Analysis for each of the chronic respiratory diseases was considered separately. We contacted study authors to obtain any missing numerical outcome data or confirm data only reported in conference abstracts. Where studies were clinically homogeneous (in terms of population, intervention, and comparison), we combined individual study estimates in a meta-analysis. Studies including stable patients and those post exacerbation were included in the same analysis, as we were not aware of evidence indicating MCID achievement differed across these groups, however we considered this as a potential source of heterogeneity for exploration in subgroup analysis where indicated. We used random-effects models to incorporate between-study heterogeneity (i.e. assumption that the studies may have heterogeneous, but related, intervention effect estimates due to the clinical nature of the intervention). A single numerical estimate of effect (relative risk) of achieving the MCID in those who attended pulmonary rehabilitation versus those who did not, and in those attending centre versus home-based pulmonary rehabilitation were calculated. Adverse events were intended to be interpreted as the number of participants experiencing one or more event (relative risk) but there was limited homogenous data to consider meta-analysis. Statistical heterogeneity in all meta-analyses was interpreted by the I² value. In meta-analyses where I² was greater than 40%, potential sources of the statistical heterogeneity were explored. We used the five GRADE considerations (study limitations, consistency of effort, imprecision, indirectness and publication bias) to assess the quality of a body of evidence as it relates to studies that contributed data to the meta-analyses for primary outcomes. Summary of findings tables were produced using GRADEpro software to document the certainty of evidence assessments with all explanations to downgrade the evidence reported in footnotes.

Results

After duplicates were removed, searches identified 5465 records for screening, of which 5124 records were excluded based on title or abstract. Full texts were sought for the remaining 341 records of which 49 trials (55 reports) met the eligibility criteria (Figure 1). See supplementary appendix for full list of included studies (Table S6). Of the 49 included trials, 42 reported adverse event data and only 16 reported exercise capacity, health related quality of life or symptom control data according to MCID for meta-analyses.^{22,23,35–48}

Figure 1.

PRISMA flow diagram.

Characteristics of included studies

The 49 included trials were published between 2004 and 2023 (Tables 1 and 2), with a total of 4921 participants randomised. Of the included studies, 35 focused on COPD, 11 on ILD, 2 on bronchiectasis and 1 a mixed population including all three diseases. For the studies that recruited COPD participants only, 31 were during stable disease (mild to very severe) and 4 were following acute exacerbation. Study sample sizes varied between 12 and 375 participants.

Table 1.

Characteristics of studies comparing pulmonary rehabilitation to usual care.

Author	Participants		Exercise training component				Additional
Author	n	Diagnosis	Frequencydays/week	Intensity	Time session; total	Type	Additional
Centre-based pulmonary rehabilitation versus usual care
Baumann 2012	100	COPD	1	Borg 4-6	20-60 min; 8-18 weeks	Endurance/resistance	Br, Bc, Ed, Ps, R
Bernocchi 2016	112	COPD	3-7	Moderate- high Borg	45-105 min	Endurance/resistance	Am, Ed, Ts
Casaburi 2014	53	COPD	3	60%–80% of 1RM	3-4 sets of 5 exercises; 10 weeks	Resistance	Ed
Casey 2013	350	COPD	2	Borg 4	60 min; 8 weeks	Endurance/resistance	Am, Br, Ed, Sm, Ts
Dale 2014	35	ILD	3	80% 6MWT; 60% peak workload	≥30 min; 8 weeks	Endurance/resistance	None
Deepak 2014	60	AECOPD	Not specified	Not specified	120 min; 12 weeks	Endurance/resistance	Ac, Br, Ed, Ps, Sm
Dowman 2017	142	ILD	2	70%–80% peak workload; Borg RPE 12-14	≥30 min; 8 weeks	Endurance/resistance	Ed, Ox, Sm
Eaton 2009	97	AECOPD	2-7	Not specified	60 min; 8 weeks	Endurance/resistance	Ed, Ox, Sm
Faulkner 2010	20	COPD	1	Not specified	Not specified; 8 weeks	Endurance/resistance	Am, Ed, Sm
Gottlieb 2011	61	COPD	2	Bore RPE 16-17	7-31 weeks	Endurance/resistance	Ed, Br, Bc, Ns, Sc
Hoff 2007	12	COPD	3	85%–90% 1RM	8 weeks	Resistance	None
Holland 2008	57	ILD	2	80% of 6MWT speed	≥30 min; 8 weeks	Endurance/resistance	Ox
Kataoka 2023	88	ILD	2	80% peak workload; 80% of 6MWT speed	≥30 min; 12 weeks	Endurance/resistance	None
Ku 2017	40	ILD	2	Not specified	120 min; 8 weeks	Endurance/resistance	Am, Br, Ed, Ox
Lee 2022	17	COPD	5	40%–60% peak VO2; 60%–80% 1RM	60 min; 8 weeks	Endurance/resistance	None
Maglakelidze 2022	60	COPD	2	65%–85% of their maximal ISWT	90 min; 8 weeks	Endurance/resistance	Ed, Sm
Majewska-Pulsakowska 2016	43	COPD	3	Not specified	23-45 min; 8 weeks	Endurance	None
Man 2004	42	AECOPD	2	Not specified	60 min; 8 weeks	Endurance/Resistance	Ed, Sm
Naz 2018	18	ILD	2	Borg 4-6	Not specified; 12 weeks	Endurance/resistance	Am, Br, Ox
Nyberg 2014	44	COPD	3	Borg ≥4-	60 min; 8 weeks	Resistance	Ed
O’Shea 2007	54	COPD	1	Not specified	12 weeks	Resistance	None
Perez-Bogerd 2018	60	ILD	2-3	60%–75% peak workload	24 weeks	Endurance/resistance	Bc, Ed, Ot, Ps
Vainshelboim 2014	34	ILD	3	Borg 3-5	60 min; 12 weeks	Endurance/resistance	Br, Ox, Sm
Vasilopoulou 2017	150	COPD	3	100% peak workload	45 min (intervals); 8 weeks	Endurance/resistance	Br, Ed, Sm
Wallaert 2020	38	ILD	3	Not specified	≥30 min; 8 weeks	Endurance/resistance	Ed, Sm, Ps
Wootton 2014	143	COPD	3	80% of 6MWT speed; Borg 3-4	30-45 min; 8 weeks	Endurance	None
Home-based pulmonary rehabilitation versus usual care
Benzo 2016	215	COPD	7	Not specified	20 min; not specified	Endurance/resistance	Br, Sm, Ts
Benzo 2021	154	COPD	6	Not specified	20 min; 8 weeks	Endurance	Am, Sm Tm, Ts
Benzo 2022	375	COPD	6	Not specified	12 weeks	Endurance	Am, Sm, Tm, Ts, R
Bourne 2022	193	COPD	Not specified	Not specified	Not specified; 5 months	Endurance/resistance	Am, Ed, Sm
Cedeño de Jesús 2022	34	Bronchiectasis	3-5	Borg ≥4-	≥20 min; 8 weeks	Endurance/resistance	Ac, Ed, Sm, Ts
Cerdan-de-las-Heras 2021	29	ILD	3-5	Not specified	10-20 min; 12 weeks	Endurance/resistance	Ed, Sm, Tm
Cerdan-de-las-Heras 2022	30	ILD	3-5	Not specified	10-20 min; 12 weeks	Endurance/resistance	Ed, Sm, Tm
Chen 2018	55	COPD	3	Not specified	20-30 min; 12 weeks	Resistance	Ed, Ps, Sm
Johnson-Warrington 2016	78	AECOPD	7	Not specified	Not specified	Endurance/resistance	Ed, Sm, Ts
Jose 2021	63	Bronchiectasis	3	60%–80% MIST cadence; 70% peak isometric force	50 min; 8 weeks	Endurance/resistance	Am, Ed, Ts
Lahham 2020	58	COPD	5	80% 6MWT speed	≥30 min; 8 weeks	Endurance/resistance	Am, Ed, Sm, Ts
Mitchell 2014	184	COPD	7	Not specified	Not specified; 6 weeks	Endurance/resistance	Am, Ed Sm, Ts
Tsai 2017	37	COPD	3	Borg 3-4	≥20 min; 8 weeks	Endurance/resistance	Ed
Zanaboni 2023	120	COPD	3-5	80% 6MWT speed; Borg 4-6	≥30 min; 2 years	Endurance/resistance	Am, Ed, Sm, Tm

Ac: airway clearance; Am: activity monitoring; Bc: behavioural counselling; Br: breathing techniques; Ed: education; Ns: Nutritional support; Ot: occupational therapy; Ox: oxygen supplementation; Ps: Psychosocial support; R: Relaxation techniques; Sc: smoking cessation; Sm: self-management training; Ts: telephone support; Tm: telemonitoring.

Table 2.

Characteristics of studies comparing home-based pulmonary rehabilitation to centre-based pulmonary rehabilitation.

Author	Population		Home-based (exercise training and additional components)						Centre-based (exercise training and additional components)
Author	N	Diagnosis	Frequencydays/week	Intensity		Timesession; total	Type	Additional components	Frequencydays/week	Intensity	TimeSession; total	Type	Additional components
Bourne 2017	90	COPD	2-5		Not specified	12-42 min; 6 weeks	Endurance/resistance	Ed, Sm	2	Not specified	12-42 min; 6 weeks	Endurance/resistance	Ed, Sm
Cerdan-de-las-Heras 2022	54	COPD	3-5		Not specified	10-20 min; 8 weeks	Endurance/resistance	Ed, Tm	2	Not specified	60 min; 8 weeks	Not specified	Ed
Cox 2022	142	Mixed	2		Borg 3-4	30 min; 8 weeks	Endurance/resistance	Am, Ed, Sm	2	Borg 3-4	30 min; 8 weeks	Endurance/resistance	Am, Ed, Sm
Ercin 2020	55	COPD	3		Not specified	Not specified; 8 weeks	Endurance	Br, Ed, Sm	7	50%–70% peak workload	30 min; 8 weeks	Endurance	Br, Ed
Hansen 2020/2023	134	COPD	3		Not specified	30 min; 8 weeks	Endurance/resistance	Ed, Sm	2	Borg 4-7; 40%–80% 1RM	40-60 min; 10-12 weeks	Endurance/resistance	Ed, Sm
Holland 2017	166	COPD	5		80% of 6MWT speed	30 min; 8 weeks	Endurance/resistance	Am, Ed, Sm, Ts	2	80% of 6MWT speed	≥30 min; 8 weeks	Endurance/resistance	Ed, Sm
Horton 2018	287	COPD	7		85% of predicted peak oxygen uptake	30 min; 7 weeks	Endurance/resistance	Am, Ed, Sm, Ts	3	85% of predicted peak oxygen uptake	≥30 min; 7 weeks	Endurance/resistance	Am, Ed, Sm
Maltais 2008	252	COPD	3		60% of peak workload	70 min; 8 weeks	Endurance/resistance	Ed, Sm	3	80% of peak workload	55-60 min; 8 weeks	Endurance/resistance	Ed, Sm
Widyastuti 2018	40	COPD	7		Fastest step pace possible	30 min; 6 weeks	Endurance	Am	3	80% of 6MWT speed	30 min; 6 weeks	Endurance	Am

Am: activity monitoring; Br: breathing techniques; Ed: education; Sm: self-management training. Tm: telemonitoring. Ts: telephone support.

All trials, except one cluster randomised trial,⁴⁹ comprised of allocation at an individual level. Included comparisons were centre-based pulmonary rehabilitation versus usual care (n = 26 studies), home-based pulmonary rehabilitation versus usual care (n = 14), or home-based pulmonary rehabilitation versus centre-based pulmonary rehabilitation (n = 9). Exercise sessions varied in frequency, from once weekly to daily exercise. Desired exercise intensity was not reported in all studies, but where reported varied between moderate and high intensity (Table 1). The most common duration of rehabilitation programs was 8 weeks (range 6 weeks to 2 years). Duration of exercise sessions varied from 10 to 120 min. The exercise modality in studies included endurance training only (n = 7) resistance training only (n = 6) or both (n = 36). For the studies comparing centre versus home rehabilitation, the exercise component of home programs were reported to be bi-weekly supervised sessions at home (n = 1), one or two supervised face-to-face introductory or supervised sessions and unsupervised thereafter with or without telephone follow-up (n = 5), a home visit followed by remote supervision via videoconferencing (n = 1) or entirely unsupervised with use of written or online resources and/or telephone calls (Table 2). The components delivered alongside exercise training for centre or home-based rehabilitation are reported in Table 2. The usual care group of eligible comparisons received advice, counselling or instructions on physical activity, education, airway clearance, breathing techniques and/or structured phone call follow-up.

The primary outcome measures most reported according to MCID were 6MWD and CRQ. All included studies used and MID of 0.5 points on the CRQ^{22,23,36,39,42–45} however, the MCID thresholds for the 6MWD varied across studies including 54 m³⁸, 25 m,^37,47 26 m⁴¹, 30 m^{22,23,44,46,48,} and 29-34 m³⁹. Thirty-seven of the included trials reported safety data. These studies covered the entire range of eligible study populations and comparisons, but the unit of classification (combined study population, at group level, for rehabilitation groups only) and type of event (serious adverse events only, any adverse events) varied in the reported data.

Risk of bias

Risk of bias assessments of studies included in the meta-analyses are presented alongside forest plots (Figures 2–4, S1-S4). The domains most assessed as unclear or high risk were allocation concealment and blinding of outcome assessment.

Figure 2.

Meta-analysis of the number of participants to achieve MCID in 6MWT following A) pulmonary rehabilitation vs usual care in COPD; B) pulmonary rehabilitation vs usual care in ILD; or C) home-based pulmonary rehabilitation vs centre-based pulmonary rehabilitation. Events = number of participants in group to achieve MCID; Totals = total number of participants in group.

Figure 3.

Meta-analysis of the number of participants to achieve MCID following pulmonary rehabilitation vs usual care in COPD in A) CRQ-Dyspnea B) CRQ-Fatigue C) CRQ-emotional function; or D) CRQ-Mastery. Events = number of participants in group to achieve MCID; Totals = total number of participants in group.

Figure 4.

Meta-analysis of the number of participants to achieve MCID following home-based pulmonary rehabilitation vs centre-based pulmonary rehabilitation in A) CRQ-Dyspnoea B) CRQ-Fatigue C) CRQ-Emotional Function; or D) CRQ-Mastery. Events = number of participants in group to achieve MCID; Totals = total number of participants in group.

Data synthesis

Primary outcomes

One trial³⁵ did not have MCID data available (CRQ domains) in a format that could be combined with other study level estimates, resulting in 15 trials with data on the number of participants achieving MCID in clinical outcomes for comparisons of pulmonary rehabilitation versus usual care or centre-based pulmonary rehabilitation versus home-based pulmonary rehabilitation. All study level data of primary outcomes including full range of reported proportions of people achieving MCIDs with centre-based rehabilitation, home-based rehabilitation and usual care are presented in Table 3, with meta-analyses undertaken according to type of chronic respiratory disease and comparison.

Table 3.

Percentage of participants achieving minimal clinical important differences in exercise capacity and health-related quality of life.

Pulmonary rehabilitation (PR) vs. usual care (UC)
Study	6MWD		ISWT		ESWT		CRQ-D		CRQ-F		CRQ-E		CRQ-M		SGRQ
Study	PR	UC	PR	UC	PR	UC	PR	UC	PR	UC	PR	UC	PR	UC	PR	UC
Benzo 2022							30	18	38	18	33	16	44	27
Cedeno de Jesus 2022	75	47
Deepak 2014	32	0													82	4
Dowman 2017	33	15					42	30	59	23	45	38	57	33
Gottlieb 2011															23	35
Johnson-Warrington 2016			50	41	50	47	63	37	92	57	63	57	73	73
Lahham 2020	43	38					44	42	44	42	32	23	56	54
Mitchell 2014			20	10	35	17	63	45	47	33	32	25	35	29
Perez-Bogerd 2018	37	15
Vasilopoulou 2017	57	4

Study	6MWD		ISWT		ESWT		CRQ-D		CRQ-F		CRQ-E		CRQ-M		SGRQ
Study	CBPR	HBPR	CBPR	HBPR	CBPR	HBPR	CBPR	HBPR	CBPR	HBPR	CBPR	HBPR	CBPR	HBPR	CBPR	HBPR
Centre-based pulmonary rehabilitation (CBPR) vs. home-based pulmonary rehabilitation (HBPR)
Cox 2022	41	41					59	57	55	50	41	41	52	35
Hansen 2020/2023	42	34
Holland 2017	37	46					56	60	55	54	42	44	54	56
Horton 2018							59	54
Widyastuti 2018	72	44

6MWD: six-minute walk distance, ISWT: incremental shuttle walk test, ESWT: endurance shuttle walk test, CRQ-D: chronic respiratory questionnaire-dyspnoea; CRQ-F: chronic respiratory questionnaire-fatigue; CRQ-E: chronic respiratory questionnaire-emotional function; CRQ-M: chronic respiratory questionnaire-mastery; SGRQ: St georges respiratory questionnaire.

Exercise capacity

Pulmonary rehabilitation versus usual care

6MWD

Six trials reported the proportion of participants achieving the MCID for 6MWD.^{37–39,44,46,47} In COPD, a higher proportion of participants achieved the MCID for 6MWD with pulmonary rehabilitation (50%) compared to usual care (10%), but this was not statistically significant (risk ratio (RR) = 5.51, 95% confidence intervals (95% CI) 0.69 to 44.06 (3 studies, 247 participants) (Figure 2(A)). There was evidence of substantial heterogeneity (I² = 84%; p = 0.002). Stratified analysis according to severity of COPD (Figure 2(A)), revealed a greater number of participants achieving the MCID with pulmonary rehabilitation (vs usual care) in trials including moderate-severe COPD (57% vs 5%) (14.18, 3.61 to 55.73) or following AECOPD (32% vs 0%) (19.00, 1.16 to 311.46) but not mild COPD (43% vs 38%) (1.14, 0.56 to 2.34). Certainty of evidence in COPD was low due to risk of bias and imprecision (Table S8). In ILD^39,46 a greater number of pulmonary rehabilitation participants achieved the MCID compared to usual care (34% vs 15%) (2.24, 1.29 to 3.90, 2 studies, 192 participants, I² = 0%) (Figure 2(B)). Certainty of evidence was moderate (Table S9). A single trial in bronchiectasis³⁷ favoured an effect of home-based pulmonary rehabilitation compared to usual care (75% vs 47%) but this was not statistically significant (1.61, 0.87 to 2.96, 1 trial, 31 participants). Certainty of evidence in bronchiectasis was downgraded to very low due to risk of bias, indirectness and imprecision (Table S10).

ISWT

Meta-analysis of two COPD trials^43,45 revealed a greater number of pulmonary rehabilitation participants achieving the MCID compared to usual care (26% vs 16%), but this effect was not statistically significant (1.50, 0.92 to 2.45, I² = 0%, Figure S1). Certainty of evidence was low due to indirectness and imprecision (Table S8).

ESWT

Meta-analysis of two COPD trials^43,45 also favoured a greater number of rehabilitation participants achieving the MCID compared to usual care (37% vs 22%), but this effect was not statistically significant and there was substantial heterogeneity (1.53, 0.80 to 2.91, I² = 56%, Figure S2). Certainty of evidence was downgraded to very low due to inconsistency, indirectness and imprecision (Table S8).

Centre-based pulmonary rehabilitation vs home-based pulmonary rehabilitation

Four trials^22,23,41,48 reported the proportion of participants achieving the MCID for 6MWD. There was no statistically significant difference in the number of participants achieving MCID for those who completed centre-based programs (43%) and those who completed home-based programs (41%) (0.93, 0.71 to 1.22, I² = 28%, 4 trials, 410 participants) (Figure 2(C)). Certainty of evidence was low due to risk of bias and imprecision (Table S11).

Health-related quality of life

Pulmonary rehabilitation versus usual care

CRQ-dyspnoea

Five trials reported the proportion of participants achieving the MCID for CRQ-Dyspnoea score.^{36,39,43–45} In COPD,^36,43–45 a greater number of participants achieved the MCID with pulmonary rehabilitation compared to usual care (43% vs 29%), which was statistically significant with no apparent heterogeneity (1,46, 1.20 to 1.78, 4 trials, 670 participants) (Figure 3(A)). Certainty of evidence was moderate (Table S8). One trial in ILD³⁹ had a similar estimate of effect for number of participants achieving the MCID with pulmonary rehabilitation compared to usual care (42% vs 30%), but this trial alone was not statistically significant (1,42, 0.89 to 2.26, 1 trial, 133 participants). Certainty of evidence was low due to indirectness and imprecision (Table S9).

CRQ-fatigue

Five trials reported the proportion of participants achieving the MCID for CRQ-Fatigue score.^{36,39,43–45} In COPD ^36,43–45 a greater number of participants achieved the MCID with pulmonary rehabilitation compared to usual care (45% vs 27%), which was statistically significant with no apparent heterogeneity (1.61, 1.26 to 2.08, I² = 37%, 4 trials, 665 participants) (Figure 3(B)). Certainty of evidence was moderate (Table S8). One trial in ILD³⁹ had a larger estimate of effect than the COPD trials for the number of participants achieving the MCID with pulmonary rehabilitation compared to usual care (59% vs 23%), with this trial alone also being statistically significant (2.53, 1.56 to 4.12, 1 trial, 128 participants). Certainty of evidence was moderate (Table S9).

CRQ-emotional function

Five trials reported the proportion of participants achieving the MCID for CRQ-Emotional Function score.^{36,39,43–45} In COPD,^36,43–45 a greater number of participants achieved the MCID with pulmonary rehabilitation compared to usual care (35% vs 23%), which was statistically significant with no apparent heterogeneity (1.45, 1.06 to 1.98, I² = 39%, 4 trials, 670 participants) (Figure 3(C)). Certainty of evidence was moderate (Table S8). One trial in ILD³⁹ had a similar estimate of effect for number of participants achieving the MCID with pulmonary rehabilitation compared to usual care (45% vs 38%), but this trial alone was not statistically significant (1.20, 0.79 to 1.81, 1 trial, 128 participants). Certainty of evidence was low due to indirectness and imprecision (Table S9).

CRQ-mastery

Five trials reported the proportion of participants achieving the MCID for CRQ-Mastery score.^{36,39,43–45} In COPD ^36,43–45 a greater number of pulmonary rehabilitation participants achieved the MCID compared to usual care (45% vs 34%) but this effect was not statistically significant and there was evidence of moderate heterogeneity (1.22, 0.94 to 1.57, I² = 49%, 4 trials, 670 participants) (Figure 3(D)). Certainty of evidence was very low due to inconsistency, indirectness and imprecision (Table S8). One trial in ILD³⁹ showed a greater number of participants achieving the MCID with pulmonary rehabilitation compared to usual care (57% vs 33%), which was statistically significant (1.70, 1.13 to 2.54, 1 trial, 128 participants). Certainty of evidence was moderate (Table S9).

SGRQ-total

Two trials^38,40 reported the proportion of participants achieving the MCID for SGRQ for those that completed pulmonary rehabilitation (82% and 23%) and those in usual care (4% and 35%). One trial included participants following AECOPD and another included stable, moderate COPD. The contrasting estimates of effect in these trials meant that meta-analysis was deemed inappropriate.

Centre-based pulmonary rehabilitation versus home-based pulmonary rehabilitation

CRQ-dyspnoea

Three trials reported the proportion of participants who achieved the MCID in CRQ-Dyspnoea score.^22,23,42 There was no statistically significant difference in the number of participants achieving MCID for those that completed centre-based programs (58%) and those that completed home-based programs (57%) (0.99, 0.84 to 1.16, I² = 0%, 3 trials, 447 participants) (Figure 4(A)). Certainty of evidence was moderate (Table S11).

CRQ-fatigue

Two trials reported the proportion of participants who achieved the MCID in CRQ-Fatigue score.^22,23 There was no statistically significant difference in the number of participants achieving MCID for those that completed centre-based programs (55% and 55%) and those that completed home-based programs (50% and 54%) (0.95, 0.77 to 1.18, I² = 0%, 2 trials, 284 participants) (Figure 4(B)). Certainty of evidence was low due to indirectness and imprecision (Table S11).

CRQ-emotional function

Two trials reported the proportion of participants who achieved the MCID in CRQ-Emotional Function score^22,23 There was no statistically significant difference in the number of participants achieving MCID for those that completed centre-based programs (41% and 42%) and those that completed home-based programs (41% and 44%) (1.07, 0.82 to 1.41, I² = 0%, 2 trials, 280 participants) (Figure 4(C)). Certainty of evidence was low due to indirectness and imprecision (Table S11).

CRQ-mastery

Two trials reported the proportion of participants who achieved the MCID in CRQ-Mastery.^22,23 There was no statistically significant difference in the number of participants achieving MCID for those that completed centre-based programs (52% and 54%) and those that completed home-based programs (35% and 56%) (0.87, 0.57 to 1.31, I² = 65%, 2 trials, 283 participants), however there was evidence of a substantial heterogeneity with one trial favouring an effect of centre-based pulmonary rehabilitation (Figure 4(D)). Certainty of evidence was downgraded to very low due to inconsistency, indirectness and imprecision (Table S11).

Secondary outcomes

Symptom control

Pulmonary rehabilitation versus usual care

No trials comparing pulmonary rehabilitation to usual care reported symptom data according to achievement of MCID.

Centre-based pulmonary rehabilitation versus home-based pulmonary rehabilitation

mMRC

Two trials reported the proportion of participants who achieved the MCID for mMRC.^22,48 There was no statistically significant difference in the number of participants achieving MCID for those that completed centre-based programs (9% and 61%) and those that completed home-based programs (10% and 28%) (0.67, 0.28 to 1.61, I² = 43%, 2 trials, 171 participants) (Figure S4). The estimate of effect did favour centre-based pulmonary rehabilitation but there was moderate heterogeneity between the two trials.

CAT

Two trials reported the proportion of participants who achieved the MCID for CAT.^41,48 There was no statistically significant difference in the number of participants achieving MCID for those that completed centre-based programs (27% and 83%) and those that completed home-based programs (36% and 72%) (1.01, 0.69 to 1.48, I² = 35%, 2 trials, 157 participants) (Figure S5).

Adverse events

Of the 42 trials that reported safety data, 38 (90%) reported zero adverse events or serious adverse events related to pulmonary rehabilitation (Table S7).

Pulmonary rehabilitation vs. usual care

Two trials^49,50 reported mild events related to exercise testing and 2 trials^51,52 reported mild temporary events during delivery of rehabilitation (Table S7).

Centre-based pulmonary rehabilitation versus home-based pulmonary rehabilitation

Two trials^21,53 reported mild events, with 1 trial²¹ reporting such events in both groups whilst the other trial⁴⁴ only observing events in the centre-based rehabilitation group.

Discussion

Pulmonary rehabilitation is a fundamental treatment with well-accepted improvements in important outcomes for people with chronic respiratory diseases that remains underused.^7–11 In an era of personalised medicine and the emergence of choice in newer pulmonary rehabilitation models, it is a high priority to identify who is most likely to achieve success in different models.^7,20

This systematic review included 49 trials conducted in 4921 people with stable COPD, AECOPD, ILD or bronchiectasis. To the best of our knowledge, this is the first review to provide single numerical estimates of effect of the number of people to achieve MCID in functional capacity, quality of life or respiratory symptoms with pulmonary rehabilitation compared to usual care and demonstrate that current estimates suggest achievement of MCID is similar between centre and home-based pulmonary rehabilitation models. However, the proportion of participants who achieved the MCIDs was broad (32% to 75% for exercise capacity, 23% to 92% for health-related quality of life). Adverse events are uncommon in pulmonary rehabilitation trials and when they do occur are mild and temporary.

The findings of this review provide evidence for informed decisions in clinical practice during referral and enrolment to pulmonary rehabilitation by identifying the proportion of people who will achieve a meaningful change in outcomes. This concept may be easier to consider and provides a more personalised understanding of the benefits of pulmonary rehabilitation. Shared decision-making interventions that can utilise such evidence in chronic respiratory disease are limited but have demonstrated potential in improving health-related outcomes,⁵⁴ and development of these interventions for pulmonary rehabilitation is progressing.^55–57

National clinical audits of pulmonary rehabilitation services in the UK have previously reported ∼60% of people with stable COPD achieve improvements in functional capacity,^16,58–60 quality of life and symptoms that meet the MCID. Such estimates have become benchmarks against which individual health services can compare their outcomes to.⁶⁰ This review determined a similar number of people with stable COPD (∼50%–60%) achieve MCID in outcomes, but only for functional capacity, dyspnoea, and fatigue. For functional capacity outcomes in our analyses of pulmonary rehabilitation versus usual care we did not find statistically significant between-group differences. This differs from previous analyses ^8–11 and likely reflects the loss of statistical power when using a dichotomous outcome, as well as heterogeneity across trials. This limitation did not affect analyses of dyspnoea and fatigue, where heterogeneity was lower. This evidence was judged to be of low-to-moderate certainty in COPD, as was the evidence for these outcomes when estimating the effect of pulmonary rehabilitation in ILD and when comparing centre-based to home-based pulmonary rehabilitation. The evidence was very uncertain, however, on the effect of pulmonary rehabilitation on the number of people achieving a MCID in disease mastery and ESWT in COPD, or 6MWT in bronchiectasis.

Our data demonstrate that in the context of randomised controlled trials, some improvement can be seen with usual care alone. This may be attributed to behaviour changes associated with clinical trial participation for which patient reported outcomes are particularly susceptible. For functional capacity, it is possible that performing a baseline exercise test may influence exercise behaviour and thereby confound control outcome data.⁶¹ All trials in this review included a practice exercise test at baseline except one ^53. It is worthy to note that MCID data reporting in randomised trials is substantially lower than the total number of trials reported in previous reviews. The amount of trial data available in emerging areas in stable COPD (e.g. home-based vs centre-based pulmonary rehabilitation) was comparable to the evidence base of more established areas (e.g. pulmonary rehabilitation vs usual care). Given the timespan of the evidence synthesised, the MCID thresholds varied across the trials, and future updates of the evidence could consider other approaches such as individual patient meta-analysis whereby original data are sought directly from the researchers responsible for the randomised controlled trials. However, the fact that many of trials were published more than 10 years ago may make this difficult. Future trials can add new evidence by reporting clinical outcomes according to the number of participants achieving the MCID in addition to mean measures of effect for both established and newer outcomes measures such as the mMRC and CAT tool. This recommendation will improve the certainty of evidence in achieving MCID and is also supported by a recent multistakeholder consensus process that identified exercise capacity, health-related quality of life and symptoms within a core outcome set to increase consistency among clinical trials of pulmonary rehabilitation and help to benchmark service delivery.⁶² The estimates of effect presented in this review and their 95% confidence intervals can help inform sample size calculations for future trials. The relatively low proportion of participants who achieved the MCID for 6MWT (50%) suggests that optimisation of exercise training strategies is required, and should be addressed by future research.

Pulmonary rehabilitation is considered a safe treatment for chronic respiratory disease, however previous reviews have infrequently collated data on adverse events⁸ or were not able to identify trials that reported adverse event data.¹¹ The variation in the level of reporting safety data restricted any formal statistical analysis in this review, however the available data indicates that adverse events are uncommon and temporary across rehabilitation models and disease categories. It is recommended that future trials measure and report on all adverse events (intervention related or not) at an individual group level so the likelihood of any harms in conventional or emerging models of pulmonary rehabilitation are accurate. Like previous systematic reviews of pulmonary rehabilitation,^8–11 allocation concealment and blinding of outcome assessment were the common domains at high risk of bias. Ensuring the highest quality of trial conduct and reporting in all other domains is paramount irrespective of the pulmonary rehabilitation model being investigated.

We note the following limitations. Our data synthesis on achievement of MCID in clinical outcomes was largely based on trials in stable COPD, which limits generalising the estimates of effect to other contexts, particularly in the comparison of centre and home-based pulmonary rehabilitation where there were no trials focused on people with a primary diagnosis of ILD or bronchiectasis or an acute exacerbation setting. We did not include trials where the majority of participants had a diagnosis of asthma due to weak recommendations in international guidelines ⁶³ and limited implementation in clinical practice. Specific thresholds for MCIDs of some outcomes varied between studies and the exact MCID are likely to evolve over time. Hence, we would recommend use of both absolute number of participants and relative differences between comparison groups when interpreting the number of people achieving MCIDs. Not all included trials met the definition of pulmonary rehabilitation, however all trials included in our analysis incorporated the core components in their intervention protocols, except two that involved endurance training only. ^36,48 It should be acknowledged that 40% and 60% of the trials included in the comparison of pulmonary rehabilitation versus usual care and centre and home-based pulmonary rehabilitation respectively involved members of the review team. However, no authors were involved in data extraction or risk of bias assessment on their own trials. We did not search bibliographic databases from inception and instead first collated the evidence from the most recent Cochrane reviews of pulmonary rehabilitation or exercise training within the Cochrane database of systematic reviews and updated searches from the last search date of these reviews. We are confident our approach did not miss out any available evidence given that these reviews followed best-practice methodology and we were able to verify both the included and excluded trials from these reviews. Our protocol was registered before the availability of Cochrane’s Risk of Bias 2.0 tool, hence the risk of bias judgements were not focused on a specific result from the included studies.

Conclusion

The available evidence suggests that centre-based and home-based pulmonary rehabilitation models are safe and lead to comparable number of people with chronic respiratory disease achieving clinically meaningful changes in important outcomes. Future trials, which are likely to be head-to-head comparisons of different pulmonary rehabilitation models, should look to report outcomes according to minimal clinically important thresholds so that treatment decisions on pulmonary rehabilitation can be fully informed and personalised across all chronic respiratory diseases.

Supplemental Material

Supplemental Material - Clinically important changes and adverse events with centre-based or home-based pulmonary rehabilitation in chronic respiratory disease: A systematic review and meta-analysis

Supplemental Material for Clinically important changes and adverse events with centre-based or home-based pulmonary rehabilitation in chronic respiratory disease: A systematic review and meta-analysis by Janet Bondarenko, Simone Dal Corso, Michael P Dillon, Sally Singh, Belinda R Miller, Caroline Kein, Anne E Holland and Arwel W Jones in Chronic Respiratory Disease.

Footnotes

Declaration of conflicting interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iDs

Janet Bondarenko

Arwel W Jones

Data availability statement

All study data used for analyses are visible in tables and figures. Template Cochrane data extraction form is available at .

Supplemental Material

Supplemental material for this article is available online.

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