Outpatient vs. home-based pulmonary rehabilitation in COPD: a randomized controlled trial
verfasst von:
Júlio C. Mendes de Oliveira, Fernando S. Studart Leitão Filho, Luciana M. Malosa Sampaio, Ana C. Negrinho de Oliveira, Raquel Pastrello Hirata, Dirceu Costa, Claudio F. Donner, Luís V. F. de Oliveira
Chronic obstructive pulmonary disease (COPD) is a common cause of morbidity and mortality affecting a large number of individuals in both developed and developing countries and it represents a significant financial burden for patients, families and society. Pulmonary rehabilitation (PR) is a multidisciplinary program that integrates components of exercise training, education, nutritional support, psychological support and self-care, resulting in an improvement in dyspnea, fatigue and quality of life. Despite its proven effectiveness and the strong scientific recommendations for its routine use in the care of COPD, PR is generally underutilized and strategies for increasing access to PR are needed. Home-based self-monitored pulmonary rehabilitation is an alternative to outpatient rehabilitation. In the present study, patients with mild, moderate and severe COPD submitted to either an outpatient or at-home PR program for 12 weeks were analyzed.
Methods
Patients who fulfilled the inclusion criteria were randomized into three distinct groups: an outpatient group who performed all activities at the clinic, a home-based group who performed the activities at home and a control group. PR consisted of a combination of aerobic exercises and strengthening of upper and lower limbs 3 times a week for 12 weeks.
Results
There was a significant difference in the distance covered on the six-minute walk test (p < 0.05) and BODE index (p < 0.001) in the outpatient and at-home groups after participating in the rehabilitation program compared to baseline.
Conclusion
A home-based self-monitoring pulmonary rehabilitation program is as effective as outpatient pulmonary rehabilitation and is a valid alternative for the management of patients with COPD.
Introduction
Chronic obstructive pulmonary disease (COPD) is a common cause of illness and death that affects a large and increasing number of individuals in both developed and developing countries. Estimates suggest that COPD will become the 3rd most common cause of death in the world and 5th most common cause of illness in the next 20 years [1, 2].
Pulmonary rehabilitation (PR) is a multidisciplinary intervention that integrates physical exercise, nutritional therapy, patient education and psychological support [3‐7]. Evidence indicates that PR offers numerous clinical benefits, such as improved health-related quality of life, a reduction in anxiety and depression, increased tolerance to physical exercise and a reduction in the number of hospitalizations and days of hospital stay per year [3, 4]. However, despite the strong scientific recommendations for its routine use in the treatment of COPD, PR is generally underutilized [5‐7]. A survey carried out in 2005 in Canada demonstrated that only 1-2% of the Canadian population with COPD has access to rehabilitation programs [8]. Similar statistics are reported for other countries [7, 9].
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A search of the scientific literature revealed few controlled studies that demonstrate the benefits of self-monitored pulmonary rehabilitation programs for patients with COPD. The majority of these studies demonstrate the effectiveness of home-based PR, with similar results to those obtained in a clinical setting involving the direct supervision of physiotherapists [8‐11]. The aim of the present study was to carry out a comparative analysis of patients with COPD submitted to PR in a clinical setting and at home.
Methods
Study design
A randomized controlled prospective study with a consecutive sample was carried out. The study received approval from the Ethics Committee of the Nove de Julho University (Brazil) under protocol number 306654/2008. All participants gave their informed consent agreeing to participate in the study and were permitted to abandon the study at any time with no negative consequences.
The initial sample was made up of 216 patients who sought treatment at a private pulmonology clinic in the city of Cascavel (southern Brazil). The patients were randomized electronically by a computer into three groups as follows: outpatient rehabilitation, at-home rehabilitation and a control group. The primary outcome was the difference in distance walked on the six-minute walk test (6MWT). The secondary outcome was the variation in the BODE index.
Patients
The following were the inclusion criteria: COPD based on the GOLD classification [1]; clinical stability in the eight weeks prior to the study (no reports of worsening of dyspnea, increased phlegm production or phlegm purulence). The exclusion criteria were: hospitalization; COPD instability; presence of neuromuscular disease, associated respiratory disease, orthopedic or neurological disease that affected gait; recent impairment due to comorbidities, such as myocardial infarction, heart failure, stroke or neoplasm; prior pneumonectomy or other thoracic surgery. The presence of stable comorbidities was not considered an exclusion criterion as most patients with COPD are elderly and commonly affected by multiple comorbidities [12]. All patients who sought care at the clinic and fulfilled these criteria were considered eligible for the study.
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Measurements
All patients underwent a physical and spirometric evaluation [13], determination of weight and height for the calculation of the body mass index (BMI), assessment with the modified Medical Research Council (MMRC) scale [14] and the 6MWT, based on the recommendations of the American Thoracic Society [15]. The BODE index was determined at this time using the variables identified in this baseline evaluation, as previously described [16]. The BODE index is a multidimensional 10-point scale based on four variables: FEV1 (as percent predicted), distance walked in 6 minutes (expressed in meters), MMRC dyspnea scale, and the body-mass index, in which higher scores indicate a higher risk of death (see Table 1). Two duly trained health care professionals were responsible for the evaluations, which were performed by the same evaluators for all patients.
Table 1
Parameters and scoring system of the bodymass, airflow obstruction, dyspnea and exercise capacity (BODE) index*
Variable
Points on BODE Index
0
1
2
3
FEV1 (% of predicted)†
≥ 65
50-64
36-49
≤ 35
Distance walked in 6 min (m)
≥ 350
250-349
150-249
≤ 149
MMRC dyspnea scale‡
0-1
2
3
4
Body-mass index§
> 21
≤ 21
* Cutoff values for the assignment of points are shown for each variable.
Total possible BODE score ranges from 0 to 10.
† Forced expiratory volume in 1 second (FEV1) categories are based on stages identified by the American Thoracic Society.
‡ Scores on the modified Medical Research Council (MMRC) dyspnea scale can range from 0 to 4, with a score of 4 indicating that the patient is too breathless to leave the house or becomes breathless when dressing or undressing.
§ The values for body-mass index were 0 or 1 because of the inflection point in the inverse relation between survival and body-mass index at a value of 21.
The outpatient group performed all the PR activities in the clinic under the supervision of a physiotherapist. The at-home group performed the same PR activities unsupervised at home. The control group did not perform any PR activities and was merely accompanied clinically. The PR program lasted 12 weeks, after which the individuals were evaluated a second time. At the end of the study, all participants were encouraged to continue the PR activities at home. Telephone contact was made each month by a blind evaluator, who inquired about the general health status of the individuals, adverse effects and the continuity of the physical activities. Figure 1 displays the flowchart of the study. All patients (in the three groups) were treated with bronchodilators associated to inhaled corticoids when needed, in accordance with the GOLD guidelines [1].
Figure 1
Flowchart of study design.
×
Interventions
Educational program
During the initial evaluations, all patients took part in an educational program in the auditorium at the clinic, where they received information on the development and progression of COPD, its treatment (both pharmacological and non-pharmacological), the correct use of oxygen for oxygen-dependent patients and the importance of an exercise-based rehabilitation program. All patients received a chart containing the content of the educational program.
Outpatient pulmonary rehabilitation program
The outpatient group performed a combination of aerobic and strengthening exercises three mornings a week for three months. Each session was made up of active warm-up exercises, strengthening of upper and lower limbs, aerobic exercises and stretching. The warm-up phase consisted of intercalated callisthenic exercises for different muscle groups, based on the tolerance of each patient.
The upper limb exercises were performed with hand weights while seated comfortably and consisted of 10 repetitions of elbow flexion, 10 repetitions of elbow abduction, 10 repetitions of shoulder abduction and 10 repetitions of shoulder flexion. The lower limb exercises were performed with ankle weights while patients were seated comfortably and consisted of 10 repetitions of hip flexion and 10 repetitions of knee extension. These exercises were performed to the maximal range of motion of each patient, with diaphragm and pursed-lips breathing. The initial load was 50% of the maximal load achieved on the maximal repetition test (1MR) for the upper and lower limbs [4], with an increase of 0.5 Kg every two weeks until reaching the tolerance limit of each patient. The test for the determination of 1MR consisted of a brief five-minute warm up with upper limb exercises (Kabat diagonals and shoulder flexion-extension), followed by a progressive increase in load until reaching the greatest load moved throughout the total joint range [17].
Aerobic exercise consisted of walking on a tread-mill for 30 minutes at an intensity of 60 to 80% of maximal heart rate reached on the 6MWT, which was monitored throughout the training. Patients with oxyhemoglobin desaturation (SpO2 ≤ 88%) induced by the initial 6MWT session and those who were already oxygen dependent used oxygen supplementation in order to maintain SpO2 ≥ 92%. In cases of severe dyspnea or complications (dizziness, unusual discomfort in the precordial region or lower limbs), the exercise was immediately interrupted and the patient was evaluated by a pneumologist.
Home pulmonary rehabilitation program
The at-home group performed the same combination of upper and lower-limb strengthening exercises as the outpatient group for the same amount of time. In cases in which the patient was unable to afford the hand and ankle weights, weights were provided by the clinic for the same function. The patients in this group initially received training from a specialized health care professional at the pneumology clinic and were instructed to follow the proposed protocol at home. Aerobic exercise was performed by means of walks on flat ground at 60 to 80% of the maximal heart rate reached on the 6MWT performed at the clinic. A heart monitor (Polar S810, Polar®, Finland) provided by the clinic to all patients was used to monitor heart rate. A log was designed and the patients were instructed to fill it out at the end of each training session.
During the 12-week period, the individuals received telephone calls from the same professional at the clinic in order to follow up on the load increase, detect problems, clarify questions and reinforce the importance of the rehabilitation. The patients were instructed, in the case of a high degree of dyspnea or any other symptoms of respiratory distress, to reduce the intensity of exercise or cease the exercise and contact the pneumologist. The criteria for at-home oxygen therapy and the protocol for increasing the load on the upper and lower limb exercises were the same as those for the outpatient group.
Statistical analysis
The sample size was calculated based on the study by Shahin et al. [18], in which the standard deviation on the post-home rehabilitation 6MWT was 19 meters. Considering a clinically significant difference of 54 meters [19], α = 5% and 90% power, it was determined that a minimum of 23 patients was needed for each group. The Kolmogorov-Smirnov test was used to test the normality of the distribution of the variables studied. For the intra-group comparisons, Student's paired t-test was used for variables with parametric distribution; the Mann-Whitney test was used for variables with non-parametric distribution. Inter-group comparisons were performed using one-way analysis of variance (ANOVA) and Tukey's post test was used for paired comparisons whenever ANOVA rejected the null hypothesis. The Kruskal-Wallis test was used for inter-group comparisons of variables with non-parametric distribution and the Mann-Whitney test was used for paired comparisons when the null hypothesis was rejected. The chi-square test was used to test associations between groups and intensity of symptoms/hospitalization. All analyses were carried out using the Statistical Package for the Social Sciences, version 13.0 for Windows (SPSS, Chicago, IL, USA), with the level of significance set at 5%.
Results
Between January 2007 and May 2009, 216 consecutive patients who sought treatment at the Institute of the Lung, Cascavel, PR, Brazil were evaluated and 117 were considered eligible for the study (Figure 1). These patients were divided into three groups: 42 in the at-home group, 46 in the outpatient group and 29 in the control group. After the study had begun, seven patients in the at-home group and 19 in the outpatient group abandoned the study. Moreover, follow up losses occurred with two patients in the at-home group and four in the outpatient group.
Patient characteristics
Table 2 shows the demographic and anthropometric data of the study population. Mean age was 69.2 ± 8.7 years. Mean weight was 67.8 ± 17.4 Kg. Males accounted for 76.5% of the sample. The main cause related to the development of COPD was past or present smoking habits (94.1% of cases); three such cases were likely due to second-hand smoke. Mean tobacco smoke exposure was 43.6 ± 34.4 pack years. Another, less frequent cause was exposure to biomass (wood-burning stove and crop burning), which occurred in three patients (3.5%). Mean BMI was 24.5 ± 5.7 kg/m2; 66 patients (77.6%) had a BMI > 21 kg/m2.
Table 2
Patient characteristics of the three study groups
Characteristics
At-home n = 33
Outpatient n = 23
Control n = 29
Age (years)
66.4 ± 9.5
71.3 ± 6.7
70.8 ± 8.7
Gender (male/female)
27/6
19/4
19/10
Weight (Kg)
70.0 ± 18.7
66.1 ± 13.0
66.7 ± 19.1
Height (cm)
166.9 ± 9.2
167.0 ± 8.5
162.9 ± 10.7
BMI (kg/m2)
25.0 ± 6.2
23.5 ± 4.2
24.6 ± 6.3
Smoker (ex and current)
32 (97%)
20 (86.9%)
28 (96.5%)
Pack years
61.0 ± 41.9
24.0 ± 16.6
32.7 ± 19.4
Data expressed as mean ± standard deviation or percentage (in parentheses).
Definition of abbreviation: BMI, body mass index.
Table 3 shows the clinical characteristics of the patient population. Cough was the most common symptom (90.5%), followed by dyspnea (74.1%), wheezing (71.8%) and bronchial secretion (36.5%). Mean post-bronchodilator forced expiratory volume in one second (FEV1) in % of predicted value was 46.5 ± 22.0%, with the majority of patients in more advanced stages (GOLD III and IV respectively 34.1% and 28.2%). At the beginning of the study, 40 patients (47.0% of the sample) were on long-term home oxygen therapy.
Table 3
Clinical characteristics at baseline evaluation of the three study groups
Variables
At-home n = 33
Outpatient n = 23
Control n = 29
Dyspnea - MRC 0
8 (24.2)
6 (26.1)
8 (27.6)
Dyspnea - MRC 1
9 (27.3)
8 (34.8)
8 (27.6)
Dyspnea - MRC 2
10 (30.3)
5 (21.7)
10 (34.5)
Dyspnea - MRC 3
6 (18.2)
4 (17.4)
2 (6.9)
Dyspnea - MRC 4
0 (0)
0 (0)
1 (3.4)
Cough
31 (93.9)
20 (86.9)
26 (89.6)
Secretion
12 (36.4)
8 (34.8)
11 (37.9)
Wheezing
26 (78.8)
15 (65.2)
20 (69.0)
Post-bronchodilator spirometry
FVC (L)
2.19 ± 0.71
2.51 ± 0.82
2.22 ± 0.55
FVC (%)
68.7 ± 30.2
79.1 ± 30.0
69.9 ± 28.0
FEV1 (L)
1.31 ± 0.76
1.32 ± 0.68
0.99 ± 0.46
FEV1 (%)
47.5 ± 23.3
51.5 ± 23.9
41.4 ± 18.4
FEV1/FVC (%)
69.1 ± 21.8
65.1 ± 24.5
59.2 ± 20.6
COPD stage
GOLD I
4 (12.1)
2 (8.7)
2 (6.9)
GOLD II
8 (24.2)
10 (43.5)
6 (20.7)
GOLD III
11 (33.3)
5 (21.7)
13 (44.8)
GOLD IV
10 (30.3)
6 (26.1)
8 (27.6)
BODE
4 (0-7)
4 (0-8)
4 (1-9)
Data expressed as absolute number and percentage (in parentheses) or mean ± standard deviation.
Definition of abbreviatons: COPD, chronic obstructive pulmonary disease; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; GOLD, Global initiative for chronic obstructive lung disease; MRC, Medical Research Council.
In the intra-group comparisons, the variation in the distance walked on the 6MWT at the end of the 12-week period was clinically significant in the outpatient group (93.6 ± 70.6 meters, p < 0.05) and at-home group (73.2 ± 50.2 meters, p < 0.05) in relation to the initial results (Figure 2).
Figure 2
Intra-group results of distance walked on six-minute walk test before and after rehabilitation program.
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There was no significant difference in the improvement on the 6MWT between the outpatient and at-home groups (p = 0.44). The control group demonstrated no change on the 6MWT at the end of the study (Figure 3).
Figure 3
Variation on six-minute walk test between groups before and after rehabilitation program.
×
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There was a significant reduction in the BODE index in the outpatient and at-home groups at the end of the 12-week period (p < 0.001) and the patients in the control group also demonstrated a significant improvement (p = 0.01) (Figure 4). In the inter-group comparisons, there was no significant difference in the variation in BODE index between the outpatient and at-home groups (p = 0.90), whereas both these groups achieved a significantly greater reduction in the index in comparison to the control group (p = 0.010 and p = 0.016, respectively).
Figure 4
Bode index variation before and after rehabilitation program.
×
Discussion
PR focuses on the multiple needs of patients with COPD and is one of the approaches to reducing disability stemming from this progressive, chronic disease [4, 20]. However, there is limited availability of PR programs in most countries and few patients are submitted to this treatment modality [7‐9].
Moreover, PR carried out in a clinical setting and based on hospital guidelines requires qualified health care professionals, equipment and facilities, which are expensive to maintain and this cost contributes toward the reduction in the availability of PR at health care services [5‐7].
The 6MWT is a widely accepted method for determining functional capacity for exercise, being commonly used in field studies due to its low-cost, reproducibility, objectivity and easy application in relation to patient age and education level [15, 21]. It has also proven to be a predictor of post-pulmonary rehabilitation survival [16, 22]. According to Weisman et al., the 6MWT has proven more sensitive in detecting decline in SpO2 than a maximal increment test on cycle ergometer for patients with COPD [23].
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In the present study, the variation in the distance walked on the 6MWT following participation in the PR program was statistically significant in both the outpatient and at-home groups in comparison to the control group (p < 0.05). The mean variation was 93.61 ± 70.57 meters in the outpatient group and 73.21 ± 50.21 meters in the at-home group. According to Redelmeier et al., an increase in the distance walked on the 6MWT of at least 54 meters over baseline values is clinically important in terms of the improvement in physical capacity [19]. This has been confirmed in a number of studies assessing PR programs [24, 25].
The BODE index is considered a better predictor of the risk of mortality due to both respiratory and non-respiratory causes when compared to FEV1 alone [16]. In the present study, all groups demonstrated a reduction in the BODE index. However, the reduction was significantly greater in the outpatient and at-home groups. The fact that an improvement in the BODE index was found in all groups, including the control group, is probably due to the fact that all patients, regardless of the rehabilitation modality, were rigorously treated with bronchodilators and inhaled corticosteroids, with an optimization of their pharmacological management during the course of the study.
For all the variables analyzed, the clinical benefits achieved with PR performed in the clinical setting were not significantly greater than those achieved in the self-monitored home modality. This demonstrates the efficacy of the home modality for the management of patients with COPD, which allows clinical benefits, lower costs and possibly greater adherence due to the non-necessity of transportation to specialized clinics. Two previous studies have assessed the effectiveness of self-monitored home PR programs, but neither of them used a control group [27, 28]. In a multicenter randomized clinical trial, Maltais et al. found that both outpatient and at-home PR interventions were equally effective in promoting a clinical improvement in dyspnea [26].
Another positive aspect of our study is that the dropout rate was notably less in the at-home group than in the outpatient group (7 vs. 19). This difference is likely due to the fact that carrying out a rehabilitation program at home is logistically easier for patients than travelling to a hospital clinic 3 times a week.
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The present study had some limitations. The study was carried out at a single center, more specifically in a specialist pulmonology clinic, and subjects in the different groups were not matched for age, BMI, smoking status, FEV1, or baseline 6MWD. Moreover, there was no evaluation of health-related quality of life, which is another clinically important outcome.
Conclusion
The present study, despite the above limitations, demonstrates that a self-monitored home pulmonary rehabilitation program can achieve similar results to a supervised outpatient pulmonary rehabilitation program and is a valid alternative in the therapeutic approach to patients with COPD. The data we provide show that self-monitored exercise, truly home-based, following a short period of instruction and education, can achieve equivalent benefits in exercise capacity and body-index scores. Considering the limited access to pulmonary rehabilitation programs worldwide, offering patients the opportunity of a home-based rehabilitation program can overcome the problems related to outpatient rehabilitation (i.e. it is costly to provide and many patients have problems travelling to the center several times per week). Hence, a broad-scale use of the home program is recommended, as this treatment modality is not limited by geographic location and would enable a greater access of patients with COPD to pulmonary rehabilitation.
Conflict of interests statement
None of the authors has any conflict of interest to declare in relation to the subject matter of this manuscript.
Note
Study based on Julio Cesar Mendes de Oliveira's master's degree dissertation presented in 2009 to the Postgraduate Program in Rehabilitation Sciences of the Nove de Julho University (Brazil).
Acknowledgements
This study received support from the Brazilian fostering agencies Fundação de Amparo a Pesquisa do Estado de São Paulo and Conselho Nacional de Desenvolvimento Científico e Tecnológico. The authors Dirceu Costa and Luis V. Franco de Oliveira are respectively PQI and PQII research productivity grant awardees from the Conselho Nacional de Desenvolvimento Científico e Tecnológico, Brazil.
Open Access
This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License (
https://creativecommons.org/licenses/by/2.0
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Outpatient vs. home-based pulmonary rehabilitation in COPD: a randomized controlled trial
verfasst von
Júlio C. Mendes de Oliveira Fernando S. Studart Leitão Filho Luciana M. Malosa Sampaio Ana C. Negrinho de Oliveira Raquel Pastrello Hirata Dirceu Costa Claudio F. Donner Luís V. F. de Oliveira
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