| Literature DB >> 25416306 |
Christine Råheim Borge1, Kåre Birger Hagen, Anne Marit Mengshoel, Ernst Omenaas, Torbjørn Moum, Astrid Klopstad Wahl.
Abstract
BACKGROUND: This paper reviews evidence and quality of Systematic Reviews (SRs) on the effects of breathing control exercises (BCEs) and respiratory muscle training (RMT) on breathlessness/dyspnea and other symptoms, and quality of life (QOL) for individuals with chronic obstructive pulmonary disease (COPD).Entities:
Mesh:
Year: 2014 PMID: 25416306 PMCID: PMC4258938 DOI: 10.1186/1471-2466-14-184
Source DB: PubMed Journal: BMC Pulm Med ISSN: 1471-2466 Impact factor: 3.317
Figure 1Description of breathing control exercises and respiratory muscle training.
AMSTAR score in the different reviews
| AMSTAR criteria | Holland et al. 2012[ | Roberts et al. 2009[ | Geddes et al. 2008[ | Gosselink et al. 2011[ | O’Brian et al. 2008[ | Shoemaker et al. 2009[ | Thomas et al. 2010[ |
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| Yes | Yes | Yes | Yes | Yes | Yes | Yes |
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| Yes | Ca | Yes | Yes | Yes | Ca | Yes |
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| Yes | Yes | Yes | Yes | Yes | Yes | Yes |
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| Yes | No | No | Yes | No | No | No |
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| Yes | No | No | Yes | No | No | Yes |
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| Yes | No | Yes | Yes | Yes | Yes | Yes |
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| Yes | Yes | Yes | Yes | Yes | Yes | Yes |
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| Yes | Yes | No | No | No | Yes | Yes |
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| Yes | Na | Yes | Yes | Yes | No | Yes |
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| Yes | Na | No | Yes | Ca | No | Yes |
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| Yes | No | Yes | Yes | No | No | No |
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| 11 | 4 | 7 | 10 | 6 | 5 | 9 |
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| High | Low | Moderate | High | Moderate | Moderate | High |
Yes = 1, No = 0, Cannot answer (Ca) = 0, Not applicable (Na) = 0.
AMSTAR score of 0–4 = low quality, AMSTAR score of 5–8 = moderate quality, AMSTAR score of 9–11 = high quality.
Descriptive information of included systematic reviews
| Author and year | Aim, sources of electronic literature search (year) and language of search |
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| Holland et al. (2012) [ |
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| Roberts et al. (2009) [ |
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| Geddes et al. (2008) [ |
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| Gosselink et al. (2011) [ |
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| DocOnline, ATS and ERS congress (Years: 2000–2008) | |
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| O’Brian et al. (2008) [ |
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| Shoemaker et al. (2009) [ |
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| Thomas et al. (2010) [ |
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NR: Not registered, *Severity and/or age not registered, FEV1%: predicted forced expiratory volume in one second.
Outcome measures and main effects in the included SR’s
| Authors (year) | BCE or RMT | I and C group (design of comparison) | Intervention descriptor and duration | Outcome variable (measure) | No. of trials (No. of subjects) | Pooled statistics on main effect variables MD/WMD/NU and/or SES (95%CI), p-value, (Effect in favor of intervention or control) | Authors’ comments on quality measure | Authors’ conclusion |
|---|---|---|---|---|---|---|---|---|
| Holland et al. (2012) [ | DB, PLB, YB | PLB compared with no BE (RCT) | 8 -12 weeks training | Dyspnea (BS) | 2 (19) | NQPD (NS) | Low QOE* | The effects of breathing exercises on breathlessness and well-being were variable. |
| Dyspnea (UCSD Shortness of Breath Questionnaire) | 2 (19) | NQPD (NS) | Low QOE* | |||||
| Dyspnea (MRCS) | 1 (30) | NQPD (I) | NR | |||||
| Dyspnea (Hiratsuka Scale) | 2 (60) | MD -12.94 (-22.29, -3.60), p = 0.0066, (I) | Low QOE* | |||||
| Health condition (Hiratsuka Scale) | 2 (60) | MD 6.19 (-5.24,17.61), p = 0.29 (NS) | NR | |||||
| Mood (Hiratsuka Scale) | 2 (60) | MD 1.08 (-9.60,11.75), p = 0.84 (NS) | NR | |||||
| Social function (Hiratsuka Scale) | 2 (60) | MD 11.69 (-0.91,24.28), p = 0.069 (NS) | NR | |||||
| House work (Hiratsuka Scale) | 2 (60) | MD 15.58 (0.5,30.66), p = 0.043 (C) | NR | |||||
| Headache (Hiratsuka Scale) | 2 (60) | MD -3.30 (-12.37,5.77), p = 0.48 (NS) | NR | |||||
| Appetite (Hiratsuka Scale) | 2 (60) | MD 8.42 (-5.3,22.15), p = 0.23 (NS) | NR | |||||
| Well being (Hiratsuka Scale) | 2 (60) | MD 0.09 (-9.80,9.98), p = 0.99 (NS) | NR | |||||
| QOL (Cai scale) | 1 (89) | NQPD (I) | NR | |||||
| DB compared with no BE (RCT) | 4-12 weeks training | Dyspnea (MRCS) | 1(30) | NQPD (NS) | Moderate QOE* | |||
| QOL (St. George RQ) | 1(30) | NQPD (I) | Moderate QOE* | |||||
| Yoga compared with no BE (RCT) | 12 weeks training | Dyspnea intensity (BS) | 1 (29) | NQPD (NS) | Low QOE* | |||
| Dyspnea distress (BS) | 1 (29) | NQPD (NS) | Low QOE* | |||||
| Dyspnoea-related QOL | 1 (29) | NQPD (NS) | NR | |||||
| Health QOL (St. George RQ) | 1 (45) | NQPD (I) | Moderate QOE* | |||||
| PLB compared with EMT (RCT) | 4-12 weeks training | Dyspnea (BS, SOBQ) | 2 (17) | NQPD (I (PLB) on 12 weeks, NS on 4 weeks) | Low QOE* | |||
| Low QOE* | ||||||||
| Dypsnea (UCSD Shortness of Breath Questionnaire) | 2 (17) | NQPD (NS) | ||||||
| DB, PLB and nutritional (RCT) | NR | QOL (Cai scale) | 1 (71) | NQPD (NS) | NR | |||
| Roberts. et al. (2009) [ | PLB | PLB during everyday activities or during exercise (PP) | NR in table # | Dyspnea (BS) | 5 (110) | 40% relief (range 0%–to 63%) # (NR) | Low and moderate QOE # ** | PLB has a role in the symptomatic management of stable COPD. |
| Geddes et al. (2008) [ | IMT | Inspiratory muscle training versus intervention sham (RCT) | Intensity ≥30%–60% or max load, Pimax (threshold) 15–30 minutes 1–2 pr. day, 3–7 days pr. week for 5–24 weeks. | Dyspnea (BS) | 4 (99) | WMD -1.76, (-2.35, -1.16), | No score given. Descriptive summary of the MQ is provided. | IMT improves measure of quality of life and decreases dyspnea for adults with stable COPD. |
| p <0.00001, (I) | ||||||||
| Dyspnea (TDI focal score) | 5 (96) | WMD 2.55, (0.92, 4.19), p = 0.002, (I) | ||||||
| 60% MVV (normocapnic hyperpnea tube breathing) 15 minutes × 2 pr. day, 7 days a week for 5 weeks. | Dyspnea (TDI functional impairment) | 3 (56) | WMD 0.72, (0.14, 1.31), p = 0.02, (I) | |||||
| Dyspnea (TDI magnitude of task) | 3 (56) | WMD 0.74, (0.49, 1.0), p <0.00001, (I) | ||||||
| Dyspnea (TDI magnitude of effort) | 3 (56) | WMD 0.48, (0.24, 0.72), p <0.0001, (I) | ||||||
| Quality of life (CRQ total score) | 2 (69) | WMD 0.33, (0.19, 0.47), p <0.00001, (I) | ||||||
| Gosselink et al. (2011) [ | IMT | IMT versus control (RCT) | Intensity ≥30%, Pimax (threshold load) or endurance training in controlled manner (inclusion criteria), 15–90 minute × 2–3 pr. day, 5–7 days a week, for 4 weeks to 12 months.## | Dyspnea (BS) | 14(NR) | NU -0.9, SES -0.45, (-0.66 to -0.24), | MQ score from 30–83% (median 59%) of the maximum score.** | IMT improves dyspnea and health QOL. |
| p <0.001, (I) | ||||||||
| Dyspnea (TDI score) | 4 (NR) | NU +2.8, SES 1.58, (0.86–2.3), | ||||||
| p <0.001, (I) | ||||||||
| Dyspnea (CRQ) | 9 (NR) | NU +1.1, SES 0.34, (-0.03–0.71), | ||||||
| p = 0.068, (I) | ||||||||
| Quality of life (CRQ score) | 9 (NR) | NU +3.8, SES 0.34, (0.09–0.6), p = 0.007, (I) | ||||||
| Fatigue (CRQ score) | 10 (NR) | NU + 0.9, SES 0.27, (0.03–0.5), | ||||||
| p = 0.024, (I) | ||||||||
| Emotion (CRQ score) | 10 (NR) | NU + 0.5, SES 0.19, (-0.04–0.42), | ||||||
| p = 0.107 | ||||||||
| Mastery (CRQ score) | 10 (NR) | NU–0.005, SES 0.09, (-0.14–0.33), p = 0.432 | ||||||
| O’Brien et al. (2008) [ | IMT | Combined IMT and exercise versus exercise alone (RCT) | Intensity 30%, Pimax-60% (threshold), 30 minutes × 1 pr. day 5 days a week for 16 weeks. <72% MVV (Normocapnic hyperventilation) 1–20 minutes × 1 pr. day, 3 days a week for 8 weeks. | Quality of life CRQ dyspnea | 2 (57) | WMD -1.94, (-2.88, -1.01), p <0.0001, (I) | No score given. MQ information given in a table in the SR. | Results of dyspnea and QOL are less clear. Further trials are required. |
| Quality of life CRQ fatigue | 2 (57) | WMD -0.23, (-3.85, 3.4), p = 0.9 | ||||||
| Shoemaker et. al. (2009) [ | IMT | IMT versus control | Intensity load 17-100% Pimax, 15–30 minutes daily, 3–7 days a week for 8–24 weeks | Dyspnea (during IMT) | 3 (85) | NQPD ## | Score 40-90% level 1b **** | IMT improve dyspnea and QOL in COPD patients |
| QOL | 6 (188) | NQPD ## | ||||||
| Thomas et al. (2010) [ | IMT | IMT at home versus control (RCT) | No information on intensity, 30–60 minutes pr. day × 3–6 pr. week, for 3–12 months. | Dyspnea (TDI score) | 3 (57) | MD 2.36 (0.76, 3.96), p = 0.004, (I) ## | Score of 5 in one study and 7 in two studies.*** | IMT may improve breathlessness during activities of daily living in severe COPD. |
BCE: Breathing control exercise, BS: Borg Score (range 0–10), C: Control, CI: Confidence interval, CRQ: Chronic Respiratory Questionnaire (range 0–7), DB: Diaphragmatic breathing, EMT: Expiratory muscle training, I: Intervention, IMT: Inspiratory muscle training, MD: Mean difference, MRCS: Medical Research Council Score, MQ: Methodological quality, N: Number, NQPD = No quantitative pooling data, NR: Not registered, NS: Not significant, NU: Natural units, PLB: Pursed-lip breathing, QOE: Quality of evidence, RCT: Randomized controlled trial, RQ: Respiratory Questionnaire, SES: Summary effect size, SOBS: Shortness of Breath Score, St. George RQ: St. George Respiratory Questionnaire (range 0–100), TDI: Transition Dyspnea Index (range -9–9), UCSD Shortness of Breath Questionnaire: University of California San Diego Shortness of Breath Questionnaire (range 0–120), WMD: Weighted mean difference, YB: Yoga breathing.
*Used the GRADE Working grades of evidence (High quality: further research is very unlikely to change our confidence in the estimate of effect; Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate; Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and not likely to change the estimate).
**Used a modification of the framework for methodological quality used by Smith et al.
***Used PEDro methodological quality score (range 0–10). Higher scores indicate better quality.
**** Used the evaluation scale developed by Medlicott and Harris. Scores: 80–100% = strong quality; 60–79% = moderate quality; <59 = low quality. Studies with weak methodological rigor were assigned an evidence level of 2b.
#Difficulty reading information from tables and text.
##Single studies not reported due to difficulties of reading out the exact design and effect from text and/or tables.
Figure 2Flow chart of inclusion and exclusion process.