QUESTIONS: What is the immediate effect of a single 45-minute session of transcutaneous electrical nerve stimulation over acupoints (Acu-TENS) on lung function and dyspnoea in patients with chronic obstructive pulmonary disease? DESIGN: Randomised, placebo-controlled trial with concealed allocation, participant blinding, assessor blinding, and intention-to-treat analysis. PARTICIPANTS: Forty-six ambulatory patients with a mean age of 75 years, with stage I or II chronic obstructive pulmonary disease, and with no previous experience of TENS or acupuncture. INTERVENTION: The experimental group received 45 minutes of Acu-TENS over acupoint Ex-B1 bilaterally (0.5 'cun' lateral to the spinous process of the 7(th) cervical vertebra) while the control group received placebo-TENS with identical electrode placement but no electrical output despite a flashing light indicating stimulus delivery. OUTCOME MEASURES: Lung function was measured as FEV1 and FVC while dyspnoea was measured using a shortness of breath 100-mm visual analogue scale. RESULTS: After 45 minutes of Acu-TENS, the experimental group had increased FEV1 by 0.12 litres (95% CI 0.07 to 0.15) and decreased dyspnoea by 10.7 mm (95% CI -13.9 to -7.6) more than the control group. The effect on FVC was only small (mean difference 0.05 litres, 95% CI -0.01 to 0.10). CONCLUSION: Acu-TENS may be a useful non-invasive adjunctive intervention in the management of dyspnoea in patients with chronic obstructive pulmonary disease. This study suggests that the effect of long-term Acu-TENS warrants further investigation.
RCT Entities:
QUESTIONS: What is the immediate effect of a single 45-minute session of transcutaneous electrical nerve stimulation over acupoints (Acu-TENS) on lung function and dyspnoea in patients with chronic obstructive pulmonary disease? DESIGN: Randomised, placebo-controlled trial with concealed allocation, participant blinding, assessor blinding, and intention-to-treat analysis. PARTICIPANTS: Forty-six ambulatory patients with a mean age of 75 years, with stage I or II chronic obstructive pulmonary disease, and with no previous experience of TENS or acupuncture. INTERVENTION: The experimental group received 45 minutes of Acu-TENS over acupoint Ex-B1 bilaterally (0.5 'cun' lateral to the spinous process of the 7(th) cervical vertebra) while the control group received placebo-TENS with identical electrode placement but no electrical output despite a flashing light indicating stimulus delivery. OUTCOME MEASURES: Lung function was measured as FEV1 and FVC while dyspnoea was measured using a shortness of breath 100-mm visual analogue scale. RESULTS: After 45 minutes of Acu-TENS, the experimental group had increased FEV1 by 0.12 litres (95% CI 0.07 to 0.15) and decreased dyspnoea by 10.7 mm (95% CI -13.9 to -7.6) more than the control group. The effect on FVC was only small (mean difference 0.05 litres, 95% CI -0.01 to 0.10). CONCLUSION: Acu-TENS may be a useful non-invasive adjunctive intervention in the management of dyspnoea in patients with chronic obstructive pulmonary disease. This study suggests that the effect of long-term Acu-TENS warrants further investigation.
Authors: Wing-Wa Leung; Alice Y M Jones; Simon S M Ng; Cherry Y N Wong; Janet F Y Lee Journal: World J Gastroenterol Date: 2013-01-21 Impact factor: 5.742
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