Literature DB >> 11666098

Long-term effects of spinal cord stimulation on myocardial ischemia and heart rate variability: results of a 48-hour ambulatory electrocardiographic monitoring.

F Di Pede1, G Zuin, F Giada, G Pinato, G Turiano, M Bevilacqua, R Cazzin, A Raviele.   

Abstract

BACKGROUND: Spinal cord stimulation (SCS) has analgesic properties and may be used to treat pain in patients with therapeutically refractory angina who are unsuitable for myocardial revascularization. Some studies have also demonstrated an anti-ischemic effect. The aim of this study was to evaluate the long-term persistence of the effects of SCS on myocardial ischemia and on heart rate variability.
METHODS: Fifteen patients (9 males, 6 females, mean age 76 +/- 8 years, range 58-90 years) with severe refractory angina pectoris (Canadian class III-IV), on optimal pharmacological therapy, unsuitable for myocardial revascularization and treated with SCS for a mean follow-up of 39 +/- 27 months (range 9-92 months) were studied. Eleven patients had had a previous myocardial infarction and 5 a coronary artery bypass graft. The mean ejection fraction was 54 +/- 7% (range 36-65%). All patients underwent 48-hour ambulatory ECG monitoring and were randomly assigned to 24 hours without SCS (off period) and 24 hours with SCS (on period). The primary endpoints were: number of ischemic episodes, total duration of ischemic episodes (min), and total ischemic burden (mV*min).
RESULTS: The heart rate was not statistically different during the off and on SCS periods (median 64 and 67 b/min respectively). The number of ischemic episodes decreased from a median of 6 (range 0-29) during the off period to 3 (range 0-24) during the on period (p < 0.05). The total duration of ischemic episodes decreased from a median of 29 min (range 0- 186 min) during the off period to 16 min (range 0-123 min) during the on period (p < 0.05). The total ischemic burden decreased from a median of 2.5 mV*min (range 0-19.5 mV*min) during the off period to 0.8 mV*min (range 0-13 mV*min) during the on period (p = NS). The heart rate variability parameters were similar during the on and off periods.
CONCLUSIONS: SCS exerts long-term anti-ischemic effects.

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Mesh:

Year:  2001        PMID: 11666098

Source DB:  PubMed          Journal:  Ital Heart J        ISSN: 1129-471X


  5 in total

1.  Thoracic spinal cord stimulation improves functional status and relieves symptoms in patients with refractory angina pectoris: the first placebo-controlled randomised study.

Authors:  Stephan Eddicks; Klaus Maier-Hauff; Michael Schenk; Andreas Müller; Gert Baumann; Heinz Theres
Journal:  Heart       Date:  2007-01-19       Impact factor: 5.994

2.  The effectiveness and cost-effectiveness of spinal cord stimulation for refractory angina (RASCAL study): study protocol for a pilot randomized controlled trial.

Authors:  Sam Eldabe; John Raphael; Simon Thomson; Andrea Manca; Mark de Belder; Rajesh Aggarwal; Matthew Banks; Morag Brookes; Susan Merotra; Rashidat Adeniba; Ed Davies; Rod S Taylor
Journal:  Trials       Date:  2013-02-22       Impact factor: 2.279

3.  Spinal cord stimulation versus other therapies in patients with Refractory Angina: A meta-analysis.

Authors:  Shaocheng Wang; Qixian Li; Hongwei Fang; Hao Yang; Diansan Su; Yuan-Xiang Tao; Zhankui Wang; Xiangrui Wang; Zhongwei Yang
Journal:  Transl Perioper Pain Med       Date:  2017

4.  Spinal cord stimulation in the treatment of refractory angina: systematic review and meta-analysis of randomised controlled trials.

Authors:  Rod S Taylor; Jessica De Vries; Eric Buchser; Mike J L Dejongste
Journal:  BMC Cardiovasc Disord       Date:  2009-03-25       Impact factor: 2.298

5.  The effect of electrical neurostimulation on collateral perfusion during acute coronary occlusion.

Authors:  Jessica de Vries; Rutger L Anthonio; Mike J L Dejongste; Gillian A Jessurun; Eng-Shiong Tan; Bart J G L de Smet; Ad F M van den Heuvel; Michiel J Staal; Felix Zijlstra
Journal:  BMC Cardiovasc Disord       Date:  2007-06-27       Impact factor: 2.298

  5 in total

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