Safety of supervised exercise therapy in patients with intermittent claudication

被引:54
作者
Gommans, Lindy N. M. [1 ]
Fokkenrood, Hugo J. P. [1 ,2 ]
van Dalen, Hendrika C. W. [1 ]
Scheltinga, Marc R. M. [3 ,4 ]
Teijink, Joep A. W. [1 ,2 ]
Peters, Ron J. G. [5 ]
机构
[1] Catharina Hosp, Dept Vasc Surg, POB 1350, NL-5602 ZA Eindhoven, Netherlands
[2] Maastricht Univ, Care & Publ Hlth Res Innovat CAPHRI Res Sch, NL-6200 MD Maastricht, Netherlands
[3] Maastricht Univ, Cardiovasc Res Inst Maastricht CARIM Res Sch, NL-6200 MD Maastricht, Netherlands
[4] Maxima Med Ctr, Dept Vasc Surg, Veldhoven, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, NL-1105 AZ Amsterdam, Netherlands
关键词
PERIPHERAL ARTERIAL-DISEASE; PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY; QUALITY-OF-LIFE; SILENT-MYOCARDIAL-ISCHEMIA; ENDOTHELIAL GROWTH-FACTOR; HOME-BASED EXERCISE; OCCLUSIVE DISEASE; REHABILITATION PROGRAM; TREADMILL EXERCISE; SKELETAL-MUSCLE;
D O I
10.1016/j.jvs.2014.08.070
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Supervised exercise therapy (SET) is recommended as the primary treatment for patients with intermittent claudication (IC). However, there is concern regarding the safety of performing SET because IC patients are at risk for untoward cardiovascular events. The Dutch physical therapy guideline advocates cardiac exercise testing before SET, if indicated. Perceived uncertainties concerning safety may contribute to the underuse of SET in daily practice. The objective of this review was to analyze the safety of supervised exercise training in patients with IC. Methods: Two authors independently studied clinical trials investigating SET. Data were obtained from MEDLINE, EMBASE, and The Cochrane Central Register of Controlled Trials. Complication rates were calculated and expressed as number of events pernumber of patient-hours. The usefulness of cardiac screening before SET was evaluated in a subanalysis. Results: Our search strategy revealed 2703 abstracts. We selected 121 articles, of which 74 met the inclusion criteria. Studies represent 82,725 hours of training in 2876 IC patients. Eight adverse events were reported, six of cardiac and two of noncardiac origin, resulting in an all-cause complication rate of one event per 10,340 patient-hours. Conclusions: SET can safely be prescribed in patients with IC because an exceedingly low all-cause complication rate was found. Routine cardiac screening before commencing SET is not required. Our results may diminish perceived uncertainties regarding safety and will possibly increase the use of SET in daily practice.
引用
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页码:512 / +
页数:9
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