Impact of Enhanced External Counter-pulsation Therapy on Glycaemic Control in People With Prediabetes and Type 2 Diabetes Mellitus: A Systematic Review and Meta-analysis

Q2 Medicine European Endocrinology Pub Date : 2023-01-01 DOI:10.17925/ee.2023.19.2.8
Lakshmi Nagendra, Deep Dutta, Meha Sharma, Harish Bg
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Abstract

Background: Enhanced external counter-pulsation (EECP) therapy is approved for refractory angina in coronary artery disease (CAD). EECP is being explored as a treatment modality in type 2 diabetes mellitus (T2DM). Methods: The Embase, Web of Science, Cochrane Library, MEDLINE (PubMed), ClinicaltTrials. gov, CNKI database, Clinical Trials Registry-India (CTRI), and Google Scholar databases were searched for randomized controlled trials (RCTs) involving patients receiving EECP therapy in the intervention arm. The primary outcome was the changes in glycated haemoglobin (HbA1c). The secondary outcomes were the changes in blood glucose parameters, inflammatory markers and any adverse events. Results: Data from 3 RCTs involving 71 people with T2DM/prediabetes was analysed to find out the impact of EECP therapy compared with placebo. As compared with placebo, patients receiving EECP had significantly lower HbA1C immediately after completion of therapy (mean difference [MD] -0.70%, 95% confidence interval (CI) -0.95. -0.45;p<0.00001), at 2–4 weeks post completion of therapy (MD -1.04%, 95%CI -1.32. -0.77; p<0.00001) and 7–12 weeks after therapy completion (MD -0.98%, 95% CI -1.22, -0.74; p<0.00001). EECP therapy was well tolerated without any increased side effects (risk ratio 2.36, 95% CI 0.11–52.41; p=0.59. Conclusion: EECP therapy is effective in blood glucose and pressure lowering over at least 7–12 weeks of therapy completion. Blood glucose and pressure should be monitored with suitable modulation of drug doses to prevent hypoglycaemia and hypotension in patients with angina undergoing EECP therapy. The PROSPERO registration number is CRD42023434533
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强化外抗搏动治疗对糖尿病前期和2型糖尿病患者血糖控制的影响:一项系统综述和荟萃分析
背景:增强体外反搏(EECP)疗法被批准用于治疗冠状动脉疾病(CAD)难治性心绞痛。EECP作为2型糖尿病(T2DM)的一种治疗方式正在被探索。方法:Embase, Web of Science, Cochrane Library, MEDLINE (PubMed), ClinicaltTrials。我们检索了在干预组中接受EECP治疗的患者的随机对照试验(rct),检索了CNKI数据库、Clinical Trials Registry-India (CTRI)和Google Scholar数据库。主要终点是糖化血红蛋白(HbA1c)的变化。次要结果是血糖参数、炎症标志物和任何不良事件的变化。结果:我们分析了3项随机对照试验的数据,涉及71例T2DM/前驱糖尿病患者,以找出与安慰剂相比,EECP治疗的影响。与安慰剂相比,接受EECP的患者在治疗完成后立即的HbA1C显著降低(平均差[MD] -0.70%, 95%可信区间(CI) -0.95)。-0.45;p<0.00001),在治疗完成后2-4周(MD -1.04%, 95%CI -1.32)。-0.77;p<0.00001)和治疗完成后7-12周(MD -0.98%, 95% CI -1.22, -0.74;术中,0.00001)。EECP治疗耐受性良好,无副作用增加(风险比2.36,95% CI 0.11-52.41;p = 0.59。结论:EECP治疗在治疗完成后至少7-12周内血糖和血压降低是有效的。应监测血糖和血压,适当调节药物剂量,以防止心绞痛患者接受EECP治疗时出现低血糖和低血压。普洛斯彼罗注册号是CRD42023434533
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European Endocrinology
European Endocrinology Medicine-Endocrinology, Diabetes and Metabolism
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