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个性化身体康复计划的耐受性在患者依赖于因诺托普的支持与终端阶段慢性心力衰竭的患者
M A Bortsova1, E A Demchenko1, P A Fedotov1
1Almazov National Medical Research Center, St-Petersburg.
Kardiologiia
|December 13, 2023
概括
个性化身体康复计划是安全的,并且对于需要内支持的末期慢性心力衰竭 (CHF) 患者来说是可以容忍的. 这种方法不会增加不良事件,使其成为改善患者结果的可行选择.
科学领域:
- 心脏病学 心脏病学
- 康复医学 康复医学 康复医学
- 运动生理学 运动生理学
背景情况:
- 末期慢性心力衰竭 (CHF) 患者通常需要内支持 (例如,多布他胺,多巴胺).
- 在这个弱势群体中,身体康复计划 (PRP) 的作用仍在调查中.
- 评估PRP的安全性和耐受性对于优化CHF管理至关重要.
研究的目的:
- 评估个性化身体康复计划 (PRP) 的耐受性.
- 评估因诺托普依赖的末期慢性心力衰竭 (CHF) 患者的安全性和不良事件 (AEs).
- 为了确定是否持续的无otropic 支持违反了PRP.
主要方法:
- 对120名男性 (18-65岁) 进行前性随机研究,射出分数≤30%.
- 第1组 (40名患者):内支持+PRP;第2组 (40名患者):内支持,没有PRP;第3组 (40名患者):没有内支持+PRP.
- PRP持续时间:6个月;评估运动强度,SPO2和乳酸水平.
主要成果:
- 第1组和第3组 (PRP组) 在没有危及生命的AEs的课程中参加了>80%.
- 在PRP组之间进行比较的运动强度和博格度量得分 (p>0.05).
- 在运动期间,SpO2没有显著下降 (<93%);在PRP组中,乳酸水平仍然可控.
结论:
- 个性化6个月PRP在依赖异基的末期CHF患者中耐受良好,符合安全标准.
- 在这个群体中,PRP不会增加与CHF或康复相关的副作用.
- 如果没有运动不耐受或严重的AEs,那么内托普支持 (dobutamine/dopamine) 不是PRP的禁忌.
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