Squeo Maria Rosaria, Di Giacinto Barbara, Perrone Marco Alfonso, Santini Massimo, Sette Maria Luisa, Fabrizi Emanuele, Vaquer Antonia, Parisi Attilio, Spataro Antonio, Biffi Alessandro
Institute of Sports Medicine, Sport e Salute, 00197 Rome, Italy.
Department of Cardiology and University Sports Centre, University of Rome Tor Vergata, 00133 Rome, Italy.
J Cardiovasc Dev Dis. 2022 Jun 6;9(6):182. doi: 10.3390/jcdd9060182.
: The "FIDE Project" (Fitness Implantable DEvice) was organized by the Institute of Sports Medicine and Science and the World Society of Arrhythmias with the aim of demonstrating the usefulness of exercise training in improving functional capacity in patients with implantable cardiac devices. : Thirty sedentary patients were selected for the project (25 males and 5 females), with a mean age of 73 ± 5 years (range 44-94 years). Twenty-five were implanted with a Pacemaker (PM) and five with an Implantable Cardioverter Defibrillator (ICD). Atrial fibrillation/atrial flutter was present in ten (34%) patients, post-ischemic dilated cardiomyopathy in five (17.2%), sick sinus syndrome in six (20,7%), complete atrium-ventricular block in six (20.7%), hypertrophic cardiomyopathy in one (3.4%) and recurrent syncope in one (3.4%). The baseline assessment comprised cardiovascular examination, resting and stress ECG, cardiopulmonary exercise testing (V ̇O2peak), strength assessment of different muscle groups, and a flexibility test. The same measurements were repeated after 15-20 consecutive training sessions, over a 2-month period. The exercise prescription was set to 70-80% of HRR (Heart rate reserve) and to 50-70% of 1RM (1-repetition maximum, muscular force). The training protocol consisted of two training sessions per week performed in our institute, 90 min for each (warm-up, aerobic phase, strength phase and stretching) and one or more at home autonomously. : The cardiopulmonary testing after the training period documents a significant improvement in V ̇O2peak (15 ± 4 mL/kg/min vs. 17 ± 4; = 0.001) and in work load (87 ± 30 watts vs. 108 ± 37; = 0.001). Additionally, strength capacity significantly increased after the cardiac rehabilitation program, (quadriceps: 21 ± 18 kg vs. 29 ± 16 kg, = 0.00003). Flexibility tests show a positive trend, but without statistical significance (sit-and-reach test: -19 ± 11 cm vs. -15 ± 11.7 cm; back-scratch test: -19 ± 11.6 cm vs. -15 ± 10 cm; lateral flexibility right -44 ± 1.4 cm vs. -43 ± 9.5 cm; left -43 ± 5 vs. -45 ± 8.7 cm). : A brief period of combined aerobic, strength and flexibility exercise training (FIDE project) proved to be effective and safe in improving functional capacity in patients with cardiac implantable devices.
“FIDE项目”(可植入健身设备)由运动医学与科学研究所和世界心律失常学会组织,旨在证明运动训练对改善植入心脏设备患者的功能能力的有效性。该项目选取了30名久坐不动的患者(25名男性和5名女性),平均年龄为73±5岁(年龄范围44 - 94岁)。其中25人植入了起搏器(PM),5人植入了植入式心律转复除颤器(ICD)。10名(34%)患者存在心房颤动/心房扑动,5名(17.2%)患者患有缺血性扩张型心肌病,6名(20.7%)患者患有病态窦房结综合征,6名(20.7%)患者患有完全性房室传导阻滞,1名(3.4%)患者患有肥厚型心肌病,1名(3.4%)患者有反复晕厥。基线评估包括心血管检查、静息和应激心电图、心肺运动测试(最大摄氧量)、不同肌肉群的力量评估以及柔韧性测试。在为期2个月的时间里,连续进行15 - 20次训练课程后重复相同的测量。运动处方设定为心率储备(HRR)的70 - 80%和1次重复最大值(1RM,肌肉力量)的50 - 70%。训练方案包括每周在我们研究所进行两次训练课程,每次90分钟(热身、有氧运动阶段、力量阶段和伸展),以及一次或多次自主在家训练。训练期后的心肺测试表明,最大摄氧量有显著改善(15±4毫升/千克/分钟对17±4;P = 0.001),工作负荷也有显著改善(87±30瓦对108±37;P = 0.001)。此外,心脏康复计划后力量能力显著提高(股四头肌:21±18千克对29±16千克,P = 0.00003)。柔韧性测试显示出积极趋势,但无统计学意义(坐位体前屈测试:-19±11厘米对-15±11.7厘米;背部抓挠测试:-19±11.6厘米对-15±10厘米;右侧侧方柔韧性-44±1.4厘米对-43±9.5厘米;左侧-43±5对-45±8.7厘米)。一段简短的有氧、力量和柔韧性联合运动训练期(FIDE项目)被证明对改善植入心脏设备患者的功能能力是有效且安全的。