Abstract
Chronic heart failure (HF) is a major cause of morbidity, mortality, disability, and health care costs. A hallmark feature of HF is severe exercise intolerance, which is multifactorial and stems from central and peripheral pathophysiological mechanisms. Exercise training is internationally recognized as a Class 1 recommendation for patients with HF, regardless of whether ejection fraction is reduced or preserved. Optimal exercise prescription has been shown to enhance exercise capacity, improve quality of life, and reduce hospitalizations and mortality in patients with HF. This article will review the rationale and current recommendations for aerobic training, resistance training, and inspiratory muscle training in patients with HF. Furthermore, the review provides practical guidelines for optimizing exercise prescription according to the principles of frequency, intensity, time (duration), type, volume, and progression. Finally, the review addresses common clinical considerations and strategies when prescribing exercise in patients with HF, including considerations for medications, implantable devices, exercise-induced ischemia, and/or frailty.
Keywords: Cardiac rehabilitation, Aerobic training, Resistance training, Inspiratory muscle training, Cardiorespiratory fitness, Physical therapy
Introduction
Chronic heart failure is a major global public health problem affecting over 64 million people worldwide and over 6 million in the United States [1, 2]. Heart failure (HF) is associated with significant morbidity, mortality, and health care costs [1]. Additionally, the prevalence of HF is projected to increase due to the aging of the population and improved survival due to improved treatment of ischemic heart disease and evidence-based treatments including guideline directed medical therapy [1]. The phenotype of HF has expanded to HF with preserved ejection fraction (HFpEF), HF with mildly reduced ejection fraction (HFmrEF) along with HF with reduced ejection fraction (HFrEF), classified according to ejection fraction ranges [3]. Approximately 50% of patients have HFrEF with a relatively stable prevalence compared to rapidly increasing prevalence of HFpEF which is projected to become the most common form of HF [1]. HFpEF is more likely to affect older individuals as well as women with significant and severe comorbidities, and to date there are no effective treatments for HFpEF, which contributes to its high morbidity and mortality [4, 5]. HF is defined as a clinical syndrome encompassing structural and functional abnormalities, elevated brain natriuretic peptide, and pulmonary or systemic congestion [3]. The hallmark symptom of HFrEF and HFpEF phenotypes is severe exercise intolerance, which is multifactorial and stems from central and peripheral pathophysiological mechanisms such as impaired cardiac and pulmonary reserve, excessive systemic vascular resistance and impaired vasodilatory capacity, abnormal redistribution of blood flow and muscle perfusion, and reduced mitochondrial density/volume and skeletal muscle function [6, 7]. Fortunately, the body of evidence to date demonstrates improvements in exercise capacity following exercise training programs as well as attenuation of left ventricular remodelling, improvements in quality of life, and reductions in cardiovascular and all-cause hospitalizations [8–13]. Exercise training also improves exercise capacity and quality of life for patients with HFpEF, although the impact on or improvement in diastolic function has yet to be demonstrated [14]. Herein we provide guidance and rationale for prescribing exercise in patients with HF.
Commencing an exercise program
Guidelines for the management of patients with HF recommend exercise training for clinically stable patients, regardless of whether ejection fraction is reduced or preserved [15, 16]. However, the term ‘stable’ HF can be ambiguous without a universal consensus on the definition, making it challenging to determine the appropriate timeframe for when patients with HF can commence an exercise program. The American Heart Association (AHA) and American College of Cardiology (ACC) guidelines recommend exercise training as a Class 1 indication for HF patients who are stable and on optimal guideline directed medical therapy [15]. The Centers for Medicare & Medicaid Services (CMS) in the United States define ‘stable’ as “patients who have not had recent (≤6 weeks) or planned (≤6 months) major cardiovascular hospitalizations or procedures” [17]. This timeframe was based on criteria from the HF Action Trial [18], and therefore patients with HF in the United States undergo a 6-week clinical stabilization period before coverage for exercise-based cardiac rehabilitation is available. The European Society of Cardiology (ESC) guidelines recommend exercise training for stable HF patients, where stable is defined as symptoms and signs remaining generally unchanged for at least 1 month [16]. A randomized controlled trial by Australian researchers [19] found exercise training as part of a multidisciplinary HF disease management program soon after hospital discharge (commenced within 4–8 weeks) to be feasible and safe, including both supervised exercise intervention and home-based exercise control groups. There were no adverse events related to exercise training in 178 patients with either HFrEF or HFpEF, despite patients being recently hospitalized and having high rates of comorbidities (diabetes, chronic lung disease, and musculoskeletal disorders). The study found no difference in the primary outcome (death and hospital readmissions) between supervised and home-based control exercise groups, although patients meeting exercise guidelines of 150min/week (supervised or home-based) had a significantly lower rates of death or hospital readmissions at 3-months and 6-months than patients who did not meet exercise guidelines. Therefore, instead of determining whether patients are clinically stable to commence exercise training, it would be more pragmatic to individually assess patients for any contraindications to exercise training and signs or symptoms of decompensated HF (Table 1) [20]. A recent international report designed to establish universal definitions and classifications of HF proposes that decompensated HF represents both acute decompensation due to an inciting event, or chronic/progressive worsening of HF signs and symptoms despite ongoing therapy, which requires urgent intervention, hospitalization, or rapid escalation of therapies including advanced therapies [3].
Table 1:
Absolute Contraindications |
Early phase after acute coronary syndrome (within 2 days) |
Ongoing unstable angina |
Uncompensated heart failure |
Acute thrombophlebitis or recent embolism (pulmonary or systemic) |
Active endocarditis Acute myocarditis or pericarditis |
Acute aortic dissection |
Symptomatic severe aortic stenosis |
Acute systemic illness or fever |
Uncontrolled hypertension (≥180 mmHg systolic or ≥110mmHg diastolic blood pressure at rest) |
Uncontrolled sinus tachycardiac (resting heart rate >120 beats.min–1) |
Uncontrolled or life-threatening atrial or ventricular dysrhythmias (including new onset atrial fibrillation/flutter) |
Third-degree atrioventricular block without pacemaker |
Uncontrolled diabetes mellitus |
Orthostatic drop in blood pressure (>20mmHg) with symptoms |
Progressive worsening of exercise tolerance or dyspnea at rest or on exertion over previous 3–5 days |
Significant ischemia at low work rates (<2 METs or 50 Watts) |
Relative Contraindications (increased risk) |
≥1.8 kg or 3 lbs increase in body mass over previous 1–3 days |
Concurrent continuous or intermittent dobutamine therapy |
Decrease in systolic blood pressure with exercise |
New York Heart Association Functional Class IV |
Complex ventricular arrhythmias at rest or appearing with exertion |
Supine resting heart rate ≥100 beats.min–1 |
Pre-existing co-morbidities limiting exercise tolerance |
Severe hypertrophic obstructive cardiomyopathy |
Symptoms or indications of worsening heart failure |
≥1.8 kg or 3 lbs increase in body mass over previous 1–3 days |
Worsening dyspnea (on exertion or rest) |
Excessive fatigue, lack of energy |
Swelling of legs, abdomen |
Productive cough |
Increased urination, particularly at night (nocturia) |
Difficulty sleeping due to breathing problems (orthopnea) |
Difficulty concentrating |
Shock from an implantable cardiac defibrillator |
While acute decompensated HF (ADHF) is currently recognized as a contraindication to exercise training, The Rehabilitation Therapy in Older Acute HF Patients (REHAB-HF) Trial is currently investigating whether exercise-based rehabilitation (focusing on improved balance, strength, mobility, and endurance) commenced during an admission for ADHF, may improve physical function and reduce future re-hospitalizations in older patients (>60 years) [23]. The REHAB-HF pilot study demonstrated feasibility and safety of rehabilitation compared with usual care, and a trend toward improved physical function and decreased hospitalizations [23]. Moreover, a recent study by Delgado et al [24] found early exercise therapy for inpatients recovering from acutely decompensated HF to be safe and efficacious for improvements in functional capacity compared with usual care. This study employed careful screening criteria prior to exercise training, excluding patients from their scheduled exercise session if they had ongoing intravenous infusion of inotropic medications, continuous oxygen therapy >3L/min, systolic blood pressure >180mmHg or <80mmHg, dysrhythmias and/or precordial pain in the prior 24-hours, acute pulmonary edema or glycemic decompensation within the prior 12-hours, or osteoarticular pathology impairing exercise performance [24]. Exercise training was supervised and physiological responses were routinely measured, with exercise termination criteria in line with that of the American College of Sports Medicine (Table 2) [21].
Table 2:
Onset of angina or other symptoms of cardiac insufficiency |
≥1.0 mm ST-segment depression, horizontal or downsloping) |
Systolic blood pressure ≥250mmHg or diastolic blood pressure ≥115mmHg |
Decrease in systolic blood pressure >10mmHg during exercise with increasing workload |
Increased frequency of ventricular dysrhythmias |
Other significant electrocardiogram disturbances (e.g. second- or third-degree atrioventricular block, atrial fibrillation, supraventricular tachycardia, complex ventricular ectopy). |
Other signs/symptoms of exercise intolerance (e.g. light-headedness, cyanosis, shortness of breath) |
Exercise Assessment and Programming
Prior to starting exercise or sports participation it is important to review the patient’s medical history and medications, assess for exercise contraindications, encourage optimization and adherence of medical therapy, and perform baseline assessments [16, 18, 25–27]. Conducting baseline exercise assessment is valuable for determining risk and prognosis, optimal training intensity, and effectiveness of an exercise training program. A symptom-limited cardiopulmonary exercise test (CPET) is the gold standard assessment for patients with HF, to provide information regarding the degree of cardiac and/or pulmonary impairment in addition to an objective measure of cardiorespiratory fitness expressed as peak oxygen uptake (VO2peak) and other prognostic markers such as ventilatory efficiency (VE/VCO2 slope) and oscillatory ventilation [26]. Although CPET is not routinely available for many cardiac rehabilitation programs, standard graded maximal or submaximal exercise testing without gas exchange measurements can still be valuable to provide an estimate of cardiorespiratory fitness, and assess physiological responses to exercise (e.g. symptoms, heart rate, blood pressure, cardiac rhythm) and to guide exercise prescription [22]. The six-minute walk test is widely used within cardiac rehabilitation programs and has been shown to have similar prognostic utility to CPET for all-cause mortality and hospitalization [28]. However, as the 6-minute walk test is self-paced and does not rigorously evaluate the cardiorespiratory system, its use for establishing the optimal training intensity can be limited and may result in under-prescription of exercise intensity [29, 30]. Muscle strength can be assessed as a measure of physical function (e.g. handgrip, quadriceps) to determine effectiveness of an exercise training program, as well as quantification for the basis of resistance training prescription [31]. For exercise prescription, the 1-repetition maximum (1RM) or estimated 1RM (from <10RM test) is the most practical method for determining the resistance training load, ideally performed for each targeted muscle group [22, 31]. Identification of frailty can be accomplished through scales such as the Fried, Edmonton, or Clinical Frailty Scale [32–34]. 5-m gait speed is a physical and objective test that measures functional mobility, and in older adults an improvement of 0.1 m/s in gait speed predicted a substantial reduction in mortality compared with other measures of physical function (including the Short Physical Performance Battery) [35].
Contraindications to exercise
Overall risk of exercise is low when pre-participation assessment and risk factor management is done properly, even for exercise at higher intensities and in more severe cases of HF [36, 37]. Prior to commencing an exercise training program, patients should be assessed for exercise contraindications (Table 1). Furthermore, ongoing assessment for signs of clinical instability or decompensated HF (e.g. weight gain, resting heart rate >100bpm, sudden worsening of symptoms or exercise intolerance) should be conducted throughout an exercise program with immediate referral to the patient’s primary physician if identified [7].
Cardiovascular signs and symptoms that should be used to guide exercise intensity limits are outlined in Table 2. For low-risk patients, monitoring of heart rate, cardiac rhythm, and blood pressure is appropriate for initial sessions at commencement of exercise training, while educating patients about how to self-monitor exercise intensity and recognize signs and symptoms of exercise limits (e.g. excessive fatigue, angina, or light-headedness) [21]. Perspectives on the need for continuous telemetry during exercise-based cardiac rehabilitation have changed within the past few decades. It was previously recommended by the American College of Cardiology and other guidelines that patients undertaking cardiac rehabilitation should have ECG monitoring for the first 6–12 sessions, however it is now recognized that most patients can exercise safely without continuous telemetry [7]. Minimizing the use of telemetry for low-risk patients can help reduce costs for cardiac rehabilitation programs, reduce time burden for cardiac rehabilitation staff, and encourage patients that they can exercise independently and safely without specialized monitoring. However, HF patients with a higher risk profile that should be considered for longer ECG monitoring include survivors of sudden cardiac death, patients with an implantable cardiac defibrillator (ICD), severely depressed left ventricular function (ejection fraction <25%), severe coronary artery disease (CAD), or abnormal hemodynamic responses to exercise (e.g. exercise-induced hypotension) [7].
Importance of Exercise Intensity
In the HF-Action Trial, the magnitude of improvement in VO2peak with exercise training was a strong, independent predictor of prognosis with each 6% increase in VO2peak associated with a 7% reduction in all-cause mortality and an 8% reduction in cardiovascular mortality or hospitalization [38]. Furthermore, the HF-Action Trial showed that during a baseline CPET, VO2peak (ml.kg.min−1), percentage of predicted VO2peak, and exercise duration were the strongest predictors of mortality in patients with HFrEF [39]. Several studies have demonstrated the importance of exercise training intensity for improving VO2peak in patients with HF [40–42]. In a large meta-regression analysis of studies involving patients with HF or CAD, Uddin et al [41] demonstrated that each 10% increase in exercise intensity as percentage of VO2peak (%VO2peak) or percentage of heart rate peak (%HRpeak), was associated with a 1.0 ml.kg.min−1 increase in VO2peak following CR. Specifically in patients with HFrEF, Ismail et al [40] found that exercise interventions of high intensity improved VO2peak by 23% compared with exercise interventions of vigorous intensity (8% improvement), moderate intensity (13% improvement), or low intensity (3% improvement).
Since high intensity exercise cannot be sustained continuously for long periods, high intensity interval training (HIIT), also referred to as aerobic interval training, involves alternating bouts of high intensity exercise interspersed with lower intensity recovery exercise. The optimal HIIT protocol for patients with HF, regarding interval duration and intensity, remains equivocal [43, 44]. A common protocol is the 4×4 Norwegian model, involving four bouts of 4-minute high intensity intervals (90–95% HRpeak) interspersed with 3-minute active recovery intervals (50–70% HRpeak) [45]. In patients with HFrEF, Wisløff et al [45] demonstrated substantial improvements in VO2peak and endothelial function with HIIT compared with moderate intensity continuous training (MICT) and no-exercise control. Furthermore, only HIIT reversed left ventricular remodelling [45]. Subsequent meta-analyses have confirmed a superior effect of HIIT for improving VO2peak compared with MICT in patients with HFrEF [44, 46, 47]. However, the large multi-center SMARTEX HF Study [48] failed to replicate findings that HIIT provides superior improvements in VO2peak than MICT in HFrEF. In the SMARTEX HF Study, poor adherence to the prescribed intensity was a major limitation with 51% of HIIT patients exercising below prescribed targets and 80% of MICT patients exercising above the prescribed target [48]. Furthermore, workload progression per training session was substantially less than smaller studies in HFrEF that showed superiority of HIIT compared with MICT for improving VO2peak (~0.5 Watts per session vs 2 Watts per session) [49]. In patients with HFpEF, Donelli da Silveira et al [50] demonstrated a superior effect of HIIT for improving VO2peak compared with MICT; however, these findings were not replicated in the large multi-center OptimEX-Clin Study [51]. While Donelli da Silveira et al [50] demonstrated excellent adherence to exercise intensity in their HIIT and MICT groups, the OptimEX-Clin Study [51] did not report any results pertaining to the fidelity of training intensity [51]. To date, there are no studies comparing HIIT protocols in patients with HF, and therefore the optimal HIIT protocol for HFrEF and HFpEF is unknown. In the meta-analysis by Pattyn et al [44] sub-group analyses indicated that total energy expenditure and the extent of exercise intensity during the HIIT protocol appears to have a greater influence on changes in VO2peak than interval duration alone.
Principles of exercise prescription
There are several therapeutic goals of exercise training in patients with HF: To reduce the symptoms of HF (e.g. fatigue, dyspnea, exercise intolerance); Increase exercise capacity to improve autonomy with daily living activities and quality of life; Reduce the risk of future clinical events and mortality; and improving pathophysiology (e.g. cardiac remodelling, skeletal muscle capacity, autonomic function) [22, 52]. It is also important to consider specific goals of the patient (e.g. returning to work, carrying out independent activities, rejoining friends on the golf course) as these can provide functional outcomes of exercise training and can be valuable motivators for the patient to maintain regular exercise and physical activity [7].
The fundamental components of exercise prescription involve frequency, intensity, time (duration), type (mode), volume, and progression, commonly known as the FITT-VP principles [21]. When these principles are applied effectively, exercise training provides a sufficient stimulus to promote beneficial physiological adaptations. There is no ‘one size fits all’ approach to exercise training in patients with HF, and instead an individualized approach is recommended [20]. Due to differences in pathophysiology, comorbidities, medications, and prior exercise experience, patients may differ in their ability to tolerate the same relative intensity [7]. Furthermore, patient preferences, availability of equipment/facilities, and behavioral characteristics of the patient should be considered to facilitate long-term adherence to exercise training [20, 52]. Table 3 outlines recommended ranges for frequency, intensity, time (duration), type, and progression, for aerobic training, resistance training, and inspiratory muscle training in patients with HF. The total volume of exercise (aerobic and resistance training combined) should be progressed to 3–7 MET-hr (or 180–420 MET-minutes) per week and exceeded if tolerated [53]. In clinical practice, metabolic equivalents (METs) can be estimated from a Compendium of Physical Activities [54] or treadmill and cycle workload equations [55, 56]. The MET value of the activity is then multiplied by the time spent in the activity (hours or minutes) to calculate the MET-hrs or MET-minutes accumulated.
Table 3:
Training parameter | Initial Prescription*** | Optimal Progression |
---|---|---|
Aerobic Training | ||
Frequency | 2-3 days/week | Moderate intensity: 3-7 days/week High intensity: 1-3 days/week |
Intensity | 40-50% VO2R or HRR; 45-55% VO2peak; RPE 11-12. Until 20 minutes duration is achieved May use short intervals if unable to maintain continuous exercise. |
Continuous: 70-80% VO2R, or HRR; 75-85% VO2peak; RPE 11-14. High intensity intervals: 80-90% VO2R, or HRR; 85-95% VO2peak; RPE 15-17. |
Time (duration) | Session total: 15-30 minutes Work intervals: 20-30 seconds or longer (1-2 minutes) as tolerated. | Session total: 45-60 minutes High intensity intervals: 1-4 minutes interval duration (3-6 repeated bouts) |
Type (mode) | Dynamic, rhythmic activities involving lower or upper body such as treadmill walking, cycling, arm ergometer. |
Dynamic, rhythmic activities involving lower and/or upper body such as treadmill walking/jogging, cycling, rowing, stepper, elliptical, arm ergometer). |
Resistance Training | ||
Frequency | 2-3 non-consecutive days/week | |
Intensity | <30% 1-RM; RPE 11-12 | 40-70% 1-RM; RPE 12-15 |
Time (duration) | 1-2 sets/day for each muscle group, 5-10 repetitions, 4-6 exercises | 2-3 sets/day for each muscle group, 8-15 repetitions, 8-10 exercises |
Type (mode) | Fixed weight machines, resistance bands, handheld weights, or bodyweight exercise. Commence with isolated muscles. |
Fixed weight machines, resistance bands, handheld weights, or bodyweight exercise. |
Inspiratory Muscle Training | ||
Frequency | Standard protocol: 6-7 days/week (twice daily) High intensity protocol: 3-5 days/week |
|
Intensity | Standard protocol: 50% of PImax High intensity protocol: 20-30% PImax |
Standard protocol: 50% of PImax High intensity protocol: 40-70% PImax |
Time (duration) | Session total: 20-30 minutes Standard protocol: 30 breaths (twice daily) High intensity protocol: 2-minutes of work, 1-minute recovery, repeated 7 times |
|
Type (mode) | Pressure threshold device |
Adapted from Keteyian et al [22], Piepoli et al [52], Meyer [57], and American College of Sports Medicine [21].
Abbreviations: HRpeak: peak heart rate; HRR: Heart rate reserve; MET: Metabolic equivalent; VO2peak: peak oxygen uptake; PImax: Maximal inspiratory mouth pressure; RM: repetition maximum; RPE: rating of perceived exertion 6-20 Borg Scale.
Start at lower end of intensity ranges for deconditioned or high-risk patients.
Early Mobilization
Early mobilization and gentle calisthenic exercises should begin as soon as possible once patients are hemodynamically stable, to prevent muscle wasting, improve movement coordination, and enhance respiratory capacity [20]. To commence inpatient rehabilitation, patients should not have any contraindications to exercise (Table 1) and should meet the additional following criteria: 1) no new or recurrent chest pain (within 8-hrs); 2) stable or falling creatinine kinase and troponin values; 3) no decompensated HF (e.g. resting dyspnea or bibasilar rates); and 4) normal cardiac rhythm and stable electrocardiogram (within 8-hrs) [21]. The optimal dose of exercise for inpatient rehabilitation is unknown. Current guidelines by the American College of Sports Medicine recommend a progression from self-care activities (sitting, standing, toileting) to range of motion upper body exercises performed without weight and short to moderate distance walking (minimal to no assistance) performed under supervision up to four times per day [21]. Patients should be monitored for new cardiovascular signs or symptoms (e.g. chest pain, shortness of breath, palpitations, fatigue) along with electrocardiogram (rhythm disturbances, ST segment changes) and appropriate hemodynamic responses (e.g. heart rate, systolic blood pressure) [21]. Table 2 outlines the signs or symptoms for terminating exercise during inpatient rehabilitation.
Aerobic training
All exercise sessions should include 5–10 minutes of warm-up and cool-down activities including dynamic and static stretching, and aerobic activities of a very light or light intensity [21]. Exercise prescription recommendations for aerobic training are outlined in Table 3. Aerobic training should involve activities that employ large muscle groups in a rhythmic manner such as walking, cycling, rowing, stepping, swimming, or arm ergometry. A pragmatic approach is to begin with lower or upper body exercises that are easily learned (treadmill, cycling, arm ergometry), particularly for deconditioned patients [20], and then progress to more challenging exercises that involve lower and upper body exercise (rowing, elliptical machines). Most patients can commence their training with several 5–15-minute periods at a lower intensity either on the same piece of equipment or divided into 2 to 3 modalities [22]. For patients who are unable to maintain exercise continuously early on in their program, moderate intensity intervals (or intermittent exercise) can be employed with low-intensity recovery periods (passive if required), gradually increasing the exercise period and reducing the recovery period over time [7, 58]. Continuous training of moderate-vigorous intensities (at steady state energy metabolism) can typically be performed for prolonged periods (45–60 minutes). This type of training is the most established form of exercise prescription for patients with HF, with demonstrated efficacy and safety [18, 20, 59]. A graded maximal exercise test provides the best foundation for safe and effective exercise, allowing for the determination of exercise intensity as percentage of maximal oxygen uptake reserve (%VO2R), percentage of peak oxygen uptake (%VO2peak), or percentage of maximal heart rate reserve (%HRR) where gas exchange data are unavailable. The use of %HRR (Karvonen formula) is preferred to %HRpeak since %HRR accounts for the dynamic change between resting and peak values, rather than a static peak HR, reflecting the relative intensity more accurately [21, 60, 61]. Current guidelines recommend an optimal exercise intensity for continuous aerobic exercise to be at a moderate-vigorous level in the range of 70–80% VO2R or HRR or a rating of perceived exertion (RPE) of 12–14 on the Borg 6–20 scale [21, 22, 52]. Intensity can be gradually increased from a low intensity (40–50% VO2R or HRR) to a moderate intensity (60% VO2R or HRR; ~first ventilatory threshold), and then progressed as tolerated to a moderate-vigorous intensity (70–80% VO2R or HRR; ~ second ventilatory threshold) [21, 52]. Exercise intensity can be the most challenging component of exercise prescription as the same relative intensity can have a varied tolerance between different patients, as well as by the same patient based on factors such as time of day, environment (temperature, humidity, air quality), and time since medications were taken [7]. Therefore, it is often practical to prescribe an intensity range approximately 5% below or above the desired intensity [7]. In the absence of a graded exercise test or maximal heart rate data, or for patients with atrial fibrillation, frequent ectopy, or marked chronotropic intolerance (<85% of predicted HRpeak), exercise intensity may be guided by an RPE of 11–14 (6–20 Borg Scale) and a target heart rate of 20–30 beats.min−1 above rest [21, 22]. There are no data to support the use of estimated maximal heart rate equations in patients with HF [21]. Frequency of exercise training can commence at 2–3 days/week (rest days in between as needed), with the goal to increase frequency to 3–5 days/week or preferably all days of the week [52].
Progression of exercise programming is vital for ensuring beneficial adaptations with exercise training and improvements in exercise capacity [62, 63]. At the same time, progression that is too rapid may result in adverse effects such as cardiovascular symptoms, orthopedic injury, delayed muscle soreness, or failure to recover from an exercise session [62]. In general, it is recommended to only change one FITT component at a time, and exercise duration should be progressed to a desired level (by 1–5 min per session) before increasing exercise intensity and frequency [22, 31, 62]. Increases in duration and intensity of 5–10% per session are typically well tolerated [62].
Guidelines suggest HIIT can be included 1–3 days/week in patients with HF, typically using MICT and HIIT during alternate exercise sessions [22, 52, 62]. Studies involving patients with HF have prescribed high intensity intervals within the range of 70–90% VO2peak, 75–90% HRR, or 80–95% HRpeak [30, 44]. During the initial weeks of exercise training, sustaining high intensity exercise for longer than 1–2 minutes may be challenging for HF patients, particularly those who are exercise naïve, have comorbidities, or a higher degree of exercise intolerance [64]. To gradually introduce HIIT, prescription can commence with shorter interval durations (1–2 minutes) and progress to longer interval durations (3–4 minutes) as exercise intolerance and fitness level improves [30]. While vigorous activities can acutely increase the risk of sudden cardiac death and myocardial infarction in susceptible persons, this risk is typically greater in adults who are less physically fit and active [65]. Moreover, it is important to highlight that for patients with HF many activities of daily living can require efforts equivalent to a vigorous intensity [43]. HIIT has shown a low rate of major adverse events in patients with HF and CAD when applied in cardiac rehabilitation settings with baseline exercise testing [66]. Recent ESC guidelines [67] outline that high intensity exercise is appropriate for HF patients who are stable, without high risk atherosclerotic lesions or exercise-induced dysrhythmias. Appropriate progression of exercise from low-moderate intensity to moderate-vigorous intensity before commencing HIIT (as outlined in Table 3) is a sensible approach to assess the exercise response, improve exercise tolerance and physical fitness, and minimize musculoskeletal injuries [30].
Resistance Training
Resistance training is a key component of the exercise program for HF patients to counteract skeletal muscle myopathy and increase muscular strength and endurance [68–70]. The resistance training prescription should be individualized and tailored to the findings of the baseline assessments and the presence of frailty. Resistance training exercises can generally be added within 2–4 weeks of starting the aerobic exercise program or sooner according to clinical judgement [71]. Patients should be instructed to avoid the Valsalva maneuver (holding their breath during exhale) during resistance training exercises. Proper lifting technique and training should be provided including the instruction to exhale during the concentric phase and inhale in the eccentric phase of the lift [70]. Table 3 provides recommendations for initial prescription aimed at improving muscular endurance starting with low weights and high repetitions with a preference for dynamic exercises (e.g. chair sit-to-stand, leg press, chest press, bicep curl, tricep extension, knee flexion/extension, latissimus pulldown, etc.). In those that are severely deconditioned the initial exercises can be prescribed unilaterally or as segmental training working the limbs individually to allow for peripheral adaptations without inhibition from the impaired cardiac output [70]. Mode of exercise can begin with hand-held weights or resistance bands and progress from unilateral to bilateral exercises (in severely deconditioned) and eventually to weight machines. Weight machines are safe and aid in proper lifting form and technique. In those that are more conditioned, progression of the resistance training program can transition from the initial low workload phase to an endurance phase (30–40% 1-RM, 12–25 reps, RPE 12–15) followed by the strength phase at higher intensity (40–60% 1-RM; 8–15 repetitions; RPE >15) [20, 52]. Circuit weight training is a viable option and has been associated with 13% improvement in VO2peak [72]. The exercises should be progressed gradually and include functional movements that will aid in completing activities of daily living [73].
Inspiratory Muscle Training
Inspiratory muscle weakness is prevalent in patients with HFrEF and HFpEF [74, 75]. Those with inspiratory muscle weakness are more likely to have impaired mobility and greater risk of myocardial infarction, and increased rates of all-cause and cardiovascular mortality and stroke [76–79]. Therefore, inspiratory muscle training (IMT) is an additional element to consider in the exercise prescription. In the absence of a standardized IMT prescription, the current evidence includes recommendations for both a ‘Standard’ prescription and a ‘High Intensity’ prescription. The ‘Standard’ prescription recommends 30 dynamic efforts twice daily, 6–7 days per week for 4–10 or more weeks using a pressure-threshold device at a load equivalent to 50% of maximal inspiratory pressure (MIP or PImax) [80–82]. The IMT prescription is progressed by instructing the individual to increase the load so that completion of the 30 breaths is at the limit of their tolerance [82]. This prescription was associated with improvements in MIP, reductions in sense of dyspnea, and exercise capacity as measured by VO2peak and 6-minute walk test [83–87]. The ‘High Intensity’ prescription recommends two minutes of loaded inspirations with one minute of recovery, repeated seven times, performed 3–5 days per week for at least 8 weeks at a threshold-load starting at 20–30% PImax and progressing to 70% of baseline PImax by the third or fourth session [88]. Further progression is achieved by increasing the load such that they are only able to complete the final two minute interval [88]. Improvements in MIP, dyspnea, fatigue, and six-minute walk distance were achieved with this protocol [89]. The European Secondary Prevention Guidelines recommend a more gradual approach to load progression, starting with a gradual increase in load every 7–10 days from 30% PImax to 60% PImax [52].
Clinical Considerations
Medications
For patients with HFrEF, guideline-directed medical therapy currently includes four major classes of medications: 1) β-adrenergic receptor blockers (β-blocker); 2) sodium-glucose cotransporter 2 inhibitor; 3) mineralocorticoid receptor antagonist; and 4) either angiotensin-converting enzyme inhibitor, angiotensin receptor blocker, or angiotensin receptor-neprilysin inhibitor, depending on New York Heart Association Stage [15]. In addition to reducing mortality, hospitalizations, and disease progression, these medications help to reduce myocardial load and improve exercise tolerance [15, 21]. For exercise testing and training, patients should be instructed to take their medications as prescribed. Patients on β-blockers can have an attenuated heart rate response to exercise, with the extent depending on the dose and timing in relation to exercise [21]. If β-blocker dose changes during an exercise program, a new graded exercise test is recommended to establish the new maximal heart rate, however if this is not feasible, noting the heart rate response at the workload most recently used to determine the new heart rate target [21]. Mineralocorticoid receptor antagonists are a type of diuretic, which are used to lower blood pressure and prevent fluid overload. Diuretics can increase the risk of volume depletion, orthostatic hypotension, and dehydration [21]. Blood pressure response with exercise and in recovery should be monitored along with symptoms of dizziness or light-headedness, and an extended cool-down period can be helpful to prevent post-exercise hypotension [21].
Implantable Devices
Exercise training can be performed safely in patients with a pacemaker or an ICD [90]; however, certain considerations should be taken into account. Rigorous upper extremity exercises should be avoided for at least 3–4 weeks following implantation (e.g. swimming, bowling, elliptical machines, rowing, lifting weights, golf) [21, 22]. Exercise testing is strongly recommended to assess rate responsiveness and optimize the heart rate response [21]. It is important that the pacemaker or ICD programming settings are optimized (upper rate limit and rate responsiveness) to maximize a patient’s ability to perform activities and exercise effectively [7]. If a patient’s heart rate does not increase with exercise testing, then exercise training should be postponed until the exercise sensing mechanism (to movement or respiration) has been adjusted by the device specialist [21]. Exercise specialists should be familiar with the reason for ICD implantation, the triggers for dysrhythmia (e.g. ischemia or specific heart rate), the individual intervention threshold, and the sequence of therapy (monitoring zone, anti-tachycardia pacing, shocks) [20, 22]. Heart rate monitoring is advisable when exercise is prescribed close to the device’s programmed intervention zone. Exercise should be prescribed at an intensity where maximal training heart rate is 10–20 beats.min−1 below the programmed threshold for ICD intervention [20, 21]. For patients who have a history of symptomatic dysrhythmias or ICD discharges, exercise modalities should be chosen in which short loss of consciousness would be less harmful (e.g. cycling or arm ergometry), and water exercise should be avoided unless supervised [20].
Exercise-induced ischemia
For patients with exercise-induced ischemia or angina, exercise intensity should be set to elicit a heart rate 10 beats.min−1 below the threshold of ischemia or angina symptoms [21]. A longer warm-up time can increase time to ischemia and the ischemic threshold, which is thought to be due to a slower rise in cardiac workload from improved myocardial perfusion and preconditioning [91]. For patients who experience angina with exercise below the recommended intensity targets or routine daily activities, the use of prophylactic sublingual nitroglycerin (taken 10 minutes before the start of exercise) may be a strategy that exercise specialists or cardiac rehabilitation staff can discuss with the patient’s physician, which can typically allow patients to exercise without symptoms and at slightly higher workloads [22, 92]. Since nitroglycerin has a vasodilatory effect which can cause patients to feel light-headed, patients should be seated when administered, and additional blood pressure monitoring may be needed before and after administration, and prior to commencing exercise.
Frailty/cachexia/sarcopenia
There is a bidirectional relationship between HF and frailty such that older individuals with HF are at risk of developing frailty and frail older individuals are at risk of developing HF [93]. An estimated 45% of patients with HF have concurrent frailty identifying a significant area of focus for exercise prescription [94, 95]. Cardiac rehabilitation and exercise training programs are uniquely designed to counteract and address the components of frailty that have significant crossover with HF comorbidities (sarcopenia, limited mobility/sedentary lifestyle, fatigue, cognitive impairment, mood disorders and/or depression, self-efficacy, and quality of life) [96]. The exercise prescription should be tailored by shifting the time spent in aerobic, strength, and balance/flexibility components [97]. In those identified as pre-frail the exercise prescription has a greater focus initially on resistance training (20 minutes; 80% 1-RM; 2–3 times per week), balance exercises (20 minutes; 2–3 times per week), and only 10 minutes of aerobic exercise [97]. For individuals with frailty, the overall exercise time decreases to 45 minutes with a shift in aerobic exercise duration back to 20 minutes, a reduction of resistance training to 10 minutes, and the remaining 15 minutes as balance/flexibility exercises [97].
Conclusion
Evidence-based guidelines for exercise training in patients with HF recommend a combination of aerobic, resistance, and inspiratory muscle training. Following the FITT-VP principles of exercise prescription, with a particular focus on progression to optimal levels, helps to produce a sufficient stimulus for promoting beneficial physiological adaptations that lead to improvements in exercise capacity, HF symptoms, and prognosis. There is no ‘one size fits all’ approach to exercise training in patients with HF. This review has provided rationale and outlined exercise prescription recommendations and practical strategies to adapt exercise training prescription based on degree of exercise intolerance, medications, and other clinical considerations for HF patients.
Funding/Acknowledgments:
Jenna L. Taylor is supported by the National Institute on Aging (1R21AG073726) and Jonathon Myers is funded by the Department of Veterans Affairs, Veterans Health Administration, Rehabilitation Research & Development Service.
Footnotes
Conflicts of Interest: The authors declare no conflict of interest.
References
- 1.Savarese G, et al. , Global burden of heart failure: A comprehensive and updated review of epidemiology. Cardiovasc Res, 2022. [DOI] [PubMed] [Google Scholar]
- 2.Virani SS, et al. , Heart Disease and Stroke Statistics—2020 Update: A Report From the American Heart Association. Circulation, 2020. 141(9): p. e139–e596. [DOI] [PubMed] [Google Scholar]
- 3.Bozkurt B, et al. , Universal definition and classification of heart failure: a report of the Heart Failure Society of America, Heart Failure Association of the European Society of Cardiology, Japanese Heart Failure Society and Writing Committee of the Universal Definition of Heart Failure. European Journal of Heart Failure, 2021. 23(3): p. 352–380. [DOI] [PubMed] [Google Scholar]
- 4.Oktay AA, Rich JD, and Shah SJ, The Emerging Epidemic of Heart Failure with Preserved Ejection Fraction. Current Heart Failure Reports, 2013. 10(4): p. 401–410. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Upadhya B, et al. , Exercise intolerance in heart failure with preserved ejection fraction: more than a heart problem. J Geriatr Cardiol, 2015. 12(3): p. 294–304. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Del Buono MG, et al. , Exercise Intolerance in Patients With Heart Failure: JACC State-of-the-Art Review. J Am Coll Cardiol, 2019. 73(17): p. 2209–2225. [DOI] [PubMed] [Google Scholar]
- 7.Myers J, Principles of exercise prescription for patients with chronic heart failure. Heart Fail Rev, 2008. 13(1): p. 61–8. [DOI] [PubMed] [Google Scholar]
- 8.Taylor RS, et al. , Exercise-Based Rehabilitation for Heart Failure: Cochrane Systematic Review, Meta-Analysis, and Trial Sequential Analysis. JACC Heart Fail, 2019. 7(8): p. 691–705. [DOI] [PubMed] [Google Scholar]
- 9.Sagar VA, et al. , Exercise-based rehabilitation for heart failure: systematic review and meta-analysis. Open Heart, 2015. 2(1): p. e000163. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Haykowsky MJ, et al. , A Meta-Analysis of the Effect of Exercise Training on Left Ventricular Remodeling in Heart Failure Patients: The Benefit Depends on the Type of Training Performed. Journal of the American College of Cardiology, 2007. 49(24): p. 2329–2336. [DOI] [PubMed] [Google Scholar]
- 11.Lewinter C, et al. , Exercise-based cardiac rehabilitation in patients with heart failure: a meta-analysis of randomised controlled trials between 1999 and 2013. Eur J Prev Cardiol, 2015. 22(12): p. 1504–12. [DOI] [PubMed] [Google Scholar]
- 12.Pandey A, et al. , Exercise training in patients with heart failure and preserved ejection fraction: meta-analysis of randomized control trials. Circ Heart Fail, 2015. 8(1): p. 33–40. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Edwards JJ and O’Driscoll JM, Exercise Training in Heart failure with Preserved and Reduced Ejection Fraction: A Systematic Review and Meta-Analysis. Sports Med Open, 2022. 8(1): p. 76. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Taylor RS, et al. , Effects of exercise training for heart failure with preserved ejection fraction: A systematic review and meta-analysis of comparative studies. International Journal of Cardiology, 2012. 162(1): p. 6–13. [DOI] [PubMed] [Google Scholar]
- 15.Heidenreich PA, et al. , 2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation, 2022. 145(18): p. e895–e1032. [DOI] [PubMed] [Google Scholar]
- 16.Ponikowski P, et al. , 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur Heart J, 2016. 37(27): p. 2129–2200. [DOI] [PubMed] [Google Scholar]
- 17.Jacques L, Jensen TS,. Schafer J, Decision Memo for Cardiac Rehabilitation (CR) Programs — Chronic Heart Failure (CAG-00437N). Centers for Medicare and Medicaid Services, Editor. 2014: Baltimore, MD. [Google Scholar]
- 18.O’Connor CM, et al. , Efficacy and safety of exercise training in patients with chronic heart failure: HF-ACTION randomized controlled trial. Jama, 2009. 301(14): p. 1439–50. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Mudge AM, et al. , Addition of Supervised Exercise Training to a Post-Hospital Disease Management Program for Patients Recently Hospitalized With Acute Heart Failure: The EJECTION-HF Randomized Phase 4 Trial. JACC Heart Fail, 2018. 6(2): p. 143–152. [DOI] [PubMed] [Google Scholar]
- 20.Piepoli MF, et al. , Exercise training in heart failure: from theory to practice. A consensus document of the Heart Failure Association and the European Association for Cardiovascular Prevention and Rehabilitation. Eur J Heart Fail, 2011. 13(4): p. 347–57. [DOI] [PubMed] [Google Scholar]
- 21.American College of Sports Medicine., ACSM’s guidelines for exercise testing and prescription. 11th ed. Guidelines for exercise testing and prescription. 2022, Philadelphia, PA: Lippincott Williams & Wilkins. [Google Scholar]
- 22.Keteyian SJ, et al. , Incorporating patients with chronic heart failure into outpatient cardiac rehabilitation: practical recommendations for exercise and self-care counseling-a clinical review. J Cardiopulm Rehabil Prev, 2014. 34(4): p. 223–32. [DOI] [PubMed] [Google Scholar]
- 23.Reeves GR, et al. , A Novel Rehabilitation Intervention for Older Patients With Acute Decompensated Heart Failure: The REHAB-HF Pilot Study . JACC Heart Fail, 2017. 5(5): p. 359–366. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Delgado BM, et al. , Early rehabilitation in cardiology - heart failure: The ERIC-HF protocol, a novel intervention to decompensated heart failure patients rehabilitation. Eur J Cardiovasc Nurs, 2020. 19(7): p. 592–599. [DOI] [PubMed] [Google Scholar]
- 25.Piepoli MF, et al. , Exercise training meta-analysis of trials in patients with chronic heart failure (ExTraMATCH). Bmj, 2004. 328(7433): p. 189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Corrà U, et al. , Role of cardiopulmonary exercise testing in clinical stratification in heart failure. A position paper from the Committee on Exercise Physiology and Training of the Heart Failure Association of the European Society of Cardiology. Eur J Heart Fail, 2018. 20(1): p. 3–15. [DOI] [PubMed] [Google Scholar]
- 27.Scherr J, et al. , Associations between Borg’s rating of perceived exertion and physiological measures of exercise intensity. Eur J Appl Physiol, 2013. 113(1): p. 147–55. [DOI] [PubMed] [Google Scholar]
- 28.Forman DE, et al. , 6-min walk test provides prognostic utility comparable to cardiopulmonary exercise testing in ambulatory outpatients with systolic heart failure. J Am Coll Cardiol, 2012. 60(25): p. 2653–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Ingle L and Carroll S, Cardiac rehabilitation and exercise training. Heart, 2013. 99(17): p. 1298. [DOI] [PubMed] [Google Scholar]
- 30.Taylor JL, Bonikowske AR, and Olson TP, Optimizing Outcomes in Cardiac Rehabilitation: The Importance of Exercise Intensity. Front Cardiovasc Med., 2021. 8(985). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Hansen D, et al. , Exercise intensity assessment and prescription in cardiovascular rehabilitation and beyond: why and how: a position statement from the Secondary Prevention and Rehabilitation Section of the European Association of Preventive Cardiology. Eur J Prev Cardiol., 2021. [DOI] [PubMed] [Google Scholar]
- 32.Fried LP, et al. , Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci, 2001. 56(3): p. M146–56. [DOI] [PubMed] [Google Scholar]
- 33.Rockwood K, et al. , A global clinical measure of fitness and frailty in elderly people. Canadian Medical Association Journal, 2005. 173(5): p. 489–495. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Rolfson DB, et al. , Validity and reliability of the Edmonton Frail Scale. Age Ageing, 2006. 35(5): p. 526–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Hardy SE, et al. , Improvement in usual gait speed predicts better survival in older adults. J Am Geriatr Soc, 2007. 55(11): p. 1727–34. [DOI] [PubMed] [Google Scholar]
- 36.Rognmo Ø, et al. , Cardiovascular risk of high- versus moderate-intensity aerobic exercise in coronary heart disease patients. Circulation, 2012. 126(12): p. 1436–40. [DOI] [PubMed] [Google Scholar]
- 37.Ellingsen Ø, et al. , High-Intensity Interval Training in Patients With Heart Failure With Reduced Ejection Fraction. Circulation, 2017. 135(9): p. 839–849. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Swank AM, et al. , Modest increase in peak VO2 is related to better clinical outcomes in chronic heart failure patients: results from heart failure and a controlled trial to investigate outcomes of exercise training. Circ Heart Fail, 2012. 5(5): p. 579–85. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Keteyian SJ, et al. , Variables Measured During Cardiopulmonary Exercise Testing as Predictors of Mortality in Chronic Systolic Heart Failure. J Am Coll Cardiol, 2016. 67(7): p. 780–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Ismail H, et al. , Exercise training program characteristics and magnitude of change in functional capacity of heart failure patients. Int J Cardiol, 2014. 171(1): p. 62–5. [DOI] [PubMed] [Google Scholar]
- 41.Uddin J, et al. , Predictors of exercise capacity following exercise-based rehabilitation in patients with coronary heart disease and heart failure: A meta-regression analysis. Eur J Prev Cardiol, 2016. 23(7): p. 683–93. [DOI] [PubMed] [Google Scholar]
- 42.Mitchell BL, et al. , What is the effect of aerobic exercise intensity on cardiorespiratory fitness in those undergoing cardiac rehabilitation? A systematic review with meta-analysis. British Journal of Sports Medicine, 2019. 53(21): p. 1341. [DOI] [PubMed] [Google Scholar]
- 43.Haykowsky MJ, et al. , Heart Failure: Exercise-Based Cardiac Rehabilitation: Who, When, and How Intense? Can J Cardiol, 2016. 32(10 Suppl 2): p. S382–s387. [DOI] [PubMed] [Google Scholar]
- 44.Pattyn N, Beulque R, and Cornelissen V, Aerobic Interval vs. Continuous Training in Patients with Coronary Artery Disease or Heart Failure: An Updated Systematic Review and Meta-Analysis with a Focus on Secondary Outcomes. Sports Med, 2018. 48(5): p. 1189–1205. [DOI] [PubMed] [Google Scholar]
- 45.Wisløff U, et al. , Superior cardiovascular effect of aerobic interval training versus moderate continuous training in heart failure patients: a randomized study. Circulation, 2007. 115(24): p. 3086–3094. [DOI] [PubMed] [Google Scholar]
- 46.Haykowsky MJ, et al. , Meta-analysis of aerobic interval training on exercise capacity and systolic function in patients with heart failure and reduced ejection fractions. Am J Cardiol, 2013. 111(10): p. 1466–9. [DOI] [PubMed] [Google Scholar]
- 47.Edwards J, et al. , Exercise Mode in Heart Failure: A Systematic Review and Meta-Analysis. Sports Med Open, 2023. 9(1): p. 3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Ellingsen Ø, et al. , High Intensity Interval Training in Heart Failure Patients with Reduced Ejection Fraction. Circulation, 2017. 135(9): p. 839–849. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Wisloff U, Lavie CJ, and Rognmo O, Letter by Wisloff et al Regarding Article, “High-Intensity Interval Training in Patients With Heart Failure With Reduced Ejection Fraction”. Circulation, 2017. 136(6): p. 607–608. [DOI] [PubMed] [Google Scholar]
- 50.Donelli da Silveira A, et al. , High-intensity interval training is effective and superior to moderate continuous training in patients with heart failure with preserved ejection fraction: A randomized clinical trial. European Journal of Preventive Cardiology, 2020. 27(16): p. 1733–1743. [DOI] [PubMed] [Google Scholar]
- 51.Mueller S, et al. , Effect of High-Intensity Interval Training, Moderate Continuous Training, or Guideline-Based Physical Activity Advice on Peak Oxygen Consumption in Patients With Heart Failure With Preserved Ejection Fraction: A Randomized Clinical Trial. JAMA, 2021. 325(6): p. 542–551. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Ambrosetti M, et al. , Secondary prevention through comprehensive cardiovascular rehabilitation: From knowledge to implementation. 2020 update. A position paper from the Secondary Prevention and Rehabilitation Section of the European Association of Preventive Cardiology. Eur J Prev Cardiol, 2020: p. 2047487320913379. [DOI] [PubMed] [Google Scholar]
- 53.Keteyian SJ, et al. , Relation between volume of exercise and clinical outcomes in patients with heart failure. J Am Coll Cardiol, 2012. 60(19): p. 1899–905. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Ainsworth BE, et al. , 2011 Compendium of Physical Activities: A Second Update of Codes and MET Values. Medicine & Science in Sports & Exercise, 2011. 43(8). [DOI] [PubMed] [Google Scholar]
- 55.Kokkinos P, et al. , New Generalized Equation for Predicting Maximal Oxygen Uptake (from the Fitness Registry and the Importance of Exercise National Database). Am J Cardiol., 2017. 120(4): p. 688–692. [DOI] [PubMed] [Google Scholar]
- 56.Kokkinos P, et al. , A new generalized cycle ergometry equation for predicting maximal oxygen uptake: The Fitness Registry and the Importance of Exercise National Database (FRIEND). Eur J Prev Cardiol., 2018. 25(10): p. 1077–1082. [DOI] [PubMed] [Google Scholar]
- 57.Meyer K, Exercise training in heart failure: recommendations based on current research. Med Sci Sports Exerc, 2001. 33(4): p. 525–31. [DOI] [PubMed] [Google Scholar]
- 58.Meyer K, et al. , Physical responses to different modes of interval exercise in patients with chronic heart failure--application to exercise training. Eur Heart J, 1996. 17(7): p. 1040–7. [DOI] [PubMed] [Google Scholar]
- 59.Bozkurt B, et al. , Cardiac Rehabilitation for Patients With Heart Failure: JACC Expert Panel. Journal of the American College of Cardiology, 2021. 77(11): p. 1454–1469. [DOI] [PubMed] [Google Scholar]
- 60.Carvalho VO and Mezzani A, Aerobic exercise training intensity in patients with chronic heart failure: principles of assessment and prescription. Eur J Cardiovasc Prev Rehabil, 2011. 18(1): p. 5–14. [DOI] [PubMed] [Google Scholar]
- 61.Zweerink A, et al. , Chronotropic Incompetence in Chronic Heart Failure. Circulation: Heart Failure, 2018. 11(8): p. e004969. [DOI] [PubMed] [Google Scholar]
- 62.Squires RW, et al. , Progression of Exercise Training in Early Outpatient Cardiac Rehabilitation: AN OFFICIAL STATEMENT FROM THE AMERICAN ASSOCIATION OF CARDIOVASCULAR AND PULMONARY REHABILITATION. Journal of Cardiopulmonary Rehabilitation and Prevention, 2018. 38(3). [DOI] [PubMed] [Google Scholar]
- 63.Haeny T, et al. , The Influence of Exercise Workload Progression Across 36 Sessions of Cardiac Rehabilitation on Functional Capacity. J Cardiovasc Dev Dis, 2019. 6(3). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Gayda M, et al. , Comparison of Different Forms of Exercise Training in Patients With Cardiac Disease: Where Does High-Intensity Interval Training Fit? Can J Cardiol, 2016. [DOI] [PubMed] [Google Scholar]
- 65.Thompson PD, et al. , Exercise and acute cardiovascular events placing the risks into perspective: a scientific statement from the American Heart Association Council on Nutrition, Physical Activity, and Metabolism and the Council on Clinical Cardiology. Circulation, 2007. 115(17): p. 2358–2368. [DOI] [PubMed] [Google Scholar]
- 66.Wewege Michael A, et al. , High-Intensity Interval Training for Patients With Cardiovascular Disease—Is It Safe? A Systematic Review. J Am Heart Assoc, 2018. 7(21): p. e009305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Pelliccia A, et al. , 2020 ESC Guidelines on sports cardiology and exercise in patients with cardiovascular disease: The Task Force on sports cardiology and exercise in patients with cardiovascular disease of the European Society of Cardiology (ESC). European Heart Journal, 2021. 42(1): p. 17–96. [DOI] [PubMed] [Google Scholar]
- 68.Pu CT, et al. , Randomized trial of progressive resistance training to counteract the myopathy of chronic heart failure. J Appl Physiol (1985), 2001. 90(6): p. 2341–50. [DOI] [PubMed] [Google Scholar]
- 69.Warburton DER, et al. , Central haemodynamics and peripheral muscle function during exercise in patients with chronic heart failure. Applied Physiology, Nutrition, and Metabolism, 2007. 32(2): p. 318–331. [DOI] [PubMed] [Google Scholar]
- 70.Volaklis KA and Tokmakidis SP, Resistance exercise training in patients with heart failure. Sports Med, 2005. 35(12): p. 1085–103. [DOI] [PubMed] [Google Scholar]
- 71.Williams MA, et al. , Resistance exercise in individuals with and without cardiovascular disease: 2007 update: a scientific statement from the American Heart Association Council on Clinical Cardiology and Council on Nutrition, Physical Activity, and Metabolism. Circulation, 2007. 116(5): p. 572–84. [DOI] [PubMed] [Google Scholar]
- 72.Maiorana A, et al. , The effect of combined aerobic and resistance exercise training on vascular function in type 2 diabetes. J Am Coll Cardiol, 2001. 38(3): p. 860–6. [DOI] [PubMed] [Google Scholar]
- 73.Savage PA, et al. , Effect of resistance training on physical disability in chronic heart failure. Med Sci Sports Exerc, 2011. 43(8): p. 1379–86. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Hamazaki N, et al. , Prevalence and prognosis of respiratory muscle weakness in heart failure patients with preserved ejection fraction. Respiratory Medicine, 2020. 161: p. 105834. [DOI] [PubMed] [Google Scholar]
- 75.Nakagawa NK, et al. , Risk Factors for Inspiratory Muscle Weakness in Chronic Heart Failure. Respiratory Care, 2020. 65(4): p. 507. [DOI] [PubMed] [Google Scholar]
- 76.Meyer FJ, et al. , Respiratory muscle dysfunction in congestive heart failure: Clinical correlation and prognostic significance. Circulation, 2001. 103(17): p. 2153–2158. [DOI] [PubMed] [Google Scholar]
- 77.Buchman AS, et al. , Pulmonary function, muscle strength and mortality in old age. Mechanisms of Ageing and Development, 2008. 129(11): p. 625–631. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Buchman AS, et al. , Respiratory Muscle Strength Predicts Decline in Mobility in Older Persons. Neuroepidemiology, 2008. 31(3): p. 174–180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 79.van der Palen J, et al. , Respiratory muscle strength and the risk of incident cardiovascular events. Thorax, 2004. 59(12): p. 1063. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Volianitis S, et al. , Inspiratory muscle training improves rowing performance. Medicine and Science in Sports and Exercise, 2001. 33(5): p. 803–809. [DOI] [PubMed] [Google Scholar]
- 81.Romer LM and McConnell AK, Specificity and reversibility of inspiratory muscle training. Medicine and Science in Sports and Exercise, 2003. 35(2): p. 237–244. [DOI] [PubMed] [Google Scholar]
- 82.Smith JR and Taylor BJ, Inspiratory muscle weakness in cardiovascular diseases: Implications for cardiac rehabilitation. Prog Cardiovasc Dis, 2022. 70: p. 49–57. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 83.Dall’Ago P, et al. , Inspiratory Muscle Training in Patients With Heart Failure and Inspiratory Muscle Weakness: A Randomized Trial. Journal of the American College of Cardiology, 2006. 47(4): p. 757–763. [DOI] [PubMed] [Google Scholar]
- 84.Cahalin LP, Semigran MJ, and Dec GW, Inspiratory Muscle Training in Patients With Chronic Heart Failure Awaiting Cardiac Transplantation: Results of a Pilot Clinical Trial. Physical Therapy, 1997. 77(8): p. 830–838. [DOI] [PubMed] [Google Scholar]
- 85.Mancini DM, et al. , Benefit of Selective Respiratory Muscle Training on Exercise Capacity in Patients With Chronic Congestive Heart Failure. Circulation, 1995. 91(2): p. 320–329. [DOI] [PubMed] [Google Scholar]
- 86.Weiner P, et al. , The effect of specific inspiratory muscle training on the sensation of dyspnea and exercise tolerance in patients with congestive heart failure. Clinical Cardiology, 1999. 22(11): p. 727–732. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 87.Johnson PH, Cowley AJ, and Kinnear WJM, A randomized controlled trial of inspiratory muscle training in stable chronic heart failure. European Heart Journal, 1998. 19(8): p. 12491253. [DOI] [PubMed] [Google Scholar]
- 88.Sturdy G, et al. , Feasibility of High-Intensity, Interval-Based Respiratory Muscle Training in COPD. Chest, 2003. 123(1): p. 142–150. [DOI] [PubMed] [Google Scholar]
- 89.Hill K, et al. , High-intensity inspiratory muscle training in COPD. European Respiratory Journal, 2006. 27(6): p. 1119–1128. [DOI] [PubMed] [Google Scholar]
- 90.Piccini JP, et al. , Exercise training and implantable cardioverter-defibrillator shocks in patients with heart failure: results from HF-ACTION (Heart Failure and A Controlled Trial Investigating Outcomes of Exercise TraiNing). JACC Heart Fail, 2013. 1(2): p. 142–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.Tomai F, et al. , Mechanisms of the warm-up phenomenon. Eur Heart J, 1996. 17(7): p. 1022–7. [DOI] [PubMed] [Google Scholar]
- 92.Hambrecht R, Berra K, and Calfas KJ, Managing Your Angina Symptoms With Nitroglycerin. Circulation, 2013. 127(22): p. e642–e645. [DOI] [PubMed] [Google Scholar]
- 93.Goldwater DS and Pinney SP, Frailty in Advanced Heart Failure: A Consequence of Aging or a Separate Entity? Clin Med Insights Cardiol, 2015. 9(Suppl 2): p. 39–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 94.Denfeld QE, et al. , The prevalence of frailty in heart failure: A systematic review and meta-analysis . Int J Cardiol, 2017. 236: p. 283–289. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Reeves GR, et al. , Comparison of Frequency of Frailty and Severely Impaired Physical Function in Patients ≥60 Years Hospitalized With Acute Decompensated Heart Failure Versus Chronic Stable Heart Failure With Reduced and Preserved Left Ventricular Ejection Fraction. Am J Cardiol, 2016. 117(12): p. 1953–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 96.Afilalo J, Evaluating and Treating Frailty in Cardiac Rehabilitation. Clin Geriatr Med, 2019. 35(4): p. 445–457. [DOI] [PubMed] [Google Scholar]
- 97.Bray NW, et al. , Exercise prescription to reverse frailty. Appl Physiol Nutr Metab, 2016. 41(10): p. 1112–1116. [DOI] [PubMed] [Google Scholar]