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Journal of Geriatric Cardiology : JGC logoLink to Journal of Geriatric Cardiology : JGC
. 2016 Jul;13(5):450–457. doi: 10.11909/j.issn.1671-5411.2016.05.004

Submaximal oxygen uptake kinetics, functional mobility, and physical activity in older adults with heart failure and reduced ejection fraction

Scott L Hummel 1,2, John Herald 1, Craig Alpert 1, Kimberlee A Gretebeck 3, Wendy S Champoux 4, Donald R Dengel 5, Peter V Vaitkevicius 6, Neil B Alexander 1,2
PMCID: PMC4984569  PMID: 27594875

Abstract

Background

Submaximal oxygen uptake measures are more feasible and may better predict clinical cardiac outcomes than maximal tests in older adults with heart failure (HF). We examined relationships between maximal oxygen uptake, submaximal oxygen kinetics, functional mobility, and physical activity in older adults with HF and reduced ejection fraction.

Methods

Older adults with HF and reduced ejection fraction (n = 25, age 75 ± 7 years) were compared to 25 healthy age- and gender-matched controls. Assessments included a maximal treadmill test for peak oxygen uptake (VO2peak), oxygen uptake kinetics at onset of and on recovery from a submaximal treadmill test, functional mobility testing [Get Up and Go (GUG), Comfortable Gait Speed (CGS), Unipedal Stance (US)], and self-reported physical activity (PA).

Results

Compared to controls, HF had worse performance on GUG, CGS, and US, greater delays in submaximal oxygen uptake kinetics, and lower PA. In controls, VO2peak was more strongly associated with functional mobility and PA than submaximal oxygen uptake kinetics. In HF patients, submaximal oxygen uptake kinetics were similarly associated with GUG and CGS as VO2peak, but weakly associated with PA.

Conclusions

Based on their mobility performance, older HF patients with reduced ejection fraction are at risk for adverse functional outcomes. In this population, submaximal oxygen uptake measures may be equivalent to VO2 peak in predicting functional mobility, and in addition to being more feasible, may provide better insight into how aerobic function relates to mobility in older adults with HF.

Keywords: Aging, Congestive heart failure, Mobility, Oxygen uptake, The elderly

1. Introduction

Heart failure (HF) affects over 5 million Americans, 70% of which are over the age of 60. The aging of the population and increased prevalence of HF risk factors has translated into an overall increase in the prevalence of older adults living in the community with HF. Over the last several decades, major outcomes (such as mortality and rehospitalization) have improved only modestly in older adults with HF, possibly related to the impact of concurrent frailty and multimorbidity.[1],[2] A key contributor to frailty, mobility disability, is a key risk factor for mortality in older adults with HF.[3],[4] Physical activity is reduced and sedentary behavior is increased in individuals with cardiovascular disease, particularly in those with HF.[5]

Decreased peak oxygen consumption (VO2peak) is a strong prognostic indicator for mortality in HF patients.[6] However, the relationship between VO2peak and self-reported measures of functional disability and physical activity in older HF patients is not strong.[7] Most daily mobility tasks performed by older adults require submaximal, rather than maximal, oxygen uptake. In physically impaired older adults, submaximal testing is less demanding, carries lower risk, and may be less dependent on participant motivation. In mobility-impaired older adults without HF, oxygen uptake kinetics during the onset of and recovery from submaximal exercise are more predictive of functional mobility than VO2peak.[8],[9] Compared to healthy controls, HF patients' time constants of oxygen uptake kinetics are increased before and after submaximal as well as after maximal exercise.[10],[11] These time constants predict key measures and outcomes in HF, including neurohormonal activation,[12] cardiac output,[13] functional class,[14] hospitalization[15] and survival,[16] the latter better than VO2peak.[17]

The purpose of this study was to examine the relationships between VO2peak, submaximal oxygen uptake kinetics, functional mobility, and self-reported physical activity in older adults with HF. To our knowledge, there are no studies that evaluate the relationships of submaximal oxygen uptake kinetics to functional mobility or self-reported physical activity in HF. Based on previous studies and compared to healthy age-and gender-matched controls, we expected older adults with HF to have slower oxygen uptake kinetics, poorer functional mobility and lower self-reported physical activity. The key hypothesis of the present study was that functional mobility and reported physical activity would correlate more strongly with submaximal oxygen uptake kinetics than VO2peak, and that this relationship would be stronger in older adults with HF than in healthy controls.

2. Methods

2.1. Participants

Two groups of community dwelling volunteers aged 65 or older, one with HF and reduced ejection fraction and the other healthy controls, were screened by a nurse practitioner for an aerobic exercise trial focusing on functional mobility outcomes. HF participants were referred from HF clinics to the study nurse practitioner, who reviewed the medical record and recent diagnostic tests and then performed a focused history and physical examination to determine inclusion into the study. All participants signed informed consent forms approved by the University of Michigan Institutional Review Board.

HF inclusion criteria were: left ventricular ejection fraction < 40%; New York Heart Association (NYHA) Class II-III symptom duration greater than 3 months; on ACC/AHA guideline medications for 3 months with stable/optimal dosing for at least one month. HF group exclusion criteria were: exercise-induced sustained arrhythmia or myocardial ischemia (symptoms or ischemic changes on EKG); symptomatic arrhythmia that had not been addressed with the use of a pacemaker or implantable defibrillator if appropriate; atrial fibrillation with poor rate control; high-grade AV block; symptomatic obstructive valvular disease; and severe renal (serum creatinine > 3.0) or hepatic (transaminases > 4 × normal) disease. Exclusion criteria for HF and controls were: alcohol intake > 3 ounces/day; recent (within the past six months) myocardial infarction, coronary artery bypass graft surgery or stroke; uncontrolled hypertension; substantial dementia [Mini-Mental Status Examination (MMSE) < 24/30]; hemiplegia or lower limb amputation; current participation in intensive aerobic exercise program or physical therapy more than 30 min three times per week; severe orthopedic or musculoskeletal conditions that limited weight bearing; and other acute medical conditions.

Age- and gender-matched healthy controls had no significant cardiopulmonary, musculoskeletal, or neurological findings, and took no beta blocker or nitrate medications.

2.2. Assessments

2.2.1. Self-reported function

Self-reported disability was assessed using the Established Populations for the Epidemiologic Study of the Elderly (EPESE) questionnaire which includes 15 activities of daily living and the Rosow-Breslau and Nagi mobility-relevant items (including walking one half mile, walking up and down a flight of stairs, and moving heavy objects such as carrying a bag of groceries). Items were scored and summed on a scale of disability or difficulty present (1) or absent (0). Total EPESE score could range from 0−15 with a higher score representing greater self-reported disability.[18],[19]

The HF group was further evaluated by the Kansas City Cardiomyopathy Questionnaire (KCCQ). The KCCQ included items assessing physical limitations (amount of limitation of basic activities such as dressing, walking, yard work); symptoms (frequency and severity of symptoms such as shortness of breath or foot swelling); social interference (limitation of social activities such as hobbies or visiting family and friends); and quality of life (enjoyment, discouragement and satisfaction living with HF symptoms). Functional status (combination of physical limitation and symptom domains) and clinical (combination of physical limitation, symptom, social interference and quality of life domains) scores were calculated for the present study. The KCCQ is scored from 0–100 with greater scores indicating higher levels of function and lower symptom burden.[20]

2.2.2. Physical activity

The Community Healthy Activities Model Program for Seniors (CHAMPS) questionnaire was used to measure physical activity.[21] Participants rated their participation (i.e., frequency and duration) in light, moderate and vigorous physical activities during a typical week over the past four weeks. The estimated kilocalories expended per week in moderate (and greater) intensity and total activities were calculated. Moderate intensity physical activity included activities with an intensity of three or more metabolic equivalents (METs) such as brisk walking, jogging, golfing without a cart, tennis, heavy household chores and gardening.[19] Total activities score included the aforementioned moderate to vigorous activities as well as lower intensity physical activities such as light housework, yoga, stretching/flexibility exercises, and leisure walking. The CHAMPS has adequate test-retest reliability (ICC ranging from 0.67 to 0.76) and excellent established construct validity.[21],[22]

2.2.3. Treadmill tests

Participants first practiced walking on the treadmill and with a face mask to assess oxygen uptake. Oxygen uptake (VO2) was assessed breath by breath using a SensorMedics Vmax Cardiopulmonary Exercise System (Yorba Linda, CA).

Submaximal test: participants exercised at a submaximal load [1mph (miles per hour), 0 grade] to determine their submaximal test VO2peak and submaximal oxygen uptake kinetics. Prior to walking on the treadmill, participants stood on a platform immediately above the treadmill belt for 3 min to determine their baseline oxygen consumption. Participants then stepped off the platform onto the moving treadmill and performed a 6-min walk, and then stood quietly for the 3-min recovery period.

Maximal test: following the submaximal testing and rest period, a symptom-limited maximum-exercise tolerance test was performed to determine maximal test VO2peak. Due to our experience in maximal exercise testing of mobility-impaired older adults, a modified Balke treadmill test was utilized, starting at participants' selected comfortable walking speed and 0 grade and then increasing the grade by 2% every 2 min until exhaustion.[11] Of note, the meananaerobic threshold (AT) for the HF group was 11.0 with percent AT (AT divided by VO2peak) 74.1%, suggesting that the low HF group VO2peak shown below did not represent a true VO2max.

2.2.4. Functional mobility assessments

A series of functional mobility assessments were performed during a second laboratory visit. These tasks were chosen because of the likelihood that they reflected aspects of daily walking and standing balance needs. Get-up-and-go test (GUG). Participants rose from a standard chair, walked 3 m, turned around, walked back 3 m, and sat back in the chair.[23] The maximum time allowed was set at 30 s. One practice trial preceded the actual trial analyzed. Unipedal stance (US). Participants stood, up to a maximum of 30 s, with arms crossed over chest and foot of choice on the floor with the other leg at least two inches from the weight bearing leg and from the floor. Three trials were performed, alternating the weight bearing foot, with the best time used for the data analysis. Comfortable gait speed (CGS, m/s) was determined by having participants walk at their usual pace over 10 m. The actual timed portion was 6.1 m, with a section before and after the timed portion to reduce the effects of acceleration upon starting and deceleration upon stopping.

2.3. Data analysis

The HF group was compared to controls in self-reported function, physical activity, functional mobility and oxygen uptake using independent t-tests. Pearson's correlation was used to evaluate the relationships between these variables according to group (HF and controls). Since body mass index (BMI) can affect exercise capacity, all of the HF-control group relationships were further explored using ANOVA to control for BMI.

Submaximal oxygen uptake kinetics: the 3-min (baseline) values for oxygen uptake during rest were defined as the average values obtained from 120 s to 180 s during the period when the participant was standing on the elevated platform. The 6-min (end-exercise) values for oxygen uptake during the submaximal walk on the treadmill were defined as the average values obtained from 300–360 s during the exercise period. The 3-min recovery values were also determined as the average values obtained from 120–180 s of the recovery period. The time constant of oxygen uptake kinetics at the onset of exercise, tcdeficit, was determined by fitting a monoexponential function to the oxygen uptake response using the value at rest as the baseline.[9] The general form of this equation can be written as Y(t) = ΔY(steady state)(1–e−(kt)) where Y(t) is the VO2 above baseline at any time (t), ΔY is the steady state increase in Y for VO2, and k is the rate constant of the reaction with the dimension of t−1. The monoexponential model with delay is appropriate to characterize the parameters of the kinetic response in older participants.[24] The time constant of oxygen uptake kinetics upon recovery from the exercise, the excess post-exercise oxygen consumption (tcEPOC), was determined using the same method. This method appropriately models the submaximal oxygen uptake kinetics following exercise in older cardiac patients.[25] Test-retest reliability for two separate determinations of oxygen uptake kinetics is excellent (r = 0.96) for maximal graded exercise testing.[26]

3. Results

3.1. Participant description

Participant characteristics for the HF group (n = 25) and controls (n = 25) appear in Table 1. The mean age for both groups was 75 ± 7 with 92% males. The HF group had higher BMI and disability scores (EPESE), and higher total number of chronic conditions such as hypertension and diabetes. The HF group mean KCCQ functional status and clinical scores (67 and 68, respectively) were analogous to a stable outpatient HF cohort reported previously.[22] The HF patients were well-managed medically according to treatment guidelines: nearly all were taking both β-blockers (88%) and angiotension-converting enzyme inhibitor (88%), and 44% were taking aldosterone inhibitors. Most of the HF patients reported a history of coronary artery disease (88%), hypertension (88%), and arrhythmias (76%), while a smaller percentage (48%) reported a history of diabetes.

Table 1. Group characteristics.

Characteristics Control, n = 25 HF, n = 25 P value
BMI 27.2 ± 0.7 32.3 ± 1.4 0.002
EPESE 1.6 ± 03 4.7 ± 0.9 0.005
Total chronic conditions 1.0 ± 0.2 3.3 ± 0.3 0.03
Etiology HF, ischemic/non-ischemic 72%/28%
Left ventricular ejection fraction 25 ± 2
KCCQ functional status score 67 ± 2.8
KCCQ clinical score 68 ± 2.7

Data are presented as mean ± SE unless other indicated. BMI: body mass index; EPESE: established populations for the epidemiologic study of the elderly (higher score indicates more disability); HF: heart failure; KCCQ: Kansas City cardiomyopathy questionnaire (higher score indicates higher levels of function and fewer symptoms).

3.2. VO2peak and submaximal oxygen-uptake kinetics

The mean VO2peak of 12.9 was 43% lower in the HF group than the control group (see Table 2). The time constant at onset of exercise, tcdeficit, was twice as high in HF as in controls (P = 0.002). The time constant upon recovery from exercise, tcEPOC, was 55% higher in HF compared to controls (P = 0.001).

Table 2. Peak oxygen uptake and oxygen uptake kinetics for peak and submaximal treadmill test.

Variable Control (n = 25) HF (n = 25) P-value
Maximal treadmill test
 VO2peak, mL/kg per min 22.5 ± 1.2 12.9 ± 0.7 0.0001
Submaximal treadmill test
 VO2peak, mL/kg per min 7.4 ± 0.3 7.2 ± 0.3 0.57
 tcdeficit 29.9 ± 3.6 60.0 ± 8.3 0.002
 tcEPOC 33.8 ± 3.1 52.2 ± 3.8 0.001

Data are presented as mean ± SE. tcdeficit: lag in oxygen uptake at the beginning of exercise (oxygen deficit); tcEPOC: excess oxygen uptake above rest following exercise (excess post-exercise oxygen consumption); VO2peak: peak oxygen uptake.

3.3. Functional mobility performance and physical activity

Compared to controls, the HF group had significantly worse performance on GUG, CGS, and US tests (See Table 3).

Table 3. Functional mobility and self reported physical activity.

Variable Control (n = 25) HF (n = 25) P value
Functional mobility
 GUG, s 10.4 ± 0.4 14.3 ± 1.7 0.03
 CGS, m/s 1.2 ± 0.1 0.9 ± 0.1 0.0001
 Impaired US (% of group able only < 5 s) 22% (5/23) 71% (15/21) 0.002*
Self-reported physical activity
 CHAMPS (kcal/day, total) 3421 ± 428 1893 ± 353 0.01
 CHAMPS (kcal/day, ≥ moderate) 2024 ± 296 796 ± 219 0.004

Data are presented as mean ± SE unless other indicated. *Fisher's exact test. CGS: comfortable gait speed; EPESE: established populations for the epidemiologic study of the elderly (higher score indicates more disability); CHAMPS: community healthy activities model program for seniors (daily physical activity reported as expenditure of total kilocalories and kilocalories for intensity of activity at a level of moderate or more); GUG: get up and go; US: unipedal stance.

In addition, the HF group reported much lower total physical activity, particularly moderate or greater intensity physical activity, compared to control. Table 4 shows the relationships between VO2peak, submaximal oxygen uptake kinetics, functional mobility, and physical activity. In controls, VO2peak was more strongly associated with functional mobility and physical activity (r = 0.48−0.72) than were measures of submaximal oxygen uptake kinetics, tcdeficit and tcEPOC (r = 0.14−0.39). Among the HF, tcdeficit and tcEPOC correlations (r = 0.48−0.57) with GUG and CGS were similar to those with VO2peak (r = 0.45−0.59). Therefore, in HF, submaximal oxygen kinetics were as strongly related to functional mobility measures as VO2peak. However, in HF, neither VO2peak nor the submaximal oxygen kinetics measures were strongly related to self-reported total or moderate intensity physical activity. Despite the significantly greater BMI in HF than controls (see Table 1), all of the HF-control group differences cited below remained significant after using ANOVA to control for the covariate BMI.

Table 4. Relationships between VO2peak on peak treadmill, submaximal oxygen uptake kinetics, functional mobility, and physical activity.

Variable VO2peak tcdeficit tcEPOC
Controls
 VO2peak –0.55 –0.47
Functional mobility
 GUG –0.57* 0.37 0.30
 CGS 0.54* –0.39 –0.30
 US 0.48* –0.14 –0.04
Physical activity
 CHAMPS (total) 0.63* –0.21 –0.11
 CHAMPS (≥ moderate) 0.72* –0.29 –0.22
CHF
 VO2peak –0.37 –0.40
Functional mobility
 GUG –0.45* 0.48* 0.11
 CGS 0.59* –0.57* –0.58*
 US 0.32 0.25 0.20
Physical activity
 CHAMPS (total) 0.04 0.1 –0.05
 CHAMPS (≥ moderate) 0.13 0.19 –0.03

*P < 0.05. CHF: congestive heart failure; CHAMPS: community healthy activities model program for seniors; CGS: comfortable gait speed; GUG: get up and go; tcdeficit: lag in oxygen uptake at the beginning of exercise (oxygen deficit); tcEPOC: excess oxygen uptake above rest following exercise (excess post-exercise oxygen consumption); US: unipedal stance; VO2peak: peak oxygen uptake.

4. Discussion

The HF participants, as expected, demonstrated significant impairments in VO2peak, submaximal oxygen uptake kinetics, and functional mobility compared with age and gender-matched controls. In controls, VO2peak was more strongly related to functional mobility and physical activity than submaximal oxygen kinetics. In the HF group, submaximal oxygen uptake kinetics were as strongly related to functional mobility as VO2peak. These data are consistent with previous findings by our group that submaximal oxygen kinetics are as strongly related to functional mobility as VO2peak in mobility-impaired individuals without heart failure.[9] The present study now provides vital data in HF patients who as well.

Aside from the practical advantages in using a submaximal test instead of a maximal test, submaximal oxygen kinetics may also provide a better mechanistic link to determine the relationship between aerobic function and daily mobility in HF. A delay in oxygen kinetics in HF (specifically in tcdeficit) reflects a delay in muscular oxygen uptake,[27] and muscular function is considered the key factor in performing daily mobility tasks. Furthermore, the calculation for oxygen uptake kinetics on recovery adds additional information, addressing the oxygen debt that needs to be repaid after exercise and that reflects oxygen delivery and oxygen utilization to muscles and changes in muscle composition from type I to less efficient type IIb fiber type.[28] Finally, in addition to prognostic value in HF (see introduction), oxygen uptake kinetics may be a key outcome for training in HF because of these skeletal muscle oxygen utilization issues.[29]

Given their poor performance in maximal treadmill and functional mobility tests, HF patients are at high risk of adverse functional outcomes. In particular, disability, hospitalization, and institutionalization are more likely to occur in older adults with mean VO2peak < 18 mL/kg per min, and mean CGS <1 m/s.[18],[30] Moreover, with a mean GUG > 13.5 and the majority of the HF group only able to stand < 5 s in US, patients with HF are at high risk for falls,[31] and injurious falls in particular.[32] Compounding this issue is that patients with HF commonly have gait abnormalities, such as in step variability,[33] increasingly recognized as a significant predictor of falls.[34] A recent paper linked HF to an increased incidence of hip fractures,[35] but did not consider impaired postural control and gait disturbances as potential underlying causes.

In the present study, a self-report instrument was administered according to American Heart Association (AHA) statement algorithms for physical activity measurement.[36] There are advantages and disadvantages of different physical activity measurement techniques, as recently reviewed in an AHA scientific statement.[36] Physical activity in HF as evaluated by self-reported questionnaire relates to VO2peak, especially with activities greater than 3 METs.[37],[38] Similarly, accelerometric measures associate with VO2peak, 6-min walk distance, and subsequent morbid events.[39],[40]

The HF group in this study reported low physical activity, expending only 796 kcal/week in moderate and vigorous activity and 1893 total kcal/week. Nevertheless, a number of HF participants with very low self-reported physical activity paradoxically had relatively higher VO2peak. The reason for this is not entirely clear but may reflect the gap between usual activity, where patients tend to restrict their activity to manage symptoms, and residual capacity, where patients are willing work harder and endure more symptoms under supervised maximal treadmill conditions.[41]

Alternatively, the lack of correlation may indicate a limitation in use of self reported physical activity measures, and suggests that future studies might also utilize more objective measures of physical activity such as accelerometers. Based on a recent comparison,[42] self-report of physical activity was reasonably successful in classifying HF patients with minimal symptoms (NYHA class I) and those with symptoms during less than usual activity (NYHA class III), whereas accelerometry independently predicted VO2peak and was better at identifying NYHA class III patients. Advantages and disadvantages of both measures continue to be identified, although the CHAMPS questionnaire used in the present study is well-established and recommended for older adults.[43] The present study reports baseline data for an exercise intervention to improve mobility as well as physical activity, and thus self-reported physical activity was important for customization of the intervention and a primary focus for repeated assessment. Future studies in older adults should consider using both CHAMPS and accelerometry, as providing complementary information.[44]

Finally, other factors may account for more modest relationships between measured aerobic function and physical activity in HF. Of the oxygen uptake and kinetics measures, only VO2peak correlated significantly with KCCQ, and only with the overall clinical summary score (r = 0.54, P < 0.05). The clinical summary score reflects a number of behavioral and health status assessments, including self-reported physical limitations, symptoms, social interference and quality of life. Other studies confirm that behavioral measures, such as self efficacy, predict physical activity in HF better than VO2peak.[45] Given modest associations between health and functional status in HF and VO2peak, laboratory exercise tolerance may not be a good reflection of how patients perceive their capacity to undertake daily activities.[7]

One other possible explanation of the relationship between aerobic function and physical activity relates to the workload of the maximal and submaximal tests. The submaximal test at 1 mph presents a minimal load to the controls but a more substantial load to the HF, particularly those with more advanced HF,[46] and thus the VO2 levels measured in the HF are more physiologically (and functionally) meaningful. Daily tasks require more effort and oxygen uptake for HF than healthy controls.[47] Reproducibility for submaximal oxygen uptake kinetics may decrease at lower loads, particularly for healthy adults.[10] Recent work highlights the use of six minute walk distance as a predictor for HF mortality and hospitalization.[48] The six minute walk test has been used with accelerometry to provide additional telehealth information about step count and overall activity level,[49] and with oxygen kinetics analysis using a portable gas analyzer as a predictor of HF adverse outcomes.[50] In both these situations, the distance covered during the six minute walk (and thus the work accomplished) can vary, making these outcomes somewhat difficult to interpret.

Other measures of submaximal oxygen uptake that relate to important clinical outcomes may also be considered. Individualization of submaximal load based on other measurements such as anaerobic threshold may be more physiologically meaningful but may be difficult to obtain in older HF patients.[51] Using portable measurement devices, others have reported that percent of peak VO2 utilized during activities of daily living, even when self-paced, is higher in HF patients than controls.[47] Finally, estimation of the oxygen uptake efficiency slope uses an extrapolation of oxygen utilization at certain percentages of maximal testing, and holds promise in use with HF patients,[52] and in predicting HF patient survival.[53] Whether the oxygen uptake efficiency slope is a better predictor of mobility function and physical activity than oxygen uptake kinetics remains to be determined.

Limitations of these data include the modest sample size of self-selected volunteers for this pilot exploratory study. A larger sample size of more representative participants should be considered in future study replication.

In conclusion, based on their mobility task performance, older HF patients with reduced ejection fraction are at risk for adverse functional outcomes. In this population, submaximal oxygen uptake measures may be equivalent to VO2peak in predicting functional mobility, and in addition to being more feasible, may provide better insight into how aerobic function relates to mobility in older adults with HF.

Acknowledgments

The authors acknowledge primary support of the Department of Veterans Affairs Research and Development and additional support from the National Institute of Aging (NIA) Michigan Claude Pepper Older Americans Independence Center (AG08808 and AG024824). Dr. Hummel is supported by a K23 Mentored Patient-Oriented Career Development Award HL109176 from the National Heart Lung and Blood Institute (NHLBI). Dr. Alexander was a recipient of a K24 Mid-Career Investigator Award in Patient-Oriented Research AG109675 from NIA. Dr. Gretebeck was the recipient of an American Diabetes Association Junior Faculty Award (1-06-JF-20). The assistance of Nicole Osevala, Mark Hofmeyer, Becky Cleland, Diane Scarpace, Nancy Ambrose-Gallagher, Ravinder Goswami, and Eric Pear in participant recruitment, assessment, and data collection is gratefully acknowledged. The authors do not receive any financial benefit from the study results or funding sources.

References

  • 1.Murad K, Kitzman DW. Frailty and multiple comorbidities in the elderly patient with heart failure: implications for management. Heart Fail Rev. 2012;17:581–588. doi: 10.1007/s10741-011-9258-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Jha S, Ha H, Hickman L, et al. Frailty in advanced heart failure: A systematic review. Heart Fail Rev. 2015;20:553–560. doi: 10.1007/s10741-015-9493-8. [DOI] [PubMed] [Google Scholar]
  • 3.Cacciatore F, Abete P, Mazzella F, et al. Frality predicts long-term mortality in elderly subjects with chronic heart failure. Eur J Clin Invest. 2005;35:723–730. doi: 10.1111/j.1365-2362.2005.01572.x. [DOI] [PubMed] [Google Scholar]
  • 4.Chaudhry SI, Wang Y, Gill TM, et al. Geriatrics conditions and subsequent mortality in older patients with heart failure. J Am Coll Cardiol. 2010;55:309–316. doi: 10.1016/j.jacc.2009.07.066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Evenson KR, Butler EN, Rosamond WD. Prevalence of physical activity and sedentary behavior among adults with cardiovascular disease in the United States. J Cardiopulm Rehab Prevention. 2014;34:406–419. doi: 10.1097/HCR.0000000000000064. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Lund LH, Aaronson KD, Mancini DM. Validation of peak exercise oxygen consumption and the heart failure survival score for serial risk stratification in advanced heart failure. Am J Cardiol. 2005;95:734–741. doi: 10.1016/j.amjcard.2004.11.024. [DOI] [PubMed] [Google Scholar]
  • 7.Myers J, Zaheer N, Quaglietti S, et al. Association of functional and health status measures in heart failure. J Cardiac Failure. 2006;6:439–445. doi: 10.1016/j.cardfail.2006.04.004. [DOI] [PubMed] [Google Scholar]
  • 8.Whipp BJ, Wasserman K. Oxygen-uptake kinetics for various intensities of constant-load work. J Appl Physiol. 1972;33:351–356. doi: 10.1152/jappl.1972.33.3.351. [DOI] [PubMed] [Google Scholar]
  • 9.Alexander NB, Dengel DR, Olson RJ, et al. Oxygen-uptake (VO2) kinetics and functional mobility performance in impaired older adults. J Gerontol A Biol Sci Med Sci. 2003;8:734–739. doi: 10.1093/gerona/58.8.m734. [DOI] [PubMed] [Google Scholar]
  • 10.Sietsema KE, Ben-Dov MD, Zhang YY, et al. Dynamics of oxygen uptake for submaximal exercise and recovery in patients with chronic heart failure. Chest. 1994;105:1693–1700. doi: 10.1378/chest.105.6.1693. [DOI] [PubMed] [Google Scholar]
  • 11.Nanas S, Nanas J, Kassiotis C, et al. Early recovery of oxygen kinetics after submaximal exercise test predicts functional capacity in patients with chronic heart failure. Eur J Heart Fail. 2001;3:685–692. doi: 10.1016/s1388-9842(01)00187-8. [DOI] [PubMed] [Google Scholar]
  • 12.Brunner-Larocca HP, Weilenmann D, Follath F, et al. Oxygen uptake kinetics during low exercise in patients with heart failure: relation to neurohormones, peak oxygen concentration and clinical findings. Heart. 1999;31:121–127. doi: 10.1136/hrt.81.2.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Matsumoto A, Itoh H, Yokoyama I, et al. Kinetics of oxygen uptake at onset of exercise related to cardiac output, but not to arteriovenous oxygen difference in patients with chronic heart failure. Am J Cardiol. 1999;83:1573–1576. doi: 10.1016/s0002-9149(99)00154-x. [DOI] [PubMed] [Google Scholar]
  • 14.Belardinelli R, Zhang Y, Wasserman K, et al. A four-minute submaximal constant work rate exercise test to assess cardiovascular functional class in chronic heart failure. Am J Cardiol. 1998;81:1210–1214. doi: 10.1016/s0002-9149(98)00093-9. [DOI] [PubMed] [Google Scholar]
  • 15.Brunner-La Rocca HP, Weilenmann D, Schalcer C. Prognostic significance of oxygen uptake kinetics during low level exercise in patients with heart failure. Am J Cardiol. 1999;84:741–744. doi: 10.1016/s0002-9149(99)00426-9. [DOI] [PubMed] [Google Scholar]
  • 16.Koike A, Koyama Y, Itoh H. Prognostic significance of cardiopulmonary exercise testing for 10-year survival in patients with mild-moderate heart failure. J Circ. 2000;64:915–920. doi: 10.1253/jcj.64.915. [DOI] [PubMed] [Google Scholar]
  • 17.Shalcher C, Rickli H, Brehm M, et al. Delayed oxygen uptake kinetics during low-intensity exercise are related to poor prognosis in patients with mild-to-moderate congestive heart failure. Chest. 2003;124:580–586. doi: 10.1378/chest.124.2.580. [DOI] [PubMed] [Google Scholar]
  • 18.Morey MC, Pieper CF, Cornoni-Huntley J. Is there a threshold between peak oxygen uptake and self-reported physical functioning in older adults? Med Sci Sports Exerc. 1998;30:1223–1229. doi: 10.1097/00005768-199808000-00007. [DOI] [PubMed] [Google Scholar]
  • 19.Smith LA, Branch LG, Scherr PA. Short-term variability of measures of physical function in older people. J Am Geriatr Soc. 1990;38:993–998. doi: 10.1111/j.1532-5415.1990.tb04422.x. [DOI] [PubMed] [Google Scholar]
  • 20.Green CP, Porter CB, Bresnahan DR, et al. Development and evaluation of the Kansas City Cardiomyopathy Questionnaire: a new health status measure for heart failure. J Am Coll Cardiol. 2000;35:1245–1255. doi: 10.1016/s0735-1097(00)00531-3. [DOI] [PubMed] [Google Scholar]
  • 21.Stewart AL, Mills KM, King AC, et al. CHAMPS physical activity questionnaire for older adults: outcomes for interventions. Med Sci Sports Exerc. 2001;33:1126–1141. doi: 10.1097/00005768-200107000-00010. [DOI] [PubMed] [Google Scholar]
  • 22.Harada ND, Chiu V, King AC, et al. An evaluation of three self-report physical activity instruments for older adults. Med Sci in Sports Exerc. 2001;33:962–970. doi: 10.1097/00005768-200106000-00016. [DOI] [PubMed] [Google Scholar]
  • 23.Podsiadlo D, Richardson S. The timed ‘Up & Go’; A test of basic functional mobility for frail elderly persons. J Am Geriatr Soc. 1991;39:142–148. doi: 10.1111/j.1532-5415.1991.tb01616.x. [DOI] [PubMed] [Google Scholar]
  • 24.Cunningham DA, Himann JE, Paterson DH, et al. Gas exchange dynamics with sinusoidal work in young and elderly women. Resp Physiol. 1993;91:43–56. doi: 10.1016/0034-5687(93)90088-r. [DOI] [PubMed] [Google Scholar]
  • 25.Koike A, Hiroe M, Marumo F. Delayed kinetics of oxygen uptake during recovery after exercise in cardiac patients. Med Sci Sports Exerc. 1998;30:185–189. doi: 10.1097/00005768-199802000-00002. [DOI] [PubMed] [Google Scholar]
  • 26.Cohen-Solal A, Laperche T, Morvan D, et al. Prolonged kinetics of recovery of oxygen consumption after maximal graded exercise in patients with chronic heart failure. Circulation. 1995;91:2924–2932. doi: 10.1161/01.cir.91.12.2924. [DOI] [PubMed] [Google Scholar]
  • 27.Koike A, Hiroe M, Adachi H, et al. Oxygen uptake kinetics are determined by cardiac function at onset of exercise rather than peak exercise in patients with prior myocardial infarction. Circulation. 1994;90:2324–2332. doi: 10.1161/01.cir.90.5.2324. [DOI] [PubMed] [Google Scholar]
  • 28.Mitchell SH, Steele NP, Leclerc KM, et al. Oxygen cost of exercise is increased in heart failure after accounting for recovery costs. Chest. 2003;124:572–579. doi: 10.1378/chest.124.2.572. [DOI] [PubMed] [Google Scholar]
  • 29.Sarma S, Levine BD. Soothing the sleeping giant: improving skeletal muscle oxygen kinetics and exercise intolerance in HFpEF. J Appl Physiol. 2015;119:734–738. doi: 10.1152/japplphysiol.01127.2014. [DOI] [PubMed] [Google Scholar]
  • 30.Studenski S, Perera S, Wallace D, et al. Physical performance measures in the clinical setting. J Am Geriatr Soc. 2003;51:314–322. doi: 10.1046/j.1532-5415.2003.51104.x. [DOI] [PubMed] [Google Scholar]
  • 31.Shumway-Cook A, Brauer S, Woollacott M. Predicting the probability for falls in community-dwelling older adults using the timed get up and go test. Phys Ther. 2000;80:896–903. [PubMed] [Google Scholar]
  • 32.Vellas BJ, Wayne SJ, Romero L, et al. One-leg balance is an important predictor of injurious falls in older persons. J Am Geriatr Soc. 1997;45:735–738. doi: 10.1111/j.1532-5415.1997.tb01479.x. [DOI] [PubMed] [Google Scholar]
  • 33.Hausdorff JM, Forman DE, Ladin Z, et al. Increased walking variability in elderly persons with congestive heart failure. J Am Geriatr Soc. 1994;42:1056–1061. doi: 10.1111/j.1532-5415.1994.tb06209.x. [DOI] [PubMed] [Google Scholar]
  • 34.Hausdorff JM, Rios DA, Edelberg HK. Gait variability and fall risk in community-living older adults: a 1-year prospective study. Arch Phys Med Rehabil. 2001;82:1050–1056. doi: 10.1053/apmr.2001.24893. [DOI] [PubMed] [Google Scholar]
  • 35.Van Diepen S, Majumdar SR, Bakal JA, et al. Heart failure is a risk factor for orthopedic fracture: A population-based analysis of 16 294 patients. Circulation. 2008;118:1946–1952. doi: 10.1161/CIRCULATIONAHA.108.784009. [DOI] [PubMed] [Google Scholar]
  • 36.Strath S, Kaminsky LA, Ainsworth BE, et al. Guide to the assessment of physical activity: clinical and research applications. Circulation. 2013;128:2259–2279. doi: 10.1161/01.cir.0000435708.67487.da. [DOI] [PubMed] [Google Scholar]
  • 37.Garet M, Barthelemy JC, DeGache F, et al. A questionnaire-based assessment of daily physical activity in heart failure. Eur J Heart Fail. 2004;6:577–584. doi: 10.1016/j.ejheart.2003.11.022. [DOI] [PubMed] [Google Scholar]
  • 38.Chryssanthopoulos SN, Dritsas A, Cokkinos DV. Activity questionnaires; a useful tool in assessing heart failure patients. Intl J Cardiol. 2005;105:294–299. doi: 10.1016/j.ijcard.2004.12.046. [DOI] [PubMed] [Google Scholar]
  • 39.Jehn M A, Schmidt-Trucksäss A, Schuster T, et al. Daily walking performance as an independent predictor of advanced heart failure: prediction of exercise capacity in chronic heart failure. Am Heart J. 2009;157:292–298. doi: 10.1016/j.ahj.2008.10.006. [DOI] [PubMed] [Google Scholar]
  • 40.Howell J, Strong BM, Weisenberg J, et al. Maximum daily 6 minutes of activity: an index of functional capacity derived from actigraphy and its application to older adults with heart failure. J Am Geriatr Soc. 2010;58:931–936. doi: 10.1111/j.1532-5415.2010.02805.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Oka RK, Stotts NA, Dae MW, et al. Daily physical activity levels in congestive heart failure. Am J Cardiol. 1993;71:921–925. doi: 10.1016/0002-9149(93)90907-t. [DOI] [PubMed] [Google Scholar]
  • 42.Jehn M, Schmidt-Trucksass A, Hanssen H, et al. Association of physical activity and prognostic parameters in elderly patients with heart failure. J Aging Phys Act. 2011;19:1–15. doi: 10.1123/japa.19.1.1. [DOI] [PubMed] [Google Scholar]
  • 43.Falck RS, McDonald SM, Beets MW, et al. Measurement of physical activity in older adult interventions: a systematic review. Br J Sports Med. 2016;50:464–470. doi: 10.1136/bjsports-2014-094413. [DOI] [PubMed] [Google Scholar]
  • 44.Colbert LH, Matthews CE, Havighurst TC, et al. Comparative validity of physical activity measures in older adults. Med Sci Sports Exerc. 2011;43:867–876. doi: 10.1249/MSS.0b013e3181fc7162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Oka RK, Gortner SR, Stotts NA, et al. Predictors of physical activity in patients with chronic heart failure secondary to either ischemic or idiopathic dilated cardiomyopathy. Am J Cardiol. 1996;77:159–163. doi: 10.1016/s0002-9149(96)90588-3. [DOI] [PubMed] [Google Scholar]
  • 46.Jehn M, Halle M, Schuster T, et al. The six-minute walk test in heart failure: is it a maximum or submaximum exercise test? Eur J Appl Physiol. 2009;107:317–323. doi: 10.1007/s00421-009-1128-0. [DOI] [PubMed] [Google Scholar]
  • 47.Spruit MA, Wouters EFM, Eterman RMA, et al. Task-related oxygen uptake and symptoms during activities of daily life in CHF patients and healthy subjects. Eur J Appl Physiol. 2011;111:1679–1686. doi: 10.1007/s00421-010-1794-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Forman DE, Fleg JL, Kitzman DW, et al. 6-min walk test provides utility comparable to cardiopulmonary exercise testing in ambulatory outpatients with systolic heart failure. J Am Coll Card. 2012;60:2653–2661. doi: 10.1016/j.jacc.2012.08.1010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Jehn M, Schmidt-Trucksäess A, Schuster T, et al. Accelerometer-based quantification of 6-minute walk test performance in patients with chronic heart failure: applicability in telemedicine. J Card Fail. 2009;15:334–340. doi: 10.1016/j.cardfail.2008.11.011. [DOI] [PubMed] [Google Scholar]
  • 50.Kern L, Condrau S, Baty F, et al. Oxygen kinetics during 6-minute walk tests in patients with cardiovascular and pulmonary disease. BMC Pulm Med. 2014;14:167. doi: 10.1186/1471-2466-14-167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Cohen-Solal A, Aupeiti JF, Gueret P, et al. Can anaerobic threshold be used as an endpoint for therapeutic trials in heart failure? Eur Heart J. 1994;15:236–241. doi: 10.1093/oxfordjournals.eurheartj.a060482. [DOI] [PubMed] [Google Scholar]
  • 52.Van Laethem C, Bartunek J, Goethals M, et al. Oxygen uptake efficiency slope, a new submaximal parameter in evaluating exercise capacity in chronic heart failure exercise. Am Heart J. 2005;149:175–180. doi: 10.1016/j.ahj.2004.07.004. [DOI] [PubMed] [Google Scholar]
  • 53.Davies LC, Wensel R, Georgiadou P, et al. Enhanced prognostic value from cardiopulmonary exercise testing in chronic heart failure by non-linear analysis: oxygen uptake efficiency slope. Am Heart J. 2006;27:684–690. doi: 10.1093/eurheartj/ehi672. [DOI] [PubMed] [Google Scholar]

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