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Construct and Predictive Validity of a Self-Reported Measure of Preclinical Mobility Limitation
Minna Mänty, Ari Heinonen, Raija Leinonen, Timo Törmäkangas, Ritva Sakari-Rantala, Mirja Hirvensalo, Mikaela B. von Bonsdorff, Taina Rantanen
Archives of Physical Medicine and Rehabilitation
September 2007 (Vol. 88, Issue 9, Pages 1108-1113)
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Abstract Weiss CO, Hoenig HM, Fried LP. Compensatory strategies used by older adults facing mobility disability. Preclinical disability in mobility tasks can be recognized by asking people without overt mobility disability whether they have changed the way, either the manner or the frequency, of doing a mobility task because of a health or physical condition. Like other compensatory strategies, preclinical mobility disability has a dual nature as both a risk marker associated with impairment or limitation and a mediating factor affecting the natural history of disability. The method of ascertaining preclinical disability through self-report has been shown to have construct validity, to be reliable, and to identify people at an elevated risk of developing overt mobility disability over 1 to 2 years. Many worthy research questions in this field remain to be addressed, especially regarding qualitative heterogeneity (doing more vs doing less) and interactions among compensatory strategies. Nonetheless, there is sufficient evidence to apply what is known about preclinical disability to screening in clinical settings. This area of research and practice constitutes an opportunity for physical medicine and rehabilitation and geriatric medicine to jointly make a large beneficial impact on population health through strategies to prevent disability because rapidly growing numbers of older adults will experience this early and potentially malleable stage. THE SCIENCE IS DEVELOPED and the opportunities are large for physical medicine and rehabilitation (PM&R) and geriatric medicine to join productively in the prevention of mobility disabilities, now also called restricted participation in mobility tasks,1 in older adults. The prevention of morbidity in older adults is finally recognized as a primary public health target. For example, the U.S. Department of Health and Human Services estimated that the dollar costs of disabilities in the United States equal heart disease and are 1.75 times those of cancer.2 Mobility disabilities are concentrated in, although not limited to,3 older age groups whose numbers will grow dramatically in coming years. Because at least half of mobility disabilities develop gradually and progressively, there is a substantial opportunity for primary or secondary prevention even in old age.4, 5, 6 In this issue, Mänty et al7 provide findings from a European sample that extend and confirm previous work on the detectable nature of preclinical changes such as compensatory strategies that presage the development of disability.8 Mobility disability is a spectrum ranging from having difficulty with mobility only in highly challenging terrain to being bed bound. Simplifying this complex process into 3 major steps (none, preclinical disability, overt disability) appears to be useful. Thus, preclinical disability refers to mobility changes experienced in day-to-day life before they become overt disability. Preclinical disability in mobility tasks can be recognized by asking people without overt mobility problems whether they have changed the way, either the manner or the frequency, of doing a mobility task because of a health or physical condition. This simple question has been shown to identify older persons with intermediate levels of measured activity limitations (leg strength, balance, self-selected walking speed) compared with robust or disabled persons,9 to be reliable,10 and to have good construct validity.11, 12 Most importantly, across multiple studies, preclinical disability has been shown to identify people at an elevated risk of developing mobility disability.13, 14, 15, 16 Self-reported preclinical disability predicts disability independently of other risk factors, including disease and impairments, and as well, or better, than performance tests.13, 14, 17 Mänty et al7 provide additional data by examining baseline then follow-up in a Finnish trial of women (75%) and men aged 75 to 81 years. They found that preclinical disability was associated with an intermediate level of leg extensor muscle power and maximal walking speed at baseline compared with robust and disabled groups and an elevated risk of new disability at 2 years compared with robust older adults. We propose that the study of preclinical mobility disability has reached a late adolescence full of promise. Taken together, these findings motivate us to ask whether we know enough to move forward clinically, screening for preclinical disability in older adults, and who should respond to this challenge. Do We Know Enough About Preclinical Disability?  As developed and implemented, preclinical disability is a method for identifying precursors to disability through ascertainment of compensatory strategies when disability is not yet present. Thus, the approach offers a preventive framework and the opportunity for early intervention. For many daily tasks, there are alternative ways of getting things done. A compensatory strategy can be defined as a way of achieving a result that is adopted frequently in the face of a physical impairment or limitation and under usual conditions. Compensatory strategies are also usually recognizable as something healthy people do not “normally” do. As an example, most people do not use a cane to walk. At one time, canes were used often as a fashion statement. Now, they are used to compensate for an activity limitation related to walking. Under demanding conditions, such as climbing across jagged boulders, even the healthiest person would appreciate a cane; in contrast, on a flat, nonslippery surface, a cane be recognized as a compensatory strategy. General categories of compensation for mobility include behavioral adaptations, using technology or environmental supports, and receiving human help.18, 19 Gignac et al20 applied the Baltes’s theory of selective optimization with compensation to mobility disability, classifying a wide range of adaptations. By using their scheme, preclinical disability encompasses a range of adaptations, including “selection” by performing the activity less often, “optimization” by planning activities to avoid problems, “compensation” by using assistive devices, and “receiving help.” Approaching preclinical disability at this conceptual level leads to consideration of the complexity of the issue; preclinical disability has a dual nature with compensation as both a risk marker associated with impairment or limitation and a mediating risk factor affecting the natural history of disability. A large amount of potential heterogeneity among such compensations remains to be understood. Most importantly, perhaps, are the qualitative differences between strategies that leverage abilities to overcome threats to activity and participation in life and strategies that consist of decreasing task demands. Does a compensatory strategy lead to less or more activity? Some gerontologists believe that people on the chronic pathway to disability should “use it or lose it!” Is relying on someone’s arm for support when walking fearful walking, and does it lead to using one’s own physiologic systems for balance less and walking less? Or, does it lead to overcoming barriers and walking more? Thus, there are many worthy future research questions regarding mobility compensations, some of which will require advanced methods because of compensations’ complex, nonindependent, nature. Why does someone start to compensate? What are the downstream effects of spontaneous compensations? What are the tradeoffs between different compensatory strategies? Can distinct contributions from diseases, changes in energy utilization and metabolism, psychologic factors, and environmental and social variables as causes of compensation and disability be identified? How do these factors affect the gradual transition from preclinical disability to overt disability? The interaction between the individual and his/her environment is an emphasis of the new World Health Organization conceptual model of disability1 and a research area that will surely lead to theoretical and practical insights into how to apply more potent therapeutic strategies. Nonetheless, we propose that enough is known already about preclinical disability to move forward to translational research and clinical application. Should We Be Screening?  To chart directions about the way forward in applying knowledge about preclinical disabilities in clinical settings to improve the health of older adults, a review of the 4 criteria for screening provides a useful structure. Is the Outcome a Significant (Prevalent and Potent) Public Health Burden?  Should the outcome be rare enough, even a near-perfect screening test can be more likely to lead to a false-positive than a true-positive. In this case, mobility disability is a huge public health burden, with a prevalence on the order of 30% to 50% in adults 65 years and older.21 Furthermore, the prevalence of preclinical disabilities in mobility tasks is considerable, ranging from approximately 20% to 40% in prior studies and 31% to 55% in the sample of adults age over 75 reported by Mänty et al7 in this issue. Is There an Acceptable Level of Potential Harm?  Some screening tests lead to dangerous procedures or treatments and serious psychologic burden. These concerns are mitigated if the consequence of screening is tailored recommendations for physical activity, as in this case. Low risk from resulting interventions lowers the bar for screening. Although we should not minimize the need to carefully monitor for adverse effects in trials of physical activity in older adults, the level of concern about potential harm is arguably acceptable in this case. Can a Treatable Preclinical Phase Be Identified Accurately?  This screening criterion is poorly suited to preclinical disability because mobility disability is a latent construct with no criterion standard. However, the epidemiologic studies of predictive validity mentioned previously form a reasonable basis for moving forward. In addition, nomograms are available, providing screening accuracy data for clinical use.17 Perhaps ironically, a challenge to establishing the accuracy of measures of preclinical disability lies in the fact that many older adults experience fluctuations in health status. For example, the risk of disability among women with preclinical disability has been found to be 26% to 31% at 18 months, depending on the item measured. The likelihood of improvement or recovery to reporting no preclinical disability was 31% to 34%.13 Similarly, substantial rates of recovery have been found for disability. If some would get better on their own, should we be intervening? Several considerations are relevant. Periods of transient disability followed by recovery form one of the strongest risk factors for recurrent and persistent disability.22, 23 We do not yet know who will spontaneously recover or if such recovery will be optimal. Furthermore, increasing physical activity as an intervention leads to multiple benefits across a range of physiologic systems and dimensions of health, beyond benefits in mobility, forming the basis of a strong argument for tailored activity interventions in the presence of preclinical disability. Is Early Intervention More Effective Than Waiting for Overt Presentation?  There may be sufficient data to move toward effectiveness trials targeting preclinical disability. In a trial of prehabilitation, a home-based intervention was found to benefit older adults who were able to perform an out-and-back 10-foot walk test in less than 10 seconds or able to rise from a chair with arms folded. Notably, the intervention was not effective in those who were unable to do both.24 In a study by Mann et al,25 home visits by an occupational therapist providing assistive technology and environmental modifications to increase function and safety reduced the rate of functional decline. There are other examples, both from epidemiologic studies and interventions, suggesting that restorative therapy alone may miss opportunities to prevent disability. Preclinical disability aims to identify people in a transitional zone, functionally, who are not already near the benefit ceiling from an intervention, yet not so sick that recovery to a previous state of functioning is much less likely to occur. The Benefit Will Be Large  In the Women’s Health and Aging Study II, the probability of becoming disabled in women with preclinical disability was 26% to 31% at 18 months versus 7% to 12% in those with no preclinical disability.13 The risk difference between these groups was therefore 14% to 24%. An intervention with the modest expectation of altering this outcome in 1 in 4 people would be associated with an absolute risk reduction of one fourth of 14% to 24% or 3.5% to 6%. The corresponding number needed to treat (NNT) is 17 to 29. By comparison, the NNT with a statin to prevent a generous composite measure of death or a nonfatal stroke or heart attack is estimated to be 35.26 These rough calculations provide some perspective on the potential for clinical benefit from treating preclinical disability. However, these figures do not consider that only small proportions of the population are either very active or very physically disabled, and the vast majority fall closer to the middle and are more likely to benefit from an intervention than those at the extremes. As is the case in treating blood pressure, focusing public health efforts on middle values (blood pressures in the low-abnormal or even high-normal range) would lead to massive population benefits because that is where most of the population lies. Similarly, effective efforts to treat preclinical disability in older adults will have a large impact on the health of our aging population. Who Can Respond to This Challenge?  PM&R and geriatric medicine offer complementary and overlapping expertise important to the treatment of physical disability in later life. Physiatrists are trained in the mechanistic treatment of impairments and limitations, focused primarily on restorative therapy or tertiary prevention, especially after an acute illness or injury, and are comfortable with the empirical nature of prescribing and adjusting therapeutic regimens to maximize activity for a patient. Geriatricians bring knowledge gained from identifying and intervening on multifactorial syndromes and age-related diseases that interact to create nonspecific clinical presentations, such as fatigue, and lead to aggregate outcomes such as disability, experience in the prevention of disability and in prioritizing among many possible medical treatments, and skill minimizing adverse reactions to medical treatment. The geriatricians’ focus is often on primary and secondary prevention. Collaboration between rehabilitation and geriatrics experts now tends to occur only during acute rehabilitation. Extending this collaboration to other settings is needed to make even larger gains in population health. More than ever, collaborative clinical and research efforts joining PM&R and geriatric medicine are likely to make contributions that, in the context of a demographic imperative to ameliorate health in later life, will lead to large public benefit. References  1. 1World Health Organization. International classification of functioning, disability, and health. Geneva: WHO; 2001;. 2. 2Kirschstein R. Disease-specific estimates of direct and indirect costs of illness and NIH support. Bethesda: Department of Health and Human Services; 2000;. 3. 3Iezzoni LI, McCarthy EP, Davis RB, Siebens H. Mobility difficulties are not only a problem of old age. J Gen Intern Med. 2001;16:235–243. MEDLINE |
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4. 4Ferrucci L, Guralnik JM, Simonsick E, Salive ME, Corti C, Langlois J. Progressive versus catastrophic disability: a longitudinal view of the disablement process. J Gerontol A Biol Sci Med Sci. 1996;51:M123–M130. MEDLINE 5. 5Guralnik JM, Ferrucci L, Balfour JL, Volpato S, Di Iorio A. Progressive versus catastrophic loss of the ability to walk: implications for the prevention of mobility loss. J Am Geriatr Soc. 2001;49:1463–1470. MEDLINE |
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6. 6Onder G, Penninx BW, Ferrucci L, Fried LP, Guralnik JM, Pahor M. Measures of physical performance and risk for progressive and catastrophic disability: results from the Women’s Health and Aging Study. J Gerontol A Biol Sci Med Sci. 2005;60:74–79. MEDLINE 7. 7Mänty M, Heinonen A, Leinone R, et al. Construct and predictive validity of a self-reported measure of preclinical mobility limitation. Arch Phys Med Rehabil. 2007;88:1108–1113. Abstract | Full Text |
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8. 8Fried LP, Herdman SJ, Kuhn KE, Rubin G, Turano K. Preclinical disability: hypotheses about the bottom of the iceberg. J Aging Health. 1991;3:285–300.
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9. 9Fried LP, Young Y, Rubin G, Bandeen-Roche KWHAS II Collaborative Research Group. Self-reported preclinical disability identifies older women with early declines in performance and early disease. J Clin Epidemiol. 2001;54:889–901. Abstract | Full Text |
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10. 10Miller DK, Andresen EM, Malmstrom TK, Miller JP, Wolinsky FD. Test-retest reliability of subclinical status for functional limitation and disability. J Gerontol B Psychol Sci Soc Sci. 2006;61:S52–S56. MEDLINE 11. 11Petrella JK, Cress ME. Daily ambulation activity and task performance in community-dwelling older adults aged 63-71 years with preclinical disability. J Gerontol A Biol Sci Med Sci. 2004;59:264–267. MEDLINE 12. 12Miller DK, Wolinsky FD, Malmstrom TK, Andresen EM, Miller JP. Inner city, middle-aged African Americans have excess frank and subclinical disability. J Gerontol A Biol Sci Med Sci. 2005;60:207–212. MEDLINE 13. 13Fried LP, Bandeen-Roche K, Chaves PH, Johnson BA. Preclinical mobility disability predicts incident mobility disability in older women. J Gerontol A Biol Sci Med Sci. 2000;55:M43–M52. MEDLINE 14. 14Wolinsky FD, Miller DK, Andresen EM, Malmstrom TK, Miller JP. Further evidence for the importance of subclinical functional limitation and subclinical disability assessment in gerontology and geriatrics. J Gerontol B Psychol Sci Soc Sci. 2005;60:S146–S151. MEDLINE 15. 15West SK, Munoz B, Rubin GS, Bandeen-Roche K, Broman AT, Turano KA. Compensatory strategy use identifies risk of incident disability for the visually impaired. Arch Ophthalmol. 2005;123:1242–1247. MEDLINE |
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16. 16Wolinsky FD, Miller DK, Andresen EM, Malmstrom TK, Miller JP, Miller TR. Effect of subclinical status in functional limitation and disability on adverse health outcomes 3 years later. J Gerontol A Biol Sci Med Sci. 2007;62:101–106. MEDLINE 17. 17Chaves PH, Garrett ES, Fried LP. Predicting the risk of mobility difficulty in older women with screening nomograms: the Women’s Health and Aging Study II. Arch Intern Med. 2000;160:2525–2533. MEDLINE |
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18. 18Agree EM, Freedman VA. A comparison of assistive technology and personal care in alleviating disability and unmet need. Gerontologist. 2003;43:335–344. MEDLINE 19. 19Hoenig H, Ganesh SP, Taylor DH, Pieper C, Guralnik J, Fried LP. Lower extremity physical performance and use of compensatory strategies for mobility. J Am Geriatr Soc. 2006;54:262–269. MEDLINE |
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20. 20Gignac MA, Cott C, Badley EM. Adaptation to chronic illness and disability and its relationship to perceptions of independence and dependence. J Gerontol B Psychol Sci Soc Sci. 2000;55:P362–P372. MEDLINE 21. 21Shumway-Cook A, Ciol MA, Yorkston KM, Hoffman JM, Chan L. Mobility limitations in the Medicare population: prevalence and sociodemographic and clinical correlates. J Am Geriatr Soc. 2005;53:1217–1221. MEDLINE |
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22. 22Valderrama-Gama E, Damian J, Guallar E, Rodriguez-Mañas L. Previous disability as a predictor of outcome in a geriatric rehabilitation unit. J Gerontol A Biol Sci Med Sci. 1998;53:M405–M409. MEDLINE 23. 23Gill TM, Kurland B. The burden and patterns of disability in activities of daily living among community-living older persons. J Gerontol A Biol Sci Med Sci. 2003;58:70–75. MEDLINE 24. 24Gill TM, Baker DI, Gottschalk M, Peduzzi PN, Allore H, Byers A. A program to prevent functional decline in physically frail, elderly persons who live at home. N Engl J Med. 2002;347:1068–1074.
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25. 25Mann WC, Ottenbacher KJ, Fraas L, Tomita M, Granger CV. Effectiveness of assistive technology and environmental interventions in maintaining independence and reducing home care costs for the frail elderly (A randomized controlled trial). Arch Fam Med. 1999;8:210–217. MEDLINE |
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26. 26Bandolier. Statins. Bandolier J [serial online]. 1998;47(Jan). Available at: http://www.jr2.ox.ac.uk/bandolier/band47/b47-2.html. Accessed June 29, 2007. a Division of Geriatric Medicine & Gerontology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD b Center on Aging and Health, Johns Hopkins Medical Institutions, Baltimore, MD c Department of Medicine/Geriatrics, Duke University Medical Center, Durham, NC d Physical Medicine & Rehabilitation Service, Durham Veterans Administration Medical Center, Durham, NC. Correspondence to Carlos O. Weiss, MD, MHS, Div of Geriatric Medicine, Mason F. Lord, West Tower, # 711, Baltimore, MD 21224-2734. Reprints are not available from the authors.
See original article, p 1108. Supported in part by the National Institutes of Disability and Rehabilitation Research, RERC on Wheeled Mobility (grant no. H133E030035-04). No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the author(s) or upon any organization with which the author(s) is/are associated. PII: S0003-9993(07)01261-0 doi:10.1016/j.apmr.2007.07.007 © 2007 American Congress of Rehabilitation Medicine and the American Academy of Physical Medicine and Rehabilitation. Published by Elsevier Inc. All rights reserved. | |
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