Background
Frailty is characterized by a loss of strength, endurance, physical ability and cognitive function, which results in an increased risk of vulnerability to disease, dependence, and death [
1,
2]. Frail adults are at increased risk of falls, disability, hospitalization, admission to long-term care and mortality [
3‐
5]. Independent of the number and severity of comorbidities measured by the Charlson Index, frail older adults who are hospitalized for an acute illness have a two-fold higher risk of mortality prior to discharge, compared to non-frail adults [
5]. Healthcare spending is highest for frail older adults due to use of more expensive and intensive services [
6], and adults over age 75 years with multiple comorbidities account for 60% of emergency room and hospital resource use [
7]. These frail older adults with multiple comorbidities can be seen by geriatricians and supporting healthcare practitioners in geriatric medicine out-patient clinics based in acute care settings and in the community [
8]. Screening patients in a clinical setting will help identify frail patients at high-risk for negative health outcomes and provide an opportunity to intervene and prevent the progression of frailty [
9].
Although the negative consequences of frailty are well-established [
3,
4], there is no gold standard method that is consistently used by researchers and clinicians to assess frailty. This may be because frailty is a multidimensional concept involving many physical, psychological and social aspects of health [
1]. The Comprehensive Geriatric Assessment (CGA) is arguably the best way to assess overall health of an older adult, and the CGA is a multidisciplinary diagnostic procedure used to identify care needs and formulate future care plans for older adults [
10]. However, conducting the CGA is resource intensive and does not objectively classify frail and non-frail patients by providing an overall frailty score. It may be advantageous for out-patient clinic staff to easily and quickly assess frailty for the purposes of diagnosing frailty, screening patients for clinical trials and quantifying the impact of interventions on frailty status [
11].
There are over 25 subjective and objective frailty assessment methods [
12]. Two methods that focus on physical frailty are the Cardiovascular Health Study (CHS) frailty phenotype method (Fried’s phenotype method) [
3], which is the most widely cited method [
13] and the Short Performance Physical Battery (SPPB) [
14]. These tools are extensively published on for the assessment of frailty [
3,
15‐
18], however, the components of the assessments differ, which may have implications on the feasibility of incorporating these assessments into clinical practice. The Fried phenotype method considers weight loss, exhaustion, physical activity level, grip strength, and walking speed, whereas the SPPB is a test of walking speed, balance and ability to complete chair stands. Although the Fried phenotype method predominantly assesses physical frailty, it has good construct validity [
3], convergent validity [
19], concurrent validity [
20] and predictive validity [
21] for assessing frailty. Moreover, the tool has been shown to be sensitive to change following an intervention in frail patients [
9]. The SPPB has been identified as one of the best physical performance tests to identify frail adults [
18]. It is one of the primary outcomes of interest in large, multicomponent trials in older adults [
22]. Like the Fried phenotype method, the SPPB has good concurrent validity when compared to other measures of frailty [
15,
16], internal consistency [
23], and satisfactory short (1 week) and long-term (6 month) reliability [
24,
25].
The primary aim of this study was to determine the prevalence of frailty using the two methods, and agreement between the methods. The secondary aim was to determine the feasibility of assessing frailty at a geriatric out-patient clinic.
Discussion
In this cohort of older adults at a geriatric out-patient clinic, the prevalence of frailty was 35% according to Fried’s phenotype method, and 50% according to the SPPB. There was fair to moderate agreement between assessment methods. At least 90% of enrolled participants agreed to be assessed for frailty, which suggests that according to our criteria for feasibility, it is feasible to assess frailty in a geriatric out-patient clinic.
This study showed that most patients attending the out-patient clinic were frail or pre-frail. Cognitive impairment was also evident in approximately 50% of our participants, which may contribute to the development of frailty [
35]. However, we found that cognitive impairment was equally common in the pre-frail and non-frail groups. We were unable to discern the directionality of the relationship between cognitive impairment and frailty, given the small sample size and cross-sectional design, and this should be explored in a larger study. Similar to our findings, Tavassoli and colleagues found that 39% and 54% of older patients attending a geriatric clinic were pre-frail or frail, respectively, according to Fried’s phenotype method [
8]. In addition, 75% of the participants had an SPPB score ≤ nine [
8]. Kim and colleagues found that among older men attending a geriatric out-patient clinic, 34% were considered to be frail and 50% were considered to be pre-frail according to Fried’s phenotype method [
36]. The high prevalence of frailty and pre-frailty in our study indicates a need to intervene to prevent further health declines and disability. An intervention similar to that described by Cameron and colleagues would be ideal, as components of physical frailty (i.e.
, gait speed, physical activity level) and SPPB scores improved after 12 months of a tailored, multifaceted intervention based on baseline frailty characteristics [
31].
When identifying frail participants, there was fair to moderate agreement between methods used. These findings are similar to those reported by Theou et al. and Islam et al. who both showed agreement between Fried’s phenotype method and other frailty assessment methods (i.e.
, Clinical Frailty Scale) [
17,
37]. While the relationship between SPPB and frailty has been reported [
15], this is the first study to examine the agreement between the SPPB and other frailty assessment tools, using the SPPB cut-offs for frail and pre-frail. Given that physical activity and gait speed are important indicators of frailty [
38], it is not surprising that agreement between the SPPB and Fried’s phenotype method is fair to moderate. Our findings show that for identifying frail or pre-frail older adults, either method could be used, but consideration should be given to other aspects of feasibility.
In a clinical setting similar to our study, Kim and colleagues explored the feasibility of assessing frailty using Fried’s phenotype method in 162 male veterans attending a geriatric clinic [
36]. While no criterion for feasibility was stated, the authors concluded that it is feasible to assess frailty using Fried’s phenotype method, but that the assessment took approximately 15-20 min [
36]. Another recent study revealed that Fried’s phenotype method takes 10 min or less to administer [
39]. One of the more time consuming components of Fried’s phenotype method may be the Minnesota Leisure Time Activity Questionnaire. Fried’s phenotype method has been modified over 200 times, with the physical activity and weight loss components being modified most often [
40]. Eckel and colleagues developed a modified six-item physical activity questionnaire, based on the Minnesota Leisure Time Activity Questionnaire, and found that scores obtained from the modified version were predictive of scores obtained with the original questionnaire [
41]. We also question the validity of this questionnaire for a geriatric out-patient population, as many participants received a score of frail on this component of the assessment because an energy expenditure of zero kilocalories per week was recorded. It may be that the activities captured on the questionnaire are not appropriate for an older geriatric out-patient clinic population, and another method of assessing activity level, such as the Physical Activity Scale for the Elderly (PASE) may be more appropriate [
42]. In another feasibility study, Maxwell and colleagues aimed to determine the feasibility of assessing frailty in hospitalized older adults in 5 min or less using the Vulnerable Elders Survey (VES-13), Barthel Index and Life Space Assessment questionnaires [
43]. The main barrier to participant enrollment was the absence of a surrogate respondent to provide consent and assist with the questionnaires [
43]. Also, like our study, a research assistant was responsible for completing the assessments, which resulted in a high completion rate. However, having a dedicated person responsible for assessing frailty is not sustainable in most healthcare settings, therefore, future studies should investigate the feasibility of clinic staff completing the assessments. Given that we found that agreement between methods is fair to moderate and there were no adverse events reported for either method, clinical staff should consider the added time that administering the Fried phenotype method may take [
36], the differences in equipment requirements (i.e.
, grip strength dynamometer), and appropriateness of the physical activity questionnaire that is part of the Fried phenotype method. Clinicians may also want to consider other contributors to frailty, such as weight loss and exhaustion, which aren’t directly assessed using the SPPB. In addition to considering aspects of feasibility, Norman and Streiner suggest that in judging the appropriateness of a tool for a clinical setting, the validity (concurrent, predictive, convergent, content validity) and reliability (internal consistency and stability) of the assessment method should be considered [
44]. Many of these features are also highlighted as key criteria for frailty assessment tools, with the addition of a tool’s ability to predict patient response to therapy, be supported by biologic mechanisms, be feasibly applied, and to align with the purpose (i.e., risk prediction) of assessing frailty [
1,
13,
39].
There are various strengths to this study. We objectively assessed feasibility using criteria set a priori
, and we assessed frailty using two characteristically different, yet valid and reliable methods. The Fried’s phenotype method that was used was not modified from the original method, which is rare as Theou and colleagues reported that only 24 of 264 studies assessed frailty using the original method [
40]. We also investigated the agreement between the assessment methods based on published cut-offs for frailty and pre-frailty, whereas other studies have reported the agreement for the frailty category only, or have not included the SPPB in agreement analyses.
There are also study limitations to acknowledge. This study used a small sample of participants from one geriatric out-patient clinic and all assessments were performed by a research assistant. We would have preferred to have clinic staff complete the frailty assessments and use additional geriatric clinic sites. These factors would improve the generalizability of our results to other clinic settings that don’t have access to additional resources, such as a research assistant. However, by involving a research assistant, we were able to assess frailty on over 90% of study participants who met the study criteria. The high prevalence of frailty and pre-frailty in this population provides rationale to involve clinic staff in assessing frailty in the future. The study was also conducted between 2013 and 2014, and occurred intermittently over 9 months. While we don’t believe that the feasibility results would differ if recruitment occurred contiguously over the study period, the prevalence of frailty may be underestimated as lower activity levels, exhaustion, weight loss and falls may be more common during the winter months. In addition, the frailty assessment tools that were selected do not specifically assess cognitive and social aspects of health, which may also contribute to frailty. Finally, members of the interdisciplinary team excluded patients from the study if they deemed the participant unfit to participate, which included some patients with severe cognitive impairment and/or no legally authorized representative present at the appointment to provide consent. Therefore, we may have excluded some of the most frail patients.