Frailty and adverse drug effects are linked in the fact that polypharmacy is correlated with the severity of frailty; however, a causal relation has not been proven in older people with clinically manifest frailty.
A literature search was performed in Medline to detect prospective randomized controlled trials (RCTs) testing the effects of pharmacological interventions or medication optimization in older frail adults on comprehensive frailty scores or partial aspects of frailty that were published from January 1998 to October 2019.
Twenty-five studies were identified, 4 on comprehensive frailty scores and 21 on aspects of frailty. Two trials on comprehensive frailty scores showed positive results on frailty although the contribution of medication review in a multidimensional approach was unclear. In the studies on aspects related to frailty, ten individual drug interventions showed improvement in physical performance, muscle strength or body composition utilizing alfacalcidol, teriparatide, piroxicam, testosterone, recombinant human chorionic gonadotropin, or capromorelin. There were no studies examining negative effects of drugs on frailty.
So far, data on a causal relationship between drugs and frailty are inconclusive or related to single-drug interventions on partial aspects of frailty. There is a clear need for RCTs on this topic that should be based on a comprehensive, internationally consistent and thus reproducible concept of frailty assessment.
Frailty has been defined by the World Health Organization as a ‘progressive age-related decline in physiological systems that results in decreased reserves of intrinsic capacity, which confers extreme vulnerability to stressors and increases the risk of a range of adverse health outcomes’ [1, 2]. While there is still some debate concerning a more precise definition of frailty, this widely recognized definition of frailty was also implemented by the first joint action (JA) on the prevention of frailty, ADVANTAGE [1, 2]. The prevalence of frailty increases with age (about 11% in community-dwelling older adults [3,4,5,6]); frailty is a dynamic process and older people are commonly staged as being robust/non-frail, prefrail, or frail [3, 5]. The presence of frailty in older adults has been associated with serious adverse clinical outcomes including, falls, disability, hospitalization, nursing home admissions, and even mortality [3, 4, 7].
There are many instruments designed to define and measure frailty or different aspects of frailty including its physical, cognitive, social, environmental, and emotional domains [8, 9]. The most commonly used instruments are the frailty phenotype and the Frailty Index . However, according to the ADVANTAGE JA initiative, validated instruments such as the Short Physical Performance Battery (SPPB), the Edmonton Frail Scale, (The Rockwood) Clinical frailty Scale, or PRISMA-7 which do not require special equipment and take less than 10 min to complete are useful for frailty screening and preferable to others across clinical settings [1, 2].
In a previous publication examining the association of polypharmacy (i.e., often defined as ≥ 5 daily medications) and hyperpolypharmacy (i.e., ≥ 10 daily medications) with frailty, we found that polypharmacy is common in prefrail and frail adults and that robust/non-frail persons with polypharmacy are at significantly higher odds for developing prefrailty compared to those not exposed to polypharmacy . This association between polypharmacy, inappropriate prescribing, and frailty has been corroborated by several systematic reviews that suggest, but do not prove, that a reduction of polypharmacy may prevent or improve frailty or aspects of frailty [11,12,13]. In this context, an important limitation of interpreting evidence from observational studies on medications and frailty has to be noted: clinicians often selectively discontinue/de-prescribe in those who are frailest, thereby creating a bias regarding applicability to frail people at large. As these associations do not provide insights on the causal relationship between medications and frailty, more research is required to address this interaction that could reflect medications being increased to cope with frailty or frailty as a consequence of medications. A lack of evidence on pharmacological interventions for the management of frailty has been anticipated, and already been indicated in literature [14,15,16]. Therefore, a systematic review was performed to identify evidence on pharmacological interventions and frailty or aspects of frailty from randomized controlled trials (RCT). Approaches to tackle polypharmacy and inappropriate drug treatment (medication optimization), as well as single-drug interventions (pharmacological interventions) aimed at improving clinically manifest frailty as a primary or secondary outcome, were searched for by addressing both key aspects of medication-frailty interactions: aggravating or improving frailty through medication.
This systematic review was performed according to the methodological manuals of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA ). The PRISMA checklist and PICOs are provided in Supplementary data 1 & 2. It was an initiative of the European Geriatric Medicine Society (EuGMS) special interest group (SIG) on Pharmacology.
Search terms were proposed by two authors (FP and MW) to all EuGMS Pharmacology special interest group members for discussion and amendment. The resultant search terms (Supplementary Material 3), combinations, and limitations were developed and used to search MEDLINE, from January 1998 up to and including 14th October 2019. The key themes in our search were frailty and medicines (including polypharmacy and inappropriate prescribing), and only randomized controlled trials (RCT) were included.
Publications describing the impact of medication optimization or single-drug interventions on frailty or aspects of frailty in older adults (≥ 60 years old, except one study ), evaluated through a randomized controlled trial were examined. A broad definition of medication optimization was used including not only medication review, but also educational interventions, care coordination, use of technology, or ‘brown bag’ analyses.
Studies concerning non-geriatric or non-frail (at baseline) patients were excluded, as were studies without measurement of frailty or aspects of frailty, or studies measuring quality of life without providing a separate analysis of the intervention on the aforementioned aspects of frailty. These exclusion criteria also applied to nursing homes, though a considerable rate of frail patients is to be expected there, but the measurement of interventional improvements is not possible without baseline data on frailty. Studies focusing on treatment of diseases such as most oncology trials, association studies, or studies without differences in medications between the control and intervention group were also excluded (Fig. 1). There were no exclusions regarding the language.
The search results were exported by FP from PubMed to a Word file (Microsoft, Redmond, Washington). Subsequently, two reviewers (FP, MW) independently screened the titles and abstracts of the manuscripts to identify relevant publications describing the impact of medication optimization or drug treatment on frailty or aspects of frailty in randomized controlled trials. Each record generating uncertainty regarding inclusion or exclusion criteria was discussed by FP and MW in order to reach consensus about inclusion.
Data extraction and synthesis
The following data were extracted from the selected publications: PubMed ID (PMID), first author, publication year, type of population, mean age of study participants and standard deviation if provided, number of study participants, female gender, outcome relating to a common frailty score/instrument, outcome(s) relating to partial aspects of frailty, short description of the intervention and its duration, positive outcome(s) relating to frailty or aspects of frailty. Methodological quality, or risk of bias of clinical trials, was calculated by using a three-item questionnaire, known as the Jadad score . Drop-outs/withdrawals, randomization, blinding, and the quality of latter two items are assessed and a score derived ranging from 0 (very poor) to 5 (rigorous) . In the assessment of the trials, positive study outcomes corresponded to at least one primary or secondary endpoint exposing a significant improvement by the intervention (i.e., p < 0.05).
Measurement of frailty or aspects of frailty considered for study selection and data extraction
Measurement of frailty corresponded to highly cited  or other commonly used/recommended (by ADVANTAGE JA) frailty instruments [5, 14]. The following tools were considered to be comprehensive frailty scores: (physical) frailty phenotype (PFP, also known as Fried Frailty Criteria), Deficit Accumulation Index (DAI), Frailty index, Electronic Frailty Index, Gill Frailty Measure, Frailty/Vigor assessment, (The Rockwood) Clinical Frailty Scale, Brief Frailty Instrument, Vulnerable Elders Survey (VES-13), Fatigue, Resistance, Ambulation Illness, Loss of Weight Index (FRAIL Index), Inter-Frail, Sherbrooke Postal Questionnaire, Groningen Frailty Indicator, Study of Osteoporotic Fractures frailty criteria, Tilburg Frailty Indicator, Edmonton Frailty Scale, Frail Scale, Short Physical Performance Battery (SPPB), PRISMA-7, Multidimensional Prognostic Index, Geriatric 8 frailty questionnaire for oncology (G8), Kihon Checklist, Frailty Risk score, Hospital Frailty Risk Score, and Winograd Screening Instrument.
The aspects of frailty considered to be relevant included physical performance/function, body composition, body weight/weight loss, cognition, exhaustion/fatigue, and muscle strength. We particularly focused on the following assessments: gait speed, walking speed, activities of daily living (ADL), instrumental activities of daily living (IADL), Timed Up and Go test (TUG), handgrip strength, and Mini Mental State Examination (MMSE).
The search yielded 291 studies, of which 255 were excluded at the abstract level (Fig. 1). The remaining 36 studies were reviewed in full-text and 11 were excluded based on the abovementioned criteria from this systematic review, leading to the selection of 25 articles [18, 21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44]. Finally, only 4 of the 25 studies measured the frailty status by a ‘comprehensive’ frailty instrument as an endpoint, and the remaining 21 studies detected changes in partial aspect(s) of frailty as an outcome (Table 1). The total number of study participants, types of intervention, number of trials with positive outcome(s), and the number of trials with a Jadad score ≥ 3 (a trial with a score above 2 is considered to have a high quality ) are provided in Table 1.
Studies including a comprehensive frailty score as an outcome (n = 4)
In only two out of the four studies [23, 24] with a comprehensive frailty score, a significant improvement of the frailty status by a multidisciplinary intervention that included medication review was demonstrated. Both studies used the Short Physical Performance Battery (SPPB) as frailty instrument and applied a multidimensional intervention (Supplementary Table 1a & 1b). In the study conducted by Romera-Liebana et al.  which recruited frail older persons living in the community, a 12-week intervention was utilized consisting of exercise training, intake of high protein nutritional drinks/supplements, memory training, and medication review. Other aspects of frailty (handgrip strength, Functional Reach Test, Unipodal Station Test, and several neuropsychological performance tests) were measured or performed in addition to the SPPB. In this trial, handgrip strength, Functional Reach Test, and the neuropsychological performance tests improved significantly (p < 0.05) in the intervention group as compared to the control group. However, this study had a Jadad score of 2, suggesting poor quality. The other study conducted by Matchar et al.  recruited participants who visited an emergency department for a fall-related injury and were discharged home. A tailored program of physical therapy for 3 months plus screening and follow-up for vision, polypharmacy, and environmental hazards for 6 months was employed. With a Jadad score of 3, the trial was of better quality than the Romera-Liebana study . SPPB was a secondary outcome which significantly more deteriorated in the control group as compared to the intervention group.
The remaining two studies [21, 22] both used the frailty phenotype (Fried Frailty Criteria) to measure frailty; one study also used SPPB. The study which used SPPB in addition to the frailty phenotype was a single-drug intervention in males (testosterone versus placebo) ; the other trial utilized a multidimensional intervention consisting of comprehensive geriatric assessment and appropriate intervention by medication adjustment, exercise instruction, nutrition support, physical rehabilitation, social worker consultation, and specialty referral in community-dwelling older persons. These studies showed no improvement of the comprehensive frailty score. A significant increase in lean body mass by testosterone was observed in one study ; this trial had a higher Jadad score as compared to the multi-interventional trial (3 versus 1).
In those 11 studies that included a ‘medication review’ [for categorization see 46], this was a comprehensive prescription review in 1 case, an adherence review in 1 case, a clinical medication review in 7 cases, and others in 2 cases. It was performed by clinicians with different professional backgrounds (multidisciplinary in 6 cases, geriatricians only, GPs only or nurses only in 1 case each) and by physicians and pharmacists or by pharmacists only in 1 case each. Initial access to past medical records was provided in five cases (Supplementary Table 1b).
Studies including an aspect of frailty as an outcome (n = 21)
The majority (n = 13) of the trials which only addressed single or multiple aspects of frailty as an endpoint were single-drug interventions [18, 26, 28, 30, 32, 33, 35,36,37,38,39,40, 42], and in ten of these trials, a significant improvement of some aspects of frailty was demonstrated. Only three trials [32, 38, 39] failed in this regard. Eight trials on single-drug interventions had a Jadad score of 3 or more [26, 28, 29, 32, 35, 36, 39, 40].
In only two of the 21 studies which focused on aspects of frailty, a medication optimization process represented the intervention [27, 28]. These studies showed no impact of the intervention on the aforementioned aspects of frailty.
There were six multi-interventional trials [25, 31, 34, 41, 43, 44] with aspects of frailty as an endpoint; except for , they used medication review/optimization as one part of the intervention. Only three of them (including ref. 28) showed a positive impact on some aspects of frailty [25, 34]. However, the Jadad score was below 3 in three of these studies [31, 43, 44].
Supplementary Table 1a & 1b summarizes the 25 randomized trials found in this review and provides relevant details about these studies including type of study population, intervention, the nature of medication review (if applied), outcomes, and quality of the trial according to the Jadad score .
An overview of frailty aspects considered in these 25 studies and the frequency and types of interventions with and without significantly positive impact on aspect(s) of frailty are provided in Table 2.
Physical performance was measured in 17 studies and improved in 9 of them:
in two studies involving complex interventions,
in one study involving an early switch to oral treatment with diuretics in patients with heart failure and
in one study utilizing a home-based support program.
Single-drug interventions with positive impact on physical performance tested
alfacalcidol (a vitamin D analog),
teriparatide (an anabolic parathyroid hormone fragment),
piroxicam (a nonsteroidal anti-inflammatory drug),
testosterone (an anabolic steroid) or
capromorelin (a growth hormone secretagogue).
Four of ten interventional trials on muscle strength (including handgrip) showed positive results. In two of these trials, a complex intervention was evaluated; in two other trials, alfacalcidol or testosterone was applied in the intervention group.
Body composition and body weight were positively affected in six of seven interventional trials measuring these parameters. The trials with positive outcomes used single drugs (5)/nutritional supplementation (1) as intervention. The successful single drugs were testosterone in three studies and capromorelin or recombinant human chorionic gonadotropin in one study each.
Cognition, behavioral disturbances, and/or depression were improved in only 2 of 13 trials. One of these trials utilized a complex intervention and the other a home-based support program. Activities of daily living (ADL) and/or instrumental activities of daily living (iADL) improved in three out of five studies. In one of these studies, the early switch to oral diuretics in patients with heart failure positively affected the outcomes and the other two were based on complex interventions. Fatigue was ameliorated by piroxicam, while two other trials with fatigue as an outcome showed no significant improvement. Anorexia was positively influenced by a chemotherapy regimen (MVP: mitomycin-C, vinblastine, cisplatin) as compared to MVC (mitomycin-C, vinblastine, carboplatin) in patients with advanced non-small cell lung cancer.
The present systematic review showed that among the identified 25 studies, only 2 trials on comprehensive frailty scores reported positive results though the contribution of medication review was unclear in a multidimensional approach. In addition, the studies were heterogeneous regarding the nature of the medication review used (Supplementary Table 1b) and, thus, do not allow for identifying the most recommendable type of medication review. In the studies on frailty aspects, ten single-drug interventions were positive for physical performance, muscle strength, or body composition. There were no studies on negative effects of drugs on frailty. To our knowledge, this is the first systematic review addressing the impact of drug interventions on frailty or aspects of frailty.
The association of frailty and drugs has been described repeatedly in the literature, including a recent review by this group . As many medications may cause mental/cognitive and/or physical deterioration, a causal relation between those drugs and major aspects of frailty is plausible. Such side effects or adverse effects constitute the most important reasons to classify them as “potentially inappropriate medications” (PIMs) in PIM lists like the US Beers criteria . Conversely, medications may positively alter aspects of age-related frailty such as acetylcholine esterase inhibitors, angiotensin-converting enzyme (ACE) inhibitors, appetite enhancers, or nutritional supplements/vitamins to increase muscle strength, all of which have been shown to elicit effects principally relevant to frailty. Some of these medications are positively labeled, i.e., to be encouraged in the FORTA (Fit fOR The Aged) list (labels A or B ), a positive/negative drug list for age appropriateness of drugs or are recommended in START criteria . It is obvious that frequent medication reviews (every 3–6 months) addressing over- and undertreatment issues are always desirable in multimorbid older patients to avoid noxious side effects and to provide chances of positively labeled drugs, apart from dealing with those aspects of frailty.
It is clearly important to search for evidence to support these bi-directional claims of impact of medication on aspects of frailty. The outcome of this search is, however, very limited as mentioned above. Thus, the impact of medication review in general and of specific medication avoidance in particular on frailty in older people is largely unknown. Randomized controlled trials involving increasing numbers of representative older people using structured medication reviews or individual drug trials as single interventions for frailty are clearly needed. A key driver in this regard could be the European Medicine Agency in that it encourages the use of SPPB or gait speed as instruments in pre- and post-authorization studies for medicine registration across all therapeutic areas .
The 21 trials on particular aspects of frailty were more conclusive in that 10 trials with positive outcomes tested single-drug interventions. The medications with positive effects on physical performance, muscle strength, body composition, and fatigue were alfacalcidol, teriparatide, piroxicam, testosterone, recombinant human chorionic gonadotropin, and capromorelin. Notably, none of them proved to be beneficial to improve comprehensive frailty scores. A strong biological understanding of frailty based on basic research is needed before more focused and presumably more successful treatment strategies may be developed.
Many of the trials (N = 10) found in this systematic review are of low methodological quality according to the Jadad score, a finding that emphasizes the lack of compelling data and strategies.
It is remarkable that no prospective RCT-derived evidence was found for the potentially harmful effects of medications on frailty symptoms. There is abundant literature on potentially harmful drugs, such as those that predispose to falls, delirium or dementia, drugs that may even increase mortality (e.g., sedative antihistamines) [51, 52]. However, none of them clearly describe the worsening of aspects of frailty or the use of a comprehensive frailty score according to the criteria of this systematic review. For instance, falls are not included in most frailty concepts, but usually considered as an outcome of frailty.
From the findings of the present systematic review, it appears that a classic prospective, controlled RCT designed to examine the harmful effects of medications in age-related frailty would be ethically questionable as it would involve placing already incapacitated patients at potentially higher risk if still exposed to potentially harmful drugs in the control group. Thus, other trial designs (for example, stepped-wedge design) and/or other interventions such as re-prescribing (the replacement of inappropriate medications by better alternatives for the treatment of a given disease, thus reflecting the combined optimization of both over- and undertreatment issues) based on medication reviews would be more acceptable from an ethical perspective. As is evident from this systematic review, such trials should involve singular interventions since multiple interventions would be difficult to relate to specific impacts. In addition, to identify culprit drugs, such trials have to be large enough to provide information on the contribution of particular drugs or drug classes such as sedatives or antihypertensives on particular elements of the frailty syndrome.
An additional point of attention in designing such trials is the heterogeneity of frailty definitions and frailty assessment scores that measure different aspects of frailty in a non-specific manner. Importantly, a recent review comparing 35 different frailty scores concluded that “research results based on different frailty scores cannot be compared or pooled” . In this regard, recent efforts have been made in trying to find a consensus for functional status across available assessments of physical function or physical frailty . It is also highly likely that such trials would have to be international, involving cooperative consortia with considerable public funding. Clearly, pharmaceutical companies will not be motivated to funding trials on negative outcomes of certain drugs. Furthermore, most of those drugs under suspicion in relation to age-related frailty are generic, further minimizing the level of interest among pharmaceutical companies in funding RCT investigation of the kind.
This systematic review was restricted to MEDLINE entries and to prespecified search terms; thus, relevant literature may have been overlooked. However, the likelihood of missing relevant trials with only one entry, for example exclusively reported in EMBASE, was considered to be low as most trials have multiple citations referring to each other. Unpublished studies were not searched for, e.g., by contacting study investigators or sponsors. The interpretation of results was mainly done by two researchers who may have misinterpreted some findings. Besides, publication bias might be present, i.e., lack of publication of trials with neutral or even negative effects on frailty or frailty components.
In summary, this review shows that there is virtually no prospective evidence for causal pharmacological effects on frailty with the exception of few trials demonstrating the positive impact of medications on partial aspects of frailty. Dedicated, large prospective trials are urgently needed to identify both the deleterious and/or beneficial effects of drugs on frailty.
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Conflict of interest
MW was employed by AstraZeneca R&D, Mölndal, as director of discovery medicine (=translational medicine) from 2003 to 2006, while on sabbatical leave from his professorship at the University of Heidelberg. Since returning to this position in January 2007, he has received lecturing and consulting fees from Sanofi-Aventis, Bayer, Berlin-Chemie, Boehringer-Ingelheim, Aspen, Novartis, Takeda, Roche, Pfizer, Bristol-Myers, Daichii-Sankyo, Lilly, Otsuka, Novo-Nordisk, Shire, and LEO Pharma. AC received lecturing and consulting fees from Bristol Myers Squibb, Nestle and MSD. MD has received lecturing and consulting fees from Daiichi-Sankyo and Novartis. FP, MP, AG, ANP, DOM, GZ, HB, JBB, JMS, KI, MAF, MSB, NVDV, PC, CR, JASR, TF, TVDC, ACJ, GO, RJVM, WK, KWT, PG, GS, JPB, DD, HG, AP, AM, and ER declare that they have no conflict of interest.
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Pazan, F., Petrovic, M., Cherubini, A. et al. Current evidence on the impact of medication optimization or pharmacological interventions on frailty or aspects of frailty: a systematic review of randomized controlled trials. Eur J Clin Pharmacol 77, 1–12 (2021). https://doi.org/10.1007/s00228-020-02951-8
- Medication optimization
- Inappropriate drug treatment
- Older people