Evidence map›Paper›PMID 35349875›Full record

Trial reportArchives of gerontology and geriatrics

The association between polypharmacy, frailty and disability-free survival in community-dwelling healthy older individuals.

A R M Saifuddin Ekram, Robyn L Woods, Joanne Ryan, Sara E Espinoza, Julia F M Gilmartin-Thomas, Raj C Shah, Raaj Mehta, Bharati Kochar, Judy A Lowthian, Jessica Lockery and 5 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Archives of gerontology and geriatrics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 2 countries.

A R M Saifuddin EkramSchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia. Electronic address: saifuddin.ekram@monash.edu.
Robyn L WoodsSchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia.
Joanne RyanSchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia.
Sara E EspinozaSam and Ann Barshop Institute, UT Health San Antonio Texas Research Park Campus, San Antonio, TX, USA; Geriatrics Research, South Texas Veterans Health Care System, San Antonio, Texas, USA.
Julia F M Gilmartin-ThomasSchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia; College of Health and Biomedicine, and Institute for Health & Sport, Victoria University, Victoria, Australia; Australian Institute for Musculoskeletal Science, Victoria, Australia.
Raj C ShahRush Alzheimer's Disease Center, Rush University, Chicago, IL, USA.
Raaj MehtaClinical & Translational Epidemiology Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Bharati KocharClinical & Translational Epidemiology Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Judy A LowthianSchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia; Bolton Clarke Research Institute, Bolton Clarke, Burwood Highway, Forest Hill, Victoria, Australia.
Jessica LockerySchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia.
Suzanne OrchardSchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia.
Mark NelsonMenzies Research Institute, University of Tasmania, Churchill Ave, Hobart, Tasmania, Australia.
Michelle A FravelDepartment of Pharmacy Practice and Science, College of Pharmacy, The University of Iowa, Iowa City, IA, USA.
Danny LiewSchool of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, St Kilda, Victoria 3004, Australia.
Michael E ErnstDepartment of Pharmacy Practice and Science, College of Pharmacy, The University of Iowa, Iowa City, IA, USA; Department of Family Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Monash University · AUHarvard University · USUniversity of Iowa · USAustralian Institute for Musculoskeletal Science · AURush University · USSouth Texas Veterans Health Care System · USUniversity of Tasmania · AU

Funding

ASPirin in Reducing Events in the ElderlyU01AG029824 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI MCNEIL, JOHN JAMES, MURRAY, ANNE M · 2009 to 2018
$64.6M
Main Administrative CoreU19AG062682 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI CHAN, ANDREW T, MCNEIL, JOHN JAMES · 2019 to 2023
$42.9M
NIA NIH HHS U01 AG029824NIA NIH HHS U19 AG062682
6 · The paper itself

Abstract

objectivesPolypharmacy and frailty are two common geriatric conditions. In community-dwelling healthy older adults, we examined whether polypharmacy is associated with frailty and affects disability-free survival (DFS), assessed as a composite of death, dementia, or persistent physical disability.

methodsWe included 19,114 participants (median age 74.0 years, IQR: 6.1 years) from ASPirin in Reducing Events in the Elderly (ASPREE) clinical trial. Frailty was assessed by a modified Fried phenotype and a deficit accumulation Frailty Index (FI). Polypharmacy was defined as concomitant use of five or more prescription medications. Multinomial logistic regression was used to examine the cross-sectional association between polypharmacy and frailty at base line, and Cox regression to determine the effect of polypharmacy and frailty on DFS over five years.

resultsIndividuals with polypharmacy (vs. <5 medications) were 55% more likely to be pre-frail (Relative Risk Ratio or RRR: 1.55; 95%Confidence Interval or CI:1.44, 1.68) and three times more likely to be frail (RRR: 3.34; 95%CI:2.64, 4.22) according to Fried phenotype. Frailty alone was associated with double risk of the composite outcome (Hazard ratio or HR: 2.16; 95%CI: 1.56, 2.99), but frail individuals using polypharmacy had a four-fold risk (HR: 4.24; 95%CI: 3.28, 5.47). Effect sizes were larger when frailty was assessed using the FI.

conclusionPolypharmacy was significantly associated with pre-frailty and frailty at baseline. Polypharmacy-exposed frailty increased the risk of reducing disability-free survival among older adults. Addressing polypharmacy in older people could ameliorate the impact of frailty on individuals' functional status, cognition and survival.

Indexed as

FrailtyAgedCross-Sectional StudiesFrail ElderlyGeriatric AssessmentHumansIndependent LivingPolypharmacyASPREEDisability-free survivalFrailty indexFried phenotypePolypharmacy

Identifiers

PMID35349875
PMCPMC9437977
OpenAlexW4220969512

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.