Evidence map›Paper›PMID 41222603›Full record

ArticleInternational journal of clinical pharmacy2026

Responsiveness and minimum important change of the Pharmacotherapeutic Symptom Evaluation-20-Australian version: a tool for measuring changes in medicine-related symptoms over time.

Abebe Basazn Mekuria, Andre Q Andrade, Renly Lim, Debra Rowett, Mariann Hedström, Elizabeth E Roughead

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Article in International journal of clinical pharmacy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Abebe Basazn MekuriaQuality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, Adelaide, 5001, Australia. abebe.mekuria@mymail.unisa.edu.au.ORCID http://orcid.org/0000-0003-2909-2001
Andre Q AndradeQuality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, Adelaide, 5001, Australia.
Renly LimQuality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, Adelaide, 5001, Australia.
Debra RowettQuality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, Adelaide, 5001, Australia.
Mariann HedströmDepartment of Public Health and Caring Sciences, Section of Caring Sciences, Uppsala University, BMC, Husargatan 3, 75122, Uppsala, Sweden.
Elizabeth E RougheadQuality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, Adelaide, 5001, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMonitoring patient-reported symptoms over time may support early detection of medicine-related harms. The Pharmacotherapeutic Symptom Evaluation-20-Australian version (PHASE-20-Australian version) is an 11-point rating scale designed for longitudinal monitoring of medicine-related symptoms; however, its responsiveness and minimum important change (MIC) have not been established.

aimTo evaluate the responsiveness and MIC of the PHASE-20-Australian version for monitoring changes in medicine-related symptoms over time.

methodA prospective cohort study was conducted among Australian adults (≥ 18 years) taking medications. Participants completed the PHASE-20-Australian version at baseline and follow-up and reported perceived symptom changes using the Global Rating Scale (GRS) at follow-up. Responsiveness was assessed by correlating score changes with the GRS and calculating the area under the receiver operating characteristic (ROC) curve (AUC). MIC was estimated using ROC anchor-based and 0.5 standard deviation (SD) distribution-based methods and then compared with the Smallest Detectable Change (SDC).

resultsAmong 102 participants, 52% were aged ≥ 60 years and 65.7% were female. Strong correlations were observed for overall score changes (rho = 0.815) with the GRS as well as for 84.2% of individual symptoms (rho = 0.701-0.897). The tool demonstrated good to strong discriminative ability (AUC = 0.739-0.975 for improvement; 0.764-0.977 for deterioration), with sensitivity and specificity ≥ 0.75 for 16 symptoms. The MIC values ranged from 0.5 to 1.5 using the ROC method and 0.9-1.8 using the 0.5 SD approach. The estimated MIC values exceeded the SDC for 84.2% of symptoms. Limited responsiveness (rho < 0.7, AUC < 0.7) and MIC values below the SDC were noted for forgetful, swollen legs/ankles and frequent urination/incontinent of urine.

conclusionThe PHASE-20-Australian version is responsive for most symptoms, with a clinically meaningful change of approximately 2.0 points on a 0-10 scale. The estimated MIC is applicable at the individual level, although caution is needed for symptoms with an MIC below the SDC.

Indexed as

Drug-Related Side Effects and Adverse ReactionsSymptom AssessmentAdultAgedAustraliaCohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedProspective StudiesTime FactorsAdverse drug eventsLongitudinal monitoringMinimum important changePatient-reported outcomesPHASE-20ResponsivenessSurvey

Identifiers

PMID41222603
PMCPMC12992458

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