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Polypharmacy Among Internal Medicine Patients

Polypharmacy and Associated Risk Factors and Clinical Outcomes for Internal Medicine Patients Discharged From Hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05756400
Enrollment
85942
Registered
2023-03-06
Start date
2023-01-01
Completion date
2024-05-01
Last updated
2024-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Internal Medicine

Keywords

Polypharmacy, Potentially Inappropriate Medication List, Risk Factors, Cinical Outcomes, Predication on Medication Related Harm, Discharge, Inappropriate Prescribing, Drug-related side effects and adverse reaction,, Readmisson, Patient discharge, Prediction tool, Start and stop, Beers

Brief summary

The World Health Organisation Patient Safety Challenge: Medication Without Harm has brought our attention to the importance of medication-related harm as a global public health issue. One of the major contributing factors is polypharmacy, the usage of multiple medicines at the same time. People are getting older and living longer with chronic diseases; they need more medications, which frequently leads to polypharmacy. Subsequently, they are at more risk of medication-related harm. The planned project is an epidemiological study on polypharmacy, medication appropriateness, risk factors, and clinical outcomes post-discharge from a hospital for internal medicine patients. The study group hypothesise that pre- and post-admission polypharmacy and potentially inappropriate prescribing is common, especially among older patients, patients with a high comorbidity and frailty burden. Our hypothesis is additionally that preadmission polypharmacy and potentially inappropriate prescribing is associated with higher short- and long-term mortality, a longer primary hospitalization length of stay, and a higher risk of readmission.

Detailed description

This is an observational, retrospective, single-centered study using clinical data from the patient's medical record from the hospital, the national prescription database of the Directorate of Health, and the ICD-10 codes from primary care records. For this analysis, medicines will be classified into drug classes based on the first five characters of their WHO Anatomical Therapeutic Chemical (ATC) code. The prevalence (pre) and incidence (post) of polypharmacy (≥5 or more regular medicines) and hyper-polypharmacy (≥10 regular medicines) will be calculated. Potentially inappropriate prescribing will be assessed in individuals ≥65 years, applying Beers 2019, Start and Stopp 2014, explicit prescribing criteria. The analysis will be restricted to older individuals, as Beers criteria have not been validated in younger age groups. The anticholinergic burden will be assessed for all individuals ≥18 years will be assessed by applying the anticholinergic burden scale, and the PRIME tool will be applied to predict the likelihood of medication-related harm post-discharge. The PRIME tool consists of eight variables drawn from clinical, medication, and psychosocial domains. Applied at the point of discharge, it provides the absolute risk of an individual older adult experiencing medication-related harm during the eight weeks after discharge from acute hospital admission. This stratification is important in order to deliver targeted interventions in resource-limited healthcare settings.

Interventions

None listed

Sponsors

University of Iceland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Population-based cohort study that included all patients ≥18 years hospitalized in internal medicine ward at Landspitali - The National University Hospital of Iceland during the study period 1st January 2010 and 31st December 2020

Exclusion criteria

* Under 18 years of age

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of polypharmacyTwo years, one year pre-admission and one year post-admisson, 2010-2020Polypharmacy measured by by the number of different ATC classes of medications filled in the year preceding and year following surgery. Polypharmacy further quantified into categories of non-polypharmacy (\<5), polypharmacy (5-9) and hyper-polypharmacy (≥10).

Secondary

MeasureTime frameDescription
Potentially inappropriate prescribing by Beers criteria 20192010-2020The association of potentially inappropriate prescribing by applying Beers criteria 2019 with polypharmacy (summary score, yes/no)
Anticholinergic burden by applying the Anticholinergic burden scale2010-2020The association of anticholinergic burden by applying the Anticholinergic burden scale with polypharmacy ((summary score, yes/no)
Demographics2010-2020Gender (male, female),age (years), comorbidity based on the International Statistical Classification of Diseases, and Related Health Problems, ninth or tenth revision, ICD9/10 classification system
Incidence of polypharmacyTwo years, one year pre-admission and one year post-admisson, 2010-2020Polypharmacy measured by by the number of different ATC classes of medications filled in the year preceding and year following surgery. Polypharmacy further quantified into categories of non-polypharmacy (\<5), polypharmacy (5-9) and hyper-polypharmacy (≥10).
Drug classes2010-2020Drug classes based on ATC-codes on filled medications from the Prescription Medicines Registry and association with polypharmacy
Clinical outcomes2010-2020Mortality (short-and long-term mortality) Length of hospital stay (number of days, ≥ ten days) Readmission (number of days until readmission, readmission \<30 days)
Comorbidity burden2010-2020The association of comorbidity burden will be described by calculating the Charlson Comorbidity Index and Elixhauser comorbidity index (summary score) with polypharmacy ((summary score, yes/no)

Countries

Iceland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026