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Medication (de)prescribing in hospitalized geriatric patients with sarcopenia, less is more?

Medication (de)prescribing in hospitalized geriatric patients with sarcopenia, less is more? - (De)prescribing in hospitalized sarcopenic geriatric patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON53702
Enrollment
160
Registered
2022-12-19
Start date
2023-03-03
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

stoppen/ starten/ dosisaanpassing van medicatie bij acuut zieke sarcopene geriatrische patienten met polyfarmacy en diverse uitgebreide co-morbiditeit waarbij de betrokken aandoeningen heel divers kunnen zijn en de reden van de medicatie wijziging ook verschillend kan zijn. medication adjustment in older frail hospitalized patients with low muscle strength and muscle mass using at least 5 different medications. (de)prescribing in acutely ill hospitalized sarcopenic geriatric patients with polyp

Interventions

Medication review in patients randomised to the IG group will be performed according to the principles of DPA and in the CG this will be performed following the SSA approach.

Sponsors

Zuyderland Medisch Centrum
Lead Sponsor

Eligibility

Age
65 Years to 99 Years

Inclusion criteria

Inclusion criteria: frail older adults, 70 Y and older with sarcopenia and polypharmacy admitted to the acute care hospital ward because of an acute medical problem

Exclusion criteria

Exclusion criteria: If a patient is not instructable. If a patient has an implantable cardioverter defibrillator (ICD) or no informed consent or if there is no (legal) representative with informed consent if the patient is (temporary) incapacitated. Patients in a palliative phase will be excluded from this study, since most medication will be stopped in a palliative setting. Finally, patients with an expected admission time of less than 48 hours will be excluded due to logistic reasons (48 hours are needed to screen for suitability, minimum of 24 hours to consider participation).

Design outcomes

Primary

MeasureTime frame
number and type of medication stopped during medication review and not restarted within 1, 3 and 6 months

Secondary

MeasureTime frame
Secondary endpoints: number and severity of Adverse Drug Reactions (ADR) and complications due to medication (e.g. delirium or falls), hospital readmission, quality of life (QoL) and mortality

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)