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Medication Review in Chronic Complex or Polymedicated Patients After Hospital Discharge.

Effects of Interdisciplinary Medication Review in Chronic Complex Patients or Patients With Polypharmacy After Hospital Discharge

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05799430
Enrollment
372
Registered
2023-04-05
Start date
2023-04-15
Completion date
2024-07-31
Last updated
2023-09-15

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

Conditions

Disease, Chronic, Medication Review, Polypharmacy

Keywords

Medication Review, Polypharmacy

Brief summary

The goal of this prospective multicentre clustered randomized controlled trial is to evaluate the effect on new hospitalization episodes of a multidisciplinary medication review in primary care patients with polypharmacy or chronic complex conditions after hospital discharge. The multidisciplinary team will be integrated by a family physician (FP), a primary care nurse (PCN) and a primary care pharmacist (PCP). Patient will be adults aged 65 years and older. Polypharmacy refers to the use of 10 or more drugs based on information in electronic prescription software. Research questions are: In elderly patients with polypharmacy, which is the effect of an interdisciplinary medication review after hospital discharge in comparison with standard care, in terms of: * new hospitalization episodes? * number of drugs prescribed? * prescribed drugs adequacy?

Detailed description

Centres will be randomized to medication review intervention or usual care group. Eligible patients will be ask for informed consent. For patients in the intervention group, PCP will collect information about prescribed medication and diseases from the electronic health record and e-prescribing application. The medication review in primary care will be focus to reconcile the medications the patient was taking prior to admission and those initiated in hospital, with the medications they should be taking post-discharge to ensure all changes are intentional and that discrepancies are resolved as soon as possible. The review process will include detection of potential drugs interactions, wrong doses, lack of adherence (based on dispensing recorded data) and adequacy to explicit criteria for potentially inappropriate prescriptions included in different tools: a) STOPP-STAR, STOPP-Pal, LESS-CHRON lists; b) Guideline for Medication Review in Primary Care, a local publication and c) Medication review in patients with polypharmacy. A list of drugs frequently associate with potentially inappropriate prescriptions. Andalusian health Service). PCP will write a report to communicate the results of medication review to primary care physician and nurse. The multidisciplinary team will define a personalized therapeutic plan to be implemented for every patient. Patients in the control group will receive usual care.

Interventions

FP communicate to the PCP patients recently discharged. The medication review process consists in 5 steps: 1. PCP perform a structured drug review based on information from health record and e-prescribing application. The drug review comprise the appraisal of potentially inappropriate medication based on lists of explicit criteria. 2. PCP communicates and discuss the results of medication review with GP and PCN, in a brief meeting face-to-face, with possible adaptation of the recommendations. 3. FP, PCN and PCP agree on a personalized therapeutic plan for the patient that includes actions to optimize the therapy. 4. FP and PCN share plan with the patient and/or carer with possible adaptation of the recommendations and agree about actions to be implemented. 5. FP and PCN communicate to PCP final agreement with patient and/or carer 6. FP and/or PCN follow-up implantation of agreed recommendations using standard health care procedures

BEHAVIORALControl group

Usual care by FP an PCN

Sponsors

Andalusian Health Service
CollaboratorOTHER_GOV
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Intervention model description

A cluster-randomized control trial

Eligibility

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

Inclusion criteria

\- Hospital discharge in the last 48 h and one of the following conditions: * Polypharmacy: ten o more drugs prescribed in a chronic schedule OR * Complez Chronic Condition

Exclusion criteria

* Patients in last days of life * Major mental health disorder * Patient on dialysis * Organ transplant patients

Design outcomes

Primary

MeasureTime frameDescription
Number of hospitalization episodes12 monthsRegistered in Electronic Health Record. In emergency department or in hospital service
Length of Hospital Stay12 monthsRegistered in Electronic Health Record.

Secondary

MeasureTime frameDescription
Number of potentially inappropriate drugs12 monthsTotal number of potentially inappropriate prescribed drugs based on explicit criteria
Healthcare utilisation12 monthsNumber of visits to primary care services (family physician or primary care nurse) and hospital services (non emergency and without hospitalization)
Number of medications12 monthsTotal number of drugs chronically prescribed (treatment length: unless 120 days)
Number of proposal about treatment improvement agreed with primary care team7 daysNumber of proposal about treatment improvement agreed with primary care team in a face face meeting
Number of proposal about treatment improvement accepted by the patient or care7 daysNumber of proposal about treatment improvement agreed with primary care team in a face face meeting
Mortality12 monthDead for any cause
Number of proposal about treatment improvement7 daysNumber of proposal about treatment improvement included in PCP report

Countries

Spain

Contacts

Primary ContactTeresa Molina-López, Pharm Dr
mariat.molina.sspa@juntadeandalucia.es637642 411+
Backup ContactDaniel Palma-Morgado, Pharm G
daniel.palma.sspa@juntadeandalucia.es

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026