The goal of this cluster randomized controlled trial is to compare transitional multidisciplinary pharmacotherapeutic care (TMPC) with usual care in patients aged 70 years or older with polypharmacy, admitted to the hospital via the emergency department for longer than 24 hours and that have an elevated risk of drug related readmissions. The primary aims of the study are: * To assess whether TMPC leads to a decrease in number of DRreAs compared to usual care during the first 30 days after index hospitalisation. * To assess whether TMPC is cost-effective Participants will receive TMPC in hospitals allocated to the intervention. TMPC will be executed by a pharmacotherapeutic team, it consists of the following four elements: * pharmacotherapeutic analysis * transitional multidisciplinary discussion * pharmacotherapeutic care interview and discussion with the patient * discharge note with the pharmacotherapeutic care plan Researchers will compare TMPC with usual care to assess the effect and cost-effectiveness of TMPC.
Rationale: Polypharmacy poses an ongoing healthcare challenge, as it is associated with negative outcomes such as adverse drug events, lower quality of life and mortality. These risks are especially elevated for the frail and old, leading to high numbers of drug related admissions (DRAs) and unplanned emergency department visits. Approximately half of the DRAs are potentially preventable, and therefore a possible target point for interventions. Unfortunately, until now, despite multiple efforts to decrease drug related harm, the number of drug related admissions has not decreased. Several studies have previously investigated the effect of a structured medication review with varying success. Identified strengths were multicomponent approaches, multidisciplinary approaches and selection of specifically high-risk patients. The LIMONCELLO study will take this into account and will study a multidisciplinary multicomponent intervention with focus on transitional care in a patient population that is most likely to benefit from this intervention. It is hypothesised that transitional multidisciplinary pharmacotherapeutic care (TMPC) is superior in preventing drug related readmissions (DRreAs) compared to usual care. Objective: The LIMONCELLO study aims to assess the effect and cost-effectiveness of TMPC compared to usual care. Study design: This is a cluster randomised controlled trial, a cluster will be defined at the hospital level, with each cluster randomly allocated to the intervention or control group. Patients aged 70 years or older with polypharmacy, admitted to the hospital via the emergency department for longer than 24 hours, with completed medication verification and with an elevated risk of drug related readmissions (calculated by use of the DRA prediction model, an algorithm developed by the OPERAM study group) will be included. Participants in intervention hospitals will receive TMPC during index hospitalisation. TMPC consists of four elements: pharmacotherapeutic analysis, transitional multidisciplinary discussion, pharmacotherapeutic care interview and discussion with the patient, and a discharge note with the pharmacotherapeutic care plan. The comparator is usual care as is provided in the participating hospitals. Follow-up will be 1 year, participants will be called 30 days, 3 months and 12 months after index hospitalisation. Statistical considerations: 16 clusters will participate in the study, requiring a total of 161 patients per cluster to be included, 2,576 participants in total. Results will be analysed by intention-to-treat analysis and per-protocol analysis. For the primary outcome, drug related readmissions, a generalized linear mixed model with a binomial distribution and logit link function will be used for the analysis on an individual level, adjusting for clustering.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
2,576
A structured medication review with improved transitional care and multidisciplinary collaboration. TMPC consists of the following four elements: 1. A structured pharmacotherapeutic analysis 2. A transitional multidisciplinary discussion.The treating physician in the hospital will be involved. The general practitioner and community pharmacist will be consulted. 3. An interview and discussion with the patient and/or legal representative by a member of the Pharmacotherapy-team, which will be performed before the patient is discharged from the hospital. 4. A discharge note with the pharmacotherapeutic care plan. This will be sent to the community pharmacist and the general practitioner.
Canisius Wilhelmina Ziekenhuis
Nijmegen, Gelderland, Netherlands
Radboudumc
Nijmegen, Gelderland, Netherlands
Amphia ziekenhuis
Breda, North Brabant, Netherlands
Catharina Ziekenhuis
Eindhoven, North Brabant, Netherlands
Amsterdam UMC - location VUMC
Amsterdam, North Holland, Netherlands
Amsterdam UMC- location AMC
Amsterdam, North Holland, Netherlands
Zaans Medisch Centrum
Zaandam, North Holland, Netherlands
Ziekenhuisgroep Twente
Almelo, Overijssel, Netherlands
Deventer Ziekenhuis
Deventer, Overijssel, Netherlands
Universitair Medisch Centrum Groningen
Groningen, Provincie Groningen, Netherlands
...and 6 more locations
Number of Drug Related Readmissions in the first 30 days after index hospitalisation
Whether readmission is drug related will be assessed with AT-HARM10
Time frame: 30 days after index hospitalisation
Number of Drug Related Readmissions at 3 and 12 months after index hospitalisation
Whether readmission is drug related will be assessed with AT-HARM10
Time frame: 3 and 12 months after index hospitalisation
Duration of hospitalisation of Drug Related Readmission
Whether readmission is drug related will be assessed with AT-HARM10
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Time to first Drug Related Readmission
Whether readmission is drug related will be assessed with AT-HARM10
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Number of Emergency Department visits
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Number of all-cause hospital readmissions
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Healthcare costs
In euros, assessed with the iMTA Medical Consumption Questionnaire (iMCQ)
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Quality of Life measured with EQ-5D-5L
Measured by 5-level EuroQol-5 domains (EQ-5D-5L) questionnaire
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Cost-effectiveness
In euro per Quality Adjusted Life Year (QALY) gained, by combining costs and quality of life measurements
Time frame: During the 12 month follow-up
Number of regular medications
Based on number of regular medications in the medication list
Time frame: At discharge from index hospitalisation and 30 days, 3 months and 12 months after index hospitalisation
Number and type of recommendations in the intervention group
Based on documented recommendations made during TMPC
Time frame: At discharge from index hospitalisation
Number of implemented recommendations
The number of differences between the pharmacotherapeutic plan composed by the P-team and the participant's current medication list at each time point
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Activities of Daily Living
Measured with Katz-6 ADL questionnaire
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Number of patients living independently
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Number of falls
Time frame: 30 days, 3 months and 12 months after index hospitalisation
Mortality
Time frame: 30 days, 3 months and 12 months after index hospitalisation
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