Evaluation of the Impact of a Collaboration Between Hospital and Community Pharmacists at Hospital Discharge

ConditionPolypharmacy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorPharmacie des Hopitaux de l'Est Lemanique

About this trial

The aim of this study is to evaluate the impact of an enhanced collaboration between a hospital pharmacist and a community pharmacist during hospital discharge. For patients taking multiple medications, hospitalization often involves numerous changes to their treatment regimen. For community pharmacies, discharge prescriptions are often complex, and they sometimes lack the information that pharmacists need to deliver the treatment as safely as possible. As a result, there is a risk of medication errors, and a risk for patients. We aim to evaluate the benefits of this collaboration for adult patients admitted to the internal medicine ward of a regional hospital who are taking seven or more drugs and are being discharged to home.

The main question it aims to answer is : Does the enhanced collaboration reduce the number of drug-related problems encountered by community pharmacists with discharge prescriptions ? Researchers will compare patients when a hospital pharmacist is involved during the discharge process and when he or she is not involved, which corresponds to normal care.

The hospital pharmacist will not perform the intervention directly on the patient, but only with the community pharmacy. Once they agree to participate in the study, patients will only have to go to their usual community pharmacy after discharge and accept that the hospital transmits medical information to their usual pharmacy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients admitted to the internal medicine ward for more than 48 hours

Patients prescribed seven or more drugs at the time of screening

Patients discharged to home

Patients able to give informed consent as documented by signature

Disqualifiers

Patient discharged to another hospital, nursing home or rehabilitation clinic

Refusal of the community pharmacy to participate

Inability to sign consent and follow the procedures of the study, due to language problems, psychological disorders, dementia, alterations of consciousness and lack of judgement

Trial design

Design model

Parallel

Treatments tested in this trial

  • Support of the hospital pharmacist for the medication management at hospital discharge

    Other intervention

    1\) The hospital pharmacist calls the community pharmacy the day before discharge to order unusual or specific medications 2) The day of discharge, the hospital pharmacist performs a medication reconciliation in collaboration with the hospital physician 3) Once completed, the discharge prescription is sent to the community pharmacy before the patient is discharged. 4) The hospital pharmacist calls the community pharmacy to provide additional information about the patient and the prescription and to answer any questions. Additional information will help the community pharmacist to understand the prescription : administrative data, clinical data, medication-related information, patient follow-up and patient concerns.

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: Control armNo intervention 0 interventions
Group B: Intervention armExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Number of drug-related problems on the hospital discharge prescription

Community pharmacists will assess the number of drug-related problems (DRP) on the discharge that they faced when preparing the discharge medication. They will have to use the PharmDISC system, which is a validated tool for referencing drug-related problems faced in the community which was adapted from the drug-related problems classification system of the Pharmaceutical Care Network Europe (PCNE). Community pharmacists will also document the intervention performed for each DRP, and the resolution (yes/no) of the DRP.

Time frame
7 days after hospital discharge

Secondary outcomes

1

Patient's satisfaction

Patients' satisfaction related to their visit at the pharmacy after hospital discharge will be assessed using a questionnaire. Patients will be contacted via email or telephone

Time frame
7 days after hospital discharge
2

Community pharmacists' satisfaction

The satisfaction of community pharmacists with the service provided by the hospital pharmacist at patient discharge will be evaluated

Time frame
Through study completion, approximately 6 months
3

30 day readmission rate

Number of participants with hospital emergency department visits and hospital readmission in the same hospital within 30 days of discharge

Time frame
30 days after hospital discharge

Other outcomes

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