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临床试验/NCT06902779
NCT06902779终止不适用

Enhanced Collaboration Between Hospital and Community Pharmacists to Improve the Hospital Discharge Process

Pharmacie des Hopitaux de l'Est Lemanique3 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年9月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
70
试验地点
3
主要终点
Number of drug-related problems on the hospital discharge prescription

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Control arm

No Intervention

Participants in the control arm will benefit from the usual standard of care currently provided in routine clinical practice. Physicians performs medication reconciliation on their own and hand-out the prescription to the patient the day of discharge. The patient then goes to the pharmacy for a classical drug dispensation.

Intervention arm

Experimental

Participants in the intervention group will benefit from the hospital pharmacist's support to optimize medication management and ensure a safe and effective discharge process.

干预措施: Support of the hospital pharmacist for the medication management at hospital discharge (Other)

结局指标

主要结局

Number of drug-related problems on the hospital discharge prescription

时间窗: 7 days after hospital discharge

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.

次要结局

  • Patient's satisfaction(7 days after hospital discharge)
  • Community pharmacists' satisfaction(Through study completion, approximately 6 months)
  • 30 day readmission rate(30 days after hospital discharge)

研究者

发起方
Pharmacie des Hopitaux de l'Est Lemanique
申办方类型
Other
责任方
Sponsor

研究点 (3)

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