Poland Integrated Medicines Management (PL-IMM) - Study Assessing the Provision of Complex Clinical Pharmacy Services to Hospitalized Patients

Wroclaw Medical University

Status: Not yet enrolling

Conditions: Acute Admitted Multimorbid Patients

Treatments: Behavioral: multidisciplinary treatment

Study type: Interventional

Funder types: Other

Identifiers

NCT07159932

KB 47O/2O23N

Details and patient eligibility

About

The aim of the study is to assess whether the involvement of a clinical pharmacist in patient care at every stage of hospitalization, from admission to discharge, will improve the quality of healthcare services provided in clinical and economic terms. As part of the research study, we will randomly assign you to two different groups.

Within one group, a pharmacist will be involved in the process of caring for you throughout your hospital stay. The pharmacist will participate in medical rounds, verify medications upon admission to the hospital, check current test results and medical orders regarding pharmacotherapy, verify medications upon discharge and provide advice on the use of medications. All activities will be carried out in consultation with other medical staff. The aim is to check whether such a model of patient care increases safety and leads to improved pharmacotherapy for patients, and also has a positive effect on patient satisfaction and compliance with therapeutic recommendations. Additionally, the opinion of the medical staff and the economic aspects of this solution will be assessed. Within the second group, you will receive standard care offered by the hospital. In the case of both groups, after the hospitalization is completed, the pharmacist will contact you after 1, 3, 6 months to verify your health condition - he or she will ask about any hospitalizations, complications, side effects, and additional visits to the doctor.

Full description

Despite the benefits of clinical pharmacy services demonstrated in numerous publications and their implementation in many countries around the world, Poland has still not achieved nationwide implementation. There is also a lack of scientific data at the national level showing the benefits of including a pharmacist in the patient facing activities. Therefore, this RCT aimes to determine if pharmacist input at each stage of hospitalization, from admission to discharge, can result in an enhanced level of patient care when compared to standard care as measured by a number of clinical and economic outcomes. Given the aforementioned, the objective of this research is to:

1. Primary outcome: Determine the incidence of hospital, emergency department and other unscheduled visits after discharge from hospital during the 6 months follow-up period.

2. Secondary outcome: Assess the length of stay (LoS) in hospital.

3. Additional outcomes:

   • Evaluate the service by determining the frequency and type of interventions performed, their acceptance and influence on the quality of pharmacotherapy.
   • Assess the perception of the service by patients.
   • Assess the perception of the service by healthcare professionals.
   • Estimate the potential financial benefits of the service.

Enrollment: 610 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Patients meeting the following inclusion criteria:

• ≥18 years old and an acute admission to the hospital fulfilling at least one of the following criteria:

• taking ≥4 medicines
• taking high risk medicines listed in the medicines reconciliation standard of Polish Society of Clinical Pharmacy (….)
• medicine related admission to the hospital within last 12 months
• chronic kidney or liver disease
• after solid organ transplantation

Exclusion criteria

• age below 18 years old
• pregnancy
• resident of long-term care facility
• unable to express informed consent to participate in the research
• expected survival less than 6 months

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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610 participants in 2 patient groups

Control group

No Intervention group

Description:

Standard care during hospital stay, without pharmacist involved

Pharmacist intervention - IMM

Experimental group

Description:

A pharmacist is included in the multidisciplinary treatment team during the hospital stay

Treatment:

Behavioral: multidisciplinary treatment