The Pharmacist in the Acute Geriatric Inpatient Treatment Team

Overview

This trial investigates the effects of a comprehensive pharmaceutical assessment in an acute care geriatric hospital on the number of hospital readmissions and patient's days spent at home.

Full Title of Study: “The Pharmacist in the Acute Geriatric Inpatient Treatment Team – Impact on Re-hospitalization and Trans-sectoral Communication”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: September 20, 2019

Detailed Description

Drug-related problems are common in elderly patients. These problems can not only be regarded from a medical or economical point of view (i.e. hospitalization, drug related deaths, longer hospital stays and increased healthcare costs) but also from a patient centered perspective: Drug therapy may not be sufficiently explained by health care practitioners, patients might suffer from side effects, the number of different medications could be too large and their intake schedule too difficult, all of this leading to a reduced adherence. In addition, medication histories are rarely accurate in older patients and doctor's letters do not always meet the requirements of a complex drug therapy. At the transition from inpatient to outpatient treatment this can lead to a significant loss of information and subsequently cause patient harm. In Germany, clinical, ward-based pharmacists are not yet established in contrast to other countries (i.e. Great Britain, Canada and Australia). However, the implementation of a clinical pharmacist may particularly address the problems described above. The present study therefore describes the implementation of a comprehensive pharmaceutical assessment in an acute care geriatric hospital. The above mentioned pharmaceutical assessment consists of the following steps: First, the pharmacist will obtain the patient's medication history following the protocol of "best possible medication history" (WHO). Furthermore, he will ascertain the patient's adherence to his/her drug regime. With the information obtained, he will then carry out a thorough medication review (regarding interactions, contraindications, suitability for the elderly, dosage regimes, etc.) in order to develop a suggestion for the best possible drug regime, which is discussed with the treating physician. In addition, he will also observe possible side effects and provide information on the background and significance of every single drug to the patient and/or his/her care-giver. Furthermore, the handling of difficult devices (i.e. insulin pens, inhalators and transdermal therapeutic systems) will be individually explained. Finally, the pharmacist will prepare a distinctive paragraph in the medical discharge report in which he explains the changes in the medication regime during the inpatient period to the general practitioner and will also elaborate possible interactions and problems concerning the patient's medication (pharmaceutical council). The main outcome to be evaluated will be the number of hospital readmissions and drug related hospital readmissions within six months after discharge (recorded at one, three and six months). The secondary outcome will be the days spent at home (also recorded at one, three and six months), time to readmission, changes in medication within six months and the acceptance of the supposed medication regime by the general practitioner (GP). The study will be conducted as a before and after comparison in which the steps described above will be implemented successively: In the first phase (140 patients planned for an observation period of eight months), patients will receive standard care and the pharmacist will only obtain the medication history shortly after admission. Results and discrepancies will be discussed with the attending physician of the hospital. After discharge, described outcomes will be documented. In the second phase (140 patients planned for an observation period of eight months), the pharmacist will conduct all of the activities described above. The outcomes will be documented as in phase one. We expect that the comprehensive pharmaceutical assessment in the second phase will lead to a better coordination regarding the medication regime, enhance the patient's knowledge of their medication, thus improving their adherence to the therapy and that the pharmaceutical council will ensure a better trans-sectoral communication to the GP with a higher acceptance of the supposed drug regime in the doctor's letter. All these improvements combined might reduce hospital readmissions and increase the patient's days spent at home.

Arms, Groups and Cohorts

  • Control group
    • First observational period: Standard care without an advising pharmacist, 140 patients
  • Implementation group
    • Second observational period: Standard care with an advising pharmacist, 140 patients
  • Learning success group
    • Second observational period: Standard care without an advising pharmacist, 30 patients

Clinical Trial Outcome Measures

Primary Measures

  • Drug related re-hospitalization
    • Time Frame: 6 months
    • Number of re-hospitalizations with causal relation to one or more medicinal products, to examine the potential effect of an advising pharmacist

Secondary Measures

  • Overall re-hospitalization
    • Time Frame: 6 months
    • Overall number of re-hospitalizations within the observational period per patient
  • Days spent at home
    • Time Frame: 6 months
    • Number of days within the observational period not spent in a hospital, short-term care facility, rehabilitation centre, day-care hospital, emergency department or other medical facilities
  • Period of time until the potential re-hospitalization into the inpatient sector
    • Time Frame: 6 months
    • Time between the discharge and a potential re-hospitalization per patient
  • Acceptance of the recommended medication plan by the further treating primary care physicians
    • Time Frame: 6 months
    • Adoption of the medication plan, recommended in the doctor’s letter, by the further treating primary care physicians
  • Time required for the pharmacists support
    • Time Frame: 6 months
    • Expenditure of time, required for the pharmacists support, per patient within the implementation group
  • Completeness of the pharmaceutical anamnesis in the course of the inpatient admission
    • Time Frame: 6 months
    • Comparison between the pharmaceutical anamnesis conducted by the doctor and the pharmacist, respectively
  • Evaluation of the clinical relevance of the medicinal products, which were not assessed by the doctors
    • Time Frame: 6 months
    • The evaluation will be conducted by an interdisciplinary group using the focus group method.

Participating in This Clinical Trial

Inclusion Criteria

  • Geriatric complex treatment (Operation and procedure code (German: "Operationen- und Prozedurenschl├╝ssel", OPS) 8-550) – In-patient stay for at least 7 days – Written informed consent of the patient or the legal representative – Existing concomitant drug therapy at the time of the inpatient admission Exclusion Criteria:

  • Patients, that were already included in the study beforehand – Patients classified as terminally ill by the medical staff – Patients, that are incapable to give their informed consent and who do not have a legal representative

Gender Eligibility: All

Minimum Age: 70 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Prof. Dr. med. Cornelius Bollheimer
  • Provider of Information About this Clinical Study
    • Sponsor-Investigator: Prof. Dr. med. Cornelius Bollheimer, Univ.-Prof. Dr. med., Klinikdirektor – RWTH Aachen University
  • Overall Official(s)
    • Cornelius Bollheimer, Prof. Dr., Study Director, University Hospital RWTH Aachen

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.