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Optimizing Drug-Therapy in Patients 80 Years and Older

U

Uppsala University Hospital

Status

Completed

Conditions

Drug-Related Problems

Treatments

Other: Drug review 80+ -To reduce usage of hospital care

Study type

Interventional

Funder types

Other

Identifiers

NCT00661310
Uppsala80

Details and patient eligibility

About

The purpose of this study is to measure the effects of an enhanced service where a pharmacists is part of the healthcare team on the ward (focusing on drug-related problems and transferring information between primary and secondary care). Primary outcome measure is visits to hospital during a 12-month follow-up period, and the population is patients 80 years and older.

Full description

Optimising drug-therapy for patients, 80 years and older, to reduce hospital visits

Background and Objective:

Results from a pilot-study performed in 2004 at the Academic Hospital, Uppsala, including 214 consecutive patients (80 years old or older) showed that 9.4%-13.6% of the patients were acutely admitted to hospital due to a drug related problem1. Other similar international studies show that the frequency of drug-related hospital admissions stands for at least 14% of the acute admissions (14%-30.4%). Of these admissions it was estimated that 32%-69% were preventable 2,3,4.

A study from Antrim Hospital, Northern Ireland, showed that pharmacists´ involvement in the health care team can reduce the number of acute hospital admissions and improve quality of drug use5.

In view of these findings this study was initiated in 2005 with fundings from the Drug and Therapeutics committee, the County Council of Uppsala, the Division of Acute-Medicine and the Pharmacy Department at the Academic Hospital in Uppsala

Aim and objectives:

The Study Aim was to optimize drug-prescribing and drug use for patients 80 years and older.

The main objective was to reduce the number of hospital visits for patients 80-years old or older.

Design:

A randomized, controlled trial including 400 patients (200+200). Patients in the intervention group (I) received a patient interview on admission, drug counseling on discharge and a drug review - all performed by a clinical pharmacist. Patients in the control group (C) received standard care, without pharmacists´ involvement.

Patients were included between Oct 2005 and June 2006.

Setting:

Two wards at the Division of Acute-Medicine at Uppsala University Hospital, Sweden

Main Outcome Measures:

  1. Frequency of hospital visits 12 months after (last included patient) discharge from hospital for (I) and (C).

Enrollment

400 patients

Sex

All

Ages

80+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 80 years and older
  • Acute admission to study ward

Exclusion criteria

  • <80 years
  • Scheduled admission
  • Previously admitted to studyward during study period

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

400 participants in 2 patient groups

I
Experimental group
Description:
Intervention by team consisting of Doctor, pharmacist and nurse
Treatment:
Other: Drug review 80+ -To reduce usage of hospital care
C
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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