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Clinical and Economic Impact of Interventions by a Clinical Pharmacist on Antibiotic Use on Surgical Wards

Clinical and Economic Impact of Interventions by a Clinical Pharmacist on Antibiotic Use on Surgical Wards

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00431483
Enrollment
779
Registered
2007-02-05
Start date
2007-02-28
Completion date
2008-02-29
Last updated
2013-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bacterial Infections

Keywords

antibacterial agents, surgery, pharmacist, economics, pharmaceutical

Brief summary

The purpose of this study is to establish the impact of a pharmacist's recommendations regarding choice, dosing and duration of antibiotic therapy on quality and cost of antibiotic treatment on surgical wards.

Detailed description

Inappropriate or incorrect use of antibacterials exerts selection pressure on pathogens potentiating emergence of resistance, puts patients at risk for unnecessary adverse drug reactions and potentially prolongs the length of stay in hospital thus increasing healthcare costs. In an effort to improve the quality of antibiotic drug therapy on surgical wards of a large university hospital, specific consulting by a clinical pharmacist was established. The objective of this study is to assess the impact of pharmaceutical consulting on the quality and costs of antibiotic use in surgical wards. Comparison: Within a control period the current pattern of antibiotic use is monitored. During the intervention period, the impact of the interventions made by the clinical pharmacist on antibiotic use is examined. One ward serves as a parallel control group; no intervention is being made on this ward throughout this study.

Interventions

BEHAVIORALpharmaceutical consulting

to measure if information and advice by a pharmacist has an impact on quality and quantity of prescribed antibacterials

Sponsors

Ludwig-Maximilians - University of Munich
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* female and male patients receiving antibiotics for a proven or suspected infection on designated surgical wards

Exclusion criteria

* patients under 18 * patients unable or unwilling to consent to their data being evaluated * patients receiving antibiotics perioperatively as prophylaxis * patients receiving antibiotics for less than 48hrs

Design outcomes

Primary

MeasureTime frame
overall duration of antibiotic therapy during study periodFeb 2008

Secondary

MeasureTime frameDescription
iv to oral switchFeb 2008number of courses of iv antibiotics switched to oral antibiotics; duration of iv treatment
compliance of treatment with hospital formulary for antibiotic therapyFeb 2008
cost of antibiotic therapyFeb 2008
number and duration of therapy with antibiotics with redundant spectraFeb 2008

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026