Related Experiment Videos
A required course in the development, implementation, and evaluation of clinical pharmacy services
Monica L Skomo1, Khalid M Kamal, Hildegarde J Berdine
1Mylan School of Pharmacy, Duquesne University, USA. skomo@duq.edu
American Journal of Pharmaceutical Education
|February 14, 2009
Summary
This study developed a pharmacy practice course to teach students business planning for clinical services. The course successfully equipped students with skills for evidence-based programs and efficient resource utilization.
Area of Science:
- Pharmacy Education
- Clinical Pharmacy Services
- Health Economics
Background:
- Pharmacy students require training in business planning to effectively develop and implement clinical services.
- Pharmacoeconomic evaluations are crucial for demonstrating the value of pharmacy interventions.
Purpose of the Study:
- To create, implement, and evaluate a mandatory course for pharmacy students focused on business planning for clinical pharmacy services.
- The course aimed to equip students with the ability to develop, implement, and assess clinical pharmacy services using a business plan model.
Main Methods:
- Course content covered business planning (literature evaluation, market analysis, marketing strategy) and pharmacoeconomic evaluations (cost-minimization, cost-benefit, cost-effectiveness, cost-utility analysis, HRQoL).
- Assessment included objective exams, participation, a group project, and peer evaluations for 153 students.
Main Results:
- Students achieved high scores on objective exams (mean 82-85/100), group projects (183.5/200), and participation (46.1/50).
- Peer evaluations also indicated positive performance, with a mean score of 30.8/31.7.
Conclusions:
- The course successfully provided pharmacy students with a framework for developing and implementing evidence-based disease management programs.
- It also prepared students to ensure efficient and cost-effective resource utilization in patient care settings.
Related Concept Videos
Dosage Regimens: Designs and Approaches
Designing a dosage regimen, which refers to the manner of drug administration, is a complex process involving the selection of drug dose, route, and frequency. This process is underpinned by pharmacokinetic parameters derived from tests and population averages. These parameters are then tailored to patient-specific variables such as diagnosis, demographics, and allergy status. Once therapy commences, therapeutic response monitoring is critical and achieved through clinical and physical...
Preclinical Development: Overview
Preclinical development consists of a series of tests that ensure the safety and efficacy of a new therapeutic compound before it is tested in humans. There are four main phases to this process. First, safety pharmacology tests are conducted to ensure the drug does not produce any acutely harmful effects. These tests examine parameters such as bronchoconstriction, cardiac dysrhythmias, blood pressure changes, and ataxia. Next, preliminary toxicological testing is performed to determine the...
Drug Administration and Therapy Phases: Overview
Drugs, the chemical agents used in diagnosing, treating, or preventing diseases, undergo a four-phase process of development: pharmaceutic, pharmacokinetics, pharmacodynamics, and therapeutic.
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
Clinical Trials: Overview
Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
Clinical Trials
Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
There are four phases in a clinical trial. A phase one...
Nursing Clinical Information System
Nursing Clinical Information System (NCIS)
A Nursing Clinical Information System (NCIS) is a specialized type of healthcare information system tailored to meet the unique needs of nursing practice. It incorporates the principles of nursing informatics to streamline information management and improve the quality of care delivery.
Critical attributes of NCIS include:
A Nursing Clinical Information System (NCIS) is a specialized type of healthcare information system tailored to meet the unique needs of nursing practice. It incorporates the principles of nursing informatics to streamline information management and improve the quality of care delivery.
Critical attributes of NCIS include: