教学生兽医专业人员关于药物监测:对英国兽医教育工作者进行的一项调查
Heather Grieve1, Martin Hawes2, Catherine Hemingway3
1Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Journal of veterinary pharmacology and therapeutics
|February 27, 2026
概括
兽医专业人员需要更好的药物监测培训,以改善药物不良事件 (ADE) 报告. 目前英国的培训主要是教学性的,几乎没有机会实践提交ADE报告.
科学领域:
- 兽医医学 兽医医学 兽医医学
- 药物监督 药物监督 药物监督
- 药品安全 药品安全
背景情况:
- 兽医专业人员报告药物不良事件 (ADE) 对于监测销售的兽医产品的安全性和有效性至关重要.
- 然而,大量的兽医ADEs仍未报告.
- 人类医疗保健中已经探索了药监督教育,以提高报告率.
研究的目的:
- 了解目前为英国的兽医学生提供的药监督培训.
- 为兽医专业人员提供改进的药监监课程的设计提供信息.
主要方法:
- 在英国的兽医教育工作者中进行了一项调查.
- 从培训提供者那里收到17个回复 (6个是兽医外科医生,11个是兽医护士).
主要成果:
- 所有被调查的学生都接受了一些药监督培训,主要是教学.
- 只有29.4%的受访者报告说,学生有机会提交实践ADE报告.
- 培训似乎缺乏实际应用和现实世界的例子.
结论:
- 目前英国的兽医药监督培训主要是理论性的.
- 建议通过现实世界的ADE示例和实践报告机会来提高实践技能.
- 需要进一步探索学生的知识,态度和感知,以提高培训质量.
相关概念视频
Vaccinations
Overview
Drug Regulation
Drug regulation encompasses the management of drug usage by evaluating its safety and efficacy through assessments conducted by regulatory authorities. Regrettably, the history of drug regulation is marred by several catastrophic events. One such incident is the Elixir Sulfanilamide tragedy, in which the toxic compound diethyl glycol was included in a sweet-tasting medication, leading to numerous fatalities. This event prompted the enactment of the Food, Drug, and Cosmetic Act in 1938. Under...
Pharmacovigilance
Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Pharmacokinetics: Overview
Pharmacokinetics is a scientific discipline that focuses on the journey of a drug within the body, encompassing four key stages: absorption, distribution, metabolism, and elimination. The first stage, absorption, involves the drug's transfer into the bloodstream. Several factors dictate the extent and speed of this process. For example, the liver often metabolizes oral drugs before they reach systemic circulation, leading to only partial absorption. In contrast, intravenous (IV) administration...
Biopharmaceutics and Pharmacokinetics: Overview
Understanding drugs, drug products, and their performance in pharmaceutical science is pivotal. Drugs, whether simple molecules or complex compounds, are designed to interact with the body's biological systems to diagnose, treat, or prevent diseases. Drug products include various delivery systems such as tablets, capsules, injections, and inhalers. The performance of these drug products is gauged by their ability to deliver the active ingredient to the desired site of action at the appropriate...
Pharmaceutical Poisoning: Potential Scenarios
Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...


