认可的助产士在澳大利亚处方计划药物:一个范围审查
Elizabeth Hull1, Roslyn Donnellan-Fernandez1, Carolyn Hastie2
1School of Nursing and Midwifery, Griffith University, Logan campus, Queensland, Australia.
Women and birth : journal of the Australian College of Midwives
|November 8, 2023
概括
认可的助产士提高了妇女的药物获取,但他们的处方受到限制性政策和系统性障碍的阻碍. 需要进一步的研究和政策变化,以优化澳大利亚的助产士处方.
科学领域:
- 孕产妇健康 孕产妇健康
- 药理学 药理学是指药理学的学科.
- 卫生政策 卫生政策
背景情况:
- 澳大利亚的认可助产士有权对计划药物进行处方.
- 它们可以改善妇女获得药物的机会,并得到医疗保险折扣的支持.
- 立法不一致和政策障碍阻碍了他们的处方做法.
研究的目的:
- 审查和综合有关澳大利亚认可助产士处方计划药物的现有文献.
- 确定当前助产士处方实践中的关键主题和挑战.
- 为未来的政策和实践发展提供信息.
主要方法:
- 使用乔安娜·布里格研究所的方法进行了范围审查.
- 在CINAHL,PubMed,Science Direct和Medline数据库中进行了搜索.
- 对2016年至2023年间发表的七篇同行评审文章进行了定性内容分析.
主要成果:
- 认可的助产士显著增加了妇女获得处方药的机会.
- 制药福利计划提出了限制,限制了助产士的处方范围.
- 处方受组织结构和专业关系的影响.
结论:
- 处方权力提高了认可助产士的实践,角色满意度和及时患者获得药物的机会.
- 障碍包括制药福利计划,配方限制和医疗服务政策.
- 进一步发展教育,消除障碍和安全演示对于充分利用至关重要.
更多相关视频
相关概念视频
Drug Classes and Categories
2.0K
Drugs can be classified according to their chemical composition or their intended therapeutic application. For instance, anti-infective agents that possess the ability to eliminate pathogens or suppress their growth and reproduction can be grouped based on the organisms they target or their chemical structure. Furthermore, drugs can be divided into prescription, nonprescription, or controlled substances. Prescription medications, such as antibiotics, require oversight from a licensed healthcare...
2.0K
Drug Administration and Therapy Phases: Overview
483
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...
483
Pharmacovigilance
860
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...
860
Drug Control Governance: Regulatory Bodies and Their Impact
163
Drug control governance involves the oversight and regulation of pharmaceuticals to ensure their safety and efficacy while preventing illegal drug use and trafficking. Regulatory bodies, including the US Food and Drug Administration (FDA) and the European Union's European Medicines Agency (EMA), play a central role in this process. These agencies evaluate the safety and efficacy of drugs before they can be marketed. They fund clinical trials and assess the benefits and risks associated with...
163
Opioid Analgesics: Synthetic and Semisynthetic Opioids
310
Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
310
Drug Dosage Regimen: Overview
3.6K
A drug dosage regimen describes the specific instructions and schedule for administering a drug to a patient. It considers factors such as drug dosage, frequency, route of administration, and duration of treatment. Designing an appropriate dosage regimen for a patient aims to achieve a target drug concentration at the site of action.
Typically, the starting dose and dosing interval are guided by the manufacturer's recommendations based on clinical trials conducted during and after drug...
Typically, the starting dose and dosing interval are guided by the manufacturer's recommendations based on clinical trials conducted during and after drug...
3.6K


