Related Experiment Videos
Recent developments in podiatric prescribing in the UK and Australia
Mark F Gilheany1, Alan M Borthwick
1Podiatrists Registration Board of Victoria, Melbourne, Victoria, Australia.
Journal of Foot and Ankle Research
|December 17, 2009
Summary
Recent policy changes in Australia and the UK are expanding podiatrists' access to restricted medicines, reflecting broader healthcare workforce reforms. This commentary examines the potential impacts of these significant shifts for allied health professionals.
Area of Science:
- Healthcare Policy
- Pharmacy Practice
- Allied Health Workforce Development
Background:
- Recent policy shifts in Australia have substantially increased podiatrists' access to restricted medicines.
- Simultaneously, the UK Department of Health has focused on prescribing and medicine access for allied health professionals, including podiatrists.
Purpose of the Study:
- To explore the potential implications of these concurrent policy changes regarding medicine access for podiatrists.
- To contextualize these changes within broader healthcare workforce reshaping initiatives.
Main Methods:
- Commentary based on analysis of recent policy developments in Australia and the UK.
- Review of healthcare policies related to allied health professional scope of practice.
Main Results:
- The changes in Australia align with national healthcare policies aimed at workforce reform.
- The UK's focus on allied health prescribing indicates a growing trend in medicine access expansion.
Conclusions:
- Expanded medicine access for podiatrists signifies a significant evolution in allied health roles.
- These changes necessitate careful consideration of their impact on healthcare delivery and patient outcomes.
Related Concept Videos
01:31Diabetic Foot Ulcer
Definition A diabetic foot ulcer (DFU) is a chronic, non-healing wound that develops in individuals with diabetes. It typically occurs on pressure-bearing areas such as the heel, metatarsal heads, or hallux, and carries a high risk of infection and amputation.Pathophysiology • The development of DFUs can be explained by four interconnected mechanisms: neuropathy, ischemia, infection, and impaired wound healing. • Neuropathy is the most common factor. Sensory neuropathy reduces pain perception,...
01:02Prescription, Nonprescription and Orphan Drugs
Prescription drugs require a prescription from a medical practitioner and can only be obtained from a pharmacy. They have many applications, including treating pain, anxiety, and hypertension.
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
01:19Pharmacovigilance
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...
01:15Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions
PK–PD modeling has significantly influenced FDA regulatory decisions, particularly drug approval, dosage optimization, and labeling. These models integrate pharmacokinetics (PK) and pharmacodynamics (PD) to predict drug behavior and effects, aiding in optimizing dosing regimens and enhancing the probability of clinical trial success.One notable example is Nesiritide (Natrecor®), a recombinant human brain natriuretic peptide for treating acute decompensated congestive heart failure (CHF).
01:03Drug Control Governance: Regulatory Bodies and Their Impact
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 a...
01:25Drug 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...