为四个东南亚国家的牙医提供数字药物工具的可接受性和可用性
Leanne Teoh1, Ruby Biezen2, Marietta Taylor1
1Melbourne Dental School, University of Melbourne, Melbourne, Australia.
International dental journal
|January 15, 2026
概括
在东南亚的牙医中,MIMS Drugs4dent 工具表现出高度的接受度和可用性. 将药物数据库本地化可能会增强其改善该地区牙科处方实践的潜力.
科学领域:
- 牙科 牙科是指牙科的专业.
- 数字健康数字健康
- 药理学 药理学是指药理学的学科.
背景情况:
- 抗菌素耐药性是一个关键的全球卫生问题,特别是在东南亚.
- 缺乏牙科专用药物资源阻碍了牙医有效的药物管理.
- MIMS Drugs4dent工具是为了帮助澳大利亚牙医优化处方,而开发出来的.
研究的目的:
- 评估MIMS Drugs4dent工具在印度尼西亚,马来西亚,新加坡和泰国的牙医实践者的接受度和可用性.
- 评估牙医从业人员目前用于药物信息的资源.
- 探索数字工具在改善东南亚牙科处方方面的潜力.
主要方法:
- 一项涉及四个东南亚国家的牙医从业者的横截面研究.
- 参与者使用MIMS Drugs4dent一个月.
- 在线调查评估了可接受性和可用性,并对药物信息来源进行了定性主题分析.
主要成果:
- 很高的参与者同意 (超过93%),MIMS Drugs4dent改善了指导方针的遵守和获得牙科药物信息.
- 对该工具的易用性和信息检索速度有强烈的共识 (超过88%).
- 偏好本地化药物数据库和移动友好的版本,报告了62个不同来源的药物信息.
结论:
- 在试验中,MIMS Drugs4dent表现出高的可接受性和可用性.
- 建议与国家特定的药物数据库进行调整,以便在牙科中更广泛地实施.
- 将牙科护理纳入数字健康战略对于应对区域卫生挑战至关重要.
相关概念视频
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...
01:20Measurement of Bioavailability: Pharmacodynamic Methods
Pharmacodynamic methods provide insights into a drug's effects on physiological processes over time and play a crucial role in understanding bioavailability and therapeutic efficacy. These methods can be broadly classified into acute pharmacological and therapeutic response approaches, each with distinct mechanisms and applications.The acute pharmacological response method directly correlates a drug's physiological effects, such as ECG or pupil diameter changes, to its time course in the body.
01:14Drug Dissolution: Requirements and Profile Comparison
The acceptance criteria for dissolution profile data are anchored in Q values, representing the percentage of drug dissolved within a specified period. This assessment unfolds in three stages:First Stage: The test passes if all six drug dosage units are equal to or greater than Q plus 5%; otherwise, the sample proceeds to the second stage.Second Stage: The average of twelve units must be equal to or greater than Q, with no unit falling below Q - 15% to pass; if not, it progresses to the final...
01:26Pharmaceutical Equivalents
As defined by regulatory standards, pharmaceutical equivalents require generic drug products to have identical dosage forms and chemically identical active pharmaceutical ingredients (APIs). They must adhere to compendial or applicable standards for potency, content uniformity, disintegration times, and dissolution rates. In the case of modified-release dosage forms, variations in drug content are permissible as long as the delivered amount remains consistent with the innovator drug product.
01:01Dosage Regimens: Partial Pharmacokinetic Parameters
It is not uncommon for complete drug pharmacokinetic profiles to remain elusive in pharmacokinetics. This necessitates certain educated assumptions by pharmacokineticists to determine appropriate dosage regimens without comprehensive pharmacokinetic data from animal or human studies. One prevalent assumption is setting the bioavailability factor, denoted as F, to 1 or 100%. This assumption caters to the scenario where a drug doesn't achieve full systemic absorption, resulting in the patient...
01:23Oral Drug Delivery Systems: Introduction
Oral drug delivery is the most common route of administration due to its convenience, cost-effectiveness, and high patient compliance. It enables precise formulation to ensure proper drug dosage and bioavailability. The development of oral dosage forms considers drug properties such as solubility, stability, and absorption to optimize therapeutic efficacy.Tablets, capsules, liquids, and chewable formulations enhance drug stability, mask undesirable tastes, and improve patient experience.