在门诊护理中对SGLT-2抑制剂的坚持影响因素的预测建模:从处方索赔的洞察力 数据分析 数据分析
Nadia Khartabil1, Candis M Morello2, Etienne Macedo3
1Center of Graduate Studies, West Coast University, Los Angeles, CA 90004, USA.
Pharmacy (Basel, Switzerland)
|April 26, 2024
概括
在患有2型糖尿病,心力衰竭或慢性病的患者中,可以预测对-葡萄糖共运输体2抑制剂 (SGLT2i) 的坚持. 一个决策树模型确定了糖化血红蛋白,年龄,性别和保险作为SGLT2i坚持的关键预测因素.
科学领域:
- 药理学和治疗学 药理学和治疗学
- 慢性疾病管理中的现实世界证据
- 卫生信息学和预测建模
背景情况:
- -葡萄糖携带载体2抑制剂 (SGLT2i) 为患有2型糖尿病 (T2D),心力衰竭 (HF) 和慢性病 (CKD) 的患者提供心血管和代谢益处.
- 现实世界数据有限,可以预测SGLT2i在门诊环境中的坚持.
- 了解坚持预测因素对于优化治疗结果至关重要.
研究的目的:
- 使用电子健康记录开发和验证SGLT2i遵守的预测模型.
- 确定影响SGLT2i遵守的关键人口,临床和保险相关因素.
- 评估坚持对血糖控制和功能的影响.
主要方法:
- 在2020年1月至2021年4月期间,在加州大学圣地亚哥卫生部对174名成年患者进行了SGLT2i的回顾性研究.
- 通过覆盖日数比例 (PDC) 测量依从性.
- 采用简单的决策树模型,分析了21个变量,包括HbA1c,GFR,年龄,性别,种族/种族和保险计划.
主要成果:
- 决策树模型实现了 74% 和 82% 的曲线下面面积 (AUC) 准确度.
- 遵守的关键预测因素包括糖化血红蛋白 (HbA1c),年龄,性别和保险计划支付金额.
- 坚持是与HbA1c成反比例的,与计划支付金额成正比的. 不符合标准的患者HbA1c较高,EGFR较低.
结论:
- 一个简单的决策树模型有效预测SGLT2i在门诊患者的坚持.
- 预测模型可以帮助临床医生识别有风险的患者,并定制干预措施以改善遵守.
- 优化SGLT2i坚持对于有效管理T2D,HF和CKD至关重要.
相关概念视频
Factors Influencing Drug Absorption: Disease States and Pharmacology
503
Multiple disease states can significantly influence the oral drug absorption process by affecting blood flow and the functionality of the gastrointestinal (GI) system. Various GI diseases, including conditions that alter GI motility, such as diarrhea, decreased acid secretions (achlorhydria), and infections, have been associated with reduced drug absorption.
Substances such as alcohol and specific drugs, including antineoplastics, can also negatively impact drug absorption. For instance,...
Substances such as alcohol and specific drugs, including antineoplastics, can also negatively impact drug absorption. For instance,...
503
Factors Influencing Drug Absorption: Pharmaceutical Parameters
133
Solid dosage forms such as tablets and capsules undergo rigorous manufacturing processes to ensure stability and effectiveness. Their dissolution and absorption properties are influenced significantly by the choice of excipients (inactive ingredients that serve various roles in the formulation), and the methodology applied during production. The manufacturing parameters, such as compression force and granulation techniques, significantly affect dissolution rates. Elevated compression forces...
133
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
125
Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
125
Drug Absorption: Factors Affecting GI Absorption
3.9K
The process of oral drug absorption can be influenced by several factors. Weakly acidic drugs tend to be absorbed more readily from the stomach due to their nonionized state. However, absorption may be less efficient in the upper intestine, where drugs are often ionized. Interestingly, despite the stomach's apparent advantage for drug absorption, its mucous layer can hinder diffusion. Its surface area is also smaller than the intestine's, which can further slow down the absorption rate.
3.9K
Factors Influencing Drug Absorption: Presystemic Elimination
214
The pharmacokinetic journey of oral drugs begins with a crucial first pass through the hepatic portal system, called the first-pass effect. This first pass significantly impacts bioavailability — the proportion of a drug that enters systemic circulation and is available for therapeutic action. The primary route sees the drug absorbed by intestinal membranes and then shunted to the liver via the hepatic portal vein. Here, pre-systemic elimination occurs as drugs face metabolism or biliary...
214
Physiological Pharmacokinetic Models: Incorporating Hepatic Transporter-Mediated Clearance
38
Drug transporters are critical in drug absorption, distribution, and excretion processes. They should be included in physiological-based pharmacokinetic (PBPK) models, which help predict human drug disposition. However, predicting this is challenging during drug development, especially when liver transport is involved. However, with a realistic representation of body transport processes, an accurate model may be possible.
A recent model describes pravastatin's hepatobiliary excretion,...
A recent model describes pravastatin's hepatobiliary excretion,...
38


