儿科牙科的高风险药物:模式,结果和临床影响
Journal of the American Dental Association (1939)
|October 13, 2025
概括
涉及阿片类药物的儿科牙科诊所显示,过量或持续使用的风险为10%,特别是在幼儿中. 对儿童来说,更安全的阿片类药物和非阿片类药物止痛药的处方至关重要.
科学领域:
- 儿科牙科 儿科牙科
- 药理学 药理学是指药理学的学科.
- 公共卫生 公共卫生
背景情况:
- 像阿片类药物和二类药物这样的高风险药物在儿科牙科护理中很常见.
- 对这些药物的处方模式和儿童的不良后果尚不清楚.
研究的目的:
- 评估在儿科牙医诊所处方高风险药物的频率.
- 确定与接受这些药物的儿童不良后果相关的因素.
主要方法:
- 分析MarketScan数据 (2014-2019) 对18岁以下的患者进行牙科检查的分析.
- 定义的高风险药物 (二,巴比图拉特,阿片类药物) 和复合结果 (住院治疗,ED/紧急护理访问在7天内).
- 检查了阿片类药物特定的结果 (过量服用,持续使用),并使用了统计分析的概括估计方程.
主要成果:
- 0.72%的儿科牙科访问涉及高风险药物;4.3%导致复合结果.
- 与阿片类药物相关的结果发生在10.1%的阿片类药物处方牙科诊所.
- 增加不良结果的几率与特定的年龄组,性别,慢性疾病和护理环境有关.
结论:
- 十分之一的儿科牙科诊所使用阿片类药物处方导致过量或持续使用,特别是在年幼的儿童中.
- 在儿童阿片类药物处方和推广基于指南的非阿片类止痛药方面迫切需要谨慎.
- 建议包括遵守指导方针,非阿片类药物疼痛管理,以及为更安全的儿科牙科处方提供者教育.
相关概念视频
Pharmacokinetics in Pediatric Patients: Drug Excretion
212
In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
212
Pharmacokinetics in Pediatric Patients: Drug Distribution
252
Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
252
Drug Dosing: Infants and Children
253
Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
253
Pharmacokinetics in Pediatric Patients: Drug Metabolism
192
In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
192
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
242
Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
242
Factors Affecting Drug Response: Overview
3.0K
When it comes to infants and young children, they are typically administered smaller doses of medication in comparison to adults. This is primarily because their organ functions still need to fully develop, meaning their bodies are not as efficient at metabolizing or eliminating drugs. Additionally, their blood-brain barrier is more permeable than in adults. As a result, high concentrations of drugs can easily penetrate the central nervous system (CNS), potentially leading to neurological...
3.0K


