影响口腔大气管的因素 保持类型:尖端或尖端
Kendrea L Focht Garand1, Mary Catherine Reilly1, Dahye Choi1
1Department of Speech Pathology and Audiology, University of South Alabama, Mobile.
Perspectives of the ASHA special interest groups
|June 5, 2023
概括
在健康的成年人中,在吞过程中常见的是尖端球囊握住. 老年人和男性更有可能表现出特定的玻尿酸保持类型,影响典型的吞行为.
科学领域:
- 吞生理学 吞生理学
- 脱的生物力学
- 成人语音和听力科学 听力科学
背景情况:
- 了解典型的吞机制对于识别吞障碍至关重要.
- 吞的口腔阶段的关键方面,即玻尿酸保持位置,可以变化.
- 年龄和性别等因素可能会影响这些行为.
研究的目的:
- 为了检查年龄,性别和吞任务如何影响健康成年人的玻尿酸保持位置.
- 为了研究玻尿酸保持位置和特定的修改巴吞损伤概况 (MBSImP) 评分之间的关系.
主要方法:
- 对195名健康成年人的视频光学吞研究进行了回顾性分析.
- 对各种液体一致性和体积的玻尿酸保持类型 (倾斜型和倾斜型) 的分类.
- 后勤回归和费舍尔的精确测试被用于统计分析.
主要成果:
- 在95%的吞任务中观察到倾斜螺栓保持类型.
- 老年人更有可能使用倾斜型用于薄和蜂蜜加厚的液体.
- 男性在特定任务中更倾向于使用型.
结论:
- 尖头螺栓保持是健康成年人的主要模式.
- 年龄和性别是影响玻尿酸保持类型的重要因素.
- 这些发现有助于为吞行为提供规范性数据.
相关概念视频
One-Compartment Open Model for IV Bolus Administration: General Considerations
258
The one-compartment model is a pharmacokinetic tool that models the body as a single, uniform compartment, facilitating the understanding of drug distribution and elimination. This model is particularly beneficial for intravenous (IV) bolus administration, where the drug rapidly circulates throughout the body.
The drug's presence in the body is defined by an equation representing the difference between the rates of drug entry and exit. Key parameters—elimination rate constant,...
The drug's presence in the body is defined by an equation representing the difference between the rates of drug entry and exit. Key parameters—elimination rate constant,...
258
Two-Compartment Open Model: IV Bolus Administration
589
The two-compartment model for intravenous (IV) bolus administration illustrates drug distribution in the body, subdividing it into central and peripheral compartments. This model operates on the concept of two-compartment kinetics. The drug's plasma concentration shows a bi-exponential decline following IV bolus administration, signaling the presence of two disposition processes: distribution and elimination.
The disparity between drug input and the sum of drug transfer rates between...
The disparity between drug input and the sum of drug transfer rates between...
589
One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution
356
The one-compartment open model is a simplified approach used in pharmacokinetics to understand the distribution and elimination of a drug administered through an intravenous bolus. This model assumes rapid drug dispersal throughout the body and elimination using a first-order process. Key pharmacokinetic parameters, such as the elimination rate constant (k), half-life (t1/2), and the apparent volume of distribution (Vd), can be estimated from this model. The elimination rate is calculated...
356
Factors Influencing Drug Absorption: Pharmaceutical Parameters
157
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...
157
The Tongue and Taste Buds
37.0K
The surface of the tongue is covered with various small bumps called papillae, which either distribute what has been ingested (filiform papillae) or contain the sensory taste (or gustatory) receptor cells (fungiform, circumvallate, and foliate papillae). Embedded within each taste-related papilla are the taste buds—clusters of 30 to 100 gustatory receptor cells.
37.0K
Factors Affecting Dissolution: Particle Size and Effective Surface Area
903
Dissolution kinetics, an essential aspect of oral drug delivery, is significantly influenced by the drug's particle size. According to the Noyes-Whitney dissolution model, the dissolution rate correlates directly with the drug's surface area. The larger the surface area, the higher the drug's solubility in water, leading to a faster drug dissolution rate. Reducing particle size increases the effective surface area, enhancing the dissolution process. Micronization and nanosizing are...
903


