3.26 : Regime de Dosagem de Medicamentos: Visão Geral

A drug dosage regimen describes the specific instructions and schedule for administering a drug to a patient. It considers factors such as drug dosage, frequency, route of administration, and duration of treatment. Designing an appropriate dosage regimen for a patient aims to achieve a target drug concentration at the site of action.

Typically, the starting dose and dosing interval are guided by the manufacturer's recommendations based on clinical trials conducted during and after drug development. However, several additional parameters influence regimen design. Firstly, the drug's pharmacokinetic parameters, such as absorption, distribution, and elimination, need to be assessed in the patient. The half-life of a drug determines the dosing interval, as it represents the time taken for the drug concentration to reduce by half. Drugs with shorter half-lives often require more frequent dosing to maintain therapeutic levels.

Patient parameters, such as age, weight, gender, and nutritional status, can also impact the drug dosage regimen. Pathophysiologic conditions like renal dysfunction, hepatic disease, or congestive heart failure can alter the normal pharmacokinetic profile, requiring careful dose adjustments. Personal lifestyle factors like smoking, alcohol abuse, and obesity are known to affect drug pharmacokinetics.

Lastly, patient compliance plays a crucial role in achieving therapeutic outcomes. Noncompliance, or the lack of adherence to the prescribed medication regimen, can hinder the effectiveness of the treatment.