Peak-to-trough ratio

From WikiMD's Food, Medicine & Wellness Encyclopedia

Peak-to-trough ratio is a pharmacokinetic parameter that is used to describe the fluctuation of drug concentration in the body over a dosing interval. It is calculated as the ratio of the maximum (peak) concentration (Cmax) to the minimum (trough) concentration (Cmin) of a drug in the body. The peak-to-trough ratio is an important factor in determining the dosing regimen of a drug and can influence the efficacy and safety of the drug.

Calculation[edit | edit source]

The peak-to-trough ratio is calculated by dividing the maximum concentration of the drug (Cmax) by the minimum concentration of the drug (Cmin). This ratio provides a measure of the fluctuation of drug concentration in the body over a dosing interval.

Importance[edit | edit source]

The peak-to-trough ratio is an important factor in determining the dosing regimen of a drug. A high peak-to-trough ratio may indicate a large fluctuation in drug concentration, which could lead to periods of sub-therapeutic or toxic drug levels. Conversely, a low peak-to-trough ratio may indicate a more constant drug concentration, which could lead to more consistent therapeutic effects.

Factors affecting peak-to-trough ratio[edit | edit source]

Several factors can affect the peak-to-trough ratio, including the absorption, distribution, metabolism, and excretion (ADME) of the drug, the dosing regimen, and individual patient factors. For example, drugs that are rapidly absorbed and eliminated will have a higher peak-to-trough ratio than drugs that are slowly absorbed and eliminated.

Clinical implications[edit | edit source]

The peak-to-trough ratio can have important clinical implications. For example, drugs with a high peak-to-trough ratio may be associated with a higher risk of adverse effects, while drugs with a low peak-to-trough ratio may be associated with a lower risk of adverse effects. Therefore, understanding the peak-to-trough ratio can help clinicians optimize drug therapy and minimize the risk of adverse effects.

See also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD