Related Experiment Video
Updated: Aug 14, 2026

Stepwise Dosing Protocol for Increased Throughput in Label-Free Impedance-Based GPCR Assays
Published on: February 21, 2020
TESS-based dose-response using pediatric clonidine exposures
Blaine E Benson1, Daniel A Spyker, William G Troutman
1New Mexico Poison and Drug Information Center and University of New Mexico College of Pharmacy, Albuquerque, 87131, USA. jebenson@salud.unm.edu
Insights
This study shows that data from the American Association of Poison Control Centers Toxic Exposure Surveillance System (TESS) can establish a dose-response relationship for pediatric clonidine poisoning. This helps understand clonidine toxicity in children.
Area of Science:
- Toxicology
- Pediatric Emergency Medicine
- Data Science in Healthcare
Background:
- The toxic and lethal doses of clonidine in children are not well-defined.
- Accurate dose-response data is crucial for managing pediatric clonidine exposures.
Purpose of the Study:
- To determine if the Toxic Exposure Surveillance System (TESS) database can be used to establish a dose-response relationship for clonidine exposure in children.
- To analyze pediatric clonidine poisoning cases to identify factors influencing medical outcomes.
Main Methods:
- Retrospective analysis of 3,458 single-substance clonidine exposures in children under 6 years old reported to TESS (2000-2003).
- Logistic regression was used to examine the relationship between clonidine dose (microg/kg), dose certainty, and medical outcome severity.
- Medical outcomes were categorized (Arrest, Major, Moderate, Mild, No effect), with respiratory arrest as the most severe.
Main Results:
- The logistic regression model demonstrated a statistically significant relationship between medical outcome and both the logarithm of the dose per kilogram and the certainty of the dose (P < 0.0001).
- Specifically, Log dose/kg (P = 0.0000) and Certainty (P = 0.045) were significant predictors of medical outcome.
Conclusions:
- The Toxic Exposure Surveillance System (TESS) database is a valuable resource for establishing a statistically sound dose-response relationship for pediatric clonidine poisoning.
- These findings can inform clinical management and public health strategies for clonidine overdose in children.
Objective:
The toxic and lethal doses of clonidine in children are unclear. This study was designed to determine whether data from the American Association of Poison Control Centers Toxic Exposure Surveillance System (TESS) could be utilized to determine a dose-response relationship for pediatric clonidine exposure.
Methods:
3,458 single-substance clonidine exposures in children <6 years of age reported to TESS from January 2000 through December 2003 were examined. Dose ingested, age, and medical outcome were available for 1550 cases. Respiratory arrest cases (n = 8) were classified as the most severe of the medical outcome categories (Arrest, Major, Moderate, Mild, and No effect). Exposures reported as a "taste or lick" (n = 51) were included as a dose of 1/10 of the dosage form involved. Dose ranged from 0.4 to 1980 (median 13) microg/kg. Weight was imputed based on a quadratic estimate of weight for age. Dose certainty was coded as exact (26% of cases) or not exact (74%). Medical outcome (response) was examined via logistic regression using SAS JMP (release 5.1).
Results:
The logistic model describing medical outcome (P < 0.0001) included Log dose/kg (P = 0.0000) and Certainty (P = 0.045).
Conclusion:
TESS data can provide the basis for a statistically sound description of dose-response for pediatric clonidine poisoning exposures.
Related Concept Videos
Dose Response Curve: Conventional Versus Nonmonotonic
Drug Dosing: Infants and Children
Dose-Response Relationship: Overview
Desensitization and Tachyphylaxis
Several...
Dosage Regimens: Designs and Approaches
Factors Affecting Drug Response: Overview
