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Rapid drug desensitization in children: A single-center experience
Çağrı Torun Özel1, Aslı Kuzu Kuşaklı1, Azize Pınar Metbulut2
1Department of Pediatric Allergy and Immunology, Ankara Bilkent City Hospital, Ankara, Türkiye.
Insights
Pediatric rapid drug desensitization (RDD) is highly effective and safe for children with drug hypersensitivity reactions (HSRs). This study shows over 99% success, making RDD a reliable option when other treatments fail.
Area of Science:
- Pediatric Allergy and Immunology
- Clinical Pharmacology
- Immunology
Background:
- Drug hypersensitivity reactions (HSRs) in children often lead to essential treatment cessation.
- Pediatric data on rapid drug desensitization (RDD) are limited, despite its importance for safe re-exposure.
Purpose of the Study:
- To evaluate the efficacy and safety of RDD in a pediatric population.
- To analyze the outcomes of RDD across various drug classes in children.
Main Methods:
- Retrospective analysis of 59 pediatric patients (0-18 years) undergoing RDD.
- Reviewed 1978 RDD procedures using 62 protocols for 27 different drugs.
- Analyzed demographics, HSR characteristics, premedication, and breakthrough reactions (BRs).
Main Results:
- Over 99% success rate with 1977 out of 1978 protocols successfully completed.
- Only one patient required treatment modification; 58 patients completed desensitization.
- Breakthrough reactions (BRs) occurred in 0.6% of procedures, mostly mild-to-moderate and manageable.
Conclusions:
- Pediatric RDD demonstrates high efficacy (>99%) and a favorable safety profile.
- RDD is a reliable therapeutic option for children with drug hypersensitivity when alternatives are unavailable.
- This study represents one of the largest pediatric RDD series, supporting its clinical utility.
Background:
Drug hypersensitivity reactions (HSRs) in children often necessitate discontinuation of essential therapies. Rapid drug desensitization (RDD) is a key strategy to enable safe re-exposure; however, pediatric data remain limited.
Methods:
This retrospective study included 59 pediatric patients (0-18 years) who underwent RDD between September 2019 and January 2025 at a tertiary pediatric allergy center. Demographics, HSR characteristics, premedication strategies, desensitization protocols, and breakthrough reactions (BRs) were analyzed. A total of 1978 procedures were performed using 62 protocols for 27 different drugs, including antimicrobials, enzyme replacement therapies (ERTs), immunomodulators, chemotherapeutics, and other agents.
Results:
Fifty-nine patients underwent 1978 RDD procedures. Of these, 58 patients successfully completed desensitization, while treatment modification was required in one patient. In total, 1977 protocols were successfully completed, with only one protocol failure, corresponding to an overall success rate exceeding 99%. BRs reactions occurred in 0.6% (n = 12) of procedures; most were mild to moderate and effectively managed without discontinuation of the protocol. Premedication regimens were individualized according to the drug administered and patient characteristics.
Conclusion:
This study represents one of the largest pediatric RDD series to date, demonstrating high efficacy and a favorable safety profile across a wide range of drug classes. Pediatric RDD should be considered a reliable therapeutic option in children with drug hypersensitivity when alternatives are lacking.
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