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Defining risk factors for red man syndrome in children and adults
Angela L Myers1, Andrea Gaedigk, Hongying Dai
1Department of Pediatrics, Medical Research, Children's Mercy Hospitals and Clinics and the University of Missouri-Kansas City, Kansas City, MO 64108, USA. amyers@cmh.edu
Insights
Red man syndrome (RMS) is a common adverse reaction in children receiving vancomycin. Risk factors include Caucasian ethnicity, older age, prior RMS, and higher vancomycin doses, while African American race is protective.
Area of Science:
- Pediatric Pharmacology
- Clinical Toxicology
- Pharmacovigilance
Background:
- Red man syndrome (RMS) is a known vancomycin adverse reaction in children, but its prevalence, characteristics, and risk factors remain unclear.
- Understanding these factors is crucial for safe vancomycin administration in pediatric populations.
Purpose of the Study:
- To determine the prevalence, characteristics, and risk factors for RMS in pediatric patients receiving vancomycin.
- To investigate potential contributing genetic factors to RMS development.
Main Methods:
- A multicenter retrospective study involving 546 pediatric patients (0.5-21 years) who received intravenous vancomycin.
- Data collection included chart reviews and parent/nurse reports for demographic and symptom data.
- Genotype analysis focused on single nucleotide polymorphisms within the histamine pathway.
Main Results:
- RMS occurred in 14% of pediatric vancomycin recipients.
- Common symptoms included rash, pruritus, and flushing without hypotension.
- Identified risk factors: Caucasian ethnicity, age > 2 years, prior RMS, higher vancomycin dose/concentration, and antihistamine use. African American race was protective.
- No significant association found between RMS and genetic variants in the histamine pathway.
Conclusions:
- Red man syndrome is a frequent adverse event in children treated with vancomycin.
- Key risk factors identified include Caucasian ethnicity, age, prior RMS, and vancomycin administration parameters.
- Genetic factors within the histamine pathway do not appear to be major contributors to RMS risk in this population.
Background:
Red man syndrome (RMS) is a well-known adverse reaction that occurs in pediatric patients receiving vancomycin, yet reported prevalence is varied, and characteristics and risk factors are not well understood. Our objective was to determine the prevalence, characteristics and risk factors for RMS in pediatric patients receiving vancomycin, including contributing genetic factors.
Methods:
A multicenter retrospective study of 546 subjects (0.5-21 years) who received at least 1 dose of intravenous vancomycin was conducted. Demographic and symptom data were collected through chart review and parent/nurse report. Genotype analysis included 10 single nucleotide polymorphisms in the histamine pathway.
Results:
RMS was observed in 77 (14%) subjects receiving vancomycin. Forty percent of subjects with RMS symptoms developed rash, pruritis and flushing, without hypotension. Antecedent antihistamine use was identified as a risk factor for RMS (P < 0.001). Multivariate regression analysis identified age > 2 years (P = 0.008), previous RMS (P < 0.001), vancomycin dose (P = 0.02) and vancomycin concentration (P = 0.017) as RMS risk factors, whereas African American race was protective (P = 0.011). We observed an apparent association between RMS and a single nucleotide polymorphism in the diamine oxidasegene (P = 0.044); however, no associations were revealed by multifactor dimensionality reduction analysis.
Conclusions:
RMS is a common adverse event in children receiving vancomycin. Identified risk factors are Caucasian ethnicity, age ≥ 2 years, previous RMS history, vancomycin dose ≥ 10 mg/kg, vancomycin concentration ≥ 5 mg/mL and antecedent antihistamine use. Known genetic variants in histamine metabolism or receptors do not appear to be substantial contributors to risk of RMS.
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