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Published on: November 16, 2016
Comparative study of cefuroxime axetil versus amoxicillin in children with early Lyme disease
Stephen C Eppes1, Judith A Childs
1Alfred I. DuPont Hospital for Children, Division of Infectious Diseases, Wilmington, DE 19899, USA. seppes@nemours.org
Insights
Cefuroxime axetil is a safe and effective oral treatment for early Lyme disease in children. This study found it comparable to amoxicillin, offering an alternative for those who cannot tolerate amoxicillin.
Area of Science:
- Pediatric Infectious Diseases
- Antimicrobial Therapy
- Lyme Disease Research
Background:
- Doxycycline, effective for early Lyme disease (LD) in adults, is often avoided in children due to toxicity.
- Amoxicillin is the standard treatment for pediatric LD, but alternatives are needed for intolerant patients.
- Cefuroxime axetil shows comparable efficacy to doxycycline in adult LD cases.
Purpose of the Study:
- To compare the efficacy and safety of two cefuroxime axetil dosages against amoxicillin for treating early Lyme disease in children.
- To evaluate cefuroxime axetil as a potential alternative oral therapy for pediatric Lyme disease.
Main Methods:
- Randomized, unblinded study involving children aged 6 months to 12 years with erythema migrans.
- Comparison of cefuroxime axetil (20 mg/kg/d and 30 mg/kg/d) versus amoxicillin (50 mg/kg/d), all for 20 days.
- Evaluations included serologic testing, safety, tolerability, and efficacy assessments over a 1-year follow-up period.
Main Results:
- Erythema migrans resolution at treatment completion: 67% (amoxicillin), 92% (low-dose cefuroxime), 87% (high-dose cefuroxime).
- Constitutional symptom resolution: 100% (amoxicillin), 69% (low-dose cefuroxime), 87% (high-dose cefuroxime).
- All patients experienced good outcomes; mild diarrhea was the most common side effect, with no hypersensitivity reactions.
Conclusions:
- Both amoxicillin and cefuroxime axetil appear to be safe and efficacious treatments for early pediatric Lyme disease.
- Cefuroxime axetil presents a viable alternative oral therapy for children unable to tolerate amoxicillin.
- Further studies with larger cohorts are needed to establish statistically significant differences between the treatments.
Abstract:
Cefuroxime axetil has been shown to have efficacy comparable to doxycycline in adults with early Lyme disease (LD). Because of toxicity, doxycycline is usually avoided in children. For children who are unable to tolerate amoxicillin, there is currently no proven alternative oral therapy for LD. This randomized, unblinded study compared 2 dosage regimens of cefuroxime axetil (20 mg/kg/d and 30 mg/kg/d) with amoxicillin (50 mg/kg/d), each given for 20 days. Children were enrolled if they were 6 months to 12 years of age, had erythema migrans, and met other eligibility requirements. Serologic testing occurred at entry and after 6 months. Follow-up evaluations for safety, tolerability, and efficacy occurred at 10 and 20 days, 6 months, and 1 year. Forty-three children were randomized (13 in the amoxicillin group, 15 in each cefuroxime axetil group); 39 completed 12 months of follow-up. At the completion of treatment, there was total resolution of erythema migrans in 67% of the amoxicillin group, 92% of the low-dose cefuroxime group, and 87% of the high-dose cefuroxime group, and resolution of constitutional symptoms occurred in 100%, 69%, and 87%, respectively. All patients had a good outcome, with no long-term problems associated with LD. One patient, who was well at the first 2 follow-up visits, was treated with doxycycline because of new constitutional symptoms. Mild diarrhea occurred in a small number of participants in each group (1 patient was diagnosed and treated for Clostridium difficile-associated diarrhea, which occurred after completing the full course of study medication). No hypersensitivity reactions occurred. The number of patients in this trial was not sufficient to demonstrate a statistically significant difference between the 3 groups; however, both amoxicillin and cefuroxime axetil seem to be safe, efficacious treatments for children with early LD.
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