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Early vancomycin therapy and adverse outcomes in children with pneumococcal meningitis
Steven C Buckingham1, Jonathan A McCullers, Jorge Luján-Zilbermann
1Department of Pediatrics, University of Tennessee Health Science Center, Le Bonheur Children's Medical Center, Memphis, Tennessee, USA. sbuckingham@utmem.edu
Insights
Early vancomycin in pediatric pneumococcal meningitis did not improve outcomes but increased hearing loss risk. Delaying vancomycin may be safer for children with suspected meningitis.
Area of Science:
- Pediatric Infectious Diseases
- Clinical Pharmacology
- Neurology
Background:
- Pneumococcal meningitis in children often treated with vancomycin and cephalosporins.
- The impact of vancomycin timing on treatment outcomes is not well understood.
Purpose of the Study:
- To investigate the association between vancomycin administration timing and outcomes in pediatric pneumococcal meningitis.
Main Methods:
- Retrospective review of medical records for 114 children with pneumococcal meningitis.
- Vancomycin start time defined as hours from cephalosporin initiation.
- Outcomes assessed included death, sensorineural hearing loss, and neurologic deficits.
Main Results:
- No significant association found between vancomycin start time and death or neurologic deficits.
- Shorter vancomycin start times (<1 hour) were linked to a higher incidence of hearing loss.
- Hearing loss was independently associated with vancomycin start time <2 hours.
Conclusions:
- Early vancomycin therapy in pediatric pneumococcal meningitis is not clinically beneficial and increases hearing loss risk.
- Consider delaying vancomycin for at least 2 hours after initial cephalosporin dose in children with suspected meningitis.
Background:
Experts recommend that children with suspected pneumococcal meningitis should empirically receive combination therapy with vancomycin plus either ceftriaxone or cefotaxime. The relationship between timing of the first dose of vancomycin relative to other antibiotics and outcome in these children, however, has not been addressed.
Methods:
Medical records of children with pneumococcal meningitis at a single institution from 1991-2001 were retrospectively reviewed. Vancomycin start time was defined as the number of hours from initiation of cefotaxime or ceftriaxone therapy until the administration of vancomycin therapy. Outcome variables were death, sensorineural hearing loss, and other neurologic deficits at discharge. Associations between independent variables and outcome variables were assessed in univariate and multiple logistic regression analyses.
Results:
Of 114 subjects, 109 received empiric vancomycin therapy in combination with cefotaxime or ceftriaxone. Ten subjects (9%) died, whereas 37 (55%) of 67 survivors who underwent audiometry had documented hearing loss, and 14 (13%) of 104 survivors were discharged with other neurologic deficits. Subjects with hearing loss had a significantly shorter median vancomycin start time than did those with normal hearing (<1 vs 4 hours). Vancomycin start time was not significantly associated with death or other neurologic deficits in univariate or multivariate analyses. Multiple logistic regression revealed that hearing loss was independently associated with vancomycin start time <2 hours, blood leukocyte count <15000/microL, and cerebrospinal fluid glucose concentration <30 mg/dL.
Conclusions:
Early empiric vancomycin therapy was not clinically beneficial in children with pneumococcal meningitis but was associated with a substantially increased risk of hearing loss. It may be prudent to consider delaying the first dose of vancomycin therapy until > or =2 hours after the first dose of parenteral cephalosporin in children beginning therapy for suspected or confirmed pneumococcal meningitis.
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