Impact of an institutional guideline on the care of neonates at risk for herpes simplex virus in the emergency department

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Background and Objectives: Herpes simplex virus (HSV) is rare in neonates but carries significantmorbidity andmortality in that group. Emergency department (ED) clinicians have little guidance to decide when to test for HSVand give acyclovir.We created an institutional guideline to provide guidance in patients younger than 6 weeks. Our objective was to evaluate whether guideline implementation affected the ED's decision to test for HSV, and ED use of HSV polymerase chain reactions (PCRs) and acyclovir. Methods: We reviewed charts for patients 1 year before implementation and 1 year after implementation of our guideline. Inclusion criteria were younger than 60 days, admitted through the ED, symptom onset younger than 6 weeks, and any one of the following criteria: (1) ED blood culture obtained, (2) ED or inpatient HSV PCR obtained, and (3) ED or inpatient acyclovir treatment. Premature patients and transfer patientswere excluded. We compared whether the decision to initiate HSV testing, ED use of HSV PCRs, serum alanine aminotransferase, and acyclovir use changed post-guideline implementation. Results: We reviewed 173 charts pre-implementation and 129 postimplementation. We found a significant decrease in ED testing for HSV among patients who did not meet guideline criteria (P < 0.01). We saw an improvement in the use of alanine aminotransferase among patients who met criteria for testing (P = 0.02), but no change in the use of HSV PCRs or acyclovir use among tested patients. Conclusions: Guideline implementation reduced HSV evaluations in low-risk patients, but did not improve test utilization or acyclovir administration among those tested. Additional work is needed to improve guideline utilization.

Original languageEnglish
Pages (from-to)396-401
Number of pages6
JournalPediatric emergency care
Issue number6
StatePublished - 2017


  • Herpes simplex virus
  • acyclovir
  • guideline
  • neonate
  • polymerase chain reaction


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