Oral Acyclovir Suppression and Neurodevelopment after Neonatal Herpes

Neonates with HSV and CNS involvement or skin, eye, and mouth disease were treated with IV acyclovir for 2 to 3 weeks, then acyclovir suppressive therapy or placebo for 6 months. Infants receiving acyclovir suppressive therapy had better neurodevelopmental outcomes. The outcomes of neonatal herpes s...

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Veröffentlicht in:The New England journal of medicine 2011-10, Vol.365 (14), p.1284-1292
Hauptverfasser: Kimberlin, David W, Whitley, Richard J, Wan, Wen, Powell, Dwight A, Storch, Gregory, Ahmed, Amina, Palmer, April, Sánchez, Pablo J, Jacobs, Richard F, Bradley, John S, Robinson, Joan L, Shelton, Mark, Dennehy, Penelope H, Leach, Charles, Rathore, Mobeen, Abughali, Nazha, Wright, Peter, Frenkel, Lisa M, Brady, Rebecca C, Van Dyke, Russell, Weiner, Leonard B, Guzman-Cottrill, Judith, McCarthy, Carol A, Griffin, Jill, Jester, Penelope, Parker, Misty, Lakeman, Fred D, Kuo, Huichien, Lee, Choo Hyung, Cloud, Gretchen A
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Sprache:eng
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Zusammenfassung:Neonates with HSV and CNS involvement or skin, eye, and mouth disease were treated with IV acyclovir for 2 to 3 weeks, then acyclovir suppressive therapy or placebo for 6 months. Infants receiving acyclovir suppressive therapy had better neurodevelopmental outcomes. The outcomes of neonatal herpes simplex virus (HSV) disease are dependent on the extent of the disease. 1 Approximately 30% of babies with disseminated disease die, but only 20% of survivors have neurologic sequelae. 2 In contrast, only 6% of babies with central nervous system (CNS) disease die, but approximately 70% have permanent neurologic impairment. 2 Skin, eye, and mouth disease is not associated with death, and neurologic impairment is rare with this manifestation of neonatal herpes. 3 HSV establishes latency in sensory ganglia, with periodic reactivation and recurrence of localized disease. 4 , 5 Whether the virus subclinically reactivates in the brain after neonatal HSV . . .
ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa1003509