1989
DOI: 10.1001/archderm.1989.01670230090016
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Successful Treatment of Progressive Acyclovir-Resistant Herpes Simplex Virus Using Intravenous Foscarnet in a Patient With the Acquired Immunodeficiency Syndrome

Abstract: We report a case of orofacial herpes simplex virus (HSV) infection that was progressive despite multiple courses of acyclovir sodium in a patient with the acquired immunodeficiency syndrome. The viral isolate was shown to be resistant to acyclovir in vitro, but proved susceptible to vidarabine and foscarnet sodium (trisodium phosphonoformate). The patient failed to respond to a 2-week course of intravenous vidarabine. However, rapid improvement in the orofacial lesion occurred with intravenous foscarnet. Most … Show more

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Cited by 21 publications
(3 citation statements)
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References 9 publications
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“…Herpes strains can become resistant to acyclovir, and HSV infection due to acyclovir-resistant virus is most commonly treated with foscarnet or cidofovir. Response of classic cutaneous herpes to foscarnet is relatively rapid (7–10 days) [13, 14]. However, foscarnet and cidofovir are potentially nephrotoxic and require intravenous administration.…”
Section: Discussionmentioning
confidence: 99%
“…Herpes strains can become resistant to acyclovir, and HSV infection due to acyclovir-resistant virus is most commonly treated with foscarnet or cidofovir. Response of classic cutaneous herpes to foscarnet is relatively rapid (7–10 days) [13, 14]. However, foscarnet and cidofovir are potentially nephrotoxic and require intravenous administration.…”
Section: Discussionmentioning
confidence: 99%
“…The drug acts as a noncompetitive inhibitor of the DNA pol enzymatic activity by binding directly to its pyrophosphate binding site and blocking the cleavage of pyrophosphate from the nucleoside triphosphate, thus impeding further elongation of the viral DNA (Arduino & Porter, 2008;Piret & Boivin, 2011;Poole & James, 2018). Studies in HIV positive individuals and HSCT recipients, including isolated cases reports as well as randomized phase II trials, show that intravenous administration of FOS is effective in treating severe ACVr HSV-1 and -2 mucocutaneous lesions, since it reduces viral shedding along with the size and duration of lesions (Chatis et al, 1989;Iino et al, 1996;MacPhail et al, 1989;Naik et al, 1995;Sall et al, 1989;Verdonck et al, 1993), being more efficacious and showing less toxicity compared to vidarabine (Safrin et al, 1991). A few reports have also shown good results using FOS cream 1%-2.4% for the treatment of orogenital and cutaneous ACVr HSV lesions (Heidenreich et al, 2020;Javaly et al, 1999;Pechère et al, 1998; Table 1).…”
Section: Foscarnet (Fos)mentioning
confidence: 99%
“…Similar sensitivity and clinical responsiveness to foscarnet sodium have been docu¬ mented in acyclovir-resistant strains of herpes sim¬ plex virus. 13 …”
mentioning
confidence: 99%