Acyclovir is an agent used to treat infections caused by the herpes simplex virus (HSV). It is FDA approved to treat genital herpes and HSV encephalitis. Non-FDA approved indications are mucocutaneous HSV, herpes zoster (shingles) and varicella zoster (chickenpox). Acyclovir is the first line treatment for HSV encephalitis. Currently, there are no other medications indicated for the treatment of this condition.
Despite the long term use of acyclovir to treat HSV encephalitis, there has not been a systematic review regarding the efficacy of this disease/treatment combination. Current systematic reviews to address its safety and efficacy are currently ongoing, with the primary outcome being mortality rate. A secondary outcome measure is the quality of life.
HSV keratitis has been shown to respond to oral acyclovir and topical steroids in pediatric patients.
In patients with human immunodeficiency virus (HIV), acyclovir is sometimes used to treat eczema herpeticum. It is also used to prevent infections of the skin, eyes, nose, and mouth. Eczema herpeticum is rare but rapidly progressive if untreated. Those with extensive involvement, systemic symptoms or decreased oral intake should undergo admission for intravenous acyclovir treatment. Also, acyclovir treats oral hairy leukoplakia.
Acyclovir has been proven useful in treating myelopathy secondary to varicella zoster infection. In a small case series, researching patients from 1994 to 2014 with laboratory-confirmed VZV and MRI confirmed myelopathy, marked improvement of symptoms was the outcome in most patients within 2 months.
Brachial plexus neuritis secondary to VZV infection and visceral disseminated VZV infection (characteristic features are abdominal and absence of skin lesions) has also responded to acyclovir, alleviating all symptoms.
In recipients of hematopoietic stem cell transplantation, herpes simplex virus and varicella zoster reactivation may respond to treatment with acyclovir prophylaxis. Prophylactic use of acyclovir should be considered in HSV-1 and HSV-2-seropositive organ recipients as well. Diseases from such viruses have decreased secondary to this intervention. However, a breakthrough infection may occur. Not surprisingly, HSV and VZV infection is not uncommon in patients that have discontinued acyclovir prophylaxis.
Another form of prophylactic acyclovir use is juvenile-onset recurrent respiratory papillomatosis. In a prospective observational study involving 21 patients, oral acyclovir was a postoperative adjuvant. It was shown to decrease the recurrence of papillomas and thus decrease the need for successive surgeries and associated operative risks.
VZV infections have many complications, including cerebellitis. Treating the source infection has been shown to decrease the complication burden as well. A 2019 case report, for instance, describes a patient presenting with truncal ataxia. After intravenous acyclovir treatment, the patient was free of neurologic disability and his cerebellitis.  Similarly, paresis secondary to dermatomal herpes zoster infections has been shown to respond to oral acyclovir. This is a rare complication of herpes zoster when the virus affects motor nerve fibers in addition to/instead of the dorsal root ganglion.
Acyclovir is an antiviral agent that incorporates itself into viral DNA. It inhibits DNA synthesis and viral replication after it is converted to acyclovir triphosphate by cellular enzymes. Acyclovir is a synthetic purine nucleoside analog that demonstrates in vitro and in vivo inhibitory activity against both herpes simplex virus types 1 (HSV-1), 2 (HSV-2), and varicella-zoster virus (VZV).
Acyclovir administration may be oral or intravenous.
For limited mucocutaneous lesions, acyclovir can be administered orally. In cases in which there is disseminated, visceral or CNS involvement, the acyclovir administration should be intravenous.
When taken orally, acyclovir may be taken with or without food 2 to 5 times a day for 5 to 10 days as well as up to 12 months to prevent outbreaks of genital herpes.
Intravenous administration should be done via IV infusion only, over 1 hour at a constant rate to prevent renal damage. Medication should be in a diluted D5W solution or 0.9% NaCl to a final concentration of less than or equal to 7 mg/mL.
Most commonly, patients experience malaise.
Less commonly patients experience inflammation or phlebitis at the infusion site, nausea, vomiting, transaminitis, and rash (including Steven-Johnson syndrome) when taken intravenously. Rotating infusion sites and decreasing final infusion concentration less than 10 mg/mL can help prevent inflammation/phlebitis at the infusion site.. Patients also may experience nausea, vomiting, diarrhea, headache when taken orally.
Least commonly, patients experience abdominal pain, aggression/confusion, agitation, alopecia, anaphylaxis, anemia, angioedema, anorexia, ataxia, coma, disseminated intravascular coagulation (DIC), dizziness and fatigue.
In certain pediatric patients, acyclovir has been shown to decrease hemoglobin levels and the absolute neutrophil count.
The only absolute contraindication to acyclovir is hypersensitivity.
Cautions include renal failure/impairment, immunocompromised host, potential risk of thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS)).
Regarding pregnancy and lactation, acyclovir has been shown to cross the placenta. Acyclovir's manufacturer recommends caution with use during pregnancy as well as only using it when necessary and indicated, as there have only been a few studies conducted. Specifically, cases of HSV hepatitis have been treated during pregnancy. Although rare, this condition can become disseminated and fatal in pregnant patients. Although all 56 patients studied had transaminitis, only 18.2% had a vesicular rash. For patients that were treated with acyclovir empirically, it conferred no risks to the fetus. Acyclovir also has been shown to enter breast milk but is generally considered compatible with breastfeeding.
Patients should be monitored for adverse effects such as malaise, inflammation or phlebitis at infusion site, nausea, vomiting, rash (including Steven-Johnson syndrome), transaminitis, nausea, vomiting, diarrhea, headache, abdominal pain, aggression/confusion, agitation, alopecia, anaphylaxis, anemia, angioedema, anorexia, ataxia, coma, disseminated intravascular coagulation (DIC), dizziness and fatigue.
Acute kidney injury (AKI) is the most significant side effect from parenteral acyclovir administration. The incidence of AKI is comparable to other nephrotoxic medications such as aminoglycosides. Patients with CKD are at higher risk. Dose adjustment of acyclovir for ideal body weight and baseline renal function is imperative. A study regarding the pharmacokinetics of acyclovir demonstrated that a patient's glomerular filtration and tubular secretion contribute to its renal excretion.
Also, a recent retrospective case-control study over four years showed a statistically significant association between obesity and nephrotoxicity (odds ratio 3.2, 95% CI 1.19 to 8.67). Similarly, and not surprisingly, a similar association was observed between those receiving concomitant vancomycin (odds ratio 4.73, 95% CI, 1.57 to 14.25). Cautions should be taken accordingly when administering intravenous acyclovir to such higher risk patients.
Administering intravenous acyclovir requires interdisciplinary effort and communication. It is not a benign drug, having potential side effects such as phlebitis, hypersensitivity, and AKI. Therefore, pharmacists, physicians, and nurses must work together to achieve adequate and non-toxic dosing. Dose adjustments for ideal body weight and baseline renal function are necessary. Also, patients must undergo monitoring for signs/symptoms of hypersensitivity and phlebitis, specifically at the infusion site. Interprofessional teamwork between each healthcare provider for a patient can help minimize and prevent the adverse effects of intravenous administration of acyclovir.
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