Evidence map›Paper›PMID 42809744›Full record

ReviewReviews in medical virology2026

Continuous Intravenous Acyclovir as Outpatient Parenteral Antimicrobial Therapy for HSV and VZV Neurological Infections: A Case Series With Pharmacokinetic and Cost Evaluation, and Review of Literature.

Irene G Manders, Eline L van Tuinen, Martijn Weisfelt, Marco Goeijenbier, Jayant S Kalpoe, Steven F L van Lelyveld, Eric C M van Gorp, Ken Ho Hua

Abstract readReviewCase Reports
In one paragraph

Review in Reviews in medical virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Irene G MandersDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-7857-7198
Eline L van TuinenPharmacy Spaarne Gasthuis, Haarlem, the Netherlands.ORCID https://orcid.org/0000-0001-6859-8123
Martijn WeisfeltSpaarne Gasthuis, Department of Neurology, Haarlem, the Netherlands.
Marco GoeijenbierDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-3165-8193
Jayant S KalpoeRegional Public Health Laboratory Kennemerland, Department of Medical Microbiology, Haarlem, the Netherlands.ORCID https://orcid.org/0000-0003-4549-7236
Steven F L van LelyveldSpaarne Gasthuis, Department of Internal Medicine, Haarlem, the Netherlands.ORCID https://orcid.org/0000-0001-9153-8196
Eric C M van GorpDepartment of Viroscience, Erasmus MC, Rotterdam, the Netherlands.
Ken Ho HuaPharmacy Spaarne Gasthuis, Haarlem, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Varicella zoster virus (VZV) and herpes simplex virus (HSV) are major causes of viral meningitis and encephalitis. Standard intermittent intravenous acyclovir requires hospitalisation, reducing patient comfort and prolonging admissions. Continuous infusion may maintain therapeutic plasma and cerebrospinal fluid (CSF) concentrations while enabling treatment through Outpatient Parenteral Antimicrobial Therapy (OPAT). Objectives to evaluate the feasibility, pharmacokinetic target attainment, and cost reduction of continuous intravenous acyclovir for HSV and VZV neurological infections in an OPAT setting. We conducted a case series of eight patients with HSV or VZV neurological infections who received continuous intravenous acyclovir through our OPAT programme after initial hospital-based therapy. Steady-state plasma concentrations were measured to assess pharmacokinetic target attainment. Costs were calculated based on daily costs of discontinued inpatient care and OPAT. Existing literature on continuous intravenous acyclovir and acyclovir in OPAT was reviewed. No persistent complications associated with continuous intravenous acyclovir administration were observed. All patients completed treatment with good clinical responses; one had persistent ptosis, and another developed postherpetic neuralgia. Acyclovir plasma concentrations remained above the therapeutic threshold in all seven measured cases, suggesting adequate CSF exposure. Hospital admissions were shortened, with no readmissions. The acyclovir OPAT programme led to cost savings of 3486 EUR per patient. Despite this small case series, continuous intravenous acyclovir appears to be feasible for treating HSV and VZV neurological infections in an OPAT setting, with potential benefits in patient comfort, healthcare costs, and hospital resource utilization. Larger studies are warranted to assess safety and efficacy.

Indexed as

AcyclovirAmbulatory CareAntiviral AgentsHerpes SimplexAdministration, IntravenousAdolescentAdultAgedAged, 80 and overFemaleHerpesvirus 3, HumanHumansInfusions, IntravenousMaleMiddle AgedOutpatientsAcyclovirAntiviral Agentsacyclovircontinuousencephalitisherpes simplex virusherpes zoster ophthalmicusmeningitisOPAToutpatient parenteral antimicrobial therapysteady‐state plasma concentrationvaricella zoster virus

Identifiers

PMID42809744
PMCPMC13623296

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.