Acyclovir treatment of varicella-zoster virus meningeal infections and acute kidney injury: a multicentre case series study.

Varicella-zoster virus acute kidney injury acyclovir encephalitis meningitis

Journal

Infectious diseases (London, England)
ISSN: 2374-4243
Titre abrégé: Infect Dis (Lond)
Pays: England
ID NLM: 101650235

Informations de publication

Date de publication:
31 May 2024
Historique:
medline: 1 6 2024
pubmed: 1 6 2024
entrez: 1 6 2024
Statut: aheadofprint

Résumé

Systematic treatment with intravenous acyclovir is usually given when varicella zoster virus (VZV) DNA is isolated in cerebrospinal fluid (CSF), indicating central nervous system (CNS) involvement. Our study aimed to describe therapeutic management and acute kidney injury (AKI) occurrence during acyclovir treatment of VZV infection with CNS involvement. Multicentre, retrospective study including all patients from 2010 to 2022 with VZV DNA in CSF. Patient management and outcomes were compared according to clinical presentation and indications for intravenous acyclovir: i) definite (encephalitis, myelitis or stroke, peripheral nervous system (PNS) with ≥ 2 roots, herpes zoster ≥ 3 dermatomes, immunosuppression), ii) questionable (1 or 2 dermatomes) or iii) no indication (other situations). 154 patients were included (median age 66 (interquartile range 43-77), 87 (56%) males); 60 (39%) had encephalitis, myelitis or stroke, 35 (23%) had PNS involvement, 37 (24%) had isolated meningitis, 14 (9%) had isolated cutaneous presentation, and 8 (5%) had other presentations. Overall, 128 (83%) received intravenous acyclovir for more than 72 h. AKI occurred in 57 (37%) patients. Finally, 42 (27%) and 25 (16%) patients had respectively no or a questionable indication for intravenous acyclovir, while 29 (69%) and 23 (92%) of them received it for more than 72 h, with AKI in 13 (35%) and 13 (52%) patients, respectively. In-hospital mortality was 12% ( Intravenous acyclovir is widely prescribed when VZV DNA is isolated in CSF, regardless of the clinical presentation, with a high rate of AKI. Further studies are needed to better define the value of intravenous acyclovir in isolated VZV meningitis.

Sections du résumé

BACKGROUND UNASSIGNED
Systematic treatment with intravenous acyclovir is usually given when varicella zoster virus (VZV) DNA is isolated in cerebrospinal fluid (CSF), indicating central nervous system (CNS) involvement. Our study aimed to describe therapeutic management and acute kidney injury (AKI) occurrence during acyclovir treatment of VZV infection with CNS involvement.
METHODS UNASSIGNED
Multicentre, retrospective study including all patients from 2010 to 2022 with VZV DNA in CSF. Patient management and outcomes were compared according to clinical presentation and indications for intravenous acyclovir: i) definite (encephalitis, myelitis or stroke, peripheral nervous system (PNS) with ≥ 2 roots, herpes zoster ≥ 3 dermatomes, immunosuppression), ii) questionable (1 or 2 dermatomes) or iii) no indication (other situations).
RESULTS UNASSIGNED
154 patients were included (median age 66 (interquartile range 43-77), 87 (56%) males); 60 (39%) had encephalitis, myelitis or stroke, 35 (23%) had PNS involvement, 37 (24%) had isolated meningitis, 14 (9%) had isolated cutaneous presentation, and 8 (5%) had other presentations. Overall, 128 (83%) received intravenous acyclovir for more than 72 h. AKI occurred in 57 (37%) patients. Finally, 42 (27%) and 25 (16%) patients had respectively no or a questionable indication for intravenous acyclovir, while 29 (69%) and 23 (92%) of them received it for more than 72 h, with AKI in 13 (35%) and 13 (52%) patients, respectively. In-hospital mortality was 12% (
CONCLUSIONS UNASSIGNED
Intravenous acyclovir is widely prescribed when VZV DNA is isolated in CSF, regardless of the clinical presentation, with a high rate of AKI. Further studies are needed to better define the value of intravenous acyclovir in isolated VZV meningitis.

Identifiants

pubmed: 38822453
doi: 10.1080/23744235.2024.2355989
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-9

Auteurs

Myriam Contamine (M)

Department of Infectious Diseases, Dijon-Bourgogne University Hospital, Dijon, France.

Florence Ader (F)

Department of Infectious Diseases, Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

Quentin Lepiller (Q)

Laboratory of virology, Besançon University Hospital, Besançon, France.

Benoit Martha (B)

Department of Infectious Diseases, William Morey Hospital, Chalon sur Saône, France.

Joséphine Cagnon-Chapalain (J)

Department of Infectious Diseases, Macon Hospital, Macon, France.

Paul Leturnier (P)

Infectious and Tropical Diseases Unit, Cayenne General Hospital, Cayenne, French Guiana.
Cayenne General Hospital, INSERM, Cayenne, French Guiana.

Emilie Frober (E)

Laboratory of virology, Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.

Kevin Bouiller (K)

Department of infectious and tropical diseases, Université de Franche-Comté, CHU Besançon, UMR-CNRS 6249 Chrono-environnement, Besançon, France.

Christine Binquet (C)

CHU Dijon-Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France.
LabEx LipSTIC, University of Burgundy, Dijon, France.
Lipness Team, INSERM Research Centre LNC-UMR1231 and LabEx LipSTIC, University of Burgundy, Dijon, France.

Christelle Auvray (C)

Laboratory of virology, Dijon-Bourgogne University Hospital, Dijon, France.

Lionel Piroth (L)

Department of Infectious Diseases, Dijon-Bourgogne University Hospital, Dijon, France.
CHU Dijon-Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France.
LabEx LipSTIC, University of Burgundy, Dijon, France.

Mathieu Blot (M)

Department of Infectious Diseases, Dijon-Bourgogne University Hospital, Dijon, France.
CHU Dijon-Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France.
LabEx LipSTIC, University of Burgundy, Dijon, France.
Lipness Team, INSERM Research Centre LNC-UMR1231 and LabEx LipSTIC, University of Burgundy, Dijon, France.

Classifications MeSH