Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/111983
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dc.contributor.authorTerheyden, Patrick-
dc.contributor.authorSunderkötter, Cord-
dc.contributor.authorSöhngen, Franz-Dietmar-
dc.contributor.authorGolle, Linda-
dc.contributor.authorSchimo, Sonja-
dc.contributor.authorBaron, Ralf-
dc.contributor.authorMaihöfner, Christian Gert-
dc.contributor.authorBinder, Andreas-
dc.contributor.authorPönisch, Wolfram-
dc.date.accessioned2023-11-27T07:29:19Z-
dc.date.available2023-11-27T07:29:19Z-
dc.date.issued2023-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/113941-
dc.identifier.urihttp://dx.doi.org/10.25673/111983-
dc.description.abstractIntroduction: Immunocompromised patients are at increased risk for herpes zoster (HZ)-associated complications. Despite standard therapy with systemic antiviral drugs and analgesics, complications are frequently encountered, including generalization of lesions or persistent neuropathic pain, so-called post-herpetic neuralgia (PHN). Given the scarcity of literature and awareness of therapeutic options to improve patient outcomes, especially for vulnerable patient groups, here we describe a strategy based on early intensification of treatment with a varicella zoster virus-specific hyperimmunoglobulin (VZV-IgG), which is approved in the adjuvant treatment of HZ. Methods: For this case series, we selected four cases of HZ in patients with impaired immunity due to hemato-oncologic disease or immunosuppressive treatment who presented with either existing generalized lesions and/or severe pain or with other risk factors for a complicated HZ course such as PHN. They were considered to be representative examples of different patient profiles eligible for intensification of treatment by the addition of VZV-IgG to virostatic therapy. Case Report: All patients showed a rapid response to combined treatment with VZV-IgG and a virostatic agent. In two patients who had generalized lesions, the formation of new lesions ceased 1 day after VZV-IgG infusion. One patient, with mantle cell lymphoma, achieved complete healing of the lesions 9 days after diagnosis of HZ, a rare occurrence compared to similar cases or cohorts. A patient with HZ in the cervical region showed a good response after a single dose of VZV-IgG. None of the patients developed post-zoster-related complications. Combination therapy of a virostatic agent and VZV-IgG was well tolerated in these four cases. Conclusion: This case series demonstrates highly satisfactory treatment effectiveness and tolerability for VZV-IgG in the adjuvant treatment of immunocompromised HZ patients and supports early intensification of HZ therapy in patients at high risk of severe disease progression.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/-
dc.subject.ddc610-
dc.titleVaricella zoster virus-specific hyperimmunoglobulin in the adjuvant treatment of immunocompromised herpes zoster patients : a case serieseng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleDermatology and therapy-
local.bibliographicCitation.volume13-
local.bibliographicCitation.pagestart2461-
local.bibliographicCitation.pageend2471-
local.bibliographicCitation.publishernameSpringer-
local.bibliographicCitation.publisherplaceHeidelberg-
local.bibliographicCitation.doi10.1007/s13555-023-01019-6-
local.openaccesstrue-
dc.identifier.ppn1871246733-
cbs.publication.displayform2023-
local.bibliographicCitation.year2023-
cbs.sru.importDate2023-11-27T07:28:45Z-
local.bibliographicCitationEnthalten in Dermatology and therapy - Heidelberg : Springer, 2011-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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