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dc.contributor.authorMateo-Casas, M
dc.contributor.authorReyes, S
dc.contributor.authorDe Trane, S
dc.contributor.authorEdwards, F
dc.contributor.authorEspasandin, M
dc.contributor.authorAnjorin, G
dc.contributor.authorBaker, D
dc.contributor.authorSchmierer, K
dc.contributor.authorGiovannoni, G
dc.date.accessioned2020-11-12T16:46:06Z
dc.date.available2020-09-30
dc.date.available2020-11-12T16:46:06Z
dc.date.issued2020-10-09
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/68267
dc.description.abstractObjective: To describe a fatal case of influenza A pneumonia in a patient with severe lymphopenia after receiving subcutaneous cladribine to treat her multiple sclerosis (MS). Methods: Case report. Results: A 53-year-old woman developed fatal influenza pneumonia associated with grade 4 lymphopenia two months after receiving a total dose of 60mg subcutaneous cladribine. Despite treatment with oseltamivir, her condition deteriorated and the patient passed away after developing respiratory failure. Conclusion: Cladribine-related lymphopenia is usually mild to moderate, however severe lymphopenia may occur. People with MS, especially those who are immunosuppressed, should be offered the inactivated influenza vaccine annually.en_US
dc.format.extent100279 - ?
dc.languageeng
dc.relation.ispartofeNeurologicalSci
dc.rightsCC BY-NC-ND license
dc.rightsAttribution-NonCommercial-NoDerivs*
dc.rights.urihttp://creativecommons.org/licenses/BY-NC-ND/4.0/*
dc.subjectAdverse eventen_US
dc.subjectCladribineen_US
dc.subjectDisease-modifying treatmenten_US
dc.subjectInfluenza A virusen_US
dc.subjectLymphopeniaen_US
dc.subjectMultiple Sclerosisen_US
dc.titleSevere lymphopenia after subcutaneous cladribine in a patient with multiple sclerosis: To vaccinate or not?en_US
dc.typeArticleen_US
dc.rights.holder© 2020 Published by Elsevier B.V.
dc.identifier.doi10.1016/j.ensci.2020.100279
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33163633en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume21en_US
dcterms.dateAccepted2020-09-30
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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