Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12289
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dc.contributor.authorBroadley, Simon Aen
dc.contributor.authorBarnett, Michael Hen
dc.contributor.authorBoggild, Mikeen
dc.contributor.authorBrew, Bruce Jen
dc.contributor.authorButzkueven, Helmuten
dc.contributor.authorHeard, Roberten
dc.contributor.authorHodgkinson, Suzanneen
dc.contributor.authorKermode, Allan Gen
dc.contributor.authorLechner-Scott, Jeannetteen
dc.contributor.authorMacdonell, Richard A Len
dc.contributor.authorMarriott, Marken
dc.contributor.authorMason, Deborah Fen
dc.contributor.authorParratt, Johnen
dc.contributor.authorReddel, Stephen Wen
dc.contributor.authorShaw, Cameron Pen
dc.contributor.authorSlee, Marken
dc.contributor.authorSpies, Judithen
dc.contributor.authorTaylor, Bruce Ven
dc.contributor.authorCarroll, William Men
dc.contributor.authorKilpatrick, Trevor Jen
dc.contributor.authorKing, Johnen
dc.contributor.authorMcCombe, Pamela Aen
dc.contributor.authorPollard, John Den
dc.contributor.authorWilloughby, Ernesten
dc.date.accessioned2015-05-16T01:57:06Z
dc.date.available2015-05-16T01:57:06Z
dc.date.issued2014-06-30en
dc.identifier.citationJournal of Clinical Neuroscience 2014; 21(11): 1857-65en
dc.identifier.govdoc24993136en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12289en
dc.description.abstractIn this third and final part of our review of multiple sclerosis (MS) treatment we look at the practical day-to-day management issues that are likely to influence individual treatment decisions. Whilst efficacy is clearly of considerable importance, tolerability and the potential for adverse effects often play a significant role in informing individual patient decisions. Here we review the issues surrounding switching between therapies, and the evidence to assist guiding the choice of therapy to change to and when to change. We review the current level of evidence with regards to the management of women in their child-bearing years with regards to recommendations about treatment during pregnancy and whilst breast feeding. We provide a summary of recommended pre- and post-treatment monitoring for the available therapies and review the evidence with regards to the value of testing for antibodies which are known to be neutralising for some therapies. We review the occurrence of adverse events, both the more common and troublesome effects and those that are less common but have potentially much more serious outcomes. Ways of mitigating these risks and managing the more troublesome adverse effects are also reviewed. Finally, we make specific recommendations with regards to the treatment of MS. It is an exciting time in the world of MS neurology and the prospects for further advances in coming years are high.en
dc.language.isoenen
dc.subject.otherEvidence-based medicineen
dc.subject.otherGuidelineen
dc.subject.otherMultiple sclerosisen
dc.subject.otherReviewen
dc.subject.otherTreatmenten
dc.titleTherapeutic approaches to disease modifying therapy for multiple sclerosis in adults: an Australian and New Zealand perspective: part 3 treatment practicalities and recommendations.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Clinical Neuroscienceen
dc.identifier.affiliationDepartment of Neurology, Eastern Health and Monash University, 2/5 Arnold Street, Box Hill VIC 3128, Australiaen
dc.identifier.affiliationWestmead Clinical School, University of Sydney, NSW, Australiaen
dc.identifier.affiliationSouth Western Sydney Clinical School, University of New South Wales, NSW, Australiaen
dc.identifier.affiliationCentre for Neuromuscular and Neurological Disorders, University of Western Australia, WA, Australiaen
dc.identifier.affiliationHunter Medical Research Institute, The University of Newcastle, New Lambton, NSW, Australiaen
dc.identifier.affiliationDepartment of Neurology, Gold Coast University Hospital, Southport, QLD, Australiaen
dc.identifier.affiliationMelbourne Brain Centre, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationCentral Clinical School, University of Sydney, NSW, Australiaen
dc.identifier.affiliationBrain and Mind Research Institute, University of Sydney, Camperdown, NSW, Australiaen
dc.identifier.affiliationDepartment of Neurology and St Vincent's Centre for Applied Medical Research, St Vincent's Hospital, University of New South Wales, Darlinghurst, NSW, Australiaen
dc.identifier.affiliationFlinders Medical Centre, Flinders University, SA, Australiaen
dc.identifier.affiliationSchool of Medicine, Deakin University, Victoria, Australiaen
dc.identifier.affiliationMenzies Research Institute, University of Tasmania, TAS, Australiaen
dc.identifier.affiliationFlorey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationUniversity of Queensland Centre for Clinical Research, QLD, Australiaen
dc.identifier.affiliationDepartment of Neurology, The Townsville Hospital, Douglas, QLD, Australiaen
dc.identifier.affiliationSchool of Medicine, Griffith University, Gold Coast Campus, QLD 4222, Australiaen
dc.identifier.affiliationDepartment of Neurology, Christchurch Hospital, Christchurch, New Zealand.en
dc.identifier.affiliationDepartment of Neurology, Auckland City Hospital, Auckland, New Zealand.en
dc.identifier.doi10.1016/j.jocn.2014.01.017en
dc.description.pages1857-65en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/24993136en
dc.type.austinJournal Articleen
local.name.researcherMacdonell, Richard A L
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptNeurology-
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