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dc.contributor.authorMcGeachan, AJ
dc.contributor.authorHobson, EV
dc.contributor.authorAl-Chalabi, A
dc.contributor.authorStephenson, J
dc.contributor.authorChandran, S
dc.contributor.authorCrawley, F
dc.contributor.authorDick, D
dc.contributor.authorDonaghy, C
dc.contributor.authorEllis, CM
dc.contributor.authorGorrie, G
dc.contributor.authorHanemann, CO
dc.contributor.authorHarrower, T
dc.contributor.authorJung, A
dc.contributor.authorMalaspina, A
dc.contributor.authorMorrison, KE
dc.contributor.authorOrrell, RW
dc.contributor.authorTalbot, K
dc.contributor.authorTurner, MR
dc.contributor.authorWilliams, TL
dc.contributor.authorYoung, CA
dc.contributor.authorShaw, PJ
dc.contributor.authorMcDermott, CJ
dc.date.accessioned2020-01-13T14:14:28Z
dc.date.issued2017-08-31
dc.description.abstractFailure to clear oral secretions can be debilitating for patients with amyotrophic lateral sclerosis (ALS), but the treatment of this symptom is poorly defined and there is no consensus on best practice. The objective of this study was to identify the treatments that are commonly prescribed, and to describe how experienced clinicians manage a patient with treatment resistant symptoms. Twenty-three clinicians were approached, of which 19 from 16 centres across the UK provided case report forms for a total of 119 ALS patients identified as having problematic oral secretions. The use of five anticholinergics, salivary gland botulinum toxin injections, conservative management approaches and carbocisteine were reported. Of the 72 patients who were evaluated following the initiation of a first anticholinergic, 61% had symptomatic improvement. Only 19% of patients achieved symptomatic improvement with the use of an alternative anticholinergic when an initial anticholinergic achieved no symptomatic improvement. Problems with thick and thin secretions often coexisted, with 37% of patients receiving treatment for both types of problem. In conclusion, a variety of treatment options are employed by expert clinicians for problematic oral secretions in ALS patients. The variation in management highlights the need for further prospective research in this area.en_GB
dc.identifier.citationVol. 18, pp. 1 - 9en_GB
dc.identifier.doi10.1080/21678421.2016.1221433
dc.identifier.urihttp://hdl.handle.net/10871/40393
dc.language.isoenen_GB
dc.publisherInforma Healthcareen_GB
dc.rights© 2016 World Federation of Neurology on behalf of the Research Group on Motor Neuron Diseasesen_GB
dc.subjectSecretion managementen_GB
dc.subjectsialorrhoeaen_GB
dc.subjectanticholinergicsen_GB
dc.subjectbotulinum toxinen_GB
dc.titleA multicentre evaluation of oropharyngeal secretion management practices in amyotrophic lateral sclerosisen_GB
dc.typeArticleen_GB
dc.date.available2020-01-13T14:14:28Z
dc.identifier.issn2167-8421
dc.descriptionThis is the author accepted manuscript. The final version is available from the publisher via the DOI in this recorden_GB
dc.identifier.journalAmyotrophic Lateral Sclerosis and Frontotemporal Degenerationen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
pubs.euro-pubmed-idMED:27579520
dcterms.dateAccepted2016-08-01
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2017-08-31
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-01-13T14:09:54Z
refterms.versionFCDAM
refterms.dateFOA2020-01-13T14:14:33Z
refterms.panelAen_GB


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