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dc.contributor.authorHarris, Linda
dc.contributor.authorGraham, Sophie
dc.contributor.authorMacLachlan, Sharon
dc.contributor.authorExuzides, Alex
dc.contributor.authorJacob, Saiju
dc.date.accessioned2024-03-04T15:23:27Z
dc.date.available2024-03-04T15:23:27Z
dc.date.issued2022-05-09
dc.identifier.citationHarris L, Graham S, MacLachlan S, Exuzides A, Jacob S. A retrospective longitudinal cohort study of the clinical burden in myasthenia gravis. BMC Neurol. 2022 May 9;22(1):172. doi: 10.1186/s12883-022-02692-4en_US
dc.identifier.eissn1471-2377
dc.identifier.doi10.1186/s12883-022-02692-4
dc.identifier.pmid35534810
dc.identifier.urihttp://hdl.handle.net/20.500.14200/3853
dc.description.abstractBackground: Patients with generalized myasthenia gravis (MG) often experience debilitating exacerbations, with the possibility of life-threatening respiratory crises requiring hospitalization. Long-term longitudinal studies are needed to understand the burden of MG, including in patients whose disease is refractory to conventional treatment. Methods: A retrospective, longitudinal, cohort study was conducted of patients in England aged ≥ 18 years with treatment-refractory or non-refractory MG, using data recorded during 1997-2016 in the Clinical Practice Research Datalink and the Hospital Episode Statistics databases. A control cohort of patients without MG, matched to the patients in the treatment-refractory MG cohort, was also identified. Outcome measures included myasthenic crises, MG exacerbations, MG-related hospitalizations, comorbidities, and all-cause mortality. Descriptive statistics were calculated for the overall MG population. For continuous variables, between-cohort comparisons were made using t tests for normally distributed data and Mann-Whitney U tests for non-normally distributed data. For categorical data, the comparisons were made by chi-squared tests. Differences in clinical outcomes between cohorts were modeled using negative binomial regression. Results: A total of 1149 patients with MG were included. Overall, 18.4% of patients experienced myasthenic crises, 24.6% experienced exacerbations, and 38.6% underwent MG-related hospitalizations. Most of these events occurred within 2-3 years of diagnosis. Patients with MG refractory to conventional treatment (n = 66) experienced more exacerbations and MG-related hospitalizations than patients with non-refractory disease (n = 1083). Patients with refractory MG experienced a higher frequency of renal disease and hypertension compared with patients with non-refractory MG, and with matched patients without MG. They were also more likely to have diabetes and congestive heart failure than the matched controls. Rates of all-cause mortality during the follow-up period did not differ between patients with refractory MG and non-refractory MG. Conclusions: These results show that conventional treatments for MG are not adequately managing patients' symptoms and that patients with refractory MG are more likely to experience certain comorbidities than those with non-refractory MG or matched controls without MG. Future research should focus on the impact of newer targeted therapies on long-term clinical outcomes and comorbid conditions.en_US
dc.language.isoenen_US
dc.publisherBMCen_US
dc.relation.urlhttps://bmcneurol.biomedcentral.com/en_US
dc.rights© 2022. The Author(s).
dc.subjectNeurologyen_US
dc.titleA retrospective longitudinal cohort study of the clinical burden in myasthenia gravis.en_US
dc.typeArticle
dc.source.journaltitleBMC Neurology
dc.source.volume22
dc.source.issue1
dc.source.beginpage172
dc.source.endpage
dc.source.countryEngland
rioxxterms.versionNAen_US
dc.contributor.trustauthorJacob, Saiju
dc.contributor.departmentNeurologyen_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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