Please use this identifier to cite or link to this item: https://doi.org/10.1159/000452285
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dc.titlePrognostic factors and pattern of long-term recovery with MLC601 (NeuroAiD™) in the Chinese medicine NeuroAiD efficacy on stroke recovery - Extension study
dc.contributor.authorVenketasubramanian, N
dc.contributor.authorLee, C.F
dc.contributor.authorYoung, S.H
dc.contributor.authorTay, S.S
dc.contributor.authorUmapathi, T
dc.contributor.authorLao, A.Y
dc.contributor.authorGan, H.H
dc.contributor.authorBaroque, A.C
dc.contributor.authorNavarro, J.C
dc.contributor.authorChang, H.M
dc.contributor.authorAdvincula, J.M
dc.contributor.authorMuengtaweepongsa, S
dc.contributor.authorChan, B.P.L
dc.contributor.authorChua, C.L
dc.contributor.authorWijekoon, N
dc.contributor.authorDe Silva, H.A
dc.contributor.authorHiyadan, J.H.B
dc.contributor.authorSuwanwela, N.C
dc.contributor.authorWong, K.S.L
dc.contributor.authorPoungvarin, N
dc.contributor.authorEow, G.B
dc.contributor.authorChen, C.L.H
dc.date.accessioned2020-10-23T02:35:38Z
dc.date.available2020-10-23T02:35:38Z
dc.date.issued2017
dc.identifier.citationVenketasubramanian, N, Lee, C.F, Young, S.H, Tay, S.S, Umapathi, T, Lao, A.Y, Gan, H.H, Baroque, A.C, Navarro, J.C, Chang, H.M, Advincula, J.M, Muengtaweepongsa, S, Chan, B.P.L, Chua, C.L, Wijekoon, N, De Silva, H.A, Hiyadan, J.H.B, Suwanwela, N.C, Wong, K.S.L, Poungvarin, N, Eow, G.B, Chen, C.L.H (2017). Prognostic factors and pattern of long-term recovery with MLC601 (NeuroAiD™) in the Chinese medicine NeuroAiD efficacy on stroke recovery - Extension study. Cerebrovascular Diseases 43 (43497) : 36-42. ScholarBank@NUS Repository. https://doi.org/10.1159/000452285
dc.identifier.issn10159770
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179244
dc.description.abstractBackground: The Chinese Medicine NeuroAiD Efficacy on Stroke recovery - Extension (CHIMES-E) study is among the few acute stroke trials with long-term outcome data. We aimed to evaluate the recovery pattern and the influence of prognostic factors on treatment effect of MLC601 over 2 years. Methods: The CHIMES-E study evaluated the 2 years outcome of subjects aged ≥18 years with acute ischemic stroke, National Institutes of Health Stroke Scale (NIHSS) score 6-14, pre-stroke modified Rankin Scale (mRS) score ≤1 included in a multicenter, randomized, double-blind, placebo-controlled trial of MLC601 for 3 months. Standard stroke care and rehabilitation were allowed during follow-up with mRS score being assessed in-person at month (M) 3 and by telephone at M1, M6, M12, M18 and M24. Results: Data from 880 subjects were analyzed. There was no difference in baseline characteristics between treatment groups. The proportion of subjects with mRS score 0-1 increased over time in favor of MLC601 most notably from M3 to M6, thereafter remaining stable up to M24, while the proportion deteriorating to mRS score ?2 remained low at all time points. Older age (p < 0.01), female sex (p = 0.06), higher baseline NIHSS score (p < 0.01) and longer onset to treatment time (OTT; p < 0.01) were found to be predictors of poorer outcome at M3. Greater treatment effect, with more subjects improving on MLC601 than placebo, was seen among subjects with 2 or more prognostic factors (OR 1.65 at M3, 1.78 at M6, 1.90 at M12, 1.65 at M18, 1.39 at M24), especially in subjects with more severe stroke or longer OTT. Conclusions: The sustained benefits of MLC601 over 2 years were due to more subjects improving to functional independence at M6 and beyond compared to placebo. Selection of subjects with poorer prognosis, particularly those with more severe NIHSS score and longer OTT delay, as well as a long follow-up period, may improve the power of future trials investigating the treatment effect of neuroprotective or neurorestorative therapies. © 2016 The Author(s) Published by S. Karger AG, Basel.
dc.publisherS. Karger AG
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectmlc601
dc.subjectneuroprotective agent
dc.subjectunclassified drug
dc.subjectherbaceous agent
dc.subjectNeuroaid
dc.subjectneuroprotective agent
dc.subjectadult
dc.subjectArticle
dc.subjectbrain ischemia
dc.subjectcerebrovascular accident
dc.subjectChinese medicine
dc.subjectcontrolled study
dc.subjectfemale
dc.subjectfollow up
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmiddle aged
dc.subjectmulticenter study (topic)
dc.subjectNational Institutes of Health Stroke Scale
dc.subjectpriority journal
dc.subjectprognosis
dc.subjectrandomized controlled trial (topic)
dc.subjectRankin scale
dc.subjectstroke rehabilitation
dc.subjecttime to treatment
dc.subjectaged
dc.subjectAsia
dc.subjectcerebrovascular accident
dc.subjectclinical trial
dc.subjectconvalescence
dc.subjectdisability
dc.subjectdouble blind procedure
dc.subjectmulticenter study
dc.subjectodds ratio
dc.subjectpathophysiology
dc.subjectprocedures
dc.subjectpsychology
dc.subjectrandomized controlled trial
dc.subjectrisk factor
dc.subjecttime factor
dc.subjecttreatment outcome
dc.subjectAged
dc.subjectAsia
dc.subjectDisability Evaluation
dc.subjectDouble-Blind Method
dc.subjectDrugs, Chinese Herbal
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNeuroprotective Agents
dc.subjectOdds Ratio
dc.subjectRecovery of Function
dc.subjectRisk Factors
dc.subjectStroke
dc.subjectStroke Rehabilitation
dc.subjectTime Factors
dc.subjectTreatment Outcome
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.contributor.departmentPHARMACOLOGY
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1159/000452285
dc.description.sourcetitleCerebrovascular Diseases
dc.description.volume43
dc.description.issue43497
dc.description.page36-42
dc.published.statePublished
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