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Glucose Modifies the Effect of Endovascular Thrombectomy in Patients With Acute Stroke.
Chamorro, Ángel; Brown, Scott; Amaro, Sergio; Hill, Michael D; Muir, Keith W; Dippel, Diederik W J; van Zwam, Wim; Butcher, Ken; Ford, Gary A; den Hertog, Heleen M; Mitchell, Peter J; Demchuk, Andrew M; Majoie, Charles B L M; Bracard, Serge; Sibon, Igor; Jadhav, Ashutosh P; Lara-Rodriguez, Blanca; van der Lugt, Aad; Osei, Elizabeth; Renú, Arturo; Richard, Sébastien; Rodriguez-Luna, David; Donnan, Geoffrey A; Dixit, Anand; Almekhlafi, Mohammed; Deltour, Sandrine; Epstein, Jonathan; Guillon, Benoit; Bakchine, Serge; Gomis, Meritxell; du Mesnil de Rochemont, Richard; Lopes, Demetrius; Reddy, Vivek; Rudel, Gernot; Roos, Yvo B W E M; Bonafe, Alain; Diener, Hans-Christoph; Berkhemer, Olvert A; Cloud, Geoffrey C; Davis, Stephen M; van Oostenbrugge, Robert; Guillemin, Francis; Goyal, Mayank; Campbell, Bruce C V; Menon, Bijoy K.
Afiliação
  • Chamorro Á; From the Department of Neuroscience, Comprehensive Stroke Center, Hospital Clinic, University of Barcelona, Barcelona, Spain (A.C., S.A., A.R.).
  • Brown S; August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain (A.C., S.A., A.R.).
  • Amaro S; Altair Biostatistics, St Louis Park, MN (S. Brown).
  • Hill MD; From the Department of Neuroscience, Comprehensive Stroke Center, Hospital Clinic, University of Barcelona, Barcelona, Spain (A.C., S.A., A.R.).
  • Muir KW; August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain (A.C., S.A., A.R.).
  • Dippel DWJ; Calgary Stroke Program, Departments of Clinical Neurosciences, Medicine, Community Health Sciences, and Radiology (M.D.H.), Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Canada.
  • van Zwam W; Institute of Neuroscience and Psychology, University of Glasgow, Scotland, United Kingdom (K.W.M.).
  • Butcher K; Department of Neurology (D.W.J.D., E.O., O.A.B.), Erasmus MC University Medical Center, Rotterdam, the Netherlands.
  • Ford GA; Department of Radiology (W.v.Z.), Maastricht University Medical Center Maastricht, the Netherlands.
  • den Hertog HM; Division of Neurology, Department of Medicine, University of Alberta, Edmonton, Canada (K.B.).
  • Mitchell PJ; Stroke Unit, Oxford University Hospitals and Division of Medical Sciences, Oxford University, United Kingdom (G.A.F.).
  • Demchuk AM; Department of Neurology, Isala Klinieken, Zwolle, the Netherlands (H.M.d.H.).
  • Majoie CBLM; Department of Neurology, Medisch Spectrum Twente, Enschede, Netherlands (H.M.d.H., E.O.).
  • Bracard S; Department of Radiology, Royal Melbourne Hospital (P.J.M.), University of Melbourne, Parkville, Australia.
  • Sibon I; Calgary Stroke Program, Departments of Clinical Neurosciences and Radiology (A.M.D., M.A., M. Goyal, B.K.M.), Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Canada.
  • Jadhav AP; Department of Radiology (C.B.L.M.M., O.A.B.), Academic Medical Center Amsterdam, the Netherlands.
  • Lara-Rodriguez B; Department of Diagnostic and Interventional Neuroradiology, INSERM U 947 (S. Bracard), Université de Lorraine and University Hospital of Nancy, France.
  • van der Lugt A; Stroke Unit University and University Hospital of CHU Bordeaux, France (I.S.).
  • Osei E; Department of Neurology, University of Pittsburgh, PA (A.P.J.).
  • Renú A; Department of Neurology, Hospital Universitari de Bellvitge (HUB), Spain (B.L.-R.).
  • Richard S; Department of Radiology (A.v.d.L., O.A.B.), Erasmus MC University Medical Center, Rotterdam, the Netherlands.
  • Rodriguez-Luna D; Department of Neurology (D.W.J.D., E.O., O.A.B.), Erasmus MC University Medical Center, Rotterdam, the Netherlands.
  • Donnan GA; Department of Neurology, Medisch Spectrum Twente, Enschede, Netherlands (H.M.d.H., E.O.).
  • Dixit A; From the Department of Neuroscience, Comprehensive Stroke Center, Hospital Clinic, University of Barcelona, Barcelona, Spain (A.C., S.A., A.R.).
  • Almekhlafi M; August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain (A.C., S.A., A.R.).
  • Deltour S; Department of Neurology, University Hospital of Nancy, France (S.R.).
  • Epstein J; Stroke Unit, Neurology Department, Vall d'Hebron University Hospital, Spain (D.R.-L.).
  • Guillon B; The Florey Institute of Neuroscience and Mental Health (G.A.D.), University of Melbourne, Parkville, Australia.
  • Bakchine S; University of Newcastle upon Tyne, United Kingdom (A.D.).
  • Gomis M; Calgary Stroke Program, Departments of Clinical Neurosciences and Radiology (A.M.D., M.A., M. Goyal, B.K.M.), Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Canada.
  • du Mesnil de Rochemont R; Urgences Cerebro-Vasculaires Sorbonne University and Pitié-Salpêtrière Hospital, APHP, Paris, France (S.D.).
  • Lopes D; INSERM CIC 1433 Clinical Epidemiology (J.E.), Université de Lorraine and University Hospital of Nancy, France.
  • Reddy V; Stroke Unit, University and University Hospital of Nantes, France (B.G.).
  • Rudel G; Neurology-Stroke Unit University and University Hospital of Reims, France (S. Bakchine).
  • Roos YBWEM; Stroke Unit, Hospital Universitari Germans Trias i Pujol, Badalona, Barcelona, Spain (M. Gomis).
  • Bonafe A; Institute of Neuroradiology, Klinikum der Goethe-Universität, Frankfurt, Germany (R.d.M.d.R.).
  • Diener HC; Rush Medical Center Chicago, IL (D.L.).
  • Berkhemer OA; Department of Neurology, University of Pittsburgh Medical Center, PA (V.R.).
  • Cloud GC; Department of Neurology, Klinikum Dortmund, Germany (G.R.).
  • Davis SM; Department of Neurology (Y.E.W.E.M.R.), Academic Medical Center Amsterdam, the Netherlands.
  • van Oostenbrugge R; Department of Neuroradiology, Hôpital Gui-de-Chauliac, Montpellier, France (A.B.).
  • Guillemin F; Department of Neurology, University Hospital Essen University Duisburg-Essen, Germany (C.D.).
  • Goyal M; Department of Neurology (D.W.J.D., E.O., O.A.B.), Erasmus MC University Medical Center, Rotterdam, the Netherlands.
  • Campbell BCV; Department of Radiology (A.v.d.L., O.A.B.), Erasmus MC University Medical Center, Rotterdam, the Netherlands.
  • Menon BK; Department of Radiology (C.B.L.M.M., O.A.B.), Academic Medical Center Amsterdam, the Netherlands.
Stroke ; 50(3): 690-696, 2019 03.
Article em En | MEDLINE | ID: mdl-30777000
ABSTRACT
Background and Purpose- Hyperglycemia is a negative prognostic factor after acute ischemic stroke but is not known whether glucose is associated with the effects of endovascular thrombectomy (EVT) in patients with large-vessel stroke. In a pooled-data meta-analysis, we analyzed whether serum glucose is a treatment modifier of the efficacy of EVT in acute stroke. Methods- Seven randomized trials compared EVT with standard care between 2010 and 2017 (HERMES Collaboration [highly effective reperfusion using multiple endovascular devices]). One thousand seven hundred and sixty-four patients with large-vessel stroke were allocated to EVT (n=871) or standard care (n=893). Measurements included blood glucose on admission and functional outcome (modified Rankin Scale range, 0-6; lower scores indicating less disability) at 3 months. The primary analysis evaluated whether glucose modified the effect of EVT over standard care on functional outcome, using ordinal logistic regression to test the interaction between treatment and glucose level. Results- Median (interquartile range) serum glucose on admission was 120 (104-140) mg/dL (6.6 mmol/L [5.7-7.7] mmol/L). EVT was better than standard care in the overall pooled-data analysis adjusted common odds ratio (acOR), 2.00 (95% CI, 1.69-2.38); however, lower glucose levels were associated with greater effects of EVT over standard care. The interaction was nonlinear such that significant interactions were found in subgroups of patients split at glucose < or >90 mg/dL (5.0 mmol/L; P=0.019 for interaction; acOR, 3.81; 95% CI, 1.73-8.41 for patients < 90 mg/dL versus 1.83; 95% CI, 1.53-2.19 for patients >90 mg/dL), and glucose < or >100 mg/dL (5.5 mmol/L; P=0.004 for interaction; acOR, 3.17; 95% CI, 2.04-4.93 versus acOR, 1.72; 95% CI, 1.42-2.08) but not between subgroups above these levels of glucose. Conclusions- EVT improved stroke outcomes compared with standard treatment regardless of glucose levels, but the treatment effects were larger at lower glucose levels, with significant interaction effects persisting up to 90 to 100 mg/dL (5.0-5.5 mmol/L). Whether tight control of glucose improves the efficacy of EVT after large-vessel stroke warrants appropriate testing.
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Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Glicemia / Trombectomia / Acidente Vascular Cerebral / Procedimentos Endovasculares / Hiperglicemia Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Eixos temáticos: Pesquisa_clinica Base de dados: MEDLINE Assunto principal: Glicemia / Trombectomia / Acidente Vascular Cerebral / Procedimentos Endovasculares / Hiperglicemia Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article