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Time to Reperfusion and Treatment Effect for Acute Ischemic Stroke: A Randomized Clinical Trial.
Fransen, Puck S S; Berkhemer, Olvert A; Lingsma, Hester F; Beumer, Debbie; van den Berg, Lucie A; Yoo, Albert J; Schonewille, Wouter J; Vos, Jan Albert; Nederkoorn, Paul J; Wermer, Marieke J H; van Walderveen, Marianne A A; Staals, Julie; Hofmeijer, Jeannette; van Oostayen, Jacques A; Lycklama À Nijeholt, Geert J; Boiten, Jelis; Brouwer, Patrick A; Emmer, Bart J; de Bruijn, Sebastiaan F; van Dijk, Lukas C; Kappelle, L Jaap; Lo, Rob H; van Dijk, Ewoud J; de Vries, Joost; de Kort, Paul L M; van den Berg, J S Peter; van Hasselt, Boudewijn A A M; Aerden, Leo A M; Dallinga, René J; Visser, Marieke C; Bot, Joseph C J; Vroomen, Patrick C; Eshghi, Omid; Schreuder, Tobien H C M L; Heijboer, Roel J J; Keizer, Koos; Tielbeek, Alexander V; den Hertog, Heleen M; Gerrits, Dick G; van den Berg-Vos, Renske M; Karas, Giorgos B; Steyerberg, Ewout W; Flach, H Zwenneke; Marquering, Henk A; Sprengers, Marieke E S; Jenniskens, Sjoerd F M; Beenen, Ludo F M; van den Berg, René; Koudstaal, Peter J; van Zwam, Wim H.
Afiliación
  • Fransen PS; Department of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands2Department of Radiology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Berkhemer OA; Department of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands3Department of Radiology, Academic Medical Center, Amsterdam, the Netherlands.
  • Lingsma HF; Department of Public Health, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Beumer D; Department of Neurology, Maastricht University Medical Center, Cardiovascular Research Institute Maastricht, Maastricht, the Netherlands.
  • van den Berg LA; Department of Neurology, Academic Medical Center, Amsterdam, the Netherlands.
  • Yoo AJ; Texas Stroke Institute, Plano.
  • Schonewille WJ; Department of Neurology, St Antonius Hospital, Nieuwegein, the Netherlands.
  • Vos JA; Department of Radiology, St Antonius Hospital, Nieuwegein, the Netherlands.
  • Nederkoorn PJ; Department of Neurology, Academic Medical Center, Amsterdam, the Netherlands.
  • Wermer MJ; Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands.
  • van Walderveen MA; Department of Radiology, Leiden University Medical Center, Leiden, the Netherlands.
  • Staals J; Department of Neurology, Maastricht University Medical Center, Cardiovascular Research Institute Maastricht, Maastricht, the Netherlands.
  • Hofmeijer J; Department of Neurology, Rijnstate Hospital, Arnhem, the Netherlands.
  • van Oostayen JA; Department of Radiology, Rijnstate Hospital, Arnhem, the Netherlands.
  • Lycklama À Nijeholt GJ; Department of Radiology, Medisch Centrum Haaglanden, the Hague, the Netherlands.
  • Boiten J; Department of Neurology, Medisch Centrum Haaglanden, the Hague, the Netherlands.
  • Brouwer PA; Department of Radiology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Emmer BJ; Department of Radiology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • de Bruijn SF; Department of Neurology, Haga Hospital, the Hague, the Netherlands.
  • van Dijk LC; Department of Radiology, Haga Hospital, the Hague, the Netherlands.
  • Kappelle LJ; Department of Neurology, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Lo RH; Department of Radiology, University Medical Center Utrecht, Utrecht, the Netherlands.
  • van Dijk EJ; Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • de Vries J; Department of Neurosurgery, Radboud University Medical Center, Nijmegen, the Netherlands.
  • de Kort PL; Department of Neurology, St Elisabeth Hospital, Tilburg, the Netherlands.
  • van den Berg JS; Department of Neurology, Isala Klinieken, Zwolle, the Netherlands.
  • van Hasselt BA; Department of Radiology, Isala Klinieken, Zwolle, the Netherlands.
  • Aerden LA; Department of Neurology, Reinier de Graaf Gasthuis, Delft, the Netherlands.
  • Dallinga RJ; Department of Radiology, Reinier de Graaf Gasthuis, Delft, the Netherlands.
  • Visser MC; Department of Neurology, VU Medical Center, Amsterdam, the Netherlands.
  • Bot JC; Department of Radiology, VU Medical Center, Amsterdam, the Netherlands.
  • Vroomen PC; Department of Neurology, University Medical Center Groningen, Groningen, the Netherlands.
  • Eshghi O; Department of Radiology, University Medical Center Groningen, Groningen, the Netherlands.
  • Schreuder TH; Department of Neurology, Atrium Medical Center, Heerlen, the Netherlands.
  • Heijboer RJ; Department of Radiology, Atrium Medical Center, Heerlen, the Netherlands.
  • Keizer K; Department of Neurology, Catharina Hospital, Eindhoven, the Netherlands.
  • Tielbeek AV; Department of Radiology, Catharina Hospital, Eindhoven, the Netherlands.
  • den Hertog HM; Department of Neurology, Medical Spectrum Twente, Enschede, the Netherlands.
  • Gerrits DG; Department of Radiology, Medical Spectrum Twente, Enschede, the Netherlands.
  • van den Berg-Vos RM; Department of Neurology, St Lucas Andreas Hospital, Amsterdam, the Netherlands.
  • Karas GB; Department of Radiology, St Lucas Andreas Hospital, Amsterdam, the Netherlands.
  • Steyerberg EW; Department of Public Health, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • Flach HZ; Department of Neurology, Reinier de Graaf Gasthuis, Delft, the Netherlands.
  • Marquering HA; Department of Radiology, Academic Medical Center, Amsterdam, the Netherlands39Department of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, the Netherlands.
  • Sprengers ME; Department of Radiology, Academic Medical Center, Amsterdam, the Netherlands.
  • Jenniskens SF; Department of Radiology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Beenen LF; Department of Radiology, Academic Medical Center, Amsterdam, the Netherlands.
  • van den Berg R; Department of Radiology, Academic Medical Center, Amsterdam, the Netherlands.
  • Koudstaal PJ; Department of Neurology, Erasmus MC University Medical Center Rotterdam, Rotterdam, the Netherlands.
  • van Zwam WH; Department of Radiology, Maastricht University Medical Center, Maastricht, the Netherlands.
JAMA Neurol ; 73(2): 190-6, 2016 Feb.
Article en En | MEDLINE | ID: mdl-26716735
IMPORTANCE: Intra-arterial treatment (IAT) for acute ischemic stroke caused by intracranial arterial occlusion leads to improved functional outcome in patients treated within 6 hours after onset. The influence of treatment delay on treatment effect is not yet known. OBJECTIVE: To evaluate the influence of time from stroke onset to the start of treatment and from stroke onset to reperfusion on the effect of IAT. DESIGN, SETTING, AND PARTICIPANTS: The Multicenter Randomized Clinical Trial of Endovascular Treatment of Acute Ischemic Stroke in the Netherlands (MR CLEAN) was a multicenter, randomized clinical open-label trial of IAT vs no IAT in 500 patients. The time to the start of treatment was defined as the time from onset of symptoms to groin puncture (TOG). The time from onset of treatment to reperfusion (TOR) was defined as the time to reopening the vessel occlusion or the end of the procedure in cases for which reperfusion was not achieved. Data were collected from December 3, 2010, to June 3, 2014, and analyzed (intention to treat) from July 1, 2014, to September 19, 2015. MAIN OUTCOMES AND MEASURES: Main outcome was the modified Rankin Scale (mRS) score for functional outcome (range, 0 [no symptoms] to 6 [death]). Multiple ordinal logistic regression analysis estimated the effect of treatment and tested for the interaction of time to randomization, TOG, and TOR with treatment. The effect of treatment as a risk difference on reaching independence (mRS score, 0-2) was computed as a function of TOG and TOR. Calculations were adjusted for age, National Institutes of Health Stroke Scale score, previous stroke, atrial fibrillation, diabetes mellitus, and intracranial arterial terminus occlusion. RESULTS: Among 500 patients (58% male; median age, 67 years), the median TOG was 260 (interquartile range [IQR], 210-311) minutes; median TOR, 340 (IQR, 274-395) minutes. An interaction between TOR and treatment (P = .04) existed, but not between TOG and treatment (P = .26). The adjusted risk difference (95% CI) was 25.9% (8.3%-44.4%) when reperfusion was reached at 3 hours, 18.8% (6.6%-32.6%) at 4 hours, and 6.7% (0.4%-14.5%) at 6 hours. CONCLUSION AND RELEVANCE: For every hour of reperfusion delay, the initially large benefit of IAT decreases; the absolute risk difference for a good outcome is reduced by 6% per hour of delay. Patients with acute ischemic stroke require immediate diagnostic workup and IAT in case of intracranial arterial vessel occlusion. TRIAL REGISTRATION: trialregister.nl Identifier: NTR1804.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Reperfusión / Isquemia Encefálica / Activador de Tejido Plasminógeno / Accidente Cerebrovascular / Fibrinolíticos Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Neurol Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Reperfusión / Isquemia Encefálica / Activador de Tejido Plasminógeno / Accidente Cerebrovascular / Fibrinolíticos Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Neurol Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos