Response of Blood Pressure and Blood Glucose to Treatment With Recombinant Tissue-Type Plasminogen Activator in Acute Ischemic Stroke Evidence From the Virtual International Stroke Trials Archive

被引:10
|
作者
Kerr, Daniel M. [1 ]
Fulton, Rachael L. [1 ]
Higgins, Peter [1 ]
Bath, Philip M. W. [2 ]
Shuaib, Ashfaq [3 ]
Lyden, Patrick [4 ]
Lees, Kennedy R. [1 ]
机构
[1] Univ Glasgow, Western Infirm, Inst Cardiovasc & Med Sci, Glasgow G11 6NT, Lanark, Scotland
[2] Univ Nottingham, Stroke Trials Unit, Div Stroke, Nottingham NG7 2RD, England
[3] Univ Alberta, Stroke Res Program, Edmonton, AB, Canada
[4] Univ Calif San Diego, Dept Neurol, San Diego, CA 92103 USA
关键词
cerebral infarct; hyperglycemia; hypertension; stroke care; thrombolysis; STRESS HYPERGLYCEMIA; OUTCOMES; RECANALIZATION; THROMBOLYSIS; MANAGEMENT; ALTEPLASE; PROFILES; NINDS; ECASS; TIME;
D O I
10.1161/STROKEAHA.111.627059
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Elevations in blood pressure (BP) and blood glucose are common during stroke and may represent a stress response secondary to the acute neurological deficit. If so, they should settle more completely in recombinant tissue-type plasminogen activator (rtPA)-treated patients in association with improved neurological status. Methods-We performed a controlled comparison of 24-hour declines in BP and glucose in rtPA-treated and control patients from the Virtual Stroke International Stroke Trial Archive (VISTA) database. Twenty-four-hour falls in BP and glucose were compared using multiple regression to account for baseline imbalances. The logarithmic transformation of glucose was used and 24-hour differences expressed as ratios of 24 hours to admission geometric means. Two-way analysis of variance was used to test for interaction between rtPA and early improvement for 24-hour falls in BP and blood glucose. Results-BP analysis included 5406 patients (rtPA=41%) and glucose analysis 4288 (rtPA=37%). rtPA-treated patients were younger, less likely to have a history of hypertension or diabetes, and had more severe strokes on admission. BP and glucose were lower at baseline in rtPA-treated patients than control subjects. On regression, rtPA predicted significantly greater 24-hour falls in systolic BP (beta=3.9; 95% CI, 2.8-5.0), diastolic BP (beta=3.1; 95% CI, 2.4-3.9), and glucose (beta=0.97; 95% CI, 0.95-0.99). rtPA did not interact with early neurological improvement for 24-hour falls in systolic BP (P=0.72), diastolic BP (P=0.79), or blood glucose (P=0.51). Conclusions-A stress response does not appear to be the principal cause of elevations in BP and glucose during stroke. (Stroke. 2012;43:399-404.)
引用
收藏
页码:399 / 404
页数:6
相关论文
共 50 条
  • [21] Use of tissue-type plasminogen activator for acute ischemic stroke - The Cleveland area experience
    Katzan, IL
    Furlan, AJ
    Lloyd, LE
    Frank, JI
    Harper, DL
    Hinchey, JA
    Hammel, JP
    Qu, A
    Sila, CA
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (09): : 1151 - 1158
  • [22] Vepoloxamer Enhances Fibrinolysis of tPA (Tissue-Type Plasminogen Activator) on Acute Ischemic Stroke
    Wang, Chunyang
    Huang, Rui
    Li, Chao
    Lu, Mei
    Emanuele, Martin
    Zhang, Zheng Gang
    Chopp, Michael
    Zhang, Li
    STROKE, 2019, 50 (12) : 3600 - 3608
  • [23] Strategies Used by Hospitals to Improve Speed of Tissue-Type Plasminogen Activator Treatment in Acute Ischemic Stroke
    Xian, Ying
    Smith, Eric E.
    Zhao, Xin
    Peterson, Eric D.
    Olson, DaiWai M.
    Hernandez, Adrian F.
    Bhatt, Deepak L.
    Saver, Jeffrey L.
    Schwamm, Lee H.
    Fonarow, Gregg C.
    STROKE, 2014, 45 (05) : 1387 - 1395
  • [24] Influence of Obesity on Effectiveness of Intravenous Tissue-Type Plasminogen Activator in Acute Ischemic Stroke
    Schlick, Konrad
    Raman, Rema
    Hemmen, Thomas
    Meyer, Brett
    Meyer, Dawn
    Ernstrom, Karin
    Ovbiagele, Bruce
    NEUROLOGY, 2012, 78
  • [25] Effectiveness of tissue-type plasminogen activator for acute ischemic stroke: Consequences of protocol violation
    Karbalai, H
    Demchuk, AM
    Hoyte, KM
    Klein, GM
    Feasby, TE
    Buchan, AM
    STROKE, 1999, 30 (01) : 248 - 248
  • [26] Quality improvement and tissue-type plasminogen activator for acute ischemic stroke - A Cleveland update
    Katzan, IL
    Hammer, MD
    Furlan, AJ
    Hixson, ED
    Nadzam, DM
    STROKE, 2003, 34 (03) : 799 - 800
  • [27] Impact of Time to Treatment on Tissue-Type Plasminogen Activator-Induced Recanalization in Acute Ischemic Stroke
    Muchada, Marian
    Rodriguez-Luna, David
    Pagola, Jorge
    Flores, Alan
    Sanjuan, Estela
    Meler, Pilar
    Boned, Sandra
    Alvarez-Sabin, Jose
    Ribo, Marc
    Molina, Carlos A.
    Rubiera, Marta
    STROKE, 2014, 45 (09) : 2734 - 2738
  • [28] ApoE phenotype and the effectiveness of intravenous tissue-type plasminogen activator in acute ischemic stroke
    Broderick, J
    Lu, M
    Jackson, C
    Pancioli, A
    Tilley, BC
    Fagan, SC
    Kothari, R
    Levine, SR
    Marler, JR
    Lyden, PD
    Haley, EC
    Brott, T
    Grotta, JC
    ANNALS OF NEUROLOGY, 2000, 48 (03) : 421 - 421
  • [29] NURR1 Involvement in Recombinant Tissue-Type Plasminogen Activator Treatment Complications After Ischemic Stroke
    Merino-Zamorano, Cristina
    Hernandez-Guillamon, Mar
    Jullienne, Amandine
    Le Behot, Audrey
    Bardou, Isabelle
    Pares, Mireia
    Fernandez-Cadenas, Israel
    Giralt, Dolors
    Carrera, Caty
    Ribo, Marc
    Vivien, Denis
    Ali, Carine
    Rosell, Anna
    Montaner, Joan
    STROKE, 2015, 46 (02) : 477 - 484
  • [30] Contemporary trends in recombinant tissue-type plasminogen activator utilization for ischemic stroke in the United States
    Kassab, M. Yassin
    Jani, V.
    Lahewala, S.
    Patel, A.
    Arora, S.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2015, 357 : E422 - E422