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    JAMA. 2000 Mar 1;283(9):1151-8.

    Use of tissue-type plasminogen activator for acute ischemic stroke: the Cleveland area experience.

    Source

    Cerebrovascular Center, Cleveland Clinic Foundation, OH 44195, USA. katzani@ccf.org

    Abstract

    CONTEXT:

    Little is known regarding outcomes after intravenous tissue-type plasminogen activator (IV tPA) therapy for acute ischemic stroke outside a trial setting.

    OBJECTIVE:

    To assess the rate of IV tPA use, the incidence of symptomatic intracerebral hemorrhage (ICH), and in-hospital patient outcomes throughout a large urban community.

    DESIGN:

    Historical prospective cohort study conducted from July 1997 through June 1998.

    SETTING:

    Twenty-nine hospitals in the Cleveland, Ohio, metropolitan area.

    PATIENTS:

    A total of 3948 patients admitted to a study hospital with a primary diagnosis of ischemic stroke (International Classification of Diseases, Ninth Revision, Clinical Modification code 434 or 436).

    MAIN OUTCOME MEASURES:

    Rate of IV tPA use and occurrence of symptomatic ICH among patients treated with tPA; proportion of patients receiving tPA whose treatment deviated from national guidelines; in-hospital mortality among patients receiving tPA compared with that among ischemic stroke patients not receiving tPA and with mortality predicted by a model.

    RESULTS:

    Seventy patients (1.8%) admitted with ischemic stroke received IV tPA. Of those, 11 patients (15.7%; 95% confidence interval [CI], 8.1%-26.4%) had a symptomatic ICH (of which 6 were fatal) and 50% (95% CI, 37.8%-62.2%) had deviations from national treatment guidelines. In-hospital mortality was significantly higher among patients treated with tPA (15.7%) compared with patients not receiving tPA (5.1%, P<.001) and compared with the model's prediction (7.9%; P<.006).

    CONCLUSIONS:

    A small proportion of patients admitted with acute ischemic stroke in Cleveland received tPA; they experienced a high rate of ICH. Cleveland community experience with tPA for acute ischemic stroke may differ from that reported in clinical trials.

    Comment in

    PMID:
    10703777
    [PubMed - indexed for MEDLINE]

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