THE EFFECTS OF TISSUE-PLASMINOGEN ACTIVATOR, STREPTOKINASE, OR BOTH ON CORONARY-ARTERY PATENCY, VENTRICULAR-FUNCTION, AND SURVIVAL AFTER ACUTE MYOCARDIAL-INFARCTION

被引:0
|
作者
ROSS, AM
SIMOONS, ML
LUNDERGAN, C
THOMPSON, M
REINER, J
DEYCHAK, Y
ROHRBECK, S
COYNE, K
WALKER, P
CHO, S
GREENHOUSE, S
LEE, K
GRANGER, C
WILDERMANN, N
FINK, C
HARRY, S
ALLISON, D
DRAOUI, Y
COSTIGAN, G
FOX, D
LEMPEL, M
WILLIAMS, M
ROSS, J
FLOURA, R
HICKS, J
VANDEBRAND, M
BALK, A
RODENBURG, L
BAARDMAN, T
HOEKMAN, I
AMO, D
VANOOSTEROM, I
VANHESSEM, G
DEZWART, I
JANSSEN, M
DEPUI, A
TERWOGT, C
HOUWELING, J
CORBEAU, N
IWEMA, J
PAMEIJER, J
DEJONG, R
TOPOL, E
CALIFF, R
ARMSTRONG, PW
AYLWARD, P
BARBASH, G
BATES, E
BETRIU, A
BOISSEL, J
机构
[1] GEORGE WASHINGTON UNIV, ANGIOG SUBSTUDY COORDINATING CTR, WASHINGTON, DC 20052 USA
[2] GEORGE WASHINGTON UNIV, CORE LAB, WASHINGTON, DC 20052 USA
[3] NON-N AMER ANGIOG COORDINATING CTR CARDIALYSIS, ROTTERDAM, NETHERLANDS
[4] ST MARYS HOSP, ROCHESTER, NY 14611 USA
[5] GEORGE WASHINGTON UNIV HOSP, WASHINGTON, DC 20037 USA
[6] TULSA REG MED CTR, TULSA, OK USA
[7] MCKAY DEE HOSP, OGDEN, UT USA
[8] ST VINCENTS MED CTR, JACKSONVILLE, FL USA
[9] E ALABAMA MED CTR, OPELIKA, AL USA
[10] ST MARYS HOSP, TUCSON, AL USA
[11] PROCTOR COMMUNITY HOSP, PEORIA, IL USA
[12] MERCY HOSP, PITTSBURGH, PA 15219 USA
[13] MT CLEMENS GEN HOSP, MT CLEMENS, MI USA
[14] UNIV HOSP CLEVELAND, CLEVELAND, OH 44106 USA
[15] SPARTENBURG REG MED CTR, SPARTANBURG, SC USA
[16] UNIV COMMUN HOSP, TAMPA, FL USA
[17] HUMANA MED CITY, DALLAS, TX USA
[18] LAHEY CLIN MED CTR, BURLINGTON, MA USA
[19] UNIV MICHIGAN HOSP, ANN ARBOR, MI 48109 USA
[20] MOTHER FRANCES HOSP, TYLER, TX USA
[21] ST MARKS HOSP, SALT LAKE CITY, UT USA
[22] CRAWFORD W LONG MEM HOSP, ATLANTA, GA USA
[23] HAHNEMANN UNIV, PHILADELPHIA, PA 19102 USA
[24] SIOUX VALLEY HOSP, SIOUX FALLS, SD USA
[25] ST JOSEPHS HOSP, SAVANNAH, GA USA
[26] OCHSNER FDN HOSP, NEW ORLEANS, GA USA
[27] GOOD SAMARITAN HOSP, CINCINNATI, OH 45220 USA
[28] MCLEOD REG MED CTR, FLORENCE, SC USA
[29] EVANSTON HOSP CORP, EVANSTON, IL 60201 USA
[30] ST AGNES MED CTR, PHILADELPHIA, PA USA
[31] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, RICHMOND, VA 23298 USA
[32] GLENBROOK HOSP, GLENVIEW, IL USA
[33] SHADEYSIDE HOSP, PITTSBURGH, PA USA
[34] TERRE HAUTE REG HOSP, TERRE HAUT, IN USA
[35] LUTHERAN HOSP, FT WAYNE, IN USA
[36] MEM MED CTR, CORPUS CHRISTI, TX USA
[37] SWEDISH AMER HOSP, ROCKFORD, IL USA
[38] SPOHN HOSP, CORPUS CHRISTI, TX USA
[39] MCKENNAN HOSP, SIOUX FALLS, SD USA
[40] NO MICHIGAN HOSP, PETOSKEY, MI USA
[41] HACKENSACK MED CTR, HACKENSACK, NJ USA
[42] LAKESIDE VET AFFAIRS MED CTR, CHICAGO, IL USA
[43] HOP COCHIN, F-75674 PARIS 14, FRANCE
[44] HOP TENON, F-75970 PARIS 20, FRANCE
[45] CHU CAEN, F-14033 CAEN, FRANCE
[46] HOP HAUT LEVEQUE, PESSAC, FRANCE
[47] HOP HAUTE PIERRE, STRASBOURG, FRANCE
[48] HOP PURPAN, TOULOUSE, FRANCE
[49] HOP TROUSSEAU, TOURS, FRANCE
[50] HOP HOTEL DIEU, RENNES, FRANCE
来源
NEW ENGLAND JOURNAL OF MEDICINE | 1993年 / 329卷 / 22期
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Although it is known that thrombolytic therapy improves survival after acute myocardial infarction, it has been debated whether the speed with which coronary-artery patency is restored after the initiation of therapy further affects outcome. Methods. To study this question, we randomly assigned 2431 patients to one of four treatment strategies for reperfusion: streptokinase with subcutaneous heparin; streptokinase with intravenous heparin; accelerated-dose tissue plasminogen activator (t-PA) with intravenous heparin; or a combination of both activators plus intravenous heparin. Patients were also randomly assigned to cardiac angiography at one of four times after the initiation of thrombolytic therapy: 90 minutes, 180 minutes, 24 hours, or 5 to 7 days. The group that underwent angiography at 90 minutes underwent it again after 5 to 7 days. Results. The rate of patency of the infarct-related artery at 90 minutes was highest in the group given accelerated-dose t-PA and heparin (81 percent), as compared with the group given streptokinase and subcutaneous heparin (54 percent, P<0.001), the group given streptokinase and intravenous heparin (60 percent, P<0.001), and the group given combination therapy (73 percent, P = 0.032). Flow through the infarct-related artery at 90 minutes was normal in 54 percent of the group given t-PA and heparin but in less than 40 percent of the three other groups (P<0.001). By 180 minutes, the patency rates were the same in the four treatment groups. Re-occlusion was infrequent and was similar in all four groups (range, 4.9 to 6.4 percent). Measures of left ventricular function paralleled the rate of patency at 90 minutes; ventricular function was best in the group given t-PA with heparin and in patients with normal flow through the infarct-related artery irrespective of treatment group. Mortality at 30 days was lowest (4.4 percent) among patients with normal coronary flow at 90 minutes and highest (8.9 percent) among patients with no flow (P = 0.009). Conclusions. This study supports the hypothesis that more rapid and complete restoration of coronary flow through the infarct-related artery results in improved ventricular performance and lower mortality among patients with myocardial infarction. This would appear to be the mechanism by which accelerated t-PA therapy produced the most favorable outcome in the GUSTO trial.
引用
收藏
页码:1615 / 1622
页数:8
相关论文
共 50 条
  • [2] ACHIEVEMENT OF CORONARY-ARTERY PATENCY BY USE OF ANISOYLATED PLASMINOGEN STREPTOKINASE ACTIVATOR COMPLEX IN ACUTE MYOCARDIAL-INFARCTION
    HILLIS, WS
    HORNUNG, RS
    HOGG, KJ
    HOCKINGS, N
    BURNS, JMA
    DUNN, FG
    DRUGS, 1987, 33 : 117 - 123
  • [3] TISSUE-PLASMINOGEN ACTIVATOR VS PLACEBO AND STREPTOKINASE IN ACUTE MYOCARDIAL-INFARCTION
    VAHANIAN, A
    ARCHIVES DES MALADIES DU COEUR ET DES VAISSEAUX, 1986, 79 (04): : 532 - 532
  • [4] HEPARIN AND INFARCT CORONARY-ARTERY PATENCY AFTER STREPTOKINASE IN ACUTE MYOCARDIAL-INFARCTION
    MAHAN, EF
    CHANDLER, JW
    ROGERS, WJ
    NATH, HR
    SMITH, LR
    WHITLOW, PL
    HOOD, WP
    REEVES, RC
    BAXLEY, WA
    AMERICAN JOURNAL OF CARDIOLOGY, 1990, 65 (15): : 967 - 972
  • [5] PREDICTING EXTENT OF CORONARY-ARTERY DISEASE AND VENTRICULAR-FUNCTION AFTER ACUTE MYOCARDIAL-INFARCTION
    GIBSON, RS
    TAYLOR, GJ
    STEBBINS, P
    BERGER, BC
    WATSON, DD
    BELLER, GA
    CLINICAL RESEARCH, 1979, 27 (05): : A727 - A727
  • [6] IMPROVED VENTRICULAR-FUNCTION AFTER EARLY CORONARY-ARTERY RECANALIZATION IN ACUTE MYOCARDIAL-INFARCTION
    KUCK, KH
    MATHEY, D
    POLSTER, J
    BLEIFELD, W
    ZEITSCHRIFT FUR KARDIOLOGIE, 1980, 69 (10): : 713 - 713
  • [7] STREPTOKINASE OR TISSUE PLASMINOGEN-ACTIVATOR AND LEFT-VENTRICULAR FUNCTION AFTER MYOCARDIAL-INFARCTION
    WILLNER, RL
    NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (10): : 688 - 688
  • [8] STREPTOKINASE, BUT NOT TISSUE-PLASMINOGEN ACTIVATOR, ATTENUATES PLATELET-AGGREGATION IN PATIENTS WITH ACUTE MYOCARDIAL-INFARCTION
    KARLBERG, KE
    CHEN, J
    HAGERMAN, I
    BERGSTROM, K
    WALLIN, R
    SALDEEN, T
    SYLVEN, C
    JOURNAL OF INTERNAL MEDICINE, 1993, 234 (05) : 513 - 519
  • [9] STREPTOKINASE AND TISSUE PLASMINOGEN-ACTIVATOR IN ACUTE MYOCARDIAL-INFARCTION
    BREWER, CC
    MARKIS, JE
    HEART & LUNG, 1986, 15 (06): : 552 - 558
  • [10] COMPARISON OF ACCELERATED TISSUE-PLASMINOGEN ACTIVATOR WITH STREPTOKINASE FOR TREATMENT OF SUSPECTED MYOCARDIAL-INFARCTION
    KELLETT, J
    CLARKE, J
    MEDICAL DECISION MAKING, 1995, 15 (04) : 297 - 310