LONG-TERM OUTCOME AFTER INTRAVENOUS MAGNESIUM-SULFATE IN SUSPECTED ACUTE MYOCARDIAL-INFARCTION - THE 2ND LEICESTER INTRAVENOUS MAGNESIUM INTERVENTION TRIAL (LIMIT-2)

被引:163
作者
WOODS, KL [1 ]
FLETCHER, S [1 ]
机构
[1] UNIV LEICESTER,DEPT MED & THERAPEUT,LEICESTER LE1 7RH,ENGLAND
关键词
D O I
10.1016/S0140-6736(94)92024-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The second Leicester Intravenous Magnesium Intervention Trial (LIMIT-2) examined the effect of an intravenous regimen of magnesium sulphate in 2316 patients with suspected acute myocardial infarction. Treatment, according to a double-blind randomised protocol, was started with a loading injection, before any thrombolytic therapy, and continued with a maintenance infusion for a further 24 h. Cause-specific mortality of randomised patients has now been examined over 1.0-5.5 (mean 2.7) years of follow-up. Mortality rate from ischaemic heart disease was reduced by 21% (95% CI 5-35%, p=0.01) and all-cause mortality rate reduced by 16% (2-29%, p=0.03) in magnesium-treated patients. Magnesium protects the contractile function of the myocardium from reperfusion injury (''stunning'') in experimental models; this observation accords with the 25% (7-39%, p=0.009) reduction in early left ventricular failure in the magnesium group of LIMIT-2. For such protection to occur, magnesium must be raised by the time of reperfusion since the injury is immediate. In the clinical context the timing of magnesium treatment in relation to thrombolytic therapy or spontaneous reperfusion is likely to be critical. The early benefits of this simple and safe intervention are reflected in improved long-term survival.
引用
收藏
页码:816 / 819
页数:4
相关论文
共 28 条
[1]  
ADAMS JH, 1979, THROMB HAEMOSTASIS, V42, P603
[2]  
AHMAD EN, 1991, FASEB J, V5, pA1045
[3]   MARKED REDUCTION OF FREE-RADICAL GENERATION AND CONTRACTILE DYSFUNCTION BY ANTIOXIDANT THERAPY BEGUN AT THE TIME OF REPERFUSION - EVIDENCE THAT MYOCARDIAL STUNNING IS A MANIFESTATION OF REPERFUSION INJURY [J].
BOLLI, R ;
JEROUDI, MO ;
PATEL, BS ;
ARUOMA, OI ;
HALLIWELL, B ;
LAI, EK ;
MCCAY, PB .
CIRCULATION RESEARCH, 1989, 65 (03) :607-622
[4]   MECHANISM OF MYOCARDIAL STUNNING [J].
BOLLI, R .
CIRCULATION, 1990, 82 (03) :723-738
[5]   MAGNESIUM AND REPERFUSION OF ISCHEMIC RAT-HEART AS ASSESSED BY P-31-NMR [J].
BORCHGREVINK, PC ;
BERGAN, AS ;
BAKOY, OE ;
JYNGE, P .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (01) :H195-H204
[6]   PREVALENCE OF TOTAL CORONARY-OCCLUSION DURING THE EARLY HOURS OF TRANSMURAL MYOCARDIAL-INFARCTION [J].
DEWOOD, MA ;
SPORES, J ;
NOTSKE, R ;
MOUSER, LT ;
BURROUGHS, R ;
GOLDEN, MS ;
LANG, HT .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (16) :897-902
[7]   MODULATION OF SEVERITY OF REPERFUSION STUNNING IN THE ISOLATED RAT-HEART BY AGENTS ALTERING CALCIUM FLUX AT ONSET OF REPERFUSION [J].
DUTOIT, EF ;
OPIE, LH .
CIRCULATION RESEARCH, 1992, 70 (05) :960-967
[8]   MYOCARDIAL RECOVERY DURING POSTISCHEMIC REPERFUSION - EFFECTS OF NIFEDIPINE, CALCIUM AND MAGNESIUM [J].
FERRARI, R ;
ALBERTINI, A ;
CURELLO, S ;
CECONI, C ;
DILISA, F ;
RADDINO, R ;
VISIOLI, O .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1986, 18 (05) :487-498
[9]  
Fibrinolytic 'Therapy Trialists' (FTT) Collaborative Group, 1994, LANCET, V343, P311
[10]  
GERTZ SD, 1987, MAGNESIUM, V6, P225