BMJ 1996;312:1637-1641 (29 June)

Papers

Prospective evaluation of eligibility for thrombolytic therapy in acute myocardial infarction

John K French, cardiologist,a Barbara F Williams, research nurse,a Hamish H Hart, physician,b Susan Wyatt, research nurse,b June E Poole, rehabilitation nurse,c Christine Ingram, charge nurse,d Christopher J Ellis, cardiologist,d Miles G Williams, cardiologist,c Harvey D White, director of coronary care and cardiovascular research a

a Coronary Care Unit, Green Lane Hospital, Auckland, New Zealand, b Coronary Care Unit, North Shore Hospital, Auckland, c Coronary Care Unit, Middlemore Hospital, Auckland, d Coronary Care Unit, Auckland Hospital, Auckland

Correspondence to: Dr John French, Cardiology Department, Green Lane Hospital, Epsom, Auckland 1003, New Zealand.

Abstract

Objective: To determine the proportion of patients presenting with acute myocardial infarction who are eligible for thrombolytic therapy.
Design: Cohort follow up study.
Setting: The four coronary care units in Auckland, New Zealand.
Subjects: All 3014 patients presenting to the units with suspected myocardial infarction in 1993.
Main outcome measures: Eligibility for reperfusion with thrombolytic therapy (presentation within 12 hours of the onset of ischaemic chest pain with ST elevation >/=2 mm in leads V1-V3, ST elevation >/=1 mm in any other two contiguous leads, or new left bundle branch block); proportions of (a) patients eligible for reperfusion and (b) patients with contraindications to thrombolysis; death (including causes); definite myocardial infarction.
Results: 948 patients had definite myocardial infarction, 124 probable myocardial infarction, and nine ST elevation but no infarction; 1274 patients had unstable angina and 659 chest pain of other causes. Of patients with definite or probable myocardial infarction, 576 (53.3%) were eligible for reperfusion, 39 had definite contraindications to thrombolysis (risk of bleeding). Hence 49.7% of patients (537/1081) were eligible for thrombolysis and 43.5% (470) received this treatment. Hospital mortality among patients eligible for reperfusion was 11.7% (55/470 cases) among those who received thrombolysis and 17.0% (18/106) among those who did not.
Conclusions: On current criteria about half of patients admitted to coronary care units with definite or probable myocardial infarction are eligible for thrombolytic therapy. Few eligible patients have definite contraindications to thrombolytic therapy. Mortality for all community admissions for myocardial infarction remains high.

Key messages

  • Less than 10% of patients eligible for reperfusion have contraindications to thrombolysis

  • The hospital mortality for all patients with acute myocardial infarction remains high (14%)

  • Better treatments are required to reduce mortality in both reperfusion eligible and reperfusion ineligible patients

Introduction

Because of the mortality benefit conferred by thrombolytic therapy in acute myocardial infarction1 2 3 4 5 6 strategies must be aimed at delivering treatment to the maximum number of eligible patients presenting to hospital from the general community. The proportion of patients eligible for thrombolytic therapy reportedly varies from 15-16%7 8 to 79%.9 These figures are affected by whether eligibility is based on admission electrocardiographic and time window criteria or a discharge diagnosis of myocardial infarction. Patients entering thrombolytic trials such as the fourth international study of infarct survival,9 which reported 79% utilisation of thrombolytic therapy, may represent only a subset of those who present to general hospitals with suspected myocardial infarction. This is within the range (70-80%) suggested by Ketley and Woods10 11 as the likely optimum rate of eligibility for thrombolytic therapy and less than the National Health Service recommended rate (90%).12 By contrast, some studies reporting low rates of thrombolytic use may have excluded potentially eligible patients--for example, elderly patients, diabetic patients, or patients treated by primary angioplasty.7 8

To determine the eligibility of consecutive, un-selected patients with suspected acute myocardial infarction presenting to community hospitals for reperfusion with thrombolytic therapy we prospectively evaluated patients presenting to the four coronary care units in Auckland, New Zealand, in 1993.

Methods

The coronary care units accepted patients of any age with suspected myocardial infarction unless cardiopulmonary resuscitation was precluded by comorbidity. Patients considered to have unstable angina at presentation were also usually admitted to the units. The recommended time window and electrocardiographic criteria for thrombolytic therapy were presentation within 12 hours of symptom onset with either ST elevation >/=1 mm in at least two leads (>/=2 mm in leads V1-V3)5 13 or new onset left bundle branch block.6 Specific contraindications included uncontrolled hypertension (blood pressure >/= 180/110 mm Hg which could not be lowered); surgery, trauma, or invasive procedures within two weeks; prolonged (15 minutes or more) or traumatic cardiopulmonary resuscitation; known haemostatic disorder; haemorrhagic diabetic retinopathy; recent gastrointestinal or genitourinary bleeding; or stroke within six months.

Definite myocardial infarction was defined as two of the following: 20 minutes or more of ischaemic chest pain; peak creatine kinase activity >/= twice normal; development of Q waves or persistent T wave changes in the electrocardiogram. When creatine kinase activity was increased to less than twice normal for our laboratory and there were no evolutionary Q waves or persistent T wave changes probable myocardial infarction was diagnosed. Patients who presented with ST elevation and received thrombolytic therapy but did not have peak creatine kinase activity >300 U/l were recorded as having aborted infarction.

Data were collected prospectively. A family history of premature coronary heart disease was defined as sudden death, myocardial infarction, or angina in mother or sisters aged under 60 or in father or brothers aged under 55. Hypertension was recorded as currently receiving treatment. Smoking was defined as current or having quit for less than one month. A history of dyslipidaemia was not recorded. The time to hospital admission and time to thrombolytic therapy from the onset of pain were also recorded. Cardiogenic shock was defined as hypotension with systolic blood pressure </=90 mm Hg for >/=30 minutes with evidence of hypoperfusion despite correction of reversible factors. Heart failure was defined as radiological evidence of pulmonary interstitial or alveolar oedema.

The significance of categorical variables was determined by {chi}2 test and of continuous variables by Student's t test. 95% Confidence intervals were calculated when appropriate.

Results

Admissions to the coronary care units in 1993 included 1072 patients with probable or definite myocardial infarction, 1274 patients with unstable angina pectoris, and 659 patients considered to have other causes for their chest pain (fig 1). Additionally, nine patients who presented with ST elevation had no increase in creatine kinase activity or persistent electrocardiographic changes after thrombolytic therapy. Patients with unstable angina pectoris and chest pain of other causes are excluded from this study. Mean hospital stay was 7.4 (SD 5.3) days. Table 1 gives the baseline characteristics of the patients with myocardial infarction.



View larger version (19K):
[in this window]
[in a new window]
 
Fig 1--Flow chart of 3014 patients admitted with suspected or established myocardial infarction or unstable angina


Table 1--Baseline characteristics
----------------------------------------------------------------------------------
                           Definite             Probable
                          infarction           infarction               Total*
                           (n = 948)            (n = 124)             (n = 1081)
----------------------------------------------------------------------------------
Mean (SD) age (years)       64 (12)              65 (11)                64 (12)
No (%) male                672 (71)              88 (71)               766 (71)
No (%) with previous
  infarction               208 (22)              36 (29)               247 (23)
No (%) with angina         301 (32)              58 (47)               363 (34)
No (%) with hypertension   332 (35)              48 (39)               384 (36)
No (%) with diabetes       106 (11)              18 (15)               124 (11)
No (%) smokers             332 (35)              41 (33)               375 (35)
No (%) with family
  history of premature
  coronary heart disease   252 (27)              34 (27)               288 (27)
No (%) with previous
  percutaneous
  transluminal coronary
  angioplasty               18 (2)                1 (1)                 19 (2)
No (%) with previous
  coronary artery bypass
  grafting                  44 (5)                10 (8)                55 (5)
----------------------------------------------------------------------------------
*Includes nine patients with ST elevation and no increase in creatine
kinase activity who received thrombolytic therapy (aborted infarction).

ELIGIBILITY FOR THROMBOLYTIC THERAPY

Five hundred and seventy six patients (53.3%; 95% confidence interval 50.3% to 56.2%) fulfilled the time and electrocardiographic criteria for eligibility for reperfusion, including 12 patients (2.1%; 1.2% to 3.6%) with new onset left bundle branch block. Of reperfusion eligible patients, 39 (6.8%; 5.0% to 9.1%) had definite contraindications to thrombolytic therapy (table 2). Additionally, at the physicians' discretion eight patients who were eligible for reperfusion but had a history of peptic ulceration (six), non-haemorrhagic diabetic retinopathy (one), and advanced oropharyngeal carcinoma (one) were not given thrombolytic therapy. Of all patients who fulfilled the electrocardiographic and time window criteria for thrombolytic therapy, 470 (81.6%; 78.2% to 84.6%) received thrombolytic therapy; 455 (79.0%) received streptokinase and 15 (2.6%) recombinant tissue plasminogen activator. One patient who had surgery 10 days previously was treated by primary angioplasty. Table 3 lists the characteristics of patients eligible for reperfusion who did and did not receive thrombolytic therapy.


Table 2--Reasons for non-use of thrombolysis in patients
eligible by time and electrocardiographic criteria (n = 106)
-----------------------------------------------------------------
                                              No of patients
-----------------------------------------------------------------
Contraindications to therapy
Hypertension (blood pressure >180/110 mm Hg)        3
Recent surgery or trauma*                          17
Recent gastrointestinal or genitourinary bleeding   7
Stroke                                             11
Bleeding diathesis                                  1
-----------------------------------------------------------------
Total                                              39
-----------------------------------------------------------------
Relative contraindications
Previous peptic ulcer disease                       6
Diabetic retinopathy                                1
Cancer                                              1
-----------------------------------------------------------------
Total                                               8
-----------------------------------------------------------------
Diagnostic uncertainty
? Dissection                                        4
? Pericarditis                                      1
Transient or borderline ST elevation               15
? New left or right bundle branch block            12
-----------------------------------------------------------------
Total                                              32
-----------------------------------------------------------------
Other
Severe comorbid disease                             3
Age+                                                5
Physician discretion+                              12
Shock+                                              1
Unknown                                             6
-----------------------------------------------------------------
Total                                              27
-----------------------------------------------------------------
*Includes five traumatic cardiac arrests.
+See discussion.


Table 3--Characteristics and outcome of patients
presenting within 12 hours and with ST elevation or new
onset left bundle branch block in electrocardiogram
-----------------------------------------------------------------
                                                         No
                                  Thrombolytic      thrombolytic
                                    therapy            therapy
                                    (n = 470)          (n = 106)
-----------------------------------------------------------------
Mean (SD) age (years)                64 (11)            66 (12)
No (%) male                         337 (72)            66 (62)
No (%) with previous infarction      88 (19)            36 (34)
No (%) with angina                  125 (27)            39 (37)
No (%) with hypertension            157 (33)            43 (41)
No (%) with diabetes                 40 (9)             18 (17)
No (%) smoking                      170 (36)            33 (31)
Mean (SD) peak creatine
 kinase (U/I)                     2250 (1704)         1637 (1325)
No (%) with previous
 percutaneous transluminal
 coronary angioplasty                5 (1)               2 (2)
No (%) with previous coronary
 artery bypass grafting             18 (4)               8 (8)
Mortality                           55 (12)             18 (17)

Of the 948 patients with a discharge diagnosis of definite myocardial infarction, 534 (56.3%; 53.2% to 59.5%) fulfilled electrocardiographic and time window criteria for thrombolytic therapy and 428 of these patients (80.2%; 76.6% to 83.3%) received thrombolytic therapy.

THROMBOLYTIC THERAPY IN PATIENT SUBGROUPS

Of patients who were eligible for reperfusion on electrocardiographic and time window criteria, 50 (23.0%; 17.9% to 29.1%) of 217 aged 70 or more did not receive thrombolytic therapy as compared with 56 (15.6%; 12.2% to 19.7%) of 359 aged under 70 ({chi}2 = 4.51; P = 0.03). This difference could not be attributed to decreased utilisation of thrombolytic therapy among eligible elderly women compared with elderly men (71/94 (75.5%; 65.9% to 83.2%) v 96/123 (78.0%; 69.9% to 84.5%)). There was a trend towards decreased utilisation of thrombolytic therapy among eligible women (women 133/173 (76.9%; 70.0% to 82.6%); men 337/403 (83.6%; 79.7% to 86.9%)) ({chi}2 = 3.5; P = 0.06). Thrombolytic therapy was also used less commonly in patients with diabetes than in non-diabetic patients (40/58 (69.0%; 56.0% to 79.5%) v 430/518 (83.0%; 79.5% to 86.0%)) ({chi}2 = 6.8; P = 0.02).

PATIENTS PRESENTING LATE OR WITHOUT ST ELEVATION

One hundred and fifty six patients (14.4%; 12.5% to 16.7%) (including 26 with presumed new onset left bundle branch block) were eligible for reperfusion on electrocardiographic criteria but presented more than 12 hours after symptom onset. Of these patients, 36 (23.1%) received thrombolytic therapy and 120 (76.9%) did not. Twenty three of 349 patients (6.6%) presenting with ST depression, T wave inversion, or a normal electrocardiogram received thrombolytic therapy (table 4).


Table 4--Mortality according to presenting electrocardiogram, age, and thrombolytic therapy. Figures are percentages (whole numbers in
parentheses)
---------------------------------------------------------------------------------------------------------------------------------------------------------------------
                                 Thrombolytic therapy                       No thrombolytic therapy                               Total
---------------------------------------------------------------------------------------------------------------------------------------------------------------------
                                     Age (years)                                  Age (years)                                   Age (years)
---------------------------------------------------------------------------------------------------------------------------------------------------------------------
                          <55      55-69        >/=70    All ages     <55       55-69       >/=70     All ages      <55       55-69       >/=70        All ages
---------------------------------------------------------------------------------------------------------------------------------------------------------------------
ST elevation or bundle
  branch block </= 12      1.9       8.7         21.6       11.7       5.9        7.7        28.0        17.0        2.4        8.5         23.0          12.7
  hours                 (2/108)   (17/195)    (36/167)   (55/470)    (1/17)     (3/39)     (14/50)    (18/106)     (3/125)   (20/234)    (50/217)      (73/576)
ST elevation or bundle
  branch block >12         0        12.5        27.3       13.9       18.2       18.4       28.3        23.3        12.9       16.7        28.2          21.2
  hours*                 (0/9)     (2/16)      (3/11)     (5/36)     (4/22)     (7/38)     (17/60)    (28/120)     (4/31)     (9/54)     (20/71)       (33/156)
ST depression            50.0        0          60.0       44.4        0          7.4       20.7        13.7        5.3        7.1         23.0          15.4
                         (1/2)     (0/2)        (3/5)      (4/9)     (0/17)     (4/54)     (17/82)    (21/153)     (1/19)     (4/56)     (20/87)       (25/162)
T wave inversion or
  normal                   0         0          20.0        7.1        0          2.6        9.1        3.5           0         2.4        10.2          3.7
  electrocardiogram+     (0/3)     (0/6)        (1/5)      (1/14)    (0/53)     (2/76)      (4/44)    (6/173)      (0/56)     (2/82)     (5/49)        (7/187)
---------------------------------------------------------------------------------------------------------------------------------------------------------------------
*Or time not specified.
+Includes paced rhythm.

MORTALITY

Patients presenting with ST elevation or new onset left bundle branch block within 12 hours had an overall hospital mortality of 12.7% (73/576 cases; 95% confidence interval 10.2% to 15.6%). Of these deaths, 55 (11.7%; 9.1% to 14.9%) occurred among the 470 patients given thrombolytic therapy and 18 (17.0%; 11.0% to 25.3%) among the 106 not given thrombolytic therapy (table 4). Mortality among patients presenting more than 12 hours after symptom onset with ST elevation or new onset left bundle branch block was 21.2% (33/156 cases; 15.4% to 28.3%). Of the entire cohort of 1081 patients, 138 died (overall mortality 12.8%; 10.9% to 14.9%). Among the 948 patients with definite myocardial infarction (age range 24-94 years) and 124 patients with probable myocardial infarction were 130 (13.7%; 95% confidence interval 11.5% to 15.9%) and eight (6.5%; 2.2% to 10.8%) respectively. The most common cause of death was cardiogenic shock (55 cases; 39.9%) or heart failure (30; 21.7%) (table 5). Confirmed or presumed cardiac rupture occurred in 17 cases (12.3%) and one patient died of a haemorrhagic stroke after thrombolytic therapy.


Table 5--Causes of death
-----------------------------------------------------
                                      No of patients
-----------------------------------------------------
Cardiogenic shock                           55
Congestive heart failure                    30
Confirmed rupture                            5
Presumed rupture*                           12
Ventricular arrhythmia                      17
Unwitnessed death                            2
Other cardiovascular                        13
No data                                      4
-----------------------------------------------------
Total                                      138
-----------------------------------------------------
*Electromechanical dissociation.

Discussion

For reperfusion therapy with thrombolytic agents to significantly reduce overall hospital mortality from myocardial infarction we need to rapidly identify and treat patients who may benefit. The electrocardiographic criteria that we used for eligibility for thrombolytic therapy have been accepted internationally.5 13 Nevertheless, they differed slightly from those used in the Gruppo Italiano per lo Studio della Streptochinasi nell'Infarto Miocardico (GISSI) and other studies of thrombolytic therapy (table 6). Most studies included patients with ST elevation, though there were two minor differences in the electrocardiographic criteria: >/=1 mm versus >/=2 mm ST elevation in leads V4-V6 and one or more versus two or more leads showing ST elevation. Some studies, however, including the second international study of infarct survival (ISIS-2), did not use electrocardiographic criteria, whereas others such as the GISSI-I study included patients with ST depression.


Table 6--Eligibility criteria for thrombolytic therapy from clinical trials
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
                             Time from                     ST elevation
                             symptom    ----------------------------------------------------  Amount of ST
                               onset       Limb leads      Leads V1-V3     Leads V4-V6         depression                                             Drug (intravenous
Trial                         (hours)         (No)            (No)            (No)            (No of leads)               Other                    unless otherwise stated)
------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
GISSI1                  </=12       >/=1 mm (1)       >/=2 mm (1)     >/=2 mm (1)          As for ST                  --                   Streptokinase
                                                                                                elevation
USIM28                  </=4        >/=1 mm (1)       >/=2 mm (1)     >/=2 mm (1)          As for ST                  --                   Urokinase
                                                                                                elevation
Interuniversity29       </=4        >/=1 mm (1)       >/=2 mm (1)     >/=2 mm (1)         Not eligible                --                   Intracoronary + intravenous
                                                                                                                                                   streptokinase
AIMS30                  </=6        >/=1 mm (2)       >/=2 mm (2)     >/=2 mm (2)         Not eligible                --                   Anisoylated plasminogen
                                                                                                                                                   streptokinase activator complex
ISIS-22                 </=24            --               --              --                 --          Acute infarction clinically       Streptokinase
                                                                                                                    suspected
ASSET31                 </=5             --               --              --                 --          Acute infarction clinically       Tissue plasminogen activator
                                                                                                                    suspected
EMERAS32                6-24             --               --              --                 --          Acute infarction clinically       Streptokinase
                                                                                                                    suspected
LATE16                  6-24        >/=1 mm (2)       >/=2 mm (2)     >/=2 mm (2)         >/=2 mm (2)    Abnormal Q or T waves             Tissue plasminogen activator
                                                                                                                (>/=2 leads)
Western                      </=12       >/=1 mm (2)       >/=1.5 mm (2)   >/=1 mm (2)         Not eligible   One lead with ST elevation if no  Intracoronary streptokinase
 Washington4                                                                                              Q waves or hyperacute T waves
White et al5 13        </=6        >/=1 mm (2)       >/=2 mm (2)     >/=1 mm (2)         Not eligible                --                   Streptokinase
ISAM3                   </=6        >/=1 mm (1)       >/=2 mm (1)     >/=2 mm (1)         Not eligible                --                   Streptokinase

We evaluated prospectively eligibility for reperfusion therapy with thrombolytic agents and utilisation of this treatment in patients admitted from the community with suspected acute myocardial infarction. Patients were admitted irrespective of age provided that they had no serious comorbidity that might have made admission to a coronary care unit inappropriate. We did not collect data on patients with chest pain admitted direct to medical wards. Nor did we collect data on patients admitted direct to medical wards with other symptoms, such as confusion or breathlessness, who later turned out to have myocardial infarction.

Of patients admitted to coronary care units, 53.3% (576/1081) presented within 12 hours of symptom onset and had ST elevation or new left bundle branch block in the electrocardiogram, thus fulfilling our usual criteria for eligibility for reperfusion therapy.5 13 A total of 6.8% (39) of these eligible patients had definite contraindications to thrombolytic therapy. Of patients with a discharge diagnosis of definite myocardial infarction, 56.3% (534/948) were eligible for thrombolytic therapy on time and electrocardiographic criteria. This figure is lower than that reported (79%).9 These ISIS study differences may relate either to patient selection or to whether eligibility is based on time and electrocardiographic criteria at admission or on a discharge diagnosis of myocardial infarction. Patients with a discharge diagnosis of myocardial infarction include many without ST elevation or new left bundle branch block in the electrocardiogram at presentation, resulting in a smaller proportion of reperfusion eligible patients.

In this study 32.3% of patients (349/1081) with definite or probable myocardial infarction presented with ST depression, T wave inversion, or a normal electrocardiogram. There is no evidence for the efficacy of thrombolytic therapy in reducing mortality in patients with these electrocardiographic criteria.6

In the GISSI-I study roughly one fifth of patients had no ST elevation in the electrocardiogram and 13.8% had contraindications to streptokinase1 whereas GISSI-2 required ST elevation in only one lead and 10.3% of patients had contraindications to thrombolysis.14

CAUTIONS WITH THROMBOLYTIC THERAPY

In the early years of clinical treatment with thrombolytic agents there was caution about its use in older patients, in patients presenting after six hours, and in those with relative contraindications.15 The fibrinolytic therapy trialists' overview found a significant reduction in mortality with thrombolytic therapy in patients irrespective of age--namely, 15 (SD 4) lives saved per 1000 aged under 55; 21 (5) lives saved per 1000 aged 55-64; 37 (6) lives saved per 1000 aged 65-74; 13 (14) lives saved per 1000 aged 75 and over.6 Our findings show that thrombolytic therapy remains underutilised in elderly patients who may otherwise be eligible on time and electrocardiographic criteria. Also some patients presenting after 12 hours benefit from reperfusion therapy with thrombolytic agents,16 though predicting which patients may benefit at admission may be difficult.

Concern about the risk of retinal haemorrhage in diabetic patients with retinopathy17 probably explains the decreased use of thrombolysis in these patients. Recent evidence suggests that the risk of this complication may be low18 and if it occurs it can usually be treated without long term loss of vision.19 Because diabetic patients are at high absolute risk6 they should be considered for thrombolytic therapy irrespective of retinopathy.

Other potential bleeding risks, including traumatic cardiopulmonary resuscitation (four (0.4%) cases excluded in this study) and menstruation (none excluded), have been considered contraindications to thrombolytic therapy. Several reports suggest that these are only relative contraindications and that the risks of major bleeding are small.20 21 22 23 The role of reperfusion strategies in cardiogenic shock requires definition. Finally, patients who are eligible for thrombolytic therapy on electrocardiographic and time window criteria but who have definite contraindications to thrombolytic therapy should not be denied reperfusion therapy and should have primary angioplasty. Only one patient in this series was referred for primary angioplasty in these circumstances and potentially others could have been considered.

In addition to absolute contraindications to thrombolytic therapy, there are numerous relative contraindications, including pancreatitis, the presence of left atrial thrombus, infective endocarditis, pregnancy, oral anticoagulant therapy, and advanced liver disease. Overall these relative contraindications are uncommon. The possible risks and likely benefits of treatment need to be assessed and considered individually in each patient. Having considered absolute and relative contraindications, there remained 59 patients (10.2%) who were eligible for thrombolytic therapy on time and electrocardiographic criteria but who did not receive this treatment. Most commonly either these patients had equivocal or transient ST elevation or there were other, unstated physicians' reasons for withholding treatment. Also, some patients had differential diagnoses which may have precluded thrombolysis. The overall rate of non-administration of reperfusion therapy (roughly 10%) among otherwise eligible patients is low compared with recent registry data in the same era.24

The hospital mortality in this series among patients considered eligible for reperfusion was 13.7% (95% confidence interval 11.5% to 15.9%); 11.7% among patients who received thrombolysis, 17.0% among those who did not. These results are similar to recent reports of European registries.25 26 The respective 30 and 35 day death rates were about 7% in the global utilisation of streptokinase and tissue plasminogen activator for occluded coronary arteries study27 and the fourth international study of infarct survival.9 This suggests that patients randomised in trials represent a subgroup of patients presenting to community hospitals with suspected acute myocardial infarction.

In conclusion, the community hospital mortality from myocardial infarction remains high. Definite contraindications to thrombolysis are uncommon but only half of patients with suspected acute myocardial infarction and slightly more with definite myocardial infarction fulfil current eligibility criteria. Thrombolytic therapy should be used as widely and expeditiously as possible in these patients. Other strategies should be directed at facilitating hospital admission, and in order to lower overall community death rates additional treatments are required for patients not considered eligible for thrombolytic therapy.

We thank Loretta Bush and Judy Grant for help with data collection and the nurses and physicians who cared for patients.

Funding: This work was supported in part by a grant from the Health Research Council of New Zealand.

Conflict of interest: None.

  1. Gruppo Italiano per lo Studio della Streptochinasi nell'Infarto Miocardico (GISSI). Effectiveness of intravenous thrombolytic treatment in acute myocardial infarction. Lancet 1986;i:397-402.
  2. ISIS-2 (Second International Study of Infarct Survival) Collaborative Group. Randomised trial of intravenous streptokinase, oral aspirin, both, or neither among 17 187 cases of suspected acute myocardial infarction: ISIS-2. Lancet 1988;ii:349-60.
  3. ISAM Study Group. A prospective trial of intravenous streptokinase in acute myocardial infarction (ISAM): mortality, morbidity, and infarct size at 21 days. N Engl J Med 1986;314:1465-71. [Abstract]
  4. Kennedy JW, Ritchie JL, Davis KB, Stadius ML, Maynard C, Fritz JK. Western Washington randomized trial of intracoronary streptokinase in acute myocardial infarction: a 12-month follow-up report. N Engl J Med 1985;312:1073-8. [Abstract]
  5. White HD, Norris RM, Brown MA, Takayama M, Maslowski A, Bass NM, et al. Effect of intravenous streptokinase on left ventricular function and early survival after acute myocardial infarction. N Engl J Med 1987;317:850-5. [Abstract]
  6. Fibrinolytic Therapy Trialists' (FTT) Collaborative Group. Indications for fibrinolytic therapy in suspected acute myocardial infarction: collaborative overview of early mortality and major morbidity results from all randomised trials of more than 1000 patients. Lancet 1994;343:311-22. [Medline]
  7. Behar S, Abinader E, Caspi A, David D, Flich M, Friedman Y, et al. Frequency of use of thrombolytic therapy in acute myocardial infarction in Israel. Am J Cardiol 1991;68:1291-4. [Medline]
  8. Cragg DR, Friedman HZ, Bonema JD, Jaiyesimi IA, Ramos RG, Timmis GC, et al. Outcome of patients with acute myocardial infarction who are ineligible for thrombolytic therapy. Ann Intern Med 1991;115:173-7.
  9. ISIS-4 (Fourth International Study of Infarct Survival) Collaborative Group. ISIS-4: a randomised factorial trial assessing early oral captopril, oral mononitrate, and intravenous magnesium sulphate in 58 050 patients with suspected acute myocardial infarction. Lancet 1995;345:669-85. [Medline]
  10. Ketley D, Woods KL. Impact of clinical trials on clinical practice: example of thrombolysis for acute myocardial infarction. Lancet 1993;342:891-4. [Medline]
  11. Woods KL, Ketley D. Thrombolysis and acute myocardial infarction. Lancet 1994;343:232-3.
  12. Haines A, Jones R. Implementing findings of research. BMJ 1994;308:1488-92. [Free Full Text]
  13. White HD, Rivers JT, Maslowski AH, Ormiston JA, Takayama M, Hart HH, et al. Effect of intravenous streptokinase as compared with that of tissue plasminogen activator on left ventricular function after first myocardial infarction. N Engl J Med 1989;320:817-21. [Abstract]
  14. Gruppo Italiano per lo Studio della Sopravvivenza nell'Infarto Miocardico. GISSI-2: a factorial randomised trial of alteplase versus streptokinase and heparin versus no heparin among 12 490 patients with acute myocardial infarction. Lancet 1990;336:65-71. [Medline]
  15. Muller DWM, Topol EJ. Selection of patients with acute myocardial infarction for thrombolytic therapy. Ann Intern Med 1990;113:949-60.
  16. LATE Study Group. Late assessment of thrombolytic efficacy (LATE) study with alteplase 6-24 hours after onset of acute myocardial infarction. Lancet 1993;342:759-66. [Medline]
  17. Ward H, Yudkin JS. Thrombolysis in patients with diabetes: withholding treatment is probably mistaken: patients should be given a choice. BMJ 1995;310:3-4. [Free Full Text]
  18. Barbash GI, White HD, Modan M, Van de Werf F, for Investigators of the International Tissue Plasminogen Activator/Streptokinase Mortality Trial. Significance of diabetes mellitus in patients with acute myocardial infarction receiving thrombolytic therapy. J Am Coll Cardiol 1993;22:707-13. [Abstract]
  19. Thompson JT, de Bustros S, Michels RG, Rice TA. Results and prognostic factors in vitrectomy for diabetic vitreous hemorrhage. Arch Ophthalmol 1987;105:191-5. [Abstract/Free Full Text]
  20. Scholz KH, Tebbe U, Herrmann C, Wojcik J, Lingen R, Chemnitius JM, et al. Frequency of complications of cardiopulmonary resuscitation after thrombolysis during acute myocardial infarction. Am J Cardiol 1992;69:724-8. [Medline]
  21. Neches RB, Goldfarb AM, Saviano GJ. Thrombolytic therapy in acute myocardial infarction following prolonged cardiopulmonary resuscitation. Clin Cardiol 1991;14:616-9. [Medline]
  22. Tenaglia AN, Califf RM, Candela RJ, Kereiakes DJ, Berrios E, Young SY, et al. Thrombolytic therapy in patients requiring cardiopulmonary resuscitation. Am J Cardiol 1991;68:1015-9. [Medline]
  23. Karnash SL, Granger CB, White HD, Woodlief LH, Topol EJ, Califf RM, et al. Treating menstruating women with thrombolytic therapy: insights from the global utilization of streptokinase and tissue plasminogen activator for occluded coronary arteries (GUSTO-I) trial. J Am Coll Cardiol 1995;26:1651-6. [Abstract]
  24. Rogers WJ, Bowlby LJ, Chandra NC, French WJ, Gore JM, Lambrew CT, et al. Treatment of myocardial infarction in the United States (1990 to 1993): observations from the national registry of myocardial infarction. Circulation 1994;90:2103-14. [Abstract/Free Full Text]
  25. Rustige J, Schiele R, Burczyk U, Koch A, Tebbe U, Senges J, et al. High hospital mortality despite frequent use of thrombolysis in acute myocardial infarction [Abstract]. Eur Heart J 1995;16(suppl):9.
  26. Gottlieb S, Hod H, Barbash G, Cohen M, Boyko V, Behar S, et al. National survey on the use of thrombolysis and invasive procedures in acute myocardial infarction in Israel in 1994 [Abstract]. Eur Heart J 1995;16(suppl):9.
  27. GUSTO Investigators. An international randomized trial comparing four thrombolytic strategies for acute myocardial infarction. N Engl J Med 1993;329:673-82. [Abstract/Free Full Text]
  28. Rossi P, Bolognese L, on behalf of Urochinasi per via Sistemica nell'Infarto Miocardico (USIM) Collaborative Group. Comparison of intravenous urokinase plus heparin versus heparin alone in acute myocardial infarction. Am J Cardiol 1991;68:585-92. [Medline]
  29. Simoons ML, Serruys PW, van den Brand M, Bar F, de Zwaan C, Res J, et al. Improved survival after early thrombolysis in acute myocardial infarction: a randomised trial by the Interuniversity Cardiology Institute in the Netherlands. Lancet 1985;ii:578-82.
  30. AIMS Trial Study Group. Effect of intravenous APSAC on mortality after acute myocardial infarction: preliminary report of a placebo-controlled clinical trial. Lancet 1988;i:545-9.
  31. Wilcox RG, von der Lippe G, Ollson CG, Jensen G, Skene AM, Hampton JR. Trial of tissue plasminogen activation for mortality reduction in acute myocardial infarction: Anglo-Scandinavian study of early thrombolysis (ASSET). Lancet 1988;ii:525-30.
  32. EMERAS (Estudio Multicentrico Estreptoquinasa Republicas de America del Sur) Collaborative Group. Randomised trial of late thrombolysis in patients with suspected acute myocardial infarction. Lancet 1993;342:767-72. [Medline]
(Accepted 24 April 1996)


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to StumbleUpon StumbleUpon   Add to Technorati Technorati    What's this?

Relevant Article

Data on eligibility for thrombolytic treatment cannot be generalised
Adam D Timmis
BMJ 1996 313: 941. [Extract] [Full Text]

This article has been cited by other articles:

  • (2005). Reperfusion in acute myocardial infarction. DTB 43: 49-53 [Abstract] [Full text]  
  • Schomig, A., Mehilli, J., Antoniucci, D., Ndrepepa, G., Markwardt, C., Di Pede, F., Nekolla, S. G., Schlotterbeck, K., Schuhlen, H., Pache, J., Seyfarth, M., Martinoff, S., Benzer, W., Schmitt, C., Dirschinger, J., Schwaiger, M., Kastrati, A., for the Beyond 12 hours Reperfusion AlternatiVe Ev, (2005). Mechanical Reperfusion in Patients With Acute Myocardial Infarction Presenting More Than 12 Hours From Symptom Onset: A Randomized Controlled Trial. JAMA 293: 2865-2872 [Abstract] [Full text]  
  • Kastrati, A., Mehilli, J., Nekolla, S., Bollwein, H., Martinoff, S., Pache, J., Schuhlen, H., Seyfarth, M., Gawaz, M., Neumann, F.-J., Dirschinger, J., Schwaiger, M., Schomig, A., STOPAMI-3 Study Investigators, (2004). A randomized trial comparing myocardial salvage achieved by coronary stenting versus balloon angioplasty in patients with acute myocardial infarction considered ineligible for reperfusion therapy. J Am Coll Cardiol 43: 734-741 [Abstract] [Full text]  
  • Cohen, M., Gensini, G. F., Maritz, F., Gurfinkel, E. P., Huber, K., Timerman, A., Krzeminska-Pakula, M., Santopinto, J., Hecquet, C., Vittori, L., on behalf of the TETAMI Investigators, (2003). Prospective Evaluation of Clinical Outcomes After Acute ST-Elevation Myocardial Infarction in Patients Who Are Ineligible for Reperfusion Therapy: Preliminary Results From the TETAMI Registry and Randomized Trial. Circulation 108: III-14-21 [Abstract] [Full text]  
  • Schomig, A., Ndrepepa, G., Mehilli, J., Schwaiger, M., Schuhlen, H., Nekolla, S., Pache, J., Martinoff, S., Bollwein, H., Kastrati, A. (2003). Therapy-Dependent Influence of Time-to-Treatment Interval on Myocardial Salvage in Patients With Acute Myocardial Infarction Treated With Coronary Artery Stenting or Thrombolysis. Circulation 108: 1084-1088 [Abstract] [Full text]  
  • Hyde, T A, French, J K, Wong, C-K, Edwards, C, Whitlock, R M L, White, H D (2003). Associations between ST depression, four year mortality, and in-hospital revascularisation in unselected patients with non-ST elevation acute coronary syndromes. Heart 89: 490-495 [Abstract] [Full text]  
  • Wilkinson, J, Foo, K, Sekhri, N, Cooper, J, Suliman, A, Ranjadayalan, K, Timmis, A D (2002). Interaction between arrival time and thrombolytic treatment in determining early outcome of acute myocardial infarction. Heart 88: 583-586 [Abstract] [Full text]  
  • Wong, C.-K., French, J.K., Andrews, J., Frey, M.J., Adgey, A.A.J., Aylward, P.E., White, H.D. (2002). Usefulness of the presenting electrocardiogram in predicting myocardial salvage with thrombolytic therapy in patients with a first acute myocardial infarction. Eur Heart J 23: 399-404 [Abstract] [Full text]  
  • Mehilli, J., Kastrati, A., Dirschinger, J., Pache, J., Seyfarth, M., Blasini, R., Hall, D., Neumann, F.-J., Schomig, A. (2002). Sex-Based Analysis of Outcome in Patients With Acute Myocardial Infarction Treated Predominantly With Percutaneous Coronary Intervention. JAMA 287: 210-215 [Abstract] [Full text]  
  • Sayer, J W, Archbold, R A, Wilkinson, P, Ray, S, Ranjadayalan, K, Timmis, A D (2000). Prognostic implications of ventricular fibrillation in acute myocardial infarction: new strategies required for further mortality reduction. Heart 84: 258-261 [Abstract] [Full text]  
  • Jacobs, A. K., French, J. K., Col, J., Sleeper, L. A., Slater, J. N., Carnendran, L., Boland, J., Jiang, X., LeJemtel, T., Hochman, J. S., for the SHOCK Investigators, (2000). Cardiogenic shock with non-ST-segment elevation myocardial infarction: a report from the SHOCK Trial Registry. J Am Coll Cardiol 36: 1091-1096 [Abstract] [Full text]  
  • Hourigan, C T, Mountain, D, Langton, P E, Jacobs, I G, Rogers, I R, Jelinek, G A, Thompson, P L (2000). Changing the site of delivery of thrombolytic treatment for acute myocardial infarction from the coronary care unit to the emergency department greatly reduces door to needle time. Heart 84: 157-163 [Abstract] [Full text]  
  • French, J. K., Hyde, T. A., Straznicky, I. T., Andrews, J., Lund, M., Amos, D. J., Zambanini, A., Ellis, C. J., Webber, B. J., McLaughlin, S. C., Whitlock, R. M. L., Manda, S. O. M., Patel, H., White, H. D. (2000). Relationship between corrected TIMI frame counts at three weeks and late survival after myocardial infarction. J Am Coll Cardiol 35: 1516-1524 [Abstract] [Full text]  
  • Capewell, S, Pell, J.P, Morrison, C, McMurray, J (1999). Increasing the impact of cardiological treatments. How best to reduce deaths. Eur Heart J 20: 1386-1392 [Abstract]  
  • French, J. K., Hyde, T. A., Patel, H., Amos, D. J., McLaughlin, S. C., Webber, B. J., White, H. D. (1999). Survival 12 years after randomization to streptokinase: the influence of thrombolysis in myocardial infarction flow at three to four weeks. J Am Coll Cardiol 34: 62-69 [Abstract] [Full text]  
  • Gottlieb, S., Boyko, V., Harpaz, D., Hod, H., Cohen, M., Mandelzweig, L., Khoury, Z., Stern, S., Behar, S., for the Israeli Thrombolytic Survey Group, (1999). Long-term (three-year) prognosis of patients treated with reperfusion or conservatively after acute myocardial infarction. J Am Coll Cardiol 34: 70-82 [Abstract] [Full text]  
  • Brown, N, Melville, M, Gray, D, Young, T, Skene, A M, Wilcox, R G, Hampton, J R (1999). Relevance of clinical trial results in myocardial infarction to medical practice: comparison of four year outcome in participants of a thrombolytic trial, patients receiving routine thrombolysis, and those deemed ineligible for thrombolysis. Heart 81: 598-602 [Abstract] [Full text]  
  • Mahon, N G, O'Rorke, C, Codd, M B, McCann, H A, McGarry, K, Sugrue, D D (1999). Hospital mortality of acute myocardial infarction in the thrombolytic era. Heart 81: 478-482 [Abstract] [Full text]  
  • French, J. K., Amos, D. J., Williams, B. F., Cross, D. B., Elliott, J. M., Hart, H. H., Williams, M. G., Norris, R. M., Ashton, N. G., Whitlock, R. M. L., McLaughlin, S. C., White, H. D. (1999). Effects of early captopril administration after thrombolysis on regional wall motion in relation to infarct artery blood flow. J Am Coll Cardiol 33: 139-145 [Abstract] [Full text]  
  • White, H. D., Van de Werf, F. J. J. (1998). Thrombolysis for Acute Myocardial Infarction. Circulation 97: 1632-1646 [Abstract] [Full text]  
  • Barron, H. V., Bowlby, L. J., Breen, T., Rogers, W. J., Canto, J. G., Zhang, Y., Tiefenbrunn, A. J., Weaver, W. D. (1998). Use of Reperfusion Therapy for Acute Myocardial Infarction in the United States : Data From the National Registry of Myocardial Infarction 2. Circulation 97: 1150-1156 [Abstract] [Full text]  
  • Purcell, I F, Newall, N, Farrer, M (1997). Change in ST segment elevation 60 minutes after thrombolytic initiation predicts clinical outcome as accurately as later electrocardiographic changes. Heart 78: 465-471 [Abstract] [Full text]  
  • SMYTH, D. W, ELLIOTT, J. M (1997). Treating coronaries, at home or away?. Heart 78: 329-330 [Full text]  
  • Timmis, A. D (1996). Data on eligibility for thrombolytic treatment cannot be generalised. BMJ 313: 941c-941 [Full text]  
  • (1996). Eligibility for Thrombolysis. Journal Watch Cardiology 1996: 7-7 [Full text]  



Access jobs at BMJ Careers
Whats new online at Student 

BMJ