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J Am Coll Cardiol, 2002; 39:1723-1728 © 2002 by the American College of Cardiology Foundation |
* Department of Cardiology, Isala Clinics location "de Weezenlanden," Zwolle, Netherlands
Manuscript received July 12, 2001; revised manuscript received March 4, 2002, accepted March 13, 2002.
* Reprint requests and correspondence: Dr. Menko-Jan de Boer, Department of Cardiology, Isala Klinieken lokatie "de Weezenlanden," Groot Wezenland 20, 8011 JW, Zwolle, Netherlands.
ereis{at}planet.nl
| Abstract |
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BACKGROUND: The benefit of reperfusion therapy in elderly patients with AMI is uncertain, although elderly people account for a large proportion of deaths.
METHODS: We randomly assigned a total of 87 patients with an AMI who were older than 75 years to treatment with angioplasty or intravenous (IV) streptokinase. Clinical outcome was measured by taking the end points of death and the combination of death, reinfarction or stroke during follow-up.
RESULTS: The primary end point, a composite of death, reinfarction or stroke, at 30 days had occurred in 4 (9%) patients in the angioplasty group as compared with 12 (29%) in the thrombolysis group (p = 0.01, relative risk [RR]: 4.3, 95% confidence interval [CI]: 1.2 to 20.0). At one year the corresponding figures were 6 (13%) and 18 (44%), respectively (p = 0.001, RR: 5.2, 95% CI: 1.7 to 18.1).
CONCLUSIONS: In this series of patients with AMI who were older than 75 years, primary coronary angioplasty had a significant clinical benefit when compared with IV streptokinase therapy.
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| Methods |
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Inclusion criteria were as follows: symptoms of AMI that persisted for more than 30 min accompanied by an elevation of more than 1 mm (0.1 mV) in the ST segment in two or more contiguous electrocardiographic leads; and presentation within 6 h after the onset of symptoms (or between 6 h and 24 h, if there was evidence of continuing ischemia). Contraindication to thrombolytic therapy was defined as previous stroke or other known intracranial disease, recent trauma or surgery, refractory hypertension (systolic
180 mm Hg, diastolic
110 mm Hg), active bleeding or prolonged cardiopulmonary resuscitation. Before randomization we recorded each patients age, gender, Killip class on admission (16), electrocardiographic site of infarction, history of previous infarction, heart rate, time of onset of symptoms and time of hospital admission. The catheterization laboratory and the dedicated house staff were available 24 h, 7 days a week.
All patients received 450 mg of aspirin intravenously, followed by 80 mg of aspirin per day orally and IV nitroglycerin in a dose designed to maintain a systolic blood pressure of 110 mm Hg. Intravenous heparin was given in a dose designed to maintain the activated partial thromboplastin time between two and three times the normal value for at least two days. This partial thromboplastin time was measured twice a day. Patients assigned to streptokinase received 1.5 million U intravenously over a period of 1 h. In patients assigned to angioplasty treatment, coronary angiography was performed as soon as possible. Both coronary arteries were visualized; left ventriculography was not performed routinely. Coronary angioplasty was performed at the investigators discretion using any approved techniques and devices. Patients who received a stent were treated with ticlopidine, 250 mg, twice a day for two weeks. All cineangiograms were reviewed by two experienced investigators not involved in other parts of the study. Flow through the IRV was scored according to the Thrombolysis In Myocardial Infarction (TIMI) flow grading, before and after the angioplasty procedure (17). Agreement on flow and extent of coronary artery disease was reached in all cases. The time from admission to the initiation of therapy was calculated as the time to the start of the streptokinase infusion or the first balloon inflation.
Recurrent AMI was defined as chest pain, changes in the ST-T segment and a second increase in the creatine kinase level to more than two times the upper limit of normal or an increase of >200 U/l over the previous value if the level had not dropped below the upper limit of normal.
The primary end point was the composite of death, reinfarction or stroke at 30 days after randomization. The secondary end points were:
The study protocol was approved by the institutional ethics committee, and all patients gave oral informed consent. Before randomization it was ascertained that a catheterization laboratory was immediately available for coronary intervention. Randomization was performed using a telephone randomization service and was stopped early (April 1999) because a significant difference in the primary end point was found. Follow-up data were collected in March 2000. All clinical and outpatient records were reviewed, and general practitioners were contacted by telephone.
Statistical analysis.
All end points were analyzed according to the principle of intention-to-treat. A chi-square statistic was calculated to test differences between proportions with calculations of relative risks (RR) and exact 95% confidence intervals (CIs). Fisher exact test was used if there was an expected cell value of <5. The Student t test or the Mann-Whitney U test was used to compare continuous values. Survival and survival without recurrent infarction or stroke were calculated by the Kaplan-Meier product-limit method (19). Survival analysis over the total follow-up period was also performed by fitting Cox proportional hazards model (20). Because of the small sample size, this was not used as a multivariate model but enabled us to calculate hazard ratios, which may be interpreted as RRs, with 95% CIs. Continuous variables are summarized by using medians (with 25th, 75th percentiles) unless otherwise indicated; discrete variables are represented as frequencies and percentages. A p value of
0.05 was considered to indicate statistical significance.
The sample size was estimated on the basis of the following assumption: the 30-day incidence of death, reinfarction or stroke in the thrombolysis group would be 30%, whereas this incidence in the angioplasty group would be 15% (14,21). At alpha-level 5% and beta-level 20%, the number of patients required was 266, with 133 patients in each group.
| Results |
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The in-hospital mortality of the 77 patients not included in our study was 21%, and their baseline characteristics are given in Table 3. They were compared with baseline characteristics and in-hospital outcome of the study patients.
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| Discussion |
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In the initial phase after the index infarction, infarct size, as was estimated from cumulative LDH release in the plasma, was lower in the angioplasty treated patients, although this did not reach the level of significance. There was no difference in mean ejection fraction measured with radionuclide techniques between the two groups. This apparent lack of benefit with regard to direct myocardial salvage may be a similar finding as was observed when comparing thrombolytic therapy with placebo treatment (22).
In our experience with angioplasty, we did not encounter specific age-related problems with performing angioplasty in old patients as was reflected in the short time from hospital admission to first balloon inflation. All noncerebral bleedings in the angioplasty group were related to the arterial puncture site, and this occurs more frequently in the elderly (13). The main reason for excluding patients from our study was the high incidence of nonconclusive ECGs, and the number of patients with previous AMI in this group was significantly higher.
Other studies. Recently, the benefits of thrombolytic therapy in the elderly were questioned based on data from the Medicare Cooperative Cardiovascular Project registry (8). This observational survey concerned 7,864 patients age 76 to 86 years from a retrospective cohort study but does not represent randomized data. Although older patients from the same registry, who received thrombolytic therapy or primary angioplasty, had a lower mortality at one year compared with those who did not receive a reperfusion strategy, only those treated with primary angioplasty had better survival at 30 days (23,24).
The number of elderly patients with symptomatic coronary artery disease and the relative number of older patients being treated in Western society is steadily increasing (2527). Approximately 30% of all patients presenting with AMI are >75 years old (27). However, in most studies of reperfusion therapy in AMI, elderly people are excluded or represent a very small minority of the study population. In a pooled analysis of three randomized studies of primary angioplasty versus thrombolysis in elderly patients (>70 years), angioplasty was more effective (14). Furthermore, the high incidence of comorbidity and contraindications for thrombolytic therapy makes primary angioplasty an attractive reperfusion modality in this patient group. On the other hand, data from a recently published pooled analysis of the PAMI study group indicate that elderly patients still remain at an increased risk of death, bleeding, stroke and other complications despite treatment with primary angioplasty (28).
Some limitations of our study should be noted. In contrast with multicenter trials that have included large numbers of patients undergoing reperfusion therapy for AMI, our study included only 87 patients from a single institution. A trial comparing angioplasty with pharmacologic reperfusion therapy cannot be blinded. Furthermore, the high success rates associated with primary angioplasty and subsequent clinical outcome are directly related to technical skills and experience of operators in high volume interventional centers (2931).
Conclusions
In this series of patients with AMI who were older than 75 years, primary coronary angioplasty had a significant clinical benefit when compared with IV streptokinase therapy.
Our data stress the need for a large community-based multicenter trial to confirm our conclusion that primary coronary angioplasty may be the reperfusion therapy of choice in elderly patients.
| Acknowledgments |
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| References |
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