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Heart. Jan 2006; 92(1): 117–118.
PMCID: PMC1861002

Primary percutaneous coronary intervention for patients with acute ST elevation myocardial infarction with and without diabetes mellitus

Patients with acute ST segment elevation myocardial infarction (STEMI) with diabetes mellitus (DM) have an increased mortality and morbidity when compared with patients without DM.1 Information is limited about clinical outcome of with STEMI and DM treated with reperfusion. Furthermore, patients with DM have a higher rate of thrombolysis failure.2,3 Information is also limited on long term outcome of patients with DM treated with primary percutaneous coronary intervention (PCI),4 which is the reperfusion treatment of choice.5

We therefore studied one year mortality among patients with and without DM in a large cohort of patients with acute STEMI treated with primary PCI. Furthermore, we studied the impact of preadmission treatment for DM, either oral medication or with insulin.

METHODS

Between January 1997 and December 2002, 1463 consecutive and unselected patients were admitted to our hospital with acute STEMI. Of the 1463 patients, 17 were lost to follow up and for another 138 patients data about DM status was not available. The remaining 1308 patients constituted the study cohort. Follow up information was obtained one year after the initial event by written questionnaire sent to all patients. If necessary outpatients' reports were reviewed and general practitioners were contacted by telephone. Baseline clinical and angiographic data were collected prospectively on a dedicated database. The patients were categorised as being without DM or as having an established diagnosis of DM at admission. Patients with DM were categorised according to preadmission treatment: either with oral medication or diet controlled DM (non‐insulin dependent DM (NIDDM)) or with insulin (insulin dependent DM (IDDM)). IDDM comprised both type 1 and type 2 DM. Patients treated with insulin in combination with oral medication were categorised as having IDDM.

To find independent predictors of one year mortality we performed multivariate analysis with a Cox proportional hazards regression model.

RESULTS

Of the 1308 patients, 174 (13.3%) had a confirmed diagnosis of DM at admission. Patients with DM were older (< 60 years; 44.4% v 64.4%, p < 0.001) and fewer of them were men (64.9% v 74.9%, p  =  0.006) or smokers (34.5% v 55.2%, p < 0.001). More of the patients with DM were hypertensive (49.4% v 31.7%, p < 0.001), had a previous coronary event (previous PCI, STEMI, or coronary bypass grafting: 40.8% v 20.3%, p < 0.001), or had a long ischaemic time (> 3 hours) (54.7% v 44.3%, p  =  0.027) compared with patients without DM. Patients with DM had a higher incidence of cardiogenic shock at admission (13.2% v 8.3%, p  =  0.034) and more of them needed intra‐aortic balloon counter pulsation (12.1% v 5.6%, p < 0.001). Patients with DM had more multivessel disease (55.7% v 37.9%, p < 0.001) and coronary calcifications (27.6% v 19.5%, p  =  0.014) but fewer successful PCI procedures (86.6% v 95.2%, p < 0.001) compared with patients without DM. Mortality after one year's follow up was 8.9% (n  =  113) in the whole cohort, 17.8% for patients with DM, and 7.2% for patients without DM (OR 2.9, 95% CI 1.8 to 4.3, p < 0.001). Of the 174 patients with DM, 126 (72.4%) were taking oral treatment (NIDDM) and 48 (27.8%) were taking insulin (IDDM) at admission. Baseline and angiographic characteristics did not differ between patients with IDDM and those with NIDDM. IDDM patients tended to have more coronary calcifications (37.5% v 23.8%, p  =  0.071) and less successful PCI (81.3% v 88.9%, p  =  0.184) than patients with NIDDM. Mortality was 27.1% for patients with IDDM and 14.3% for patients with NIDDM (OR 2.2, 95% CI 1.0 to 5.0, p < 0.05). Multivariate analysis showed that significant independent predictors for mortality were cardiogenic shock at presentation, PCI failure, IDDM, NIDDM, and coronary calcifications (table 11).

Table thumbnail
Table 1 Independent predictors of one year mortality in 1308 patients with ST elevation myocardial infarction treated with primary percutaneous coronary intervention

DISCUSSION

This study confirms that even with the reperfusion treatment of choice, patients with STEMI and DM have a greater long term mortality than do patients without DM. They have different baseline characteristics from patients without DM. Patients with DM also present with a higher incidence of cardiogenic shock, possibly at least partly due to a longer ischaemic time. Furthermore, more patients with than without DM had PCI failure possibly also as a consequence of a longer ischaemic time. Some angiographic differences may also partly explain the difference in PCI success. Both coronary calcifications and a higher rate of multivessel disease are also associated with more complicated PCI procedures and were more common among patients with DM.

The second finding is that preadmission treatment for DM is an independent predictor for one year mortality. Patients requiring insulin have longstanding type 1 DM or type 2 DM without adequate glycaemic regulation with oral medication. These patients with IDDM mostly have longstanding DM and mortality of those with type 2 DM receiving insulin at admission is about four times higher than that of patients without DM and two times higher than that of patients with DM taking oral medication at admission. In our study about 13% of the patients had a previous diagnosis of DM. Of all the patients with DM about 28% were taking insulin at admission, in agreement with large registries.

As a limitation, we did not routinely estimate haemoglobin A1c or test for DM on admission or during follow up. Despite the relatively large sample size, the absolute number of patients in each DM category is somewhat small. Only 23% of all patients were treated with abciximab.

Patients with acute STEMI with diagnosed DM more often present with cardiogenic shock and have more severe coronary disease and PCI failure. After primary PCI for STEMI, the one year mortality rate is 7.2% for patients without DM and 17.8% for patients with DM. For patients with DM taking oral medication at the time of admission for STEMI, the one year mortality is 14.3% and for those taking insulin mortality is 27.1%. Preadmission treatment for DM is an independent predictor of one year mortality. Even after primary PCI for acute STEMI, patients with DM treated with insulin form a subgroup with a mortality about four times higher than that of patients without DM and two times higher than that of patients with DM treated with oral medication in daily, real life clinical practice.

Abbreviations

DM - diabetes mellitus

IDDM - insulin dependent diabetes mellitus

NIDDM - non‐insulin dependent diabetes mellitus

PCI - percutaneous coronary intervention

STEMI - ST segment elevation myocardial infarction

Footnotes

There are no conflicts of interest or financial disclosure

References

1. Mak K H, Moliterno D J, Granger C B. et al Influence of diabetes mellitus on clinical outcome in the thrombolytic era of acute myocardial infarction. GUSTO‐I Investigators. Global utilization of streptokinase and tissue plasminogen activator for occluded coronary arteries. J Am Coll Cardiol 1997. 30171–179.179. [PubMed]
2. Hsu L F, Mak K H, Lau K W. et al Clinical outcomes of patients with diabetes mellitus and acute myocardial infarction treated with primary angioplasty or fibrinolysis. Heart 2002. 88260–265.265. [PMC free article] [PubMed]
3. Zairis M N, Lyras A G, Makrygiannis S S. et al Type 2 diabetes and intravenous thrombolysis outcome in the setting of ST elevation myocardial infarction. Diabetes Care 2004. 27967–971.971. [PubMed]
4. Timmer J R, Ottervanger J P, Thomas K, on behalf of the Zwolle myocardial infarction study group et al Long‐term, cause‐specific mortality after myocardial infarction in diabetes. Eur Heart J 2004. 25926–931.931. [PubMed]
5. Keeley E C, Boura J A, Grines C L. Primary angioplasty versus intravenous thrombolytic therapy for acute myocardial infarction: a quantitative review of 23 randomised trials. Lancet 2003. 36113–20.20. [PubMed]

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