>
To better explore the effectiveness of drug-eluting stents in the "real-world" of high-risk patients, we should focus on registry results.12-14 Unlike randomized studies, registries have almost no inclusion criteria, thus producing a larger study population that more closely resembles the population seen in daily practice. Since patient inclusion is generally voluntary, there may be an inherent patient enrollment bias in any registry. However, a registry is often the only way to create evidence in highly adverse clinical situations that are normally excluded in industry-sponsored randomized studies. The study from Berenguer et al15 published in this issue of our journal is a welcome addition to the literature.
Berenguer et al15 have assessed the usefulness of sirolimus-eluting stents among diabetic patients with complex lesions by conducting a substudy of a single-center registry of complex lesions treated with these devices.16 Complex stenosis was defined as stenosis presenting any of the following anatomical conditions associated with a high risk of restenosis: location in the left main sten, bifurcations, lesions longer than 18 mm, calcified lesions, stenosis of the proximal left anterior descending artery, restenotic lesions, total occlusions, ostial lesions, and stenosis in vessels of less than 2.75 mm. In all 260 lesions treated, target vessel failure at 1 year as the primary event and angiographic evidence of restenosis at 6 months were then compared between nondiabetic, non-insulin-dependent diabetic mellitus (NIDDM), and insulin-dependent diabetic mellitus (IDDM) patients. The patients with insulin-dependent diabetes presented significantly greater late luminal loss and a higher incidence of restenosis (trend at the limit of significance). Nevertheless, these findings did not result in an increase in the rate of target vessel revascularization (6.5% in type 1 diabetes, 5.8% in NIDDM, and 3.8% in non-diabetics; P=NS). Likewise, the incidence of target vessel failure showed only a tendency (P=.07) to be higher in patients with IDDM. Lastly, and most importantly, the multivariate analysis eliminated IDDM as an independent predictor of restenosis and target vessel failure. This fact is not as surprising if the baseline data are analyzed for both groups (Tables 1-4 of the study). Patients with IDDM were typically women, hypertensive, with a history of coronary artery bypass grafting, peripheral vascular disease, heart failure, and ejection fraction <50%, and presented significantly longer lesions. Finally, an analysis of the cause of target vessel failure (Table 5 of the study) showed that this was basically due to a trend toward a higher incidence of cardiac death that was not related to a higher incidence of infarction in the target vessel (stent thrombosis) or a higher incidence of clinical restenosis. This appears to be logical, when considering that this patient group has poorer clinical characteristics. Therefore, in my opinion, the data from this registry do not show that sirolimus-eluting stents imply a poorer clinical progress in patients with IDDM, but rather that these patients are those who worsen (greater number of deaths) despite receiving a stent, with an incidence of clinical restenosis similar to that of nondiabetic or NIDDM patients.
Although a decrease in the efficacy of sirolimus-eluting stents could not be proven among IDDM diabetics due to the design of this registry, we should ask whether or not the clinical data support the concept of sirolimus resistance in these patients.
In the SIRIUS study, insulin-dependent patients did not present any improvement in the angiographic restenosis parameters when the stent was analyzed together with its margins. Nevertheless, when the analysis only looks at the stent, which is where the antiproliferative potency of the drug is determined, there was a significant decrease in late luminal loss and incidence of restenosis. This "margin effect" is attributed to technical problems (geographic miss) rather than ineffectiveness of the drug.17
The randomized, multicenter DIABETES study18 included high-risk diabetic patients, a group that is highly comparable to the patients in the present study. The mean reference diameter was 2.34 mm for all patients and 2.24 mm for insulin-dependent patients. Contrary to the authors' description, chronic total occlusions (13% of the lesions included) and patients with renal failure (32% of the patients) were not excluded. In addition, 43% of the lesions were longer than 20 mm and 65% of the patients presented multivessel disease. In this context, the incidences of restenosis and late luminal loss were comparable among IDDM and NIDDM patients. In reality, the decrease in risk was greater in insulin-dependent patients due to an increase in the incidence of restenosis in the group treated with conventional stents. Therefore, this is further evidence for the "neutralizing" effect of sirolimus-eluting stents in a high-risk group.
Finally, if we analyze the results of the 293 diabetic patients included in the Research and T-Search registries,19 similar data are obtained to those of the Berenguer et al study.15 The patients with insulin-dependent diabetes presented a worse clinical outcome (27% of major cardiac adverse events at 1 year versus 14.6% in patients with type 2 diabetes; P=.091). In the multivariate analysis, however, treatment of the left main sten and the left anterior descending artery, renal failure, and female sex were identified as independent predictors of failure at 1 year of follow-up, whereas the need for insulin was not statistically significant.
Based on the current evidence, because of their greater comorbidity, diabetic patients who require insulin should benefit from integral medical treatment beyond a purely cardiologic approach, in which treatment is more careful, more controlled and probably multidisciplinary. Likewise, from the standpoint of percutaneous revascularization, they should receive, almost universally and as standard therapy, implantation of a drug-eluting stent.
Correspondence: Dr. M. Sabaté.
Unidad de Hemodinámica. Hospital de la Santa Creu i Sant Pau.
Sant Antoni Maria Claret, 167. 08025 Barcelona. España.
E-mail: msabatet@santpau.es