Babak A. Vakili
Albert Einstein College of Medicine
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Featured researches published by Babak A. Vakili.
Arteriosclerosis, Thrombosis, and Vascular Biology | 2004
David L. Brown; Kavita Desai; Babak A. Vakili; Chadi Nouneh; Hsi-Ming Lee; Lorne M. Golub
Background—Vulnerable plaque demonstrates intense inflammation in which macrophages secrete matrix metalloproteinases (MMPs) that degrade the fibrous cap, ultimately leading to rupture, in situ thrombosis, and an associated clinical event. Thus, inhibition of MMP activity or more general suppression of vascular inflammation are attractive targets for interventions intended to reduce plaque rupture. We hypothesized that subantimicrobial doses of doxycycline (SDD) (20 mg twice daily) would benefit patients with coronary artery disease by reducing inflammation and MMP activity and thus possibly prevent coronary plaque rupture events. Methods and Results—We conducted a prospective, randomized, double-blind, placebo-controlled pilot study of 6 months of SDD or placebo treatment to reduce inflammation and prevent plaque rupture events. A total of 50 patients were enrolled, of whom 24 were randomized to placebo and 26 to SDD. At 6 months, there was no difference in the composite endpoint of sudden death, fatal myocardial infarction (MI), non-fatal MI, or troponin-positive unstable angina in SDD compared with placebo-treated patients (8.4% versus 0%, P =0.491). Biochemical markers of inflammation were assessed in plasma at study entry and after 6 months of therapy in 30 patients. In SDD-treated patients, high-sensitivity C-reactive protein (CRP) was reduced by 46% from 4.8±0.6 &mgr;g/mL to 2.6±0.4 &mgr;g/mL (P =0.007), whereas CRP was not significantly reduced in placebo patients. Interleukin (IL)-6 decreased from 22.1±3.7 pg/mL at baseline to 14.7±1.8 pg/mL at 6 months in SDD-treated patients (P =0.025) but did not decrease significantly in placebo-treated patients. On zymography, pro-MMP-9 activity was reduced 50% by SDD therapy (P =0.011), whereas it was unchanged by placebo treatment. Conclusion—SDD appears to exert potentially beneficial effects on inflammation that could promote plaque stability. These findings should be investigated in a larger study.
Catheterization and Cardiovascular Interventions | 2003
Olga Dynina; Babak A. Vakili; James Slater; Warren Sherman; Kumar L. Ravi; Stephen Green; Timothy A. Sanborn; David L. Brown
Coronary heart disease is the leading cause of death among the elderly (> 65 years) and the very elderly (> 85 years). Little information is available regarding the outcome of very elderly patients referred for PCI in the current era of improved techniques, devices, and pharmacotherapy. The objective of the current study was to evaluate the clinical characteristics and outcomes of very elderly patients ≥ 85 years of age in a large, contemporary, multi‐institutional PCI database. Five hospitals in the New York City metropolitan area contributed these prospectively defined data elements on consecutive patients undergoing PCI from 1 January 1998 to 1 October 1999. Of 10,847 patients, 5,341 (49%) were younger than 65 years, 3,342 (31%) were 65–74 years, 1,885 (17%) were 75–84 years, and 279 (2.6%) were at least 85 years of age. Following PCI, the very elderly developed stroke (P < 0.001) and renal failure requiring dialysis (P = 0.002) more commonly than younger patients following PCI. The very elderly had a significantly increased in‐hospital mortality rate at 2.5% (P < 0.001). However, on multivariate analysis, age ≥ 85 years was not an independent predictor of in‐hospital mortality (OR = 1.22; 95% CI = 0.37–4.07). The very elderly should not be refused PCI on the basis of advanced age alone. Cathet Cardiovasc Intervent 2003;58:351–357.
American Journal of Cardiology | 2003
Babak A. Vakili; Robert C. Kaplan; James Slater; Warren Sherman; Kumar L. Ravi; Stephen Green; Timothy A. Sanborn; David L. Brown
It is unknown whether the benefits of parenteral platelet glycoprotein (GP) IIb/IIIa inhibitors as an adjunct to percutaneous coronary intervention (PCI) demonstrated in randomized clinical trials extend to patients treated outside the setting of clinical trials. A contemporary registry of 10,847 consecutive PCI procedures was analyzed to determine the effect of GP IIb/IIIa inhibitor treatment on in-hospital major adverse coronary events ([MACEs] composite of death, urgent coronary artery bypass surgery, periprocedural myocardial infarction, abrupt closure, and stent thrombosis). In this registry, GP IIb/IIIa inhibitors were administered to 20.1% of patients. These patients were younger, more often men, and less often hypertensive than untreated patients. GP IIb/IIIa inhibitor-treated patients were more likely to present with acute myocardial infarction or unstable angina. Stents were placed in 79% of patients treated with GP IIb/IIIa inhibitors. MACEs occurred in 7.8% of GP IIb/IIIa inhibitor-treated patients compared with 3.8% of untreated patients (p <0.001). After multivariable adjustment for the propensity of GP IIb/IIIa inhibitor treatment as well as other possible confounders and interactions known to influence MACEs, GP IIb/IIIa inhibitor treatment was associated with a 57% increase in the risk of a MACE (odds ratio 1.57, 95% confidence interval 1.22 to 2.03; p = 0.0004). In a data set consisting of patients with a high degree of acuity predominantly treated with stent placement, GP IIb/IIIa inhibitor treatment is associated with an increase in thrombotic complications of PCI.
American Journal of Cardiology | 2000
Babak A. Vakili; David L. Brown
This study compared the in-hospital outcomes of patients treated with or without stent placement during mechanical revascularization for acute myocardial infarction. After correction for differences in baseline characteristics, patients treated with stent placement had lower in-hospital mortality.
Journal of the American College of Cardiology | 2015
Nandkishore Ranadive; Babak A. Vakili; Brandon Berry
In 2012, our practice started a program with the goal to improve blood pressure (BP) control for patients through interactive educational seminars. The 90-minute group sessions consisted of disease education for hypertension, as well as promoting healthy lifestyles through education on heart healthy
American Heart Journal | 2001
Babak A. Vakili; Peter M. Okin; Richard B. Devereux
Diabetes Care | 2004
Sean R. Wilson; Babak A. Vakili; Warren Sherman; Timothy A. Sanborn; David L. Brown
Journal of Invasive Cardiology | 2002
Vs. Srinivas; Babak A. Vakili; David L. Brown
Kardiologia | 2003
Sean R. Wilson; Babak A. Vakili; Robert C. Kaplan; Warren Sherman; Kumar L. Ravi; Timothy A. Sanborn; David L. Brown
Journal of the American College of Cardiology | 2003
Babak A. Vakili; Warren Sherman; Kumar L. Ravi; Timothy A. Sanborn; David L. Brown