Ahmad Khraisat
Rosalind Franklin University of Medicine and Science
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Featured researches published by Ahmad Khraisat.
Clinical Cardiology | 2009
Sarabjeet Singh; Rohit Arora; Kamna Handa; Ahmad Khraisat; Nagapradeep Nagajothi; Janos Molnar; Sandeep Khosla
Animal studies have suggested dramatic improvement in cardiac function after acute myocardial infarction (AMI) through regeneration of the myocardium or neovascularization by transfer of cells derived from bone marrow (BMC) generated clinical studies. Recently published small sized studies have yielded mixed results, leaving the question unanswered.
American Journal of Therapeutics | 2008
Nagapradeep Nagajothi; Sasikanth Adigopula; Saravanan Balamuthusamy; Jose-Luis E Velazquez-Cecena; Kalpana Raghunathan; Ahmad Khraisat; Sarabjeet Singh; Janos Molnar; Sandeep Khosla; Daniel Benatar
A recent meta-analysis suggested that the use of rosiglitazone increases the risk of myocardial infarction (MI) in patients with type 2 diabetes mellitus. It is unclear whether this is a class effect of thiazolidinediones (TZD). We did a meta-analysis to evaluate cardiovascular outcomes with the use of pioglitazone. Randomized, controlled trials in which pioglitazone was compared with placebo or other hypoglycemic agents were considered for analysis. Studies were included if the data for MI were available. Studies were identified with use of relevant search words in Medline, Pubmed, EMBASE, CINAHL, and Cochrane databases. Data abstraction was done by 2 individual authors using a standardized protocol. The relative risk across all study groups was computed by the Mantel-Haenszel method, and interstudy heterogeneity was assessed by the χ2 method. All results were computed according to 95% confidence intervals. Five trials (N = 9965) met the inclusion criteria for analysis. The relative risk for MI was 0.86 (0.69-1.07; P = 0.17). The relative risks for stroke and revascularization were 0.79 (0.61-1.02; P = 0.07) and 0.40 (0.13-1.23; P = 0.11), respectively. Pioglitazone does not increase the risk for MI and may decrease the risk for stroke and revascularization.
Journal of Cardiovascular Pharmacology and Therapeutics | 2007
Sarabjeet Singh; Rohit Arora; Ahmad Khraisat; Kamna Handa; Amol Bahekar; Atul Trivedi; Sandeep Khosla
The purpose of this article was to determine the incidence of in-stent thrombosis (IST) after coronary stent implantation in patients with cocaine abuse. A retrospective review was done of medical records of consecutive patients who underwent coronary stent implantation for obstructive coronary artery disease at a single inner-city institution from January 1997 to October 2006. Patients with temporal cocaine use were identified by positive urine drug screen. IST was confirmed angiographically. Of the 81 patients with active cocaine use that underwent coronary stent implantation, 4 (5%) suffered IST (mean period from stent implantation, 28.5 ± 14 days). All procedures were performed successfully and received intravenous IIb/IIIa antagonist intraprocedurally. All patients were prescribed dual antiplatelet therapy with aspirin and clopidogrel at discharge; however, all 4 patients that suffered from IST continued cocaine abuse were noncompliant with the prescribed dual antiplatelet therapy. Of these 4 patients, 2 presented with ST segment elevation myocardial infarction (50%), whereas 2 presented with non-ST-segment elevation myocardial infarction (50%). One was managed medically. Two received repeat percutaneous coronary intervention, and 1 underwent coronary artery bypass surgery. The patient that underwent surgery died in the postoperative period. The remaining 3 patients survived. Patients with active cocaine abuse who undergo successful coronary stent revascularization have a high (5%) incidence of stent thrombosis. A majority of patients that suffer stent thrombosis continue cocaine abuse and are noncompliant with antiplatelet therapy.
Archives of Medical Research | 2008
Jose-Luis E Velazquez-Cecena; Sandeep Sharma; Nagapradeep Nagajothi; Ahmad Khraisat; Sandeep Khosla; Rohit Arora; Daniel Benatar
BACKGROUND Distinct hemodynamic patterns determined by impedance cardiography (ICG) have been found to be superior to clinical assessment for the identification of patients at risk for heart failure decompensation in the outpatient setting. Correlation of these hemodynamic patterns with serum brain natriuretic peptides (BNP) and left ventricular end diastolic pressure (LVEDP) has not been established. We evaluated the correlation of low-, intermediate- and high-risk groups for acute decompensation of heart failure (ADHF) as determined by ICG parameters with LVEDP and serum BNP. METHODS Consecutive patients referred for cardiac catheterization with echocardiographic diagnosis of left ventricle dysfunction (systolic or diastolic) or history of congestive heart failure (CHF) underwent ICG evaluation, serum BNP measurement, and LVEDP by cardiac catheterization. Three groups at different levels of risk for ADHF were determined according to ICG parameters: thoracic fluid content (TFC) and stroke volume index (SVI); low risk (low TFC, high SVI), intermediate risk (low-low or high-high TFC and SVI, respectively), and high risk (high TFC and low SVI). RESULTS Sixty three patients were included in the present study. Mean LVEDP and serum BNP levels were 20.2 +/- 8.2 mmHg and 814 +/- 1005 pg/mL, respectively, in the high-risk group in comparison to 12.3 +/- 6.2 mmHg and 53 +/- 38 pg/mL in the low-risk group (p = 0.01 and p = 0.009). CONCLUSIONS Patients with ICG parameters that represent high risk for ADHF have higher levels of serum BNP and LVEDP in comparison with patients who have intermediate- or low-risk ICG parameters for ADHF.
The American Journal of Medicine | 2008
Nagapradeep Nagajothi; Ahmad Khraisat; Jose-Luis E Velazquez-Cecena; Rohit Arora; Kalpana Raghunathan; Ravi Patel; Ritesh Parajuli
Journal of The Cardiometabolic Syndrome | 2008
Eshraq Al-Jaghbeer; Ahmad Khraisat; Sant P. Singh
Circulation | 2008
Rohit Bhuriya; Ahmad Khraisat; Janos Molnar; Bharti Chaudhari; Monica Stancu; Param Singh; Rohit Arora; Sandeep Khosla
Circulation | 2008
Rohit Bhuriya; Ahmad Khraisat; Janos Molnar; Bharti Chaudhari; Monica Stancu; Navdeep Gupta; Rohit Arora; Sandeep Khosla
The American Journal of Medicine | 2007
Ahmad Khraisat; Sarabjeet Singh; Rohit Arora; Eshraq Al-Jaghbeer
Experimental & Clinical Cardiology | 2007
Ahmad Khraisat; Tejal Shah; Jose-Luis E Velazquez-Cecena; Nagapradeep Nagajothi; Eshraq Al-Jaghbeer; Daniel Benatar; Rohit Arora