Browsing by Author "Kushwaha, Sudhir S. (57202372712)"
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Publication Sex Related Differences in the Risk of Antibody-Mediated Rejection and Subsequent Allograft Vasculopathy Post-Heart Transplantation: A Single-Center Experience(2016) ;Grupper, Avishay (12801212800) ;Nestorovic, Emilija M. (56090978800) ;Daly, Richard C. (24549959300) ;Milic, Natasa M. (7003460927) ;Joyce, Lyle D. (7006287983) ;Stulak, John M. (6508029937) ;Joyce, David L. (7102255807) ;Edwards, Brooks S. (7202177472) ;Pereira, Naveen L. (7005220422)Kushwaha, Sudhir S. (57202372712)Background. Pregnancies may result in antibodies against HLA, a risk factor for antibody-mediated rejection (AMR) and subsequent cardiac allograft vasculopathy (CAV) after heart transplantation (HTx). The aim of this study was to evaluate sex differences in the incidence of AMR events and subsequent risk of CAV among HTx recipients. Methods. The study comprised 160 patients (51 [32%] women) who underwent HTx in 2008 to 2014. The cumulative effect of AMR events was calculated by AMR score (sum of myocardial biopsy grading divided by number of biopsies taken during 3 years post-HTx). Results. Females had higher levels of anti-HLA I antibodies pre-HTx compared to males which was associated with a history of pregnancies, total number of children and with a higher AMR score at 6 months post-HTx (P < 0.05). Women demonstrated a significant increase in the total incidence of AMR events (27 vs. 7%, P = 0.001) and in AMR scores at 6, 12, 24 and 36 months post-HTx compared to men (P < 0.05). There were no differences in cellular rejection between the groups. A history of AMR events was associated with a significantly increased risk of severe CAV onset (hazard ratio, 7.0; 95% confidence interval, 1.5-31.5; P = 0.012). Conclusions. Women are at higher risk for AMR post-HTx which subsequently increases their risk for CAV. Females recipients may benefit from closer surveillance to identify AMR at an earlier stage post-HTx, and targeted immunosuppressive therapy to attenuate the development of CAV. Copyright © 2016 The Authors. - Some of the metrics are blocked by yourconsent settings
Publication Successful establishment of a left ventricular assist device program in an emerging country: One year experience(2018) ;Nestorovic, Emilija (56090978800) ;Schmitto, Jan D. (6507654381) ;Kushwaha, Sudhir S. (57202372712) ;Putnik, Svetozar (16550571800) ;Terzic, Dusko (57195538891) ;Milic, Natasa (7003460927) ;Mikic, Aleksandar (57214281171) ;Markovic, Dejan (26023333400) ;Trifunovic, Danijela (9241771000) ;Ristic, Arsen (7003835406)Ristic, Miljko (57214043577)Background: The primary goal of this study was to evaluate the outcomes of patients with end-stage heart failure (HF) who underwent continuous flow left ventricular assist device (CF-LVAD) in a developing country and to compare to those reported by more developed countries. The secondary goal was on determining factors that may be connected to improved survival. Methods: We prospectively analyzed 47 consecutive patients who underwent CF-LVAD at our institution. After one year the survival and adverse event profiles of patients were evaluated. At 3, 6 and 12 months, the cardiac, renal and liver function outcomes were assessed. Results: The 30-day, 6-month and 1-year survival rates were 89%, 85% and 80%, respectively. A significant improvement in dimensions and ejection fraction of left ventricle, BNP, functional capacity, blood urea nitrogen (BUN) and total bilirubin (P < 0.05 for all) were noticed 3 months post-CF-LVAD implantation, and patients were stable throughout the entire first year follow up. In the group of patients with baseline renal dysfunction (RD) there were significant improvements of renal function (P=0.004), with no changes on follow up. 57% of patients exhibited some kind of adverse event, commonly in the form of bleeding. In multivariate Cox regression analysis renal failure was found to be as an independent risk factor for the overall survival (HR =13.1, P < 0.001). Conclusions: In conclusion, our data extends previous findings from centers of developed countries, that CF-LVAD is an adequate treatment option for patients suffering from end-stage HF, and encourages expansion of CF-LVAD implantation in developing countries with nascent HT program. © Journal of Thoracic Disease.
