Stated Ballyhoo Of Torin 1

Матеріал з HistoryPedia
Перейти до: навігація, пошук

""Knecht KR, Alexander ML, Swearingen CJ, Frazier EA. NTproBNP as a marker of rejection in pediatric heart transplant recipients. Abstract:? Acute rejection is a major morbidity in heart transplant recipients; diagnosis Torin 1 molecular weight is difficult, and rejection must often be treated reactively. Various serum biomarkers have been investigated for non-invasive monitoring of the cardiac allograft. NTproBNP is produced by the ventricular myocardium and may increase with evolving rejection allowing earlier diagnosis. Retrospective review of serum NTproBNP levels in pediatric heart transplant recipients has been carried out to evaluate the association with episodes of acute rejection. Repeated measures logistic regression was used to model associations for variables with first rejection and within an individual for change in NTproBNP and first rejection. Odds ratios for rejection risk given an increase in serum NTproBNP were calculated. Correlation of NTproBNP levels with renal function as estimated by modified Schwartz equation was performed to look for confounding. Higher serum NTproBNP level was associated with increased risk of rejection, but intersubject variability was Floctafenine wide. However, increase in an individual subject��s serum level showed increased risk of rejection, greater with greater rise. Serum NTproBNP levels appear not greatly affected by renal function. NTproBNP shows promise in surveillance for pediatric heart transplant recipients. The greatest use appears to be in following trends for an individual instead of using an absolute value. ""Herlenius G, Hansson S, Krantz M, Olausson M, Kullberg-Lindh C, Friman S. Stable long-term renal function after pediatric liver transplantation. Pediatr Transplantation 2010: 14:409�C416. ? 2010 John Wiley & Sons A/S. Abstract:? Long-term exposure to calcineurin inhibitors increases the risk of CKD in children after LT. The aims of this study were to study renal function by measuring GFRm before and yearly after LT, to describe the prevalence of CKD (stage III: GFR 30�C60 mL/min/1.73?m2) and to investigate if age and underlying liver disease had an impact on long-term renal function. Thirty-six patients with a median age of 2.9?years selleck compound (0.1�C16?yr) were studied. Median follow-up was 6.5 (2�C14?yr). GFRm decreased significantly during the first six months post-transplantation with 23% (p?