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Mark A. Schnitzler

Researcher at Saint Louis University

Publications -  268
Citations -  14664

Mark A. Schnitzler is an academic researcher from Saint Louis University. The author has contributed to research in topics: Transplantation & Kidney transplantation. The author has an hindex of 61, co-authored 254 publications receiving 13236 citations. Previous affiliations of Mark A. Schnitzler include Washington University in St. Louis & Barnes-Jewish Hospital.

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Diabetes mellitus after kidney transplantation in the United States.

TL;DR: The authors’ analysis of risk factors for new-onset diabetes and its clinical implications provides valuable evidence on this important issue, and highlights the need for management strategies that minimize risk of diabetes developing after transplantation.
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Incidence of BK with tacrolimus versus cyclosporine and impact of preemptive immunosuppression reduction.

TL;DR: Whether intensive monitoring and discontinuation of mycophenolate (MMF) or azathioprine (AZA), upon detection of BK viremia, could prevent BK nephropathy with tacrolimus (FK506) versus cyclosporine (CyA) is investigated.
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OPTN/SRTR 2012 Annual Data Report: kidney.

TL;DR: Kidney transplant is one of the most cost‐effective surgical interventions; however, average reimbursement for recipients with primary Medicare coverage from transplant through 1 year posttransplant was comparable to the 1‐year cost of care for a dialysis patient.
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Incidence and cost of new onset diabetes mellitus among U.S. wait-listed and transplanted renal allograft recipients.

TL;DR: While NodM had an incidence of approximately 6% per year among wait‐listed dialysis patients, NODM over the first 2 years post‐transplant had an occurrence of almost 18% and 30% among patients receiving cyclosporine and tacrolimus, respectively.
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A randomized, double-blinded comparison of thymoglobulin versus atgam for induction immunosuppressive therapy in adult renal transplant recipients

TL;DR: Brief (7-day) induction with Thymoglobulin resulted in less frequent and less severe rejection, a better event-free survival, less cytomegalovirus disease, fewer serious adverse events, but more frequent early leukopenia than induction with Atgam.