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1.
Clin Transplant ; 28(8): 897-905, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24931144

ABSTRACT

Predicting graft outcome after renal transplantation based on donor histological features has remained elusive and is subject to institutional variability. We have shown in a retrospective study that the Maryland Aggregate Pathology Index score reliably predicts graft outcome. We sought to validate the scoring system in our center and a second transplant center. We analyzed 140 deceased donor kidneys pre-implantation biopsies from center 1 and 65 from center 2. The patients had a mean follow-up of 695 ± 424 and 656 ± 305 d respectively. Although MAPI scores were similar, there were significant differences in donor and recipient parameters between both centers. Despite this, MAPI was predictive of graft outcome for both centers by Cox univariate, multivariate and time dependent ROC analysis. For center 1 and 2, three yr graft survival within each MAPI group was statistically equivalent. The three-yr graft survival at center 1 for low, intermediate, and high MAPI groups were 84.3%, 56.5%, and 50.0%, respectively, p ≤ 0.0001, and at center 2 were 83.3%, 33.3%, and 33.3%, p = 0.006. MAPI, which is based on a pre-implantation biopsy, demonstrated similar predictive and outcome results from both centers. As expanded criteria donors (ECD) criteria have redefined marginal kidneys, MAPI has the potential to further define ECD kidneys, increase utilization, and ultimately improve outcomes.


Subject(s)
Graft Rejection/diagnosis , Graft Survival , Kidney Failure, Chronic/surgery , Kidney Transplantation/methods , Preimplantation Diagnosis/methods , Female , Follow-Up Studies , Glomerular Filtration Rate , Graft Rejection/mortality , Humans , Kidney Function Tests , Male , Maryland , Middle Aged , Patient Selection , Preimplantation Diagnosis/statistics & numerical data , Prognosis , Risk Factors
2.
Expert Opin Drug Saf ; 9(6): 959-69, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20521865

ABSTRACT

IMPORTANCE OF THE FIELD: BK virus has emerged as an important cause of graft dysfunction and failure in renal transplant recipients. Risk factors for BK virus nephropathy (BKN) are not well established, but evidence suggests that it is the result of a complex interplay between multiple donor- and recipient-related factors. AREAS COVERED IN THIS REVIEW: The purpose of this article is to review the current understanding on the effect of various immunosuppressive agents on BK viral replication and the results of different reported immunosuppression reduction protocols. WHAT THE READER WILL GAIN: The intensity of overall immunosuppression has been accepted as a major risk factor for the development of BKN. We review the data regarding the contribution of different anti-rejection agents to the risk of BK virus-induced graft injury. TAKE HOME MESSAGE: Although reduction in immunosuppression on detection of BK viral replication appears to be the most successful means in preserving allograft function, data are emerging that support the stronger association of the disease with tacrolimus, in contrast to mycophenolate compounds. Therefore, initial dose reduction for tacrolimus may be more beneficial than this anti-metabolite preemptively or after diagnosis of BKN.


Subject(s)
BK Virus , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/therapeutic use , Kidney Diseases/chemically induced , Polyomavirus Infections/chemically induced , Tumor Virus Infections/chemically induced , BK Virus/immunology , BK Virus/metabolism , Graft Rejection , Humans , Immunosuppression Therapy/adverse effects , Kidney Diseases/etiology , Kidney Diseases/virology , Kidney Transplantation/adverse effects , Lymphocyte Depletion/adverse effects , Polyomavirus Infections/etiology , Polyomavirus Infections/virology , Risk Factors , Tumor Virus Infections/etiology , Tumor Virus Infections/virology
4.
Pharmacotherapy ; 29(10): 1270-2, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19792996

ABSTRACT

Hyperkalemia is an electrolyte abnormality that can lead to severe consequences. Paralysis induced by hyperkalemia has been described in only a few reports. We describe a 60-year-old man who experienced paralysis presumably due to hyperkalemia. He presented to the emergency department with severe weakness in all extremities. The patient's serum potassium concentration was greater than 8 mEq/L and his serum creatinine concentration was 7 mg/dl. Findings on electrocardiography were abnormal. Of note, his drug therapy included lisinopril and naproxen. After treatment for hyperkalemia, the patient's symptoms resolved; however, he was admitted for further workup for renal failure. The patient was discharged after approximately 1 week with a diagnosis of end-stage renal disease. Use of the Naranjo adverse drug reaction probability scale indicated a probable relationship (score of 5) between the patient's paralysis and hyperkalemia. Although hyperkalemia as a cause of paralysis is extremely rare, clinicians should be aware of this potentially life-threatening, noncardiac toxicity.


Subject(s)
Hyperkalemia/complications , Paralysis/etiology , Creatinine/blood , Humans , Hyperkalemia/etiology , Kidney Failure, Chronic/complications , Lisinopril/adverse effects , Male , Middle Aged , Naproxen/adverse effects
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