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2.
Exp Clin Transplant ; 19(7): 732-735, 2021 07.
Article in English | MEDLINE | ID: mdl-31580237

ABSTRACT

With the rising incidence of end-stage renal disease in the United States, patients needing renal transplants are waiting longer for increasingly scarce grafts. Formerly, the general practice was to avoid organs with tumors for transplant because of the risk of malignancy transmission to the recipient. However, with comprehensive donor selection and a small-sized primary tumor, the positive outcomes of transplant outweigh the risks of transmission after a partial nephrectomy. In our case, a 31-year-old woman, the daughter of the recipient, underwent a laparoscopic nephrectomy with an existing 8-mm tumor later confirmed as renal cell carcinoma. An ex vivo tumor enucleation was performed before the allograft was transplanted into the 69-year-old patient with endstage renal disease. At last follow-up, graft function has remained excellent with no evidence of local recurrence or metastasis in both the donor and recipient. Here, we describe our case and perform a literature review on the incidence and management of renal allografts with incidentally detected renal cell carcinoma during transplant.


Subject(s)
Carcinoma, Renal Cell , Kidney Failure, Chronic , Kidney Neoplasms , Kidney Transplantation , Adult , Aged , Allografts/pathology , Carcinoma, Renal Cell/pathology , Carcinoma, Renal Cell/surgery , Female , Humans , Kidney Failure, Chronic/complications , Kidney Failure, Chronic/diagnosis , Kidney Failure, Chronic/surgery , Kidney Neoplasms/pathology , Kidney Transplantation/adverse effects , Male , Nephrectomy/adverse effects , Treatment Outcome , United States
3.
Acad Med ; 95(10): 1492-1494, 2020 10.
Article in English | MEDLINE | ID: mdl-32520751

ABSTRACT

The COVID-19 pandemic has presented unprecedented challenges and opportunities for medical schools in the United States. In this Invited Commentary, the authors describe a unique collaboration between the University of Massachusetts Medical School (UMMS), the only public medical school in the state; the University of Massachusetts Memorial Medical Center (UMMMC); and the Commonwealth of Massachusetts. Through this partnership, UMMS was able to graduate fourth-year medical students 2 months early and deploy them to UMMMC to care for patients and alleviate workforce shortages during the COVID-19 surge, which peaked in Massachusetts in April 2020. The authors describe how they determined if students had fulfilled graduation requirements to graduate early, what commencement and the accompanying awards ceremony looked like this year as virtual events, the special emergency 90-day limited license these new graduates were given to practice at UMMMC during this time, and the impact these new physicians had in the hospital allowing residents and attendings to be redeployed to care for COVID-19 patients.


Subject(s)
Health Workforce/legislation & jurisprudence , Licensure/legislation & jurisprudence , Pandemics/legislation & jurisprudence , Physicians/supply & distribution , Students, Medical/legislation & jurisprudence , Betacoronavirus , COVID-19 , Coronavirus Infections , Humans , Massachusetts/epidemiology , Physicians/legislation & jurisprudence , Pneumonia, Viral , SARS-CoV-2 , Schools, Medical , United States
4.
Clin J Am Soc Nephrol ; 9(3): 583-9, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24482066

ABSTRACT

BACKGROUND AND OBJECTIVES: BK virus reactivation in kidney transplant recipients can lead to progressive allograft injury. Reduction of immunosuppression remains the cornerstone of treatment for active BK infection. Fluoroquinolone antibiotics are known to have in vitro antiviral properties, but the evidence for their use in patients with BK viremia is inconclusive. The objective of the study was to determine the efficacy of levofloxacin in the treatment of BK viremia. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Enrollment in this prospective, multicenter, double-blinded, placebo-controlled trial occurred from July 2009 to March 2012. Thirty-nine kidney transplant recipients with BK viremia were randomly assigned to receive levofloxacin, 500 mg daily, or placebo for 30 days. Immunosuppression in all patients was adjusted on the basis of standard clinical practices at each institution. Plasma BK viral load and serum creatinine were measured monthly for 3 months and at 6 months. RESULTS: At the 3-month follow-up, the percentage reductions in BK viral load were 70.3% and 69.1% in the levofloxacin group and the placebo group, respectively (P=0.93). The percentage reductions in BK viral load were also equivalent at 1 month (58% versus and 67.1%; P=0.47) and 6 months (82.1% versus 90.5%; P=0.38). Linear regression analysis of serum creatinine versus time showed no difference in allograft function between the two study groups during the follow-up period. CONCLUSIONS: A 30-day course of levofloxacin does not significantly improve BK viral load reduction or allograft function when used in addition to overall reduction of immunosuppression.


Subject(s)
Anti-Infective Agents/therapeutic use , BK Virus/drug effects , Kidney Transplantation/adverse effects , Levofloxacin/therapeutic use , Polyomavirus Infections/drug therapy , Tumor Virus Infections/drug therapy , Viremia/drug therapy , BK Virus/pathogenicity , Biomarkers/blood , Creatinine/blood , Double-Blind Method , Female , Humans , Immunosuppressive Agents/adverse effects , Linear Models , Male , Middle Aged , Polyomavirus Infections/diagnosis , Polyomavirus Infections/virology , Prospective Studies , Time Factors , Treatment Outcome , Tumor Virus Infections/diagnosis , Tumor Virus Infections/virology , United States , Viral Load , Viremia/diagnosis , Viremia/virology
5.
Am J Kidney Dis ; 39(6): 1310-2, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12046047

ABSTRACT

A 51-year-old white woman 6 months status post cadaveric renal transplant developed a mild case of primary varicella-zoster (VZ). It is hypothesized that the limited nature of her illness was due to infection with vaccine-type VZ virus instead of wild-type VZ. Approximately 1 month prior, she had daily household contact with a child who had developed a rash after immunization with live attenuated varicella vaccine. This case highlights several important questions. Should special precautions be undertaken with renal transplant recipients naive to varicella infection after vaccination of household contacts? Should pretransplant immunization with varicella vaccine be performed routinely in naive patients? Should naive patients transplanted and maintained on immunosuppressive therapy be vaccinated? Until there are clinical trials to answer these questions, it may be instructive to consider the recommendations for pediatric and immunocompromised patients.


Subject(s)
Herpes Zoster/etiology , Immunocompromised Host , Kidney Transplantation/immunology , Chickenpox Vaccine/adverse effects , Family Health , Female , Herpes Zoster/transmission , Herpesvirus 3, Human , Humans , Middle Aged , Vaccination/adverse effects , Vaccines, Attenuated/adverse effects
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