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Cytomegalovirus serologic matching in deceased donor kidney allocation optimizes high- and low-risk (D+R- and D-R-) profiles and does not adversely affect transplant rates.
Lockridge, Joe; Roberts, Daniel; Olyaei, Ali; Noble, Brie N; Langewisch, Eric; Rehman, Shehzad; Stack, Megan; Scott, David; Orloff, Susan; Shaut, Carley; Gardner, Brent; Bennett, William; Norman, Doug.
Afiliação
  • Lockridge J; Division of Nephrology, Oregon Health and Science University, Portland, Oregon, USA.
  • Roberts D; Section of Nephrology, VA Medical Center, Portland, Oregon, USA.
  • Olyaei A; Division of Nephrology, Oregon Health and Science University, Portland, Oregon, USA.
  • Noble BN; School of Pharmacy, Oregon Health and Science University, Portland, Oregon, USA.
  • Langewisch E; Department of Pharmacy Practice, OSU College of Pharmacy, Portland, Oregon, USA.
  • Rehman S; Department of Pharmacy Practice, OSU College of Pharmacy, Portland, Oregon, USA.
  • Stack M; Division of Nephrology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
  • Scott D; Division of Nephrology, Oregon Health and Science University, Portland, Oregon, USA.
  • Orloff S; Section of Nephrology, VA Medical Center, Portland, Oregon, USA.
  • Shaut C; Division of Nephrology, Oregon Health and Science University, Portland, Oregon, USA.
  • Gardner B; Division of Surgery, Oregon Health and Science University, Portland, Oregon, USA.
  • Bennett W; Division of Surgery, Oregon Health and Science University, Portland, Oregon, USA.
  • Norman D; Laboratory of Immunogenetics, Oregon Health and Science University, Portland, Oregon, USA.
Am J Transplant ; 20(12): 3502-3508, 2020 12.
Article em En | MEDLINE | ID: mdl-32372499
ABSTRACT
Cytomegalovirus (CMV) is a major cause of infection-related morbidity and mortality in kidney transplantation. The most significant risk for developing CMV infection after transplant depends upon donor (D) and recipient (R) CMV serostatus. In 2012, our Organ Procurement Organization (OPO) began a novel pretransplant CMV prevention strategy via matching deceased kidney donors and recipients by CMV serostatus. Prior to the matching protocol, our distribution of seropositive and seronegative donors and recipients was similar to the United States at large. After the matching protocol, high-risk D+R- were reduced from 18.5% to 2.9%, whereas low-risk D-R- were increased from 13.5% to 24%. There was no adverse effect on transplant rates and no differential effect on waiting times for R+ vs R- after the protocol was implemented. This protocol could be implemented on a regional or national level to optimize low and high-risk CMV seroprofiles and potentially improve CMV-related outcomes in kidney transplantation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Rim / Infecções por Citomegalovirus Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Rim / Infecções por Citomegalovirus Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article