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Risk Factors and Outcomes of Ganciclovir-Resistant Cytomegalovirus Infection in Solid Organ Transplant Recipients.
Fisher, Cynthia E; Knudsen, Janine L; Lease, Erika D; Jerome, Keith R; Rakita, Robert M; Boeckh, Michael; Limaye, Ajit P.
Afiliação
  • Fisher CE; Division of Allergy and Infectious Diseases, University of Washington.
  • Knudsen JL; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center.
  • Lease ED; Division of Allergy and Infectious Diseases, University of Washington.
  • Jerome KR; Division of Allergy and Infectious Diseases, University of Washington.
  • Rakita RM; Division of Pulmonary and Critical Care Medicine, University of Washington, Seattle, Washington, USA.
  • Boeckh M; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center.
  • Limaye AP; Virology Division, Department of Laboratory Medicine, University of Washington, Seattle.
Clin Infect Dis ; 65(1): 57-63, 2017 07 01.
Article em En | MEDLINE | ID: mdl-28369203
ABSTRACT

Background:

Ganciclovir-resistant (ganR) cytomegalovirus (CMV) is an emerging and important problem in solid organ transplant (SOT) recipients. Only through direct comparison of ganR- and ganciclovir-sensitive (ganS) CMV infection can risk factors and outcomes attributable specifically to ganciclovir resistance appropriately be determined.

Methods:

We performed a retrospective, case-control (13) study of SOT recipients with genotypically confirmed ganR-CMV (n = 37) and ganS-CMV infection (n = 109), matched by donor/recipient CMV serostatus, year and organ transplanted, and clinical manifestation. We used χ2 (categorical) and Mann-Whitney (continuous) tests to determine predisposing factors and morbidity attributable to resistance, and Kaplan-Meier plots to analyze survival differences.

Results:

The rate of ganR-CMV was 1% (37/3467) overall and 4.1% (32/777) among CMV donor-positive, recipient-negative patients, and was stable over the study period. GanR-CMV was associated with increased prior exposure to ganciclovir (median, 153 vs 91 days, P < .001). Eighteen percent (3/17) of lung transplant recipients with ganR-CMV had received <6 weeks of prior ganciclovir (current guideline-recommended resistance testing threshold), and all non-lung recipients had received ≥90 days (median, 160 [range, 90-284 days]) prior to diagnosis of ganR-CMV. GanR-CMV was associated with higher mortality (11% vs 1%, P = .004), fewer days alive and nonhospitalized (73 vs 81, P = .039), and decreased renal function (42% vs 19%, P = .008) by 3 months after diagnosis.

Conclusions:

GanR-CMV is associated with longer prior antiviral duration and higher attributable morbidity and mortality than ganS-CMV. Upcoming revised CMV guidelines should incorporate organ transplant-specific thresholds of prior drug exposure to guide rational ganR-CMV testing in SOT recipients. Improved strategies for prevention and treatment of ganR-CMV are warranted.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Antivirais / Ganciclovir / Infecções por Citomegalovirus / Citomegalovirus / Transplantados Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Antivirais / Ganciclovir / Infecções por Citomegalovirus / Citomegalovirus / Transplantados Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2017 Tipo de documento: Article