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Impact of valganciclovir prophylaxis duration on cytomegalovirus disease in high-risk donor seropositive/recipient seronegative heart transplant recipients.
Imlay, Hannah; Dumitriu Carcoana, Allison O; Fisher, Cynthia E; Wong, Beatrice; Rakita, Robert M; Fishbein, Daniel P; Limaye, Ajit P.
Afiliación
  • Imlay H; Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, Washington.
  • Dumitriu Carcoana AO; Division of Infectious Diseases, Department of Internal Medicine, University of Utah, Salt Lake City, Utah.
  • Fisher CE; University of Washington, Seattle, Washington.
  • Wong B; Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, Washington.
  • Rakita RM; Department of Pharmacology, University of Washington, Seattle, Washington.
  • Fishbein DP; Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, Washington.
  • Limaye AP; Division of Cardiology, Department of Medicine, University of Washington, Seattle, Washington.
Transpl Infect Dis ; 22(3): e13255, 2020 Jun.
Article en En | MEDLINE | ID: mdl-32020736
ABSTRACT

BACKGROUND:

Few data support use of 6 over 3 months of antiviral prophylaxis for cytomegalovirus (CMV) disease prevention in donor seropositive/recipient seronegative (D+R-) heart transplant recipients (HTR).

METHODS:

We retrospectively assessed CMV disease and outcomes in 310 adult HTR between July 5, 2005, and December 30, 2016, at our center. Valganciclovir (VGCV) prophylaxis was given for 3-6 months in the D+R- group. Multivariable models evaluated risk factors for CMV disease in patients who received 3 vs 6 months (±1 month) of prophylaxis, with investigation of inverse probability weighting to correct for confounding variables.

RESULTS:

The incidence of CMV disease among all patients and the D+R- group was 8.7% (27/310) and 26.5% (22/83), respectively, and included syndrome in 22.2% (6/27) and end-organ involvement in 77.8% (21/27). In a multivariable model, 6 vs 3 months of antiviral prophylaxis was not associated with reduced risk for CMV disease (OR 2.28 [95% CI 0.66, 7.91], P = .19). CMV disease in D+R- HTR was associated with higher rates of hospitalization (87.5% [14/16] vs 6.3% [1/16], P < .001) and for a longer duration than in matched D+R- controls without disease.

CONCLUSIONS:

Cytomegalovirus disease remains a major cause of morbidity in D+R- HTR. In contrast to documented benefit in D+R- lung and kidney recipients, VGCV duration of 6 months was not associated with a lower incidence of CMV disease in D+R- HTR compared to 3-month duration and should be reconsidered in this patient population.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antivirales / Trasplante de Corazón / Infecciones por Citomegalovirus / Receptores de Trasplantes / Valganciclovir Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Transpl Infect Dis Asunto de la revista: TRANSPLANTE Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antivirales / Trasplante de Corazón / Infecciones por Citomegalovirus / Receptores de Trasplantes / Valganciclovir Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Transpl Infect Dis Asunto de la revista: TRANSPLANTE Año: 2020 Tipo del documento: Article