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Retrospective Evaluation of Cystatin C as a Measure of Renal Function in Pediatric Hematopoietic Stem Cell Transplant Patients Receiving Foscarnet for Cytomegalovirus Reactivation.
Pickett, Logan R; Daukshus, Nicole P; Camacho-Bydume, Christine; Mathew, Sherry; Mauguen, Audrey; Cohen, Nina; Cancio, Maria.
Afiliação
  • Pickett LR; From the Department of Pharmacy, Children's Healthcare of Atlanta, Atlanta, Georgia.
  • Daukshus NP; Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York City, New York.
  • Camacho-Bydume C; Department of Pediatric Blood and Marrow Transplant and Cellular Therapy, Joseph M. Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, New Jersey.
  • Mathew S; Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York City, New York.
  • Mauguen A; Department of Epidemiology and Biostatistics, and.
  • Cohen N; Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York City, New York.
  • Cancio M; Stem Cell Transplantation and Cellular Therapies, MSK Kids, Memorial Sloan Kettering Cancer Center, New York City, New York.
Pediatr Infect Dis J ; 43(5): 457-462, 2024 May 01.
Article em En | MEDLINE | ID: mdl-38190640
ABSTRACT

BACKGROUND:

Cytomegalovirus (CMV) infection following allogeneic hematopoietic cell transplantation has considerable morbidity and mortality, and foscarnet is a treatment option that requires renal dose adjustment. Serum creatinine (SCr)-based estimated glomerular filtration rate (eGFR) equations are used to estimate renal function for patients receiving foscarnet, but cystatin C (cysC) has been shown as a possible alternative. Data examining cysC-based eGFR in this population is sparse. Our primary objective was to evaluate outcomes of patients treated with foscarnet dosed utilizing cysC-based eGFR versus SCr-based eGFR.

METHODS:

We analyzed patients on the transplantation and cellular therapies service at Memorial Sloan Kettering Kids from January 2011 to September 2021 who received allogeneic hematopoietic cell transplantation and ≥14 days of foscarnet for CMV infection. Patients with cysC-based eGFR were compared to a historical cohort of patients who only had SCr-based eGFR. Outcomes included time to CMV clearance, death or change in anti-CMV therapy. Cumulative incidence curves and cause-specific hazards model were used for analysis.

RESULTS:

In 61 analyzed patients, no differences were found between the cohorts in cumulative incidence of change in anti-CMV therapy ( P = 0.17) or death ( P = 0.69). After adjustment for multiple confounders, patients in the SCr cohort seemed to have a higher chance of CMV clearance compared with the cysC cohort, but the difference was not statistically significant (hazard ratio = 2.42, P = 0.089). Patients who received corticosteroids appeared to have lower incidence of CMV clearance ( P = 0.056).

CONCLUSIONS:

We did not find differences in outcomes when dosing foscarnet using cysC versus SCr for treatment of CMV infection.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por Citomegalovirus / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por Citomegalovirus / Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article