Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Clin Transplant ; 38(9): e15453, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-39229690

RESUMO

PURPOSE: Evaluate cytomegalovirus (CMV) post-prophylaxis surveillance in high-risk (D+/R-) kidney and liver transplant recipients. METHODS: Adult D+/R- patients were included if transplanted between 6/1/15 and 11/30/22 and divided into a pre-CMV-stewardship-era (6/1/15-5/31/18), CMV-stewardship-era (6/1/18-6/30/20), and a surveillance-era (7/1/2020-11/30/2022) then followed through 12 months. The primary objective was to evaluate CMV-related outcomes. The secondary objective was to assess graft and patient survival by era. RESULTS: There were 328 patients in the study period; 133 in the pre-stewardship-era, 103 in the stewardship-era, and 92 in the surveillance-era. Replication rates in the surveillance-era were significantly higher, as anticipated due to increased sampling (pre 38.4%, stewardship 33.0%, surveillance 52.2%, p = 0.02). Time from transplant to first replication was similar (pre 214.0 ± 79.0 days, stewardship 231.1 ± 65.5, surveillance 234.9 ± 61.4, p = 0.29). CMV viral load (VL) at first detection, maximum-VL, and incidence of VL > 100 000 IU/mL were numerically lower in the surveillance era, although not statistically significant. CMV end-organ disease (p < 0.0001) and ganciclovir-resistance (p = 0.002) were significantly lower in the surveillance era than in both previous eras. Rejection was not different between eras (p = 0.4). Graft (p = 0.0007) and patient survival (p = 0.008) were significantly improved in the surveillance era. CONCLUSIONS: Post-prophylaxis surveillance significantly reduced CMV end-organ disease and resistance. Despite observing increased replication rates in the surveillance era, rejection was not significantly different and there was no graft loss or patient mortality at 12 months.


Assuntos
Antivirais , Infecções por Citomegalovirus , Citomegalovirus , Farmacorresistência Viral , Ganciclovir , Rejeição de Enxerto , Sobrevivência de Enxerto , Transplante de Rim , Transplante de Fígado , Humanos , Infecções por Citomegalovirus/prevenção & controle , Infecções por Citomegalovirus/virologia , Infecções por Citomegalovirus/epidemiologia , Masculino , Feminino , Pessoa de Meia-Idade , Citomegalovirus/isolamento & purificação , Citomegalovirus/efeitos dos fármacos , Antivirais/uso terapêutico , Ganciclovir/uso terapêutico , Seguimentos , Transplante de Fígado/efeitos adversos , Fatores de Risco , Transplante de Rim/efeitos adversos , Prognóstico , Rejeição de Enxerto/prevenção & controle , Rejeição de Enxerto/etiologia , Rejeição de Enxerto/virologia , Complicações Pós-Operatórias/prevenção & controle , Adulto , Taxa de Sobrevida , Estudos Retrospectivos , Transplantados/estatística & dados numéricos
2.
J Pharm Pract ; 37(5): 1042-1043, 2024 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-38395741

RESUMO

Invasive aspergillosis (IA) is a rare and often fatal complication of immunosuppression following orthotopic heart transplant. Prophylaxis plays a crucial role in preventing the emergence of this opportunistic infection. The azole class of medications are the bellwether agents utilized in this patient population. Unfortunately, given their impact on the Cytochrome P450 enzyme system, significant fluctuations in serum tacrolimus concentrations occur when initiating and stopping azole therapy, increasing the risk for prolonged periods of sub-optimal immunosuppression. While there are recommended dosing adjustments for these transition periods based on small data sets primarily with fluconazole, there is no published literature on recommended dosing adjustments for posaconazole. Given our institution utilizes posaconazole as the primary therapeutic for aspergillosis prophylaxis, we aimed to explore and report our local data to better guide dosing decisions during these transition periods.


Assuntos
Antifúngicos , Rejeição de Enxerto , Transplante de Coração , Imunossupressores , Tacrolimo , Triazóis , Humanos , Triazóis/administração & dosagem , Triazóis/sangue , Triazóis/uso terapêutico , Tacrolimo/sangue , Tacrolimo/administração & dosagem , Rejeição de Enxerto/prevenção & controle , Antifúngicos/administração & dosagem , Antifúngicos/sangue , Antifúngicos/uso terapêutico , Imunossupressores/sangue , Imunossupressores/administração & dosagem , Imunossupressores/efeitos adversos , Aspergilose/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Feminino , Interações Medicamentosas
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA