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3.
Front Immunol ; 14: 1292648, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38264645

RESUMEN

Background: The cytomegalovirus (CMV) mismatch rate in deceased donor kidney transplant (DDKT) recipients in the US remains above 40%. Since CMV mismatching is common in DDKT recipients, the cumulative effects may be significant in the context of overall patient and graft survival. Our primary objective was to describe the short- and long-term risks associated with high-risk CMV donor positive/recipient negative (D+/R-) mismatching among DDKT recipients with the explicit goal of deriving a mathematical mismatching penalty. Methods: We conducted a retrospective, secondary analysis of the Scientific Registry of Transplant Recipients (SRTR) database using donor-matched DDKT recipient pairs (N=105,608) transplanted between 2011-2022. All-cause mortality and graft failure hazard ratios were calculated from one year to ten years post-DDKT. All-cause graft failure included death events. Survival curves were calculated using the Kaplan-Meier estimation at 10 years post-DDKT and extrapolated to 20 years to provide the average graft days lost (aGDL) and average patient days lost (aPDL) due to CMV D+/R- serostatus mismatching. We also performed an age-based stratification analysis to compare the relative risk of CMV D+ mismatching by age. Results: Among 31,518 CMV D+/R- recipients, at 1 year post-DDKT, the relative risk of death increased by 29% (p<0.001), and graft failure increased by 17% (p<0.001) as compared to matched CMV D+/R+ group (N=31,518). Age stratification demonstrated a significant increase in the risk associated with CMV mismatching in patients 40 years of age and greater. The aGDL per patient due to mismatching was 125 days and the aPDL per patient was 100 days. Conclusion: The risks of CMV D+/R- mismatching are seen both at 1 year post-DDKT period and accumulated throughout the lifespan of the patient, with the average CMV D+/R- recipient losing more than three months of post-DDKT survival time. CMV D+/R- mismatching poses a more significant risk and a greater health burden than previously reported, thus obviating the need for better preventive strategies including CMV serodirected organ allocation to prolong lifespans and graft survival in high-risk patients.


Asunto(s)
Infecciones por Citomegalovirus , Receptores de Trasplantes , Humanos , Adulto , Citomegalovirus , Estudios Retrospectivos , Sistema de Registros
4.
Front Transplant ; 2: 1237112, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38993926

RESUMEN

On July 14, 2022, the Organ Procurement and Transplantation Network's (OPTN) Membership and Professional Standards Committee (MPSC) approved bylaws including two new post-transplant performance evaluation metrics, the 90-day (90D) and 1-year conditional on the 90-day (1YC90D) graft survival hazard ratio (HR). These metrics have replaced the previous 1-year (1Y) unconditional, post-transplant graft survival HR and are used to nationally rank and identify programs for MPSC review. The MPSC's policies have major implications for all transplant programs, providers, and patients across the United States. Herein we show two significant limitations with the new evaluation criteria, arbitrary censoring periods and interdependence in the new performance metrics. We have demonstrated a strong and consistent inverse correlation between the new evaluation metrics, thus proving a lack of independence. Moreover, these two evaluation criteria are interdependent even at nominal HRs. Thus, the 90D cohort can be used to accurately predict whether the 1YC90D is above or below a given HR threshold. This could alter practice behaviors and the timing of patient event reporting, which may result in many unintended consequences related to clinical practice. Here we provide the first evidence that this new evaluation system will lead to a significant increase in the number of programs flagged for MPSC review. When this occurs, the cost of operating a transplant program will increase without a clear demonstration of an increased accuracy in identifying problematic programs.

8.
Medicina (B.Aires) ; 76(3): 159-165, June 2016. ilus, mapas
Artículo en Inglés | LILACS | ID: biblio-841564

RESUMEN

The objective of this report is to provide information on Mycobacterium tuberculosis complex infections in animals and in humans. Included is information on the susceptibility of different species as well as information on etiology, epidemiology, pathogenesis, diagnosis, prevention and control of this disease. The term One Health has been adopted to describe the unified human medical and veterinary interdisciplinary/multidisciplinary collaborative approach to zoonoses and will be critical for future endeavors in the control of the global TB epidemic. This unified paradigm is ideally suited for control of bovine TB and many other international public health and clinical health issues. Sharing resources and increasing interaction between public health and veterinary medical scientists can raise awareness of ‘shared risk' of bovine TB between humans and animals and, in resource-limited situations, can maximize use of existing infrastructure and reduce unnecessary duplication of effort in disease control programs.


El objetivo de este artículo es proporcionar información sobre las infecciones por el Complejo Mycobacterium tuberculosis en animales y en humanos. Se incluye información sobre la susceptibilidad de diferentes especies, así como sobre la etiología, epidemiología, patogenia, diagnóstico, prevención y control de esta enfermedad. La expresión UNA SALUD ha sido adoptada para describir el enfoque unificado de la medicina humana y la veterinaria, de colaboración interdisciplinaria/multidisciplinaria en las zoonosis, que puede resultar fundamental para el control de la endemia mundial de tuberculosis. Este paradigma unificado es especialmente relevante para el control de la tuberculosis bovina. Compartir recursos y lograr una mayor interacción entre la investigación en salud pública y en medicina veterinaria puede elevar la conciencia de “riesgo compartido” de la tuberculosis bovina en humanos y animales y, en situaciones de recursos limitados, puede maximizar el uso de la infraestructura existente y reducir la duplicación innecesaria de esfuerzos en los programas de control de la infección y enfermedad.


Asunto(s)
Humanos , Animales , Tuberculosis/prevención & control , Tuberculosis/veterinaria , Zoonosis/prevención & control , Salud Única , Tuberculosis/diagnóstico , Estados Unidos/epidemiología , Bovinos , Zoonosis/microbiología , Zoonosis/epidemiología , Salud Pública , Mycobacterium bovis/patogenicidad , Mycobacterium tuberculosis/patogenicidad
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