Jove
Visualize
Contáctanos
JoVE
x logofacebook logolinkedin logoyoutube logo
ACERCA DE JoVE
Visión GeneralLiderazgoBlogCentro de Ayuda JoVE
AUTORES
Proceso de PublicaciónConsejo EditorialAlcance y PolíticasRevisión por ParesPreguntas FrecuentesEnviar
BIBLIOTECARIOS
TestimoniosSuscripcionesAccesoRecursosConsejo Asesor de BibliotecasPreguntas Frecuentes
INVESTIGACIÓN
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchivo
EDUCACIÓN
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualCentro de Recursos para ProfesoresSitio de Profesores
Términos y Condiciones de Uso
Política de Privacidad
Políticas

Videos de Conceptos Relacionados

Determination of Multiple Dosing Parameters: Loading and Maintenance Doses01:25

Determination of Multiple Dosing Parameters: Loading and Maintenance Doses

284
A loading dose is an essential pharmacological strategy to rapidly achieve the target plasma drug concentration necessary for an immediate therapeutic effect. This approach is especially critical for drugs characterized by slow absorption or extended half-lives, where delaying therapeutic plasma levels could compromise treatment outcomes. By administering a loading dose, clinicians ensure a prompt onset of drug action, even for agents with complex pharmacokinetic profiles.Achieving steady-state...
284
Estimation of k and VD of Aminoglycosides01:20

Estimation of k and VD of Aminoglycosides

274
Aminoglycosides are a class of antibiotics used to treat various bacterial infections. Clinicians must determine the elimination rate constant (k) and volume of distribution (VD) to optimize therapeutic efficacy and minimize toxicity. The k value represents the rate at which the drug is removed from the body, and the VD reflects the degree to which the drug distributes into body tissues. Accurately estimating these parameters allows healthcare professionals to tailor drug dosing to individual...
274
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations01:15

Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations

288
Gentamicin, an aminoglycoside antibiotic, is commonly administered via intermittent intravenous infusion to treat severe infections. An intermittent one-hour infusion of gentamicin, administered at eight-hour intervals, allows for precise control of plasma drug concentrations, minimizing toxicity while ensuring therapeutic efficacy. Pharmacokinetic principles govern the dynamics of plasma concentrations and can be mathematically described using specific equations.The plasma drug concentration...
288
Dosage Regimens: Designs and Approaches01:28

Dosage Regimens: Designs and Approaches

386
Designing a dosage regimen, which refers to the manner of drug administration, is a complex process involving the selection of drug dose, route, and frequency. This process is underpinned by pharmacokinetic parameters derived from tests and population averages. These parameters are then tailored to patient-specific variables such as diagnosis, demographics, and allergy status. Once therapy commences, therapeutic response monitoring is critical and achieved through clinical and physical...
386
Drug Dosing in Renal Diseases: Dose Adjustments Based on Drug Clearance and Elimination Rate Constant01:25

Drug Dosing in Renal Diseases: Dose Adjustments Based on Drug Clearance and Elimination Rate Constant

261
In patients with renal disease, dosage adjustments are necessary to maintain therapeutic plasma drug concentrations and prevent toxicity or subtherapeutic exposure. Renal impairment alters drug pharmacokinetics, especially in conditions like uremia, where changes such as prolonged elimination half-life and altered apparent volume of distribution can significantly affect drug disposition. These changes require careful modification of the dosing regimen to achieve the desired clinical...
261
One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution01:09

One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution

963
The one-compartment open model is a simplified approach used in pharmacokinetics to understand the distribution and elimination of a drug administered through an intravenous bolus. This model assumes rapid drug dispersal throughout the body and elimination using a first-order process. Key pharmacokinetic parameters, such as the elimination rate constant (k), half-life (t1/2), and the apparent volume of distribution (Vd), can be estimated from this model. The elimination rate is calculated...
963

También podría leer

Artículos Relacionados

Artículos vinculados a este trabajo por autores compartidos, revista y gráfico de citas.

Ordenar por
Same author

Transformer-DAPT: AI-based dynamic assessment of ischemic and bleeding risks in patients on DAPT following PCI.

NPJ digital medicine·2026
Same author

RLBWT-based LCP computation in compressed space for terabase-scale pangenome analysis.

Bioinformatics (Oxford, England)·2026
Same author

Voriconazole Dosing and Therapeutic Drug Monitoring in Patients Before and After Liver Transplantation.

Pharmacotherapy·2026
Same author

Vision transformer autoencoders captures local and non-local features in brain imaging to reveal novel genetic associations.

Communications biology·2026
Same author

Replicability of unsupervised deep learning derived image phenotypes.

bioRxiv : the preprint server for biology·2026
Same author

Genetic architecture of white matter microstructure captured by unsupervised deep representation learning of fractional anisotropy maps.

Nature communications·2026

Video Experimental Relacionado

Updated: Feb 24, 2026

A General Method for Evaluating Deep Brain Stimulation Effects on Intravenous Methamphetamine Self-Administration
09:16

A General Method for Evaluating Deep Brain Stimulation Effects on Intravenous Methamphetamine Self-Administration

Published on: January 22, 2016

15.9K

Un marco de simulación motivado por el aprendizaje por refuerzo (RL) para evaluar estrategias de dosificación de

Bingyu Mao1, Ziqian Xie1, Laila Rasmy1

  • 1McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, Texas, United States.

AMIA ... Annual Symposium proceedings. AMIA Symposium
|February 23, 2026
PubMed
Resumen

La optimización de la dosificación de vancomicina es crucial para los resultados del paciente. Un nuevo marco de simulación que utiliza aprendizaje profundo y aprendizaje por refuerzo (RL) ayuda a determinar las mejores estrategias de dosificación para la terapia con vancomicina.

Palabras clave:
aprendizaje por refuerzosimulaciónvancomicinadosificaciónfarmacocinéticaaprendizaje profundoAUC

Más Videos Relacionados

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
11:56

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection

Published on: October 25, 2013

14.7K
Modeling Fast-scan Cyclic Voltammetry Data from Electrically Stimulated Dopamine Neurotransmission Data Using QNsim1.0
07:41

Modeling Fast-scan Cyclic Voltammetry Data from Electrically Stimulated Dopamine Neurotransmission Data Using QNsim1.0

Published on: June 5, 2017

10.4K

Videos de Experimentos Relacionados

Last Updated: Feb 24, 2026

A General Method for Evaluating Deep Brain Stimulation Effects on Intravenous Methamphetamine Self-Administration
09:16

A General Method for Evaluating Deep Brain Stimulation Effects on Intravenous Methamphetamine Self-Administration

Published on: January 22, 2016

15.9K
Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
11:56

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection

Published on: October 25, 2013

14.7K
Modeling Fast-scan Cyclic Voltammetry Data from Electrically Stimulated Dopamine Neurotransmission Data Using QNsim1.0
07:41

Modeling Fast-scan Cyclic Voltammetry Data from Electrically Stimulated Dopamine Neurotransmission Data Using QNsim1.0

Published on: June 5, 2017

10.4K

Área de la Ciencia:

  • Farmacocinética y Farmacodinámica
  • Biología Computacional
  • Aprendizaje Automático en Medicina

Sus antecedentes:

  • Lograr y mantener niveles terapéuticos de vancomicina es fundamental para la eficacia del tratamiento y la minimización de la toxicidad.
  • Las pautas existentes para la dosificación de vancomicina se basan en datos empíricos, pero las estrategias teóricas óptimas en diversas condiciones no se comprenden completamente.

Objetivo del estudio:

  • Desarrollar un nuevo marco de simulación basado en el aprendizaje por refuerzo (RL) para optimizar las estrategias de dosificación de vancomicina.
  • Integrar las pautas clínicas en un sistema de recompensa de RL utilizando el área bajo la curva de tiempo-concentración (AUC).

Principales métodos:

  • Se desarrolló un modelo farmacocinético de dos compartimentos de aprendizaje profundo (PK-RNN-2CM).
  • Se utilizaron datos específicos del paciente para generar curvas de tiempo-concentración de referencia.
  • Se simularon estrategias de dosificación de vancomicina en diversas condiciones, incluidas perturbaciones de ruido para imitar la variabilidad del mundo real.
  • Se emplearon la AUC de 24 horas y el error cuadrático medio (RMSE) como métricas de evaluación.

Principales resultados:

  • Ambos objetivos de AUC de dosis baja y dosis alta mostraron un rendimiento comparable en simulaciones sin ruido.
  • La estrategia de dosis baja logró puntuaciones de recompensa de AUC más altas en condiciones de ruido.
  • La estrategia de dosis alta demostró una mayor estabilidad en condiciones de ruido.

Conclusiones:

  • El marco de simulación desarrollado basado en RL proporciona un nuevo enfoque para optimizar la dosificación de vancomicina.
  • Esta metodología puede ayudar a refinar las estrategias de dosificación para mejorar los resultados del paciente en la terapia con vancomicina.
  • La capacidad del marco para incorporar pautas clínicas y simular la variabilidad del mundo real ofrece información valiosa para la monitorización de fármacos terapéuticos.