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June 1, 2022BMJ OpenOpen Access

Rationale and design of a prospective study evaluating population pharmacokinetics and pharmacodynamics of rivaroxaban in Chinese patients with non-valvular atrial fibrillation

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Key result

Design paper outlines a prospective study evaluating rivaroxaban PK/PD in Chinese NVAF patients.

Why the study?

Few studies have investigated the pharmacokinetics and pharmacodynamics of rivaroxaban in Chinese patients with non-valvular atrial fibrillation to provide a reference for dose selection and individualized therapy.

What are the population pharmacokinetics and pharmacodynamics of rivaroxaban in Chinese patients with non-valvular atrial fibrillation?

Population

Chinese patients with non-valvular atrial fibrillation treated with rivaroxaban

Design

Single-centre prospective study

Follow-up

3 and 6 months

Authors

XLXiaoqin LiuYZYufei ZhangHDHong-yan Ding

Discussion

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Overview

This study protocol outlines a prospective evaluation of the pharmacokinetics and pharmacodynamics of rivaroxaban in Chinese patients with non-valvular atrial fibrillation to guide individualized dosing.

Study Design

Type

Observational

Multicenter

No

Structured PICO

What are the population pharmacokinetics and pharmacodynamics of rivaroxaban in Chinese patients with non-valvular atrial fibrillation?

P
Population
Chinese patients with non-valvular atrial fibrillation (NVAF) treated with rivaroxaban
I
Intervention
Rivaroxaban
O
Outcome
Population PK-PD model of rivaroxaban (evaluating plasma concentration, factor Xa activity, prothrombin time and single-nucleotide polymorphisms)surrogate

This study protocol outlines a prospective evaluation of the pharmacokinetics and pharmacodynamics of rivaroxaban in Chinese patients with non-valvular atrial fibrillation to guide individualized dosing.

Cite This Study

Liu et al. (2022) conducted an observational in non-valvular atrial fibrillation (NVAF). Rivaroxaban was evaluated on Population pharmacokinetics and pharmacodynamics of rivaroxaban. This rationale and design paper describes a prospective study to evaluate the population pharmacokinetics and pharmacodynamics of rivaroxaban in Chinese patients with non-valvular atrial fibrillation.

synapsesocial.com/papers/6a129ddac031bb6829a6fb9fhttps://doi.org/10.1136/bmjopen-2021-058378
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Also Consider

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  1. 1Safety, pharmacokinetics and pharmacodynamics of single/multiple doses of the oral, direct Factor Xa inhibitor rivaroxaban in healthy Chinese subjects2009 · 73 citations
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  3. 3Comparisons of Rivaroxaban Following Different Dosage Criteria (ROCKET AF or J‐ROCKET AF Trials) in Asian Patients With Atrial Fibrillation2019 · 30 citations
  4. 4Low-Dose Rivaroxaban and Risks of Adverse Events in Patients With Atrial Fibrillation2019 · 57 citations
  5. 5Outcomes After Use of Standard- and Low-Dose Non–Vitamin K Oral Anticoagulants in Asian Patients With Atrial Fibrillation2018 · 93 citations