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临床试验/NCT03972644
NCT03972644招募中不适用

Danish National Randomized Study on Early Aortic Valve Replacement in Patients With Asymptomatic Severe Aortic Stenosis

Odense University Hospital2 个研究点 分布在 1 个国家目标入组 1,700 人开始时间: 2020年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,700
试验地点
2
主要终点
all-cause mortality

研究概览

简要总结

The purpose of this study is to examine the impact of early surgery in patients with asymptomatic severe aortic valve stenosis with signs of subclinical LV dysfunction despite preserved LVEF, with a watchfull waiting approach.

详细描述

Since the seminal paper by Ross and Braunwald, the development of symptoms has been regarded as one of the most important precursors of a poor outcome in aortic stenosis (AS), and is today half a century later, still the leading reason for referral for aortic valve replacement (AVR). The development of symptoms is however often preceded by structural changes in the left ventricle (LV).These changes including concentric remodeling and LV hypertrophy have been regarded as compensative measures to adapt the LV to increased ventricular afterload. Although LV hypertrophy may preserve wall-stress in the normal range and increase contractility allowing the preservation of stroke volume, this occurs at the expense of increased filling pressures. Diastolic dysfunction with increased filling pressure lead to left atrial (LA) dilatation and significantly contributes to the development of symptoms.

Despite successful surgery, AS patients have increased long-term mortality and morbidity compared to the general population, and the outcome is largely determined by the degree of preoperative structural LV and LA alterations. This has led to the theory that AVR prior to the development of symptoms could improve outcome, a view supported by prospective and retrospective studies.These studies were however small, with some important limitations. In addition, there has been a concern that operative risk and prosthetic valve related long-term morbidity and mortality does not justify surgery on every asymptomatic patient with severe AS. Numerous studies have suggested that markers of LV structure and function, particularly LA volume index,E/e' and brain natriuretic peptides (BNP) all reflecting LV filling pressures may identify patients with benefit of early AVR. Accordingly, the most recent European guideline for management of valvular disease has implemented BNP as a class IIa recommendation for AVR in asymptomatic AS patients,although no randomized studies have demonstrated that early surgery based on these markers improve prognosis.

The purpose of this study is thus to evaluate if early AVR in patients with signs of elevated LV filling pressuresmay improve long-term outcome in patients with asymptomatic severe AS, compared to conventional symptom-guided surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Severe AS defined as
  • aortic valve area (AVA) ≤1 cm2, AND
  • Transvalvular maximum velocity (Vmax) ≥3.5 m/s AND
  • AS severity evaluated severe by a heart valve team conference. In cases where severity is not unambiguous an integrative approach will be utilized combining echocardiographic markers of valve severity and LV function, and if necessary aortic valve calcification estimated by non-contrast CT.
  • Considered to be asymptomatic (estimated by a consultant in cardiology)
  • Considered to be candidate for AVR (transcatheter AVR/surgical AVR)
  • Sign of increased LV filling pressures18 or reduced longitudinal LV systolic function
  • Left atrial volume index (LAVi) > 34 ml/m2; OR
  • ratio of early diastolic peak mitral inflow velocity (E) to early mitral annulus diastolic velocity (e') ratio E/e'avg>13; OR
  • Threefold elevation in NT-proBNP compared to the upper expected age and gender value. OR
  • Age ≥18 years
  • Signed informed consent

排除标准

  • Very severe AS defined as Vmax>5 m/s.
  • Concomitant severe valvular disease other than AS
  • Previous valvular surgery
  • Estimated glomerular filtration rate<30 ml/min/m2
  • Women of childbearing potential
  • Inability to provide informed consent
  • Age>85 years.
  • Supravalvular or subvalvular AS

结局指标

主要结局

all-cause mortality

时间窗: After 379 events (approx 5 years)

All-cause mortality assessed by Danish patient records

次要结局

  • Combined endpoint(After 379 events (approx 5 years))
  • all-cause mortality in patients with low-gradient AS(After 379 events (approx 5 years))
  • Combined endpoint in low-gradient AS(After 379 events (approx 5 years))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jordi Dahl

Associate Professor, MD, Ph.D.

Odense University Hospital

研究点 (2)

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