OPTImizing Lead Placement in Patients Requiring Pacemaker After Cardiac Surgery (OPTI-PACS)
OPTIMIZING LEAD PLACEMENT IN PATIENTS REQUIRING PACEMAKER AFTER CARDIAC SURGERY
Conventional right ventricular pacing has been associated with ventricular dyssynchrony and an increased risk of pacing-induced cardiomyopathy, which may lead to worse clinical outcomes. To lessen the burden of pacing-induced cardiomyopathy, the adoption of conduction system pacing has increased in recent years. In patients with normal cardiac function, measured as left ventricular ejection fraction, the superiority of conduction system pacing is less clear. As a result, both pacing strategies remain in widespread clinical use.
Patients undergoing cardiac surgery represent a vulnerable cohort for pacing-induced cardiomyopathy, given their established structural heart disease, and postoperative atrioventricular block remains a common occurrence in these patients.
This multicenter randomized trial aims to evaluate the use of conduction system pacing, in the form of left bundle branch area pacing, versus conventional pacing in patients with normal left ventricular ejection fraction after cardiac surgery.
研究概览
详细说明
A high percentage of ventricular pacing increases the risk of pacing-induced cardiomyopathy. Pacing-induced cardiomyopathy is a syndrome defined by left ventricular dysfunction secondary to chronic right ventricular pacing, resulting in impaired outcomes. Pacing-induced cardiomyopathy is estimated to affect approximately 10-20% of patients with a high proportion of right ventricular pacing (>20%), a population that mainly consists of patients with atrioventricular block (AVB). The abnormal activation leads to prolonged electrical and mechanical activation, which results in ventricular dyssynchrony. Other important risk factors for pacing-induced cardiomyopathy include structural heart disease and reduced ejection fraction, male sex and wide, paced QRS.
Clinical practice guidelines support pacemaker implantation following cardiac surgery only for severe and non-transient bradyarrhythmias, as pacemaker implantation increases the risk of severe infections and device-related long-term complications. Evidence suggests that a substantial proportion of patients who receive a pacemaker following cardiac surgery have limited need for pacing at long-term follow-up. Thus, the risk/benefit ratio for patients following cardiac surgery differs from that of the general population, while these patients also form a vulnerable population at high risk for pacing-induced cardiomyopathy.
Over the last decade, a conduction system pacing strategy called left bundle branch area pacing (LBBAP) has been developed. In LBBAP, the pacemaker lead is inserted deep into the interventricular septum from the right ventricle to the left ventricular endocardium, targeting the left bundle and its resulting fascicles. As the current understanding of the development of pacing-induced cardiomyopathy suggests that the electrical dyssynchrony introduced by right ventricular pacing plays a crucial role, our hypothesis is that its incidence could be reduced by the favorable electrical activation achieved with LBBAP.
There are ongoing randomized controlled trials of conduction system pacing in the general population; however, none are investigating cardiac surgery patients. These patients differ substantially from the general population in age, expected long-term survival, and cardiovascular health. This increases their risk of pacing-induced cardiomyopathy and could influence the feasibility of conduction system pacing due to their otherwise impaired cardiovascular health. At the same time, their long-term pacing dependence could differ from that of the general population.
Therefore, the aim of the present multicenter randomized controlled trial is to evaluate the long-term outcomes of LBBAP versus right ventricular pacing after cardiac surgery in patients with normal left ventricular ejection fraction. A secondary aim is to assess the feasibility of LBBAP after cardiac surgery with regard to implantation success and long-term electrical parameters. The results of this trial are anticipated to provide clinically meaningful evidence to guide pacing strategy selection in this patient cohort.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Andreas S Martinsson, MD, PhD
- 电话号码:+46313427717
- 邮箱:andreas.s.martinsson@vgregion.se
研究联系人备份
- 姓名:Alice David, MD
- 电话号码:+313429684
- 邮箱:laura.david@vgregion.se
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- High degree atrioventricular block
- Cardiac surgery within 30 days of pacemaker implantation
- Written informed consent
- Current left ventricular ejection fraction at or above 50%
Exclusion Criteria:
- Any concomitant condition that results in a life expectancy of less than 1 year
- Planned for heart transplant or left ventricular assist device
- Current dialysis
- Not suitable according to the opinion of the investigators due to characteristics that interfere with the adherence to the study protocol.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器:Conventional pacing strategy
This arm will receive a conventional pacemaker lead if they have atrioventricular block after cardiac surgery
|
Conventional pacing strategy
|
|
实验性的:Left bundle branch area pacing strategy
This arm will receive a left bundle branch area pacing pacemaker lead if they have atrioventricular block after cardiac surgery
|
Conventional pacing strategy versus conduction system pacing strategy in the form of left bundle branch area pacing
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in left ventricular ejection fraction
大体时间:1 year
|
Change in left ventricular ejection fraction between enrollment and end of follow-up
|
1 year
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
全因死亡率
大体时间:1年
|
全因死亡率
|
1年
|
|
Change in left ventricular end-diastolic diameter
大体时间:1 year
|
Change in LVEDD from enrollment to end of study follow-up
|
1 year
|
|
Clinical endpoints - composite
大体时间:1 year
|
Composite of all-cause mortality, heart failure hospitalization, device-related hospitalization
|
1 year
|
|
Heart failure hospitalization
大体时间:1 year
|
Heart failure hospitalization
|
1 year
|
|
Device-related hospitalization
大体时间:1 year
|
Device-related hospitalization
|
1 year
|
|
Quality-of-life measurement
大体时间:1 year
|
Quality-of-life measurement by standardized questionnaire
|
1 year
|
合作者和调查者
调查人员
- 首席研究员:Andreas S Martinsson, MD, PhD、Sahlgrensa university hospital
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 2025-08652-01
- 2025 (美国 NIH 拨款/合同:Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 20241208 (其他赠款/资助编号:Swedish Heart- Lung Foundation)
- ALFGBG-977905 (其他赠款/资助编号:ALF Agreement (Swedish state))
- ALFGBG-1029431 (其他赠款/资助编号:ALF Agreement (Swedish state))
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计划共享个人参与者数据 (IPD)?
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