Ont Health Technol Assess Ser. 2006;6(8):1-101. Epub 2006 Mar 1.
To assess the effectiveness, cost-effectiveness, and demand in Ontario for catheter ablation of complex arrhythmias guided by advanced nonfluoroscopy mapping systems. Particular attention was paid to ablation for atrial fibrillation (AF).
Tachycardia Tachycardia refers to a diverse group of arrhythmias characterized by heart rates that are greater than 100 beats per minute. It results from abnormal firing of electrical impulses from heart tissues or abnormal electrical pathways in the heart because of scars. Tachycardia may be asymptomatic, or it may adversely affect quality of life owing to symptoms such as palpitations, headaches, shortness of breath, weakness, dizziness, and syncope. Atrial fibrillation, the most common sustained arrhythmia, affects about 99,000 people in Ontario. It is associated with higher morbidity and mortality because of increased risk of stroke, embolism, and congestive heart failure. In atrial fibrillation, most of the abnormal arrhythmogenic foci are located inside the pulmonary veins, although the atrium may also be responsible for triggering or perpetuating atrial fibrillation. Ventricular tachycardia, often found in patients with ischemic heart disease and a history of myocardial infarction, is often life-threatening; it accounts for about 50% of sudden deaths. Treatment of Tachycardia The first line of treatment for tachycardia is antiarrhythmic drugs; for atrial fibrillation, anticoagulation drugs are also used to prevent stroke. For patients refractory to or unable to tolerate antiarrhythmic drugs, ablation of the arrhythmogenic heart tissues is the only option. Surgical ablation such as the Cox-Maze procedure is more invasive. Catheter ablation, involving the delivery of energy (most commonly radiofrequency) via a percutaneous catheter system guided by X-ray fluoroscopy, has been used in place of surgical ablation for many patients. However, this conventional approach in catheter ablation has not been found to be effective for the treatment of complex arrhythmias such as chronic atrial fibrillation or ventricular tachycardia. Advanced nonfluoroscopic mapping systems have been developed for guiding the ablation of these complex arrhythmias.
Four nonfluoroscopic advanced mapping systems have been licensed by Health Canada: CARTO EP mapping System (manufactured by Biosense Webster, CA) uses weak magnetic fields and a special mapping/ablation catheter with a magnetic sensor to locate the catheter and reconstruct a 3-dimensional geometry of the heart superimposed with colour-coded electric potential maps to guide ablation. EnSite System (manufactured by Endocardial Solutions Inc., MN) includes a multi-electrode non-contact catheter that conducts simultaneous mapping. A processing unit uses the electrical data to computes more than 3,000 isopotential electrograms that are displayed on a reconstructed 3-dimensional geometry of the heart chamber. The navigational system, EnSite NavX, can be used separately with most mapping catheters. The LocaLisa Intracardiac System (manufactured by Medtronics Inc, MN) is a navigational system that uses an electrical field to locate the mapping catheter. It reconstructs the location of the electrodes on the mapping catheter in 3-dimensional virtual space, thereby enabling an ablation catheter to be directed to the electrode that identifies abnormal electric potential. Polar Constellation Advanced Mapping Catheter System (manufactured by Boston Scientific, MA) is a multielectrode basket catheter with 64 electrodes on 8 splines. Once deployed, each electrode is automatically traced. The information enables a 3-dimensional model of the basket catheter to be computed. Colour-coded activation maps are reconstructed online and displayed on a monitor. By using this catheter, a precise electrical map of the atrium can be obtained in several heartbeats.
A systematic search of Cochrane, MEDLINE and EMBASE was conducted to identify studies that compared ablation guided by any of the advanced systems to fluoroscopy-guided ablation of tachycardia. English-language studies with sample sizes greater than or equal to 20 that were published between 2000 and 2005 were included. Observational studies on safety of advanced mapping systems and fluoroscopy were also included. Outcomes of interest were acute success, defined as termination of arrhythmia immediately following ablation; long-term success, defined as being arrhythmia free at follow-up; total procedure time; fluoroscopy time; radiation dose; number of radiofrequency pulses; complications; cost; and the cost-effectiveness ratio. Quality of the individual studies was assessed using established criteria. Quality of the overall evidence was determined by applying the GRADE evaluation system. (3) Qualitative synthesis of the data was performed. Quantitative analysis using Revman 4.2 was performed when appropriate. Quality of the Studies Thirty-four studies met the inclusion criteria. These comprised 18 studies on CARTO (4 randomized controlled trials [RCTs] and 14 non-RCTs), 3 RCTs on EnSite NavX, 4 studies on LocaLisa Navigational System (1 RCT and 3 non-RCTs), 2 studies on EnSite and CARTO, 1 on Polar Constellation basket catheter, and 7 studies on radiation safety. The quality of the studies ranged from moderate to low. Most of the studies had small sample sizes with selection bias, and there was no blinding of patients or care providers in any of the studies. Duration of follow-up ranged from 6 weeks to 29 months, with most having at least 6 months of follow-up. There was heterogeneity with respect to the approach to ablation, definition of success, and drug management before and after the ablation procedure.
Evidence is based on a small number of small RCTS and non-RCTS with methodological flaws.Advanced nonfluoroscopy mapping/navigation systems provided real time 3-dimensional images with integration of anatomic and electrical potential information that enable better visualization of areas of interest for ablationAdvanced nonfluoroscopy mapping/navigation systems appear to be safe; they consistently shortened the fluoroscopy duration and radiation exposure.Evidence suggests that nonfluoroscopy mapping and navigation systems may be used as adjuncts to rather than replacements for fluoroscopy in guiding the ablation of complex arrhythmias.Most studies showed a nonsignificant trend toward lower overall failure rate for advanced mapping-guided ablation compared with fluoroscopy-guided mapping.Pooled analyses of small RCTs and non-RCTs that compared fluoroscopy- with nonfluoroscopy-guided ablation of atrial fibrillation and atrial flutter showed that advanced nonfluoroscopy mapping and navigational systems:Yielded acute success rates of 69% to 100%, not significantly different from fluoroscopy ablation.Had overall failure rates at 3 months to 19 months of 1% to 40% (median 25%).Resulted in a 10% relative reduction in overall failure rate for advanced mapping guided-ablation compared to fluoroscopy guided ablation for the treatment of atrial fibrillation.Yielded added benefit over fluoroscopy in guiding the ablation of complex arrhythmia. The advanced systems were shown to reduce the arrhythmia burden and the need for antiarrhythmic drugs in patients with complex arrhythmia who had failed fluoroscopy-guided ablationBased on predominantly observational studies, circumferential PV ablation guided by a nonfluoroscopy system was shown to do the following:Result in freedom from atrial fibrillation (with or without antiarrhythmic drug) in 75% to 95% of patients (median 79%). This effect was maintained up to 28 months.Result in freedom from atrial fibrillation without antiarrhythmic drugs in 47% to 95% of patients (median 63%).Improve patient survival at 28 months after the procedure as compared with drug therapy.Require special skills; patient outcomes are operator dependent, and there is a significant learning curve effect.Complication rates of pulmonary vein ablation guided by an advanced mapping/navigation system ranged from 0% to 10% with a median of 6% during a follow-up period of 6 months to 29 months.The complication rate of the study with the longest follow-up was 8%.The most common complications of advanced catheter-guided ablation were stroke, transient ischemic attack, cardiac tamponade, myocardial infarction, atrial flutter, congestive heart failure, and pulmonary vein stenosis. A small number of cases with fatal atrial-esophageal fistula had been reported and were attributed to the high radiofrequency energy used rather than to the advanced mapping systems.
An Ontario-based economic analysis suggests that the cumulative incremental upfront costs of catheter ablation of atrial fibrillation guided by advanced nonfluoroscopy mapping could be recouped in 4.7 years through cost avoidance arising from less need for antiarrhythmic drugs and fewer hospitalization for stroke and heart failure. Expert Opinion Expert consultants to the Medical Advisory Secretariat noted the following: Nonfluoroscopy mapping is not necessary for simple ablation procedures (e.g., typical flutter). However, it is essential in the ablation of complex arrhythmias including these:Symptomatic, drug-refractory atrial fibrillationArrhythmias in people who have had surgery for congenital heart disease (e.g., macro re-entrant tachycardia in people who have had surgery for congenital heart disease).Ventricular tachycardia due to myocardial infarctionAtypical atrial flutterAdvanced mapping systems represent an enabling technology in the ablation of complex arrhythmias. The ablation of these complex cases would not have been feasible or advisable with fluoroscopy-guided ablation and, therefore, comparative studies would not be feasible or ethical in such cases. (ABSTRACT TRUNCATED)
评估在安大略省使用先进的非荧光透视标测系统指导下进行复杂心律失常导管消融的有效性、成本效益和需求。特别关注心房颤动(房颤)的消融治疗。
心动过速 心动过速是指一组多样的心律失常,其特征为心率大于每分钟100次。它是由于心脏组织电冲动异常发放或因瘢痕导致心脏内异常电传导通路引起的。心动过速可能无症状,也可能因心悸、头痛、气短、乏力、头晕和晕厥等症状而对生活质量产生不利影响。房颤是最常见的持续性心律失常,安大略省约有99,000人受其影响。由于中风、栓塞和充血性心力衰竭风险增加,它与更高的发病率和死亡率相关。在房颤中,大多数异常心律失常起源部位位于肺静脉内,尽管心房也可能触发或维持房颤。室性心动过速常见于患有缺血性心脏病和心肌梗死病史的患者,通常危及生命;约占猝死的50%。心动过速的治疗 心动过速的一线治疗是抗心律失常药物;对于房颤,还使用抗凝药物预防中风。对于对抗心律失常药物难治或不耐受的患者,消融心律失常起源的心脏组织是唯一选择。诸如Cox-Maze手术等外科消融更具侵入性。导管消融是通过经皮导管系统在X线透视引导下输送能量(最常用的是射频),已被许多患者用于替代外科消融。然而,这种传统的导管消融方法尚未被发现对治疗慢性房颤或室性心动过速等复杂心律失常有效。已开发出先进的非荧光透视标测系统用于指导这些复杂心律失常的消融。
加拿大卫生部已批准四种非荧光透视先进标测系统:CARTO EP标测系统(由加利福尼亚州的Biosense Webster公司生产)使用弱磁场和带有磁传感器的特殊标测/消融导管来定位导管,并重建叠加有彩色编码电位图的心脏三维几何结构以指导消融。EnSite系统(由明尼苏达州的Endocardial Solutions Inc.公司生产)包括一个多电极非接触导管,可进行同步标测。一个处理单元使用电数据计算出3000多个等电位心电图,并显示在重建的心脏腔室三维几何结构上。导航系统EnSite NavX可与大多数标测导管分开使用。LocaLisa心内系统(由明尼苏达州的Medtronic Inc.公司生产)是一种导航系统,利用电场定位标测导管。它在三维虚拟空间中重建标测导管上电极的位置,从而使消融导管能够指向识别异常电位的电极。Polar Constellation先进标测导管系统(由马萨诸塞州的Boston Scientific公司生产)是一种多电极篮状导管,在8个花键上有64个电极。一旦展开,每个电极会自动追踪。该信息可计算出篮状导管的三维模型。彩色编码的激动图在线重建并显示在监视器上。通过使用该导管,在几次心跳内即可获得心房的精确电图。
对Cochrane、MEDLINE和EMBASE进行系统检索,以识别比较任何先进系统指导下的消融与透视指导下的心动过速消融的研究。纳入2000年至2005年间发表的样本量大于或等于20的英文研究。还纳入了关于先进标测系统和透视安全性的观察性研究。感兴趣的结果包括急性成功率,定义为消融后立即终止心律失常;长期成功率,定义为随访时无心律失常;总手术时间;透视时间;辐射剂量;射频脉冲数;并发症;成本;以及成本效益比。使用既定标准评估各个研究的质量。通过应用GRADE评估系统确定总体证据的质量。(3)对数据进行定性综合。在适当情况下使用Revman 4.2进行定量分析。研究质量 34项研究符合纳入标准。其中包括18项关于CARTO的研究(4项随机对照试验[RCT]和14项非RCT)、3项关于EnSite NavX的RCT、4项关于LocaLisa导航系统的研究(1项RCT和3项非RCT)、2项关于EnSite和CARTO的研究、1项关于Polar Constellation篮状导管的研究以及7项关于辐射安全性的研究。研究质量从中等到低不等。大多数研究样本量小且存在选择偏倚,所有研究中患者或医护人员均未设盲。随访时间从6周至29个月不等,大多数至少随访6个月。在消融方法、成功定义以及消融前后的药物管理方面存在异质性。
证据基于少数存在方法学缺陷的小型RCT和非RCT。先进的非荧光透视标测/导航系统提供实时三维图像,整合了解剖和电位信息,能够更好地可视化消融感兴趣区域。先进的非荧光透视标测/导航系统似乎是安全的;它们持续缩短了透视时间和辐射暴露。有证据表明,在指导复杂心律失常消融时,非荧光透视标测和导航系统可作为透视的辅助手段而非替代方法。大多数研究表明,与透视指导的标测相比,先进标测指导的消融总体失败率呈非显著降低趋势。对比较透视与非透视指导的房颤和房扑消融的小型RCT和非RCT进行汇总分析表明,先进的非荧光透视标测和导航系统:急性成功率为69%至100%,与透视消融无显著差异。3个月至19个月时的总体失败率为1%至40%(中位数为25%)。与透视指导的消融相比,先进标测指导的消融总体失败率相对降低10%,用于治疗房颤。在指导复杂心律失常消融方面比透视有额外益处。对于透视指导的消融失败的复杂心律失常患者,先进系统显示可减轻心律失常负担并减少对抗心律失常药物的需求。基于主要是观察性研究,非荧光透视系统指导的环肺静脉消融显示如下:75%至95%的患者(中位数为79%)实现无房颤(无论是否使用抗心律失常药物)。这种效果可持续至28个月。47%至95%的患者(中位数为63%)实现无抗心律失常药物的情况下无房颤。与药物治疗相比,术后28个月时患者生存率提高。需要特殊技能;患者结局依赖于操作者,且存在显著的学习曲线效应。先进标测/导航系统指导的肺静脉消融并发症发生率在6个月至29个月的随访期内为0%至10%,中位数为6%。随访时间最长的研究并发症发生率为8%。先进导管指导消融最常见的并发症是中风、短暂性脑缺血发作、心脏压塞、心肌梗死、房扑、充血性心力衰竭和肺静脉狭窄。已报告少数致命的心房 - 食管瘘病例,归因于使用的高射频能量而非先进标测系统。
基于安大略省的经济分析表明,先进非荧光透视标测指导的房颤导管消融累计增量前期成本可在4.7年内通过减少对抗心律失常药物的需求以及减少中风和心力衰竭住院次数而节省成本来收回。专家意见 医学咨询秘书处的专家顾问指出:对于简单消融手术(如典型房扑),非荧光透视标测并非必要。然而,在消融复杂心律失常时至关重要,包括这些情况:有症状的、药物难治性房颤;先天性心脏病手术后的心律失常(如先天性心脏病手术后的大折返性心动过速);心肌梗死导致的室性心动过速;非典型房扑。先进标测系统是复杂心律失常消融的一项赋能技术。对于这些复杂病例,透视指导的消融不可行或不可取,因此,在此类情况下进行比较研究不可行或不符合伦理。(摘要截断)