Results of Using Various Conduction System Pacing Options in Patients with Bradyarrhythmia

E. O. Perepeka, B. Kravchuk
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To analyze the immediate and long-term results of the use of conduction system pacing in patients with indications for permanent ventricular pacing. \nMaterials and methods. This study included 18 patients with indications for permanentventricular pacing who were operated at the National Amosov Institute of Cardiovascular Surgery of the National Academy of Medical Sciences of Ukraine in the period from 01/01/2013 to 12/31/2022, in whom permanent conduction system pacing was used. There were 17 patients with bradyarrhythmias, of these 16 (88%) suffered from high-degree AV block (including 1 patient with Frederick’s syndrome and 1 (5%) patient with atrial ϐibrillation with slow ventricular response) and 1 (5%) patient with ischemic cardiomyopathy with left bundle branch block and ϐirstdegree AV block with indications for cardiac resynchronization therapy. The mean age of the patients was 55 ± 16 years (8 men, 10 women), LVEF at the time of the intervention was 56.42 ± 9.13 %, end diastolic volume 130.2 ± 23.8 ml, end systolic volume 55.1 ± 17.7 ml, diameter of the left atrium 4.01 ± 0.6 cm. The average QRS width before implantation was 116.5 ± 27.7 ms. In 6 (33%) patients, a special delivery system (С304-L69, Medtronic in 1 patient [5%], C315HIS in 5 [27%] patients) and 4.1F active ϐixation lead Medtronic 3830 Select Secure (69 or 74 cm) were used; in other cases (66%) standard 6F leads with active ϐixation and a lumen for a stylet without a delivery system were used. \nResults. The average follow-up period after implantation of pacemaker was 36.35 ± 29.65 months. During the observation period, LVEF was 57.07 ± 5.38 %, end diastolic volume111.5 ± 18.09 ml, end systolic volume 49.5 ± 13.4 ml, diameter of the left ventricle 3.9 ± 0.5 cm. The mean duration of paced QRS was 119.1 ± 10.09 ms. In 6 patients (33%), it was possible to demonstrate a change in the QRS width when the amplitude of ventricular stimulation was reduced, with 2 variants of transitions: 1) 4 (22%) patients with a transition from non-selective His bundle pacing (NSHBP) to selective His bundle pacing (SHBP), in 2 (11%) of these patients with a transition from SHBP with correction of right bundle branch block (RBBB) to SHBP without correction of RBBB, and then loss of capture of the myocardium of the ventricles; 2) 2 patients (11%) with a transition from NSHBP to myocardial septal ventricular pacing and further with a decrease in amplitude to the loss of capture of the myocardium of the ventricles. One (5%) patient with complete heart block had permanent non-selective left bundle branch area pacing. The other 11 (61%) patients met the criteria for parahisian pacing without visible transitions with a change in the amplitude of ventricular pacing. The average global longitudinal strain was -17.6 ± 2.7 %. The average interval from the stimulus to the peak of the R-wave in lead V6, which indicated the time of left ventricular activation, was 73.2 ± 8.7 ms. Pacing parameters were standardly set according to the primary indications, but with correction of the amplitude of ventricular stimulation relative to the thresholds of pacing of the conduction system. AV delay was corrected for the latency from the stimulus to the onset of the QRS in SHBP or for the duration of the “pseudodelta” wave in NSHBP which in both cases was the duration of the H-V interval. There were no complications in the acute or long-term postoperative period. \nConclusions. Conduction system pacing is a challenge in the practice of cardiologist for treating life-threatening bradyarrhythmias and heart failure, but at the same time it is a safe method that provides physiological electrical and mechanical activation of the myocardium of the ventricles, that allows to effectively avoid the consequences of dyssynchrony due to permanent myocardial ventricular pacing.","PeriodicalId":33680,"journal":{"name":"Ukrayins''kii zhurnal sertsevosudinnoyi khirurgiyi","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ukrayins''kii zhurnal sertsevosudinnoyi khirurgiyi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30702/ujcvs/22.30(04)/pk064-94103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1

Abstract

Chronic right ventricular myocardial pacing causes an asynchronous pattern of left ventricular activation, reduces left ventricular ejection fraction (LVEF), and may be associated with worsening of clinical outcomes in the long term. Although with the emergence of algorithms that minimize ventricular pacing it became possible to reduce the percentage of paced complexes in patients with sinus node dysfunction, permanent ventricular pacing is still inevitable in patients with high-degree atrioventricular (AV) block. The use of permanent conduction system pacing is a promising method for preserving the physiological activation of the ventricular myocardium and preventing the development of heart failure due to ventricular dyssynchrony. The aim. To analyze the immediate and long-term results of the use of conduction system pacing in patients with indications for permanent ventricular pacing. Materials and methods. This study included 18 patients with indications for permanentventricular pacing who were operated at the National Amosov Institute of Cardiovascular Surgery of the National Academy of Medical Sciences of Ukraine in the period from 01/01/2013 to 12/31/2022, in whom permanent conduction system pacing was used. There were 17 patients with bradyarrhythmias, of these 16 (88%) suffered from high-degree AV block (including 1 patient with Frederick’s syndrome and 1 (5%) patient with atrial ϐibrillation with slow ventricular response) and 1 (5%) patient with ischemic cardiomyopathy with left bundle branch block and ϐirstdegree AV block with indications for cardiac resynchronization therapy. The mean age of the patients was 55 ± 16 years (8 men, 10 women), LVEF at the time of the intervention was 56.42 ± 9.13 %, end diastolic volume 130.2 ± 23.8 ml, end systolic volume 55.1 ± 17.7 ml, diameter of the left atrium 4.01 ± 0.6 cm. The average QRS width before implantation was 116.5 ± 27.7 ms. In 6 (33%) patients, a special delivery system (С304-L69, Medtronic in 1 patient [5%], C315HIS in 5 [27%] patients) and 4.1F active ϐixation lead Medtronic 3830 Select Secure (69 or 74 cm) were used; in other cases (66%) standard 6F leads with active ϐixation and a lumen for a stylet without a delivery system were used. Results. The average follow-up period after implantation of pacemaker was 36.35 ± 29.65 months. During the observation period, LVEF was 57.07 ± 5.38 %, end diastolic volume111.5 ± 18.09 ml, end systolic volume 49.5 ± 13.4 ml, diameter of the left ventricle 3.9 ± 0.5 cm. The mean duration of paced QRS was 119.1 ± 10.09 ms. In 6 patients (33%), it was possible to demonstrate a change in the QRS width when the amplitude of ventricular stimulation was reduced, with 2 variants of transitions: 1) 4 (22%) patients with a transition from non-selective His bundle pacing (NSHBP) to selective His bundle pacing (SHBP), in 2 (11%) of these patients with a transition from SHBP with correction of right bundle branch block (RBBB) to SHBP without correction of RBBB, and then loss of capture of the myocardium of the ventricles; 2) 2 patients (11%) with a transition from NSHBP to myocardial septal ventricular pacing and further with a decrease in amplitude to the loss of capture of the myocardium of the ventricles. One (5%) patient with complete heart block had permanent non-selective left bundle branch area pacing. The other 11 (61%) patients met the criteria for parahisian pacing without visible transitions with a change in the amplitude of ventricular pacing. The average global longitudinal strain was -17.6 ± 2.7 %. The average interval from the stimulus to the peak of the R-wave in lead V6, which indicated the time of left ventricular activation, was 73.2 ± 8.7 ms. Pacing parameters were standardly set according to the primary indications, but with correction of the amplitude of ventricular stimulation relative to the thresholds of pacing of the conduction system. AV delay was corrected for the latency from the stimulus to the onset of the QRS in SHBP or for the duration of the “pseudodelta” wave in NSHBP which in both cases was the duration of the H-V interval. There were no complications in the acute or long-term postoperative period. Conclusions. Conduction system pacing is a challenge in the practice of cardiologist for treating life-threatening bradyarrhythmias and heart failure, but at the same time it is a safe method that provides physiological electrical and mechanical activation of the myocardium of the ventricles, that allows to effectively avoid the consequences of dyssynchrony due to permanent myocardial ventricular pacing.
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慢性心律失常患者使用不同传导系统起搏方案的结果
慢性右心室心肌起搏导致左心室非同步激活模式,降低左心室射血分数(LVEF),并可能与长期临床结果的恶化有关。尽管随着最小化心室起搏算法的出现,降低窦房结功能障碍患者中起搏复合体的百分比成为可能,但对于高度房室传导阻滞的患者,永久性心室起搏仍然是不可避免的。使用永久性传导系统起搏是一种很有前途的方法,可以保持心室心肌的生理激活,防止由于心室非同步化引起的心力衰竭的发展。的目标。分析传导系统起搏在有永久性心室起搏指征的患者中使用的近期和长期效果。材料和方法。本研究纳入了2013年1月1日至2022年12月31日期间在乌克兰国家医学科学院国家阿莫索夫心血管外科研究所接受永久性心室起搏手术的18例有适应症的患者。慢速心律失常患者17例,其中16例(88%)为高度房室传导阻滞(包括1例弗雷德里克综合征和1例(5%)心房ϐibrillation伴心室反应缓慢),1例(5%)缺血性心肌病伴左束支传导阻滞和ϐirstdegree房室传导阻滞,需心脏再同步化治疗。患者平均年龄55±16岁(男8例,女10例),干预时LVEF 56.42±9.13%,舒张末期容积130.2±23.8 ml,收缩末期容积55.1±17.7 ml,左心房直径4.01±0.6 cm。植入前平均QRS宽度为116.5±27.7 ms。在6例(33%)患者中,使用特殊给药系统(С304-L69, 1例美敦力[5%],5例C315HIS[27%])和4.1F active ϐixation lead Medtronic 3830 Select Secure(69或74 cm);在其他情况下(66%),使用了具有活动ϐixation的标准6F引线和没有输送系统的样式管的管腔。结果。起搏器植入后平均随访36.35±29.65个月。观察期内LVEF为57.07±5.38%,舒张末期容积111.5±18.09 ml,收缩末期容积49.5±13.4 ml,左室直径3.9±0.5 cm。节律性QRS平均持续时间为119.1±10.09 ms。6例(33%),可以证明QRS宽度变化的振幅心室刺激减少时,2变种的转换:1)4(22%)患者从大众化的节奏(NSHBP)选择性包袱包踱步(SHBP), 2例(11%)患者的过渡与校正SHBP右束支块(RBBB) SHBP没有RBBB的校正,然后捕获的心室的心肌;2) 2例患者(11%)从NSHBP过渡到心肌室间隔起搏,并进一步下降到心室心肌失去俘获。1例(5%)完全性心脏传导阻滞患者行永久性非选择性左束支区起搏。其余11例(61%)患者符合旁行性起搏标准,未见心室起搏幅度变化的明显转变。整体纵向应变平均值为-17.6±2.7%。从刺激到V6导联r波峰值的平均间隔时间为73.2±8.7 ms,表明左心室的激活时间。根据主要适应症标准设定起搏参数,但相对于传导系统起搏阈值校正心室刺激幅度。AV延迟被校正为从刺激到SHBP QRS发作的潜伏期或NSHBP“伪三角洲”波的持续时间,这两种情况下都是H-V间隔的持续时间。术后急性期和远期均无并发症发生。结论。传导系统起搏在心脏病专家治疗危及生命的慢速心律失常和心力衰竭的实践中是一个挑战,但与此同时,它是一种安全的方法,可以提供心室心肌的生理电和机械激活,从而有效地避免由于永久性心肌心室起搏引起的非同步化后果。
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6 weeks
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