First Case Report of Transvenous Pacemaker Placement in a Patient with Congenital Absence of the Clavicles Due to Cleidocranial Dysplasia

Krista Diane Niezwaag, Benjamin James Kotur, A. Michaels
{"title":"First Case Report of Transvenous Pacemaker Placement in a Patient with Congenital Absence of the Clavicles Due to Cleidocranial Dysplasia","authors":"Krista Diane Niezwaag, Benjamin James Kotur, A. Michaels","doi":"10.11648/j.ccr.20210502.17","DOIUrl":null,"url":null,"abstract":"Cleidocranial dysplasia is a rare, autosomal dominant disease that is associated with clavicular absence or hypoplasia. Permanent pacemakers are most commonly implanted using percutaneous subclavian venous access. The clavicle is typically used as a bony landmark to guide venous access. Transvenous pacemaker implantation in the setting of clavicular hypoplasia, resection or other anomalies has not been described in literature. This is the first case report of a patient with clavicular absence undergoing transvenous permanent pacemaker implantation. This patient has a rare condition called cleidocranial dysplasia resulting in the congenital absence of his clavicles, along with other skeletal abnormalities. Cardiac anomalies are not associated with this disorder. This patient presented for permanent pacemaker placement in the setting of trifascicular block, symptomatic intermittent second-degree Mobitz type II atrioventricular block, and syncope. Using intra-procedural subclavian venography and intraprocedural Sonosite ultrasound imaging to identify vascular anatomy and surrounding anatomic landmarks, this patient underwent successful placement of a dual chamber transvenous pacemaker. Images from the intraprocedural venogram and the post-procedure chest x-ray illustrate the anatomy in this patient with congenital absence of the clavicles. This case has important implications in subclavian access and pacemaker placement in patients with clavicular abnormalities that may include absent, deformed, or resected clavicles.","PeriodicalId":92185,"journal":{"name":"Cardiology research and cardiovascular medicine","volume":"10 5","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cardiology research and cardiovascular medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11648/j.ccr.20210502.17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Cleidocranial dysplasia is a rare, autosomal dominant disease that is associated with clavicular absence or hypoplasia. Permanent pacemakers are most commonly implanted using percutaneous subclavian venous access. The clavicle is typically used as a bony landmark to guide venous access. Transvenous pacemaker implantation in the setting of clavicular hypoplasia, resection or other anomalies has not been described in literature. This is the first case report of a patient with clavicular absence undergoing transvenous permanent pacemaker implantation. This patient has a rare condition called cleidocranial dysplasia resulting in the congenital absence of his clavicles, along with other skeletal abnormalities. Cardiac anomalies are not associated with this disorder. This patient presented for permanent pacemaker placement in the setting of trifascicular block, symptomatic intermittent second-degree Mobitz type II atrioventricular block, and syncope. Using intra-procedural subclavian venography and intraprocedural Sonosite ultrasound imaging to identify vascular anatomy and surrounding anatomic landmarks, this patient underwent successful placement of a dual chamber transvenous pacemaker. Images from the intraprocedural venogram and the post-procedure chest x-ray illustrate the anatomy in this patient with congenital absence of the clavicles. This case has important implications in subclavian access and pacemaker placement in patients with clavicular abnormalities that may include absent, deformed, or resected clavicles.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
经静脉置放起搏器治疗锁骨发育不良所致先天性锁骨缺失的首例报道
锁骨颅骨发育不良是一种罕见的常染色体显性疾病,与锁骨缺失或发育不全有关。永久性起搏器最常用的植入方法是经皮锁骨下静脉通路。锁骨通常被用作引导静脉通路的骨标记。经静脉起搏器植入在锁骨发育不全,切除或其他异常的设置尚未在文献中描述。这是首例锁骨缺失患者接受经静脉永久性起搏器植入的病例报告。该患者患有一种罕见的锁骨颅骨发育不良,导致先天性锁骨缺失,并伴有其他骨骼异常。心脏异常与这种疾病无关。该患者在三束传导阻滞、间歇性二度Mobitz型房室传导阻滞和晕厥的情况下表现为永久性起搏器放置。通过术中锁骨下静脉造影和术中超声成像来识别血管解剖和周围解剖标志,该患者成功放置了双腔经静脉起搏器。术中静脉造影和术后胸部x线图像显示了先天性锁骨缺失的解剖结构。该病例对锁骨缺失、畸形或切除的锁骨异常患者的锁骨下通路和起搏器放置具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Cardiogenic Shock: Integrating Pathophysiology, Phenotypes, and Advanced Therapeutic Approaches The Relationship of Weekly Monitoring of the Radial Artery Pulse Harmonics during Pregnancy Process Outcomes of Complete Transcatheter versus Complete Surgical Treatment in Patients with Severe Aortic Valve Stenosis and Concomitant Coronary Artery Disease Inadvertent Massive overdose of Isoproterenol During Electrophysiology Study Treated Successfully with Intravenous Metoprolol: Two Case Reports The Relationship Between Serum Testosterone Level as an Independent Variable in Men with the Risk Factors for Coronary Artery Disease & Rehospitalization for Acute Coronary Syndrome
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1