Gradaus R, Hammel D, Kotthoff S, Böcker D
Department of Cardiology and Angiology, Westfälische Wilhelms-University, Münster, Germany.
J Cardiovasc Electrophysiol. 2001 Mar;12(3):356-60. doi: 10.1046/j.1540-8167.2001.00356.x.
The need to access the right ventricle might preclude transvenous placement of a defibrillation lead at implantable cardioverter defibrillator (ICD) placement, especially in small children or children with complex congenital heart defects. We investigated a subcutaneous array lead in addition to an abdominally placed "active can" ICD device in two children to avoid a thoracotomy.
The first child (age 12 years, 138 cm, 41 kg) had transposition of the great arteries with a subsequent surgical intra-atrial correction by the Mustard technique. The second child (age 14 years, 161 cm, 54 kg) had a single atrium and a single ventricle, d-transposition of the aorta, and atresia of the main pulmonary artery with a surgical anastomosis between the aorta and the right pulmonary artery by the Cooley technique. The defibrillation threshold was 18 J and <20 J at initial implantation and at generator replacement in the first patient and 20 J in the second patient. During follow-up of 6 years and 1 month, respectively, no ICD-related complications occurred.
In children in whom endocardial, right ventricular placement of a defibrillation lead is precluded, defibrillation is possible and safe between an abdominally placed "active can" ICD device and a subcutaneous array lead. This approach may avoid a thoracotomy in children with no possibility for transvenous ICD placement.
在植入式心脏复律除颤器(ICD)植入时,若需要进入右心室,可能无法经静脉放置除颤导线,尤其是在小儿或患有复杂先天性心脏缺陷的儿童中。我们在两名儿童中研究了一种皮下阵列导线,同时使用腹部放置的“有源罐”ICD装置,以避免开胸手术。
第一名儿童(12岁,身高138厘米,体重41千克)患有大动脉转位,随后采用Mustard技术进行了手术心房内矫正。第二名儿童(14岁,身高161厘米,体重54千克)患有单心房和单心室、主动脉d型转位以及主肺动脉闭锁,采用Cooley技术进行了主动脉与右肺动脉之间的手术吻合。第一名患者初次植入时和更换发生器时的除颤阈值分别为18焦耳和<20焦耳,第二名患者为20焦耳。在分别为期6年1个月的随访期间,未发生与ICD相关的并发症。
对于无法进行心内膜、右心室除颤导线放置的儿童,在腹部放置的“有源罐”ICD装置与皮下阵列导线之间进行除颤是可行且安全的。这种方法可避免在无法进行经静脉ICD放置的儿童中进行开胸手术。