Implantation of a left ventricular assist device to provide long-term support for end-stage Duchenne muscular dystrophy-associated cardiomyopathy

被引:18
作者
Stoller, Douglas [1 ,3 ]
Araj, Faris [1 ,3 ]
Amin, Alpesh [1 ,3 ]
Fitzsimmons, Catherine [1 ,3 ]
Morlend, Robert [1 ,3 ]
Thibodeau, Jennifer T. [1 ,3 ]
Ramaciotti, Claudio [2 ]
Drazner, Mark H. [1 ,3 ]
Meyer, Dan M. [4 ]
Mammen, Pradeep P. A. [1 ,3 ,5 ,6 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr Dallas, Heart Failure Ventricular Assist Device & Heart T, NB10-228A,5323 Harry Hines Blvd, Dallas, TX 75390 USA
[4] Methodist Hlth Syst, Lung & Vasc Serv, Dallas, TX 75203 USA
[5] Univ Texas Southwestern Med Ctr Dallas, Hamon Ctr Regenerat Sci & Med, Dallas, TX 75390 USA
[6] Univ Texas Southwestern Med Ctr Dallas, UT Southwestern Senator Paul Wellstone Muscular D, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
DMD-associated cardiomyopathy; Heart failure; LVAD support and multidisciplinary approach;
D O I
10.1002/ehf2.12160
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A young man with Duchenne muscular dystrophy presented to the UT Southwestern Neuromuscular Cardiomyopathy Clinic with advanced heart failure. Despite maximal medical therapy, his cardiac function continued to decline requiring initiation of inotrope therapy. Given the patient's clinical deterioration, a left ventricular assist device (LVAD) was implanted as destination therapy after undergoing a multidisciplinary assessment. The patient tolerated the surgical implantation of the LVAD without any significant complications, and he has had a relatively unremarkable course 38 months post-LVAD implantation. A critical factor contributing to the long-term success of this patient was the decision to select an LVAD that would not disrupt the diaphragm and thus preserve the respiratory muscle strength. This case demonstrates that permanent mechanical LVADs should be considered for appropriately selected Duchenne muscular dystrophy patients with medically refractory end-stage cardiomyopathy.
引用
收藏
页码:379 / 383
页数:5
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