Pharmacotherapeutic Management of Gastrointestinal Bleeding in Patients with Continuous-Flow Left Ventricular Assist Devices

被引:26
|
作者
Sieg, Adam C. [1 ]
Moretz, Jeremy D. [2 ]
Horn, Edward [3 ]
Jennings, Douglas L. [4 ]
机构
[1] Univ Kentucky, Dept Pharm, Lexington, KY USA
[2] Vanderbilt Univ, Med Ctr, Dept Pharm, Nashville, TN USA
[3] Allegheny Gen Hosp, Dept Pharm, Pittsburgh, PA 15212 USA
[4] Columbia Univ, Med Ctr, Dept Pharm, New York Presbyterian Hosp, New York, NY USA
来源
PHARMACOTHERAPY | 2017年 / 37卷 / 11期
关键词
gastrointestinal bleeding; octreotide; thalidomide; anticoagulation; continuous-flow left ventricular assist device; VON-WILLEBRAND-SYNDROME; ARTERIOVENOUS-MALFORMATIONS; FACTOR DEGRADATION; RISK; OCTREOTIDE; ANGIODYSPLASIA; INHIBITORS; DISEASE; SAFETY; PUMP;
D O I
10.1002/phar.2016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Continuous-flow left ventricular assist devices (CF-LVADs) have become an integral component of the management in patients with advanced heart failure, serving as destination therapy or as a bridge to heart transplantation. Despite significant advances in the design and longevity of the device, the ongoing risk for bleeding remains a significant concern. The genesis of gastrointestinal bleeding (GIB) in patients with CF-LVADs is likely multifactorial and may include components of acquired von Willebrand disease, angiodysplasia, and gastrointestinal arteriovenous malformations, as well as additional risk factors such as history of GIB and increased age. Several pharmacotherapy options have been used, but the data surrounding their overall efficacy remain sparse. The necessity for larger prospective studies is essential to further advance the management of this devastating complication. Within this review, we discuss the known pathophysiologic process of CF-LVAD-related GIB and highlight the therapeutic options discussed within the literature. In addition, we discuss potential therapeutic options based on mechanisms of action as they correlate to known pathophysiologic processes of CF-LVAD-related GIB. Finally, we provide recommendations for constructing drug therapy regimens in patients with CF-LVADs who develop GIB.
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页码:1432 / 1448
页数:17
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