Outcomes of Adult Patients with Small Body Size Supported with a Continuous-Flow Left Ventricular Assist Device

被引:14
|
作者
Lee, Sangjin [1 ]
Katz, Jason N. [2 ,3 ]
Jorde, Ulrich P. [4 ]
Moazami, Nader [5 ,6 ]
John, Ranjit [7 ]
Sundareswaran, Kartik S. [8 ]
Farrar, David J. [8 ]
Frazier, O. H. [9 ]
机构
[1] Spectrum Hlth, Richard DeVos Heart & Lung Transplant Program, Grand Rapids, MI USA
[2] Univ N Carolina, Ctr Heart & Vasc Care, Div Cardiol, Chapel Hill, NC USA
[3] Univ N Carolina, Ctr Heart & Vasc Care, Div Pulm & Crit Care Med, Chapel Hill, NC USA
[4] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Div Cardiol, Bronx, NY 10467 USA
[5] Cleveland Clin, Dept Thorac & Cardiovasc Surg, Cleveland, OH 44106 USA
[6] Cleveland Clin, Dept Biomed Engn, Cleveland, OH 44106 USA
[7] Univ Minnesota, Div Cardiothorac Surg, Minneapolis, MN USA
[8] St Jude Med, Res & Sci Affairs, St Paul, MN USA
[9] Texas Heart Inst, Ctr Cardiac Support, Cardiovasc Surg Res, Cullen Cardiovasc Res Labs, Houston, TX 77025 USA
关键词
LVAD; BSA; BMI; INTERMACS; HeartMate II; INTERMACS ANNUAL-REPORT; DRUG ADMINISTRATION-APPROVAL; CIRCULATORY SUPPORT; INTERAGENCY REGISTRY; DESTINATION THERAPY; TRANSPLANTATION; BRIDGE; HEART; FOOD;
D O I
10.1097/MAT.0000000000000430
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There is insufficient data on patients with small body size to determine if this should be considered a risk factor for continuous-flow left ventricular assist device (CF-LVAD) support. We sought to evaluate survival outcomes, adverse events, and functional status of CF-LVAD patients with body surface area (BSA) <1.5 m(2) in a large national registry. Adults with BSA <1.5 m(2) (n = 128) implanted with a HeartMate II (HMII)-LVAD from the Interagency Registry for Mechanically Assisted Circulatory Support registry from April 2008 to December 2012 formed this cohort. Outcomes were compared with HMII bridge to transplant (BTT) and destination therapy (DT) post approval studies. The majority of patients were female (n = 106, 83%). A total of 64% (n = 82) were implanted for BTT and 36% (n = 46) for DT. The median BSA (range) was 1.44 (1.19-1.49) and 1.45 (1.25-1.49) m(2) for BTT and DT, respectively. Overall survival 1 year post implant was 81% +/- 5% for BTT and 84% +/- 6% for DT. The most common adverse events for BTT and DT patients were bleeding (0.91, 0.88 events/patient year) and driveline infection (16%, 0.28 events/patient year). Six months post implantation, 87% of BTT and 77% of DT patients were New York Heart Association functional class I or II. Post implant survival, functional status improvement, and adverse event profile for adult BTT and DT HMII patients with BSA < 1.5 m(2) are favorable and comparable with outcomes published in the overall patient population.
引用
收藏
页码:646 / 651
页数:6
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