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Do vasoactive medications impact donor hearts clinical outcomes in pediatric heart transplantation?
被引:0
|作者:
Blitzer, David
[1
]
Lirette, Seth
[2
]
Kane, Lauren
[3
]
Copeland, Jack G.
[4
]
Baran, David A.
[5
]
Copeland, Hannah
[6
,7
,8
,9
,10
]
机构:
[1] Columbia Univ, Dept Surg, Div Cardiovasc Surg, New York, NY USA
[2] Fulcrum, Jackson, MS USA
[3] TransMedics Inc, Div Cardiothorac Surg, Andover, MA USA
[4] Univ Arizona, Dept Surg, Tucson, AZ USA
[5] Cleveland Clin, Heart Vasc & Thorac Inst, Weston, FL USA
[6] Lutheran Hosp, Ft Wayne, IN USA
[7] Indiana Univ Sch Med, Ft Wayne, IN USA
[8] Lutheran Hosp, Heart Transplantat & Mech Circulatory Support, IN 7910,W Jefferson Blvd,MOB 2,Suite 102, Ft Wayne, IN 46804 USA
[9] Lutheran Hosp, Extracorporeal Membrane Oxygenat, IN 7910,W Jefferson Blvd,MOB 2,Suite 102, Ft Wayne, IN 46804 USA
[10] Indiana Univ Sch Med, Surg, Ft Wayne, IN 46805 USA
关键词:
critical care;
heart donor;
heart transplant;
pediatric;
INTERNATIONAL SOCIETY;
SURVIVAL;
REGISTRY;
FAILURE;
D O I:
10.1111/petr.14500
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
ObjectivesThere is limited data examining donor vasopressor and/or inotrope medications (vasoactives) on pediatric orthotopic heart transplant (OHT) outcomes. We aim to evaluate the effects of vasoactives on pediatric OHT outcomes. MethodsThe United Network for Organ Sharing database was retrospectively reviewed from January 2000 to March 2018 for donor hearts. Exclusion criteria included multiorgan transplants and recipient age >18. Donors receiving vasoactives at the time of procurement were compared to donors not on vasoactives, including the number of vasoactives and the type. End-points of interest were survival at 30 days and 1 year as well as post-transplant rejection at 1 year. Logistic and Cox models were used to quantify survival end-points. ResultsOf 6462 donors, 3187 (49.3%) were receiving at least one vasoactive. Comparing any vasoactive medication versus none, there was no difference in 30-day survival (p = .27), 1 year survival (p = .89), overall survival (p = .68), or post-transplant rejection (p = .98). There was no difference in 30-day survival for donors receiving 2 or more vasoactive infusions (p = .89), 1 year survival (p = .53), overall survival (p = .75), or post-transplant rejection at 1 year (p = .87). Vasopressin was associated with decreased 30-day mortality (OR = 0.22; p = .028), dobutamine with decreased 1-year mortality (OR = 0.37; p = .036), overall survival (HR = 0.51; p = .003), and decreased post-transplant rejection (HR = 0.63; p = .012). ConclusionsThere is no difference in pediatric OHT outcomes when the cardiac donor is treated with vasoactive infusions at procurement. Vasopressin and dobutamine were associated with improved outcomes. This information can be used to guide medical management and donor selection.
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