Continuous perfusion of donor hearts in the beating state extends preservation time and improves recovery of function

被引:93
作者
Hassanein, WH [1 ]
Zellos, L [1 ]
Tyrrell, TA [1 ]
Healey, NA [1 ]
Crittenden, MD [1 ]
Birjiniuk, V [1 ]
Khuri, SF [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Brockton W Roxbury Vet Adm Med Ctr,Dept Surg, Boston, MA 02115 USA
关键词
D O I
10.1016/S0022-5223(98)00452-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Improving methods of donor heart preservation may permit prolonged storage and remote procurement of cardiac allografts. We hypothesized that continuous, sanguineous perfusion of the donor heart in the beating, working state may prolong myocardial preservation. Methods: We developed a portable perfusion apparatus for use in donor heart preservation. Contractile, metabolic, and vasomotor functions were monitored simultaneously in an isolated swine heart. The metabolic state was monitored by myocardial tissue pH. Vasomotor function was assessed in isolated coronary ring chambers. Hearts were randomized into 3 groups: group I(n = 5), cardioplegic arrest, 12-hour storage at 4 degrees C with modified BeIzer solution, and 2-hour sanguineous reperfusion in the working state; group II (n = 6), 12-hour continuous perfusion in the beating working state, 30 minutes of arrest (to simulate re-implantation time), and 2 hours of reperfusion, as above; group III (n = 7), coronary ring control hearts. Results: At 2 hours of reperfusion, left ventricular developed pressure in group II was higher than in group I (mean +/- standard deviation: 90 +/- 6 mm Hg, 53 +/- 15 mm Hg, P = .005). Significantly less myocardial edema was observed in group II than in group I(73% +/- 4%, 80% +/- 1% water content, P = .01). Significantly less myocardial acidosis was noted in group II than in group I during preservation (pH 7.3 +/- 0.01, 6.1 +/- 0.03, P < .001) and reperfusion (pH 7.3 +/- 0.008, 6.8 +/- 0.05, P < .001). Coronary endothelial vasomotor function was better preserved in group II than in group I as evidenced by dose-response relaxation of coronary rings to 10(-8) mol/L bradykinin (37%, 55% Delta baseline, P = .01). Conclusion: This new method extends the current preservation limit and avoids time-dependent ischemic injury, thereby allowing for distant procurement of donor organs.
引用
收藏
页码:821 / 829
页数:9
相关论文
共 23 条
[1]  
AXFORD TC, 1992, J THORAC CARDIOV SUR, V103, P902
[2]   PRINCIPLES OF SOLID-ORGAN PRESERVATION BY COLD-STORAGE [J].
BELZER, FO ;
SOUTHARD, JH .
TRANSPLANTATION, 1988, 45 (04) :673-676
[3]  
BURT JM, 1986, J THORAC CARDIOV SUR, V92, P238
[4]   Twelve-hour canine heart preservation with a simple, portable hypothermic organ perfusion device [J].
Calhoon, JH ;
Bunegin, L ;
Gelineau, JF ;
Felger, MC ;
Naples, JJ ;
Miller, OL ;
Sako, EY .
ANNALS OF THORACIC SURGERY, 1996, 62 (01) :91-93
[5]  
CHIEN S, 1991, J HEART LUNG TRANSPL, V10, P401
[6]  
CHIEN S, 1988, J THORAC CARDIOV SUR, V95, P55
[7]   CARDIAC TRANSPLANT DONOR HEART ALLOCATION BASED ON PROSPECTIVE TISSUE MATCHING [J].
DISESA, VJ ;
MULL, R ;
DALY, ES ;
EDMUNDS, LH ;
MANCINI, DM ;
EISEN, HJ .
ANNALS OF THORACIC SURGERY, 1994, 58 (04) :1050-1053
[8]  
DRINKWATER DC, 1995, J HEART LUNG TRANSPL, V14, P891
[9]   COMPARISON OF DIFFERENT TECHNIQUES OF HYPOTHERMIC PIG-HEART PRESERVATION [J].
FERRERA, R ;
LARESE, A ;
MARCSEK, P ;
GUIDOLLET, J ;
VERDYS, M ;
DITTMAR, A ;
DUREAU, G .
ANNALS OF THORACIC SURGERY, 1994, 57 (05) :1233-1239
[10]  
FOLLETTE DM, 1978, J THORAC CARDIOV SUR, V76, P604