Modified ultrafiltration attenuates dilutional coagulopathy in pediatric open heart operations

被引:55
作者
Friesen, RH
Campbell, DN
Clarke, DR
Tornabene, MA
机构
[1] Univ Colorado, Childrens Hosp, Dept Anesthesiol, Denver, CO 80218 USA
[2] Univ Colorado, Childrens Hosp, Dept Cardiothorac Surg, Denver, CO 80218 USA
关键词
D O I
10.1016/S0003-4975(97)00921-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Extreme hemodilution caused by relatively large prime volumes required for cardiopulmonary bypass in infants causes a dilutional coagulopathy, characterized by low concentrations of fibrinogen and other circulating coagulation factors. Modified ultrafiltration results in hemoconcentration and is associated with decreases in postoperative bleeding and transfusion requirements in children. This study was undertaken to quantify the effect of modified ultrafiltration on concentrations of fibrinogen, plasma proteins, and platelets in infants and small children. Methods. Twenty patients less than 15 kg were studied. Cardiopulmonary bypass circuits were primed with crystalloid solutions. Red blood cells were added during cardiopulmonary bypass for hematocrits less than 15%. Colloid solutions were not administered. Concentrations of fibrinogen, plasma proteins, and platelets, and hematocrit were measured before cardiopulmonary bypass, before modified ultrafiltration, and after modified ultrafiltration. Results. Modified ultrafiltration was associated with significant (p < 0.001) increases in hematocrit (19% +/- 6% to 31% +/- 9%), fibrinogen (65 +/- 29 to 101 +/- 45 mg/dL), and total plasma proteins (2.7 +/- 0.3 to 4.9 +/- 0.7 g/dL), but no change (p = 0.129) in platelet count. Conclusions. We conclude that modified ultrafiltration significantly attenuates the dilutional coagulopathy associated with cardiopulmonary bypass in infants. (C) 1997 by The Society of Thoracic Surgeons.
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收藏
页码:1787 / 1789
页数:3
相关论文
共 11 条
[1]   ULTRAFILTRATION AND MODIFIED ULTRAFILTRATION IN PEDIATRIC OPEN-HEART OPERATIONS [J].
ELLIOTT, MJ .
ANNALS OF THORACIC SURGERY, 1993, 56 (06) :1518-1522
[2]  
HARKER LA, 1980, BLOOD, V56, P824
[3]  
HENRIKSSON P, 1979, BRIT HEART J, V41, P23
[4]   High-volume, zero-balanced hemofiltration to reduce delayed inflammatory response to cardiopulmonary bypass in children [J].
Joumois, D ;
IsraelBiet, D ;
Pouard, P ;
Rolland, B ;
Silvester, W ;
Vouhe, P ;
Safran, D .
ANESTHESIOLOGY, 1996, 85 (05) :965-976
[5]  
JOURNOIS D, 1994, ANESTHESIOLOGY, V81, P1181, DOI 10.1097/00000542-199411000-00011
[6]   COAGULATION DEFECTS IN NEONATES DURING CARDIOPULMONARY BYPASS [J].
KERN, FH ;
MORANA, NJ ;
SEARS, JJ ;
HICKEY, PR .
ANNALS OF THORACIC SURGERY, 1992, 54 (03) :541-546
[7]   COMPARISON OF THE HEMOSTATIC EFFECTS OF FRESH WHOLE-BLOOD, STORED WHOLE-BLOOD, AND COMPONENTS AFTER OPEN-HEART-SURGERY IN CHILDREN [J].
MANNO, CS ;
HEDBERG, KW ;
KIM, HC ;
BUNIN, GR ;
NICOLSON, S ;
JOBES, D ;
SCHWARTZ, E ;
NORWOOD, WI .
BLOOD, 1991, 77 (05) :930-936
[8]  
MOHR R, 1986, J THORAC CARDIOV SUR, V92, P434
[9]  
NAIK S K, 1991, Perfusion (London), V6, P41, DOI 10.1177/026765919100600106
[10]  
NAIK SK, 1991, CIRCULATION, V84, P422