Age of transfused blood is an independent risk factor for postinjury multiple organ failure

被引:414
作者
Zallen, G
Offner, PJ
Moore, EE
Blackwell, J
Ciesla, DJ
Gabriel, J
Denny, C
Silliman, CC
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Surg, Denver Hlth Med Ctr, Denver, CO 80204 USA
[2] Bonfils Blood Ctr, Denver, CO USA
关键词
D O I
10.1016/S0002-9610(99)00239-1
中图分类号
R61 [外科手术学];
学科分类号
摘要
BACKGROUND: Blood transfusion has repeatedly been demonstrated to be an independent risk factor for postinjury multiple organ failure (MOF). Previously believed to represent a surrogate for shock, packed red blood cell (PRBC) transfusion has recently been shown to result in neutrophil priming and pulmonary endothelial cell activation. We have previously observed that the generation of inflammatory mediators is related to the length of PRBC unit storage. The purpose of this study was to determine if age of transfused PRBC is a risk factor for the development of postinjury MOF. METHODS: Using our prospective database of trauma patients at risk for developing MOF, we identified patients who developed MOF (MOF+) and received 6 to 20 units of PRBCs in the first 12 hours following injury. A similar cohort of patients, matched for ISS and transfusion requirement, who did not develop MOF (MOF-) were also identified. The age of each unit of PRBC transfused in the first 6 hours was determined, Multiple logistic regression was performed to determine if age of transfused blood is an independent risk factor. RESULTS: Sixty-three patients were identified, 23 of whom were MOF+, There was no difference in ISS and transfusion requirement between MOF+ and MOF- groups. MOF+ patients, however, were significantly older (46 +/- 4.7 years versus 33 +/- 2.3 years). Moreover, mean age of transfused blood was greater in the MOF+ patients (30.5 +/- 1.6 days versus 24 +/- 0.5 days). Similarly, the mean number of units older than 14 and 21 days old were greater in the MOF+ patients. Multivariate analysis identified mean age of blood, number of units older than 14 days, and number of units older than 21 days as independent risk factors for MOF, CONCLUSION: The age of transfused PRBCs transfused in the first 6 hours is an independent risk factor for postinjury MOF, This suggests that current blood bank processing and storage technique should be reexamined. Moreover, fresh blood may be more appropriate for the initial resuscitation of trauma patients requiring transfusion. Am J Surg, 1999;178:570-572, (C) 1999 by Excerpta Medica, Inc.
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页码:570 / 572
页数:3
相关论文
共 10 条
[1]   Cytokines in stored red blood cell concentrates: Promoters of systemic inflammation and simulators of acute transfusion reactions? [J].
Kristiansson, M ;
Soop, M ;
Saraste, L ;
Sundqvist, KG .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1996, 40 (04) :496-501
[2]   Neutrophil transmigration across monolayers of endothelial cells and airway endothelial cells is regulated by different mechanisms [J].
Liu, LX ;
Mul, FPJ ;
Kuijpers, TW ;
Lutter, R ;
Roos, D ;
Knol, EF .
CYTOKINES AND ADHESION MOLECULES IN LUNG INFLAMMATION, 1996, 796 :21-29
[3]  
Moore FA, 1997, ARCH SURG-CHICAGO, V132, P620
[4]   EVOLVING CONCEPTS IN THE PATHOGENESIS OF POSTINJURY MULTIPLE ORGAN FAILURE [J].
MOORE, FA ;
MOORE, EE .
SURGICAL CLINICS OF NORTH AMERICA, 1995, 75 (02) :257-277
[5]   Multiple organ failure can be predicted as early as 12 hours after injury [J].
Sauaia, A ;
Moore, FA ;
Moore, EE ;
Norris, JM ;
Lezotte, DC ;
Hamman, RF .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1998, 45 (02) :291-301
[6]  
SAUAIA A, 1994, ARCH SURG-CHICAGO, V129, P39
[7]   Plasma and lipids from stored packed red blood cells cause acute lung injury in an animal model [J].
Silliman, CC ;
Voelkel, NF ;
Allard, JD ;
Elzi, DJ ;
Tuder, RM ;
Johnson, JL ;
Ambruso, DR .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (07) :1458-1467
[8]   The association of biologically active lipids with the development of transfusion-related acute lung injury: A retrospective study [J].
Silliman, CC ;
Paterson, AJ ;
Dickey, WO ;
Stroncek, DF ;
Popovsky, MA ;
Caldwell, SA ;
Ambruso, DR .
TRANSFUSION, 1997, 37 (07) :719-726
[9]  
Silliman CC, 1998, TRANSFUSION, V38, p96S
[10]  
SILLIMAN CC, 1994, J LAB CLIN MED, V124, P684