Blood transfusions are associated with increased risk for development of sepsis in severely burned pediatric patients

被引:63
作者
Jeschke, Marc G. [1 ]
Chinkes, David L.
Finnerty, Celeste C.
Przkora, Rene
Pereira, Clifford T.
Herndon, David N.
机构
[1] Univ Texas, Med Branch, Shriners Hosp Children, Galveston, TX 77550 USA
[2] Univ Texas, Med Branch, Dept Surg, Galveston, TX 77550 USA
关键词
sepsis; burn; cytokines; pediatric; inflammation; trauma;
D O I
10.1097/01.CCM.0000253812.09236.98
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective. To determine the risk of developing sepsis following transfusion of blood products in severely burned pediatric patients. Design: Retrospective, cohort study. Setting. Shriners Hospital for Children and University Hospital. Patients: Severely burned pediatric patients with >30% total body surface area (TBSA) burn. Interventions. None. Measurements and Main Results: Two hundred seventy-seven pediatric burn patients over a period of 7 yrs (1997-2004) were included in the study, with 25 patients being septic at admission and therefore excluded. Patients were stratified according to TBSA burn and presence or absence of inhalation injury. The amounts of packed red blood cells (RBCs) and fresh frozen plasma (FFP) were recorded during hospital stay before the development of sepsis. Blood product administration was normalized for the number of surgeries and divided into two groups: high (RBCs >20/FFP >5) or low (RBCs <20/FFP <5) amount of blood products. Sepsis was diagnosed based on the criteria set by the Society of Critical Care Medicine in conjunction with positive blood culture or presence of organisms in the organs at autopsy. By stratifying the groups into low and high blood transfusion, we found that patients with >60% TBSA burn with inhalation injury have an 8% risk of developing sepsis in the low RBC group, which increases to 58% in the high RBC group (p <.05). Similar results were found for RBCs per operation, FFP, and FFP per operation (p <.05). There were no differences in age and gender between groups. Conclusions: Pediatric burn suffering from a 60% TBSA burn with concomitant inhalation injury are more likely to develop sepsis if they are given high amounts of blood products, indicating an immunocompromised state following blood transfusion.
引用
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页码:579 / 583
页数:5
相关论文
共 25 条
[1]  
Alvarez G, 2001, CRIT CARE, V5, P56
[2]   Red cell transfusion practice following the transfusion requirements in critical care (TRICC) study: prospective observational cohort study in a large UK intensive care unit [J].
Chohan, SS ;
McArdle, F ;
McClelland, DBL ;
Mackenzie, SJ ;
Walsh, TS .
VOX SANGUINIS, 2003, 84 (03) :211-218
[3]   The CRIT Study: Anemia and blood transfusion in the critically ill - Current clinical practice in the United States [J].
Corwin, HL ;
Gettinger, A ;
Pearl, RG ;
Fink, MP ;
Levy, MM ;
Abraham, E ;
MacIntyre, NR ;
Shabot, M ;
Duh, MS ;
Shapiro, MJ .
CRITICAL CARE MEDICINE, 2004, 32 (01) :39-52
[4]   RELATIONSHIP OF TRANSFUSION AND INFECTION IN A BURN POPULATION [J].
GRAVES, TA ;
CIOFFI, WG ;
MASON, AD ;
MCMANUS, WF ;
PRUITT, BA .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1989, 29 (07) :948-954
[5]   Effects of early excision and aggressive enteral feeding on hypermetabolism, catabolism, and sepsis after severe burn [J].
Hart, DW ;
Wolf, SE ;
Chinkes, DL ;
Beauford, RB ;
Mlcak, RP ;
Heggers, JP ;
Wolfe, RR ;
Herndon, DN .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2003, 54 (04) :755-761
[6]   Determinants of blood loss during primary burn excision [J].
Hart, DW ;
Wolf, SE ;
Beauford, RB ;
Lal, S ;
Chinkes, DL ;
Herndon, DN .
SURGERY, 2001, 130 (02) :396-402
[7]   Does transfusion practice affect mortality in critically ill patients? [J].
Hebert, PC ;
Wells, G ;
Tweeddale, M ;
Martin, C ;
Marshall, J ;
Pham, B ;
Blajchman, M ;
Schweitzer, I ;
Pagliarello, G .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 155 (05) :1618-1623
[8]  
Hebert PC, 1998, BRIT J ANAESTH, V81, P25
[9]  
Hebert PC, 2000, VOX SANG, V78, P167
[10]  
Herndon D N, 1989, J Burn Care Rehabil, V10, P309, DOI 10.1097/00004630-198907000-00004