BACKGROUND: Craniofacial reconstructive surgery for craniosynostosis is associated with large blood loss and intraoperative transfusion. This blood loss may continue through the initial postoperative period, potentially resulting in transfusion postoperatively. The purpose of this study is to determine if there is an association between any modifiable intraoperative factors and postoperative blood transfusion in this patient population. METHODS: A cohort of 55 pediatric patients who underwent primary craniofacial reconstruction at Vanderbilt Children's Hospital from January 1, 2013 to April 31, 2014 was analyzed. The authors analyzed 20 different demographic and perioperative variables for statistical associations with postoperative PRBC transfusion using multiple logistic regression with optimal models being selected by Bayesian model averaging. RESULTS: The optimal regression model only included initial PACU Hct as a predictor and showed a significant association between this variable and postoperative PRBC transfusion (odds ratio 0.69, 95% CI 0.55-0.87, P = 0.0016). Based on the average decrease in postoperative hematocrit (Hct) and the postoperative transfusion trigger, an initial PACU Hct threshold of 30 was calculated. In our patient sample, an initial PACU Hct above 30 was associated with a 50% decrease in the absolute risk of receiving a PRBC transfusion postoperatively. CONCLUSIONS: Based on this retrospective analysis, it may be justifiable to transfuse residual volume from previously exposed intraoperative PRBCs to a Hct above 30 to decrease the likelihood of subsequent blood transfusions from different donors in the postoperative period.
BACKGROUND:Craniofacial reconstructive surgery for craniosynostosis is associated with large blood loss and intraoperative transfusion. This blood loss may continue through the initial postoperative period, potentially resulting in transfusion postoperatively. The purpose of this study is to determine if there is an association between any modifiable intraoperative factors and postoperative blood transfusion in this patient population. METHODS: A cohort of 55 pediatric patients who underwent primary craniofacial reconstruction at Vanderbilt Children's Hospital from January 1, 2013 to April 31, 2014 was analyzed. The authors analyzed 20 different demographic and perioperative variables for statistical associations with postoperative PRBC transfusion using multiple logistic regression with optimal models being selected by Bayesian model averaging. RESULTS: The optimal regression model only included initial PACU Hct as a predictor and showed a significant association between this variable and postoperative PRBC transfusion (odds ratio 0.69, 95% CI 0.55-0.87, P = 0.0016). Based on the average decrease in postoperative hematocrit (Hct) and the postoperative transfusion trigger, an initial PACU Hct threshold of 30 was calculated. In our patient sample, an initial PACU Hct above 30 was associated with a 50% decrease in the absolute risk of receiving a PRBC transfusion postoperatively. CONCLUSIONS: Based on this retrospective analysis, it may be justifiable to transfuse residual volume from previously exposed intraoperative PRBCs to a Hct above 30 to decrease the likelihood of subsequent blood transfusions from different donors in the postoperative period.
Authors: Paul A Stricker; John E Fiadjoe; Todd J Kilbaugh; Eric Y Pruitt; Jesse A Taylor; Scott P Bartlett; John J McCloskey Journal: Pediatr Crit Care Med Date: 2012-11 Impact factor: 3.624
Authors: Paul A Stricker; Franklyn P Cladis; John E Fiadjoe; John J McCloskey; Lynne G Maxwell Journal: Paediatr Anaesth Date: 2011-05-20 Impact factor: 2.556
Authors: Nicholas White; Ritchie Marcus; Stephen Dover; Guirish Solanki; Hiroshi Nishikawa; Carol Millar; Edmund D Carver Journal: J Craniofac Surg Date: 2009-03 Impact factor: 1.046
Authors: A Wood; N Wilson; P Skacel; R Thomas; E Tidmarsh; C Yale; M de Silva Journal: Arch Dis Child Fetal Neonatal Ed Date: 1995-01 Impact factor: 5.747
Authors: Thanh T Nguyen; Sarah Hill; Thomas M Austin; Gina M Whitney; John C Wellons; Humphrey V Lam Journal: J Neurosurg Pediatr Date: 2015-07-31 Impact factor: 2.375