Perioperative Transfusions and Venous Thromboembolism
Annual incidence of venous thromboembolism (VTE) including postoperative VTE in hospitalized children is rising significantly. A growing body of evidence supports the role of red blood cells (RBCs) in pathologic thrombosis. In this study, we examined the association of perioperative RBC transfusion...
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Published in | Pediatrics (Evanston) Vol. 145; no. 4 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
01.04.2020
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Abstract | Annual incidence of venous thromboembolism (VTE) including postoperative VTE in hospitalized children is rising significantly. A growing body of evidence supports the role of red blood cells (RBCs) in pathologic thrombosis. In this study, we examined the association of perioperative RBC transfusion with postoperative VTE in pediatric patients.
The pediatric databases of the American College of Surgeons' National Surgical Quality Improvement Project from 2012 to 2017 were used. Multivariable logistic regression was used to examine the association between perioperative RBC transfusion status and the development of new or progressive VTE within 30 days of surgery. The analyses were age stratified, as follows: neonates (≤28 days), infants (>28 days and <1 year), and children (≥1 year).
In this study, we included 20 492 neonates, 79 744 infants, and 382 862 children. Postoperative development of VTE was reported in 99 (0.48%) neonates, 147 (0.2%) infants, and 374 (0.1%) children. In all age groups, development of VTE was significantly more common among patients with a perioperative RBC transfusion than patients without a perioperative RBC transfusion (neonates: adjusted odds ratio [aOR] = 4.1, 95% confidence interval [CI] = 2.5-6.7; infants: aOR = 2.4, 95% CI = 1.7-3.6; children: aOR = 2.2, 95% CI = 1.7-2.9). Among children who received an intra- or postoperative transfusion, the weight-based volume of RBCs (mL/kg) transfused was associated with postoperative VTE in a dose-dependent manner: second tertile (odds ratio = 2.3, 95% CI = 1.3-4.1) and third tertile (odds ratio = 4.1, 95% CI = 2.3-7.4) versus first tertile.
Perioperative RBC transfusions are independently associated with development of new or progressive postoperative VTE in children, infants, and neonates. These findings need further validation in prospective studies and emphasize the need for evidence-based perioperative pediatric blood transfusion decisions. |
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AbstractList | Annual incidence of venous thromboembolism (VTE) including postoperative VTE in hospitalized children is rising significantly. A growing body of evidence supports the role of red blood cells (RBCs) in pathologic thrombosis. In this study, we examined the association of perioperative RBC transfusion with postoperative VTE in pediatric patients.
The pediatric databases of the American College of Surgeons' National Surgical Quality Improvement Project from 2012 to 2017 were used. Multivariable logistic regression was used to examine the association between perioperative RBC transfusion status and the development of new or progressive VTE within 30 days of surgery. The analyses were age stratified, as follows: neonates (≤28 days), infants (>28 days and <1 year), and children (≥1 year).
In this study, we included 20 492 neonates, 79 744 infants, and 382 862 children. Postoperative development of VTE was reported in 99 (0.48%) neonates, 147 (0.2%) infants, and 374 (0.1%) children. In all age groups, development of VTE was significantly more common among patients with a perioperative RBC transfusion than patients without a perioperative RBC transfusion (neonates: adjusted odds ratio [aOR] = 4.1, 95% confidence interval [CI] = 2.5-6.7; infants: aOR = 2.4, 95% CI = 1.7-3.6; children: aOR = 2.2, 95% CI = 1.7-2.9). Among children who received an intra- or postoperative transfusion, the weight-based volume of RBCs (mL/kg) transfused was associated with postoperative VTE in a dose-dependent manner: second tertile (odds ratio = 2.3, 95% CI = 1.3-4.1) and third tertile (odds ratio = 4.1, 95% CI = 2.3-7.4) versus first tertile.
Perioperative RBC transfusions are independently associated with development of new or progressive postoperative VTE in children, infants, and neonates. These findings need further validation in prospective studies and emphasize the need for evidence-based perioperative pediatric blood transfusion decisions. |
Author | Ness, Paul M Gehrie, Eric A Lokhandwala, Parvez M Tobian, Aaron A R Makhani, Sarah Petersen, Molly R Goel, Ruchika Josephson, Cassandra D Frank, Steven M Shaz, Beth H Nellis, Marianne M Bloch, Evan M Patel, Eshan U Patel, Ravi M Karam, Oliver |
Author_xml | – sequence: 1 givenname: Ruchika surname: Goel fullname: Goel, Ruchika organization: Departments of Internal Medicine and Pediatrics, School of Medicine, Southern Illinois University and Mississippi Valley Regional Blood Center, Springfield, Illinois – sequence: 2 givenname: Cassandra D surname: Josephson fullname: Josephson, Cassandra D email: cjoseph@emory.edu organization: Department of Pediatrics, Children's Healthcare of Atlanta and School of Medicine, Emory University, Atlanta, Georgia – sequence: 3 givenname: Eshan U surname: Patel fullname: Patel, Eshan U organization: Division of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland – sequence: 4 givenname: Molly R surname: Petersen fullname: Petersen, Molly R organization: Division of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland – sequence: 5 givenname: Sarah surname: Makhani fullname: Makhani, Sarah organization: Herbert Wertheim College of Medicine, Florida International University, Miami, Florida – sequence: 6 givenname: Steven M surname: Frank fullname: Frank, Steven M organization: Department of Anesthesiology, Johns Hopkins Hospital, Baltimore, Maryland – sequence: 7 givenname: Paul M surname: Ness fullname: Ness, Paul M organization: Division of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland – sequence: 8 givenname: Evan M surname: Bloch fullname: Bloch, Evan M organization: Division of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland – sequence: 9 givenname: Eric A surname: Gehrie fullname: Gehrie, Eric A organization: Division of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland – sequence: 10 givenname: Parvez M surname: Lokhandwala fullname: Lokhandwala, Parvez M organization: Division of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland – sequence: 11 givenname: Marianne M surname: Nellis fullname: Nellis, Marianne M organization: Department of Pediatrics, Weill Cornell Medicine, New York, New York – sequence: 12 givenname: Oliver surname: Karam fullname: Karam, Oliver organization: Department of Pediatrics, Children's Hospital of Richmond at Virginia Commonwealth University, Richmond, Virginia; and – sequence: 13 givenname: Beth H surname: Shaz fullname: Shaz, Beth H organization: New York Blood Center, New York, New York – sequence: 14 givenname: Ravi M surname: Patel fullname: Patel, Ravi M organization: Department of Pediatrics, Children's Healthcare of Atlanta and School of Medicine, Emory University, Atlanta, Georgia – sequence: 15 givenname: Aaron A R surname: Tobian fullname: Tobian, Aaron A R organization: Division of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland |
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Title | Perioperative Transfusions and Venous Thromboembolism |
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