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1.
Ann Thorac Surg ; 113(2): e119-e121, 2022 02.
Article in English | MEDLINE | ID: mdl-33964253

ABSTRACT

This case highlights the need for accurate and rapid testing for severe acute respiratory syndrome coronavirus 2 and also underscores the need for caregivers to remain vigilant for coronavirus disease 2019 in the postoperative setting despite negative preoperative testing.


Subject(s)
COVID-19/therapy , Heart Defects, Congenital/surgery , Postoperative Complications/therapy , SARS-CoV-2 , Extracorporeal Membrane Oxygenation , Humans , Infant , Male
2.
Pediatr Crit Care Med ; 16(1): 66-74, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25319630

ABSTRACT

OBJECTIVES: To determine if a comprehensive extracorporeal membrane oxygenation anticoagulation monitoring protocol results in fewer hemorrhagic complications, reduced blood product usage, and increased circuit life. DESIGN: In September 2011, we augmented our standard extracorporeal membrane oxygenation laboratory protocol to include anti-factor Xa assays, thromboelastography, and antithrombin measurements. We performed a retrospective chart review to determine outcomes for patients placed on extracorporeal membrane oxygenation prior to and after the initiation of our anticoagulation laboratory protocol. SETTING: Tertiary care, academic children's hospital. PATIENTS: All patients who were placed on extracorporeal membrane oxygenation at our institution from January 1, 2007, to September 30, 2013. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: There were 261 extracorporeal membrane oxygenation runs before the initiation of the protocol and 105 extracorporeal membrane oxygenation runs after the initiation of the protocol. There were no major changes to our extracorporeal membrane oxygenation circuit or changes to our transfusion threshold during the study period. The indication for extracorporeal membrane oxygenation, age, and severity of illness of the patients were similar before and after protocol initiation. Median blood product usage for packed RBCs, fresh frozen plasma, platelets, and cryoprecipitate decreased significantly after protocol initiation. The occurrence of cannula site bleeding decreased from 22% to 12% (p = 0.04), and surgical site bleeding decreased from 38% to 25% (p = 0.02). Median extracorporeal membrane oxygenation circuit life increased from 3.6 to 4.3 days (p = 0.02). A trend toward increased patient survival was noted, but it did not reach statistical significance. CONCLUSIONS: We demonstrate an association between an extracorporeal membrane oxygenation anticoagulation laboratory protocol using anti-factor Xa assays, thromboelastography, and antithrombin measurements and a decrease in blood product transfusion, a decrease in hemorrhagic complications, and an increase in circuit life. To our knowledge, this is the first study to demonstrate clinical benefit associated with the use of these laboratory values for patients on extracorporeal membrane oxygenation.


Subject(s)
Anticoagulants/therapeutic use , Extracorporeal Membrane Oxygenation/adverse effects , Hemorrhage/etiology , Blood Coagulation , Blood Transfusion , Child , Child, Preschool , Female , Hospitals, Pediatric , Humans , Infant , Male , Retrospective Studies , Thrombelastography
3.
J Pediatr Hematol Oncol ; 37(1): e63-6, 2015 Jan.
Article in English | MEDLINE | ID: mdl-24878619

ABSTRACT

Ceftriaxone is a frequently used empiric antibiotic in children. Acute hemolysis is a rare side effect of ceftriaxone therapy associated with a high mortality rate. A 14-year-old boy suffering from Crohn disease developed bacterial pneumonia that was treated with ceftriaxone. We report successful management of ceftriaxone-induced hemolytic anemia (CIHA) in this patient and review the CIHA literature in pediatric patients. Early recognition of CIHA with prompt discontinuation of ceftriaxone therapy may have a beneficial role in reduction of high mortality seen in these patients.


Subject(s)
Anemia, Hemolytic/chemically induced , Anti-Bacterial Agents/adverse effects , Ceftriaxone/adverse effects , Adolescent , Anemia, Hemolytic/therapy , Humans , Male
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