2019
DOI: 10.1213/xaa.0000000000000917
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Heparin Resistance due to an Acquired Antithrombin Deficiency in a Patient With Sickle Cell Disease During a Pregnancy Complicated by Bilateral Pulmonary Emboli: A Case Report

Abstract: We report a 31-year-old woman with sickle beta thalassemia zero who presented at 21 weeks gestational age with multiple bilateral pulmonary emboli and no hemodynamic instability. Acquired antithrombin deficiency was suspected due to a refractory response to therapeutic anticoagulation with enoxaparin, unfractionated heparin, and fondaparinux, and a reduced antithrombin antigen level. At 26 4/7 weeks, she developed signs concerning for increased pulmonary clot burden. To avoid the use of alternative anticoagula… Show more

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(4 citation statements)
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“…The more common coagulopathic presentation of systemic autoimmune diseases is a hypercoagulable state. It is well described that systemic lupus erythematosus patients can develop specific antibodies such as lupus anticoagulant, antiphospholipid syndrome, antiprothrombin, and No abnormal variables documented CT: # 154,155 CFT: # [154][155][156] A: " 155 MCF: " [154][155][156][157] VET variables were more hypercoagulable in splenectomized thalassemic patients compared to nonsplenectomized 154,156,157 There is no predisposition to hypercoagulability in children with hereditary spherocytosis unless the child has had a splenectomy 158 Sickle cell disease R: # [159][160][161] K: # 160,161 A: " 159,160 MA: " 159,160 CI: " 159,160 CT: # 162 MCF: " 162,163 Sickle 162,163 No difference in VET variables between SCT and NC 161 Treatments guided by VETs:…”
Section: Systemic Autoimmune Diseasesmentioning
confidence: 99%
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“…The more common coagulopathic presentation of systemic autoimmune diseases is a hypercoagulable state. It is well described that systemic lupus erythematosus patients can develop specific antibodies such as lupus anticoagulant, antiphospholipid syndrome, antiprothrombin, and No abnormal variables documented CT: # 154,155 CFT: # [154][155][156] A: " 155 MCF: " [154][155][156][157] VET variables were more hypercoagulable in splenectomized thalassemic patients compared to nonsplenectomized 154,156,157 There is no predisposition to hypercoagulability in children with hereditary spherocytosis unless the child has had a splenectomy 158 Sickle cell disease R: # [159][160][161] K: # 160,161 A: " 159,160 MA: " 159,160 CI: " 159,160 CT: # 162 MCF: " 162,163 Sickle 162,163 No difference in VET variables between SCT and NC 161 Treatments guided by VETs:…”
Section: Systemic Autoimmune Diseasesmentioning
confidence: 99%
“…• Heparin/protamine 162,163 • Chronic transfusion therapy 159 • Exchange blood transfusion 160 • Hydroxyurea therapy 159 • Hydroxycarbamide 160 • Ameliorating therapy 160 HbSC anticardiolipin; these antibodies often result in coagulopathies. These antibodies or the disease itself pose a risk for venous thomboembolic events and pregnancy-related complications.…”
Section: Systemic Autoimmune Diseasesmentioning
confidence: 99%
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