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1.
Thromb Res ; 210: 20-25, 2022 Feb.
Article in English | MEDLINE | ID: mdl-34968851

ABSTRACT

INTRODUCTION: Venous thromboembolism (VTE) is an important cause of maternal morbidity and mortality. During pregnancy, VTE is treated with low-molecular-weight-heparin (LMWH). Studies assessing the optimal duration and peripartum management of therapeutic anticoagulation are lacking. This survey aimed to assess clinician practices for the management of anticoagulation in pregnant women with acute VTE. METHODS: An electronic survey consisting of clinical scenarios addressing anticoagulation management for VTE in pregnancy was created. The target sample was clinicians likely to be involved in the management of pregnant women with acute VTE. The survey completion rate and proportion of individuals selecting a response were determined. RESULTS: 96 respondents completed the survey including general internists (56.3%), hematologists (21.9%), and obstetricians (6.3%). In the management of a VTE in first or second trimester, most respondents preferred therapeutic LMWH until 6 weeks postpartum. In the first and second trimester, 48.0% and 37.5% of respondents, respectively, opted to reduce the dose of anticoagulation after 3 or 6 months. 29.2% of physicians opted for bridging with intravenous heparin around delivery when treating a VTE in the third trimester. 73.0% perceived an increased risk of clinically relevant non-major bleeding associated with the use of therapeutic anticoagulation in the peripartum and postpartum periods. CONCLUSIONS: The survey highlights a wide variability of practice in the management of therapeutic anticoagulation in pregnancy. Larger scale studies with relevant clinical outcomes including thrombosis and bleeding risks are needed to inform clinical practice.


Subject(s)
Venous Thromboembolism , Anticoagulants/adverse effects , Female , Heparin, Low-Molecular-Weight/therapeutic use , Humans , Pregnancy , Pregnant Women , Risk Factors , Surveys and Questionnaires , Venous Thromboembolism/etiology
3.
J Thromb Haemost ; 10(11): 2298-304, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22925003

ABSTRACT

BACKGROUND: Guidelines for perioperative warfarin management in patients with venous thromboembolic disease (VTE) are largely based on expert opinion. OBJECTIVES: To assess the effectiveness and safety of a conservative perioperative anticoagulation strategy in patients with VTE on chronic warfarin therapy. Our center uses a conservative bridging approach for chronic VTE patients consisting of withholding warfarin for 5 days preoperatively, with prophylactic low-molecular-weight heparin (LMWH) post-procedure only if patients are admitted to hospital. PATIENTS/METHODS: We performed a single-center retrospective cohort study. During the study period (1997-2011) there were 634 procedures in 416 patients that were reviewed for postoperative outcomes at 30 and 90 days. RESULTS: Of the 634 procedures, 156 procedures (24.6%) were completed as inpatients. Pre- and post-procedure LMWH bridging was used in 15 (2.4%) and 152 (24.0%) of all procedures, respectively. The 30-day VTE incidence was 0.32% (95% confidence interval [CI] 0.087-1.14), all non-fatal DVTs. The 30-day incidence of major and total bleeding events was 1.26% (95% CI 0.64-2.47) and 3.00% (95% CI 1.93-4.63), respectively. The all-cause mortality rate was 0.32% (95% CI 0.087-1.14) at 30 days; two patients died from arterial thrombosis events. CONCLUSIONS: A randomized controlled trial is needed to provide definitive conclusions but a conservative bridging approach appears promising.


Subject(s)
Anticoagulants/administration & dosage , Venous Thromboembolism/drug therapy , Warfarin/administration & dosage , Aged , Chronic Disease , Female , Hemorrhage , Heparin, Low-Molecular-Weight/administration & dosage , Humans , Incidence , Inpatients , Male , Middle Aged , Perioperative Period , Postoperative Period , Retrospective Studies , Time Factors , Treatment Outcome , Venous Thromboembolism/epidemiology
5.
Am J Physiol Gastrointest Liver Physiol ; 296(2): G399-405, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19074640

ABSTRACT

Evidence from patients with inflammatory bowel disease (IBD) and animal models suggests that inflammation alters blood flow to the mucosa, which precipitates mucosal barrier dysfunction. Impaired purinergic sympathetic regulation of submucosal arterioles, the resistance vessels of the splanchnic vasculature, is one of the defects identified during IBD and in mouse models of IBD. We hypothesized that this may be a consequence of upregulated catabolism of ATP during colitis. In vivo and in vitro video microscopy techniques were employed to measure the effects of purinergic agonists and inhibitors of CD39, an enzyme responsible for extracellular ATP catabolism, on the diameter of colonic submucosal arterioles from control mice and mice with dextran sodium sulfate [DSS, 5% (wt/vol)] colitis. Using a luciferase-based ATP assay, we examined the degradation of ATP and utilized real-time PCR, Western blotting, and immunohistochemistry to examine the expression and localization of CD39 during colitis. Arterioles from mice with DSS colitis did not constrict in response to ATP (10 microM) but did constrict in the presence of its nonhydrolyzable analog alpha,beta-methylene ATP (1 microM). alpha,beta-Methylene ADP (100 microM), an inhibitor of CD39, restored ATP-induced vasoconstriction in arterioles from mice with DSS-induced colitis. CD39 protein and mRNA expression was markedly increased during colitis. Immunohistochemical analysis demonstrated that, in addition to vascular CD39, F4/80-immunoreactive macrophages accounted for a large proportion of submucosal CD39 staining during colitis. These data implicate upregulation of CD39 in impaired sympathetic regulation of gastrointestinal blood flow during colitis.


Subject(s)
Adenosine Triphosphate/metabolism , Antigens, CD/metabolism , Apyrase/metabolism , Colitis/enzymology , Colon/blood supply , Splanchnic Circulation , Vasoconstriction , Adenosine Diphosphate/analogs & derivatives , Adenosine Diphosphate/pharmacology , Adenosine Triphosphate/analogs & derivatives , Adenosine Triphosphate/pharmacology , Animals , Antigens, CD/genetics , Antigens, Differentiation/metabolism , Apyrase/antagonists & inhibitors , Apyrase/genetics , Arterioles/immunology , Colitis/chemically induced , Colitis/physiopathology , Colon/drug effects , Colon/enzymology , Colon/innervation , Dextran Sulfate , Disease Models, Animal , Electric Stimulation , Enzyme Inhibitors/pharmacology , Macrophages/enzymology , Male , Mice , RNA, Messenger/metabolism , Splanchnic Circulation/drug effects , Submucous Plexus/enzymology , Sympathetic Nervous System/enzymology , Up-Regulation , Vasoconstriction/drug effects
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