ABSTRACT
BACKROUND: Venous thromboembolic disease (VTED) is a frequent cause of hospitalization and mortality. Whole blood viscosity (WBV) participates in the pathogenesis of thrombosis.
OBJECTIVE: To identify the most frequent etiologies and their association with WBV index (WBVI) in hospitalized patients with VTED.
MATERIAL AND METHODS: Observational, cross-sectional, retrospective, analytical study, Group 1: cases (patients diagnosed with VTED) and Group 2: controls without thrombosis. Risk factors for VTED were described and WBVI was calculated from total proteins and hematocrit. Descriptive and inferential statistics were used with Chi-squared test, Fisher's exact test, Mann Whitney U test, bivariate and multivariate logistic regression analysis.
RESULTS: We included 146 patients and 148 controls, age 46.3 ±17.7 vs. 58 ± 18.2 years, of both sexes (female, 65.1%). The most frequent etiology was neoplastic (23.3%), followed by diseases with cardiovascular risk (17.8%). Independent risk factors for VTED were age, chronic kidney disease, presence of liver disease or solid neoplasia. WBVI was similar in patients with VTED as in those without thrombosis. We found an association of the presence of deep vein thrombosis and diseases with cardiovascular risk (p = 0.040).
CONCLUSIONS: The presence of chronic kidney disease, liver disease, and solid neoplasia are independent risk factors for VTED. The WBVI is a simple and rapid diagnostic tool in the evaluation of patients with VTED.
PMID:37200530
02:33
PubMed articles on: Cancer & VTE/PE
American Society of Hematology 2023 Guidelines for Management of Venous Thromboembolism: Thrombophilia Testing
Blood Adv. 2023 May 17:bloodadvances.2023010177. doi: 10.1182/bloodadvances.2023010177. Online ahead of print.
ABSTRACT
BACKGROUND: Hereditary and acquired thrombophilia are risk factors for venous thromboembolism (VTE). Whether testing helps in guiding management decisions is controversial.
OBJECTIVE: These evidence-based guidelines from the American Society of Hematology (ASH) intend to support decision-making about thrombophilia testing.
METHODS: ASH formed a multidisciplinary guideline panel covering clinical and methodological expertise and minimizing bias from conflicts of interest. The McMaster University GRADE Centre provided logistical support, performed systematic reviews, and created evidence profiles and evidence-to-decision tables. The Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach was used. Recommendations were subject to public comment.
RESULTS: The panel agreed on 23 recommendations regarding thrombophilia testing and associated management. Nearly all recommendations are based on very low certainty in the evidence due to modeling assumptions.
CONCLUSIONS: The panel issued a strong recommendation against testing the general population before starting combined oral contraceptives (COC), and conditional recommendations for thrombophilia testing in the following scenarios: a) patients with VTE associated with non-surgical major transient or hormonal risk factors; b) patients with cerebral or splanchnic venous thrombosis, in settings where anticoagulation would otherwise be discontinued; c) individuals with a family history of antithrombin, protein C or protein S deficiency when considering thromboprophylaxis for minor provoking risk factors, and for guidance to avoid COC/HRT; d) pregnant women with a family history of high-risk thrombophilia types; e) patients with cancer at low or intermediate risk of thrombosis and with a family history of VTE. For all other questions, the panel provided conditional recommendations against testing for thrombophilia.
PMID:37195076 | DOI:10.1182/bloodadvances.2023010177
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
PubMed articles on: Cancer & VTE/PE
Temozolomide and Lomustine Induce Tissue Factor Expression and Procoagulant Activity in Glioblastoma Cells In Vitro
Cancers (Basel). 2023 Apr 18;15(8):2347. doi: 10.3390/cancers15082347.
ABSTRACT
Glioblastoma (GBM) patients have one of the highest risks of venous thromboembolism (VTE), which is even further increased upon treatment with chemotherapy. Tissue factor (TF) is the initiator of the extrinsic coagulation pathway and expressed by GBM cells. In this study, we aimed to examine the effect of routinely used chemotherapeutic agents Temozolomide (TMZ) and Lomustine (LOM) on TF procoagulant activity and expression in GBM cells in vitro. Three human GBM cell lines (U-251, U-87, U-118) were exposed to 100 µM TMZ or 30 µM LOM for 72 h. TF procoagulant activity was assessed via an FXa generation assay and TF gene and protein expression through qPCR and Western blotting. The externalization of phosphatidylserine (PS) was studied using Annexin V flow cytometry. Treatment with TMZ and LOM resulted in increased procoagulant activity in all cell lines. Furthermore, both agents induced procoagulant activity in the supernatant and tumor-cell-secreted extracellular vesicles. In line, TF gene and protein expression were increased upon TMZ and LOM treatment. Additionally, PS externalization and induction of inflammatory-associated genes were observed. Overall, the chemotherapeutic modalities TMZ and LOM induced procoagulant activity and increased TF gene and protein expression in all GBM cell lines tested, which may contribute to the increased VTE risk observed in GBM patients undergoing chemotherapy.
PMID:37190275 | PMC:PMC10137012 | DOI:10.3390/cancers15082347
02:33
In reply to this message
PubMed articles on: Cancer & VTE/PE
Cancer-Associated Thrombosis: Risk Assessment, Prevention, and Treatment
J Adv Pract Oncol. 2023 Apr;14(3):213-217. doi: 10.6004/jadpro.2023.14.3.6. Epub 2023 Apr 1.
ABSTRACT
The risk of developing venous thromboembolism (VTE) is four to seven times higher in patients with cancer than in those without. At JADPRO Live 2022, presenters discussed risk factors and assessing patients for VTE, as well as how to protect patients against VTE in both the inpatient and outpatient clinic settings. They reviewed selecting an appropriate anticoagulation treatment, including the choice of agent and duration of treatment for the patient with cancer, and finally the steps needed to assess and treat patients experiencing therapeutic anticoagulation failure.
PMID:37197728 | PMC:PMC10184841 | DOI:10.6004/jadpro.2023.14.3.6
02:33
PubMed articles on: Cancer & VTE/PE
The role of tissue factor pathway inhibitor 2 in the coagulation and fibrinolysis system
J Obstet Gynaecol Res. 2023 Apr 25. doi: 10.1111/jog.15660. Online ahead of print.
ABSTRACT
AIM: Tissue factor (TF), the primary initiator of the extrinsic coagulation pathway, contributes to the generation of a hypercoagulable and prothrombotic state in cancer patients. TF pathway inhibitor (TFPI) is a major inhibitor of TF-mediated coagulation pathway. The two proteins, TFPI1 and TFPI2, are encoded by separate genes. Indeed, various cancer patients with venous thromboembolism (VTE) had significantly lower TFPI1 levels than those without VTE. In contrast, serum TFPI2 level was found to increase in ovarian cancer patients with VTE. It remains unclear why TFPI2, unlike TFPI1, is elevated in ovarian cancer patients with VTE. The aim of this review is to explore the pathophysiological role of TFPI2 on the coagulation and fibrinolysis system.
METHODS: A literature search was performed from inception to April 30, 2022 in the PubMed and Google Scholar databases.
RESULTS: TFPI1 and TFPI2 are homologs with different protease inhibitory activities in the coagulation and fibrinolysis system. TFPI1 inhibits TF/factor VIIa (FVIIa) catalyzed factor X (FX) activation. On the other hand, TFPI2 is unlikely to affect TF-initiated thrombin generation, but it has strong inhibitory activity against plasmin. Plasmin is involved in fibrin degradation, clot lysis, and inactivation of several coagulation factors (such as FV, FVIII, FIX, and FX). TFPI2 may increase the risk of VTE by inhibiting plasmin-dependent fibrinolysis.
CONCLUSION: TFPI1 and TFPI2 may have different key functions in regulating the coagulation and fibrinolytic systems.
PMID:37186495 | DOI:10.1111/jog.15660
02:33
PubMed articles on: Cancer & VTE/PE
Growth differentiation factor-15 and prediction of cancer-associated thrombosis and mortality: A prospective cohort study
J Thromb Haemost. 2023 May 14:S1538-7836(23)00414-2. doi: 10.1016/j.jtha.2023.04.043. Online ahead of print.
ABSTRACT
BACKGROUND: Patients with cancer are at increased risk of venous and arterial thromboembolic/thrombotic events (VTE/ATE). Growth differentiation factor-15 (GDF-15) improves cardiovascular risk assessment, but its predictive utility in cancer patients remains undefined.
OBJECTIVES: To investigate the association of GDF-15 with risk of VTE, ATE, and mortality in cancer patients and its predictive utility alongside established models.
METHODS: The Vienna Cancer and Thrombosis Study (CATS), a prospective, observational cohort study of patients with newly diagnosed or recurrent cancer, followed for two years, served as the study framework. Serum GDF-15 levels at study inclusion were measured, and association with VTE, ATE, and death was determined using competing risk (VTE/ATE) or Cox regression (death) modeling. The added value of GDF-15 to established VTE-risk prediction models was assessed using the Khorana- and Vienna-CATScore.
RESULTS: Among 1,531 included patients with cancer (median age 62 years, 53% men), median GDF-15 levels were 1,004 ng/L (interquartile range, 654-1,750). Increasing levels of GDF-15 were associated with increased risk of VTE, ATE, and all-cause death [(subdistribution) HR per doubling: 1.16 (95% CI 1.03-1.32), 1.30 (1.11-1.53), and 1.57 (1.46-1.69)], respectively. After adjustment for clinically relevant covariates, the association only prevailed for all-cause death (HR: 1.21, 1.10-1.33) and GDF-15 did not improve performance of the Khorana- or Vienna-CATScore.
CONCLUSION: GDF-15 is strongly associated with survival in cancer patients, independent of established risk factors. While an association with ATE and VTE was identified in univariable analysis, GDF-15 was not independently associated with these outcomes and failed to improve established VTE prediction models.
PMID:37192696 | DOI:10.1016/j.jtha.2023.04.043
02:33
In reply to this message
PubMed articles on: Cancer & VTE/PE
Venous Thrombosis Recurrence After Catheter-Related Upper Extremity Deep Venous Thrombosis in Cancer Patients: A Retrospective Analysis
Angiology. 2023 May 17:33197231176985. doi: 10.1177/00033197231176985. Online ahead of print.
ABSTRACT
Long-term indwelling central venous catheters (CVC) are frequently used to secure vascular access to deliver injectable treatment. Catheter-related thrombosis (CRT) occurs in approximately 2-6% of cancer patients. We conducted a single-center retrospective study to assess the rate of venous thromboembolism (VTE) recurrence in cancer patients; 200 patients were included. Mean age was 56 ± 15.15 years, median follow-up duration was 16.5 [range: 10-36] months. The incidence of recurrence was estimated using Gray's method for competing risk with death as the competing event of VTE. Recurrent VTE occurred in 25.5% of patients with a median occurrence time of 6.5 [range: 5-11.25] months. In case of recurrence, 94.6% of patients were treated for cancer and 80.4% of them received anticoagulants; 4 major bleeds and 17 non-major bleeds occurred during follow-up. In multivariate analysis, previous VTE (Hazard Ratio (HR) 2.48 (95% CI 1.42-4.32) and presence of CVC (HR 5.56 (95% CI 1.96-15.75) were significant recurrence risk factors. After a first episode of CRT, 25.5% of patients experienced VTE recurrence as UEDVT in 30 cases (55.5%), PE in 17 cases (31.5%), and DVT in 7 cases (13%), mostly during anticoagulation therapy. Anticoagulation therapy does not avoid CRT in case of cancer and must be balanced with hemorrhagic risk.
PMID:37195809 | DOI:10.1177/00033197231176985
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
Photo
Not included, change data exporting settings to download.
1200×1200, 39.0 KB
02:33
PubMed articles on: Cancer & VTE/PE
Overexpression of miR-483-5p predicts venous thrombo-embolism onset in patients with lung cancer especially in high BMI cases
Acta Biochim Pol. 2023 May 16. doi: 10.18388/abp.2020_6214. Online ahead of print.
No comments:
Post a Comment
اكتب تعليق حول الموضوع