1.Risk factors for postoperative deep venous thrombosis in patients underwent craniotomy.
Renhua LI ; Na CHEN ; Chunyan YE ; Lizhe GUO ; E WANG ; Zhenghua HE
Journal of Central South University(Medical Sciences) 2020;45(4):395-399
OBJECTIVES:
To analyze the risk factors for postoperative deep vein thrombosis (DVT) in neurosurgical patients to provide the basis for the prevention of postoperative DVT.
METHODS:
A total of 141 patients underwent neurosurgery were enrolled. Thrombelastography (TEG) test was performed before and at the end of surgery. According to whether there was DVT formation after operation, the patients were divided into a thrombosis group and a non-thrombosis group. -test and rank sum test were used to compare the general clinical characteristics of the 2 groups, such as age, gender, intraoperative blood loss, -dimer, intraoperative crystal input, colloid input, blood product transfusion, operation duration, length of postoperative hospitalization. The application of chi-square test and rank-sum test were used to compared TEG main test indicators such as R and K values between the 2 groups. Logistic regression was used to analyze the possible risk factors for postoperative DVT in neurosurgical patients.
RESULTS:
There were significant differences in postoperative TEG index R, clotting factor function, intraoperative blood loss, hypertension or not, length of postoperative hospital stay, and postoperative absolute bed time (all <0.05). Logistic regression analysis showed hypercoagulability, more intraoperative blood loss and longer postoperative absolute bed time were risk factors for DVT formation after craniotomy.
CONCLUSIONS
Hypercoagulability in postoperative TEG test of patients is an important risk factor for the formation of postoperative DVT after neurosurgery, which can predict the occurrence of postoperative DVT to some extent.
Craniotomy
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adverse effects
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Humans
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Postoperative Complications
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epidemiology
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Postoperative Period
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Risk Factors
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Thrombophilia
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Venous Thrombosis
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epidemiology
;
etiology
2.Activated Protein C Anticoagulant System Dysfunction and Thrombophilia in Asia.
Naotaka HAMASAKI ; Hiroyuki KUMA ; Hiroko TSUDA
Annals of Laboratory Medicine 2013;33(1):8-13
Thrombophilia that is common among Caucasians is caused by genetic polymorphisms of coagulation factor V Leiden (R506Q) and prothrombin G20210A. Unlike that in Caucasians, thrombophilia that is common in the Japanese and Chinese involve dysfunction of the activated protein C (APC) anticoagulant system caused by abnormal protein S and protein C molecules. Approximately 50% of Japanese and Chinese individuals who develop venous thrombosis have reduced activities of protein S. The abnormal sites causing the protein S molecule abnormalities are distributed throughout the protein S gene, PROS1. One of the most common abnormalities is protein S Tokushima (K155E), which accounts for about 30% of the protein S molecule abnormalities in the Japanese. Whether APC dysfunction occurs in other Asian countries is an important aspect of mapping thrombophilia among Asians. International surveys using an accurate assay system are needed to determine this.
Asian Continental Ancestry Group
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Blood Coagulation
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Blood Proteins/genetics/metabolism
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Humans
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Protein C/genetics/*metabolism
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Protein S/chemistry/genetics/metabolism
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Thrombophilia/epidemiology/*etiology
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Venous Thrombosis/etiology/genetics
3.The prevalence of hereditary thrombophilia in the Trakya region of Turkey.
Muzaffer DEMIR ; Ozden VURAL ; Hasan SUNAR ; Armagan ALTUN ; Faruk YORULMAZ ; Gulta OZBAY
Yonsei Medical Journal 2000;41(4):436-440
The prevalences of deficiencies in antithrombin III (AT III), protein C (PC), protein S (PS) and in the activated protein C (APC) resistance in the thrombotic population of the Trakya region, Turkey were investigated. 37 patients with venous thrombosis (VT) and 17 patients with arterial thrombosis (ArT) were included in this study. The mean ages of the patients with VT and ArT were 46 years (range 20-70) and 38 years (range 32-40), respectively. The activity of AT III was measured by commercially available immuno-turbidimetric assay. The activities of PC and PS were determined by coagulometric assay. The APC resistance was measured using a modified APTT-based clotting assay. Among the VT patients, there were 2 cases (5.4%) with AT III, 5 (13.51%) with PC deficiency, 5 (13.51%) with PS deficiency and 2 (5.4%) with APC resistance. In the ArT patient group, there was 1 patient (5.88%) with AT III, 3 (17.64%) with PC deficiency, 1 (5.88%) with PS deficiency and no APC resistant patients, while there was one (2.08%) with PC deficiency and one (2.08%) with APC resistance in the control group (49 persons, mean age 41 years). The relative risk of thrombosis (odds ratio) was 1.7 in the deficiency of PC and 5.6 in the deficiency of PS. The data presented suggests that the prevalences of AT III, PC and PS deficiencies causing thrombophilia in the Trakya region of Turkey are higher than in other reported studies while the APC resistance is lower than in others. Further studies including more patients would be required to clarify these discrepancies.
Activated Protein C Resistance/complications
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Adult
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Antithrombin III Deficiency/complications
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Human
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Middle Age
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Prevalence
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Protein C Deficiency/complications
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Protein S Deficiency/complications
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Risk Factors
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Thrombophilia/epidemiology*
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Thrombosis/etiology
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Turkey/epidemiology