chronology
发表于 2025-3-26 22:19:30
An Overview of Hemostasisore blood flow. The fibrinolysis system is one of the most important requirements for clot removal. Procoagulant and anticoagulant elements interacted complicatedly to ensure an effective response to vascular injury that is limited to the injured site.
真
发表于 2025-3-27 01:38:45
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松驰
发表于 2025-3-27 06:33:12
von Willebrand Diseasere available in VWD including VWF/FVIII concentrates, recombinant VWF, desmopressin, and, in some locations, fresh frozen plasma (FFP). With timely diagnosis and appropriate management of the VWD, the burden of the disorder can be alleviated or even eliminated.
细胞
发表于 2025-3-27 10:32:01
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调味品
发表于 2025-3-27 17:29:01
Congenital Factor II Deficiencyon laboratory tests should be used for diagnose of FII deficiency. FII deficiency is suspected through prolonged prothrombin time (PT) and activated thromboplastin time (aPTT) which was confirmed by a specific FII assay. As no specific prothrombin concentrate is available, prothrombin complex concen
辩论
发表于 2025-3-27 18:42:58
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incubus
发表于 2025-3-27 23:24:19
Multiple Coagulation Factor Deficiencyused by defect of a single gene that is implicated in the process or production/activation of multiple factors. The best examples include combined FV and FVIII deficiency (F5F8D) and vitamin K-dependent coagulation factors (VKDCF) deficiency, which have been thoroughly characterized. Isolated combin
乐章
发表于 2025-3-28 05:43:26
Congenital Factor X Deficiency plasma. Then diagnosis should be confirmed by specific tests including antigenic (FX:Ag) and functional (FX:C) assays. Treatment of FX deficiency is based on replacement therapy by fresh frozen plasma (FFP) and prothrombin complex concentrate (PCC). A single-factor FX concentrate produced from huma
beta-carotene
发表于 2025-3-28 08:59:08
Congenital Factor XIII Deficiencymmended as the first-line screening test, but a significant number of countries only used clot solubility test. For the treatment of congenital FXIII deficiency, different products are available, but FXIII concentrate is the treatment of choice. For primary prophylaxis, 10–40 IU/kg FXIII concentrate
不能妥协
发表于 2025-3-28 11:40:16
Glanzmann Thrombastheniawhereas for those with more severe hemorrhage, systemic hemostatic agents including platelet concentrates and recombinant human activated factor VII (rFVIIa) are used. Currently, platelet transfusion is the standard treatment, but repeated transfusion can result in allo-immunization and refractorine