Coagulopathy usually refers to coagulation dysfunction disease, which is caused by various factors leading to the lack of coagulation factors or coagulation dysfunction, resulting in a series of bleeding or bleeding. It can be divided into congenital and hereditary coagulation dysfunction diseases, acquired Acquired coagulation disorders.

1. Congenital hereditary coagulation disorders: due to congenital factors such as gene defects, usually X chromosome carries recessive inheritance, common is hemophilia, clinical manifestations are spontaneous bleeding, hematoma, dysphagia, etc. Through laboratory examination, it can be detected that the patient's thromboplastin is poorly produced, and under the guidance of a doctor, vitamin K1, phensulfame tablets and other drugs can be supplemented to promote blood coagulation;

2. Acquired coagulation dysfunction disease: refers to coagulation dysfunction caused by drugs, diseases or poisons, etc. The more common ones are coagulation dysfunction caused by vitamin K deficiency and liver disease. It is necessary to actively treat the primary factors according to the doctor's advice. If it is caused by drugs, the drug should be appropriately reduced or stopped, and then blood coagulation factors such as vitamin K can be supplemented according to the bleeding situation, and plasma transfusion can also be used. If the thrombus is caused by coagulation dysfunction, anticoagulant therapy, such as heparin sodium and other anticoagulant drugs, is required.