Poor blood clotting. Causes.


The hemostatic system is complex, multicomponent and performs a lot of functions, the most important of which are stopping bleeding, maintaining blood in a liquid state, and participating in the healing of damage to organs and tissues.

It includes blood coagulation factors, biological molecules, platelets, vascular walls, as well as neurohumoral mechanisms that regulate the functioning of these factors. A disruption of the hemostasis system can occur when one or more components fail. As a result, the balance between coagulation and anticoagulation mechanisms is disrupted, with the development of certain consequences for the body.

All problems associated with bleeding disorders

Problems associated with bleeding disorders are usually caused by abnormal blood flow to block blood vessels when they are injured.
There are also genetic abnormalities that complicate the process of blood clotting. If everything is normal in the body, the blood at the site of the cut should thicken, that is, prevent heavy bleeding. However, in some cases, this mechanism does not work, which leads to large blood losses.

In addition, with poor blood clotting, its external loss does not always occur. Such disorders can manifest themselves in the form of internal bleeding, for example under the skin, causing hematomas, and even into the brain.

Clinical picture

Clinically, coagulation factor 12 deficiency is manifested by prolongation of bleeding time without any other symptoms of impaired hemostasis. The severity of prolongation of bleeding time depends on the type of inheritance of the genetic defect. In the dominant type, the deficiency is more pronounced; in the recessive type, it is partially compensated by other coagulation factors. Bleeding time is increased due to delayed initiation of the cascade coagulation system. Patients do not show a tendency to pathological bleeding, so the disease is often not detected or discovered by chance during laboratory examination or preoperative screening.

It seems a little paradoxical that with coagulation factor deficiency, it is not bleeding that manifests itself, but thrombosis. For example, John Hageman, after whom the coagulation factor is named, subsequently died from thromboembolism, which was complicated by a fracture of the pelvic bones. Modern published clinical cases of surgical interventions in patients with Hageman syndrome, fortunately, ended successfully. Thrombophilic disorders are associated with the fact that factor XII is involved in the destruction of blood clots by activating the kallikrein-kinin system. Active kallikrein not only triggers the generation of kinins that regulate inflammation, vascular tone and pain reactions, but also converts the inactive plasminogen protein into the active enzyme plasmin (fibrinolysin), which dissolves the fibrin part of the blood clot. Therefore, Hageman factor deficiency is associated with:

  • thrombosis
  • migrating thrombophlebitis
  • thromboembolism
  • heart attacks
  • spontaneous abortions

Causes of bleeding disorders

Typically, poor blood clotting is caused by a deficiency of anticoagulants and other substances that ensure normal blood clotting. Such substances include proteins. In the presence of certain diseases, there may be no proteins in the plasma at all. As a rule, such diseases are hereditary, for example, hemophilia.

However, abnormal blood clotting is caused not only by genetic abnormalities, but also by several other factors, such as:

• Lack of vitamin K in the body.

• Hereditary diseases: von Willebrand disease and hemophilia.

• Liver carcinoma or the presence of metastases from other organs affected by cancer.

• Infectious liver diseases, such as hepatitis.

• Diseases that cause scarring on the liver (cirrhosis).

• Long-term use of strong antibiotics or drugs aimed at combating blood clots.

• The use of anthogenesis inhibitors - drugs that slow down the development of new blood vessels.

• Thrombocytopenia is a disease in which the concentration of platelets drops to a minimum level.

• Anemia of various types.

Methods for diagnosing disorders of the hemostatic system

The following methods can be used to identify pathology:

  • determination of bleeding time (according to Duke, according to Ivey, according to Lee-White);
  • general blood test with formula;
  • determination of platelet aggregation;
  • prothrombin time (PTT) and prothrombin index (PTI);
  • activated partial thromboplastin time (aPTT), etc.

Depending on the specific disorders of the hemostatic system, the doctor may prescribe both individual indicators and a comprehensive study - a coagulogram. It includes indicators such as PTT, PTI, APTT, determination of fibrinogen and D-dimer levels, etc.

In order to confirm or refute the hereditary nature of disorders of the hemostatic system, genetic testing is prescribed. You can take it in medical genetics.

Treatment of bleeding disorders

Treatment of bleeding disorders is carried out according to the reasons that cause such an anomaly. If the disorder is caused by the presence of liver cancer, then first all therapeutic measures should be taken to remove the tumors, and then resort to medication to restore normal blood clotting. In addition, there are general methods of treating this disorder:

• Vitamin K injection.

• Transfusion of donor platelets or plasma.

• Taking medications aimed at restoring blood clotting function.

• Taking iron supplements.

• Treatment with Oprelvekin and hydroxyurea.

Vitamin K is the new black

There is also a certain fashion for laboratory research.
And if a couple of years ago omega indices were in the top, and recently vitamin D took the leading position, today our patients are increasingly being tested for vitamin K. In the USA and Canada, vitamin K is routinely prescribed to all children immediately after birth. Why is this trend only coming now, and when should you really get tested for vitamin K? Let's figure it out together with clinical laboratory diagnostic doctors Dr. Q.

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