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Birth control pills can cause thrombosis and worsen liver function in those who are prone to it. The laboratory test before prescribing the first birth control pill examines the most common predisposing factors for thrombosis as well as liver function that may be affected by long-term hormone intake.
Blood count: to determine the absolute number of formed elements in the blood, red blood cells, white blood cells and platelets. From this, the specialist may conclude that anaemia, blood loss, inflammatory processes, hematopoietic diseases and coagulation disorders, among others, may occur.
Bilirubin: is produced as a yellow breakdown of red blood cells in the spleen, liver and certain lymph nodes. Its levels may increase in cases of increased red blood cell breakdown, liver disease and biliary obstruction. Normal total bilirubin: 5 to 17 μmol/l (3 to 10 mg/l).
GOT (glutamate oxaloacetate aminotransferase): an enzyme involved in the metabolism of amino acids. It is normally present in small amounts in the blood but increases in case of organ damage. A lower GOT value can be found in pregnant women. Its normal value is 18-31 U/l in women and 18-33 U/l in men.
GPT (glutamate pyruvate aminotransferase): an enzyme produced in liver cells that shows the damage that has taken place there. Normally, it is also present in small amounts in the blood, increasing in case of damage. Its normal value is 7-30 U/l in women and 10-55 U/l in men.


GGT (gamma glutamyl transferase): an enzyme produced by the liver, pancreas and kidneys. Its value is considered when examining the liver and bile ducts. The most reliable signalling parameter. Normal value for women is 8-40 U/l, 9-50 U/l.
Alkaline phosphatase: present in greater amounts in the liver and in the cells that make up bones. Alkaline phosphatase adult normal value: 40-115 U/l
APC resistance: the assay is suitable for detecting activated protein C resistance caused by the Leiden mutation. The presence of hereditary APC-R can lead to deep vein thrombosis. This is due in most cases to the Leiden mutation.
What is Leiden mutation?
Leiden mutation is a blood clotting disorder that is of genetic origin. The so-called APC protein inhibits abnormal clotting during blood clotting by splitting clotting factor V, which is also a protein. The Leiden mutation is nothing more than a modification in the factor V gene that results in the protein not being able to be fissile. Thrombophilia, or a predisposition to thrombosis, results from this. There is an acquired and congenital thrombotic ability. The Leiden mutation is congenital, affecting women and men equally. For offspring, the risk of recurrence is 50 percent.
The test requires an empty stomach, the result is obtained after the 14th working day after the test.
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Women taking birth control pill are more likely to get venous thrombosis, regardless of known predisposing factors, than those not taking birth control pills. If someone is genetically predisposed to thrombosis, they are 30 times more likely to suffer it compared to the average population.
In case of hereditary thrombotic predisposition, the risk of deep vein thrombosis is 8 times more common inherited from one side and 80 times from both (paternal and maternal) sides.
Laboratory test items prior to prescribing the birth control pill: Blood count, Bilirubin, GOT, GPT, GGT, Alkaline phosphatase, APC resistance, and:
Protein C and Protein S: parts of the system that prevents excessive blood clots. They regulate the rate of blood clots so that blood clots only form where the injury itself is. Their low levels cause an inherited predisposition to thrombosis.
Anti-thrombin III: plays an important role in the regulation of blood coagulation processes. It blocks the action of a number of blood clotting factors (thrombin and factors IX, X, XI, XII) to prevent excessive clotting.


Prothrombin: one of the coagulation factors produced by the liver. The Prothrombin time (PI) test measures how long it takes for a clot to form in a blood sample. The PI test examines the uniform function of coagulation factors and the ability of the body to clot within a reasonable time.
APTI: activated partial thromboplastin time, which examines the function of the coagulation cascades. The so-called coagulation cascade is suitable for closing damaged tissues or injuries by blood clot formation. This promotes healing. Acquired or inherited deficiency of one or more coagulation factors causes abnormal functioning of the factors. In this case, we cannot talk about stable clot formation, i.e. increased bleeding or clotting may occur.
Prothrombin gene mutation: a genetic abnormality that leads to thrombophilia (predisposition to thrombosis).
The test requires an empty stomach, the result is obtained after the 20th working day after the test.
Informational content only The textual content published on this page is for general information purposes only and does not constitute medical advice, a diagnosis, or a treatment recommendation. Proper assessment, examination, and therapeutic decisions always require a personal medical consultation and, where appropriate, further specialist opinion. Medicare Egészségközpont Zrt. makes every reasonable effort to keep the content up to date; however, it accepts no liability for the completeness or accuracy of the information published or for consequences arising from decisions based on it.