AN OVERVIEW ON HEREDITARY AND ACQUIRED HYPERCOAGULABILITY

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Published: 2022-12-27

DOI: 10.56557/upjoz/2022/v43i243321

Page: 262-270


MOHAMMED SALAH HUSSAIN *

Department of Gastroenterology and Endoscopy, Dr. Samir Abbas Hospital, Jeddah, Saudi Arabia and Department of Internal Medicine, Faculty of Medicine, Alazhar University Hospitals, Cairo, Egypt.

SUMYA HASSAN DAWS

King Abdulaziz Hospital & Oncology Center, Saudi Arabia.

ESSA IBRAHIM ALHAZMI

Al-Qunfudah General Hospital, Saudi Arabia.

MANSOUR ABDULRAHIM JAN

Waeerah Primary Health Care, Madinah, Saudi Arabia.

SAHAD SAMI GHAMRI

King Abdulaziz University, Saudi Arabia.

KOUTHER MUTLAQ O. ALHUDIRES

King Salman Specialist Hospital, Saudi Arabia.

OSAMAH ABDULAZIZ A. ALHASSAN

Jouf University, Jouf, Saudi Arabia.

FAHAD AMJAD A. BIN HUSSAIN

Al Noor Specialist Hospital, Saudi Arabia.

ABDULLAH AMJAD A. BIN HUSSAIN

Al Noor Specialist Hospital, Saudi Arabia.

ADAWI, ZAINAB Y. NASSER

Ajyad Emergency Hospital, Saudi Arabia.

ADAWI, YAHYA AHMED M.

Baish General Hospital, Saudi Arabia.

ALQAHTANI, ABDULAZIZ KHALID A.

Khafji General Hospital, Saudi Arabia.

*Author to whom correspondence should be addressed.


Abstract

A typical definition of hypercoagulability is the predisposition to develop venous thromboembolism due to an underlying hypercoagulable state caused by hereditary or acquired blood coagulation or fibrinolysis problems. Clinical signs of hypercoagulability can be fatal or extremely damaging. About 80% to 90% of patients can have hypercoagulability diseases accurately recognised. Determining the origin of hypercoagulability may influence the kind and length of treatment for the accompanying thrombosis. As a result, hypercoagulability is not a single, unified disease process but rather a collection of risk factors that may or may not lead to thrombosis, depending on the severity and number of risk variables as well as environmental exposures. The former includes prothrombotic polymorphisms in the genes encoding for factor V (i.e., factor V Leiden) and prothrombin, as well as shortages of natural anticoagulants such antithrombin, protein C, and protein S. It also includes elevated values of clotting factors (particularly factor VIII). The latter problems mostly include hyperhomocysteinemia, acquired elevations of coagulation factors or acquired reductions of natural inhibitors, malignancy, and antiphospholipid antibody syndrome.

Keywords: Antiphospholipid syndrome, hereditary thrombophilia, risk factors, factor v leiden, thrombophilia, venous thromboembolism


How to Cite

HUSSAIN, MOHAMMED SALAH, SUMYA HASSAN DAWS, ESSA IBRAHIM ALHAZMI, MANSOUR ABDULRAHIM JAN, SAHAD SAMI GHAMRI, KOUTHER MUTLAQ O. ALHUDIRES, OSAMAH ABDULAZIZ A. ALHASSAN, FAHAD AMJAD A. BIN HUSSAIN, ABDULLAH AMJAD A. BIN HUSSAIN, ADAWI, ZAINAB Y. NASSER, ADAWI, YAHYA AHMED M., and ALQAHTANI, ABDULAZIZ KHALID A. 2022. “AN OVERVIEW ON HEREDITARY AND ACQUIRED HYPERCOAGULABILITY”. UTTAR PRADESH JOURNAL OF ZOOLOGY 43 (24):262-70. https://doi.org/10.56557/upjoz/2022/v43i243321.