Thrombophilia risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
Common risk factors in the development of acquired thrombophlias are [[trauma]], [[surgery]], [[immobility]], [[pregnancy]], [[estrogen-replacement therapy]], and [[age]]. Common risk factors in the development of inherited thrombophilias are genetic mutations in [[Factor V Leiden]] and [[Prothrombon G20210A]]. | |||
==Risk Factors== | ==Risk Factors== | ||
Common risk factors in the development of acquired thrombophlias include: | |||
* | *[[Trauma]] | ||
* | *[[Surgery]] | ||
* | *[[Immobility]] | ||
* | *[[Age]] | ||
* | *[[Hormones]] | ||
** | **[[Pregnancy]] | ||
**[[Oral_contraceptive|Oral contraceptive pills]] | |||
**[[Hormone_replacement_therapy|Hormone therapy]] | |||
Common risk factors in the development of inherited thrombophilias are genetic mutations in [[Factor V Leiden]] and [[Prothrombon G20210A]].<ref name="pmid24421360">{{cite journal| author=Cohoon KP, Heit JA| title=Inherited and secondary thrombophilia. | journal=Circulation | year= 2014 | volume= 129 | issue= 2 | pages= 254-7 | pmid=24421360 | doi=10.1161/CIRCULATIONAHA.113.001943 | pmc=3979345 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24421360 }} </ref><ref name="pmid11309638">{{cite journal| author=Seligsohn U, Lubetsky A| title=Genetic susceptibility to venous thrombosis. | journal=N Engl J Med | year= 2001 | volume= 344 | issue= 16 | pages= 1222-31 | pmid=11309638 | doi=10.1056/NEJM200104193441607 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11309638 }} </ref><ref name="pmid21340752">{{cite journal| author=Middeldorp S| title=Evidence-based approach to thrombophilia testing. | journal=J Thromb Thrombolysis | year= 2011 | volume= 31 | issue= 3 | pages= 275-81 | pmid=21340752 | doi=10.1007/s11239-011-0572-y | pmc=3056012 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21340752 }} </ref> | |||
Please see [[Thrombophilia classification|thrombophilia classification]] for a list conditions associated with acquired thrombophilias, and to the page on [[Thrombophilia_causes|causes of thrombophilia by organ system]] | |||
==References== | ==References== | ||
Revision as of 17:20, 20 July 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Asiri Ediriwickrema, M.D., M.H.S. [2]
Overview
Common risk factors in the development of acquired thrombophlias are trauma, surgery, immobility, pregnancy, estrogen-replacement therapy, and age. Common risk factors in the development of inherited thrombophilias are genetic mutations in Factor V Leiden and Prothrombon G20210A.
Risk Factors
Common risk factors in the development of acquired thrombophlias include:
Common risk factors in the development of inherited thrombophilias are genetic mutations in Factor V Leiden and Prothrombon G20210A.[1][2][3]
Please see thrombophilia classification for a list conditions associated with acquired thrombophilias, and to the page on causes of thrombophilia by organ system
References
- ↑ Cohoon KP, Heit JA (2014). "Inherited and secondary thrombophilia". Circulation. 129 (2): 254–7. doi:10.1161/CIRCULATIONAHA.113.001943. PMC 3979345. PMID 24421360.
- ↑ Seligsohn U, Lubetsky A (2001). "Genetic susceptibility to venous thrombosis". N Engl J Med. 344 (16): 1222–31. doi:10.1056/NEJM200104193441607. PMID 11309638.
- ↑ Middeldorp S (2011). "Evidence-based approach to thrombophilia testing". J Thromb Thrombolysis. 31 (3): 275–81. doi:10.1007/s11239-011-0572-y. PMC 3056012. PMID 21340752.