
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions β written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Thrombophilia history and symptoms
Introduction
Overview
Overview
A positive family history of thrombosis and individual recurrent thrombosis history is suggestive of inherited thrombophilias. Thrombophilia screening may be beneficial in these scenarios.[1][2][3]
History and Symptoms
History and Symptoms
- Clinical history:[4]
- A detailed history consisting of demographics, family history, assessment of risk factors and physical symptoms followed by a standard physical examination is required to differentiate between provoked and unprovoked thromboembolism. A provoking factor is present in up to 70% of patients suffering from venous thromboembolism (VTE).
- One in three patients reports a positive family history predicting the underlying inherited thrombophilia. Hence, patients should be asked specifically if they have a personal history of venous thromboembolism or a family history of venous thrombosis. [5]
- Additional acquired risk factors should be clearly documented which includes advancing age, a past history of venous thrombosis, immobility, trauma, surgery, nephrotic syndrome, inflammatory disorders, hormone use, pregnancy, post-partum state and obesity.
- Based on history and physical exam, the Wells score guides diagnostic workup in first time (VTE) is preferred.
- Physical signs and symptoms:
- The signs and symptoms of thrombosis vary depending on the presumed location and acuity.
- Deep Vein Thrombosis (DVT):[6]
- Patients often present with isolated extremity swelling, pain, warmth, and erythema at the site of the blockage and describes the pain as βcrampyβ located in the calf or thigh of the affected lower extremity or any extremity.
- They may exhibit a decreased range of motion of the extremity, inability to ambulate, or radiation of pain (e.g., into the groin for LE DVT extending to femoral vein).
- Acute Pulmonary Embolism (PE): [7]
- Patients may present with pleuritic chest pain, shortness of breath, fatigue, back pain, syncope, or even death if severe cases associated with hemodynamic instability or right heart strain.
- Signs include tachycardia, tachypnea, fever, and may include oxygen desaturation.
- Arterial thrombosis: They are most commonly found in cardiac or cerebrovascular vasculature. [8]
- Coronary arteries: They often report with the classic presentation of βcrushingβ left-sided chest pain or heaviness with radiation to the left arm or jaw; though atypical presentations can occur frequently.
- Cerebral arteries: It may present with ischemic stroke symptoms which include acute onset of unilateral or bilateral weakness, headache, confusion, vision changes, dysarthria, dysphagia, paresthesias, difficulty ambulating, or frank paralysis of one or more extremities.
Table 1: Clinical characteristics of patients with thrombophilia [9] [10]
| Clinical features |
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References
References
- β DeLoughery TG. Hemostasis and Thrombosis: Springer International Publishing; 2014.
- β Cohoon KP, Heit JA (2014). “Inherited and secondary thrombophilia”. Circulation. 129 (2): 254β7. doi:10.1161/CIRCULATIONAHA.113.001943. PMCΒ 3979345. PMIDΒ 24421360.
- β Seligsohn U, Lubetsky A (2001). “Genetic susceptibility to venous thrombosis”. N Engl J Med. 344 (16): 1222β31. doi:10.1056/NEJM200104193441607. PMIDΒ 11309638.
- β “Hypercoagulability – StatPearls – NCBI Bookshelf”.
- β MΓ€rz W, Nauck M, Wieland H (2000). “The molecular mechanisms of inherited thrombophilia”. Z Kardiol. 89 (7): 575β86. doi:10.1007/s003920070206. PMIDΒ 10957782.
- β Streiff, Michael B.; Agnelli, Giancarlo; Connors, Jean M.; Crowther, Mark; Eichinger, Sabine; Lopes, Renato; McBane, Robert D.; Moll, Stephan; Ansell, Jack (2016). “Guidance for the treatment of deep vein thrombosis and pulmonary embolism”. Journal of Thrombosis and Thrombolysis. 41 (1): 32β67. doi:10.1007/s11239-015-1317-0. ISSNΒ 0929-5305.
- β Streiff MB, Agnelli G, Connors JM, Crowther M, Eichinger S, Lopes R; et al. (2016). “Guidance for the treatment of deep vein thrombosis and pulmonary embolism”. J Thromb Thrombolysis. 41 (1): 32β67. doi:10.1007/s11239-015-1317-0. PMCΒ 4715858. PMIDΒ 26780738.
- β “Thrombosis – StatPearls – NCBI Bookshelf”.
- β “Guidelines on the investigation and management of thrombophilia. The British Committee for Standards in Haematology”. Journal of Clinical Pathology. 43 (9): 703β709. 1990. doi:10.1136/jcp.43.9.703. ISSNΒ 0021-9746.
- β Pinjala, R. K.; Reddy, L. R. C.; Nihar, R. P.; Praveen, G. V. A.; Sandeep, M. (2012). “Thrombophilia β How Far and How Much to Investigate?”. Indian Journal of Surgery. 74 (2): 157β162. doi:10.1007/s12262-011-0407-2. ISSNΒ 0972-2068.
- β Smalberg JH, Kruip MJ, Janssen HL, Rijken DC, Leebeek FW, de Maat MP (2011). “Hypercoagulability and hypofibrinolysis and risk of deep vein thrombosis and splanchnic vein thrombosis: similarities and differences”. Arterioscler Thromb Vasc Biol. 31 (3): 485β93. doi:10.1161/ATVBAHA.110.213371. PMIDΒ 21325670.
- β Mohanty D, Shetty S, Ghosh K, Pawar A, Abraham P (2001). “Hereditary thrombophilia as a cause of Budd-Chiari syndrome: a study from Western India”. Hepatology. 34 (4 Pt 1): 666β70. doi:10.1053/jhep.2001.27948. PMIDΒ 11584361.
- β Bombeli T, Basic A, Fehr J (2002). “Prevalence of hereditary thrombophilia in patients with thrombosis in different venous systems”. Am J Hematol. 70 (2): 126β32. doi:10.1002/ajh.10103. PMIDΒ 12111785.
- β Lussana F, Dentali F, Ageno W, Kamphuisen PW (2007). “Venous thrombosis at unusual sites and the role of thrombophilia”. Semin Thromb Hemost. 33 (6): 582β7. doi:10.1055/s-2007-985754. PMIDΒ 17768690.
- β Riva N, Ageno W (2017). “Approach to thrombosis at unusual sites: Splanchnic and cerebral vein thrombosis”. Vasc Med. 22 (6): 529β540. doi:10.1177/1358863X17734057. PMIDΒ 29202678.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Asiri Ediriwickrema, M.D., M.H.S. [2] Jaspinder Kaur, MBBS[3]
