Excessive Clotting Disorders

Excessive clotting disorders—also called hypercoagulable states or thrombophilia— increase the risk of forming blood clots in the veins or, less commonly, arteries. Clots can develop in the legs (deep vein thrombosis, DVT), travel to the lungs (pulmonary embolism, PE), or occur at unusual sites (e.g., brain veins, abdominal veins). Causes may be inherited (e.g., Factor V Leiden, Prothrombin gene variant, Protein C/S or Antithrombin deficiency) or acquired (e.g., antiphospholipid antibodies, cancer, pregnancy, surgery/immobility, estrogen-containing medications).

Ulta Lab Tests offers targeted thrombophilia testing to help you and your clinician evaluate clot risk, investigate a prior clotting event, or assess family history—delivering fast, secure results to support screening, diagnosis, and monitoring.


Signs & Symptoms (When to consider testing)

  • Possible DVT: one-sided leg swelling, pain, warmth, redness.

  • Possible PE: sudden shortness of breath, chest pain, rapid heartbeat, coughing up blood (seek emergency care).

  • Unusual-site clots: abdominal pain (splanchnic veins), severe headache or neuro symptoms (cerebral venous sinus thrombosis).

  • Pregnancy/postpartum complications: clots or recurrent miscarriages (clinician-directed thrombophilia evaluation).

  • Personal/family history: unprovoked clots at a young age (<50), repeated clots, or multiple affected relatives.

  • Provoking factors: recent surgery, trauma, long travel/immobility, estrogen therapy or oral contraceptives, active cancer.

Related search terms: thrombophilia testing, hypercoagulability panel, Factor V Leiden test, Prothrombin gene mutation test, antiphospholipid syndrome labs, Protein C/S deficiency, Antithrombin deficiency, lupus anticoagulant.


Why These Tests Matter

What thrombophilia labs can do

  • Identify inherited risks (Factor V Leiden, Prothrombin G20210A; Protein C, Protein S, Antithrombin deficiencies).

  • Detect acquired risks (antiphospholipid antibodies: lupus anticoagulant, anticardiolipin, anti–β2 glycoprotein I).

  • Provide baseline and trend data to help explain past clots and inform future risk discussions.

  • Support decisions about family screening and periprocedural/pregnancy planning (clinician-directed).

What they cannot do

  • Diagnose a current clot on their own (imaging is needed for DVT/PE).

  • Replace clinical judgment about when to test—timing matters (acute clots, pregnancy, and anticoagulants can affect some results).

  • Predict with certainty if/when a clot will occur—results must be interpreted in context.


What These Tests Measure (at a glance)

  • Genetic variants (DNA):

    • Factor V Leiden (F5 R506Q) – resistance to activated protein C.

    • Prothrombin gene (F2 G20210A) – increased prothrombin levels.

  • Natural anticoagulants (functional ± antigen):

    • Antithrombin (AT) activity/antigen – deficiency increases VTE risk.

    • Protein C activity/antigen and Protein S (free antigen/activity) – deficiencies raise clot risk.

  • Antiphospholipid antibody testing:

    • Lupus anticoagulant (e.g., DRVVT-based methods),

    • Anticardiolipin antibodies (IgG/IgM),

    • Anti–β2 glycoprotein I antibodies (IgG/IgM).
      Note: APS evaluation often requires repeat positivity ≥12 weeks apart (clinician-directed).

  • Supporting tests (ordered selectively):

    • D-dimer (active clot breakdown; nonspecific),

    • Homocysteine (selected cases),

    • JAK2 V617F for unusual-site clots when myeloproliferative neoplasm is suspected (clinician-directed),

    • PT/INR, aPTT, fibrinogen, CBC/CMP for context.


How the Testing Process Works

  1. Order online: choose a thrombophilia panel or specific tests based on your history.

  2. Visit a local lab: quick blood draw; genetic tests use standard blood samples.

  3. Get results fast: most results post within 24–48 hours (some specialized assays may vary).

  4. Review with your clinician: integrate results with history, imaging (if any), and risk factors.


Interpreting Results (general guidance)

  • Positive genetic variant (F5 or F2): indicates inherited risk; strength depends on heterozygous vs. homozygous status and other risk factors.

  • Low AT, Protein C, or Protein S levels: may indicate deficiency, but timing matters—levels can be altered by acute clot, pregnancy, liver disease, or anticoagulants (e.g., warfarin lowers Protein C/S; heparin and DOACs can affect some assays). Your clinician may repeat testing off anticoagulation.

  • Positive antiphospholipid antibodies (LA/aCL/β2GP1): suggest APS risk; persistent positivity over time is more meaningful than a single result.

  • Normal thrombophilia panel: does not eliminate clot risk; acquired triggers (surgery, hormones, immobility, cancer) remain important.

Always interpret labs with a qualified healthcare professional.


Choosing Panels vs. Individual Tests

  • Initial workup (family history/early unprovoked VTE): start with a comprehensive thrombophilia panel(F5/F2 genetics; AT, Protein C/S; antiphospholipid antibodies).

  • Pregnancy/recurrent pregnancy loss: focus on antiphospholipid antibodies (with clinician guidance); some inherited tests may be deferred or timed appropriately.

  • Unusual-site thrombosis or high hematocrit/platelets: consider JAK2 V617F and related myeloproliferative testing (clinician-directed).

  • Active symptoms of DVT/PE: pursue urgent clinical evaluation and imaging; thrombophilia testing is not for acute diagnosis.


FAQs

What are “excessive clotting disorders”?
Conditions—inherited or acquired—that increase the risk of abnormal blood clots in veins (DVT/PE) or unusual sites.

Who should be tested?
People with unprovoked or early-age clotsrecurrent clotsunusual-site thrombosisrecurrent miscarriages, or a strong family history—testing is best planned with a clinician.

Can I be tested while on blood thinners?
Some tests are affected by anticoagulants and by recent clots or pregnancy. Your clinician may time or repeat testingoff therapy for accuracy.

Does a positive result mean I will definitely get a clot?
No. It indicates increased risk, which varies by the specific finding and your other risk factors.

Is D-dimer a thrombophilia test?
No. D-dimer helps evaluate active clot formation/breakdown; it does not determine inherited risk.

How fast are results available?
Many results are ready within 24–48 hours; some specialized assays may take longer.

Should my relatives be tested?
Family testing is individualized and depends on the specific finding and family history—discuss with your clinician.


Internal Links & Cross-References

  • Blood Disorders Hub

  • Blood Coagulation

  • DIC

  • Bleeding Disorders

  • Blood Chemistry Tests

  • Blood Count (CBC)

  • Key Lab Tests: Factor V Leiden • Prothrombin (F2) Mutation • Antithrombin Activity • Protein C Activity • Protein S Free Antigen/Activity • Lupus Anticoagulant • Anticardiolipin • Anti–β2 Glycoprotein I • D-dimer • JAK2 V617F


Available Tests & Panels

Tip: Begin with a comprehensive thrombophilia panel when the history suggests inherited or acquired risk, then add targeted tests (e.g., JAK2) as guided by your clinician.

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The Antiphospholipid Antibody Panel measures autoantibodies such as anticardiolipin, beta-2 glycoprotein I, and lupus anticoagulant associated with abnormal blood clotting. Elevated levels are linked to antiphospholipid syndrome (APS), recurrent pregnancy loss, stroke, or deep vein thrombosis. This test supports evaluation of autoimmune conditions, unexplained thrombosis, and risks of vascular or pregnancy complications.


The Antithrombin III Activity Test evaluates how effectively antithrombin controls clot formation in the blood. Reduced activity may indicate a hereditary deficiency, abnormal coagulation, or increased risk for venous thrombosis. This test provides insight into clotting disorders, supports diagnosis of thrombophilia, and helps assess vascular health and systemic risks related to impaired anticoagulant activity.

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The C-Reactive Protein (CRP) Test measures CRP levels in blood to detect inflammation in the body. Elevated CRP may indicate infections, autoimmune disorders, or chronic diseases such as arthritis, cardiovascular disease, or inflammatory bowel disease. Doctors use this test to assess acute illness, monitor treatment response, and evaluate risk for heart disease. The CRP test provides key insight into inflammation, immune health, and overall wellness.

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Also Known As: CRP Test, Inflammation Test

The Cardiolipin IgG IgA IgM Antibodies Test detects autoantibodies linked to antiphospholipid syndrome (APS), a disorder that increases the risk of blood clots, stroke, and pregnancy complications. Measuring IgG, IgA, and IgM helps identify abnormal immune responses. Doctors use this test to evaluate patients with unexplained clotting, recurrent miscarriages, or autoimmune disease, guiding diagnosis and treatment of APS and related conditions.

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Panel Contains Test: Anticardiolipin Antibodies Test, aCL Antibody Test, Cardiolipin Antibodies Test

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The Cardiolipin IgA Antibody Test detects IgA antibodies to cardiolipin, helping assess clotting disorders, autoimmune disease, and vascular complications. High levels are often linked to antiphospholipid syndrome, pregnancy loss, or thrombotic conditions. This test provides insight into immune activity, coagulation balance, and systemic disorders influenced by antibody-mediated vascular dysfunction.

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The Cardiolipin IgG Antibody Test detects IgG antibodies to cardiolipin, often associated with autoimmune disease. Abnormal results may indicate antiphospholipid syndrome, blood clotting disorders, or pregnancy complications. This test provides insight into thrombotic risk, vascular health, systemic inflammation, and immune activity linked to autoimmune conditions and antibody-mediated disease.

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The Cardiolipin IgM Antibody Test measures IgM antibodies linked to antiphospholipid syndrome and autoimmune disorders. It helps evaluate unexplained blood clots, recurrent miscarriages, or abnormal clotting events. By detecting immune system activity against phospholipids, this test supports the assessment of vascular health, autoimmune activity, and risks related to thrombosis or systemic lupus erythematosus.

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Most Popular

The Ferritin Test measures ferritin, a protein that stores iron in the body, to evaluate iron levels and detect deficiency or overload. It helps diagnose anemia, iron deficiency, hemochromatosis, and chronic disease-related inflammation. Doctors often order the ferritin test to investigate fatigue, weakness, or unexplained symptoms. It is also used to monitor iron supplementation, treatment effectiveness, and overall iron metabolism health.

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Also Known As: Iron Storage Test

The Prothrombin Time with INR Test measures how long it takes blood to clot and calculates the international normalized ratio (INR) for accuracy. It is commonly used to monitor patients on blood-thinning medications like warfarin and to evaluate bleeding disorders, liver disease, or vitamin K deficiency. Doctors order this test to investigate easy bruising, frequent nosebleeds, or prolonged bleeding and to ensure safe and effective anticoagulant therapy.

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Also Known As: PT with INR Test

The Prothrombin with INR and Partial Thromboplastin Times Test measures how long blood takes to clot by evaluating PT, INR, and aPTT. Abnormal results may indicate clotting disorders, liver disease, vitamin K deficiency, or risk of bleeding and thrombosis. Doctors use this test to monitor patients on blood thinners like warfarin, assess unexplained bleeding, and evaluate clotting function. It provides critical insight into coagulation and overall blood health.

Also Known As: PT with INR and aPTT Test, PT/INR and PTT Test

Most Popular

The D-Dimer Test measures fragments of blood clots to help detect abnormal clotting activity. Elevated levels may indicate deep vein thrombosis (DVT), pulmonary embolism (PE), or disseminated intravascular coagulation (DIC). Doctors often order this test when patients have symptoms like leg pain, chest pain, or shortness of breath. Results provide vital insight into clotting risk, helping guide diagnosis and management of thrombotic disorders.

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Also Known As: Fragment D-Dimer Test, Fibrin Degradation Fragment Test

The Complete Blood Count with Differential and Platelets Test is a comprehensive blood test that checks red blood cells, white blood cells, hemoglobin, hematocrit, and platelets. The differential analyzes types of white blood cells to detect infections, anemia, clotting abnormalities, immune conditions, and certain cancers. This essential test is often ordered for routine health exams, diagnosis, and monitoring treatment progress.

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Also Known As: CBC Test, CBC with Differential and Platelets Test, CBC w/Diff and Platelets Test, Full Blood Count Test, Complete Blood Count Test

The Protein S Activity Test evaluates blood clot regulation by measuring the function of protein S, a vitamin K–dependent anticoagulant. Reduced activity may indicate inherited or acquired deficiency, leading to risk of venous thrombosis, pulmonary embolism, or recurrent clotting disorders. This test provides important insight into coagulation balance and is frequently used with other assays to clarify causes of abnormal clot formation and assess thrombotic risk.

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The Protein C Activity Test measures the activity of protein C, a natural anticoagulant that regulates blood clotting. Low activity can indicate inherited or acquired protein C deficiency, increasing the risk of abnormal clot formation, deep vein thrombosis, or pulmonary embolism. This test supports evaluation of clotting disorders and provides insight into overall coagulation balance and vascular health.

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The Protein C Activity and Antigen Test evaluates both the function and concentration of Protein C, a natural anticoagulant that helps regulate blood clot formation. Measuring protein activity and antigen levels aids in identifying inherited or acquired Protein C deficiency, assessing thrombosis risk, and supporting diagnosis of abnormal coagulation disorders or vitamin K–related conditions.


The Protein C Activity Test with Reflex to Protein C Antigen measures the functional activity of Protein C, a vitamin K–dependent anticoagulant that regulates clot formation. Low Protein C activity can increase the risk of abnormal blood clots and may result from congenital deficiency, liver disease, or vitamin K deficiency. Reflex testing to Protein C antigen helps distinguish between quantitative and functional deficiencies.


The Protein C Antigen Test measures the quantity of Protein C, a vitamin K–dependent anticoagulant that regulates clot formation. Low antigen levels may indicate inherited or acquired Protein C deficiency, which increases the risk of deep vein thrombosis or other clotting disorders. This test helps differentiate between quantitative and functional deficiencies when evaluating abnormal coagulation.

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The Factor V Leiden Mutation Analysis detects a genetic mutation in the F5 gene that increases risk of abnormal blood clotting (thrombophilia). Individuals with this mutation may be prone to deep vein thrombosis (DVT), pulmonary embolism, or pregnancy complications. Doctors use this DNA test to confirm inherited clotting disorders, assess family risk, and guide prevention strategies, including anticoagulation or lifestyle management.

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Also Known As: Factor 5 Test, Factor V Test

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The Clotting Factor VIII Activity Test measures the activity of factor VIII, a protein essential for normal blood clotting. Low activity may indicate hemophilia A or acquired deficiencies, while elevated activity is linked to clotting risk. This test helps evaluate unexplained bleeding, bruising, or thrombosis, and supports diagnosis of inherited or acquired clotting disorders, providing insight into overall hemostatic function.

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Also Known As: Coag Factor VIII Activity Test

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The Homocysteine Test measures homocysteine levels in blood to assess risk for heart disease, stroke, and vascular problems. Elevated homocysteine may result from vitamin B6, B12, or folate deficiency and is linked to blood clots, cognitive decline, and osteoporosis. Doctors use this test to evaluate cardiovascular risk, monitor nutritional deficiencies, and guide treatment for metabolic or genetic conditions affecting homocysteine metabolism.

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Also Known As: Homocysteine Cardiac Risk Test

The Lupus Anticoagulant Evaluation with Reflex measures PTT-LA and dRVVT to detect lupus anticoagulant antibodies, which increase risk of abnormal clotting. Reflex tests such as Hexagonal Phase Confirmation, Thrombin Clotting Time, and dRVVT mixing are performed if results are prolonged. Doctors use this panel to evaluate unexplained clotting, recurrent miscarriage, or autoimmune disease, aiding in diagnosis of antiphospholipid syndrome.

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Also Known As: LA Test, LAC Test, Lupus Anticoagulant Panel Test, Lupus Inhibitor Test, LA Sensitive PTT Test, PTT-LA Test,

The Methylenetetrahydrofolate Reductase (MTHFR) DNA Mutation Analysis detects genetic variants in the MTHFR gene that affect folate metabolism and homocysteine regulation. Mutations may increase risk for blood clots, cardiovascular disease, pregnancy complications, or certain neurological conditions. Doctors use this test to evaluate unexplained blood clotting, high homocysteine levels, or family history of related disorders.

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Also Known As: MTHFR Factor Test, MTHFR Mutation Test, MTHFR Gene Mutation Test, Methylenetetrahydrofolate Reductase Gene Test, MTHFR Disease Test

At least 100,000 people in the United States die from blood clots yearly, and medical treatments for them exceed $10 billion every year. 

Blood clots can happen to anybody and are often the result of excessive blood clotting disorders. Early diagnosis is critical, and that's why blood clotting tests are so important.

Millions of people struggle with blood clotting disorders, and the best thing you can do is take action. Keep reading this guide to learn everything you need to know about blood clotting disorders and blood clotting tests.

What Are Excessive Blood Clotting Disorders

Often, we don't think about the process that happens when we wound or cut ourselves. The human body is an amazing machine, and it forms blood clots to stop the bleeding. Once the bleeding stops, the body should naturally break down and remove the clots.

But when you have excessive blood clotting disorders, this process is interrupted. This excessive blood clotting can be very dangerous, causing clots to form and travel to major arteries and organs. When your blood clots too much, it's referred to as a hypercoagulable state. 

Hypercoagulable states can be severe, especially when they aren't immediately identified and treated. If you're in a hypercoagulable state, you're at an increased risk of forming clots in your major arteries and blood vessels called an embolus or thrombus.

Blood clots in the veins (venous system) travel through the bloodstream and cause deep vein thrombosis in the leg, arm, liver, lungs, or intestines. 

Risk factors for Excessive Blood Clotting Disorders

Certain risk factors can lead to excessive blood clotting. Genetic risk factors include having family members with blood clots or if you have a history of unexplained miscarriages or blood clots before the age of 40.

Acquired risk factors include dehydration, smoking, overweight or obesity, pregnancy, and birth control pills or hormone replacement therapy.

Causes of Excessive Blood Clotting Disorders

What causes excessive clotting disorders and hypercoagulable states? Usually, hypercoagulable states are either genetic or an acquired condition that results from trauma, surgery, or certain medical conditions. 

Genetic or inherited hypercoagulable conditions include:

  • Factor V Leiden, which is the most common
  • Being deficient in natural clotting proteins like antithrombin and protein C
  • Prothrombin gene mutation
  • High levels of homocysteine
  • Elevated levels of factor VIII, factor IX, and  factor XI

You can also have a hypercoagulable state if you have abnormalities in your fibrinolytic system. Your fibrinolytic system functions by removing and breaking down clots after the initial injury heals. If this system doesn't function properly, then problems start to occur. Acquired conditions that cause hypercoagulable states include:

  • Cancers, especially leukemia
  • Certain medications used to treat cancer
  • Recent surgery or trauma
  • Hormone replacement therapy
  • Obesity
  • Pregnancy
  • Recent airplane travel
  • Heart failure or a heart attack
  • Stroke
  • Prolonged bed rest
  • Liver disease
  • Vitamin K deficiency

The liver plays a huge role in the clotting process, and acute or chronic liver disease as clotting factor VIII is usually increased.

Symptoms of Excessive Blood Clotting Disorders

Symptoms of excessive blood clotting disorders depend on the type you have and what the causes are from. But typical symptoms commonly include:

  • Bleeding
  • Bruising easily
  • Leg pain, swelling, and tenderness if clots present
  • Shortness of breath
  • Chest pain
  • Feeling lightheaded and faint
  • Anxiety
  • Coughing up blood

If you have a blood clotting disorder from liver disease, you'll experience symptoms like jaundice, abdominal pain, swelling, feeling unwell, and nausea.

Diagnosis of Excessive Blood Clotting Disorders

Your doctor will first take your personal and family medical history if it's suspected you have a clotting disorder. Your doctor will ask you if you have a family history of abnormal blood clotting or a history of blood clots before the age of 50.

After discussing signs and symptoms, your doctor will likely send you laboratory testing to further evaluate your blood for potential clotting problems. 

Common lab tests include a PT-INR, aPTT, fibrinogen level, and a complete blood count. Genetic tests such as factor V Leiden will be done if you have a strong family history of blood clotting disorders.

Lab Tests for Excessive Blood Clotting Disorders

Clotting disorder lab tests are key to confirming a diagnosis. Depending on your symptoms and medical history, there are different blood tests for blood clotting disorders and blood coagulation.

First, a prothrombin time (PT) with INR is one of the first coagulation blood tests to check. The PT with INR screens for any abnormalities in your coagulation factors. This test is also used to study people with both hereditary and genetic disorders.

The partial thromboplastin time (aPTT) tests for deficiencies in coagulation factors except for factors VII and XIII.

Fibrinogen Activity Clauss test measures your level of fibrinogen. Fibrinogen is necessary to form blood clots, and deficiencies in this can lead to severe bleeding disorders.

The D-Dimer quantitative is useful for measuring the activation of the fibrinolytic system and is useful in detecting blood clots in the venous system.

factor V (Leiden) mutation analysis test checks for mutations of the factor V protein that leads to blood clotting disorders and deep venous thrombosis.

complete blood count (CBC) measures your platelets and blood components and can detect problems with your platelet levels.

Other blood tests for clotting disorders include:

FAQS About Excessive Blood Clotting Disorders

Are you wondering what deep vein thrombosis (DVT) is? A DVT is a blood clot that forms in your leg veins, usually in the calf.

What is a pulmonary embolism (PE)? A PE is caused by a blood clot that originates in your leg or groin, breaks free, and travels to the lungs' arteries.

Do men or women have more of a risk of developing blood clots? The risk between men and women is just about equal.

What can you do during travel to prevent blood clots? Be sure to stop every hour or so and stand up and stretch. Even if you're traveling in an airplane, flex your toes and move your feet and ankles regularly to keep the blood flowing.

Blood Clotting Tests at Ulta Lab Tests

Ulta Lab Tests offers highly accurate tests, allowing you to make the best decisions about your health. Here are some awesome things to love about Ulta Lab Tests:

  • Secure and confidential results
  • No need for health insurance
  • No need for a physician's referral
  • Always affordable pricing
  • A 100% satisfaction guarantee

Order your blood clotting lab tests today, and you'll have results securely online in 24 to 48 hours in most cases.

Take charge of your health and shop with Ulta Lab Tests today!

What is Deep Vein Thrombosis (DVT)? It happens when a blood clot forms in a vein. DVTs mostly occur in a deep vein in the thigh or calf. Additionally, they can occur in deep veins in other parts of the body like arms, abdomen, or pelvis. These clots slow or block blood from returning to the lungs and heart by restricting the flow of blood.  

Clots occur easily in some people than others. Excessive blood clotting disorders can lead to the occurrence of DVTs. Pre-existing conditions, lifestyle choices, or medications increase the risk of blood clots. It is rare to have a predisposition because of inherited genes.  

Deep Vein Thrombosis keeps growing if left untreated. If DVT continues to grow, it obstructs the vein and cause pain, discoloration, swelling, inflammation, and may lead to permanent damage.  An increased risk for another DVT and long-term complications, known as postthrombotic syndrome (PTS), can occur after treatment. After a DVT, PTS can lead to chronic symptoms, such as long-term swelling, aching, pain, tiredness, heaviness, darkened skin, cramping, non-specific discomfort, or bluish tinge in the affected areas like arm or leg.  

However, the clot in its original location is not the greatest danger with DVT. The greatest danger is the risk of thromboembolism, which happens when a blood vessel is obstructed in a different part of the body. Pulmonary embolism (PE) occurs when part of a blood clot blocks blood flow to the lungs by breaking off and traveling to the lungs. PE is a medical emergency because it threatens life.  

Both PE and Deep Vein Thrombosis do not form in arteries, but they form in the body’s veins. So, they are grouped into venous thromboembolism (VTE). According to the Centers for Disease Control and Prevention (CDC), VTE affects around 900,00 people in the United States. Also, VTE kills 60,000 to 100,000 of the people affected, but most people die from PE. The first symptom of around 25% of people with PE is sudden death.  

DVT causes long term complications in around 30-50% of those with DVT. DVT and/or PE will occur within ten years in about 30% of people.  

Risk Factors 

Some conditions and factors increase the risk of DVT. For people with one or more conditions or factors, this increases their risk. And the resulting risk is cumulative. For instance, having an inherited risk increases the risk if the person uses oral contraceptives or smokes.  

You are not born with the most common risk factors. You acquire them later in life. Making changes can help lower the risk of blood clots in some of these factors.  

Here are some of the acquired risk factors:

  • Age – as you get older, the risk of clots increases.  
  • Chronic conditions like lung disease, kidney diseases such as nephrotic syndrome, heart disease such as congestive heart failure, and recent or recurrent cancer.  
  • Placing catheter in a central vein – a tube, which is placed into the main vein of the body, is used to administer fluids and medications. It is usually used when DVTs occur in the upper body.  
  • Hormone estrogen increasing – Hormone estrogen increases during pregnancy and after three months of delivery, and it increases from medications such as hormone replacement therapy or estrogen-based birth control. 
  • Your history of DVT – Having a blood clot increases the risk of having another one.  
  • Immobility – sitting or staying in bed for a long period slows blood flow. Why? The calf muscles do not help in blood circulation because they do not contract. Venous stasis, which is also known as “coach-class syndrome,” happens when something slows blood flow for several hours. This usually happens when someone is put on prolonged bed rest or during a long plane ride.  
  • Surgery – orthopedic surgeries like knee or hip surgeries and surgery that involves the pelvis or abdomen may lead to an activation of tissue factors. Activation of tissue factors increases the risk of immobility during surgery and the risk of clotting.  
  • Staying in hospital – 50% of blood clots happen after surgery or after a hospital stay and when the person is staying in the hospital.  
  • Antiphospholipid syndrome (APS) – this is an excessive clotting disorder 
  • Inflammatory bowel disease 
  • Injury to the vein – blood clots are formed by an injury to the walls of veins. Muscle injuries, fractures, or other trauma can cause injury to the vein.  
  • Smoking  
  • Obesity 
  • It is rare for inherited genetic variations to increase the risk of inappropriate clotting. The following are the common inherited risk factors. 
  • Deficiency in protein S, protein C, or antithrombin  
  • Factor II mutation – prothrombin 20210 mutation 
  • Activated protein C resistance – Factor V Leiden mutation  

Signs and Symptoms  

More than half of people with DVT do not have noticeable signs and symptoms. Although some of these people have a few noticeable signs and symptoms, however, symptoms can develop suddenly or gradually if you do not have them.

Here are the signs and symptoms:

  • You will see swelling due to the buildup of fluid in the affected leg. 
  • You will feel pain or tenderness in the affected leg. If clots develop rapidly, it can cause more pain.  
  • You will see redness or warmth of the skin in the leg.  
  • The clot may break and travel to the lungs, causing a pulmonary embolism (PE). The signs and symptoms of pulmonary embolism can develop quickly. The following are the signs and symptoms of PE.  
  • Your chest pains worsen when you take a deep breath or cough  
  • You cough up blood  
  • You have difficulty breathing  
  • You experience fast or irregular heartbeat  
  • You may faint or have very low blood pressure  

Laboratory Tests 

Evaluation is done to estimate the probability of the person having DVT before doing a test. When doing an evaluation, there are so many factors, such as signs and symptoms and the person’s medical history, that are taken into consideration.  

Once the valuation is complete, a D-dimer test is first done if the person’s pre-test probability is low to medium. If the result of the D-dimer test is negative, it rules out a DVT. A DVT or any other conditioner causes a positive result. For diagnosis, this requires one or more imaging tests. 

D-dimer test is not done if the person’s pre-test probability is high for a DVT. In this case, one or more imaging tests are done.  

These are the steps from the American College of Physicians (ACP), the American Academy of Family Physicians (AAFP), and the American Society of Hematology (ASH).  

An initial evaluation can be done with some general laboratory tests. Here are some of the general laboratory tests that can be done with an initial evaluation.  

Complete blood count – the test is for evaluating blood components like cell fragments and platelets that help in blood clotting   

partial thromboplastin time (PTT) and prothrombin time (PT) – these tests are for evaluating the amount and function of the blood clotting factors.  

A person diagnosed with a DVT and does not have classic risk factors, or a person is under 50 years and has DVT, or the person in an unusual location needs more tests. Additional tests are used for determining the underlying cause. Also, these additional tests are for determining the risk of having recurrent DVTs.  

There following are the tests that are done when a person is being treated for a DVT:

Antiphospholipid antibodies like lupus anticoagulant – for diagnosing antiphospholipid syndrome (APS) 

Prothrombin 20210 mutation (factor II) and factor V Leiden – for detecting inherited risk factors. It is done if the person has a recurrent blood clot. It is not done during the first DVT.  

Treatment for a DVT and the existing blood clots can affect some tests. So, the only way to do these tests is by treating and resolving the clot. Therefore, healthcare practitioners determine the cause of a person’s DVT by ordering the following test several weeks or months later. The tests are used for detecting deficiency in blood clotting factors.  

Antithrombin  

Protein S and protein C  

Here are the tests for monitoring treatment:

PT/INR – the test is for monitoring warfarin therapy  

PTT – the test is monitoring standard heparin therapy  

Heparin anti-Xa – the test is for monitoring both standard low molecular weight heparin (LMHW) therapy and heparin therapy   

Warfarin sensitivity testing – the test is done when warfarin therapy is prescribed, and the test is for determining sensitivity and resistance to warfarin. And it helps healthcare practitioners in selecting appropriate doses.