Have You Suffered from Heparin-Induced Thrombocytopenia or Thrombosis (HIT/HITT)?
MANEY | GORDON Trial Lawyers

The Deadly 1%

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Heparin-induced thrombocytopenia (HIT) is a paradox: a drug used to prevent clots sometimes triggers an immune reaction that causes both a drop in platelets and an increased risk of dangerous thrombosis. We'll explore how HIT begins, why it’s so serious, what the data says about risk and frequency, whether it’s rising, and practical steps for patients and clinicians.

How HIT Starts: The Immune Reaction Explained

HIT is an immune-mediated reaction. When heparin is introduced into the body, it can bind to a protein called platelet factor 4 (PF4). In some people, the immune system mistakenly sees this PF4-heparin complex as a threat and produces IgG antibodies against it. These antibodies activate platelets, causing them to clump together and form clots. At the same time, platelets are consumed or destroyed, leading to thrombocytopenia (low platelet count). This paradox—low platelets but high clot risk—is what makes HIT so dangerous.

Why HIT Is Dangerous: Clots, Limb Loss, and Mortality

Once HIT antibodies are active, the risk of venous and arterial thrombosis skyrockets. Patients may develop:

  • stroke
  • heart attack
  • pulmonary embolism (PE)
  • deep vein thrombosis (DVT)
  • or limb ischemia, which can lead to amputation.

If untreated, heparin-induced thrombocytopenia can be fatal or limb-threatening. Studies show that 30–50% of HIT cases result in thrombosis, and mortality rates can reach up to 20% without prompt treatment.

HIT Statistics: How Common Is It?

HIT is uncommon but serious. Incidence varies by patient type and heparin formulation: Unfractionated heparin (UFH): 1–5% risk in surgical patients; Low-molecular-weight heparin (LMWH): <1% risk; General hospitalized population: ~0.1–1% overall. Despite its rarity, HIT is a high-stakes diagnosis because of the severe complications it can cause.

Can You Predict HIT Before It Happens?

There’s no definitive test to predict HIT before heparin exposure. However, risk factors include:

  • use of UFH over LMWH
  • female gender and older age
  • longer duration or higher doses of heparin
  • surgical patients (especially cardiac or orthopedic)
  • prior exposure to heparin (especially within the last 100 days)

Clinicians use the 4Ts score to estimate the likelihood of HIT based on:

  • thrombosis presence
  • timing of platelet drop
  • thrombocytopenia severity
  • and other causes of low platelets.

What to Do If You Suspect HIT

If you or someone you know is receiving heparin and develops a drop in platelet count, new swelling, pain, or shortness of breath, or neurologic symptoms (e.g., stroke-like signs), act fast: Notify your healthcare provider immediately, stop all heparin products, start a non-heparin anticoagulant (e.g., argatroban, fondaparinux, or DOACs under guidance), avoid platelet transfusions unless there's life-threatening bleeding, and get tested: Immunoassays for PF4-heparin antibodies and functional assays like the serotonin release assay. Taking immediate action can prevent a medical malpractice case from forming and, more importantly, keep you and your life safe.

Are You a Victim of Heparin-Induced Thrombocytopenia?

If you’ve had HIT: Wear a medical alert bracelet, ensure your medical records reflect the diagnosis, and avoid future heparin exposure.

HIT is rare but dangerous. Knowing the signs, understanding the risks, and acting quickly can save lives and limbs. If you’re undergoing treatment with heparin, stay informed and speak up if something feels off. The expert trial attorneys at MANEY | GORDON Trial Lawyers have experience handling HIT cases from across the country. Our specialization in Medical Malpractice gives us a unique perspective to fight for you and ensure you receive the justice you deserve. Contact us for a free consultation today.

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