What is the initial workup for a patient presenting with easy bruising?

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Last updated: September 24, 2025View editorial policy

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Initial Workup for Easy Bruising

The initial workup for a patient presenting with easy bruising should include a complete blood count (CBC), peripheral blood smear, prothrombin time (PT), and partial thromboplastin time (PTT) to screen for common bleeding disorders. 1, 2

History Assessment

When evaluating a patient with easy bruising, focus on:

  • Bleeding history: Pattern, frequency, and severity of bruising
  • Medication review: Anticoagulants, antiplatelets, NSAIDs, and other medications affecting hemostasis
  • Family history: Hereditary bleeding disorders
  • Timing of symptoms: Recent onset versus lifelong
  • Associated symptoms: Mucocutaneous bleeding (suggesting platelet dysfunction) versus hemarthroses/hematomas (suggesting coagulopathy)

Consider using the International Society on Thrombosis and Hemostasis bleeding assessment tool to quantify bleeding severity and indicate possible pathology 1.

Physical Examination

Focus on:

  • Distribution and characteristics of bruises
  • Mucocutaneous bleeding sites (gums, nose)
  • Joint examination for evidence of hemarthroses
  • Petechiae or purpura (suggesting platelet disorders)
  • Signs of underlying systemic disease

Laboratory Testing Algorithm

  1. First-line tests:

    • Complete blood count (CBC) with platelet count
    • Peripheral blood smear
    • Prothrombin time (PT)/International Normalized Ratio (INR)
    • Activated partial thromboplastin time (aPTT)
    • Consider fibrinogen level
  2. Interpretation and next steps:

    • Normal PT and aPTT: Suggests platelet disorder (most commonly von Willebrand disease) 1

      • Proceed with von Willebrand screen (von Willebrand factor antigen, ristocetin cofactor activity)
      • Consider platelet function studies
    • Normal PT, prolonged aPTT: Indicates deficit in the intrinsic pathway 2

      • Perform mixing study to differentiate factor deficiency from inhibitor
      • If mixing study normalizes, proceed with specific factor assays (VIII, IX, XI, XII)
    • Prolonged PT, normal aPTT: Suggests deficit in extrinsic pathway 2

      • Consider vitamin K challenge
      • Factor VII assay
    • Both PT and aPTT prolonged: Consider liver disease, DIC, or multiple factor deficiencies

      • Liver function tests
      • Fibrinogen and D-dimer levels
    • Abnormal platelet count: If low, evaluate for immune thrombocytopenia (ITP) or other causes of thrombocytopenia

Special Considerations

  • In children with bruising, always consider non-accidental injury alongside bleeding disorders 3, 4
  • Immune thrombocytopenia (ITP) is a transient, often self-resolving bleeding disorder that should be screened for at the time of presentation 3
  • If initial testing is normal but clinical suspicion remains high, referral to a hematologist is warranted for additional specialized testing 1, 2

Common Pitfalls to Avoid

  • Failing to consider medication-induced bleeding (including over-the-counter medications and supplements)
  • Overlooking the possibility of non-accidental trauma, especially in vulnerable populations
  • Assuming normal laboratory values rule out all bleeding disorders
  • Not obtaining a thorough family history, particularly important in children who may not have experienced major bleeding episodes 1

If initial testing does not reveal an etiology in a patient with high suspicion for a bleeding disorder, refer to a hematologist for additional evaluation, as some rare platelet function disorders and mild forms of von Willebrand disease may not be detected by routine testing 1, 2.

References

Research

Bleeding and Bruising: Primary Care Evaluation.

American family physician, 2024

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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