What is the normal range for Activated Clotting Time (ACT)?

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Last updated: July 25, 2025View editorial policy

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Normal Range for Activated Clotting Time (ACT)

The normal range for Activated Clotting Time (ACT) is typically 120-180 seconds in non-anticoagulated patients, with target therapeutic ranges varying by clinical context.

Normal and Therapeutic ACT Ranges by Clinical Setting

Baseline Normal Range

  • Non-anticoagulated patients: 120-180 seconds 1
  • This represents the baseline clotting time in patients not receiving anticoagulation therapy

Therapeutic Ranges by Clinical Context

Cardiopulmonary Bypass (CPB)

  • Target range: 480 seconds or higher 2
  • Historical studies initially suggested >300 seconds was adequate 2
  • Later research recommended higher targets of 400-480 seconds 2
  • Current consensus from the International Society on Thrombosis and Haemostasis (ISTH) recommends ≥480 seconds 2

Extracorporeal Membrane Oxygenation (ECMO)

  • Target range: 180-220 seconds 2
  • Some centers use lower targets (140-160 seconds) to reduce bleeding risk 2
  • Anti-Xa levels of 0.3-0.5 U/mL are preferred for monitoring when available 2

Percutaneous Coronary Intervention (PCI)

  • With glycoprotein IIb/IIIa inhibitors: 200-250 seconds 2
  • Without glycoprotein IIb/IIIa inhibitors:
    • 250-300 seconds (HemoTec device)
    • 300-350 seconds (Hemochron device) 2

Peripheral Vascular Surgery

  • Target range: >180-200 seconds (greater than twice the baseline value) 3
  • ACT <200 seconds associated with higher risk of arterial thromboembolic complications 4
  • ACT >250 seconds associated with increased bleeding complications 4

Pediatric Cardiac Surgery

  • Target range: >480 seconds for neonates, infants, and children 2
  • Some programs use >400 seconds 2

Important Considerations in ACT Measurement

Device Variability

  • Different ACT devices produce significantly different results:
    • HemoTec and Hemochron devices show poor correlation 2, 5
    • In therapeutic ranges (200-350 seconds), values are not comparable between devices 5
    • HemoTec devices demonstrate better reproducibility (coefficient of variation 2.4% vs 7.2% for Hemochron) 5

Timing Considerations

  • ACT values decrease approximately 15% when testing is delayed by 30 minutes 1
  • Immediate point-of-care testing is recommended for accurate results 1

Factors Affecting ACT Values

  • Hypothermia, hemodilution, and decreased platelet function can prolong ACT 2
  • Aprotinin prolongs celite-activated ACT but not kaolin-activated ACT 2
  • Different activators (celite vs. kaolin) and detection methods affect measurements 2

Clinical Applications and Monitoring

  • For heparin monitoring during procedures, initial ACT should be measured before heparin administration to establish baseline 3
  • Supplemental heparin is often needed within 2 hours to maintain therapeutic levels 3
  • At procedure conclusion, if ACT >150 seconds, protamine reversal should be considered 3
  • Post-procedure ACT should be obtained 15-30 minutes after reversal to detect heparin rebound 3

Remember that ACT measurements should be interpreted in the clinical context, and the specific device used for measurement should be considered when determining appropriate target ranges.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

The Additional Value of Activated Clotting Time-Guided Heparinization During Interventions for Peripheral Arterial Disease.

Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists, 2023

Research

Reproducibility and variability of activated clotting time measurements in the cardiac catheterization laboratory.

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions, 2005

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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