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Effect of body mass index on Argatroban therapy during percutaneous coronary intervention
Marcie J Hursting1, Ik-Kyung Jang
1Clinical Science Consulting, Austin, TX, USA.
Insights
Obesity does not necessitate argatroban dose adjustments during percutaneous coronary intervention (PCI). Actual body weight-based dosing and activated clotting time (ACT) targeting are effective for obese and non-obese patients undergoing PCI.
Area of Science:
- Cardiology
- Pharmacology
- Medical Research
Background:
- Obesity is prevalent in patients undergoing percutaneous coronary intervention (PCI).
- Argatroban, a direct thrombin inhibitor, is crucial for patients with or at risk of heparin-induced thrombocytopenia (HIT) during PCI.
- Its use in non-HIT patients with glycoprotein IIb/IIIa inhibition has also been explored.
Purpose of the Study:
- To investigate the impact of body mass index (BMI), particularly obesity (BMI > 30 kg/m2), on argatroban therapy efficacy and safety during PCI.
- To determine if argatroban dosing requires adjustment in obese patients undergoing PCI.
Main Methods:
- Retrospective analysis of data from previous argatroban studies in PCI patients (HIT and non-HIT groups).
- Evaluation of BMI's association with activated clotting time (ACT) response, infusion dose, and ACT decline post-PCI.
- Comparison of additional bolus frequency and clinical outcomes between obese and non-obese patients.
Main Results:
- No significant association was found between BMI and ACT response, mean infusion dose, or time to ACT normalization.
- Obese and non-obese patients required additional argatroban boluses at similar rates.
- Clinical outcomes, including ischemic complications and major bleeding, did not differ significantly between obese and non-obese groups.
Conclusions:
- Argatroban therapy, adjusted for actual body weight and targeted to ACT levels, is effective in obese patients undergoing PCI.
- Dose adjustments for obesity (BMI up to 50.9 kg/m2) are not necessary.
- Current weight-based dosing strategies are appropriate for managing argatroban in PCI patients across a wide BMI range.
Background:
Obesity is common in patients undergoing percutaneous coronary intervention (PCI). Argatroban, a direct thrombin inhibitor, is used during PCI in patients with or at risk of heparin-induced thrombocytopenia (HIT) and also has been evaluated in conjunction with glycoprotein IIb/IIIa inhibition in nonHIT patients. We investigated the effect of body mass index (BMI), and specifically obesity (BMI>30 kg/m2), on argatroban therapy during PCI.
Methods:
From previously reported studies of argatroban therapy during PCI in patients with or at risk of HIT (ie, HIT group) or in conjunction with glycoprotein IIb/IIIa inhibition (ie, nonHIT group), we identified patients with sufficient data to determine BMI. After an initial bolus of 350 microg/kg (HIT group) or 300 or 250 microg/kg (nonHIT group), patients received continuous argatroban 25-30 microg/kg/min (adjusted to achieve ACTs of 300-450 s, HIT group) or 15 microg/kg/min (target ACTs of 275-325 s, nonHIT group) during PCI, with additional 150 microg/kg boluses allowed if needed. Regression analyses evaluated relationships between patient BMI and ACT response to initial bolus administration, mean infusion dose (HIT group only), and rate of ACT decline after PCI. Frequencies of additional bolus usage and clinical outcomes were compared between obese and nonobese patients.
Results:
Our analysis population included 225 patients (85 obese) in total: 73 in the HIT group and 152 in the nonHIT group (300 microg/kg bolus, n=101; 250 microg/kg bolus, n=51), with BMIs of 16.3-50.9 kg/m2. No association was detected between BMI and the first ACT after bolus administration (median ACTs of 361, 298, and 289 s, respectively, following 350, 300, and 250 microg/kg bolus), mean infusion dose (24.2+/-4.9 microg/kg/min overall in HIT group), or time to ACTs
Conclusions:
These findings support the use of actual body weight-adjusted (and ACT-targeted) argatroban therapy during PCI and suggest that dose adjustment for obesity (BMI up to 50.9 kg/m2) is unnecessary.
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