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Heparin dosing for percutaneous coronary angioplasty: Use of body surface area to improve initial activated clotting time values

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AbstractBackground: Activated clotting time (ACT) values during percutaneous transluminal coronary angioplasty (PTCA) after the initial 10,000 U heparin bolus are often below target values of 350 or 400 s (Hemochron) and have to be supplemented with additional heparin. This study evaluated the initial 10 min post‐heparin bolus clotting time value using a body surface area (BSA)‐adjusted heparin bolus versus the traditional 10,000 U heparin bolus.Hypothesis: Body surface area adjustment of initial heparin dosing prior to PTCA will be more effective in reaching target ACT values compared with the 10,000 U heparin bolus method.Methods: Twenty‐seven patients receiving the BSA‐adjusted heparin bolus were compared with 27 age‐ and gender‐matched controls who had received the traditional heparin bolus. The adjusted heparin bolus formula used was [BSA(m2)/1.3m2] X 10,000 U of heparin.Results: The success rate at reaching the target value of 400 s was 13 of 27 (48.1%) and 2 of 27 (7.4%) for the BSA‐guided and 10,000 U heparin‐guided groups, respectively (p < 0.01). The success rate at reaching the 350 s target value was 25 of 27 (92.6%) and 6 of 27 (22.2%) for the BSA‐guided and 10,000 U heparin‐guided groups, respectively (p < 0.01). The 95% confidence intervals for the difference in success between the BSA‐guided and 10,000 U heparin‐guided groups were 0.19–0.62 and 0.52–0.89 for the 400 s and 350 s ACT targets, respectively.Conclusion: Body surface area adjustment of initial heparin dosing is a more effective method of reaching the initial ACT target values of 350 and 400 s compared with the traditional method prior to PTCA. This conclusion applies to the Hemochron ACT device and arterial samples, and adjustments may need to be made for other devices and/or venous samples.
Title: Heparin dosing for percutaneous coronary angioplasty: Use of body surface area to improve initial activated clotting time values
Description:
AbstractBackground: Activated clotting time (ACT) values during percutaneous transluminal coronary angioplasty (PTCA) after the initial 10,000 U heparin bolus are often below target values of 350 or 400 s (Hemochron) and have to be supplemented with additional heparin.
This study evaluated the initial 10 min post‐heparin bolus clotting time value using a body surface area (BSA)‐adjusted heparin bolus versus the traditional 10,000 U heparin bolus.
Hypothesis: Body surface area adjustment of initial heparin dosing prior to PTCA will be more effective in reaching target ACT values compared with the 10,000 U heparin bolus method.
Methods: Twenty‐seven patients receiving the BSA‐adjusted heparin bolus were compared with 27 age‐ and gender‐matched controls who had received the traditional heparin bolus.
The adjusted heparin bolus formula used was [BSA(m2)/1.
3m2] X 10,000 U of heparin.
Results: The success rate at reaching the target value of 400 s was 13 of 27 (48.
1%) and 2 of 27 (7.
4%) for the BSA‐guided and 10,000 U heparin‐guided groups, respectively (p < 0.
01).
The success rate at reaching the 350 s target value was 25 of 27 (92.
6%) and 6 of 27 (22.
2%) for the BSA‐guided and 10,000 U heparin‐guided groups, respectively (p < 0.
01).
The 95% confidence intervals for the difference in success between the BSA‐guided and 10,000 U heparin‐guided groups were 0.
19–0.
62 and 0.
52–0.
89 for the 400 s and 350 s ACT targets, respectively.
Conclusion: Body surface area adjustment of initial heparin dosing is a more effective method of reaching the initial ACT target values of 350 and 400 s compared with the traditional method prior to PTCA.
This conclusion applies to the Hemochron ACT device and arterial samples, and adjustments may need to be made for other devices and/or venous samples.

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