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Blood Pressure during Blood Collection and the Implication for Absolute Cardiovascular Risk Assessment
Niamh Chapman1, Dean S Picone1, Rachel E Climie1
1Menzies Institute for Medical Research, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Insights
Blood collection does not significantly alter systolic blood pressure (SBP) measurements, making it acceptable to measure BP and collect blood during the same visit for cardiovascular disease (CVD) risk assessment.
Area of Science:
- Cardiology
- Clinical Measurement
- Public Health
Background:
- Blood collection and blood pressure (BP) measurements are routinely performed together to assess cardiovascular disease (CVD) risk.
- The potential impact of blood collection on BP readings and subsequent CVD risk calculations requires investigation.
Purpose of the Study:
- To determine the effect of blood collection on BP measurements.
- To assess the subsequent impact on absolute CVD risk calculations.
Main Methods:
- Systolic BP (SBP) was measured in 45 participants (58 ± 9 years, 53% male) using standard methods.
- BP was measured immediately before, during, and after blood collection on a separate visit.
- Absolute CVD risk scores were calculated using the Framingham equation with SBP from each condition.
Main Results:
- SBP values before and during blood collection were significantly higher than after (130 ± 18 and 132 ± 19 vs. 126 ± 18 mm Hg).
- No significant differences were found between clinic SBP and blood collection SBP, or in the calculated absolute CVD risk scores.
- Good agreement was observed between risk scores calculated with clinic SBP and blood collection SBP (ICC > 0.85).
Conclusions:
- Absolute CVD risk calculations are not significantly affected by SBP measurements taken during blood collection.
- Measuring BP and collecting blood during the same consultation is acceptable for absolute CVD risk assessment.
Background:
Blood collection and blood pressure (BP) measurements are routinely performed during the same consultation to assess absolute cardiovascular disease (CVD) risk. This study aimed to determine the effect of blood collection on BP and subsequent calculation of the absolute CVD risk.
Methods:
Forty-five participants aged 58 ± 9 years (53% male) had systolic BP (SBP) measured using clinical guideline methods (clinic SBP). Then, on a separate visit, BP was measured immediately before, during, and after blood collection. Absolute CVD risk scores were calculated (Framingham equation) using SBP from each measurement condition and compared.
Results:
The prevalence of low (<10%), moderate (10-15%), and high (≥15%) absolute CVD risks among the participants was 67%, 22%, and 11%, respectively, using clinic SBP. SBP values before and during blood collection were significantly higher compared to values after blood collection (130 ± 18 and 132 ± 19 vs. 126 ± 18 mm Hg; p = 0.010 and p = 0.003, respectively). However, there were no significant differences between clinic SBP (128 ± 18 mm Hg) and blood collection SBP (p = 0.99) or the absolute CVD risk scores (7.3 ± 6.5; 7.6 ± 5.9; 7.7 ± 6.1; and 7.1 ± 5.7%, respectively; p = 0.995 for all). The mean intraclass correlation (95% CI) indicated good agreement between absolute CVD risk scores calculated with clinic SBP and each blood collection SBP (0.86 [95% CI 0.74-0.92], 0.85 [95% CI 0.71-0.91], and 0.87 [95% CI 0.76-0.93], respectively; p < 0.001, for all).
Conclusion:
Absolute CVD risk calculation is not affected by use of SBP measurements recorded at the time of blood collection. Therefore, it is acceptable to collect blood and measure BP during the same consultation for absolute CVD risk assessment.
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