A comparison between invasive and noninvasive measurement of the Hypotension Prediction Index: A post hoc analysis of a prospective cohort study.

BACKGROUND

Clinical trials and validation studies demonstrate promising hypotension prediction capability by the Hypotension Prediction Index (HPI). Most studies that evaluate HPI derive it from invasive blood pressure readings, but a direct comparison with the noninvasive alternative remains undetermined. Such a comparison could provide valuable insights for clinicians in deciding between invasive and noninvasive monitoring strategies.

OBJECTIVES

Evaluating predictive differences between HPI when obtained through noninvasive versus invasive blood pressure monitoring.

DESIGN

Post hoc analysis of a prospective observational study conducted between 2018 and 2020.

SETTING

Single-centre study conducted in an academic hospital in the Netherlands.

PATIENTS

Adult noncardiac surgery patients scheduled for over 2 h long elective procedures. After obtaining informed consent, 91 out of the 105 patients had sufficient data for analysis.

MAIN OUTCOME MEASURES

The primary outcome was the difference in area under the receiver-operating characteristics (ROC) curve (AUC) obtained for HPI predictions between the two datasets. Additionally, difference in time-to-event estimations were calculated.

RESULTS

AUC (95% confidence interval (CI)) results revealed a nonsignificant difference between invasive and noninvasive HPI, with areas of 94.2% (90.5 to 96.8) and 95.3% (90.4 to 98.2), respectively with an estimated difference of 1.1 (-3.9 to 6.1)%; P  = 0.673. However, noninvasive HPI demonstrated significantly longer time-to-event estimations for higher HPI values.

CONCLUSION

Noninvasive HPI is reliably accessible to clinicians during noncardiac surgery, showing comparable accuracy in HPI probabilities and the potential for additional response time.

TRIAL REGISTRATION

Clinicaltrials.gov (NCT03795831) https://clinicaltrials.gov/study/NCT03795831.