The performance of the heart rate variability-derived Newborn Infant Parasympathetic Evaluation Index as a measure of early postoperative pain and discomfort in infants—A prospective observational study

<p>Background: The heart rate variability-derived Newborn Infant Parasympathetic Evaluation (NIPE™) Index is a continuous noninvasive tool for the assessment of pain and discomfort in infants. Little is known about its performance in the early postoperative setting, where assessment of pain/discomfort is usually based on discontinuous observational scoring systems or personal experience of medical staff. Aims: To investigate the performance of the NIPE as a measure of early postoperative pain and/or discomfort in infants. Methods: The potential of the NIPE to detect pain/discomfort, as assessed by two clinical scoring systems (FLACC and COMFORT-B scale), was investigated in postoperative infants (0–2 years). Results: Receiver operating curve (ROC) analyses investigating the power of the NIPE to distinguish between comfort and pain/discomfort, revealed areas under the curve (AUC) of 0.77 for the FLACC, 0.81 for the COMFORT-B score, and 0.77 for a combination of FLACC &amp; COMFORT-B. Logistic regression analysis provided initial evidence that the NIPE is an independent predictor of a FLACC score ≥4 and/or a COMFORT-B score ≥17, though R² values were below.2. NIPE values associated with a FLACC ≥4 (48 [45–56]), a COMFORT-B score ≥17 (47 [42–53]), and a FLACC ≥4 &amp; COMFORT-B ≥17 (47 [42–57]) were lower than NIPE values associated with a FLACC &lt;4 (60 [53–68], 95% CI of difference −14 to −8, p &lt;.0001), a COMFORT-B score &lt;17 (61 [54–68], 95% CI of difference −16 to −10, p &lt;.0001), and a FLACC &lt;4 &amp; COMFORT-B score &lt;17 (60 [53–68], 95% CI of difference −15 to −8, p &lt;.0001). We found no evidence of a predictive value of the NIPE regarding the occurrence of pain. Conclusions: The NIPE detected pain and discomfort in infants after general anesthesia with reasonable areas under the ROC curve (±0.8), whereas it was not predictive of clinically detectable pain or discomfort.</p>

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