Vries, R. de (Rosanne) (2016) Neonatal Care: Can pain in neonates be detected by cerebral oxygenation and electrocerebral activity. thesis, Medicine.
Full text available on request.Abstract
Abstract Although interest in neonatal pain has risen in recent years and more and more negative long term consequences become known, the detection and quantification of neonatal pain still difficult. In this study we tried to examine the efficacy of the lower border and bandwidth of the aEEG signal and the regional oxygen saturation (rSO2) and fractional tissue oxygen extraction (FTOE) as measured by near-infrared spectroscopy (NIRS) in pain detection. The 3 goals were to examine the changes of rSO2, FTOE, lower border and bandwidth by 1) a painful stimulus, 2) analgesic medications and 3) to examine the effect of a painful stimulus on the neurovascular coupling. In 17 neonates, we registered 28 skin breaking procedures, that were part of routine care. Using a paired samples t-test we found a significant lower rSO2 (p<.05) and higher FTOE (p<.05) in the minute after the skin breaking event, compared to the minute before, but not in the 2, 5, 10, 20 and 60 minutes intervals around the skin breaking event. There were no significant changes in heart rate, respiratory rate, blood pressure and arterial oxygen saturation in the 1, 10, 20, 60 minute interval, nor were there any changes in lower border and bandwidth in the 10, 20 and 60 minute interval. There was a significant trend of a lower FTOE in the morphine group compared to both the sucrose and no medication group. The proportion of intact neurovascular coupling was significantly higher in the 10 minutes before the skin breaking event compared to the 10 minutes after, but no differences in other intervals were seen. We conclude that a higher FTOE and lower rSO2, in the absence of changes in peripheral arterial oxygen saturation and heart rate, indicates cerebral processing of the painful stimulus in the first minute. Further research is needed to see whether these results can be replicated with a larger sample size. Another relevant question for future research is whether and how this subclinical pain detected by NIRS should be treated.
| Item Type: | Thesis (Thesis) |
|---|---|
| Supervisor name: | Mentor: and Kooi, dr. E. M. W. |
| Faculty: | Medical Sciences |
| Date Deposited: | 25 Jun 2020 10:51 |
| Last Modified: | 25 Jun 2020 10:51 |
| URI: | https://umcg.studenttheses.ub.rug.nl/id/eprint/1220 |
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