Abstract
The objective is to assess if fetal halogen light stimulation can reduce the time needed to obtain a normal biophysical profile (BPP). Patients scheduled for a BPP and who satisfied the inclusion criteria were prospectively randomized to halogen light stimulation and no stimulation groups. The study group was exposed to handheld halogen light for 10s whenever fetal breathing, movement, or tone was absent through the first 5min of BPP. The time required to achieve complete BPP score was recorded. In patients with complete BPP score who had delivery within 1week after the test, perinatal morbidity was examined. A total of 598 patients were randomized (light=302, no light=296). There was no difference between the two groups in terms of gestational age, maternal age, body mass index, and indication for BPP except for preterm labor (light: 9%, no light: 4%, p=0.03). Among the patients who had a normal BPP score (n=507), the mean (light: 7.1±6min, no light: 12.3±8min, p<0.0001) and median (light: 4.3, no light: 8, p=0.004) time needed to complete the BPP score was significantly less in the light stimulation group than the no stimulation group. Perinatal outcomes were not different between groups who had delivery during the first week after BPP. Fetal halogen light stimulation can be utilized to reduce the time needed to complete a BPP. However, further studies should be conducted in order to determine the effect of this method on decreasing non-reassuring test results. The study was submitted to the Registry of Clinical Trials on 04/20/2017 (IRCT2017041633470N1). After IRCT registration on 06/07/2017, we recruited patients from 06/08/2017 till 10/15/2017.
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