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Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern

BACKGROUND: One of the first-line assessment tools for fetal surveillance is nonstress test (NST), although it is limited by a high rate of false-nonreactive results. This study was performed to investigate if external stimulation from vibroacoustic and halogen light could help in provoking fetal re...

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Autores principales: Rahimikian, Fatemeh, Rahiminia, Tahereh, Modarres, Maryam, Mehran, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748565/
https://www.ncbi.nlm.nih.gov/pubmed/23983739
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author Rahimikian, Fatemeh
Rahiminia, Tahereh
Modarres, Maryam
Mehran, Abbas
author_facet Rahimikian, Fatemeh
Rahiminia, Tahereh
Modarres, Maryam
Mehran, Abbas
author_sort Rahimikian, Fatemeh
collection PubMed
description BACKGROUND: One of the first-line assessment tools for fetal surveillance is nonstress test (NST), although it is limited by a high rate of false-nonreactive results. This study was performed to investigate if external stimulation from vibroacoustic and halogen light could help in provoking fetal responsiveness and altering NST results. MATERIALS AND METHODS: This is a clinical trial. Sampling was done from April to July 2010. One hundred pregnant women with nonreactive NST for 20 min were allocated in two groups: Vibroacoustic stimulated NST (VNST, n = 50) who received vibration from a standard fetal vibratory stimulator and halogen light stimulated NST (LNST, n = 50) who received a halogen light source for 3 and 10 sec, respectively. Results were compared together and then compared to biophysical profile (BPP) scores as a backup test. We used Mann-Whitney U test, Chi-square test, and Fisher's exact test to compare the variables in the two groups through SPSS version 14. P < 0.05 was considered as statistically significant. RESULTS: Following stimulations, 68% nonreactive subjects in halogen light stimulation group and 62% in vibroacoustic stimulation group changed to reactive patterns. Time to onset of the first acceleration (VNST: 2.17 min; LNST: 2.27 min) and the test duration (VNST: 4.91 min; LNST: 5.26 min) were the same in the two groups. In VNST 89.5% and in LNST 87.5% of nonreactivity followed by score 8 in BPP. There was no significant relation between stimulus NSTs and BPPs. CONCLUSION: Vibroacoustic and light stimulation offer benefits by decreasing the incidence of nonreactive results and reducing the test time. Both halogen light stimulation and vibroacoustic stimulation are safe and efficient in fetal well-being assessment services.
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spelling pubmed-37485652013-08-27 Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern Rahimikian, Fatemeh Rahiminia, Tahereh Modarres, Maryam Mehran, Abbas Iran J Nurs Midwifery Res Original Article BACKGROUND: One of the first-line assessment tools for fetal surveillance is nonstress test (NST), although it is limited by a high rate of false-nonreactive results. This study was performed to investigate if external stimulation from vibroacoustic and halogen light could help in provoking fetal responsiveness and altering NST results. MATERIALS AND METHODS: This is a clinical trial. Sampling was done from April to July 2010. One hundred pregnant women with nonreactive NST for 20 min were allocated in two groups: Vibroacoustic stimulated NST (VNST, n = 50) who received vibration from a standard fetal vibratory stimulator and halogen light stimulated NST (LNST, n = 50) who received a halogen light source for 3 and 10 sec, respectively. Results were compared together and then compared to biophysical profile (BPP) scores as a backup test. We used Mann-Whitney U test, Chi-square test, and Fisher's exact test to compare the variables in the two groups through SPSS version 14. P < 0.05 was considered as statistically significant. RESULTS: Following stimulations, 68% nonreactive subjects in halogen light stimulation group and 62% in vibroacoustic stimulation group changed to reactive patterns. Time to onset of the first acceleration (VNST: 2.17 min; LNST: 2.27 min) and the test duration (VNST: 4.91 min; LNST: 5.26 min) were the same in the two groups. In VNST 89.5% and in LNST 87.5% of nonreactivity followed by score 8 in BPP. There was no significant relation between stimulus NSTs and BPPs. CONCLUSION: Vibroacoustic and light stimulation offer benefits by decreasing the incidence of nonreactive results and reducing the test time. Both halogen light stimulation and vibroacoustic stimulation are safe and efficient in fetal well-being assessment services. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3748565/ /pubmed/23983739 Text en Copyright: © Iranian Journal of Nursing and Midwifery Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Rahimikian, Fatemeh
Rahiminia, Tahereh
Modarres, Maryam
Mehran, Abbas
Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern
title Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern
title_full Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern
title_fullStr Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern
title_full_unstemmed Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern
title_short Comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern
title_sort comparison of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748565/
https://www.ncbi.nlm.nih.gov/pubmed/23983739
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