Increased fetal heart rate variability in periventricular leukomalacia

Abstract Objective This study used quantitative analysis to determine whether increased variability in fetal heart rate (FHR) is related to the risk of developing periventricular leukomalacia (PVL). Methods We analyzed 124 FHR traces of neonates delivered preterm at 27–33 weeks’ gestation to 105 mot...

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Veröffentlicht in:Brain & development (Tokyo. 1979) 2016-02, Vol.38 (2), p.196-203
Hauptverfasser: Kurahashi, Hirokazu, Okumura, Akihisa, Kubota, Tetsuo, Kidokoro, Hiroyuki, Maruyama, Koichi, Hayakawa, Masahiro, Itakura, Atsuo, Matsuzawa, Katsuji, Yamamoto, Hiroyuki, Kato, Toru, Hayakawa, Fumio, Watanabe, Kazuyoshi
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container_end_page 203
container_issue 2
container_start_page 196
container_title Brain & development (Tokyo. 1979)
container_volume 38
creator Kurahashi, Hirokazu
Okumura, Akihisa
Kubota, Tetsuo
Kidokoro, Hiroyuki
Maruyama, Koichi
Hayakawa, Masahiro
Itakura, Atsuo
Matsuzawa, Katsuji
Yamamoto, Hiroyuki
Kato, Toru
Hayakawa, Fumio
Watanabe, Kazuyoshi
description Abstract Objective This study used quantitative analysis to determine whether increased variability in fetal heart rate (FHR) is related to the risk of developing periventricular leukomalacia (PVL). Methods We analyzed 124 FHR traces of neonates delivered preterm at 27–33 weeks’ gestation to 105 mothers. FHR traces 1–3 h before delivery were translated into power-spectrum curves using a fast Fourier transformation. The total power (the area under the curve of 1–10 cycles per minute), segmental power of every cycle per minute, peak power, and frequency edges were calculated, and their relationship with the subsequent development of PVL was examined. Results Total power was significantly higher in the PVL group ( n = 9, median 1813, range 1064–2426) compared to the non-PVL group ( n = 114, median 1383, range 381–3324, p = 0.029). Infants in the PVL group had greater segmental power in segments with 1–2, 2–3, and 9–10 cycles per minute, than those in the non-PVL group. Total power of ⩾1550 was significantly correlated with the subsequent development of PVL and premature rupture of membranes. Furthermore, the frequency of pregnancy-induced hypertension was significantly reduced in the fetuses with a total power of ⩾1550. Conclusion Our study suggests that a fetus with increased FHR variability is at risk of developing PVL. This study provides additional evidence supporting the contribution of antenatal factors to the subsequent development of PVL.
doi_str_mv 10.1016/j.braindev.2015.08.008
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Methods We analyzed 124 FHR traces of neonates delivered preterm at 27–33 weeks’ gestation to 105 mothers. FHR traces 1–3 h before delivery were translated into power-spectrum curves using a fast Fourier transformation. The total power (the area under the curve of 1–10 cycles per minute), segmental power of every cycle per minute, peak power, and frequency edges were calculated, and their relationship with the subsequent development of PVL was examined. Results Total power was significantly higher in the PVL group ( n = 9, median 1813, range 1064–2426) compared to the non-PVL group ( n = 114, median 1383, range 381–3324, p = 0.029). Infants in the PVL group had greater segmental power in segments with 1–2, 2–3, and 9–10 cycles per minute, than those in the non-PVL group. Total power of ⩾1550 was significantly correlated with the subsequent development of PVL and premature rupture of membranes. Furthermore, the frequency of pregnancy-induced hypertension was significantly reduced in the fetuses with a total power of ⩾1550. Conclusion Our study suggests that a fetus with increased FHR variability is at risk of developing PVL. This study provides additional evidence supporting the contribution of antenatal factors to the subsequent development of PVL.</description><identifier>ISSN: 0387-7604</identifier><identifier>EISSN: 1872-7131</identifier><identifier>DOI: 10.1016/j.braindev.2015.08.008</identifier><identifier>PMID: 26338690</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Fast Fourier transform ; Female ; Fetal heart rate ; Gestational Age ; Heart Rate, Fetal - physiology ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Leukomalacia, Periventricular - physiopathology ; Long-term variability ; Male ; Neurology ; Periventricular leukomalacia ; Pregnancy ; Risk Factors</subject><ispartof>Brain &amp; development (Tokyo. 1979), 2016-02, Vol.38 (2), p.196-203</ispartof><rights>The Japanese Society of Child Neurology</rights><rights>2015 The Japanese Society of Child Neurology</rights><rights>Copyright © 2015 The Japanese Society of Child Neurology. Published by Elsevier B.V. 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Methods We analyzed 124 FHR traces of neonates delivered preterm at 27–33 weeks’ gestation to 105 mothers. FHR traces 1–3 h before delivery were translated into power-spectrum curves using a fast Fourier transformation. The total power (the area under the curve of 1–10 cycles per minute), segmental power of every cycle per minute, peak power, and frequency edges were calculated, and their relationship with the subsequent development of PVL was examined. Results Total power was significantly higher in the PVL group ( n = 9, median 1813, range 1064–2426) compared to the non-PVL group ( n = 114, median 1383, range 381–3324, p = 0.029). Infants in the PVL group had greater segmental power in segments with 1–2, 2–3, and 9–10 cycles per minute, than those in the non-PVL group. Total power of ⩾1550 was significantly correlated with the subsequent development of PVL and premature rupture of membranes. Furthermore, the frequency of pregnancy-induced hypertension was significantly reduced in the fetuses with a total power of ⩾1550. Conclusion Our study suggests that a fetus with increased FHR variability is at risk of developing PVL. This study provides additional evidence supporting the contribution of antenatal factors to the subsequent development of PVL.</description><subject>Fast Fourier transform</subject><subject>Female</subject><subject>Fetal heart rate</subject><subject>Gestational Age</subject><subject>Heart Rate, Fetal - physiology</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Infant, Premature</subject><subject>Leukomalacia, Periventricular - physiopathology</subject><subject>Long-term variability</subject><subject>Male</subject><subject>Neurology</subject><subject>Periventricular leukomalacia</subject><subject>Pregnancy</subject><subject>Risk Factors</subject><issn>0387-7604</issn><issn>1872-7131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkT1v2zAQhomgReJ8_IVAYxepd6IlUkvRImjaAAE6tJ2JE3lC6dCSS0oG_O9Dw0mHLJ1ueT9wzyvELUKFgO3HTdVH8qPjfVUDNhXoCkCfiRVqVZcKJb4TK5BalaqF9YW4TGkDAFgjnIuLupVStx2sxP3DaCNTYlcMPFMo_jDFuYg0c7Gn6Kn3wc-Hwo_FjqPf8zhHb5dAsQi8PE1bCmQ9XYv3A4XENy_3Svy-__rr7nv5-OPbw92Xx9I2Ws4lompc1w0WtOUBue8ctapH56xuB6qJNCuEGrEDpdYDtr2Cjno1dNJ10Mgr8eGUu4vT34XTbLY-WQ6BRp6WZHK-rCXodZ2l7Ulq45RS5MHsot9SPBgEc2RoNuaVoTkyNKBNZpiNty8dS79l98_2Ci0LPp8EnD_de44mWc-jZecj29m4yf-_49ObCBv86C2FJz5w2kxLHDNHgybVBszP45LHIbHJG6o87zPjapt6</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Kurahashi, Hirokazu</creator><creator>Okumura, Akihisa</creator><creator>Kubota, Tetsuo</creator><creator>Kidokoro, Hiroyuki</creator><creator>Maruyama, Koichi</creator><creator>Hayakawa, Masahiro</creator><creator>Itakura, Atsuo</creator><creator>Matsuzawa, Katsuji</creator><creator>Yamamoto, Hiroyuki</creator><creator>Kato, Toru</creator><creator>Hayakawa, Fumio</creator><creator>Watanabe, Kazuyoshi</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160201</creationdate><title>Increased fetal heart rate variability in periventricular leukomalacia</title><author>Kurahashi, Hirokazu ; Okumura, Akihisa ; Kubota, Tetsuo ; Kidokoro, Hiroyuki ; Maruyama, Koichi ; Hayakawa, Masahiro ; Itakura, Atsuo ; Matsuzawa, Katsuji ; Yamamoto, Hiroyuki ; Kato, Toru ; Hayakawa, Fumio ; Watanabe, Kazuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c583t-1175d99fc08cef1eb9da67b1ddc86fa2aa8e71021190774f16b709ab7f93d9053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Fast Fourier transform</topic><topic>Female</topic><topic>Fetal heart rate</topic><topic>Gestational Age</topic><topic>Heart Rate, Fetal - physiology</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Infant, Premature</topic><topic>Leukomalacia, Periventricular - physiopathology</topic><topic>Long-term variability</topic><topic>Male</topic><topic>Neurology</topic><topic>Periventricular leukomalacia</topic><topic>Pregnancy</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kurahashi, Hirokazu</creatorcontrib><creatorcontrib>Okumura, Akihisa</creatorcontrib><creatorcontrib>Kubota, Tetsuo</creatorcontrib><creatorcontrib>Kidokoro, Hiroyuki</creatorcontrib><creatorcontrib>Maruyama, Koichi</creatorcontrib><creatorcontrib>Hayakawa, Masahiro</creatorcontrib><creatorcontrib>Itakura, Atsuo</creatorcontrib><creatorcontrib>Matsuzawa, Katsuji</creatorcontrib><creatorcontrib>Yamamoto, Hiroyuki</creatorcontrib><creatorcontrib>Kato, Toru</creatorcontrib><creatorcontrib>Hayakawa, Fumio</creatorcontrib><creatorcontrib>Watanabe, Kazuyoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Brain &amp; development (Tokyo. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kurahashi, Hirokazu</au><au>Okumura, Akihisa</au><au>Kubota, Tetsuo</au><au>Kidokoro, Hiroyuki</au><au>Maruyama, Koichi</au><au>Hayakawa, Masahiro</au><au>Itakura, Atsuo</au><au>Matsuzawa, Katsuji</au><au>Yamamoto, Hiroyuki</au><au>Kato, Toru</au><au>Hayakawa, Fumio</au><au>Watanabe, Kazuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased fetal heart rate variability in periventricular leukomalacia</atitle><jtitle>Brain &amp; development (Tokyo. 1979)</jtitle><addtitle>Brain Dev</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>38</volume><issue>2</issue><spage>196</spage><epage>203</epage><pages>196-203</pages><issn>0387-7604</issn><eissn>1872-7131</eissn><abstract>Abstract Objective This study used quantitative analysis to determine whether increased variability in fetal heart rate (FHR) is related to the risk of developing periventricular leukomalacia (PVL). Methods We analyzed 124 FHR traces of neonates delivered preterm at 27–33 weeks’ gestation to 105 mothers. FHR traces 1–3 h before delivery were translated into power-spectrum curves using a fast Fourier transformation. The total power (the area under the curve of 1–10 cycles per minute), segmental power of every cycle per minute, peak power, and frequency edges were calculated, and their relationship with the subsequent development of PVL was examined. Results Total power was significantly higher in the PVL group ( n = 9, median 1813, range 1064–2426) compared to the non-PVL group ( n = 114, median 1383, range 381–3324, p = 0.029). Infants in the PVL group had greater segmental power in segments with 1–2, 2–3, and 9–10 cycles per minute, than those in the non-PVL group. Total power of ⩾1550 was significantly correlated with the subsequent development of PVL and premature rupture of membranes. Furthermore, the frequency of pregnancy-induced hypertension was significantly reduced in the fetuses with a total power of ⩾1550. Conclusion Our study suggests that a fetus with increased FHR variability is at risk of developing PVL. This study provides additional evidence supporting the contribution of antenatal factors to the subsequent development of PVL.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26338690</pmid><doi>10.1016/j.braindev.2015.08.008</doi><tpages>8</tpages></addata></record>
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subjects Fast Fourier transform
Female
Fetal heart rate
Gestational Age
Heart Rate, Fetal - physiology
Humans
Infant
Infant, Newborn
Infant, Premature
Leukomalacia, Periventricular - physiopathology
Long-term variability
Male
Neurology
Periventricular leukomalacia
Pregnancy
Risk Factors
title Increased fetal heart rate variability in periventricular leukomalacia
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