The value of the short‐term fetal heart rate variation for timing the delivery of growth‐retarded fetuses

Objective  To assess the clinical value of the short‐term fetal heart rate variation (STV) for timing the delivery of severely growth‐retarded fetuses, many associated with pre‐eclampsia. Design  Retrospective cohort study. Setting  John Radcliffe Maternity Hospital, Oxford, UK. Population  Two hund...

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Veröffentlicht in:BJOG : an international journal of obstetrics and gynaecology 2008-08, Vol.115 (9), p.1101-1107
Hauptverfasser: Serra, V, Moulden, M, Bellver, J, Redman, CWG
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container_end_page 1107
container_issue 9
container_start_page 1101
container_title BJOG : an international journal of obstetrics and gynaecology
container_volume 115
creator Serra, V
Moulden, M
Bellver, J
Redman, CWG
description Objective  To assess the clinical value of the short‐term fetal heart rate variation (STV) for timing the delivery of severely growth‐retarded fetuses, many associated with pre‐eclampsia. Design  Retrospective cohort study. Setting  John Radcliffe Maternity Hospital, Oxford, UK. Population  Two hundred and fifty‐seven fetuses with a birthweight less than third percentile and a last computerised cardiotocography performed within 24 h of delivery. Methods  Analysis of the relationship between antepartum STV and the perinatal outcome. Main outcome measures  Stillbirth rate and the acid–base status at birth. Results  There were no stillbirths or neonatal deaths (NNDs) within 24 h in the study population. Decreasing STV was correlated with earlier deliveries (P < 0.001), lower birthweight (P < 0.001), lower umbilical artery pH at birth (P < 0.001), worse acid–base status at birth (P < 0.001) and worse postnatal outcome (P < 0.002). The STV was able to predict the presence or absence of acidaemia and metabolic acidaemia (area under the receiver operating characteristic curve 0.70 and 0.75, respectively, P < 0.001). The risk of metabolic acidaemia increased as the antepartum STV decreased, the optimum cutoff level being ≤ 3.0 milliseconds (positive and negative predictive values 64.6 and 86.6%). An STV ≤ 3.0 milliseconds was associated with markedly higher rate of metabolic acidaemia and early NNDs compared with an STV > 3.0 milliseconds (54.2 versus 10.5% and 8.3 versus 0.5%, respectively; P < 0.001). The deaths of the former group were all due to extreme prematurity and very low birthweight. Conclusions  The antepartum STV is an important marker of perinatal outcome in severely growth‐retarded fetuses. Timing the delivery of the most preterm and small fetuses remains a difficult task.
doi_str_mv 10.1111/j.1471-0528.2008.01774.x
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Design  Retrospective cohort study. Setting  John Radcliffe Maternity Hospital, Oxford, UK. Population  Two hundred and fifty‐seven fetuses with a birthweight less than third percentile and a last computerised cardiotocography performed within 24 h of delivery. Methods  Analysis of the relationship between antepartum STV and the perinatal outcome. Main outcome measures  Stillbirth rate and the acid–base status at birth. Results  There were no stillbirths or neonatal deaths (NNDs) within 24 h in the study population. Decreasing STV was correlated with earlier deliveries (P < 0.001), lower birthweight (P < 0.001), lower umbilical artery pH at birth (P < 0.001), worse acid–base status at birth (P < 0.001) and worse postnatal outcome (P < 0.002). The STV was able to predict the presence or absence of acidaemia and metabolic acidaemia (area under the receiver operating characteristic curve 0.70 and 0.75, respectively, P < 0.001). The risk of metabolic acidaemia increased as the antepartum STV decreased, the optimum cutoff level being ≤ 3.0 milliseconds (positive and negative predictive values 64.6 and 86.6%). An STV ≤ 3.0 milliseconds was associated with markedly higher rate of metabolic acidaemia and early NNDs compared with an STV > 3.0 milliseconds (54.2 versus 10.5% and 8.3 versus 0.5%, respectively; P < 0.001). The deaths of the former group were all due to extreme prematurity and very low birthweight. Conclusions  The antepartum STV is an important marker of perinatal outcome in severely growth‐retarded fetuses. Timing the delivery of the most preterm and small fetuses remains a difficult task.]]></description><identifier>ISSN: 1470-0328</identifier><identifier>EISSN: 1471-0528</identifier><identifier>DOI: 10.1111/j.1471-0528.2008.01774.x</identifier><identifier>PMID: 18715432</identifier><identifier>CODEN: BIOGFQ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acid-Base Imbalance ; Adolescent ; Adult ; Biological and medical sciences ; Birth weight ; Cardiotocography ; Clinical outcomes ; Computerised cardiotocography ; Delivery, Obstetric - methods ; Delivery. Postpartum. Lactation ; Diseases of mother, fetus and pregnancy ; Female ; fetal growth retardation ; Fetal Growth Retardation - physiopathology ; Gestational Age ; Gynecology. Andrology. Obstetrics ; Heart rate ; Heart Rate, Fetal - physiology ; Humans ; Infant, Newborn ; Male ; Medical sciences ; Obstetrics ; Pregnancy. Fetus. 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Design  Retrospective cohort study. Setting  John Radcliffe Maternity Hospital, Oxford, UK. Population  Two hundred and fifty‐seven fetuses with a birthweight less than third percentile and a last computerised cardiotocography performed within 24 h of delivery. Methods  Analysis of the relationship between antepartum STV and the perinatal outcome. Main outcome measures  Stillbirth rate and the acid–base status at birth. Results  There were no stillbirths or neonatal deaths (NNDs) within 24 h in the study population. Decreasing STV was correlated with earlier deliveries (P < 0.001), lower birthweight (P < 0.001), lower umbilical artery pH at birth (P < 0.001), worse acid–base status at birth (P < 0.001) and worse postnatal outcome (P < 0.002). The STV was able to predict the presence or absence of acidaemia and metabolic acidaemia (area under the receiver operating characteristic curve 0.70 and 0.75, respectively, P < 0.001). The risk of metabolic acidaemia increased as the antepartum STV decreased, the optimum cutoff level being ≤ 3.0 milliseconds (positive and negative predictive values 64.6 and 86.6%). An STV ≤ 3.0 milliseconds was associated with markedly higher rate of metabolic acidaemia and early NNDs compared with an STV > 3.0 milliseconds (54.2 versus 10.5% and 8.3 versus 0.5%, respectively; P < 0.001). The deaths of the former group were all due to extreme prematurity and very low birthweight. Conclusions  The antepartum STV is an important marker of perinatal outcome in severely growth‐retarded fetuses. Timing the delivery of the most preterm and small fetuses remains a difficult task.]]></description><subject>Acid-Base Imbalance</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Birth weight</subject><subject>Cardiotocography</subject><subject>Clinical outcomes</subject><subject>Computerised cardiotocography</subject><subject>Delivery, Obstetric - methods</subject><subject>Delivery. Postpartum. Lactation</subject><subject>Diseases of mother, fetus and pregnancy</subject><subject>Female</subject><subject>fetal growth retardation</subject><subject>Fetal Growth Retardation - physiopathology</subject><subject>Gestational Age</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Heart rate</subject><subject>Heart Rate, Fetal - physiology</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Obstetrics</subject><subject>Pregnancy. Fetus. 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Postpartum. Lactation</topic><topic>Diseases of mother, fetus and pregnancy</topic><topic>Female</topic><topic>fetal growth retardation</topic><topic>Fetal Growth Retardation - physiopathology</topic><topic>Gestational Age</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Heart rate</topic><topic>Heart Rate, Fetal - physiology</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Obstetrics</topic><topic>Pregnancy. Fetus. Placenta</topic><topic>Prenatal care</topic><topic>Retrospective Studies</topic><topic>short‐term FHR variation</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Serra, V</creatorcontrib><creatorcontrib>Moulden, M</creatorcontrib><creatorcontrib>Bellver, J</creatorcontrib><creatorcontrib>Redman, CWG</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>British Nursing Index</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>British Nursing Index</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>BJOG : an international journal of obstetrics and gynaecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Serra, V</au><au>Moulden, M</au><au>Bellver, J</au><au>Redman, CWG</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The value of the short‐term fetal heart rate variation for timing the delivery of growth‐retarded fetuses</atitle><jtitle>BJOG : an international journal of obstetrics and gynaecology</jtitle><addtitle>BJOG</addtitle><date>2008-08</date><risdate>2008</risdate><volume>115</volume><issue>9</issue><spage>1101</spage><epage>1107</epage><pages>1101-1107</pages><issn>1470-0328</issn><eissn>1471-0528</eissn><coden>BIOGFQ</coden><abstract><![CDATA[Objective  To assess the clinical value of the short‐term fetal heart rate variation (STV) for timing the delivery of severely growth‐retarded fetuses, many associated with pre‐eclampsia. Design  Retrospective cohort study. Setting  John Radcliffe Maternity Hospital, Oxford, UK. Population  Two hundred and fifty‐seven fetuses with a birthweight less than third percentile and a last computerised cardiotocography performed within 24 h of delivery. Methods  Analysis of the relationship between antepartum STV and the perinatal outcome. Main outcome measures  Stillbirth rate and the acid–base status at birth. Results  There were no stillbirths or neonatal deaths (NNDs) within 24 h in the study population. Decreasing STV was correlated with earlier deliveries (P < 0.001), lower birthweight (P < 0.001), lower umbilical artery pH at birth (P < 0.001), worse acid–base status at birth (P < 0.001) and worse postnatal outcome (P < 0.002). The STV was able to predict the presence or absence of acidaemia and metabolic acidaemia (area under the receiver operating characteristic curve 0.70 and 0.75, respectively, P < 0.001). The risk of metabolic acidaemia increased as the antepartum STV decreased, the optimum cutoff level being ≤ 3.0 milliseconds (positive and negative predictive values 64.6 and 86.6%). An STV ≤ 3.0 milliseconds was associated with markedly higher rate of metabolic acidaemia and early NNDs compared with an STV > 3.0 milliseconds (54.2 versus 10.5% and 8.3 versus 0.5%, respectively; P < 0.001). The deaths of the former group were all due to extreme prematurity and very low birthweight. Conclusions  The antepartum STV is an important marker of perinatal outcome in severely growth‐retarded fetuses. Timing the delivery of the most preterm and small fetuses remains a difficult task.]]></abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18715432</pmid><doi>10.1111/j.1471-0528.2008.01774.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Acid-Base Imbalance
Adolescent
Adult
Biological and medical sciences
Birth weight
Cardiotocography
Clinical outcomes
Computerised cardiotocography
Delivery, Obstetric - methods
Delivery. Postpartum. Lactation
Diseases of mother, fetus and pregnancy
Female
fetal growth retardation
Fetal Growth Retardation - physiopathology
Gestational Age
Gynecology. Andrology. Obstetrics
Heart rate
Heart Rate, Fetal - physiology
Humans
Infant, Newborn
Male
Medical sciences
Obstetrics
Pregnancy. Fetus. Placenta
Prenatal care
Retrospective Studies
short‐term FHR variation
Time Factors
title The value of the short‐term fetal heart rate variation for timing the delivery of growth‐retarded fetuses
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