Tertiary centre referral of small-for-gestational age pregnancies: A 10-year retrospective analysis
Between 1981 and 1991, 461 pregnant women between 15 and 40 weeks of gestation (mean 30 weeks) with completed follow‐up were referred to our centre for prenatal diagnosis because of a small‐for‐gestational age (SGA) fetus or combined SGA and structural abnormality. The referral diagnosis was based e...
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Veröffentlicht in: | Prenatal diagnosis 1994-02, Vol.14 (2), p.105-108 |
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description | Between 1981 and 1991, 461 pregnant women between 15 and 40 weeks of gestation (mean 30 weeks) with completed follow‐up were referred to our centre for prenatal diagnosis because of a small‐for‐gestational age (SGA) fetus or combined SGA and structural abnormality. The referral diagnosis was based either on biparietal diameter measurements or on measurement of the upper‐abdominal circumference. SGA in our centre was defined as a fetal upper‐abdominal circumference below the tenth centile. SGA was confirmed by ultrasound in 75 per cent of the fetuses, whilst combined SGA and fetal structural abnormality was substantiated in only 16 per cent of the fetuses. However, in our centre structural abnormality was detected in 34 fetuses who were referred because of SGA alone. Nearly half of the structurally normal SGA fetuses displayed a normal head‐to‐abdomen (H/A), ratio, whereas an increased H/A ratio was found in 13/15 fetuses with an abnormal karyotype. An abnormal karyotype was present in 20 fetuses, which is 7 per cent of the total SGA population. Nearly 50 per cent represented triploidy associated with oligohydramnios. SGA was confirmed by a birth weight below the tenth centile in 89 per cent, below the fifth centile in 77 per cent, and below the 2·3rd centile in 55 per cent of infants. Structural abnormality was confirmed in 65 per cent of infants, whereas in 19 per cent of infants the abnormality was missed or a misclassification was made. Perinatal mortality was 31 per cent for all SGA fetuses, 27 per cent for SGA fetuses without anomalies, and 64 per cent for SGA fetuses with structural abnormality. |
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P. ; Wladimiroff, J. W.</creator><creatorcontrib>Heydanus, R. ; van Splunder, I. P. ; Wladimiroff, J. W.</creatorcontrib><description>Between 1981 and 1991, 461 pregnant women between 15 and 40 weeks of gestation (mean 30 weeks) with completed follow‐up were referred to our centre for prenatal diagnosis because of a small‐for‐gestational age (SGA) fetus or combined SGA and structural abnormality. The referral diagnosis was based either on biparietal diameter measurements or on measurement of the upper‐abdominal circumference. SGA in our centre was defined as a fetal upper‐abdominal circumference below the tenth centile. SGA was confirmed by ultrasound in 75 per cent of the fetuses, whilst combined SGA and fetal structural abnormality was substantiated in only 16 per cent of the fetuses. However, in our centre structural abnormality was detected in 34 fetuses who were referred because of SGA alone. Nearly half of the structurally normal SGA fetuses displayed a normal head‐to‐abdomen (H/A), ratio, whereas an increased H/A ratio was found in 13/15 fetuses with an abnormal karyotype. An abnormal karyotype was present in 20 fetuses, which is 7 per cent of the total SGA population. Nearly 50 per cent represented triploidy associated with oligohydramnios. SGA was confirmed by a birth weight below the tenth centile in 89 per cent, below the fifth centile in 77 per cent, and below the 2·3rd centile in 55 per cent of infants. Structural abnormality was confirmed in 65 per cent of infants, whereas in 19 per cent of infants the abnormality was missed or a misclassification was made. Perinatal mortality was 31 per cent for all SGA fetuses, 27 per cent for SGA fetuses without anomalies, and 64 per cent for SGA fetuses with structural abnormality.</description><identifier>ISSN: 0197-3851</identifier><identifier>EISSN: 1097-0223</identifier><identifier>DOI: 10.1002/pd.1970140205</identifier><identifier>PMID: 8183846</identifier><identifier>CODEN: PRDIDM</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Adult ; Anthropometry ; Biological and medical sciences ; Birth Weight ; Chromosome Aberrations ; Diseases of mother, fetus and pregnancy ; Female ; fetal anomaly ; fetal karyotype ; Gestational Age ; Gynecology. Andrology. Obstetrics ; Humans ; Infant, Newborn ; Infant, Small for Gestational Age ; Karyotyping ; man ; Medical sciences ; Pregnancy ; Pregnancy. Fetus. Placenta ; Prenatal Diagnosis ; Retrospective Studies ; Small-for-gestational age fetuses ; Ultrasonography, Prenatal</subject><ispartof>Prenatal diagnosis, 1994-02, Vol.14 (2), p.105-108</ispartof><rights>Copyright © 1994 John Wiley & Sons, Ltd.</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4345-22ffe70b0dde851b1b20422ecb806d2ab719f4e71e777d491d8d0c532de5663d3</citedby><cites>FETCH-LOGICAL-c4345-22ffe70b0dde851b1b20422ecb806d2ab719f4e71e777d491d8d0c532de5663d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpd.1970140205$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpd.1970140205$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3945978$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8183846$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heydanus, R.</creatorcontrib><creatorcontrib>van Splunder, I. P.</creatorcontrib><creatorcontrib>Wladimiroff, J. W.</creatorcontrib><title>Tertiary centre referral of small-for-gestational age pregnancies: A 10-year retrospective analysis</title><title>Prenatal diagnosis</title><addtitle>Prenat. Diagn</addtitle><description>Between 1981 and 1991, 461 pregnant women between 15 and 40 weeks of gestation (mean 30 weeks) with completed follow‐up were referred to our centre for prenatal diagnosis because of a small‐for‐gestational age (SGA) fetus or combined SGA and structural abnormality. The referral diagnosis was based either on biparietal diameter measurements or on measurement of the upper‐abdominal circumference. SGA in our centre was defined as a fetal upper‐abdominal circumference below the tenth centile. SGA was confirmed by ultrasound in 75 per cent of the fetuses, whilst combined SGA and fetal structural abnormality was substantiated in only 16 per cent of the fetuses. However, in our centre structural abnormality was detected in 34 fetuses who were referred because of SGA alone. Nearly half of the structurally normal SGA fetuses displayed a normal head‐to‐abdomen (H/A), ratio, whereas an increased H/A ratio was found in 13/15 fetuses with an abnormal karyotype. An abnormal karyotype was present in 20 fetuses, which is 7 per cent of the total SGA population. Nearly 50 per cent represented triploidy associated with oligohydramnios. SGA was confirmed by a birth weight below the tenth centile in 89 per cent, below the fifth centile in 77 per cent, and below the 2·3rd centile in 55 per cent of infants. Structural abnormality was confirmed in 65 per cent of infants, whereas in 19 per cent of infants the abnormality was missed or a misclassification was made. Perinatal mortality was 31 per cent for all SGA fetuses, 27 per cent for SGA fetuses without anomalies, and 64 per cent for SGA fetuses with structural abnormality.</description><subject>Adult</subject><subject>Anthropometry</subject><subject>Biological and medical sciences</subject><subject>Birth Weight</subject><subject>Chromosome Aberrations</subject><subject>Diseases of mother, fetus and pregnancy</subject><subject>Female</subject><subject>fetal anomaly</subject><subject>fetal karyotype</subject><subject>Gestational Age</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Small for Gestational Age</subject><subject>Karyotyping</subject><subject>man</subject><subject>Medical sciences</subject><subject>Pregnancy</subject><subject>Pregnancy. Fetus. Placenta</subject><subject>Prenatal Diagnosis</subject><subject>Retrospective Studies</subject><subject>Small-for-gestational age fetuses</subject><subject>Ultrasonography, Prenatal</subject><issn>0197-3851</issn><issn>1097-0223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P3DAQhi3Uii6UI8dKOVS9mY4_Eju9IVqgEv2SQEhcLMeerNxmk9TOAvvvMdpoq17akw_vM-N3HkKOGZwwAP5-9CesVsAkcCj3yIJBrShwLl6QBeSECl2yV-QgpZ8Z17xW-2RfMy20rBbEXWOcgo2bwmE_RSwithij7YqhLdLKdh1th0iXmCY7haHPgV1iMUZc9rZ3AdOH4rRgQDdoYx6e4pBGdFO4x8JmepNCek1etrZLeDS_h-Tm_NP12SW9-nbx-ez0ijopZEk5b1tU0ID3mCs3rOEgOUfXaKg8t41idStRMVRKeVkzrz24UnCPZVUJLw7Ju-3eMQ6_17mxWYXksOtsj8M6GVXJWnNe_RdklVKgNcsg3YIun5WyGjPGsMq2DAPzbN-M3vyxn_k38-J1s0K_o2fdOX875zY527XxWWHaYaKWZa10xtQWewgdbv79p_n-8a8Cc-GQJnzcTdr4y1RKqNLcfr0w-scXfidv78y5eALEK6vj</recordid><startdate>199402</startdate><enddate>199402</enddate><creator>Heydanus, R.</creator><creator>van Splunder, I. P.</creator><creator>Wladimiroff, J. W.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><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>7T3</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>199402</creationdate><title>Tertiary centre referral of small-for-gestational age pregnancies: A 10-year retrospective analysis</title><author>Heydanus, R. ; van Splunder, I. P. ; Wladimiroff, J. W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4345-22ffe70b0dde851b1b20422ecb806d2ab719f4e71e777d491d8d0c532de5663d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Adult</topic><topic>Anthropometry</topic><topic>Biological and medical sciences</topic><topic>Birth Weight</topic><topic>Chromosome Aberrations</topic><topic>Diseases of mother, fetus and pregnancy</topic><topic>Female</topic><topic>fetal anomaly</topic><topic>fetal karyotype</topic><topic>Gestational Age</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infant, Small for Gestational Age</topic><topic>Karyotyping</topic><topic>man</topic><topic>Medical sciences</topic><topic>Pregnancy</topic><topic>Pregnancy. Fetus. Placenta</topic><topic>Prenatal Diagnosis</topic><topic>Retrospective Studies</topic><topic>Small-for-gestational age fetuses</topic><topic>Ultrasonography, Prenatal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heydanus, R.</creatorcontrib><creatorcontrib>van Splunder, I. P.</creatorcontrib><creatorcontrib>Wladimiroff, J. W.</creatorcontrib><collection>Istex</collection><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>Human Genome Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Prenatal diagnosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heydanus, R.</au><au>van Splunder, I. P.</au><au>Wladimiroff, J. W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tertiary centre referral of small-for-gestational age pregnancies: A 10-year retrospective analysis</atitle><jtitle>Prenatal diagnosis</jtitle><addtitle>Prenat. Diagn</addtitle><date>1994-02</date><risdate>1994</risdate><volume>14</volume><issue>2</issue><spage>105</spage><epage>108</epage><pages>105-108</pages><issn>0197-3851</issn><eissn>1097-0223</eissn><coden>PRDIDM</coden><abstract>Between 1981 and 1991, 461 pregnant women between 15 and 40 weeks of gestation (mean 30 weeks) with completed follow‐up were referred to our centre for prenatal diagnosis because of a small‐for‐gestational age (SGA) fetus or combined SGA and structural abnormality. The referral diagnosis was based either on biparietal diameter measurements or on measurement of the upper‐abdominal circumference. SGA in our centre was defined as a fetal upper‐abdominal circumference below the tenth centile. SGA was confirmed by ultrasound in 75 per cent of the fetuses, whilst combined SGA and fetal structural abnormality was substantiated in only 16 per cent of the fetuses. However, in our centre structural abnormality was detected in 34 fetuses who were referred because of SGA alone. Nearly half of the structurally normal SGA fetuses displayed a normal head‐to‐abdomen (H/A), ratio, whereas an increased H/A ratio was found in 13/15 fetuses with an abnormal karyotype. An abnormal karyotype was present in 20 fetuses, which is 7 per cent of the total SGA population. Nearly 50 per cent represented triploidy associated with oligohydramnios. SGA was confirmed by a birth weight below the tenth centile in 89 per cent, below the fifth centile in 77 per cent, and below the 2·3rd centile in 55 per cent of infants. Structural abnormality was confirmed in 65 per cent of infants, whereas in 19 per cent of infants the abnormality was missed or a misclassification was made. Perinatal mortality was 31 per cent for all SGA fetuses, 27 per cent for SGA fetuses without anomalies, and 64 per cent for SGA fetuses with structural abnormality.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>8183846</pmid><doi>10.1002/pd.1970140205</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Anthropometry Biological and medical sciences Birth Weight Chromosome Aberrations Diseases of mother, fetus and pregnancy Female fetal anomaly fetal karyotype Gestational Age Gynecology. Andrology. Obstetrics Humans Infant, Newborn Infant, Small for Gestational Age Karyotyping man Medical sciences Pregnancy Pregnancy. Fetus. Placenta Prenatal Diagnosis Retrospective Studies Small-for-gestational age fetuses Ultrasonography, Prenatal |
title | Tertiary centre referral of small-for-gestational age pregnancies: A 10-year retrospective analysis |
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