The Fetal Growth Restriction at Term Managed by Angiogenic Factors Versus Feto-Maternal Doppler (GRAFD) Trial to Avoid Adverse Perinatal Outcomes: Protocol for a Multicenter, Open-Label, Randomized Controlled Trial
Background: Fetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight and feto-maternal Doppler has a high sensitivity for adverse outcomes; however, more than 60% of fetuses are electively delivered at 37 to 38...
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Published in: | JMIR research protocols Vol. 11; no. 10; p. e37452 |
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Format: | Journal Article |
Language: | English |
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01-10-2022
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Abstract | Background: Fetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight and feto-maternal Doppler has a high sensitivity for adverse outcomes; however, more than 60% of fetuses are electively delivered at 37 to 38 weeks. On the other hand, classification using angiogenic factors seems to have a lower false-positive rate. Here, we present a protocol for the Fetal Growth Restriction at Term Managed by Angiogenic Factors Versus Feto-Maternal Doppler (GRAFD) trial, which compares the use of angiogenic factors and Doppler to manage small fetuses at term. Objective: The primary objective is to demonstrate that classification based on angiogenic factors is not inferior to estimated fetal weight and Doppler at detecting fetuses at risk of adverse perinatal outcomes. Methods: This is a multicenter, open-label, randomized controlled trial conducted in 20 hospitals across Spain. A total of 1030 singleton pregnancies with an estimated fetal weight ≤10th percentile at 36+0 to 37+6 weeks+days will be recruited and randomly allocated to either the control or the intervention group. In the control group, standard Doppler-based management will be used. In the intervention group, cases with a soluble fms-like tyrosine kinase to placental growth factor ratio ≥38 will be classified as having fetal growth restriction; otherwise, they will be classified as being small for gestational age. In both arms, the fetal growth restriction group will be delivered at ≥37 weeks and the small for gestational age group at ≥40 weeks. We will assess differences between the groups by calculating the relative risk, the absolute difference between incidences, and their 95% CIs. Results: Recruitment for this study started on September 28, 2020. The study results are expected to be published in peer-reviewed journals and disseminated at international conferences in early 2023. Conclusions: The angiogenic factor–based protocol may reduce the number of pregnancies classified as having fetal growth restriction without worsening perinatal outcomes. Moreover, reducing the number of unnecessary labor inductions would reduce costs and the risks derived from possible iatrogenic complications. Additionally, fewer inductions would lower the rate of early-term neonates, thus improving neonatal outcomes and potentially reducing long-term infant morbidities. Trial Registration: ClinicalTrials.gov NCT04502823; https://clinicaltrials.gov/ct2/show/NCT04502823 International Registered Report Identifier (IRRID): DERR1-10.2196/37452 |
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AbstractList | Background: Fetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight and feto-maternal Doppler has a high sensitivity for adverse outcomes; however, more than 60% of fetuses are electively delivered at 37 to 38 weeks. On the other hand, classification using angiogenic factors seems to have a lower false-positive rate. Here, we present a protocol for the Fetal Growth Restriction at Term Managed by Angiogenic Factors Versus Feto-Maternal Doppler (GRAFD) trial, which compares the use of angiogenic factors and Doppler to manage small fetuses at term. Objective: The primary objective is to demonstrate that classification based on angiogenic factors is not inferior to estimated fetal weight and Doppler at detecting fetuses at risk of adverse perinatal outcomes. Methods: This is a multicenter, open-label, randomized controlled trial conducted in 20 hospitals across Spain. A total of 1030 singleton pregnancies with an estimated fetal weight ≤10th percentile at 36+0 to 37+6 weeks+days will be recruited and randomly allocated to either the control or the intervention group. In the control group, standard Doppler-based management will be used. In the intervention group, cases with a soluble fms-like tyrosine kinase to placental growth factor ratio ≥38 will be classified as having fetal growth restriction; otherwise, they will be classified as being small for gestational age. In both arms, the fetal growth restriction group will be delivered at ≥37 weeks and the small for gestational age group at ≥40 weeks. We will assess differences between the groups by calculating the relative risk, the absolute difference between incidences, and their 95% CIs. Results: Recruitment for this study started on September 28, 2020. The study results are expected to be published in peer-reviewed journals and disseminated at international conferences in early 2023. Conclusions: The angiogenic factor–based protocol may reduce the number of pregnancies classified as having fetal growth restriction without worsening perinatal outcomes. Moreover, reducing the number of unnecessary labor inductions would reduce costs and the risks derived from possible iatrogenic complications. Additionally, fewer inductions would lower the rate of early-term neonates, thus improving neonatal outcomes and potentially reducing long-term infant morbidities. Trial Registration: ClinicalTrials.gov NCT04502823; https://clinicaltrials.gov/ct2/show/NCT04502823 International Registered Report Identifier (IRRID): DERR1-10.2196/37452 BACKGROUNDFetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight and feto-maternal Doppler has a high sensitivity for adverse outcomes; however, more than 60% of fetuses are electively delivered at 37 to 38 weeks. On the other hand, classification using angiogenic factors seems to have a lower false-positive rate. Here, we present a protocol for the Fetal Growth Restriction at Term Managed by Angiogenic Factors Versus Feto-Maternal Doppler (GRAFD) trial, which compares the use of angiogenic factors and Doppler to manage small fetuses at term. OBJECTIVEThe primary objective is to demonstrate that classification based on angiogenic factors is not inferior to estimated fetal weight and Doppler at detecting fetuses at risk of adverse perinatal outcomes. METHODSThis is a multicenter, open-label, randomized controlled trial conducted in 20 hospitals across Spain. A total of 1030 singleton pregnancies with an estimated fetal weight ≤10th percentile at 36+0 to 37+6 weeks+days will be recruited and randomly allocated to either the control or the intervention group. In the control group, standard Doppler-based management will be used. In the intervention group, cases with a soluble fms-like tyrosine kinase to placental growth factor ratio ≥38 will be classified as having fetal growth restriction; otherwise, they will be classified as being small for gestational age. In both arms, the fetal growth restriction group will be delivered at ≥37 weeks and the small for gestational age group at ≥40 weeks. We will assess differences between the groups by calculating the relative risk, the absolute difference between incidences, and their 95% CIs. RESULTSRecruitment for this study started on September 28, 2020. The study results are expected to be published in peer-reviewed journals and disseminated at international conferences in early 2023. CONCLUSIONSThe angiogenic factor-based protocol may reduce the number of pregnancies classified as having fetal growth restriction without worsening perinatal outcomes. Moreover, reducing the number of unnecessary labor inductions would reduce costs and the risks derived from possible iatrogenic complications. Additionally, fewer inductions would lower the rate of early-term neonates, thus improving neonatal outcomes and potentially reducing long-term infant morbidities. TRIAL REGISTRATIONClinicalTrials.gov NCT04502823; https://clinicaltrials.gov/ct2/show/NCT04502823. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID)DERR1-10.2196/37452. BackgroundFetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight and feto-maternal Doppler has a high sensitivity for adverse outcomes; however, more than 60% of fetuses are electively delivered at 37 to 38 weeks. On the other hand, classification using angiogenic factors seems to have a lower false-positive rate. Here, we present a protocol for the Fetal Growth Restriction at Term Managed by Angiogenic Factors Versus Feto-Maternal Doppler (GRAFD) trial, which compares the use of angiogenic factors and Doppler to manage small fetuses at term. ObjectiveThe primary objective is to demonstrate that classification based on angiogenic factors is not inferior to estimated fetal weight and Doppler at detecting fetuses at risk of adverse perinatal outcomes. MethodsThis is a multicenter, open-label, randomized controlled trial conducted in 20 hospitals across Spain. A total of 1030 singleton pregnancies with an estimated fetal weight ≤10th percentile at 36+0 to 37+6 weeks+days will be recruited and randomly allocated to either the control or the intervention group. In the control group, standard Doppler-based management will be used. In the intervention group, cases with a soluble fms-like tyrosine kinase to placental growth factor ratio ≥38 will be classified as having fetal growth restriction; otherwise, they will be classified as being small for gestational age. In both arms, the fetal growth restriction group will be delivered at ≥37 weeks and the small for gestational age group at ≥40 weeks. We will assess differences between the groups by calculating the relative risk, the absolute difference between incidences, and their 95% CIs. ResultsRecruitment for this study started on September 28, 2020. The study results are expected to be published in peer-reviewed journals and disseminated at international conferences in early 2023. ConclusionsThe angiogenic factor–based protocol may reduce the number of pregnancies classified as having fetal growth restriction without worsening perinatal outcomes. Moreover, reducing the number of unnecessary labor inductions would reduce costs and the risks derived from possible iatrogenic complications. Additionally, fewer inductions would lower the rate of early-term neonates, thus improving neonatal outcomes and potentially reducing long-term infant morbidities. Trial RegistrationClinicalTrials.gov NCT04502823; https://clinicaltrials.gov/ct2/show/NCT04502823 International Registered Report Identifier (IRRID)DERR1-10.2196/37452 |
Author | Sanchez, Maria Luisa Lesmes, Cristina Tubau, Albert Valiño, Nuria Teixidor, Mireia Garcia, Esperanza Sainz, Jose Antonio Hurtado, Ivan Gil, Maria M Lopez-Quesada, Eva Bonacina, Erika López, Miguel Ángel Carreras, Elena Fabre, Marta Palacios, Ana Alayon, Nicolas Chulilla, Carolina Ocaña, Vanesa Cuiña, Ana Candela-Hidalgo, Amparo Esteve, Esther Maroto, Anna Soriano, Beatriz Martin, Lourdes Ibañez, Patricia Vaquerizo, Oscar Perez, Esther Moreno, Elena Lopez, Monica Vives, Angels Borrero, Carlota Moreno, Anna Mendoza, Manel Diaz, Sonia Garcia-Manau, Pablo Gomez-Valencia, Elena Salinas-Amoros, Andrea Martin-Alonso, Raquel Alcoz, Marina Broullon, Jose Roman Morra, Francesca |
AuthorAffiliation | 17 Maternal Fetal Medicine Unit, Department of Obstetrics Consorci Sanitari de Terrassa Universitat Internacional de Catalunya Terrassa Spain 1 Maternal Fetal Medicine Unit, Department of Obstetrics Vall d’Hebron Barcelona Hospital Campus Universitat Autònoma de Barcelona Barcelona Spain 3 School of Medicine Universidad Francisco de Vitoria Madrid Spain 9 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitari Germans Trias i Pujol Universitat Autònoma de Barcelona Badalona Spain 10 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario de Cabueñes Universidad de Oviedo Gijón Spain 11 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitari Son Llàtzer Universitat de les Illes Balears Palma de Mallorca Spain 2 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario de Torrejón Madrid Spain 6 Alicante Institute for Health and Biomedical Research Alicante Spain 21 Maternal Fetal Medicine Unit, Department of Obs |
AuthorAffiliation_xml | – name: 20 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario Puerta del Mar Universidad de Cádiz Cádiz Spain – name: 14 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario de A Coruña Universidade da Coruña A Coruña Spain – name: 22 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario Nuestra Señora de Candelaria Universidad de La Laguna Santa Cruz de Tenerife Spain – name: 10 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario de Cabueñes Universidad de Oviedo Gijón Spain – name: 7 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Clínico Universitario Virgen de la Arrixaca Universidad de Murcia Murcia Spain – name: 4 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitari de Tarragona Joan XXIII Universitat Rovira i Virgili Tarragona Spain – name: 8 Maternal Fetal Medicine Unit, Department of Obstetrics Parc Taulí Hospital Universitari Universitat Autònoma de Barcelona Sabadell Spain – name: 18 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitari Mútua Terrassa Universitat de Barcelona Terrassa Spain – name: 15 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital General Universitario de Elche Universidad Miguel Hernández Elche Spain – name: 17 Maternal Fetal Medicine Unit, Department of Obstetrics Consorci Sanitari de Terrassa Universitat Internacional de Catalunya Terrassa Spain – name: 1 Maternal Fetal Medicine Unit, Department of Obstetrics Vall d’Hebron Barcelona Hospital Campus Universitat Autònoma de Barcelona Barcelona Spain – name: 13 Maternal Fetal Medicine Unit, Department of Obstetrics Fundació Althaia Universitat de Vic Manresa Spain – name: 19 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario de Getafe Universidad Europea de Madrid Getafe Spain – name: 2 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario de Torrejón Madrid Spain – name: 6 Alicante Institute for Health and Biomedical Research Alicante Spain – name: 3 School of Medicine Universidad Francisco de Vitoria Madrid Spain – name: 16 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitario Virgen de Valme Universidad de Sevilla Sevilla Spain – name: 9 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitari Germans Trias i Pujol Universitat Autònoma de Barcelona Badalona Spain – name: 11 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitari Son Llàtzer Universitat de les Illes Balears Palma de Mallorca Spain – name: 12 Aragon Institute for Health Research Department of Obstetrics Hospital Clínico Universitario Lozano Blesa Zaragoza Spain – name: 21 Maternal Fetal Medicine Unit, Department of Obstetrics Hospital Universitari de Girona Doctor Josep Trueta Universitat de Girona Girona Spain – name: 5 Department of Obstetrics Alicante University General Hospital Miguel Hernandez University Alicante Spain |
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ContentType | Journal Article |
Copyright | 2022. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Pablo Garcia-Manau, Manel Mendoza, Erika Bonacina, Raquel Martin-Alonso, Lourdes Martin, Ana Palacios, Maria Luisa Sanchez, Cristina Lesmes, Ivan Hurtado, Esther Perez, Albert Tubau, Patricia Ibañez, Marina Alcoz, Nuria Valiño, Elena Moreno, Carlota Borrero, Esperanza Garcia, Eva Lopez-Quesada, Sonia Diaz, Jose Roman Broullon, Mireia Teixidor, Carolina Chulilla, Maria M Gil, Monica Lopez, Amparo Candela-Hidalgo, Andrea Salinas-Amoros, Anna Moreno, Francesca Morra, Oscar Vaquerizo, Beatriz Soriano, Marta Fabre, Elena Gomez-Valencia, Ana Cuiña, Nicolas Alayon, Jose Antonio Sainz, Angels Vives, Esther Esteve, Vanesa Ocaña, Miguel Ángel López, Anna Maroto, Elena Carreras. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 11.10.2022. 2022 |
Copyright_xml | – notice: 2022. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: Pablo Garcia-Manau, Manel Mendoza, Erika Bonacina, Raquel Martin-Alonso, Lourdes Martin, Ana Palacios, Maria Luisa Sanchez, Cristina Lesmes, Ivan Hurtado, Esther Perez, Albert Tubau, Patricia Ibañez, Marina Alcoz, Nuria Valiño, Elena Moreno, Carlota Borrero, Esperanza Garcia, Eva Lopez-Quesada, Sonia Diaz, Jose Roman Broullon, Mireia Teixidor, Carolina Chulilla, Maria M Gil, Monica Lopez, Amparo Candela-Hidalgo, Andrea Salinas-Amoros, Anna Moreno, Francesca Morra, Oscar Vaquerizo, Beatriz Soriano, Marta Fabre, Elena Gomez-Valencia, Ana Cuiña, Nicolas Alayon, Jose Antonio Sainz, Angels Vives, Esther Esteve, Vanesa Ocaña, Miguel Ángel López, Anna Maroto, Elena Carreras. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 11.10.2022. 2022 |
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Snippet | Background: Fetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight... BACKGROUNDFetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight and... BackgroundFetal smallness affects 10% of pregnancies. Small fetuses are at a higher risk of adverse outcomes. Their management using estimated fetal weight and... |
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SubjectTerms | Acidosis Classification Fetuses Gestational age Induced labor Pregnancy Protocol |
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Title | The Fetal Growth Restriction at Term Managed by Angiogenic Factors Versus Feto-Maternal Doppler (GRAFD) Trial to Avoid Adverse Perinatal Outcomes: Protocol for a Multicenter, Open-Label, Randomized Controlled Trial |
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