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Prenatal interventions for fetal growth restriction in animal models: A systematic review.
Valenzuela, Ignacio; Kinoshita, Mari; van der Merwe, Johannes; Marsál, Karel; Deprest, Jan.
Afiliación
  • Valenzuela I; Department of Development and Regeneration, Cluster Woman and Child, Group Biomedical Sciences, KU Leuven, Herestraat 49 - Box 805, B-3000, Leuven, Belgium. Electronic address: ignaciovalenzuela7@gmail.com.
  • Kinoshita M; Fetal Medicine Research Center, BCNatal - Barcelona Center for Maternal, Fetal, and Neonatal Medicine (Hospital Clínic and Hospital Sant Joan de Déu), IDIBAPS, University of Barcelona, Barcelona, 08028, Spain; Clinical Sciences Lund, Department of Pediatrics, Lund University, 221 85, Lund, Sweden.
  • van der Merwe J; Department of Development and Regeneration, Cluster Woman and Child, Group Biomedical Sciences, KU Leuven, Herestraat 49 - Box 805, B-3000, Leuven, Belgium; Department of Obstetrics and Gynecology, Division Woman and Child, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.
  • Marsál K; Clinical Sciences Lund, Department of Obstetrics and Gynecology, Lund University, 221 85, Lund, Sweden.
  • Deprest J; Department of Development and Regeneration, Cluster Woman and Child, Group Biomedical Sciences, KU Leuven, Herestraat 49 - Box 805, B-3000, Leuven, Belgium; Department of Obstetrics and Gynecology, Division Woman and Child, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. Electroni
Placenta ; 126: 90-113, 2022 08.
Article en En | MEDLINE | ID: mdl-35796064
ABSTRACT
Fetal growth restriction (FGR) in human pregnancy is associated with perinatal mortality, short- and long-term morbidities. No prenatal therapy is currently established despite decades of research. We aimed to review interventions in animal models for prenatal FGR treatment, and to seek the next steps for an effective clinical therapy. We registered our protocol and searched MEDLINE, Embase, and The Cochrane Library with no language restrictions, in accordance with the PRISMA guideline. We included all studies that reported the effects of any prenatal intervention in animal models of induced FGR. From 3257 screened studies, 202 describing 237 interventions were included for the final synthesis. Mice and rats were the most used animals (79%) followed by sheep (16%). Antioxidants (23%), followed by vasodilators (18%), nutrients (14%), and immunomodulators (12%) were the most tested therapy. Two-thirds of studies only reported delivery or immediate neonatal outcomes. Adverse effects were rarely reported (11%). Most studies (73%), independent of the intervention, showed a benefit in fetal survival or birthweight. The risk of bias was high, mostly due to the lack of randomization, allocation concealment, and blinding. Future research should aim to describe both short- and long-term outcomes across various organ systems in well-characterized models. Further efforts must be made to reduce selection, performance, and detection bias.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atención Prenatal / Retardo del Crecimiento Fetal Tipo de estudio: Clinical_trials / Guideline / Systematic_reviews Límite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Placenta Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atención Prenatal / Retardo del Crecimiento Fetal Tipo de estudio: Clinical_trials / Guideline / Systematic_reviews Límite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Placenta Año: 2022 Tipo del documento: Article