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Disease Activity and Maternal–fetal Outcomes in Pregnant Women With Prolactinoma: A Systematic Review and Meta-analysis

dc.contributor.authorBandeira, Diego Barata [UNESP]
dc.contributor.authorAlves, Letícia Santana [UNESP]
dc.contributor.authorGlezer, Andrea
dc.contributor.authorBoguszewski, Cesar Luiz
dc.contributor.authordos Santos Nunes-Nogueira, Vania [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionEndocrine Division (SEMPR)
dc.date.accessioned2025-04-29T18:47:59Z
dc.date.issued2025-04-01
dc.description.abstractContext: Women with prolactinoma are usually infertile but can conceive after surgery or treatment with dopamine agonists. Objective: To evaluate the impact of pregnancy in prolactinoma's natural course and in maternal–fetal outcomes. Data Sources: MEDLINE, EMBASE, LILACS, and CENTRAL. Study Selection: Observational studies that included at least 3 pregnant women with prolactinoma. Data Extraction: Two independent reviewers selected studies, assessed the risk of bias, and extracted data from the included studies. Data Synthesis: Fifty-two studies were included, involving 2544 pregnancies in 1928 women. Stata Statistical Software 18 was used for proportional meta-analyses. The overall frequency of pregnant women on dopamine agonist treatment at conception was 97% and for either continuing or resuming treatment during pregnancy was 6%. The overall frequency of miscarriage was 10% (95% CI, 8-12), 3% for prematurity (95% CI, 2-5), 4% for symptomatic tumor growth during pregnancy (95% CI, 2-8), 4% for visual impairment (95% CI, 2-7), 6% for headache (95% CI, 4-9), and 4% for development of gestational diabetes (95% CI, 3-7). The overall frequency of congenital malformations was 2% (95% CI, 1-4), 2% for perinatal mortality (95% CI, 1-2), and 6% for low birth weight (95% CI, 3-9). Moreover, prolactinoma's size is a significant modifier for visual impairment. Conclusion: Pregnancy in women with prolactinoma is safe in relation to fetal and maternal outcomes with low frequencies of miscarriage, prematurity, symptomatic growth, visual impairment, headache, congenital malformations, perinatal mortality, and low birth weight.en
dc.description.affiliationDepartment of Internal Medicine São Paulo State University (UNESP) Medical School Botucatu
dc.description.affiliationNeuroendocrine Unit Division of Endocrinology and Metabolism Hospital das Clínicas University of Sao Paulo Medical School
dc.description.affiliationDepartment of Internal Medicine Federal University of Parana Endocrine Division (SEMPR)
dc.description.affiliationUnespDepartment of Internal Medicine São Paulo State University (UNESP) Medical School Botucatu
dc.format.extente1241-e1251
dc.identifierhttp://dx.doi.org/10.1210/clinem/dgae821
dc.identifier.citationJournal of Clinical Endocrinology and Metabolism, v. 110, n. 4, p. e1241-e1251, 2025.
dc.identifier.doi10.1210/clinem/dgae821
dc.identifier.issn1945-7197
dc.identifier.issn0021-972X
dc.identifier.scopus2-s2.0-105001170458
dc.identifier.urihttps://hdl.handle.net/11449/299860
dc.language.isoeng
dc.relation.ispartofJournal of Clinical Endocrinology and Metabolism
dc.sourceScopus
dc.subjectdopamine agonist
dc.subjectmeta-analysis
dc.subjectpregnancy
dc.subjectprolactinoma
dc.subjectsystematic review
dc.titleDisease Activity and Maternal–fetal Outcomes in Pregnant Women With Prolactinoma: A Systematic Review and Meta-analysisen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.author.orcid0009-0006-2887-1475[1]
unesp.author.orcid0000-0002-3389-1140[2]
unesp.author.orcid0000-0002-8201-6756[3]
unesp.author.orcid0000-0001-7285-7941[4]
unesp.author.orcid0000-0001-9316-4167[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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