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2.
Arch Gynecol Obstet ; 310(1): 427-432, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38355761

RESUMO

OBJECTIVE: To assess the association between aspartate aminotransferase (AST) to platelet count ratio index (APRI score), during the first and third trimesters of pregnancy and the development of intrahepatic cholestasis in pregnancy (ICP). METHODS: Case-control study was conducted. The study included patients diagnosed with ICP by elevated bile acids (n = 118) and a control group of women with symptoms such as elevated liver enzymes or pruritus with normal level of bile acids (n = 127) who attended a large tertiary teaching medical center between the years 2014 and 2021. The groups were compared in terms of obstetrical characteristics, perinatal outcomes, first- and third-trimester laboratory tests, and APRI scores during the first and third trimester. A receiver operating characteristic (ROC) analysis was performed to determine the APRI score cutoff value that could predict ICP. RESULTS: The third-trimester APRI scores of patients with ICP were significantly higher than those of the control group (P < 0.001). The ROC analysis revealed that the cutoff value for the APRI score was 0.42 with 65.3% sensitivity and 73.2% specificity. CONCLUSION: Our results suggest that the third-trimester APRI score is positively associated with ICP.


Assuntos
Aspartato Aminotransferases , Colestase Intra-Hepática , Complicações na Gravidez , Terceiro Trimestre da Gravidez , Curva ROC , Humanos , Feminino , Colestase Intra-Hepática/sangue , Gravidez , Aspartato Aminotransferases/sangue , Estudos de Casos e Controles , Adulto , Complicações na Gravidez/sangue , Complicações na Gravidez/diagnóstico , Contagem de Plaquetas , Terceiro Trimestre da Gravidez/sangue , Primeiro Trimestre da Gravidez/sangue , Ácidos e Sais Biliares/sangue
3.
Eur J Obstet Gynecol Reprod Biol ; 293: 44-49, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38104393

RESUMO

OBJECTIVE: To investigate adverse pregnancy outcomes in patients complicated with GDMA1 who delivered at term before or after 40 weeks of gestation. STUDY DESIGN: A population-based cohort study including all women with GDMA1 during pregnancy was conducted. Deliveries occurred between 1988 and 2016 at a large university tertiary medical center. RESULTS: During the study period, 11,765 women with GDMA1 met the inclusion criteria. Of these, 1303 (11 %) delivered after 40 weeks (post-date, study group), while 10,462 (89 %) delivered at term before 40 weeks of gestation (before date, control group). Those who delivered after 40 weeks of gestation (the study group) had a significantly lower percent of cesarean deliveries (CD), higher rates of spontaneous vaginal deliveries and induction of labor in comparison to those who delivered before 40 weeks of gestation (the control group). The control group had significantly higher rates of preeclampsia and intrauterine growth restriction than the study group. Using a multivariable logistic regression model, delivery after 40 weeks was noted as an independent protective factor for CD (adjusted OR = 0.78, 95 %CI 0.66-0.92, p value = 0.001). Delivery after 41 + 0 weeks had a significantly higher rate of CD and LGA. CONCLUSION: No significant increase in adverse pregnancy outcomes at term post-date pregnancies complicated with GDMA1 was demonstrated. Furthermore, there was no increase in the rate of CD with the increase in gestational age until 41 weeks of gestation.


Assuntos
Resultado da Gravidez , Gravidez Prolongada , Humanos , Gravidez , Feminino , Lactente , Estudos de Coortes , Estudos Retrospectivos , Resultado da Gravidez/epidemiologia , Parto Obstétrico , Idade Gestacional , Retardo do Crescimento Fetal/epidemiologia
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