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1.
J Matern Fetal Neonatal Med ; 32(2): 188-192, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-28868944

RESUMO

INTRODUCTION: Hypertensive disorders play a significant role in maternal morbidity and mortality. Limited data on prehypertension (preHTN) in pregnancy exist. We examine the risk of adverse outcomes in patients with preHTN in early (<20 weeks) versus late pregnancy (>20 weeks). MATERIALS AND METHODS: Retrospective cohort study of singleton gestations between August 2013 and June 2014. Patients were divided based on when they had the highest blood pressure in pregnancy, as defined per the Joint National Committee 7 (JNC-7). Groups were compared using χ2, Fisher's exact, Student's t-test, and Mann-Whitney U test with p < .05 used as significance. RESULTS: There were 125 control, 95 early preHTN, 136 late preHTN, and 21 chronic hypertension (CHTN). Early preHTN had an increased risk of pregnancy-related hypertension (PRH) (OR 12.26, p < .01) and composite adverse outcomes (OR 2.32, p < .01). Late preHTN had an increased risk for PRH (OR 4.39, p = .02) compared with normotensive and decreased risk for PRH (OR 0.26, p = .02), and composite adverse outcomes (OR 0.379, p = .04) compared with CHTN. Compared with late preHTN, early preHTN had more PRH (OR 2.85, p < .01), and composite adverse outcomes (OR 1.68, p = .04). CONCLUSIONS: Early prehypertension increases the risk of adverse obstetrical outcomes. Other than an increased risk of PRH, patients with late prehypertension have outcomes similar to normotensive women.


Assuntos
Resultado da Gravidez/epidemiologia , Pré-Hipertensão/epidemiologia , Pré-Hipertensão/patologia , Adulto , Idade de Início , Estudos de Casos e Controles , Feminino , Idade Gestacional , Humanos , Gravidez , Pré-Hipertensão/fisiopatologia , Estudos Retrospectivos
2.
Fetal Diagn Ther ; 42(2): 81-91, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28351027

RESUMO

BACKGROUND/OBJECTIVES: Multiple pregnancies have tripled in the United States over the past 3 decades. Attributed to increasing maternal age at delivery but more so assisted reproductive technological advances, an effort has been made to decrease twinning through elective single embryo transfer. We sought to review and evaluate risks of monochorionic twinning as a predictable consequence of increasing utilization of elective single embryo transfer on perinatal outcomes. Primary outcomes included twinning rates, fetal anomalies, growth, preterm birth, and mortality. Secondary outcomes included neurological and pulmonary disability, intrauterine growth restriction, and congenital cardiac anomalies and twin-twin transfusion syndrome. DATA SOURCES: PubMed and Embase. RESULTS: A total of 106 studies identified by systematic search met the inclusion criteria. The trend for lower numbers of embryos transferred has inadvertently led to an increase in monochorionic twinning. This is associated with worse outcomes compared to dichorionic twinning and singleton gestations for all outcomes studied. DISCUSSION: Of great concern for monochorionic twins is the risk profile of significant morbidity and mortality. Transfer of 2 embryos should be considered to avoid higher risks inherent to the shared placental phenomena related to monochorionic twins.


Assuntos
Doenças Fetais/etiologia , Resultado da Gravidez , Nascimento Prematuro/etiologia , Transferência de Embrião Único/efeitos adversos , Gêmeos Monozigóticos , Feminino , Doenças Fetais/prevenção & controle , Humanos , Recém-Nascido Prematuro , Gravidez , Gravidez de Gêmeos , Nascimento Prematuro/prevenção & controle
3.
Am J Perinatol ; 34(2): 117-122, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27322669

RESUMO

Objective Hypertensive disorders play a significant role in maternal morbidity and mortality. There is limited data on prehypertension (pre-HTN) during the first half of pregnancy. We sought to examine the risk of adverse pregnancy outcomes in patients with prehypertension in early pregnancy (<20 weeks' gestational age). Study Design A retrospective cohort study of 377 patients between 2013 and 2014. Patients were divided based on the highest blood pressure in early pregnancy, as defined per the JNC-7 criteria. There were 261 control patients (69.2%), 95 (25.2%) pre-HTN patients, and 21 (5.6%) chronic hypertension (CHTN) patients. The groups were compared using X2, Fisher's Exact, Student t-test, and Mann-Whitney U test with p < 0.05 used as significance. Results Patients with pre-HTN delivered earlier (38.8 ± 1.9 weeks vs 39.3 ± 1.7 weeks), had more pregnancy related hypertension (odds ratio [OR], 4.62; confidence interval [CI], 2.30-9.25; p < 0.01) and composite maternal adverse outcomes (OR, 2. 10; 95% CI, 1.30-3.41; p < 0.01), NICU admission (OR, 2.21; 95% CI, 1.14-4.26; p = 0.02), neonatal sepsis (OR, 6.12; 95% CI, 2.23-16.82; p < 0.01), and composite neonatal adverse outcomes (OR, 2.05; 95% CI, 1.20-3.49; p < 0.01). Conclusion Although women with pre-HTN are currently classified as normal in obstetrics, they are more similar to women with CHTN. Pre-HTN in the first half of pregnancy increases the likelihood of adverse outcomes.


Assuntos
Hipertensão Induzida pela Gravidez/epidemiologia , Complicações Cardiovasculares na Gravidez/fisiopatologia , Pré-Hipertensão/fisiopatologia , Adulto , Pressão Sanguínea , Estudos de Casos e Controles , Doença Crônica , Diabetes Gestacional/epidemiologia , Feminino , Idade Gestacional , Humanos , Hipertensão/fisiopatologia , Recém-Nascido , Unidades de Terapia Intensiva Neonatal , Parto , Admissão do Paciente/estatística & dados numéricos , Pré-Eclâmpsia/epidemiologia , Gravidez , Primeiro Trimestre da Gravidez , Segundo Trimestre da Gravidez , Nascimento Prematuro/epidemiologia , Estudos Retrospectivos , Sepse/epidemiologia
4.
Stem Cells Dev ; 25(20): 1570-1579, 2016 10.
Artigo em Inglês | MEDLINE | ID: mdl-27451014

RESUMO

Amniotic fluid contains multipotent cells and could be a source of stem cells for clinical use. Amniotic fluid cells (AFCs) are made up of a heterogeneous population of fetal cells that can be retrieved during pregnancy without ethical concerns as it is a standard clinical procedure. Studies of proliferation, multipotent marker expression, differentiation, and gene expression were performed after culturing with dexamethasone, valproic acid, and magnesium sulfate. There were correlations between known drug effects on the human fetus and changes seen in human AFCs in culture, as well as previously undescribed observations in neural and chondrogenic inducibility. Gene expression profiles confirmed these observations. AFC culture may provide a novel method to evaluate pharmacological agents before clinical use in pregnancy.

5.
Am J Obstet Gynecol ; 215(3): 401, 2016 09.
Artigo em Inglês | MEDLINE | ID: mdl-27177522
6.
Blood Coagul Fibrinolysis ; 27(5): 481-9, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27058219

RESUMO

Distribution of hereditary thrombophilic gene mutations differs globally. Prothrombin gene mutation G20210A is a common prothrombotic single-nucleotide polymorphism. In this systematic review, we provide a comprehensive report of the prevalence of prothrombin G20210A across the globe. Databases [Pubmed, Web of Science, Embase] were interrogated from their inception through December 2015 for articles reporting prothrombin G20210A prevalence rates and ethnicity. Prevalence rates were organized by continent and ethnoracial ancestry. A total of 113 articles were included with a total 61 876 participants tested for prothrombin G20210A. Reported prevalence rates varied from 0 to 15.9% among ethnic groups, with higher rates seen in the thromboembolism affected cohort compared with the unaffected cohort. Carrier rate distribution is supported by known historical migration patterns of global populations. This review of prothrombin G20210A prevalence may guide resourceful screening for identification of hereditary thrombophilia in female populations of interest with hypercoagulable states.


Assuntos
Taxa de Mutação , Polimorfismo de Nucleotídeo Único , Protrombina/genética , Trombofilia/genética , Tromboembolia Venosa/genética , Saúde da Mulher/estatística & dados numéricos , Povo Asiático , População Negra , Feminino , Expressão Gênica , Saúde Global/etnologia , Saúde Global/estatística & dados numéricos , Heterozigoto , Humanos , Prevalência , Trombofilia/diagnóstico , Trombofilia/epidemiologia , Trombofilia/etnologia , Tromboembolia Venosa/diagnóstico , Tromboembolia Venosa/epidemiologia , Tromboembolia Venosa/etnologia , População Branca , Saúde da Mulher/etnologia
7.
Am J Obstet Gynecol ; 215(3): 376.e1-7, 2016 09.
Artigo em Inglês | MEDLINE | ID: mdl-27018466

RESUMO

BACKGROUND: Mechanical alteration of the cervical angle has been proposed to reduce spontaneous preterm birth. Performance of the uterocervical angle as measured by ultrasound for predicting spontaneous preterm birth is poorly understood. OBJECTIVE: We sought to determine whether a novel ultrasonographic marker, uterocervical angle, correlates with risk of spontaneous preterm birth in a general population. STUDY DESIGN: We conducted a retrospective cohort study from May 2014 through May 2015 of singleton gestations between 16 0/7-23 6/7 weeks undergoing transvaginal ultrasound for cervical length screening. Images were remeasured for uterocervical angle between the lower uterine segment and the cervical canal. Primary outcome was prediction of spontaneous preterm birth <34 weeks and <37 weeks by uterocervical angle and secondary outcome evaluated cervical length and spontaneous preterm birth. RESULTS: A total of 972 women were studied. The rate of spontaneous preterm birth in this cohort was 9.6% for delivery <37 weeks and 4.5% for <34 weeks. Uterocervical angle of ≥95 degrees was significantly associated with spontaneous preterm birth <37 weeks with sensitivity of 80% (P < .001; confidence interval, 0.70-0.81; negative predictive value, 95%). Uterocervical angle of ≥105 degrees predicted spontaneous preterm birth <34 weeks with sensitivity of 81% (P < .001; confidence interval, 0.72-0.86; negative predictive value, 99%). Cervical length ≤25 mm significantly predicted spontaneous preterm birth <37 weeks (P < .001; sensitivity, 62%; negative predictive value, 95%) and <34 weeks (P < .001; sensitivity, 63%; negative predictive value, 97%). Regression analysis revealed a significant association of maternal age, nulliparity, race, and obesity at conception with spontaneous preterm birth and uterocervical angle. There was no correlation identified between history of dilation and curettage, abnormal Pap smear results, excisional cervical procedures, smoking, or obesity at delivery on spontaneous preterm birth and uterocervical angle. CONCLUSION: A wide uterocervical angle ≥95 and ≥105 degrees detected during the second trimester was associated with an increased risk for spontaneous preterm birth <37 and <34 weeks, respectively. Uterocervical angle performed better than cervical length in this cohort. Our data indicate that uterocervical angle is a useful, novel transvaginal ultrasonographic marker that may be used as a screening tool for spontaneous preterm birth.


Assuntos
Colo do Útero/diagnóstico por imagem , Nascimento Prematuro/diagnóstico por imagem , Adulto , Medida do Comprimento Cervical , Estudos de Coortes , Feminino , Humanos , Valor Preditivo dos Testes , Gravidez , Segundo Trimestre da Gravidez , Estudos Retrospectivos , Sensibilidade e Especificidade , Ultrassonografia
8.
Am J Obstet Gynecol ; 214(3): 321-7, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26767797

RESUMO

Stem cells are undifferentiated cells with the capacity for differentiation. Amniotic fluid cells have emerged only recently as a possible source of stem cells for clinical purposes. There are no ethical or sampling constraints for the use of amniocentesis as a standard clinical procedure for obtaining an abundant supply of amniotic fluid cells. Amniotic fluid cells of human origin proliferate rapidly and are multipotent with the potential for expansion in vitro to multiple cell lines. Tissue engineering technologies that use amniotic fluid cells are being explored. Amniotic fluid cells may be of clinical benefit for fetal therapies, degenerative disease, and regenerative medicine applications. We present a comprehensive review of the evolution of human amniotic fluid cells as a possible modality for therapeutic use.


Assuntos
Líquido Amniótico/citologia , Transplante de Células-Tronco , Amniocentese , Terapias Fetais/métodos , Humanos , Engenharia Tecidual/métodos
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