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[PMID]:29389995
[Au] Autor:Dalinjong PA; Wang AY; Homer CSE
[Ad] Endereço:Faculty of Health, University of Technology Sydney, Sydney, New South Wales, Australia.
[Ti] Título:Has the free maternal health policy eliminated out of pocket payments for maternal health services? Views of women, health providers and insurance managers in Northern Ghana.
[So] Source:PLoS One;13(2):e0184830, 2018.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:INTRODUCTION: The free maternal health policy was implemented in Ghana in 2008 under the National Health Insurance Scheme (NHIS). The policy sought to eliminate out of pocket (OOP) payments and enhance the utilisation of maternal health services. It is unclear whether the policy had altered OOP payments for services. The study explored views on costs and actual OOP payments during pregnancy. The source of funding for payments was also explored. METHODS: A convergent parallel mixed methods design, involving quantitative and qualitative data collection approaches. The study was set in the Kassena-Nankana municipality, a rural area in Ghana. Women (n = 406) who utilised services during pregnancy were surveyed. Also, 10 focus groups discussions (FGDs) were held with women who used services during pregnancy as well as 28 in-depth interviews (IDIs) with midwives/nurses (n = 25) and insurance managers/directors (n = 3). The survey was analysed using descriptive statistics, focussing on costs from the women's perspective. Qualitative data were audio recorded, transcribed and translated verbatim into English where necessary. The transcripts were read and coded into themes and sub-themes. RESULTS: The NHIS did not cover all expenses in relation to maternal health services. The overall mean for OOP cost during pregnancy was GH¢17.50 (US$8.60). Both FGDs and IDIs showed that women especially paid for drugs and ultrasound scan services. Sixty-five percent of the women used savings, whilst twenty-two percent sold assets to meet the OOP cost. Some women were unable to afford payments due to poverty and had to forgo treatment. Participants called for payments to be eliminated and for the NHIS to absorb the cost of emergency referrals. All participants admitted the benefits of the policy. CONCLUSION: Women needed to make payments despite the policy. Measures should be put in place to eliminate payments to enable all women to receive services and promote universal health coverage.
[Mh] Termos MeSH primário: Pessoal Administrativo/psicologia
Atitude
Financiamento Pessoal
Pessoal de Saúde/psicologia
Serviços de Saúde Materna/economia
Programas Nacionais de Saúde/economia
[Mh] Termos MeSH secundário: Adulto
Antimaláricos/economia
Feminino
Gana
Seres Humanos
Cobertura do Seguro
Gravidez
Inquéritos e Questionários
Ultrassonografia Pré-Natal/economia
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Antimalarials)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180309
[Lr] Data última revisão:
180309
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180202
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0184830


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[PMID]:28454690
[Au] Autor:Spiel M; Salahuddin S; Pernicone E; Zsengeller Z; Wang A; Modest AM; Karumanchi SA; Hecht JL
[Ad] Endereço:Department of Obstetrics & Gynecology, Beth Israel Deaconess Medical Center and Harvard Medical School, 330 Brookline Ave, Boston, MA 02215, USA.
[Ti] Título:Placental soluble fms-like tyrosine kinase expression in small for gestational age infants and risk for adverse outcomes.
[So] Source:Placenta;52:10-16, 2017 Apr.
[Is] ISSN:1532-3102
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:INTRODUCTION: Soluble fms-like tyrosine kinase 1 (sFLT-1) is an anti-angiogenic factor implicated in the pathogenesis of preterm preeclampsia. We evaluated sFLT-1 expression and placental pathology in pregnancies complicated by small for gestational age (SGA) infants (<10th percentile), without evidence of preeclampsia. METHODS: Clinical and histologic data were compared between groups with high or low sFLT-1 expression determined by immunohistochemistry on archived placentas. RESULTS: Nineteen of 69 placentas showed high sFLT-1 expression. The high sFLT-1 group had higher predelivery median systolic blood pressure (BP); 140 (interquartile range (IQR) 133-152) vs. 126 (118-139) mm Hg (p = 0.003), and median diastolic BP; 87 (78-94) vs. 77.5 (71-86) mm Hg (p = 0.02). Abnormal umbilical Doppler abnormalities were more prevalent; 89.5% vs. 46% (p = 0.001). These pregnancies delivered earlier; 31.9 weeks (28.3-34.7 weeks) vs. 37.1 weeks (33.7-38.7 weeks) (p < 0.001), and infants had lower birthweight; 980 grams (520-1545 grams) vs. 2087.5 grams (1455-2340 grams) (p < 0.001). Placental-weight to fetal-weight ratios, a marker of vascular insufficiency, was increased in the high sFlt-1 group: 0.18 (0.14-0.28) vs 0.15 (0.13-0.18), p = 0.03. Placentas with high sFLT-1 showed more decidual vasculopathy; 42.1% vs. 10.0% (p = 0.005), infarction; 36.8% vs. 14.0% (p = 0.048), distal villous hypoplasia; 78.9% vs. 36.0% (p = 0.001), and fetal thrombotic vasculopathy; 47.4% vs. 16.0% (p = 0.01). DISCUSSION: Placental sFLT-1 expression is upregulated in approximately 28% of non-preeclamptic pregnancies complicated by SGA infants. These pregnancies showed increased placental vascular pathology, more umbilical Doppler abnormalities, and earlier delivery with lower birthweight. A subgroup of non-preeclamptic fetal growth restriction with upregulated sFlt-1 expression may share a common pathogenic pathway with preterm preeclampsia. This subgroup is worthy of additional study.
[Mh] Termos MeSH primário: Recém-Nascido Pequeno para a Idade Gestacional/metabolismo
Placenta/metabolismo
Insuficiência Placentária/metabolismo
Regulação para Cima
Receptor 1 de Fatores de Crescimento do Endotélio Vascular/metabolismo
[Mh] Termos MeSH secundário: Adulto
Feminino
Idade Gestacional
Seres Humanos
Recém-Nascido
Placenta/diagnóstico por imagem
Placenta/patologia
Insuficiência Placentária/diagnóstico por imagem
Insuficiência Placentária/patologia
Gravidez
Ultrassonografia Doppler
Ultrassonografia Pré-Natal
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
EC 2.7.10.1 (Vascular Endothelial Growth Factor Receptor-1)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180305
[Lr] Data última revisão:
180305
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170430
[St] Status:MEDLINE


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[PMID]:29390297
[Au] Autor:Theofanakis C; Theodora M; Sindos M; Daskalakis G
[Ti] Título:Prenatal diagnosis of sirenomelia with anencephaly and craniorachischisis totalis: A case report study.
[So] Source:Medicine (Baltimore);96(50):e9020, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Sirenomelia and anencephaly are well-defined congenital malformations that usually occur independently. PATIENT CONCERNS: We report a case of combined sirenomelia, anencephaly and complete rachischisis, diagnosed in the 16th week of gestation. DIAGNOSES: To our knowledge, this is the 7th case in the literature and the first that is diagnosed so early in pregnancy. INTERVENTIONS: The final diagnosis is confirmed with radiological examination after the termination of pregnancy. OUTCOMES: Prenatal diagnosis of sirenomelia is difficult due to the presence of kidney agenesis and severe oligohydramnios. LESSONS: The combination of sirenomelia and craniorachischisis totalis is extremely rare and prenatal ultrasound scan are a challenge, even for experts in the field.
[Mh] Termos MeSH primário: Anencefalia/diagnóstico por imagem
Ectromelia/diagnóstico por imagem
Defeitos do Tubo Neural/diagnóstico por imagem
Ultrassonografia Pré-Natal
[Mh] Termos MeSH secundário: Aborto Eugênico
Feminino
Seres Humanos
Gravidez
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180301
[Lr] Data última revisão:
180301
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180203
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009020


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[PMID]:28461175
[Au] Autor:Cohen SB; Bouaziz J; Bar-On A; Schiff E; Goldenberg M; Mashiach R
[Ad] Endereço:Department of Obstetrics and Gynecology, Chaim Sheba Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Hashomer, Tel Aviv, Israel; Department of Obstetrics and Gynecology, Herzliya Medical Center, Herzliya, Israel.
[Ti] Título:In-office Hysteroscopic Extraction of Intrauterine Devices in Pregnant Patients Who Underwent Prior Ultrasound-guided Extraction Failure.
[So] Source:J Minim Invasive Gynecol;24(5):833-836, 2017 Jul - Aug.
[Is] ISSN:1553-4669
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:STUDY OBJECTIVE: To determine an effective method of intrauterine device (IUD) retrieval from pregnant women who had previous unsuccessful ultrasound-guided IUD extraction failure. DESIGN: A retrospective cohort study (Canadian task force classification II-1). SETTING: A gynecology department of an outpatient clinic. PATIENTS: Pregnant patients in their first trimester with IUD in situ who underwent prior unsuccessful ultrasound-guided IUD extraction. INTERVENTIONS: Hysteroscopic IUD extraction guided by transabdominal ultrasound. MEASUREMENTS AND MAIN RESULTS: Between 2011 and 2014, 7 of 8 pregnant patients who had undergone previous failed attempts at IUD retrieval via ultrasound guidance underwent successful removal via ultrasound-guided hysteroscopy performed without anesthesia. The sole patient with extraction failure was in her 12th week of pregnancy, and the procedure was concluded to avoid risk to the fetus. Minimal vaginal bleeding was experienced by 2 patients after the procedure. Seven of 8 patients delivered at term without any obstetric complications. One patient had a miscarriage in her 8th week of pregnancy, 2 weeks after successful IUD removal. CONCLUSION: A novel, easy outpatient hysteroscopic technique without anesthesia is presented in case of failure of previous ultrasound-guided IUD removal in early pregnancy. Results are encouraging in this difficult context.
[Mh] Termos MeSH primário: Procedimentos Cirúrgicos Ambulatórios/métodos
Remoção de Dispositivo/métodos
Histeroscopia/métodos
Dispositivos Intrauterinos
Complicações na Gravidez/cirurgia
Reoperação/métodos
Ultrassonografia de Intervenção/métodos
[Mh] Termos MeSH secundário: Aborto Espontâneo/epidemiologia
Aborto Espontâneo/etiologia
Adulto
Procedimentos Cirúrgicos Ambulatórios/efeitos adversos
Eficácia de Contraceptivos
Remoção de Dispositivo/efeitos adversos
Falha de Equipamento
Feminino
Seres Humanos
Histeroscopia/efeitos adversos
Migração de Dispositivo Intrauterino
Gravidez
Primeiro Trimestre da Gravidez
Reoperação/efeitos adversos
Estudos Retrospectivos
Ultrassonografia de Intervenção/efeitos adversos
Ultrassonografia Pré-Natal/métodos
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180223
[Lr] Data última revisão:
180223
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170503
[St] Status:MEDLINE


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[PMID]:29390455
[Au] Autor:Felix A; Hallet E; Favre A; Kom-Tchameni R; Defo A; Fléchelles O; Rosenthal JM; Douine M; Nacher M; Elenga N
[Ad] Endereço:Department of Pediatrics, Andrée Rosemon Hospital.
[Ti] Título:Cerebral injuries associated with Zika virus in utero exposure in children without birth defects in French Guiana: Case report.
[So] Source:Medicine (Baltimore);96(51):e9178, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: A major epidemic of Zika virus (ZIKV) infection occurred in French Guiana and West Indies. French national epidemiological surveillance estimated that 1650 pregnant women contracted the ZIKV during epidemic period from January 2016 to October 2016 in French Guiana. PATIENT CONCERNS: ZIKV infection during pregnancy is a cause of microcephaly and birth defects. DIAGNOSES: In this report, we describe 2 children with proven in utero ZIKV exposure. Their mothers were both symptomatic and ZIKV infection occurred early in pregnancy. Ultrasonography monitoring in utero did not show any abnormality for both patient. They were born at full-term, healthy, without any birth defects and no sign of congenital ZIKV infection. INTERVENTIONS: ZIKV was neither found on placenta fragments nor children blood and urine at birth. Their neurodevelopment outcomes in early-life fitted the expectations. As recommended in national guidelines, we performed cerebral MRIs at 2 months old, showing severe brain abnormalities, especially of white matter areas. After a large screening, we did not find any differential diagnosis for their brain lesions. OUTCOMES: We concluded it was due to their in utero ZIKV exposure. LESSONS: In this report, pathogenicity of ZIKV may involve mother's immunological response or metabolic disorder during the infection.
[Mh] Termos MeSH primário: Lesões Encefálicas/virologia
Imagem por Ressonância Magnética/métodos
Complicações Infecciosas na Gravidez/diagnóstico por imagem
Efeitos Tardios da Exposição Pré-Natal/diagnóstico por imagem
Infecção pelo Zika virus/diagnóstico
[Mh] Termos MeSH secundário: Adulto
Lesões Encefálicas/diagnóstico por imagem
Lesões Encefálicas/etiologia
Cesárea
Desenvolvimento Infantil/fisiologia
Feminino
Seguimentos
Guiana Francesa
Seres Humanos
Lactente
Recém-Nascido
Masculino
Gravidez
Complicações Infecciosas na Gravidez/virologia
Efeitos Tardios da Exposição Pré-Natal/patologia
Medição de Risco
Ultrassonografia Pré-Natal/métodos
Infecção pelo Zika virus/complicações
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180214
[Lr] Data última revisão:
180214
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180203
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009178


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[PMID]:29390414
[Au] Autor:Zhu L; Xie L
[Ad] Endereço:Ultrasound Department, Sheng Jing Hospital of China Medical University, Shenyang, Liaoning Province, People's Republic of China.
[Ti] Título:Prenatal diagnosis of Joubert syndrome: A case report and literature review.
[So] Source:Medicine (Baltimore);96(51):e8626, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:INTRODUCTION: Joubert syndrome (JS) is a rare autosomal recessive inherited disease belonging to ciliopathy with the causative mutation of genes. Except for X-linked inheritance, the high recurrence rate of a family is about 25%. After birth, it may cause a series of neurological symptoms, even with retina, kidney, liver, and other organ abnormalities, which is defined as Joubert syndrome and related disorders (JSRD). Molecular genetics research contributes to disease prediction and genetic counseling. Prenatal diagnosis is rare. Magnetic resonance imaging (MRI) is usually the first-choice diagnostic modality with typical brain images characterized by the molar tooth sign. We describe a case of JS prenatally and Dandy-Walker malformation for the differential diagnosis based on ultrasonograms. We also review the etiology, imaging features, clinical symptoms, and diagnosis of JSRD. CASE PRESENTATION: A 22-year-old woman was pregnant at 27 1/7 weeks' gestation with fetal cerebellar vermis hypoplasia. Fetal ultrasonography and MRI confirmed a diagnosis of JS at our center. The couple finally opted to terminate the fetus, which had a normal appearance and growth parameters. The couple also had an AHI1 gene mutation on chromosome 6. CONCLUSIONS: Currently, a diagnosis of JS is commonly made after birth. Fewer cases of prenatal diagnosis by ultrasonography have been made, and they are more liable to be misdirected because of some nonspecial features that also manifest in Dandy-Walker malformation, cranio-cerebello-cardiac syndrome, and so on.
[Mh] Termos MeSH primário: Anormalidades Múltiplas/diagnóstico
Proteínas Adaptadoras de Transdução de Sinal/genética
Cerebelo/anormalidades
Síndrome de Dandy-Walker/diagnóstico
Anormalidades do Olho/diagnóstico
Doenças Renais Císticas/diagnóstico
Retina/anormalidades
[Mh] Termos MeSH secundário: Anormalidades Múltiplas/diagnóstico por imagem
Cerebelo/diagnóstico por imagem
Síndrome de Dandy-Walker/complicações
Síndrome de Dandy-Walker/diagnóstico por imagem
Diagnóstico Diferencial
Anormalidades do Olho/complicações
Anormalidades do Olho/diagnóstico por imagem
Feminino
Aconselhamento Genético
Idade Gestacional
Seres Humanos
Doenças Renais Císticas/complicações
Doenças Renais Císticas/diagnóstico por imagem
Mutação
Gravidez
Retina/diagnóstico por imagem
Ultrassonografia Pré-Natal
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (AHI1 protein, human); 0 (Adaptor Proteins, Signal Transducing)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180213
[Lr] Data última revisão:
180213
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180203
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008626


  7 / 28404 MEDLINE  
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[PMID]:29290632
[Au] Autor:Markou GA; Dafereras G; Poncelet C
[Ad] Endereço:Department of Obstetrics and Gynecology, Rene-Dubos Hospital, Cergy-Pontoise, France.
[Ti] Título:Congenital Cystic Adenomatoid Malformation Diagnosed During First-Trimester Ultrasound Scan.
[So] Source:Am J Case Rep;19:1-4, 2018 Jan 01.
[Is] ISSN:1941-5923
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND Congenital cystic adenomatoid malformation (CCAM) is mostly reported from the second trimester of pregnancy. We report a case of a microcystic type of CCAM that was suggested by routine ultrasound examination at a gestational age of 12 weeks. CASE REPORT First-trimester ultrasound screening revealed the presence of a hyperechoic image that occupied the whole of the right lung, without no other any associated complications. The cardiac and aorta deviations with diaphragmatic eversion associated with a poly-hydramnios had subsequently appeared. The diagnosis of CCAM was confirmed histologically after termination of the pregnancy at 25 weeks of gestation. CONCLUSIONS CCAM may occur at a very early stage of fetal lung development.
[Mh] Termos MeSH primário: Malformação Adenomatoide Cística Congênita do Pulmão/diagnóstico por imagem
Primeiro Trimestre da Gravidez
Ultrassonografia Pré-Natal
[Mh] Termos MeSH secundário: Aborto Terapêutico
Adulto
Malformação Adenomatoide Cística Congênita do Pulmão/cirurgia
Diagnóstico Diferencial
Feminino
Seres Humanos
Gravidez
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180205
[Lr] Data última revisão:
180205
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180102
[St] Status:MEDLINE


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[PMID]:29216688
[Au] Autor:Haponiuk I; Chojnicki M; Paczkowski K; Jaworski R; Romanowicz A; Gierat-Haponiuk K
[Ad] Endereço:Department of Pediatric Cardiac Surgery, St. Adalbertus Hospital, Copernicus Ltd., Gdansk, Poland.
[Ti] Título:Symptomatic cardiac hemangioma resected on the first day of life.
[So] Source:J Card Surg;32(12):833-836, 2017 Dec.
[Is] ISSN:1540-8191
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Cardiac tumors are extremely rare in neonates. We describe the case of a right atrial hemangioma in a neonate diagnosed prenatally and successfully operated on the first day of life.
[Mh] Termos MeSH primário: Neoplasias Cardíacas/cirurgia
Hemangioma Capilar/cirurgia
[Mh] Termos MeSH secundário: Feminino
Átrios do Coração/diagnóstico por imagem
Átrios do Coração/cirurgia
Neoplasias Cardíacas/diagnóstico por imagem
Hemangioma Capilar/diagnóstico por imagem
Seres Humanos
Recém-Nascido
Gravidez
Ultrassonografia Pré-Natal
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1801
[Cu] Atualização por classe:180129
[Lr] Data última revisão:
180129
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171208
[St] Status:MEDLINE
[do] DOI:10.1111/jocs.13255


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[PMID]:29310411
[Au] Autor:Deng MX; Zou Y
[Ad] Endereço:Department of Radiology, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
[Ti] Título:Evaluating a magnetic resonance imaging of the third-trimester abdominal pregnancy: What the radiologist needs to know.
[So] Source:Medicine (Baltimore);96(48):e8986, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:INTRODUCTION: A 33-week abdominal pregnancy is an extremely rare type of ectopic pregnancy that is potentially life-threatening for the mother and fetus. Reports of using magnetic resonance imaging (MRI) in the third-trimester abdominal pregnancy are very few. PATIENT CONCERNS: A 24-year-old woman (gravida 2, para 1, living 0) at 33 weeks' gestation presented to local hospital complaining of vaginal bleeding for 2 months and lower abdominal pain for 2 days. Then, the woman was transferred to our hospital for suspected abdominal pregnancy, which was confirmed at our hospital on ultrasonography and further evaluated in detail on MRI. DIAGNOSES: The woman was diagnosed as having abdominal pregnancy. INTERVENTIONS: The woman was managed surgically, the unviable fetus was removed, and the placenta was left in situ. Then, the woman was managed with fluids, blood transfusion, antibiotics, and systemic methotrexate after surgery. OUTCOMES: At 42 days postoperatively, the affected woman was discharged in a good condition. CONCLUSIONS: By using MRI, we can accurately diagnose an abdominal pregnancy. MRI provides more details than ultrasonography, and explains the possible mechanism of abdominal pregnancy. We advocate using MRI to help surgical planning and improve outcome in cases of abdominal pregnancy.
[Mh] Termos MeSH primário: Imagem por Ressonância Magnética
Gravidez Abdominal/diagnóstico por imagem
[Mh] Termos MeSH secundário: Feminino
Seres Humanos
Laparotomia
Gravidez
Terceiro Trimestre da Gravidez
Gravidez Abdominal/cirurgia
Ultrassonografia Pré-Natal
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1801
[Cu] Atualização por classe:180116
[Lr] Data última revisão:
180116
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180110
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008986


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[PMID]:28743444
[Au] Autor:Dehaene I; Page AS; Page G
[Ad] Endereço:Ghent University Hospital, Ghent, Belgium. Electronic address: isabelle.dehaene@ugent.be.
[Ti] Título:The value of the cerebroplacental ratio in appropriate-for-gestational-age fetuses.
[So] Source:Am J Obstet Gynecol;217(5):622-623, 2017 11.
[Is] ISSN:1097-6868
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Idade Gestacional
Artérias Umbilicais
[Mh] Termos MeSH secundário: Retardo do Crescimento Fetal
Feto
Seres Humanos
Recém-Nascido Pequeno para a Idade Gestacional
Ultrassonografia Pré-Natal
[Pt] Tipo de publicação:LETTER; COMMENT
[Em] Mês de entrada:1801
[Cu] Atualização por classe:180116
[Lr] Data última revisão:
180116
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170727
[St] Status:MEDLINE



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