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1.
Prenat Diagn ; 44(6-7): 899-906, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38797960

RESUMO

OBJECTIVE: In our center, we observed an increased frequency of right aortic arch (RAA) with an agenesis of the ductus arteriosus (ADA) in prenatally diagnosed tetralogy of Fallot (ToF) and its variations. This study aimed to determine whether there is an association of RAA and ADA in fetuses with ToF. Distribution of genetic anomalies and impact on postnatal outcome were further evaluated. METHOD: Single-center retrospective observational study including pregnancies with prenatal diagnosis of ToF from 2010 to 2023. All cases were subdivided into ToF with pulmonary stenosis (PS) and pulmonary atresia (PA). Clinical and echocardiographic databases were reviewed for pregnancy outcome, genetic anomalies, and postnatal course. RESULTS: The cohort included 169 cases, 124 (73.4%) with ToF/PS and 45(26.6%) with ToF/PA. Agenesis of the ductus arteriosus was significantly associated with RAA in both subtypes of ToF (p = 0.001) compared to left aortic arch and found in 82.5% (33/40) versus 10.7% (9/84) of fetuses with ToF/PS and in 57.1% (8/14) versus 12.9% (4/31) of fetuses with ToF/PA. In both ToF/PS and ToF/PA, RAA/ADA versus RAA/patent DA revealed a significantly higher risk for the presence of genetic abnormalities, especially microdeletion 22q11.2, major aorto-pulmonary collateral arteries and a shorter time to complete surgical repair. CONCLUSION: We demonstrated a significantly increased frequency of RAA/ADA in patients with prenatally diagnosed ToF. Although this association revealed no significant impact on overall survival, the prenatal detection of RAA/ADA has implications for counseling, genetic evaluation and postnatal management.


Assuntos
Aorta Torácica , Canal Arterial , Tetralogia de Fallot , Ultrassonografia Pré-Natal , Humanos , Tetralogia de Fallot/diagnóstico por imagem , Tetralogia de Fallot/epidemiologia , Tetralogia de Fallot/genética , Feminino , Estudos Retrospectivos , Gravidez , Aorta Torácica/anormalidades , Aorta Torácica/diagnóstico por imagem , Adulto , Canal Arterial/anormalidades , Canal Arterial/diagnóstico por imagem , Atresia Pulmonar/diagnóstico por imagem , Atresia Pulmonar/diagnóstico , Recém-Nascido , Anormalidades Múltiplas/epidemiologia , Anormalidades Múltiplas/diagnóstico por imagem
3.
Sci Rep ; 11(1): 9929, 2021 05 11.
Artigo em Inglês | MEDLINE | ID: mdl-33976258

RESUMO

Maternal consumption of polyphenol-rich foods has been associated with fetal ductus arteriosus constriction (DAC), but safety of chocolate exposure in fetal life has not been studied. This experimental study tested the hypothesis that maternal cocoa consumption in late pregnancy causes fetal DAC, with possible associated antioxidant effects. Pregnant Wistar rats, at the 21st gestational day, received by orogastric tube cocoa (720 mg/Kg) for 12 h, indomethacin (10 mg/Kg), for 8 h, or only water, before cesaren section. Immediately after withdrawal, every thorax was obtained and tissues were fixed and stained for histological analysis. The ratio of the narrowest part of the pulmonary artery to the fetal ductus inner diameter and increased ductal inner wall thickness characterized ductal constriction. Substances reactive to thiobarbituric acid were quantified. Statistical analysis used ANOVA and Tukey test. Cocoa (n = 33) and indomethacin (n = 7) reduced fetal internal ductus diameter when compared to control (water, n = 25) (p < 0.001) and cocoa alone increased ductus wall thickness (p < 0.001), but no change was noted in enzymes activity. This pharmacological study shows supporting evidences that there is a cause and effect relationship between maternal consumption of cocoa and fetal ductus arteriosus constriction. Habitual widespread use of chocolate during gestation could account for undetected ductus constriction and its potentially severe consequences, such as perinatal pulmonary hypertension, cardiac failure and even death. For this reason, dietary guidance in late pregnancy to avoid high chocolate intake, to prevent fetal ductal constriction, may represent the main translational aspect of this study.


Assuntos
Chocolate/efeitos adversos , Permeabilidade do Canal Arterial/etiologia , Canal Arterial/anormalidades , Efeitos Tardios da Exposição Pré-Natal/etiologia , Animais , Constrição Patológica/etiologia , Constrição Patológica/patologia , Canal Arterial/patologia , Permeabilidade do Canal Arterial/patologia , Feminino , Doenças Fetais/etiologia , Doenças Fetais/patologia , Feto/anormalidades , Feto/patologia , Masculino , Exposição Materna/efeitos adversos , Gravidez , Efeitos Tardios da Exposição Pré-Natal/patologia , Ratos , Ratos Wistar
4.
J Med Ultrason (2001) ; 47(4): 635-640, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32725459

RESUMO

PURPOSE: To quantitatively estimate the influence of ductal shunt on cerebral blood flow and establish a new index of ultrasonography for estimating cerebral circulation without the influence of ductal shunt in newborn infants. METHODS: We retrospectively examined the records of anterior cerebral artery (ACA) and left pulmonary artery (LPA) blood flow velocity curves recorded by pulsed Doppler ultrasonography within 6 h after birth in 123 newborn infants without asphyxia (normal group) and in 31 newborn infants with asphyxia (asphyxia group). RESULTS: In the normal group, the resistance index (RI) of the ACA showed a positive correlation with the ratio of LPA diastolic-to-systolic flow velocities (LPAD/LPAS) (P < 0.001, r = 0.58), and the estimated RI (eRI) of the ACA was calculated using the following formula: Y = 0.47X + 0.67 (Y estimated RI; X LPAD/LPAS). In the asphyxia group, the RI of the ACA showed a weak correlation to base excess (BE) (P < 0.05, r = 0.46). The eRI of the ACA was calculated by the LPAD/PLAS in the asphyxia group, and the difference between the RI and eRI showed a better correlation to BE than RI (P < 0.001, r = 0.64). CONCLUSION: We determined the relation between cerebral blood flow RI and ductal shunt, and (RI - eRI) may be a new useful ultrasonographic index indicating cerebral circulation without the influence of ductal shunt in newborn infants.


Assuntos
Artéria Cerebral Anterior/diagnóstico por imagem , Asfixia Neonatal/fisiopatologia , Circulação Cerebrovascular , Artéria Pulmonar/diagnóstico por imagem , Ultrassonografia Doppler de Pulso/métodos , Artéria Cerebral Anterior/fisiopatologia , Velocidade do Fluxo Sanguíneo , Canal Arterial/anormalidades , Canal Arterial/diagnóstico por imagem , Canal Arterial/fisiologia , Feminino , Humanos , Recém-Nascido , Masculino , Artéria Pulmonar/fisiopatologia , Estudos Retrospectivos
5.
Arterioscler Thromb Vasc Biol ; 40(9): 2212-2226, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32640908

RESUMO

OBJECTIVE: The ductus arteriosus (DA) is a fetal artery connecting the aorta and pulmonary arteries. Progressive matrix remodeling, that is, intimal thickening (IT), occurs in the subendothelial region of DA to bring anatomic DA closure. IT is comprised of multiple ECMs (extracellular matrices) and migrated smooth muscle cells (SMCs). Because glycoprotein fibulin-1 binds to multiple ECMs and regulates morphogenesis during development, we investigated the role of fibulin-1 in DA closure. Approach and Results: Fibulin-1-deficient (Fbln1-/-) mice exhibited patent DA with hypoplastic IT. An unbiased transcriptome analysis revealed that EP4 (prostaglandin E receptor 4) stimulation markedly increased fibulin-1 in DA-SMCs via phospholipase C-NFκB (nuclear factor κB) signaling pathways. Fluorescence-activated cell sorting (FACS) analysis demonstrated that fibulin-1 binding protein versican was derived from DA-endothelial cells (ECs). We examined the effect of fibulin-1 on directional migration toward ECs in association with versican by using cocultured DA-SMCs and ECs. EP4 stimulation promoted directional DA-SMC migration toward ECs, which was attenuated by either silencing fibulin-1 or versican. Immunofluorescence demonstrated that fibulin-1 and versican V0/V1 were coexpressed at the IT of wild-type DA, whereas 30% of versican-deleted mice lacking a hyaluronan binding site displayed patent DA. Fibulin-1 expression was attenuated in the EP4-deficient mouse (Ptger4-/-) DA, which exhibits patent DA with hypoplastic IT, and fibulin-1 protein administration restored IT formation. In human DA, fibulin-1 and versican were abundantly expressed in SMCs and ECs, respectively. CONCLUSIONS: Fibulin-1 contributes to DA closure by forming an environment favoring directional SMC migration toward the subendothelial region, at least, in part, in combination with EC-derived versican and its binding partner hyaluronan.


Assuntos
Proteínas de Ligação ao Cálcio/metabolismo , Permeabilidade do Canal Arterial/metabolismo , Canal Arterial/metabolismo , Células Endoteliais/metabolismo , Matriz Extracelular/metabolismo , Miócitos de Músculo Liso/metabolismo , Animais , Proteínas de Ligação ao Cálcio/deficiência , Proteínas de Ligação ao Cálcio/genética , Movimento Celular , Células Cultivadas , Técnicas de Cocultura , Canal Arterial/anormalidades , Permeabilidade do Canal Arterial/genética , Permeabilidade do Canal Arterial/patologia , Células Endoteliais/patologia , Matriz Extracelular/genética , Matriz Extracelular/patologia , Humanos , Camundongos da Linhagem 129 , Camundongos Endogâmicos C57BL , Camundongos Knockout , Miócitos de Músculo Liso/patologia , NF-kappa B/metabolismo , Técnicas de Cultura de Órgãos , Proteína Quinase C/metabolismo , Ratos Wistar , Receptores de Prostaglandina E Subtipo EP4/metabolismo , Transdução de Sinais , Fosfolipases Tipo C/metabolismo
6.
World J Pediatr Congenit Heart Surg ; 11(4): NP498-NP500, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32452246

RESUMO

Actin α2 (ACTA2) is a protein crucial for proper functioning of contractile apparatus in smooth muscles. A specific mutation resulting in substitution of arginine at position 179 by histidine (p.R179 H) in ACTA2 has been shown to be associated with multisystemic smooth muscle dysfunction syndrome. Characteristic features include aneurysmal arterial disease. Due to rarity of this disease, we report a nine-year-old girl with this rare genetic variant in whom cardiovascular manifestations were identified in fetal life and who needed neonatal cardiac surgical intervention.


Assuntos
Actinas/genética , Aneurisma/genética , DNA/genética , Permeabilidade do Canal Arterial/diagnóstico , Canal Arterial/anormalidades , Mutação , Artéria Pulmonar/anormalidades , Actinas/metabolismo , Aneurisma/diagnóstico , Aneurisma/metabolismo , Análise Mutacional de DNA , Canal Arterial/diagnóstico por imagem , Permeabilidade do Canal Arterial/genética , Ecocardiografia , Feminino , Humanos , Recém-Nascido , Gravidez , Artéria Pulmonar/diagnóstico por imagem , Artéria Pulmonar/fisiopatologia , Adulto Jovem
9.
Arch Cardiovasc Dis ; 113(2): 129-141, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31753586

RESUMO

Stenting the arterial duct emerged in the early 1990s as an alternative to a variety of surgical interventions in neonates with a duct-dependent pulmonary or systemic circulation complex defect. Furthermore, palliative ductal stenting has been applied in older children with severe suprasystemic pulmonary arterial hypertension, as an alternative to surgical shunts, such as Potts anastomosis. Early results of this technique were discouraging, but by learning from the failures of the past, ductal stenting has become a reliable palliative therapy. In this review, we aim to describe the historical evolution of ductal stenting, its different clinical applications and outcomes, and future perspectives for this strategy in congenital cardiac catheterization.


Assuntos
Cateterismo Cardíaco/instrumentação , Canal Arterial , Cardiopatias Congênitas/terapia , Cuidados Paliativos , Stents , Cateterismo Cardíaco/efeitos adversos , Pré-Escolar , Tomada de Decisão Clínica , Canal Arterial/anormalidades , Canal Arterial/diagnóstico por imagem , Canal Arterial/fisiopatologia , Cardiopatias Congênitas/diagnóstico por imagem , Cardiopatias Congênitas/fisiopatologia , Humanos , Lactente , Recém-Nascido , Seleção de Pacientes , Desenho de Prótese , Fatores de Risco , Resultado do Tratamento
11.
Acta Biomed ; 90(2): 331-332, 2019 05 23.
Artigo em Inglês | MEDLINE | ID: mdl-31125014

RESUMO

Two neonates were taken shortly after birth to our unit with a prenatal diagnosis of [S,D,S] Tetralogy of Fallot with pulmonary atresia and "unusual" aorta to pulmonary connection. The echocardiogram confirmed the main diagnosis showing: a left aortic arch with a vascular connection between the right innominate artery and the origin of the right pulmonary artery in patient A; and right aortic arch with a vascular connection between the left innominate artery and the origin of the left pulmonary artery in patient B.


Assuntos
Canal Arterial/anormalidades , Imageamento Tridimensional , Tetralogia de Fallot/diagnóstico por imagem , Tetralogia de Fallot/cirurgia , Anormalidades Múltiplas/diagnóstico por imagem , Anormalidades Múltiplas/cirurgia , Procedimentos Cirúrgicos Cardíacos/métodos , Angiografia por Tomografia Computadorizada/métodos , Ecocardiografia , Feminino , Seguimentos , Cardiopatias Congênitas/diagnóstico por imagem , Cardiopatias Congênitas/cirurgia , Humanos , Recém-Nascido , Gravidez , Diagnóstico Pré-Natal/métodos , Resultado do Tratamento
12.
J Matern Fetal Neonatal Med ; 32(7): 1057-1062, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29096572

RESUMO

OBJECTIVE: To evaluate the utility of fetal cardiac magnetic resonance imaging (MRI) in diagnosing right aortic arch with mirror image branching and retroesophageal left ductus arteriosus (RLDA). METHODS: This retrospective study included six infants diagnosed with right aortic arch with mirror image branching and RLDA postnatally by cardiac computed tomography (CT) that had fetal echocardiography (echo) and MRI initially performed. The six fetal MRI cases were examined using 1.5 T MRI unit. Steady-state free precession (SSFP) sequence and single-shot turbo spin echo (SSTSE) sequence were used to evaluate the fetal great vessels and airway. The gestational age of six fetuses at time of fetal MRI ranged from 23 to 35 weeks (mean, 26.7 weeks). RESULTS: Of six cases with mirror image right aortic arch and RLDA confirmed by postnatal CT, 4/6 were correctly diagnosed by fetal cardiac MRI and 3/6 were correctly diagnosed by prenatal echo. All six cases were not associated with other congenital heart defect. All ductus arteriosus were closed after birth. CONCLUSIONS: Fetal cardiac MRI can be a useful adjunct for evaluating fetal right aortic arch with mirror-image and RLDA.


Assuntos
Aorta Torácica/anormalidades , Canal Arterial/anormalidades , Coração Fetal/diagnóstico por imagem , Imageamento por Ressonância Magnética/métodos , Diagnóstico Pré-Natal/métodos , Adulto , Aorta Torácica/diagnóstico por imagem , Canal Arterial/diagnóstico por imagem , Feminino , Idade Gestacional , Humanos , Gravidez , Estudos Retrospectivos , Tomografia Computadorizada por Raios X , Ultrassonografia Pré-Natal
13.
Rev. cuba. obstet. ginecol ; 44(2): 1-6, abr.-jun. 2018. ilus
Artigo em Espanhol | CUMED, LILACS | ID: biblio-1003947

RESUMO

Los aneurismas espontáneos del conducto arterial se detectan inusualmente de forma prenatal. Su incidencia varía entre 1,5 por ciento y 8 por ciento de los embarazos. Usualmente se solucionan espontáneamente; sin embargo, pueden presentarse complicaciones letales como trombosis, embolia y ruptura. Los casos fatales descritos son escasos, la mayoría después del nacimiento. El objetivo es presentar el reporte de autopsia de un mortinato cuya causa de muerte fue la trombosis de aneurisma del conducto arterial. La madre fue una primigesta de 22 años de edad, con embarazo de 40 semanas sin antecedentes de importancia, atendida en un hospital de tercer nivel de Bucaramanga, Santander. Le realizamos una cesárea emergente por perfil biofísico fetal alterado y bradicardia fetal. Se obtuvo un mortinato masculino sin esfuerzo respiratorio, hipotónico, cianótico, que no respondió a maniobras de reanimación. Los hallazgos de autopsia relevantes fueron: dilatación auricular derecha y dilatación preductal con trombosis del conducto cuya luz estaba completamente ocluida por un coágulo. Los aneurismas ductales prenatales son una entidad que merece más estudio para determinar estrategias de diagnóstico precoz y seguimiento, y así disminuir el riesgo de desenlaces fatales(AU)


Introduction: Spontaneous ductus arteriosus aneurysm is a condition rarely diagnosed on prenatal imaging. Literature reveals 1,5 to 8 percent incidence on pregnancies. Most cases have spontaneous resolution, nonetheless, life-threatening complications such thrombosis, embolism and rupture can occur. Fatal cases reports are scarce, most of them presenting on newborns, days to months after birth. Objective: To present the autopsy report of a stillbirth whose cause of death was thrombosis of the arterial duct aneurysm. Methods: A 22-year healthy prime mother with 40-week pregnancy was assisted at a tertiary hospital in Bucaramanga, Santander. She required emergency cesarean section due to low biophysical profile and fetal bradycardia. The newborn had no respiratory effort, was floppy, cyanotic and did not respond to resuscitation maneuvers. The relevant autopsy findings were right atrial dilatation and preductal dilation with thrombosis of the duct whose lumen was completely occluded by a clot. Conclusions: The prenatal ductal aneurysm is an entity that deserves more study to determine strategies for early diagnosis and follow-up thus decrease the risk of fatal outcomes(AU)


Assuntos
Humanos , Feminino , Gravidez , Adulto Jovem , Diagnóstico Precoce , Canal Arterial/anormalidades , Aneurisma/complicações , Natimorto/genética , Aneurisma/prevenção & controle
14.
Pediatr Cardiol ; 39(4): 665-673, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29307026

RESUMO

A right aortic arch (RAA) with a left arterial duct (LAD) together encircle the trachea and have the potential to cause tracheobronchial compression and published guidelines recommend bronchoscopy in symptomatic patients. The aim of the study was to describe the incidence of tracheal compression in a cohort of prenatally diagnosed RAA and LAD. Retrospective review of clinical course and imaging of prenatal cases of RAA and LAD assessed with flexible bronchoscopy over an 11-year period. 34 cases of prenatally diagnosed RAA with LAD underwent bronchoscopy at median age of 9 months (range 0.4-123) of whom 11 had respiratory symptoms and 23 were asymptomatic. In the neonatal period, three cases demonstrated respiratory symptoms. An aberrant left subclavian artery (ALSA) was identified in 29 cases. Pulsatile tracheal compression was identified in 32/34 (94%) cases and two cases showed normal tracheal appearances. Significant tracheal compression (> 70% occlusion) was present in 25/34 (74%) cases of which 16 were asymptomatic. Significant carinal compression (> 70% occlusion) was identified in 14/34 (42%) cases, an ALSA was observed in 13/14. Surgical relief of a vascular ring has been performed in 27 (79%) cases at a median age of 15 months (range 0.6-128 months). At surgery, a fibrous remnant of an atretic left aortic arch was identified in 11/27 (41%) cases. Significant tracheal compression may be present in infants even without symptoms. If early relief of airway compression is to be achieved to promote normal development of tracheal cartilage, early bronchoscopy should be considered.


Assuntos
Síndromes do Arco Aórtico/complicações , Broncoscopia/métodos , Doenças da Traqueia/epidemiologia , Aneurisma/complicações , Aorta Torácica/anormalidades , Síndromes do Arco Aórtico/diagnóstico , Anormalidades Cardiovasculares/complicações , Criança , Pré-Escolar , Canal Arterial/anormalidades , Feminino , Humanos , Incidência , Lactente , Masculino , Gravidez , Diagnóstico Pré-Natal/métodos , Estudos Retrospectivos , Artéria Subclávia/anormalidades , Traqueia/patologia , Doenças da Traqueia/diagnóstico , Doenças da Traqueia/etiologia
16.
Cardiol Young ; 27(7): 1280-1288, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28376948

RESUMO

BACKGROUND: The relationship between interatrial communication, ductus arteriosus, and pulmonary flow in transposition of the great arteries and intact ventricular septum may help predict postnatal desaturation. METHODS: Echocardiographic data of 45 fetuses with transposition of the great arteries and intact ventricular septum and 50 age-matched controls were retrospectively reviewed. Interatrial communication, left and right ventricular output, flow in the ductus arteriosus, as well as effective pulmonary flow were measured. Patients were divided into two groups on the basis of postnatal saturations: group 1 had saturations ⩽50% and group 2 >50%. RESULTS: Of 45 fetuses, 13 (26.7%) were classified into group 1. Compared with fetuses in group 2, they had a smaller interatrial communication (2.9 versus 4.0 mm, p=0.004) and more retrograde diastolic flow in the ductus arteriosus (92 versus 23%, p=0.002). Both groups showed a significant decrease in ductal flow compared with controls. Patients in group 2 had a higher effective pulmonary flow compared with controls. There was a mild correlation between left ventricular output and size of the interatrial communication (Spearman's rank correlation 0.44). CONCLUSION: A retrograde diastolic flow is present in most of the fetuses with postnatal desaturation. Fetuses with transposition of the great arteries have a lower flow through the ductus arteriosus compared with controls. Fetuses without restrictive foramen ovale have higher effective pulmonary flow. Peripheral pulmonary vasodilatation due to higher oxygen saturation in pulmonary arteries in the case of transposition of the great arteries could be one possible cause.


Assuntos
Canal Arterial/anormalidades , Comunicação Interatrial/diagnóstico por imagem , Ventrículos do Coração/fisiopatologia , Artéria Pulmonar/anormalidades , Transposição dos Grandes Vasos/diagnóstico por imagem , Estudos de Casos e Controles , Canal Arterial/diagnóstico por imagem , Ecocardiografia Doppler em Cores , Feminino , Humanos , Recém-Nascido , Masculino , Gravidez , Artéria Pulmonar/diagnóstico por imagem , Estudos Retrospectivos , Transposição dos Grandes Vasos/complicações , Ultrassonografia Pré-Natal
17.
Cardiol Young ; 27(5): 1026-1029, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28260552

RESUMO

We describe the case of an infant with DiGeorge syndrome born with a right aortic arch and left arterial duct. Despite the remote location of the right aortic arch from the left arterial duct, he developed coarctation of the aorta during treatment with indomethacin. This was relieved by prostaglandin treatment. This case highlights the fact that, even in the absence of an arterial duct, ductal tissue can still be present in the aorta, and cause coarctation when exposed to indomethacin. We also demonstrate the utility of prostaglandin for relief of this type of obstruction.


Assuntos
Coartação Aórtica/diagnóstico por imagem , Coartação Aórtica/tratamento farmacológico , Síndrome de DiGeorge/complicações , Indometacina/efeitos adversos , Prostaglandinas/uso terapêutico , Aorta Torácica/anormalidades , Aorta Torácica/efeitos dos fármacos , Coartação Aórtica/induzido quimicamente , Canal Arterial/anormalidades , Canal Arterial/efeitos dos fármacos , Ecocardiografia Doppler em Cores , Humanos , Recém-Nascido , Masculino
18.
Rev. cuba. obstet. ginecol ; 43(1): 0-0, ene.-mar. 2017. ilus
Artigo em Espanhol | LILACS, CUMED | ID: biblio-901291

RESUMO

Se presenta el caso de una paciente que desde la semana 20 de gestación fue diagnosticada de cólico renal con la necesidad de varios ingresos y colocación de catéter doble J por parte de Urología. La paciente recibió tratamiento con paracetamol intravenoso y oral. Los controles ecográficos obstétricos -a los largo de la gestación- fueron normales hasta que en la semana 32, cuando ingresó de nuevo por cuadro sospechoso de cólico renal tratado con Paracetamol. Se objetivan en ecografía con hallazgos compatibles con restricción precoz del ductus arterioso. Se indicó la suspensión del paracetamol y los cambios se redujeron en las 48 horas posteriores y casi desaparecieron por completo una semana tras la retirada de la medicación. La gestación llegó a término y el recién nacido presentó un ecocardiograma posnatal normal. Recomendamos la restricción de los analgésicos no opiáceos en el tercer trimestre y el seguimiento con Doppler del conducto arterioso en los casos en que se requiriera usarlos(AU)


A case is reported of a pregnant woman who was diagnosed with renal colic at 20 weeks of gestation. She needed various admissions in hospital and double J stent placement by Urology Service and she was treated with acetaminophen by both intravenous and oral ways. Obstetric ultrasound scans were normal throughout gestation until week 32, when she was admitted to hospital again for suspected renal colic. She was treated with acetaminophen. In that moment, ultrasound findings are consisted with early ductus arteriosus constriction. Acetaminophen was decided to be stopped and changes reduced in the first 48 hours and they almost disappeared after one week of medication withdrawal. Pregnancy came to term and the child was born normal. Restricting non-opioid analgesics was recommended in the third quarter, as well as following up with ductus arteriosus doppler in cases in which it is required to use them(AU)


Assuntos
Humanos , Feminino , Gravidez , Complicações na Gravidez/tratamento farmacológico , Canal Arterial/anormalidades , Acetaminofen/efeitos adversos
19.
Rev. cuba. obstet. ginecol ; 42(4): 493-501, sep.-dic. 2016. ilus
Artigo em Espanhol | LILACS | ID: biblio-845027

RESUMO

El ductus arterioso es una derivación que conecta la arteria pulmonar con el arco aórtico el que permite la descarga del ventrículo derecho sin pasar por la alta resistencia de los pulmones. La permeabilidad del conducto arterioso se mantiene durante la gestación por las prostaglandinas producidas especialmente PGE2, que circulan a nivel local, especialmente PGE2, y la baja saturación de oxígeno fetal. Se trata de una paciente que desde la semana 20 de gestación es diagnosticada de cólico renal con la necesidad de varios ingresos y colocación de catéter doble J por parte de Urología y la cual recibió tratamiento con paracetamol intravenoso y oral. Los controles ecográficos obstétricos a los largo de la gestación fueron normales hasta que en semana 32, cuando ingresa de nuevo por cuadro sospechoso de cólico renal tratado con Paracetamol, se objetivan en ecografía hallazgos compatibles con restricción precoz del ductus arterioso. Se indicó suspender el paracetamol y los cambios se redujeron en las 48 horas posteriores y casi desaparecieron por completo una semana tras la retirada de la medicación. La gestación llegó a término y el recién nacido presentó un ecocardiograma postnatal normal. Recomendamos la restricción de los analgésicos no opiáceos en el tercer trimestre y el seguimiento con Doppler del conducto arterioso en los casos en que se requiriera usarlos(AU)


Ductus arteriosus is a derivation that connects the pulmonary artery with the aortic arch and allows the discharge from the right ventricle without passing the high resistance of lungs. Permeability of the ductus arteriosus is kept during gestation because of the production of prostaglandins, particularly PGE2, which circulates locally, and the low fetal oxygen saturation. Here is a pregnant woman who, since her 20th week of gestation was diagnosed as a renal colic case. She required several admissions to hospital and placement of double J stent in the urology service and she was treated with intravenous and oral paracetamol. Obstetric ultrasound scans throughout gestation were normal until week 32, when she was admitted to hospital again for suspected renal colic and treated again with paracetamol. At that moment, findings compatible with early ductus arteriosus constriction were observed in ultrasound. It was then decided to stop the paracetamol treatment, the changes declined in the following 48 hours and they almost disappeared completely after one week after the medication withdrawal. It was finally a term pregnancy and the postnatal echocardiogram of the newborn was normal. Restricting non-opioid analgesics in the third pregnancy trimester and the follow up of the ductus arteriosus with Doppler technique when required(AU)


Assuntos
Humanos , Feminino , Gravidez , Adulto , Canal Arterial/anormalidades , Canal Arterial/efeitos dos fármacos , Acetaminofen/efeitos adversos , Complicações na Gravidez/diagnóstico por imagem , Cólica Renal/tratamento farmacológico , Acetaminofen/uso terapêutico
20.
J Card Surg ; 31(7): 461-3, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27246554

RESUMO

Isolated left subclavian artery (LSA) from the pulmonary artery (PA) is a very rare vascular anomaly. We report a case of abnormal origin of the LSA from the PA via a very large ductus arteriosus (DA) in association with a rare communication between the left common carotid artery (LCCA) and the LSA in a patient with tetralogy of Fallot. doi: 10.1111/jocs.12770 (J Card Surg 2016;31:461-463).


Assuntos
Anormalidades Múltiplas , Artéria Carótida Primitiva/anormalidades , Canal Arterial/anormalidades , Artéria Pulmonar/anormalidades , Artéria Subclávia/anormalidades , Tetralogia de Fallot/patologia , Tetralogia de Fallot/cirurgia , Artéria Carótida Primitiva/diagnóstico por imagem , Feminino , Humanos , Lactente , Artéria Subclávia/diagnóstico por imagem , Tetralogia de Fallot/diagnóstico por imagem , Tomografia Computadorizada por Raios X , Resultado do Tratamento
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