Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 34
Filtrar
Más filtros

Banco de datos
País/Región como asunto
Tipo del documento
Intervalo de año de publicación
1.
Pediatr Int ; 64(1): e15231, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-35831247

RESUMEN

BACKGROUND: We evaluated the significance of perinatal plasma natriuretic peptide (NP) levels in neonates with congenital heart defects (CHDs) or arrhythmias and determined whether measurement of perinatal plasma NP levels and echocardiographic assessment in utero could predict heart failure after birth. METHODS: The study was conducted between 2012 and 2016 to evaluate the correlation of perinatal atrial NP (ANP) and brain NP (BNP) levels at birth with the modified Ross score after birth and the cardiovascular profile (CVP) score before birth. RESULTS: A total of 122 singletons with CHDs or arrhythmias and 27 controls were analyzed. Neonatal blood sampling was performed at a median of 0.7 h (range, 0.1-1.5) after birth. The neonatal plasma ANP and BNP levels shortly after birth were significantly higher than those in the umbilical artery (UA) plasma. The ANP and BNP levels in UA and neonatal blood were correlated with the modified Ross score. The neonatal plasma ANP and BNP levels and the modified Ross scores were inversely correlated with the CVP score in neonates with CHDs or arrhythmias. The area under the receiver operating characteristic curve of UA ANP levels for predicting neonatal heart failure was highest among those for the CVP score, perinatal plasma ANP and BNP levels, and their combinations. CONCLUSIONS: The plasma ANP and BNP levels increased markedly shortly after birth. Assessment of the UA plasma ANP level at birth and the CVP score in utero may be utilized to predict neonatal heart failure.


Asunto(s)
Cardiopatías Congénitas , Insuficiencia Cardíaca , Arritmias Cardíacas , Factor Natriurético Atrial , Femenino , Cardiopatías Congénitas/diagnóstico , Insuficiencia Cardíaca/diagnóstico , Humanos , Recién Nacido , Péptido Natriurético Encefálico , Péptidos Natriuréticos , Embarazo , Vasodilatadores
2.
J Obstet Gynaecol Res ; 45(7): 1268-1276, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-30977251

RESUMEN

AIM: To predict the prognosis of infants with congenital heart disease, accurate prenatal diagnosis of structural abnormality and heart failure are both necessary. The aim of this study was to investigate whether cardiovascular profile (CVP) and biophysical profile (BP) scores are useful for predicting prognosis in infants with congenital heart defect (CHD). METHODS: A retrospective review of singletons prenatally diagnosed with CHD at a tertiary pediatric cardiac center between 2011 and 2015 was undertaken. RESULTS: A total of 202 patients with CHD were analyzed. Perinatal and infant deaths occurred in 16 (7.9%) and 10 cases (5.0%), respectively. Infants with the last CVP score ≤ 5 had 18.7-fold higher perinatal mortality than those with a last CVP score > 5 (P < 0.01). Infants with a last BP score ≤ 6 had 18.7-fold higher perinatal mortality than those with a last BP score > 6 (P < 0.01). Infants with a CVP score decrease in utero had 4.5-fold higher infant mortality than those with an increase or no change (P < 0.01). Multivariate analysis showed that single-ventricle physiology, pre-term birth at <37 weeks of gestation, last CVP score ≤ 5, and last BP score ≤ 6 were independent predictors of perinatal mortality. Single-ventricle physiology and a CVP score decrease were independent predictors of infant mortality. CONCLUSION: CVP and BP scores are useful for predicting perinatal prognosis in infants with CHD. A CVP score decrease in utero is associated with infant mortality, suggesting that serial CVP score assessment may be useful for management planning.


Asunto(s)
Sistema Cardiovascular/embriología , Corazón Fetal/diagnóstico por imagen , Cardiopatías Congénitas/mortalidad , Diagnóstico Prenatal/estadística & datos numéricos , Índice de Severidad de la Enfermedad , Femenino , Corazón Fetal/embriología , Cardiopatías Congénitas/diagnóstico , Cardiopatías Congénitas/embriología , Humanos , Lactante , Mortalidad Infantil , Recién Nacido , Masculino , Diagnóstico Prenatal/métodos , Pronóstico , Estudios Retrospectivos , Medición de Riesgo/métodos
3.
Pediatr Cardiol ; 40(6): 1322, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31218372

RESUMEN

The authors have retracted this article [1] because, contrary to the statement in the article, this research did not obtain ethics approval from the National Cerebral and Cardiovascular Center Institutional Review Board prior to submission of the manuscript to Pediatric Cardiology. All authors agree to this retraction.

4.
Circ J ; 82(10): 2619-2626, 2018 09 25.
Artículo en Inglés | MEDLINE | ID: mdl-29998930

RESUMEN

BACKGROUND: We have previously demonstrated that umbilical cord plasma natriuretic peptide (NP) levels reflect the severity of heart failure (HF) in fetuses with congenital heart defects (CHD). The aim of this study was to evaluate the significance of amniotic fluid (AF) NP levels in the assessment of HF in fetuses with CHD or arrhythmia. Methods and Results: This was a prospective observational study at a tertiary pediatric cardiac center. A total of 95 singletons with CHD or arrhythmia, and 96 controls from 2012 to 2015 were analyzed. AF concentrations of atrial NP (ANP), B-type NP (BNP) and N-terminal pro-B-type NP (NT-proBNP) at birth were compared with ultrasonographic assessment of fetal HF using the cardiovascular profile (CVP) score. Multivariate analysis showed that a CVP score ≤5 and preterm birth are independently associated with high AF NT-proBNP levels. AF NT-proBNP levels of fetuses with CHD or arrhythmia inversely correlated with CVP score (P for trend <0.01). In contrast, AF concentrations of ANP and BNP were extremely low, and it was difficult to assess the degree of fetal HF based on them. CONCLUSIONS: AF NT-proBNP concentrations increase in stepwise fashion with the severity of HF in fetuses with CHD or arrhythmia; it was the optimal NP for assessing the fetal HF.


Asunto(s)
Líquido Amniótico/química , Enfermedades Fetales/diagnóstico , Insuficiencia Cardíaca/diagnóstico , Péptido Natriurético Encefálico/análisis , Péptidos Natriuréticos/análisis , Fragmentos de Péptidos/análisis , Arritmias Cardíacas/diagnóstico , Estudios de Casos y Controles , Femenino , Cardiopatías Congénitas/diagnóstico , Humanos , Masculino , Embarazo , Estudios Prospectivos , Índice de Severidad de la Enfermedad , Ultrasonografía Prenatal
5.
Pediatr Cardiol ; 39(7): 1355-1365, 2018 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-29777280

RESUMEN

For neonates with right atrial isomerism (RAI), functional single ventricle (f-SV), and obstructive total anomalous pulmonary venous connection (TAPVC), primary TAPVC repair (TAPVCR) has a poor outcome. At our hospital, the survival rate at 1 year of such neonates undergoing primary TAPVCR between 1999 and 2010 (TAPVCR group) was 30% (3/10). Most deceased cases suffered from capillary leak syndrome and unstable pulmonary resistance after the surgeries. We sought to determine whether less invasive primary draining vein stenting (DVS) improved the outcome of these neonates. We investigated outcomes in consecutive nine such neonates (median gestational age 38 weeks, birth weight 2.8 kg, females 4) who underwent primary DVS with 6-mm-diameter Palmaz® Genesis® stents at our hospital between 2007 and 2017 (DVS group). Eight patients underwent subsequent surgeries to adjust the pulmonary flow after decreased pulmonary resistance. The survival rate at 1 year after the first interventions in the DVS group improved to 77% (7/9), although there was a difference between the interventional eras of the two groups. Of the seven patients who underwent multiple stent redilations with a larger balloon or additional stenting in other sites until the next stage of surgery at a median age of 8 months, four received a bidirectional Glenn (BDG) shunt and TAPVCR and three underwent TAPVCR, with two of those cases reaching BDG. Less invasive primary DVS improved the outcome of neonates with RAI, f-SV, and obstructive TAPVC, with many reaching BDG. Patient selection to advance toward Fontan is thought to further improve the outcome.


Asunto(s)
Procedimientos Quirúrgicos Cardiovasculares/métodos , Síndrome de Heterotaxia/cirugía , Síndrome del Corazón Izquierdo Hipoplásico/cirugía , Síndrome de Cimitarra/cirugía , Stents/efectos adversos , Procedimientos Quirúrgicos Cardiovasculares/efectos adversos , Drenaje , Femenino , Ventrículos Cardíacos/anomalías , Síndrome de Heterotaxia/complicaciones , Síndrome de Heterotaxia/mortalidad , Humanos , Lactante , Recién Nacido , Masculino , Complicaciones Posoperatorias/epidemiología , Complicaciones Posoperatorias/etiología , Venas Pulmonares/anomalías , Estudios Retrospectivos , Síndrome de Cimitarra/complicaciones , Síndrome de Cimitarra/mortalidad , Tasa de Supervivencia , Resultado del Tratamiento
6.
J Obstet Gynaecol Res ; 41(7): 1137-40, 2015 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-25772579

RESUMEN

We describe a rare case of fetal critical aortic stenosis with spontaneous relief of severe restrictive atrial communication, resulting in complete resolution of hydrops fetalis in utero. Fetal ultrasonography showed hydrops fetalis caused by critical aortic stenosis with a severely restrictive foramen ovale and severe mitral regurgitation at 23 weeks of gestation. Hydrops fetalis, however, spontaneously resolved, showing an obvious increase of flow through the foramen ovale and pulmonary vein at 26 weeks of gestation. The neonate required balloon dilation of the aortic valve and balloon atrioseptostomy immediately after birth and also received bilateral pulmonary artery banding and arterial duct stenting 1 week later. The patient was in good condition after conversion to biventricular circulation via Ross procedure at 8 months old. The present case suggests that atrioseptostomy as a fetal intervention may improve outcome in even a hydropic condition.


Asunto(s)
Anomalías Múltiples/embriología , Estenosis de la Válvula Aórtica/embriología , Cardiomiopatía Restrictiva/embriología , Foramen Oval/anomalías , Defectos del Tabique Interatrial/embriología , Hidropesía Fetal/fisiopatología , Insuficiencia de la Válvula Mitral/embriología , Anomalías Múltiples/diagnóstico por imagen , Anomalías Múltiples/cirugía , Adolescente , Estenosis de la Válvula Aórtica/diagnóstico por imagen , Estenosis de la Válvula Aórtica/cirugía , Cardiomiopatía Restrictiva/diagnóstico por imagen , Cardiomiopatía Restrictiva/cirugía , Ecocardiografía Doppler en Color , Femenino , Foramen Oval/diagnóstico por imagen , Foramen Oval/embriología , Foramen Oval/cirugía , Defectos del Tabique Interatrial/diagnóstico por imagen , Defectos del Tabique Interatrial/cirugía , Humanos , Hidropesía Fetal/diagnóstico por imagen , Recién Nacido , Japón , Insuficiencia de la Válvula Mitral/diagnóstico por imagen , Insuficiencia de la Válvula Mitral/cirugía , Embarazo , Segundo Trimestre del Embarazo , Remisión Espontánea , Índice de Severidad de la Enfermedad , Nacimiento a Término , Resultado del Tratamiento , Ultrasonografía Prenatal
8.
ACS Appl Mater Interfaces ; 15(19): 23246-23254, 2023 May 17.
Artículo en Inglés | MEDLINE | ID: mdl-37144778

RESUMEN

Thermoelectric (TE) modules are exposed to temperature gradients and repeated thermal cycles during their operation; therefore, mechanically robust n- and p-type legs are required to ensure their structural integrity. The difference in the coefficients of thermal expansion (CTEs) of the two legs of a TE module can cause stress buildup and the deterioration of performance with frequent thermal cycles. Recently, n-type Mg3Sb2 and p-type MgAgSb have become two promising components of low-temperature TE modules because of to their high TE performance, nontoxicity, and abundance. However, the CTEs of n-Mg3Sb2 and p-MgAgSb differ by approximately 10%. Furthermore, the oxidation resistances of these materials at increased temperatures are unclear. This work manipulates the thermal expansion of Mg3Sb2 by alloying it with Mg3Bi2. The addition of Bi to Mg3Sb2 reduces the coefficient of linear thermal expansion from 22.6 × 10-6 to 21.2 × 10-6 K-1 for Mg3Sb1.5Bi0.5, which is in excellent agreement with that of MgAgSb (21 × 10-6 K-1). Furthermore, thermogravimetric data indicate that both Mg3Sb1.5Bi0.5 and MgAgSb are stable in air and Ar at temperatures below ∼570 K. The results suggest the compatibility and robustness of Mg3Sb1.5Bi0.5 and MgAgSb as a pair of thermoelectric legs for low-temperature TE modules.

9.
Eur J Pediatr ; 171(2): 259-65, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21739172

RESUMEN

In infants, acute mitral regurgitation resulting from ruptured chordae tendineae is very rare, but often fatal. There are a few case reports, but the characteristics and etiology of chordae tendineae rupture have not been elucidated. Our aim was to determine the clinical characteristics of idiopathic acute mitral regurgitation due to chordal rupture in infancy. A retrospective analysis was performed on ten consecutive patients, with a mean onset age of 4.6 ± 1.3 months. Despite nonspecific initial symptoms, all patients developed respiratory distress and four required resuscitation within a few days (mean, 1.8 ± 1.8 days). Chest radiographs showed pulmonary congestion with a normal or mildly increased cardiothoracic ratio in all ten patients. Laboratory data and electrocardiograms showed nonspecific findings. Echocardiography revealed ruptured chordae in all patients; locations were anterior (50%), posterior (20%), and both (30%). Surgical intervention was performed within 24 h of admission in eight patients (mean, 3.6 ± 5.1 h). Pathological findings included inflammatory cells in six specimens and myxomatous degeneration in two. No bacteria were isolated from preoperative blood cultures, pathological tissues, or excised tissue cultures. Autoantibody levels were insignificant. Three preoperatively resuscitated patients developed neurological sequelae and arrhythmias occurred in four after mitral valve replacement. Acute onset and rapid deterioration in patients with ruptured chordae tendineae necessitates early surgical intervention to improve outcomes. Though the etiology remains unknown, onset is in infants approximately 4 months of age, suggesting a definite disease entity.


Asunto(s)
Cuerdas Tendinosas/patología , Insuficiencia de la Válvula Mitral/diagnóstico , Cuerdas Tendinosas/cirugía , Femenino , Implantación de Prótesis de Válvulas Cardíacas , Humanos , Lactante , Masculino , Anuloplastia de la Válvula Mitral , Insuficiencia de la Válvula Mitral/etiología , Insuficiencia de la Válvula Mitral/cirugía , Estudios Retrospectivos , Rotura Espontánea , Resultado del Tratamiento
10.
Circ J ; 75(2): 413-20, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21157108

RESUMEN

BACKGROUND: The extra-cardiac conduit Fontan (EC) has a lower incidence of tachyarrhythmias than other types of Fontan. However, some intrinsic arrhythmogenic conditions, such as atrial isomerism, have been associated with a high incidence of arrhythmias. METHODS AND RESULTS: We retrospectively reviewed the clinical course of the supraventricular tachyarrhythmias (SVTs) in 212 patients after an EC, compared the results according to the atrial situs and investigated the substrate of the SVTs. The atrial situs was a solitus or inversus (SS/SI) in 152 patients, right isomerism (RI) in 45 and left isomerism (LI) in 15. Twenty-four SVTs occurred in 22 (11%) patients ≥3 months after the EC. The freedom from SVT after the EC was 95%, 76% and 77% in the SS/SI, RI and LI patients at 5 years, respectively (P<0.0001). Among the 16 SVTs associated with atrial isomerism, 10 were not related to the atrioventricular (AV) node. For the atrial isomerism, the predictors of SVT ≥3 months after the EC were a history of an AV valve repair (risk ratio (RR) 1.9; P=0.02) and complications associated with sinus node dysfunction (RR 1.9; P=0.03). Death related to SVT occurred in 3 patients. CONCLUSIONS: Postoperative SVTs after the EC with an atrial isomerism were not uncommon, mostly did not involve the AV node and possibly were caused by atrial tissue damage. A comprehensive therapeutic strategy should be considered.


Asunto(s)
Procedimiento de Fontan/métodos , Atrios Cardíacos/anomalías , Complicaciones Posoperatorias/epidemiología , Situs Inversus/complicaciones , Taquicardia Supraventricular/epidemiología , Niño , Preescolar , Femenino , Estudios de Seguimiento , Humanos , Incidencia , Lactante , Estimación de Kaplan-Meier , Masculino , Complicaciones Posoperatorias/etiología , Estudios Retrospectivos , Taquicardia Supraventricular/etiología , Taquicardia Supraventricular/mortalidad
11.
J Matern Fetal Neonatal Med ; 34(12): 1883-1889, 2021 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-31414622

RESUMEN

OBJECTIVES: To evaluate the significance of natriuretic peptide (NP) levels in fetal arrhythmia. STUDY DESIGN: Cardiovascular profile (CVP) scores and umbilical vein (UV) NP levels at birth were compared by different fetal arrhythmia statuses. RESULTS: Fetal tachyarrhythmia (n = 22), bradyarrhythmia (n = 12), extrasystole (n = 12) and controls (n = 127) were enrolled in this study. Fetal antiarrhythmic therapy was performed in fetuses with tachyarrhythmia (n = 18) and bradyarrhythmia (n = 5). Fetal arrhythmias were divided into three groups: group A (arrhythmia controlled at birth, n = 17), Group B (arrhythmia uncontrolled at birth, n = 9) and Group C (fetal therapy not indicated, n = 20). Group B had significantly lower CVP scores and higher NP levels than the other two groups and controls (p < .01). Groups A and C had significantly lower CVP scores than controls, but NP levels in Groups A and C showed no differences compared with controls. CONCLUSIONS: UV NP concentrations reflect the severity of fetal arrhythmia and responses to fetal therapy.


Asunto(s)
Enfermedades Fetales , Insuficiencia Cardíaca , Arritmias Cardíacas , Femenino , Humanos , Recién Nacido , Péptidos Natriuréticos , Venas Umbilicales
12.
Sci Rep ; 10(1): 11077, 2020 Jul 06.
Artículo en Inglés | MEDLINE | ID: mdl-32632124

RESUMEN

The Pristine Mayenite Ca12Al14O33 (C12A7) Cement was simply synthesized by using solid-state reaction. The C12A7 and Graphene Oxide (GO) composites (C12A7_GO-x) with various contents of the GO suspension loading (x = 0 wt%, 1 wt%, 2 wt%, 3 wt%, and 4 wt%) were directly prepared by mixing the C12A7 and GO. X-ray diffraction results of pristine C12A7 and all C12A7_GO composites indicated a pure phase corresponding to the standard of C12A7 cement. Raman spectroscopy confirmed the existence of GO in all C12A7_GO samples. Scanning Electron Microscopy (SEM) showed the micrometer grain sizes and the occurrence of grain boundary interfaces for GO incorporation in all C12A7_GO samples. UV-Vis spectroscopy revealed the absorption value of all C12A7_GO samples and red shift near longer wavelengths when increasing the GO concentrations. The dielectric constant of C12A7_GO composites can be explained by the high density of free electron charges for the interfacial polarization on the GO surface. The maximum specific capacitance of C12A7_GO-4 electrode of 21.514 at a current density of 0.2 A g-1 can be attributed to the increase in the electrochemically active surface area for the formation of the electrical double layer capacitors behavior and the effects of high surface area GO connections. Also, the mechanical properties exhibited an increase in Vickers indenter hardness (HV) values with increasing GO contents. The highest HV value was 117.8 HV/2 kg at the C12A7_GO-4 sample. These results showed that the composite materials of the pristine C12A7 cement with GO were highly efficient. All in all, the GO material contained a high potential for enhancing low-cost cement materials in multifunctional properties such as optical, dielectric, electrochemical, and mechanical properties.

13.
Heart ; 106(12): 910-915, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32188625

RESUMEN

OBJECTIVES: von Willebrand factor (vWF) has prognostic value in patients with heart failure (HF) and in those with liver disease. Liver congestion, due to right-sided HF (RHF), is one of the major clinical pathophysiologic manifestations in adults with congenital heart disease (ACHD). The present study's purpose was to clarify the prognostic value of plasma levels of vWF antigen (vWF:Ag) in ACHD. METHODS: We measured vWF:Ag (%) in 382 consecutive patients (20 unrepaired cyanotic ACHD, 172 Fontan patients and 190 ACHD after biventricular repair) and compared the results with the clinical profiles and prognosis. RESULTS: The plasma vWF:Ag level was 130±53 (normal range: 55%-190%), and 48 patients (13%) showed high levels of vWF:Ag (≥190%). Older age, Fontan circulation, higher central venous pressure, lower arterial oxygen saturation and lower plasma levels of albumin were independently associated with high log (vWF:Ag) (p<0.05-0.0001). During the follow-up of 2.4±1.4 years, 15 patients died. High log (vWF:Ag) predicted the all-cause mortality (HR 1.63 per 0.1, 95% CI 1.40 to 1.96, p<0.0001). Specifically, patients with high vWF:Ag (≥165%) had a substantially higher risk of all-cause mortality (HR 56.4, 95% CI 11.4 to 1020, p<0.0001), and this prognostic value was independent of plasma levels of brain-type natriuretic peptide. CONCLUSIONS: High vWF:Ag may reflect RHF severity and related liver dysfunction with a strong prognostic value of all-cause mortality in ACHD. Thus, vWF:Ag might be an excellent biomarker for monitoring ACHD with RHF.


Asunto(s)
Cardiopatías Congénitas/complicaciones , Hepatopatías/diagnóstico , Pruebas de Función Hepática , Sobrevivientes , Factor de von Willebrand/metabolismo , Adulto , Biomarcadores/sangre , Femenino , Procedimiento de Fontan , Cardiopatías Congénitas/diagnóstico , Cardiopatías Congénitas/mortalidad , Cardiopatías Congénitas/cirugía , Insuficiencia Cardíaca/etiología , Humanos , Hepatopatías/sangre , Hepatopatías/etiología , Hepatopatías/mortalidad , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Pronóstico , Estudios Prospectivos , Medición de Riesgo , Factores de Riesgo , Índice de Severidad de la Enfermedad , Factores de Tiempo , Adulto Joven
14.
Circ J ; 73(11): 2135-42, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19755751

RESUMEN

BACKGROUND: Refractory arrhythmias caused by right ventricular (RV) volume overload resulting from pulmonary regurgitation are the main concern in adult patients after repair of tetralogy of Fallot (TOF). Early pulmonary valve replacement (PVR) may prevent irreversible RV dysfunction and refractory arrhythmias, so the present study evaluated the PVR outcomes in adult patients with a severely dilated RV (d-RV) and refractory arrhythmias after TOF repair. METHODS AND RESULTS: Three TOF patients with a d-RV and tachyarrhythmias underwent PVR between the ages of 28 and 38 years. All had a d-RV (RV end-diastolic volume index (RVEDVI) >200 ml/m(2)) with a polymorphic nonsustained ventricular tachycardia (NSVT). Atrial tachycardia (AT) was identified in 2 patients and they underwent radiofrequency catheter ablation. The arrhythmias in all 3 were refractory to antiarrhythmic drugs. One year after PVR, the RVEDVI, left ventricular ejection fraction, right atrial pressure, cardiac index, cardiothoracic ratio, brain natriuretic peptide levels, and peak VO(2) improved in all, but without normalization. During the 2.6-3.8 year follow-up, all experienced tachyarrhythmias (NSVT or AT), which were controlled with medication. CONCLUSIONS: PVR may be beneficial for refractory arrhythmias, even in TOF patients with a d-RV, but it is difficult to completely normalize the hemodynamics and resolve the arrhythmogenicity.


Asunto(s)
Arritmias Cardíacas/etiología , Prótesis Valvulares Cardíacas , Hipertrofia Ventricular Derecha/etiología , Hipertrofia Ventricular Derecha/cirugía , Válvula Pulmonar/cirugía , Tetralogía de Fallot/cirugía , Adulto , Arritmias Cardíacas/fisiopatología , Arritmias Cardíacas/cirugía , Bioprótesis , Ablación por Catéter , Electrocardiografía , Femenino , Humanos , Hipertrofia Ventricular Derecha/fisiopatología , Japón , Complicaciones Posoperatorias/etiología , Complicaciones Posoperatorias/cirugía , Pronóstico , Insuficiencia de la Válvula Pulmonar/etiología , Insuficiencia de la Válvula Pulmonar/cirugía , Factores de Tiempo
15.
Materials (Basel) ; 12(12)2019 Jun 17.
Artículo en Inglés | MEDLINE | ID: mdl-31212898

RESUMEN

Si-based thermoelectric materials have attracted attention in recent decades with their advantages of low toxicity, low production costs, and high stability. Here, we report recent achievements on the synthesis and characterization of Si-based thermoelectric materials. In the first part, we show that bulk Si synthesized through a natural nanostructuring method exhibits an exceptionally high thermoelectric figure of merit zT value of 0.6 at 1050 K. In the second part, we show the synthesis and characterization of nanocomposites of Si and metal silicides including CrSi2, CoSi2, TiSi2, and VSi2. These are synthesized by the rapid-solidification melt-spinning (MS) technique. Through MS, we confirm that silicide precipitates are dispersed homogenously in the Si matrix with desired nanoscale sizes. In the final part, we show a promising new metal silicide of YbSi2 for thermoelectrics, which exhibits an exceptionally high power factor at room temperature.

16.
RSC Adv ; 9(27): 15496-15501, 2019 May 14.
Artículo en Inglés | MEDLINE | ID: mdl-35514841

RESUMEN

Nanostructured bulk silicon (bulk nano-Si) has attracted attention as an advanced thermoelectric (TE) material due to its abundance and low toxicity. However, oxidization will occur easily when bulk nano-Si is synthesized by a conventional method, which deteriorates the TE performance. Various methods to prevent such oxidation have been proposed but they need specific techniques and are thus expensive. Here, we propose a simple and cost-effective method named Surface Diffusion/Sintering Doping (SDSD) to synthesize bulk nano-Si for TEs. SDSD utilizes Si nanoparticles whose surface is coated with a native thin oxide layer. SDSD is composed of two steps, (1) a molecular precursor containing a doping element is added onto the oxide layer of Si nanoparticles and (2) the nanoparticles are sintered into a bulk state. During sintering, the doping element diffuses through the oxide layer forming conductive paths, which results in a high carrier concentration as well as high mobility. Furthermore, owing to the nanostructures, low lattice thermal conductivity (κ lat) is also achieved, which is an ideal situation for TEs. In this study, we show that P-doped bulk nano-Si synthesized by SDSD shows good TE performance due to its high carrier concentration, high carrier mobility, and low κ lat. Since SDSD takes advantage of oxidization, it is cost-effective and suitable for mass production to synthesize bulk nano-Si for TEs.

17.
Heliyon ; 5(7): e02049, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31372532

RESUMEN

Liquid ZrO2 is one of the most important materials involved in severe accident analysis of a light-water reactor. Despite its importance, the physical properties of liquid ZrO2 are scarcely reported. In particular, there are no experimental reports on the viscosity of liquid ZrO2. This is mainly due to the technical difficulties involved in the measurement of thermo-physical properties of liquid ZrO2, which has an extremely high melting point. To address this problem, an aerodynamic levitation technique was used in this study. The density of liquid ZrO2 was calculated from its mass and volume, estimated based on the recorded image of the sample. The viscosity was measured by a droplet oscillation technique. The density and viscosity of liquid ZrO2 at temperatures ranging from 2753 K to 3273 K, and 3170 K-3471 K, respectively, were successfully evaluated. The density of liquid ZrO2 was found to be 4.7 g/cm 3 at its melting point of 2988 K and decreased linearly with increasing temperature, and the viscosity of liquid ZrO2 was 13 mPa at its melting point.

18.
J Matern Fetal Neonatal Med ; 32(15): 2463-2468, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29415597

RESUMEN

OBJECTIVES: Fetal cardiac rhabdomyomas are rare but well-known to be associated with arrhythmia or conduction abnormalities. However, since in utero electrophysiological information is quite limited, it remains unclear which type of rhabdomyoma will develop arrhythmia after birth. The aim of this study is to identify factors that predict postnatal arrhythmia requiring therapy in fetuses with cardiac rhabdomyoma. STUDY DESIGN: A retrospective review of infants prenatally diagnosed with cardiac rhabdomyoma was performed at our tertiary pediatric cardiac center between 1990 and 2016. Fetal arrhythmia was diagnosed using fetal echocardiography and magnetocardiography. We compared the characteristics of cases with and without antiarrhythmic therapy after birth. Cases without antiarrhythmic therapy after birth consisted of those who had postnatal arrhythmia but did not require antiarrhythmic therapy and those who had no postnatal arrhythmia. RESULTS: A total of 20 fetuses with cardiac rhabdomyoma were included in this study. Ten cases (50%) were confirmed as having tuberous sclerosis after birth. The mean gestational week at diagnosis and delivery were 32.1 ± 2.7 and 37.6 ± 2.8 weeks, respectively. Mean cardiac tumor size in utero was 21 ± 11 mm (range, 7-54 mm) in diameter. Fetal arrhythmia was found in six cases; three resolved in utero with transplacental antiarrhythmic therapy. Postnatal arrhythmia or conduction abnormalities were found in 12 cases; 7 required antiarrhythmic therapy. Cases with antiarrhythmic therapy after birth had larger cardiac tumor in utero than those without therapy (29.6 ± 12.8 mm versus 16.3 ± 5.8 mm, p < .01). Cardiac tumor size >30 mm in diameter predicted postnatal arrhythmia requiring therapy with sensitivity of 57.1% and specificity of 100%. Location and number of cardiac tumor and presence of arrhythmia or conduction abnormalities in utero were similar between the two groups. CONCLUSIONS: Cardiac rhabdomyomas >30 mm in diameter are associated with postnatal arrhythmia requiring therapy regardless of number and location.


Asunto(s)
Arritmias Cardíacas/etiología , Enfermedades Fetales/diagnóstico por imagen , Neoplasias Cardíacas/complicaciones , Rabdomioma/complicaciones , Adulto , Arritmias Cardíacas/diagnóstico por imagen , Ecocardiografía , Femenino , Neoplasias Cardíacas/diagnóstico por imagen , Humanos , Magnetocardiografía , Embarazo , Estudios Retrospectivos , Rabdomioma/diagnóstico por imagen
19.
J Matern Fetal Neonatal Med ; 31(4): 521-524, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-28140722

RESUMEN

Right pulmonary artery to left atrium communication (RPALA com) is a fatal congenital heart disease with right-to-left shunting. We present a rare case of RPALA com that was prenatally diagnosed and confirmed by autopsy. We focus on some unique echocardiographic findings for prenatal diagnosis of RPALA com by reviewing our case and the literature. Asymmetric cardiomegaly with a pear sign and dilatation of the pulmonary artery might be useful for screening tests. A larger stalk with the pear sign, high-velocity of shunt flow, and absence of a dilated pulmonary vein might support the prenatal diagnosis of RPALA com.


Asunto(s)
Corazón Fetal/anomalías , Atrios Cardíacos/anomalías , Arteria Pulmonar/anomalías , Aborto Eugénico , Ecocardiografía , Ecocardiografía Doppler en Color , Femenino , Corazón Fetal/diagnóstico por imagen , Atrios Cardíacos/diagnóstico por imagen , Humanos , Embarazo , Arteria Pulmonar/diagnóstico por imagen , Ultrasonografía Prenatal/métodos , Adulto Joven
20.
ACS Appl Mater Interfaces ; 10(50): 43682-43690, 2018 Dec 19.
Artículo en Inglés | MEDLINE | ID: mdl-30479127

RESUMEN

Ternary compounds with a tetragonal chalcopyrite structure, such as CuGaTe2, are promising thermoelectric (TE) materials. It has been demonstrated in various chalcopyrite systems, including compounds with quaternary chalcopyrite-like structures, that the lattice parameter ratio, c/ a, being exactly 2.00 to have a pseudo-cubic structure is key to increase the degeneracy at the valence band edge and ultimately achieve high TE performance. Considering the fact that ZnSnSb2 with a chalcopyrite structure is reported to have c/ a close to 2.00, it is expected to have multiple valence bands leading to a high p-type zT. However, there are no complete investigations on the high temperature TE properties of ZnSnSb2 mainly because of the difficulty of obtaining a single-phase ZnSnSb2. In the present study, pure ZnSnSb2 samples with no impurities are synthesized successfully using a Sn flux-based method and TE properties are characterized up to 585 K. Transport properties and thermal analysis indicate that the structure of ZnSnSb2 remains chalcopyrite with no order-disorder transition and clearly show that ZnSnSb2 can be made to exhibit a high zT in the low-to-mid temperature range through further optimization.

SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA