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1.
Rev. bras. ginecol. obstet ; 43(4): 283-290, Apr. 2021. tab
Artículo en Inglés | LILACS | ID: biblio-1280044

RESUMEN

Abstract Objective Cesarean section (CS) delivery, especially without previous labor, is associated with worse neonatal respiratory outcomes. Some studies comparing neonatal outcomes between term infants exposed and not exposed to antenatal corticosteroids (ACS) before elective CS revealed that ACS appears to decrease the risk of respiratory distress syndrome (RDS), transient tachypnea of the neonate (TTN), admission to the neonatal intensive care unit (NICU), and the length of stay in the NICU. Methods The present retrospective cohort study aimed to compare neonatal outcomes in infants born trough term elective CS exposed and not exposed to ACS. Outcomes included neonatal morbidity at birth, neonatal respiratory morbidity, and general neonatal morbidity. Maternal demographic characteristics and obstetric data were analyzed as possible confounders. Results A total of 334 newborns met the inclusion criteria. One third of the population study (n=129; 38.6%) received ACS. The present study found that the likelihood for RDS (odds ratio [OR]=1.250; 95% confidence interval [CI]: 0.454-3.442), transient TTN (OR=1.,623; 95%CI: 0.556-4.739), and NIUC admission (OR=2.155; 95%CI: 0.474-9.788) was higher in the ACS exposed group, although with no statistical significance. When adjusting for gestational age and arterial hypertension, the likelihood for RDS (OR=0,732; 95%CI: 0.240-2.232), TTN (OR=0.959; 95%CI: 0.297--3.091), and NIUC admission (OR=0,852; 95%CI: 0.161-4.520) become lower in the ACS exposed group. Conclusion Our findings highlight the known association between CS-related respiratory morbidity and gestational age, supporting recent guidelines that advocate postponing elective CSs until 39 weeks of gestational age.


Asunto(s)
Humanos , Femenino , Embarazo , Atención Prenatal/métodos , Síndrome de Dificultad Respiratoria del Recién Nacido/prevención & control , Cesárea/efectos adversos , Corticoesteroides/administración & dosificación , Procedimientos Quirúrgicos Electivos/efectos adversos , Resultado del Embarazo , Unidades de Cuidado Intensivo Neonatal , Estudios Retrospectivos , Edad Gestacional , Taquipnea Transitoria del Recién Nacido/prevención & control , Tiempo de Internación
2.
BMJ Case Rep ; 20162016 Jan 12.
Artículo en Inglés | MEDLINE | ID: mdl-26759440

RESUMEN

Joubert syndrome is a rare disorder, usually autosomal recessive, with a prevalence of 1:80,000 to 1:100,000. This disease presents most commonly as breathing irregularities, although the two major clinical criteria are hypotonia and developmental delay, sometimes associated with ocular movement abnormalities. The severity of the presentation varies, ranging from mild cases with normal intelligence to severe developmental delays associated with early death. We report a case of a newborn who presented to the emergency department for absent ocular fixation and torsional nystagmus without other neurological abnormalities. Her cranial MR showed cerebellar vermis agenesis and a molar tooth sign. Her laboratory evaluation, and renal and abdominal ultrasound were normal. An electroretinogram showed mixed retinal dystrophy and an AHI1 homozygous missense c.1981T>C mutation was identified (parents are carriers). Throughout infancy, she has shown mild developmental delay and hypotonia, but no respiratory abnormalities. Owing to variable expressivity, a high level of suspicion is required.


Asunto(s)
Anomalías Múltiples/diagnóstico , Encéfalo/patología , Cerebelo/anomalías , Anomalías del Ojo/diagnóstico , Enfermedades Renales Quísticas/diagnóstico , Retina/anomalías , Anomalías Múltiples/genética , Proteínas Adaptadoras Transductoras de Señales/genética , Proteínas Adaptadoras del Transporte Vesicular , Discapacidades del Desarrollo/etiología , Electrorretinografía , Anomalías del Ojo/complicaciones , Anomalías del Ojo/genética , Femenino , Humanos , Recién Nacido , Enfermedades Renales Quísticas/complicaciones , Enfermedades Renales Quísticas/genética , Imagen por Resonancia Magnética , Hipotonía Muscular/etiología , Mutación Missense , Nistagmo Patológico/etiología
3.
Einstein (Säo Paulo) ; 9(3)july-sept. 2011.
Artículo en Inglés, Portugués | LILACS | ID: lil-604966

RESUMEN

Rhizobium radiobacter (Agrobacterium radiobacter) is an aerobic Gram-negative rod belonging to Agrobacterium genus, a group of phytopathogenic bacteria present in the soil that has been implicated in human opportunistic infections. We report a clinical case of bacterial peritonitis in a 5-year-old child with chronic renal disease in peritoneal dialysis, who had a history of direct soil contact identified. The infection was treated with ceftazidime and piperaciline+tazobactam without relapses or the need to remove the peritoneal dialysis catheter.


O Rhizobium radiobacter (Agrobacterium radiobacter) é um microorganismo Gram-negativo aeróbio do gênero Agrobacterium, grupo de bactérias fitopatogénicas presentes no solo, que tem sido implicado em infecções oportunistas nos humanos. Relata-se um caso clínico de peritonite bacteriana em criança de 5 anos com doença renal crônica em diálise peritoneal, que teve um factor epidemiológico de contato direto com o solo identificado. A infecção foi tratada com ceftazidima e piperacilina+tazobactam, sem reinfecções ou necessidade de remoção do cateter de diálise peritoneal.


Asunto(s)
Humanos , Niño , Agrobacterium tumefaciens , Diálisis Peritoneal , Peritonitis
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