Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 15 de 15
Filtrar
Más filtros












Base de datos
Intervalo de año de publicación
1.
Viruses ; 16(7)2024 Jul 16.
Artículo en Inglés | MEDLINE | ID: mdl-39066300

RESUMEN

Cytomegalovirus (CMV) is the leading infectious cause of brain defects and neurological dysfunctions, including sensorineural hearing loss (SNHL). Targeted screening in neonates failing the hearing screen is currently recommended in Italy according to national guidelines. However, SNHL may not be present at birth; also, congenital CMV (cCMV) may manifest with subtle signs other than SNHL. Therefore, the inclusion of additional criteria for cCMV screening appears clinically valuable. Starting January 2021, we have implemented expanded targeted cCMV screening at our center, with testing in case of maternal CMV infection during pregnancy, inadequate antenatal care, maternal HIV infection or immunosuppression, birthweight and/or head circumference < 10th centile, failed hearing screen, and prematurity. During the first three years of use of this program (2021-2023), 940 (12.3%) of 7651 live-born infants were tested. The most common indication was birthweight < 10th centile (n = 633, 67.3%). Eleven neonates were diagnosed as congenitally infected, for a prevalence of 1.17% (95%CI 0.48-1.86) on tested neonates and of 0.14% (95%CI 0.06-0.23) on live-born infants. None of the cCMV-infected newborns had a failed hearing screen as a testing indication. Implementation of an expanded cCMV screening program appears feasible and of clinical value.


Asunto(s)
Infecciones por Citomegalovirus , Citomegalovirus , Tamizaje Neonatal , Complicaciones Infecciosas del Embarazo , Humanos , Infecciones por Citomegalovirus/congénito , Infecciones por Citomegalovirus/diagnóstico , Recién Nacido , Femenino , Tamizaje Neonatal/métodos , Embarazo , Italia/epidemiología , Citomegalovirus/genética , Citomegalovirus/aislamiento & purificación , Complicaciones Infecciosas del Embarazo/diagnóstico , Complicaciones Infecciosas del Embarazo/virología , Masculino , Pérdida Auditiva Sensorineural/virología , Pérdida Auditiva Sensorineural/diagnóstico , Prevalencia
4.
Eur J Obstet Gynecol Reprod Biol X ; 19: 100220, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-37636521

RESUMEN

Uterine arteriovenous malformations (AVMs) is a rare but high-risk cause of uterine bleeding. The clinical management of this condition is challenging, as the ultrasound picture can sometimes be unambiguously interpreted. Moreover, in the puerperium in which acquired AVMs are most frequently formed, it is necessary to discuss the correct management in a multidisciplinary and personalized manner. We present two cases of AVMs developing in the puerperium, both with a vaginal delivery and spontaneous and complete secondment. The symptom of onset was an episode of bright red blood loss in the puerperium, on the 14th and 21st postpartum days, respectively. Transvaginal ultrasound showed a hypervascularized lesion in the myometrium with turbulent vascular flow, confirmed by transabdominal ultrasound and angiography. To date, there are no guidelines on the management of MAVs. In our cases we opted for a conservative approach, in order to preserve the fertility of the patient. These experiences reported have the purpose of enriching a literature still sparse on the subject and in the future to be able to represent a fulcrum for official recommendations.

6.
Vertex ; 15(55): 38-41, 2004.
Artículo en Español | MEDLINE | ID: mdl-15085223

RESUMEN

It becomes apparent at the present level of development of the Psychiatry that it is not possible to have a unique theoretical framework or a general principle in the wide field of this discipline. In this article the various theoretical references are reviewed. In some clinical cases the author refers to the lack of a theoretical reference at all. At the present moment, the range of theoretical perspectives leads to deal with the coexistence of regional epistemologies.


Asunto(s)
Conocimiento , Psiquiatría/historia , Historia del Siglo XIX , Historia del Siglo XX , Humanos , Trastornos Mentales/historia
7.
Encephale ; 20 Spec No 3: 551-7, 1994 Nov.
Artículo en Francés | MEDLINE | ID: mdl-7843050

RESUMEN

Description of psychasthenia by P. Janet (1903) sets up at the end of a double reflection, with on the one hand a theorization of asthenia, the notion of which already occupied the medical concepts of the 18th and 19th centuries, and on the other hand a progressive attribution of neurosis to the psychiatric field. Its clinical characteristics (feelings of non-fulfillment in action and emotion, experiences of oddness and depersonalization, obsessions, phobias...) makes psychasthenia a fully-fledged illness, the psychopathological organization of which results from a decrease of psychological tension and from a loss of reality function. Since P. Janet, the term of psychasthenia has not ceased to be used, although its etiopathological references blurred behind the psychoanalytic work, and it is usually synonymous with obsessional neurosis, even with obsessional personality. Description of psychasthenia appears in these rubrics of the DSM III, even though the term itself is ignored.


Asunto(s)
Neurastenia/historia , Trastorno Obsesivo Compulsivo/historia , Francia , Historia del Siglo XVIII , Historia del Siglo XIX , Historia del Siglo XX , Humanos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...