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1.
J Minim Invasive Gynecol ; 27(2): 433-440.e1, 2020 02.
Artículo en Inglés | MEDLINE | ID: mdl-31760118

RESUMEN

OBJECTIVE: To evaluate the diagnostic accuracy of intraoperative laparoscopic imaging tools in reference to that of histopathology for detecting endometriotic lesions and to compare them with conventional white-light inspection by performing a systematic review with meta-analysis. DATA SOURCES: We searched the MEDLINE, EMBASE, and CENTRAL databases in addition to citations and reference lists until the end of February 2019. METHODS OF STUDY SELECTION: Two authors screened 1038 citations for eligibility. We included randomized controlled trials or prospective cohort studies published in English, assessing the accuracy of intraoperative imaging tools for diagnosing endometriosis during laparoscopy. We considered studies using histopathologic evaluation as a standard criterion. TABULATION, INTEGRATION, AND RESULTS: Seven studies were eligible, including 472 women and 1717 histopathologic specimens, and they involved study of the use of narrow-band imaging (2 studies), 5-aminolevulinic acid-induced fluorescence (2 studies), autofluorescence imaging (1 study), indocyanine green (1 study), and a 3-dimensional robotic laparoscopy (1 study). Two authors extracted data and assessed the validity of the included studies. Bivariate random-effects models and McNemar's test were used to compare the tests and evaluate sources of heterogeneity. Four studies were attributed a high risk of bias, and biopsies of normal-looking peritoneum were not performed to verify the results in 3 studies; both factors were identified as significant sources of heterogeneity, leading to the overestimation of the sensitivity and underestimation of the specificity of imaging tools. In all studies, additional endometriotic lesions were diagnosed with the enhanced imaging tool compared with white-light inspection alone. In the 4 studies that appropriately performed control biopsies (171 women, 448 specimens), enhanced imaging techniques were associated with a higher sensitivity and specificity compared with white-light inspection (0.84 and 0.89 compared with 0.75 and 0.76, respectively, p ≤.001). Adverse events were uncommon (n = 5) and reported only with the use of exogeneous photosensitizers. There were no reports of long-term changes in patient-reported outcomes arising from better detection of endometriosis lesions. CONCLUSION: Studies report that enhanced imaging allows for the detection of additional endometriotic lesions missed by conventional white-light laparoscopy. The benefits of finding these additional lesions using enhanced imaging compared with white-light inspection alone on long-term postoperative outcomes have not been determined, and these tools should be considered only in a research context at this time.


Asunto(s)
Diagnóstico por Imagen/métodos , Técnicas de Diagnóstico Obstétrico y Ginecológico , Endometriosis/diagnóstico , Endometriosis/cirugía , Enfermedades Peritoneales/diagnóstico , Enfermedades Peritoneales/cirugía , Biopsia , Diagnóstico por Imagen/efectos adversos , Diagnóstico por Imagen/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/efectos adversos , Técnicas de Diagnóstico Obstétrico y Ginecológico/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/normas , Técnicas de Diagnóstico Obstétrico y Ginecológico/estadística & datos numéricos , Endometriosis/patología , Femenino , Humanos , Aumento de la Imagen , Biopsia Guiada por Imagen , Periodo Intraoperatorio , Laparoscopía/métodos , Laparoscopía/estadística & datos numéricos , Imagen de Banda Estrecha , Imagen Óptica , Enfermedades Peritoneales/patología , Examen Físico/métodos , Estudios Prospectivos , Reproducibilidad de los Resultados , Sensibilidad y Especificidad
2.
J Gynecol Obstet Hum Reprod ; 46(4): 317-321, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28643658

RESUMEN

INTRODUCTION: French guidelines regarding the minimum criteria for gynaecological ultrasound were given in a recent report in 2016, by the French National College of Obstetricians and Gynaecologists (CNGOF). An accurate report is essential for the optimal care of women, especially those presenting myomas. The goal of this study was to evaluate the quality of gynaecological ultrasound reports for women with type 0 to 2 uterine myomas, referring to the items contained in the French guidelines. MATERIALS AND METHODS: A retrospective descriptive study was conducted from reports of ultrasounds performed in private offices and in the gynaecologic department of a hospital, between June 2014 and June 2016 (before the report of CNGOF). These reports involved women who underwent hysteroscopic resection of myoma(s). A search of validated items was conducted for all of the reports, and the missing items were analysed. The different types of practitioners and between hospital and private medical offices were also compared with Chi-square tests. RESULTS: A total of 138 reports were analysed; 71 were performed in private offices and 67 were performed in the gynaecologic unit of the hospital. Many items were missing in the reports, with disparities between the type of institution (private offices or hospital) and the speciality of practitioners (radiologists or gynaecologists). Specific items regarding myomas, such as the International Federation of Gynaecologists and Obstetricians (FIGO) classification or measurement of the posterior wall, were more often missing in reports from radiologists (89.7% and 79.5%, respectively) than in reports from gynaecologists (21.2% and 34.3%, respectively) (P<0.05). A significant difference was also observed for these data between private offices' reports and hospitals' reports. Items relative to ultrasound structures, such as the appearance of myomas or associated abdominal effusion, were more frequently missing in gynaecologists' reports (88.9% and 49.5%, respectively) compared to radiologists' reports (56.4% and 12.8%, respectively) (P<0.05). CONCLUSIONS: Certain items are present in all the reports, while others are insufficiently mentioned. These inequalities can be explained in part by the type of practice; however, methods to overcome these difficulties must be developed. Information campaigns to educate professionals on the minimum reporting and training conducted jointly by radiologists and gynaecologist surgeons might improve reports and improve the care of women.


Asunto(s)
Ginecología , Leiomioma/diagnóstico , Pelvis/diagnóstico por imagen , Guías de Práctica Clínica como Asunto , Ultrasonografía/normas , Neoplasias Uterinas/diagnóstico , Técnicas de Diagnóstico Obstétrico y Ginecológico/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/normas , Femenino , Francia/epidemiología , Adhesión a Directriz/estadística & datos numéricos , Ginecología/métodos , Ginecología/normas , Humanos , Leiomioma/patología , Obstetricia/métodos , Obstetricia/normas , Pautas de la Práctica en Medicina/normas , Pautas de la Práctica en Medicina/estadística & datos numéricos , Garantía de la Calidad de Atención de Salud , Estudios Retrospectivos , Sociedades Médicas/normas , Ultrasonografía/métodos , Neoplasias Uterinas/patología
3.
In. Santiesteban Alba, Stalina. Obstetricia y perinatología. Diagnóstico y tratamiento. La Habana, Ecimed, 2012. .
Monografía en Español | CUMED | ID: cum-53286
4.
5.
In. Santiesteban Alba, Stalina. Obstetricia y perinatología. Diagnóstico y tratamiento. La Habana, Ecimed, 2012. .
Monografía en Español | CUMED | ID: cum-53278
6.
Fed Regist ; 76(56): 16292-4, 2011 Mar 23.
Artículo en Inglés | MEDLINE | ID: mdl-21434456

RESUMEN

The Food and Drug Administration (FDA) is classifying the ovarian adnexal mass assessment score test system into class II (special controls). The special control that will apply to these devices is the guidance document entitled "Guidance for Industry and FDA Staff; Class II Special Controls Guidance Document: Ovarian Adnexal Mass Assessment Score Test System." The Agency is classifying these devices into class II (special controls) because special controls, in addition to general controls, will provide a reasonable assurance of safety and effectiveness of these devices and there is sufficient information to establish special controls. Elsewhere in this issue of the Federal Register, FDA is announcing the availability of a guidance document that will serve as the special control for these devices


Asunto(s)
Enfermedades de los Anexos/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/instrumentación , Seguridad de Equipos/clasificación , Inmunoensayo/instrumentación , Neoplasias Ováricas/clasificación , Enfermedades de los Anexos/sangre , Aprobación de Recursos , Técnicas de Diagnóstico Obstétrico y Ginecológico/clasificación , Femenino , Humanos , Inmunoensayo/clasificación , Neoplasias Ováricas/sangre , Estados Unidos , United States Food and Drug Administration
7.
Fed Regist ; 76(251): 82129-31, 2011 Dec 30.
Artículo en Inglés | MEDLINE | ID: mdl-22242228

RESUMEN

The Food and Drug Administration (FDA) is amending the regulation classifying ovarian adnexal mass assessment score test systems to restrict these devices so that a prescribed warning statement that addresses a risk identified in the special controls guidance document must be in a black box and must appear in all labeling, advertising, and promotional material. The black box warning mitigates the risk to health associated with off-label use as a screening test, stand-alone diagnostic test, or as a test to determine whether or not to proceed with surgery.


Asunto(s)
Enfermedades de los Anexos/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/clasificación , Neoplasias de los Genitales Femeninos/clasificación , Pruebas Inmunológicas/clasificación , Neoplasias Ováricas/clasificación , Etiquetado de Productos/legislación & jurisprudencia , Pruebas Serológicas/clasificación , Enfermedades de los Anexos/diagnóstico , Femenino , Neoplasias de los Genitales Femeninos/diagnóstico , Humanos , Pruebas Inmunológicas/instrumentación , Uso Fuera de lo Indicado/legislación & jurisprudencia , Neoplasias Ováricas/diagnóstico , Pruebas Serológicas/instrumentación
8.
Asclepio ; 62(1): 177-208, ene.-jun. 2010.
Artículo en Español | IBECS | ID: ibc-87879

RESUMEN

En este trabajo se examina la contribución del discurso médico-forense español del siglo XIX, a través de su aplicación en los casos de agresión sexual, a la legitimación del orden moral sexual de la época. Con este objetivo se analizan los principales tratados de Medicina Forense editados en nuestro país durante ese siglo (AU)


The purpose of this paper is to analyse the importance of the contribution of the Spanish forensic medical discourse in the 19th century, and its application in cases of sexual harassment, to legitimize the sexual moral value of the time. For that reason we will analyse the main forensic medicine treaties edited in Spain during this century (AU)


Asunto(s)
Humanos , Femenino , Historia del Siglo XIX , Violación/psicología , Violación/estadística & datos numéricos , Delitos Sexuales , España/etnología , Abstinencia Sexual/historia , Abstinencia Sexual/estadística & datos numéricos , Moral , Principios Morales , Agresión/ética , Violación/prevención & control , Violación/rehabilitación , Abstinencia Sexual/ética , Abstinencia Sexual/psicología , Técnicas de Diagnóstico Obstétrico y Ginecológico/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/ética
11.
Rev. ginecol. obstet ; 13(2): 108-113, abr.-maio 2002. tab
Artículo en Portugués | LILACS | ID: lil-325651

RESUMEN

As urgencias hemorragicas representam situacao de risco de vida iminente, com indices de morbidade e mortalidade relacionados a eficiencia no atendimento medico. As pacientes avaliadas no Pronto Socorro de Ginecologia e Obstetricia devem ser...


Asunto(s)
Humanos , Femenino , Morbilidad , Factores de Riesgo , Hemorragia Uterina , Servicios Médicos de Urgencia/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/clasificación , Hemorragia Uterina
12.
Rev. ginecol. obstet ; 13(2): 114-127, abr.-maio 2002. ilus, tab
Artículo en Portugués | LILACS | ID: lil-325652

RESUMEN

A distocia do biacromial e uma emergencia obstetrica geralmente inesperada, assim, o profissional que realiza atendimento obstetrico deve estar...


Asunto(s)
Humanos , Femenino , Embarazo , Complicaciones del Trabajo de Parto/clasificación , Distocia , Servicios Médicos de Urgencia/clasificación , Técnicas de Diagnóstico Obstétrico y Ginecológico/clasificación
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