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1.
Eur Rev Med Pharmacol Sci ; 25(13): 4456-4458, 2021 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-34286507

RESUMEN

Utero-Placental Apoplexy, or Couvelaire Uterus, is a third-trimester major obstetrical complication, occurring especially during labor. It consists of placental abruption followed by an acute intradecidual hemorrhage produced by the rupture of the uterus-placental spiral arterioles leading to a retroplacental hematoma. This hemorrhage infiltrates the uterine wall up to intra- and retro-peritoneal areas. We provide a case report, on which no previous literature is available, of a utero-placental apoplexy during induction of therapeutic abortion.


Asunto(s)
Aborto Terapéutico/efectos adversos , Desprendimiento Prematuro de la Placenta/etiología , Hemorragia Uterina/etiología , Desprendimiento Prematuro de la Placenta/cirugía , Adulto , Femenino , Humanos , Histerectomía , Embarazo , Salpingooforectomía , Hemorragia Uterina/cirugía
2.
Aesthetic Plast Surg ; 41(3): 700-713, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28204933

RESUMEN

BACKGROUND: The aims of our study were to identify studies that evaluated patient satisfaction after transsexual surgery, analyze existing questionnaires, and summarize their development, psychometric properties, and content. METHODS: A systematic review of the English-language literature was performed. Patient-reported outcome measures designed to assess patient satisfaction and quality of life following transsexual surgery were identified. Qualifying instruments were assessed for content and adherence to international guidelines for development and validation. RESULTS: From 796 articles, 19 studies had sufficient data and met the inclusion criteria. Included were a total of 2299 patients and 17 patient-reported outcome measures: 10 generic instruments that assessed quality of life, 4 specific for female genital or sexual satisfaction, 2 specific for transsexual body image or gender dysphoria, and 1 specific for plastic surgery. The questionnaires were analyzed by reviewers to assess the adherence to the rules of the US FDA and the Scientific Advisory Committee of the Medical Outcomes Trust. We identified 17 individual questionnaires that were included. All measures were limited by either their development, their validation, or their content. CONCLUSIONS: There is a need for a new self-assessment tool, which should include functional, psychorelational, and cosmetic components, to measure satisfaction and quality of life of patients who have undergone transsexual surgery. LEVEL OF EVIDENCE III: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .


Asunto(s)
Imagen Corporal , Medición de Resultados Informados por el Paciente , Calidad de Vida , Cirugía de Reasignación de Sexo/métodos , Personas Transgénero , Femenino , Feminidad , Humanos , Italia , Masculino , Masculinidad , Satisfacción del Paciente/estadística & datos numéricos , Cirugía de Reasignación de Sexo/psicología
3.
Eur Arch Otorhinolaryngol ; 274(4): 1807-1811, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-27798735

RESUMEN

The literature still lacks a review regarding PROs applied for rhinoplasty. Thus, we performed a systematic review of the literature to identify PROMs that assess patient satisfaction and quality of life after rhinoplasty. The aim of our study was to identify existing questionnaires and to summarize their development, psychometric properties, and content. A multi-step search of the web-based PubMed database from the National Library of Medicine was performed to identify PROMs that are designed to evaluate satisfaction and quality of life following rhinoplasty. Each potential PROM was examined by three independent reviewers for adherence to inclusion/exclusion criteria. Questionnaires included in the analysis were appraised for their adherence to international guidelines for the development and validation of health outcome questionnaires, as outlined by the Scientific Advisory Committee of the Medical Outcome Trust and the U.S. Food and Drug Administration. Our search generated a total of 457 articles, 351 that were retrieved in the primary search, and 106 that were found in the references of the first set of articles. The process of development and validation of each of the included PROMs was examined. Only ten of these were identified as surgery-specific questionnaires about rhinoplasty. These were divided into three categories: (1) functional self-assessment (Nasal Surgical Questionnaire, Nasal Obstruction Symptoms Evaluation Scale, and Nasal Obstruction Septoplasty Effectiveness); (2) aesthetic self-assessment (Utrecht Questionnaire, FACE-Q rhinoplasty module, Glasgow Benefit Inventory); and (3) aesthetic and functional self-assessment (Rhinoplasty Outcomes Evaluation), Functional Rhinoplasty Outcome Inventory 17, RHINO Scale, and Evaluation of Aesthetic Rhinoplasty Scale).


Asunto(s)
Medición de Resultados Informados por el Paciente , Satisfacción del Paciente , Rinoplastia , Estética , Humanos , Obstrucción Nasal/etiología , Nariz/cirugía , Complicaciones Posoperatorias , Calidad de Vida , Encuestas y Cuestionarios
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