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1.
BJOG ; 125(13): 1663-1670, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29697890

RESUMO

OBJECTIVE: To estimate the incidence of caesarean scar pregnancy (CSP) and to describe the management outcomes associated with this condition. DESIGN: A national cohort study using the UK Early Pregnancy Surveillance Service (UKEPSS). SETTING: 86 participating Early Pregnancy Units. POPULATION: All women diagnosed in the participating units with CSP between November 2013 and January 2015. METHODS: Cohort study of women identified through the UKEPSS monthly mailing system. MAIN OUTCOME MEASURES: Incidence, clinical outcomes and complications. RESULTS: 102 cases of CSP were reported, with an estimated incidence of 1.5 per 10 000 (95% CI 1.1-1.9) maternities. Full outcome data were available for 92 women. Management was expectant in 21/92 (23%), medical in 15/92 (16%) and surgical in 56/92 (61%). The success rates of expectant, medical and surgical management were 43% (9/21), 46% (7/15) and 96% (54/56), respectively. The complication rates were 15/21 (71%) with expectant, 9/15 (60%) with medical and 20/56 (36%) with surgical management. Discharge from care (median number of days) was 82 (range 37-174) with expectant, 21 (range 10-31) with medical and 11 (range 4-49) with surgical management. CONCLUSIONS: Surgical management appears to be associated with a high success rate, low complication rate and short post-treatment follow up. TWEETABLE ABSTRACT: Surgery for CSP appears to be successful, with low complication rates and short post-treatment follow up.


Assuntos
Cesárea/efeitos adversos , Cicatriz/complicações , Gravidez Ectópica/epidemiologia , Gravidez Ectópica/terapia , Abortivos não Esteroides/uso terapêutico , Estudos de Coortes , Dilatação e Curetagem/efeitos adversos , Feminino , Humanos , Incidência , Nascido Vivo , Metotrexato/uso terapêutico , Gravidez , Gravidez Ectópica/diagnóstico , Gravidez Ectópica/etiologia , Resultado do Tratamento , Reino Unido/epidemiologia , Conduta Expectante
2.
Eur J Obstet Gynecol Reprod Biol ; 158(2): 305-7, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21658836

RESUMO

OBJECTIVE: To determine current practice for the management of endometrial hyperplasia. STUDY DESIGN: We carried out a web-based survey of all UK consultant gynaecologists, from the Royal College of Obstetricians and Gynaecologists (RCOG) database, to evaluate the current practice and to enquire whether a trial between oral progestogens and LNG-IUS for endometrial hyperplasia is required. RESULTS: We sent 1090 email invitations and 411 (37.7%) responded to this survey. In total, 338 consultant gynaecologists, who manage patients with endometrial hyperplasia, responded to all items of the survey. The oral progestogens (33.2%) and the LNG-IUS (52.1%) were the most popular choices for managing complex endometrial hyperplasia. The majority of the gynaecologists would explore two conservative choices before embarking into performing a hysterectomy for this condition (130, 52.6%). However, for atypical hyperplasia, the majority of the gynaecologists would perform a hysterectomy (273, 83.2%) and would only consider LNG-IUS or oral progestogens as a second or third option. Two hundred forty-four (72.2%) responded that an RCT for oral progestogens versus LNG-IUS for the management of endometrial hyperplasia is required. There were 171 (50.6%) gynaecologists that would be willing to randomise in such an RCT. CONCLUSION: Our survey shows that complex endometrial hyperplasia is managed conservatively in UK, with oral progestogens or LNG-IUS, and atypical endometrial hyperplasia is managed with hysterectomy. An RCT, between oral progestogens and LNG-IUS for endometrial hyperplasia, is required to identify the optimum therapy.


Assuntos
Hiperplasia Endometrial/terapia , Hiperplasia Endometrial/diagnóstico , Feminino , Pesquisas sobre Atenção à Saúde , Humanos , Internet , Reino Unido
4.
BJOG ; 116(13): 1796-9; discussion 1799-800, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19906021

RESUMO

This study examines the validity and reliability of the British Society for Colposcopy and Cytopathology (BSCCP) objective structured clinical examination (OSCE). The BSCCP OSCE results obtained over eight OSCE circuits were analysed using SPSS 15. Face validity and content validity were established from expert opinion and blueprinting. Statistically significant difference was not shown in construct validity through level of experience (P=0.867, P=0.822, P=0.59, P=0.74, P=0.12, P=0.01; these are the P values for each of the patient interaction stations) however, concurrent validity was established against the gynaecology mini-CEX (sensitivity=1, specificity=0.8, positive predictive value=0.947, negative predictive value=1). The reliability of the OSCE's range from Cronbach's alpha of 0.617 to 0.775. The OSCE has face, content and concurrent validity.


Assuntos
Competência Clínica , Colposcopia/normas , Educação de Pós-Graduação em Medicina/métodos , Avaliação Educacional/métodos , Ginecologia/educação , Feminino , Humanos , Reprodutibilidade dos Testes , Sociedades Médicas , Reino Unido
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