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1.
Cytopathology ; 22(4): 269-75, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21771094

RESUMO

AIMS: To investigate breast fine needle aspiration (FNA) cytology in Australasia, in terms of laboratory demographics, specimens received and quality control (QC). METHODS: A questionnaire was sent to all laboratories enrolled in the FNA module of the Royal College of Pathologists of Australasia Cytopathology Quality Assurance Program (QAP), requesting information about specimens received in a 3-month period in 2001 and in 2008. RESULTS: Responses were received from 81/180 laboratories in 2001 and from 94/200 in 2008. The mean number of cases per 3 months was 137 in 2001 and 141 in 2008 and for the 42 laboratories responding on both occasions, the mean number of cases declined from 191 to 149 (P=0.001). The mean percentage of malignant cases was 11.7% in 2001 and 10.5% in 2008 and the mean percentages of unsatisfactory rates were 21.7% and 25.2%, respectively; 43.2% of laboratories in 2001 and 40.4% in 2008 reported fewer than 50 cases for the 3-month period. The unsatisfactory rate was inversely proportional to the number of cases received. Most QC (69.1% in 2001, 71.3% in 2008) was carried out by correlation with any later histology. With no histology available, 35.8% of laboratories in 2001 and 48.9% in 2008 did no further follow-up. Follow-up of all diagnostic categories increased from 30.9% in 2001 to 44% in 2008. CONCLUSIONS: Breast FNA cytology is still actively undertaken in Australasia, but numbers have declined. Unsatisfactory rates have reached the Australian recommended upper limit and are inversely proportional to the total number of cases received. Overall QC measures are unchanged and consideration of a review of breast FNA guidelines is suggested.


Assuntos
Biópsia por Agulha Fina/normas , Neoplasias da Mama/patologia , Guias de Prática Clínica como Assunto , Australásia , Feminino , Humanos , Controle de Qualidade , Inquéritos e Questionários
2.
Aust N Z J Obstet Gynaecol ; 49(6): 627-30, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20070711

RESUMO

AIM: This study was undertaken to determine if the need for red cell blood transfusion in placenta praevia could be predicted. METHODS: Data from a retrospective observational study of 246 obstetric patients, with placenta praevia, from 1999 to 2005 were analysed to generate a model to predict requirement for transfusion. RESULTS: Seventy-one patients were transfused. Independent risk factors for transfusion were gestational age at delivery of 32-35 weeks [odds ratio (OR): 2.6; 95% confidence interval (CI): 1.1-6.4] and caesarean combined with hysterectomy (OR: 29.4; 95% CI: 5.9-145.9; P < 0.001). No independent risk of transfusion was associated with maternal age, race, parity, smoking status, type of anaesthesia, caesarean combined with arterial balloon occlusion, grade of placenta, accreta and previous uterine surgery. CONCLUSIONS: Gestational age at delivery and type of surgery required are predictors of transfusion during caesarean for placenta praevia. Arterial balloon occlusion does not appear to increase transfusion risk and may be considered as one of the techniques in management.


Assuntos
Cesárea , Transfusão de Eritrócitos , Histerectomia , Placenta Prévia/cirurgia , Hemorragia Pós-Parto/epidemiologia , Hemorragia Pós-Parto/terapia , Adulto , Cesárea/efeitos adversos , Estudos de Coortes , Feminino , Idade Gestacional , Técnicas Hemostáticas , Humanos , Avaliação das Necessidades , Placenta Prévia/diagnóstico , Placenta Prévia/etiologia , Hemorragia Pós-Parto/diagnóstico , Gravidez , Estudos Retrospectivos , Fatores de Risco
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