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1.
Int J Gynaecol Obstet ; 159(3): 771-775, 2022 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-35304736

RESUMO

OBJECTIVE: To review the management, success, and complication rates of women who presented with a cesarean scar ectopic pregnancy at an Australian tertiary referral center. METHODS: A retrospective case series was undertaken. Patients were identified through the hospital's clinical information services coding system and data were collected from medical records. RESULTS: A total of 38 cases were identified. Patients who were hemodynamically stable were predominantly managed according to local expertise via intramuscular, intra-sac methotrexate or a combination of these two. In some cases, surgical management was preferred. CONCLUSION: Cesarean scar ectopic pregnancy may be managed both surgically and medically. At institutions where surgical expertise is unavailable, medical management would be valuable with few adverse outcomes identified, provided women have closely monitored follow-up.


Assuntos
Abortivos não Esteroides , Gravidez Ectópica , Gravidez , Humanos , Feminino , Cicatriz/cirurgia , Estudos Retrospectivos , Centros de Atenção Terciária , Cesárea/efeitos adversos , Austrália/epidemiologia , Gravidez Ectópica/etiologia , Gravidez Ectópica/cirurgia , Metotrexato/uso terapêutico , Abortivos não Esteroides/uso terapêutico
2.
Nanoscale ; 13(28): 12279-12287, 2021 Jul 28.
Artigo em Inglês | MEDLINE | ID: mdl-34251003

RESUMO

Rapid diagnosis of preeclampsia is necessary to ensure timely administration of appropriate care and prevent the potentially catastrophic complications of the condition affecting both mothers and babies. While the diagnostic superiority of angiogenic blood biomarkers such as placental growth factor has recently been demonstrated, there is an urgent need to develop point-of-care (PoC) technologies that allow rapid, quantitative, and accurate testing for these markers within local communities. Towards addressing this need, here we report on a fully integrated biodiagnostic platform based on nanoscale indium oxide field effect transistor (FET) sensors. The high-performance FET sensors are integrated with blood sample processing cartridges that minimize the need for operator intervention during the assay and eliminate the need for analytical equipment. Within 40 minutes and from 30 µL of blood, the FET platform could reliably measure PlGF with a limit of detection of 0.06 pg mL-1 and a five order of magnitudes dynamic range. Pilot clinical validation in four preeclamptic pregnancies confirmed that the accuracy and reliability of the FET platform, paving the way for further development to a much-needed point-of-care preeclampsia testing.


Assuntos
Pré-Eclâmpsia , Biomarcadores , Feminino , Humanos , Fator de Crescimento Placentário , Testes Imediatos , Pré-Eclâmpsia/diagnóstico , Gravidez , Reprodutibilidade dos Testes
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