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Italian Journal of Gynaecology and Obstetrics ; 34(3):154-160, 2022.
Article in English | Scopus | ID: covidwho-2057098

ABSTRACT

Objective. International studies have found an increased risk of puerperal depression during COVID-19 pandemic. The present research aims to investigate the risk of puerperal depression within the obstetrics ward of Ospedale dell’Angelo (Venice Mestre), between March and June, 2020. Patients and Methods. 98 new mothers (average age: 33 y/o, SD: 5) were asked to complete the 10 item version of the EPDS, 2-3 days after delivery and again 3 months later. Results. The percentage of women with high score is 26.5%, less than what was found in 2016. The risk of puerperal depression does not change significantly 3 months after delivery. However, high scores on EPDS do not seem to be connected either to the type of birth or to the condition of primiparity of the mothers. Conclusions. Some hypotheses have been proposed to explain the results obtained, such as quality of the assistance offered and/or the compliance and the coping skills acquired by families, which could be evaluated in future research. © 2022, EDRA S.p.A. All rights reserved.

2.
European Journal of Gynaecological Oncology ; 42(5):893-898, 2021.
Article in English | Web of Science | ID: covidwho-1503090

ABSTRACT

Objective: The detection and treatment of high-grade cervical lesions prevent the development of invasive cervical cancer. Excisional procedures can pose a risk for subsequent pregnancies, thus conservative management of Cervical Intraepithelial Neoplasia grade 2 (CIN2) lesions should be adopted in young women. The aim of our study is to evaluate the ability of viral and cellular biomarkers in predicting regression/progression of CIN2. Methods: Women aged 25 to 45 years, participating to population-based organised cervical cancer screening programmes in the Veneto Region (Italy), diagnosed with a CIN2 lesion and fitting predefined inclusion/exclusion criteria, are invited to take part in a multicentre observational longitudinal cohort study with a follow-up of 24 months. Upon signing an informed consent, women are enrolled in the study and cervical cell samples collected. Treatment is delayed and subsequently performed in the case of lesion progression, or persistence for >12 months. HPV genotyping, p16(INK4A)/ki67 expression and methylation status for L1 viral sequences and FAM19A4/miR124-2 cellular genes are determined at baseline and during follow-up, and evaluated in relation to the clinical outcome. Results: The study, registered on Clinical Trials.gov (ID: NCTo4687267), is currently ongoing. Enrolment of women aged 25-45 years started in 2019, and will continue up to the end of 2021. Discussion: Since February 2020, the Veneto Region has been hit by the COVID-19 pandemic. The enrolment of women in the study was interrupted during an initial two-month lockdown, and slowed down during the subsequent months. The12-month extension of the study period will partially counterbalance this delay.

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