Pre-eclampsia/Eclampsia in Italy Over the Years 2010-2016
Ключові слова
Анотація
Опис
Poor placentation is considered a powerful predisposing factor for pre-eclampsia. Recently, it has been suggested that the occurrence of pre-eclampsia requires a combination of an excessive or atypical maternal immune response to the trophoblast and/or exaggerated endothelial activation as well as a generalised hyper-inflammatory state resulting in endothelial dysfunction and associated increased vascular reactivity. Any factors (maternal and paternal constitutional, genetic and environmental risk factors) that enhance these responses would predispose to pre-eclampsia.
The list of predisposing factors includes: extremes of maternal age, black race, previous history of pre-eclampsia, family history of pre-eclampsia, multifetal gestation, ≥ 10 years from previous pregnancy, limited sperm exposure, first paternity, pregnancies after donor insemination (assisted reproductive technology), oocyte donation or embryo donation, chronic hypertension or renal disease, rheumatic disease, maternal low birth weight, obesity and insulin resistance, pre-gestational diabetes mellitus, increased testosterone, increased homocysteine concentration, atherosclerosis (increased triglycerides and LDL, decreased HDL), maternal infections, pre-existing thrombophilia, maternal susceptibility genes and hydropic degeneration of placenta. Finally, smoking seems to be inversely correlated with pre-eclampsia.
Pre-eclampsia can result in a fetal syndrome characterized by fetal growth restriction, reduced amniotic fluid, abnormal oxygenation, fetal demise and preterm birth. Moreover, women with pre-eclampsia are at increased risk for abruptio placentae, disseminated coagulopathy/HELLP syndrome, pulmonary oedema, acute renal failure, eclampsia, cerebral haemorrhage, death and cardiovascular or renal disease.
Early prediction of pre-eclampsia would allow for close surveillance and preventive strategies
Дати
Востаннє перевірено: | 02/29/2020 |
Перший поданий: | 11/13/2016 |
Орієнтовна реєстрація подана: | 11/29/2016 |
Опубліковано вперше: | 12/04/2016 |
Останнє оновлення надіслано: | 03/02/2020 |
Останнє оновлення опубліковано: | 03/03/2020 |
Фактична дата початку навчання: | 07/31/2016 |
Розрахункова дата первинного завершення: | 12/31/2019 |
Розрахункова дата завершення дослідження: | 12/31/2019 |
Стан або захворювання
Фаза
Критерії прийнятності
Вік, придатний для навчання | 18 Years До 18 Years |
Стать, яка підходить для вивчення | All |
Метод відбору проб | Non-Probability Sample |
Приймає здорових добровольців | Так |
Критерії | Inclusion Criteria: - Ability to read and understand the Italian language and fill in the questionnaire, including access to the Internet. - Ability of both parents to give informed consent to the processing of personal data, with the understanding that the consent could be withdrawn at any time Exclusion Criteria: - Inability to reach the patients by telephone and inform them about the study - Death or incapacitating illness of one or both parents following discharge from hospital - Refusal of one or both parents to disclose their email address |
Результат
Заходи первинного результату
1. Incidence of preeclampsia/eclampsia in Italy [Three months]
2. Aggregation of predisposing factors to pre-eclampsia / eclampsia in Italy measured by a novel multiple choice on-line questionnaire [Three months]
Заходи вторинного результату
1. Maternal outcomes measured by a novel multiple choice on-line questionnaire [Three months]
2. Fetal outcomes measured by a novel multiple choice on-line questionnaire [Three months]