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Maternal survival in pregnancy complicated by acute fatty liver of pregnancy.
Acute fatty liver of pregnancy (AFLP) is a serious complication of pregnancy. The natural history of AFLP is variable and difficult to predict. In this study, we used a statistical model to predict maternal survival in AFLP. Prospective study of a cohort of 78 women with AFLP. Survival probabilities were predicted using the mortality data of the UK Obstetrics and Gynaecology Club and other published data. A maternal mortality risk assessment model was established. Two-thirds of our patients survived. There was an increased maternal mortality in patients with preeclampsia and with a poor nutritional status. The severity of liver disease and the presence of maternal sepsis were significant predictors of maternal mortality. Maternal survival in AFLP was good, although the risk of maternal mortality in AFLP is high.Q:

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Myob Accounting Plus is great accounting software for small or medium sized businesses.. Accounting Plus V13 14 features; Fix some errors in. Add a new payroll version .Effects of growth factors on cultured rat and human Langerhans cells.
Langerhans cells (LC) migrate from the epidermis to the draining lymph nodes and function as antigen-presenting cells (APC). Upon activation by antigen, LC synthesize T-cell-derived lymphokines and inflammatory cytokines and enhance the proliferation of other APC. To assess the role of cytokines in the regulation of LC function, we used a model system in which LC can be expanded and their functional capabilities can be further studied. Epidermal sheets from rat and human neonatal epidermis were cultured and allowed to develop into a multilayered epidermis, then dissociated into single cells. The cells were grown in the presence of known growth factors (IL-1 alpha, TGF-beta, GM-CSF, and PDGF) for 72 h. The cultures were evaluated with respect to the presence of LC and their epidermal-derived cytokines (IL-1 alpha, TGF-beta, and GM-CSF). Flow cytometric analysis of the cultures showed that LC were present in both the rat and human epidermal cell cultures. The number of LC was significantly increased after culture with IL-1 alpha and TGF-beta. The addition of a growth inhibitor, PD98059 (PD), caused a significant reduction in the number of LC within the cultures. Culture with PD caused a significant reduction in the expression of IL-1 alpha and TGF-beta mRNA and protein within the epidermal cell cultures. In addition, similar to the findings in mice, culture of rat and human epidermis with PD suppressed the expression of the mRNA for GM-CSF in the epidermis. These results demonstrate that culture with IL-1 alpha and TGF-beta causes a population of LC to proliferate and suggest that PD causes a reduction in the number of activated LC by suppressing their expression of cytokines.