Background: This study is based on blow fly samples collected from 8 medico-legal cases in Tamil Nadu, India. The fly life stages were identified and the consistency of minimum post-mortem intervals (PMImin) estimated by different thermal summation-based methods was assessed.
Methods: PMImin of 8 medico-legal cases was estimated using six different thermal summation constants and lower developmental temperatures that are based on C.
Background: The World Health Organization (WHO) Labour Care Guide (LCG) is a paper-based labour monitoring tool designed to facilitate the implementation of WHO's latest guidelines for effective, respectful care during labour and childbirth. Implementing the LCG into routine intrapartum care requires a strategy that improves healthcare provider practices during labour and childbirth. Such a strategy might optimize the use of Caesarean section (CS), along with potential benefits on the use of other obstetric interventions, maternal and perinatal health outcomes, and women's experience of care.
View Article and Find Full Text PDFObjective: 1. To determine the prevalence of pre malignant cervical lesions in HIV positive women using conventional Pap smear. 2.
View Article and Find Full Text PDFTwo-dimensional liquid crystal (LC) models of interacting V-shaped bent-core molecules with two rigid rodlike identical segments connected at a fixed angle (θ=112^{∘}) are investigated. The model assigns equal biquadratic tensor coupling among constituents of the interacting neighboring molecules on a square lattice, allowing for reorientations in three dimensions (d=2, n=3). We find evidence of two temperature-driven topological transitions mediated by point disclinations associated with the three ordering directors, condensing the LC medium successively into uniaxial and biaxial phases.
View Article and Find Full Text PDFObjective: Large data on the clinical characteristics and outcome of COVID-19 in the Indian population are scarce. We analysed the factors associated with mortality in a cohort of moderately and severely ill patients with COVID-19 enrolled in a randomised trial on convalescent plasma.
Design: Secondary analysis of data from a Phase II, Open Label, Randomized Controlled Trial to Assess the Safety and Efficacy of Convalescent Plasma to Limit COVID-19 Associated Complications in Moderate Disease.