A risk ratio of 1.0 indicates identical risk among the two groups. A risk ratio greater than 1.0 indicates an increased risk for the group in the numerator, usually the exposed group. A risk ratio less than 1.0 indicates a decreased risk for the exposed group, indicating that perhaps exposure actually protects against disease occurrence. The hazard ratio (HR) is the main, and often the only, effect measure reported in many epidemiologic studies. For dichotomous, non–time-varying exposures, the HR is defined as the hazard in the exposed groups divided by the hazard in the unexposed groups. Hazard ratio (HR) is a measure of an effect of an intervention on an outcome of interest over time. Hazard ratio is reported most commonly in time-to-event analysis or survival analysis (i.e. when we are interested in knowing how long it takes for a particular event/outcome to occur). However, the Median Hazard Ratio (MHR) that corresponds to the MOR in multilevel (i.e., ‘frailty’) Cox proportional hazards regression is rarely used. Analogously to the MOR, the MHR is the median relative change in the hazard of the occurrence of the outcome when comparing identical subjects from two randomly selected different clusters The hazard ratio, sometimes called a relative hazard, is typically used to compare time to event data between two treatment groups. The hazard ratio of death for the intervention group compared with the control group was 0.46 (0.22 to 0.95). The hazard ratio in survival analysis is the effect of an exploratory? variable on the hazard or risk of an event. Hazard ratio can be considered as an estimate of relative risk, which is the risk of an event (or of developing a disease) relative to exposure. Ratios are common descriptive measures, used in all fields. In epidemiology, ratios are used as both descriptive measures and as analytic tools. As a descriptive measure, ratios can describe the male-to-female ratio of participants in a study, or the ratio of controls to cases (e.g., two controls per case). The differences between primary sites were particularly pronounced in localized disease, with a hazard ratio of 5.7 for OM, 4.3-9.0 for external genital or oral cavity MM and 19.8-90.4 for other mucosal locations. Melanomas of the pharynx, gastrointestinal, urinary tract and vagina had poor outcomes regardless of clinical stage. The risk of ASCV mortality increased in a linear manner with higher free thyroxine levels (hazard ratio, 2.41; confidence interval, 1.68-3.47 per 1 ng/dL) and lower thyroid-stimulating hormone Background: The evaluation of the proportional hazards (PH) assumption in survival analysis is an important issue when Hazard Ratio (HR) is chosen as summary measure. The aim is to assess the appropriateness of statistical methods based on the PH assumption in oncological trials. Methods: We selected 58 randomised controlled trials comparing at least two pharmacological treatments with a time
[index] [2331] [4293] [9676] [4009] [8374] [9277] [2156] [1766] [8356] [4085]
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