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It is important to note that both estimates have wide uncertainty intervals around them, and we encourage all readers Mianserin HCl to take this into account when interpreting our findings, especially in developing countries. As noted by Hser et?al. [1], the sources of our estimates of opioid dependence in global burden of disease (GBD) 2010 did not exclude problems related to pharmaceutical opioids. These opioids are important to consider in the United States, Canada and Australia and are important drivers of opioid burden in some countries in South Asia and eastern Europe. Despite these acknowledged limitations, there is public health value in producing estimates of global burden that are based upon conservative assumptions and include clearly described SCR7 levels of uncertainty. First, GBD 2010 has an important role in heightening attention to opioid dependence at global, regional and national levels. The updates that will be provided through GBD 2.0 [11] will improve upon these estimates by estimating the epidemiology and health burden of a full range of injuries and diseases, using comparable metrics and a consistent estimation framework for each disorder. If no estimates are made while we await better data to be collected, then we run the risk that the burden of opioid dependence will be ignored by policy makers. Secondly, the quantification of the uncertainty around our estimates also serves to highlight the gaps in epidemiological data. This should stimulate the efforts to undertake better studies that will produce more reliable and less uncertain estimates of the epidemiological parameters needed to estimate burden, prevalence, incidence, mortality and remission. L.D. has received untied educational grants from Reckitt Benckiser for the post-marketing surveillance of opioid Entinostat substitution therapy medications in Australia. All such studies' design, conduct and interpretation of findings are the work of the investigators; the funders had no role in those studies. ""2728" "We evaluated the efficacy of a 12-week oral treatment with azithromycin in adult patients with bronchiectasis. The objectives were to demonstrate that this treatment reduces sputum volume, improves quality of life and to assess the lengths of effects after cessation of therapy. Seventy-eight patients with bronchiectasis confirmed by high-resolution computed tomography were included in this study. Subjects received oral azithromycin or placebo in a randomized manner for 12 weeks followed by placebo for another 12 weeks. Sputum volume, St George's Respiratory Questionnaire (SGRQ) score and spirometry were recorded at baseline, 12 weeks and 24 weeks, respectively. End-point measurements were compared from baseline to the end of each study phase. Sixty-eight subjects were included in the analysis. Mean 24-h sputum volume significantly decreased (P?