41 research outputs found

    Comparison between malaria and dengue biological variables by matched bivariate analysis.

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    *<p><i>Odds ratio</i> (OR) and 95% confidence interval (95% CI) and p calculated by matched bivariate analysis.</p>**<p>p-value calculated with Wald test in matched bivariate analysis.</p><p>ALT, alanine aminotransferase; AST, aspartate aminotransferase; CRP, C-reactive protein.</p

    Comparison between malaria and dengue epidemiological and clinical variables by matched bivariate analysis.

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    *<p><i>Odds ratio</i> (OR) and 95% confidence interval (95% CI) and p calculated by matched bivariate analysis.</p>**<p>p-value calculated with Wald test in matched bivariate analysis.</p>¥<p>Inhabitants of the coast are defined as people living in Cayenne, Rémire-Montjoly, Matoury Macouria, Kourou, Irakoubo or Mana.; Other people declared to live in Cacao, Roura, Montsinnéry-Tonnégrande, Régina, Saül, St-Elie, Saint Laurent du Maroni, Apatou, Maripasoula, Papaïchton, St George de l'Oyapock, Camopi or Trois-Sauts. 4 people came from France, 1 from the French Caribbean and 1 from French Polynesia.</p><p>Bpm, beats per minut;</p>§<p>ENT symptoms, (Ear, Nose and Throat): pharyngitis, otitis and/or sinusitis).</p

    Median β coefficients estimated by multivariate logistic regression model and bootstrapping procedure.

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    *<p><i>Odds ratio</i> and 95% confidence interval and p-value calculated by matched multivariate analysis.</p><p>Matched multivariate logistic regression analysis was performed for malaria and dengue. Weights are based on the β coefficients of the logistic regression and were calculated by rounding the model coefficients to the nearest whole integer after .<i>632</i> bootstrapping (median). The weights rank the risk predictors in relative importance and dictate how one assigns integer points value for each predictor for a given patient. The assigned points are then summed to compute that individual's risk for the mixed clinical and biological malaria score values.</p

    Vaccination and follow-up schedule for study groups (created by authors using the licensed program BioRender (http://www.biorender.com).

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    Dogs without documented previous rabies vaccination (grey) received their primary vaccination (T0, grey). For group 1 follow-up blood samples were taken seven months (T7), around one year (T12-14) and 1.5 years (T18) after primary vaccination. Due to logistic restrains the follow-up sequence differs (blue) within this group between dogs from Kandal (n = 16) and dogs from Battambang (n = 205). From dogs of group 2, a blood sample (T12) was collected one year after their primary immunization to document the immune response of this primary immunization. Afterwards these dogs received a booster vaccination (green), and additional samples were collected (green) more than one year (T26) and three years (T34) after the booster vaccination to monitor its effect on the immune response.</p
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