28 research outputs found

    (A) Haematoxylin and eosin stained bone marrow trephines obtained in February 2011 showing occasional amastigotes (white arrow).

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    <p>(B) Haematoxylin and eosin stained bone marrow trephines obtained in February 2013 after liposomal daunorubicin treatment showing a heavy parasite load (black arrows).</p

    (A) Abdominal computerised tomography (CT) scanning conducted in May 2012.

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    <p>Before treatment with liposomal daunorubicin. (B) Abdominal computerised tomography (CT) scanning conducted in July 2013. After treatment with liposomal daunorubicin, demonstrating no decrease in the patient’s hepato-splenomegaly.</p

    Multivariable model of risk factors for relapse after treatment for primary VL.

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    <p>*adjusted for age, sex, year, treatment centre and all variables in table.</p><p>**excluding patients who had spleen size ‘0’ on admission (adjusted for age, sex and all variables in table).</p><p>***Wald test-for-trend across spleen size as linear variable.</p

    Trends in primary and relapse VL in Southern Sudan (1999–2007).

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    a<p>from MSF summary statistics (expressed as proportion of patients treated for primary VL, N = 11,319).</p>b<p>from MSF treatment records (proportion of primary VL patients receiving this treatment, N = 8,521).</p>c<p>from MSF summary statistics (expressed as proportion of all patients treated, N = 12,924).</p>d<p>from MSF treatment records (duration of illness self-reported by VL relapse patients, N = 589).</p>e<p>from MSF treatment records (duration of illness self-reported by primary VL patients, N = 7,841).</p>f<p>from MSF treatment records (spleen size measured in primary VL patients, N = 8,494).</p>g<p>from MSF treatment records (interval between discharge and re-admission, N = 166).</p>h<p>Annual Percentage Change (95% confidence interval) estimated from join-point regression.</p
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