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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Duong, T.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Jourdain, Gonzague</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Ngo-Giang-Huong, Nicole</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Le Coeur, Sophie</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Kantipong, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Buranabanjasatean, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Leenasirimakul, P.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ariyadej, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Tansuphasawasdikul, S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Thongpaen, S.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Lallemant, Marc</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Laboratory and clinical predictors of disease progression following initiation of combination therapy in HIV-infected adults in Thailand</title>
        <secondary-title>Plos One</secondary-title>
      </titles>
      <pages>e43375</pages>
      <dates>
        <year>2012</year>
      </dates>
      <call-num>fdi:010057241</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Plos One</full-title>
      </periodical>
      <isbn>1932-6203</isbn>
      <accession-num>ISI:000307823600074</accession-num>
      <number>8</number>
      <electronic-resource-num>10.1371/journal.pone.0043375</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010057241</url>
        </related-urls>
        <pdf-urls>
          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/divers17-09/010057241.pdf</url>
        </pdf-urls>
      </urls>
      <volume>7</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Background: Data on determinants of long-term disease progression in HIV-infected patients on antiretroviral therapy (ART) are limited in low and middle-income settings. Methods: Effects of current CD4 count, viral load and haemoglobin and diagnosis of AIDS-defining events (ADEs) after start of combination ART (cART) on death and new ADEs were assessed using Poisson regression, in patient aged &gt;= 18 years within a multi-centre cohort in Thailand. Results: Among 1,572 patients, median follow-up from cART initiation was 4.4 (IQR 3.6-6.3) years. The analysis of death was based on 60 events during 6,573 person-years; 30/50 (60%) deaths with underlying cause ascertained were attributable to infections. Analysis of new ADE included 192 events during 5,865 person-years; TB and Pneumocystis jiroveci pneumonia were the most commonly presented first new ADE (35% and 20% of cases, respectively). In multivariable analyses, low current CD4 count after starting cART was the strongest predictor of death and of new ADE. Even at CD4 above 200 cells/mm 3, survival improved steadily with CD4, with mortality rare at &gt;= 500 cells/mm 3 (rate 1.1 per 1,000 person-years). Haemoglobin had a strong independent effect, while viral load was weakly predictive with poorer prognosis only observed at &gt;= 100,000 copies/ml. Mortality risk increased following diagnosis of ADEs during cART. The decline in mortality rate with duration on cART (from 21.3 per 1,000 person-years within first 6 months to 4.7 per 1,000 person-years at &gt;= 36 months) was accounted for by current CD4 count. Conclusions: Patients with low CD4 count or haemoglobin require more intensive diagnostic and treatment of underlying causes. Maintaining CD4 &gt;= 500 cells/mm(3) minimizes mortality. However, patient monitoring could potentially be relaxed at high CD4 count if resources are limited. Optimal ART monitoring strategies in low-income settings remain a research priority. Better understanding of the aetiology of anaemia in patients on ART could guide prevention and treatment.</abstract>
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      <custom1>UR174 / UR196</custom1>
      <custom7>Thaïlande</custom7>
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