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  <title>DSpace Collection:</title>
  <link rel="alternate" href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/114" />
  <subtitle />
  <id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/114</id>
  <updated>2026-04-23T15:02:43Z</updated>
  <dc:date>2026-04-23T15:02:43Z</dc:date>
  <entry>
    <title>A Comparative Study Of Cartridge Based Nucleic Acid Amplification Testing And Auramine-Rhodamine Stain Microscopy With Culture Method In The Diagnosis Of Pulmonary Tuberculosis</title>
    <link rel="alternate" href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/4628" />
    <author>
      <name>Dr.Hajra Tasneem Masali</name>
    </author>
    <id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/4628</id>
    <updated>2026-04-02T06:00:26Z</updated>
    <published>2019-01-01T00:00:00Z</published>
    <summary type="text">Title: A Comparative Study Of Cartridge Based Nucleic Acid Amplification Testing And Auramine-Rhodamine Stain Microscopy With Culture Method In The Diagnosis Of Pulmonary Tuberculosis
Authors: Dr.Hajra Tasneem Masali
Abstract: One of the crucial step for effective tuberculosis management is to choose a Diagnostic&#xD;
method with high sensitivity and specificity. But slow growth rate of Tubercle bacilli makes the&#xD;
diagnosis more complicated and hence need of hour is improved diagnostic methods to limit&#xD;
progression and the spread of the disease. Options available among conventional laboratory&#xD;
methods are sputum microscopy and culture methods.&#xD;
 Sputum microscopy is rapid, reliable, simple &amp; reasonably costing but has poor&#xD;
sensitivity and requires multiple visits leading to higher default rate. Culture method although&#xD;
considered gold standard but it takes almost 2-6 weeks’ time to give the result and also requires&#xD;
proper infrastructure with technical expertise. But with advancement in technology CBNAAT&#xD;
also offer a better option as it is specific, automated technology utilizing DNA - PCR technique&#xD;
for identification. It is currently unique in its simplification of molecular testing. It can detect&#xD;
both M. tuberculosis and Rifampicin resistance directly from sputum in an assay fetching results&#xD;
within two hours</summary>
    <dc:date>2019-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Comparison Of Lowenstein-Jensen Medium, Middlebrook 7h10 Medium And Bact/Alert 3d For Isolation Of Mycobacterium Tuberculosis From Clinical Specimens</title>
    <link rel="alternate" href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/2446" />
    <author>
      <name>Naveen.G</name>
    </author>
    <id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/2446</id>
    <updated>2026-04-02T08:00:18Z</updated>
    <published>2012-01-01T00:00:00Z</published>
    <summary type="text">Title: Comparison Of Lowenstein-Jensen Medium, Middlebrook 7h10 Medium And Bact/Alert 3d For Isolation Of Mycobacterium Tuberculosis From Clinical Specimens
Authors: Naveen.G
Abstract: Introduction – Tuberculosis is the most common cause of death due to single infectious agent &#xD;
worldwide in adults. India alone accounts for 30% of global tuberculosis burden. There is &#xD;
manifest need for method of cultivation of mycobacteria that is reliable, economical and has &#xD;
short turnaround time.  &#xD;
 &#xD;
Objective – Present study was attempted to assess the feasibility of using MB bact and &#xD;
middlebrook7H10 as primary isolation medium for mycobacteria. It has been compared with LJ &#xD;
medium, the gold standard.  &#xD;
 &#xD;
Materials and Methods – Various clinical specimens from total of 230 clinically suspected &#xD;
cases of TB were studied. All isolates were decontaminated using modified Petroff’s method. &#xD;
Each sample was subjected to ZN staining and simultaneously inoculated onto LJ medium, &#xD;
middlebrook7H10 medium and MB bact. Growth from the culture were confirmed by ZN &#xD;
staining and speciated using biochemical reactions. &#xD;
 &#xD;
Results – Out of 230 samples screened, 116 isolates were obtained. Of the 116 all of them were &#xD;
isolated from MB bact, 82 were isolated by LJ medium and 62 were isolated by &#xD;
middlebrook7H10. 82 isolates were obtained by MB bact and LJ medium, 62 were obtained by &#xD;
middlebrook7H10 and MB bact, 58 by LJ and middlebrook7H10 and 58 by LJ medium, &#xD;
middlebrook7H10 and MB bact. Neither L J medium nor middlebrook 7H 1O medium could &#xD;
isolate mycobacteria exclusively. The average isolation time by L J, middlebrook 7H10 medium &#xD;
and MB BACT was 30.81 days,31.06 days and 18.70 days.</summary>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Serological Markers Hbsag And Hbeag In Chronic Hepatitis B Carriers And Their Correlation With Viral Load By Polymerase Chain Reaction Assay</title>
    <link rel="alternate" href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/891" />
    <author>
      <name>Borgaonkar, Rasika</name>
    </author>
    <id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/891</id>
    <updated>2026-04-02T06:06:26Z</updated>
    <published>2018-01-01T00:00:00Z</published>
    <summary type="text">Title: Serological Markers Hbsag And Hbeag In Chronic Hepatitis B Carriers And Their Correlation With Viral Load By Polymerase Chain Reaction Assay
Authors: Borgaonkar, Rasika</summary>
    <dc:date>2018-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Seroprevalence of Rubella antibodies in women of reproductive age</title>
    <link rel="alternate" href="https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/592" />
    <author>
      <name>Shilpi, Gupta</name>
    </author>
    <id>https://digitallibrary.bldedu.ac.in/xmlui/handle/123456789/592</id>
    <updated>2026-04-02T06:08:51Z</updated>
    <published>2015-01-01T00:00:00Z</published>
    <summary type="text">Title: Seroprevalence of Rubella antibodies in women of reproductive age
Authors: Shilpi, Gupta</summary>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </entry>
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