<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/css" href="https://imcjms.com/public/assets/rss.css" ?><rss version="2.0">
<channel>
    <title>IMC Journal of Medical Science</title>
    <link>https://imcjms.com/public</link>
    <description>Ibrahim Medical College Journal of Medical Science</description>

                        <item>
                <title><![CDATA[Diagnostic significance of pleural fluid adenosine deaminase activity in tuberculous pleurisy]]></title>

                                    <author><![CDATA[Sharmeen Ahmed]]></author>
                                    <author><![CDATA[Reaz Fatema]]></author>
                                    <author><![CDATA[Ahmed Abu Saleh]]></author>
                                    <author><![CDATA[Humayun Sattar]]></author>
                                    <author><![CDATA[Md. Ruhul Amin Miah]]></author>
                
                <link data-url="https://imcjms.com/public/registration/journal_full_text/40">
    https://imcjms.com/public/registration/journal_full_text/40
</link>
                <pubDate>Tue, 02 Aug 2016 10:08:02 +0000</pubDate>
                <category><![CDATA[Original Article]]></category>
                <comments><![CDATA[Ibrahim Med. Coll. J. 2011; 5(1): 1-5]]></comments>
                <description>Diagnosis
of tuberculous pleural effusion (TPE) is difficult because of its non-specific
clinical presentation and insufficient efficiency of conventional diagnostic
methods. The study was carried out to evaluate the utility of adenosine
deaminase (ADA) activity in pleural fluid for the diagnosis of TPE. ADA
activity was measured in pleural fluid of 103 pleural effusion patients by
colorimetric method using a commercial ADA assay kit. The diagnosis of TPE was
made from pleural fluid examinations (including cytology, biochemistry, and
bacteriology) and pleural biopsy. Patient with negative result of this methods
were diagnosed by response of empirical treatment. Out of 130 cases, 62 (61.1%)
had TPE and the remaining 41 (39.8%) had pleural effusion due to non
tuberculous diseases. There was statistically significant difference (p &amp;lt;
0.001) between the mean of pleural fluid ADA levels (70.82±22.54 U/L) in TPE
group and (30.07±22.93 U/L) in non-TPE group. Of 62 TPE cases, microscopy for
AFB and culture for M.tuberculosis in pleural fluid revealed positivity
in 9.6% and 22.5% cases respectively, and biopsy of pleura showed typical
epithelioid granuloma in only 43.5% cases. The cut-off value of ADA for
diagnosing TPE was 40 U/L using a ROC curve, with a sensitivity of 94% and
specificity of 88%. Positive and negative predictive value of ADA assay were
92% and 90% respectively. The overall test accuracy was 90%. Pleural fluid ADA
assay is therefore a simple, rapid, highly sensitive and specific adjunct test
for diagnosis of TPE.
Address for Correspondence:Dr. Sharmeen Ahmed,
Associate Professor, Department of Microbiology and Immunology, Bangabandhu
Sheikh Mujib Medical University(BSMMU), Shahbagh, Dhaka-1000
&amp;nbsp;
Bangladesh
ranks sixth in the world of tuberculosis (TB) disease burden with estimated
300,000 new cases and 70,000 death per year.1&amp;nbsp;Pleural tuberculosis is a
common manifestation of extrapulmonary TB and with or without pulmonary TB, is
present in around 4% of all TB cases.2&amp;nbsp;If undetected, it may resolve spontaneously,
but untreated pleural TB is a progressive disease with high recurrence rate.
Diagnosis of pleural TB is difficult because of non-specific clinical
presentation and insufficient efficiency of traditional diagnostic methods due
to paucity of bacteria in pleural cavity.3,4&amp;nbsp;Pleural biopsy has been the gold standard in
diagnosis but is invasive and often requires several attempts to locate the
infectious loci.4
Present
study tried to find out the significance of Adenosine deaminase activity in
pleural fluid for the diagnosis of tuberculous pleural effusion.
Materials and Methods
This cross sectional type of comparative study conducted in 103
pleural effusion patients admitted to in-patient departments of Bangabandhu
Shiekh Mujib Medical University (BSMMU) and National Institute of Disease of
Chest and Hospital (NIDCH) during the period of January 2008 to December 2008.
All patients underwent thoracentesis and parietal pleural biopsy with Abram’s
needle by trained physicians. Patients with empyema thoracis, haemothorax and
patients on anti-tuberculous treatment were excluded from the study.
Laboratory methods
Effusions were classified as transudates or exudates using Light’s
criteria9&amp;nbsp;and
this required a blood sample to be collected on the day of thoracentesis in
order to measure total protein and LDH. Three pieces of pleural tissue were
taken for histology.
Diagnostic criteria
Malignant pleural effusion was diagnosed when malignant tissue was
shown by pleural tissue or cytopathology. Some of the malignant cases were
diagnosed by fiber optic bronchoscopy. Effusion was considered parapneumonic
when there was an acute febrile illness associated with pneumonia and complete
response to antibiotic treatment. Rest of the non-tuberculosis patients
(nephrotic syndrome, congestive cardiac failure and rheumatoid arthritis) were
diagnosed by standard clinical procedure.
Statistical analysis
&amp;nbsp;
Out of
103 pleural effusion cases, 62 (60.1%) were diagnosed as tuberculous pleural
effusion (TPE) and 41 (39.1%) were non-TPE cases. The non-TPE cases group
included 30 (29.1%) cases with malignant pleural effusion, 8(7.7%) patients
with parapneumonic effusion and 3 cases of effusion due to nephrotic syndrome,
cardiac failure and rheumatioid arthritis each. Among the 62 of TPE, 49 (79%)
were male and 13 (21%) were female with a male female ratio 3.8:1. The mean age
of all tuberculous cases was 35.85±14.59 years.
&amp;nbsp;
Fig-1. ROC plot
of pleural fluid ADA activity. Dotted diagonal line indicates the line of no
discrimination
&amp;nbsp;
&amp;nbsp;
&amp;nbsp;
&amp;nbsp;
Discussion
TPE
represent an immunological reaction to relatively few AFB in pleural space.
Hence direct examination of pleural fluid by Ziehl-Neelsen (Z-N) staining has
low sensitivity (0-10%).14,18,19&amp;nbsp;In the present study, Z-N staining of pleural
fluid revealed positivity in 9.6% cases and pleural fluid culture yielded M.tuberculosis
in 22.5% cases. Culture requires a minimum of 10-100 viable bacilli and,
therefore, is more sensitive than Z-N staining.20&amp;nbsp;Majority of series showed
diagnostic yields of &amp;lt;30%.18,21,22&amp;nbsp;Presence of granulomatous inflammation is
frequently used as a diagnostic criteria for TPE,23,18&amp;nbsp;and biopsy of parietal
pleura showed typical epithelioid granuloma in 50% to 84% of TPE cases.23,24,25&amp;nbsp;In this study, pleural
biopsy showed diagnostic granuloma in only 43.5% of TPE cases. The low
positivity might be due to non repetition of pleural biopsy in this series.
Moreover, biopsy requires greater expertise and subject to sampling error to
locate the infection foci.4
&amp;nbsp;
&amp;nbsp;
1.&amp;nbsp;&amp;nbsp; WHO report 2008. Global
tuberculosis control, country profile, Bangladesh. Geneva WHO 2008. 
3.&amp;nbsp;&amp;nbsp; Laniado-Laborin R.
Adenosine deaminase in the diagnosis of tuberculous pleural effusion: Is it
really an ideal test? A word of caution. Chest 2005; 127: 417-8.
5.&amp;nbsp;&amp;nbsp; Barnes PF, Mistry SD,
Cooper CL, Pirmex C, Tea TH, Modlin. Compartmentalization of CD4+ T lymphocyte
subpopulation in tuberculous pleuritis. J Immunol 1989; 142:
1114-9.
7.&amp;nbsp;&amp;nbsp; Perez-Rodriguez E, Walton
IJP, Hernandez. JJS, Pallaris E, Rubi J, Castro DJ, Diaz Nuevo G. ADA1/ADAp&amp;nbsp;ratio
in pleural tuberculosis: an exellent diagnostic parameter in pleural fluid. Respir
Med 1999; 93(11): 816-21.
9.&amp;nbsp;&amp;nbsp; Light RW. Diagnoistic
principles in pleural disease. Eur Respir J 1997; 10: 476-81.
11.Riantawan P, Chaowalit P,
Wongsangiem M and Rojanaraweewong P. Diagnostic value of pleural fluid adenosine
deaminase in tuberculous pleuritis with reference to HIV coinfection and a
Bayesian analysis. Chest 1999; 116: 97-103.
13.Banales JL, Pineda PR,
Fitzgerald JM, Rubio H, Selman M, and Salazar-Lezama M. Adenosine deaminase in
the diagnosis of tuberculous pleural effusions, a report of 218 patients and
review of the literature. Chest 1991; 99: 355-7.
15.Valdes L, Jose ES, Alvarez
D, Valle JM. Adenosine deaminase (ADA) isoenzyme analysis in pleural effusions:
diagnositc role and relevance to the origin of increased ADA in tuberculous
pleurisy. Eur Respir J 1996; 9: 747-51.
17.Haque ME, Ahmad MM, Hiron
MM. Aetiological diagnosis of pleural effusion. Chest &amp;amp; Heart Journal
2000; 24(1): 1-4.
19.Escudero-Bueno C,
Garain-Clemente M, Cuesta-Castro B, et al. Cytologic and bacteriologic
analysis of fluid and pleural biopsy with cop’s needle. Arch Intern Med
1990; 150: 1190-4.
21.Liam CK, Lim KH, Wong CMM.
Tuberculous pleurisy as a manifestation of primary and reactivation disease in
a region with a high prevalence of tuberculosis. Int J Tuberc Lung Dis
1999; 3(9): 816-22.
23.Seibert AF, Haynes J,
Middleton R, Bass JB. Tuberculous pleural effusion. Twenty year experience. Chest
1991; 99: 883-6.
25.Relkin F, Aranda CP, Garay
SM, et al. Pleural tuberculosis and HIV infection. Chest 1994; 105:
1338-41.
27.Chen ML, Yu WC, Lam CW, Au
KM, Kong FY, Chan AY, Diagnostic value of pleural fluid adenosine daminase
activity in tuberculous pleuritis. Clin Chim Acta 2004; 341(1-2):
101-7.
</description>

            </item>
            
    <copyright>2026 Ibrahim Medical College. All rights reserved.</copyright>
</channel>
</rss>
