Prospective study based on the evaluation of daily and intermittent dosage regimen of anti-tubercular (ATT) drug therapy (Record no. 7876)

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control field 20190314094147.0
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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 6983
Author Sankar, V.
245 ## - TITLE STATEMENT
Title Prospective study based on the evaluation of daily and intermittent dosage regimen of anti-tubercular (ATT) drug therapy
250 ## - EDITION STATEMENT
Volume, Issue number Vol. 55 (03) March
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Drug Manufacture's Association - IDMA
Year 2018
300 ## - PHYSICAL DESCRIPTION
Pagination 49-57
520 ## - SUMMARY, ETC.
Summary, etc. Anti-TB drug induced hepatotoxicity causes treatment interruption, poor compliance, increased mortality and morbidity, and modification of treatment regimen. Hence, we need to assess the effect of dosing schedule of daily and intermittent regimens and identify patients with increased risk of developing drug induced hepatotoxicity. To determine the frequency and risk factors associated with anti-tuberculosis drug induced hepatotoxicity in daily and intermittent dosage regimen of anti- tubercular therapy, a prospective study was conducted with 130 patients diagnosed with tuberculosis, followed clinically and biochemically before and after the initiation of anti-tuberculosis drugs. Complete history including demographic details and physical examination were documented. Among 53 patients, 28.3% of the patients developed anti- tuberculosis drug induced hepatotoxicity with higher incidence in those receiving daily regimen than the intermittent regimen (P = 0.00). On comparing the site of tuberculosis, higher risk of drug induced hepatotoxicity was reported in cases with pulmonary tuberculosis (P = 0.01) than with extra-pulmonary tuberculosis. Among the 23 patients with anti– tuberculosis drug induced hepatotoxicity, 52% were noted to have moderate hepatotoxicity based on the severity grading of hepatotoxicity and 44% noted as probable based on the Roussel-Uclaf causality assessment method. Body mass index < 20kg/m2 (P = 0.042) and concomitant use of other hepatotoxic drug (P = 0.005) were risk factors for anti-TB DIH. Higher incidence of anti- tuberculosis drug induced hepatotoxicity was found in patients who received daily regimen rather than intermittent regimen. Extreme precaution should be taken in patients with body mass index < 20kg/m2 and also among those using concomitant hepatotoxic drugs
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
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Keywords Tuberculosis
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Keywords Risk factors
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 6984
Co-Author Nimitha, M.
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 6985
Co-Author Rama, P.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Mumbai Indian Drug Manufactures Association
Title Indian drugs
856 ## - ELECTRONIC LOCATION AND ACCESS
Link text Click here
URL https://www.indiandrugsonline.org/issuesarticle-details?id=Nzc1
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2019-03-28 2018056 2019-06-19 2019-03-28 Articles Abstract Database
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