Background: Multidrug resistant tuberculosis is a global threat. Effective treatment is implemented as per RNTCP guidelines. But the drugs used have great potential to develop adverse drug reactions. Such drug reactions if not managed optimally can lead to unfavourable treatment outcome. Hence, the study is to know the occurrence of adverse drug reactions. Aims: To study the occurrence of adverse drug reactions in treatment of multidrug resistant tuberculosis and hence the factors affecting the treatment. Settings and Design: Retrospective analysis of patients treated with standardised regimen for MDR-TB, as per RNTCP guidelines at a tertiary chest institute between august 2011 and December 2014. Methods and Material: Retrospective analysis of 607 patients' records reviewed for the occurrence of adverse drug reactions. All adverse reactions are noted and diagnosed either clinically or by laboratory evidence. Results: Among the 607 patients included in the study, majority had one or more adverse drug reactions. The most common was gastritis (71.7%), which was easily treatable, and the least common was visual impairment (0.2%). Only 1.7% discontinued the treatment citing adverse drug reactions and 10.5% required permanent discontinuation of the offending drug. Conclusion: Treatment of MDR-TB is challenging mainly due to the long duration of treatment and the potential adverse reactions of the drugs used. These reactions are frequent but majority of them can be successfully managed without treatment interruption. Training the peripheral health centre workers to identify and refer the patients with adverse reaction bears a major impact on treatment outcome. Keywords MDR-TB, ADR, Adherence, Outcome J. S. Akshata et al. 28
Context: To achieve good cure rate during treatment of MDR-TB, strict adherence to treatment regimen is a must. As the second line drugs have great potential to cause adverse drug reactions (ADR), identifying these adverse reactions and treating them early is major factor in preventing default. Hypothyroidism is one such ADR caused by thioamides (ethionamide, prothionamide) and paraamino salicylic acid.Aims: To study the frequency of occurrence of hypothyroidism and its implication in MDR-TB treatment.Settings and design: Retrospective analysis of 488 patients enrolled in our institute for MDR-TB treatment treated with standardised Cat IV treatment, as per RNTCP-PMDT guidelines.Methods and material: Retrospective analysis of 484 (4 had hypothyroidism before treatment initiation) patients treated in our institute was done. Thyroid function test was done at baseline and repeated when indicated by symptoms during clinical follow up. Patients developing hypothyroidism (defined as TSH > 10 microIU/ml) during treatment and the reasons for same are analysed. Its implication in treatment outcome is studied.Results: Out of the 484 study population, 19 (3.9%) had at least one documented record of TSH > 10.0 microIU/ml after treatment initiation. Median time from initiation of MDR-TB treatment to development of hypothyroidism was 153 days (range 32-441 days).Conclusions: Occurrence of hypothyroidism is rare in MDRTB treatment. But symptomatic hypothyroidism is a major factor influencing the patient compliance towards the treatment regimen. As the drugs in regimen are effective in disease treatment, the major hindrance in achieving good cure-rate is to prevent defaulters. Identifying hypothyroidism early helps to prevent default.
This pilot study was done to choose which among the five core set criteria will have more discriminating ability and which is easy to administer in a clinical setting. Forty-eight patients recently diagnosed to have rheumatoid arthritis (RA) were recruited for the study. They were assessed by a rheumatologist in each visit (initial and after 2 months of treatment), for five core measures: patient assessment, pain (measured on VAS scale), number of tender joints, health assessment questionnaire (HAQ) score, and erythrocyte sedimentation rate (ESR). All patients were treated with methotrexate 7.5 mg per week and hydroxychloroquin 400 mg per day with adequate dose of NSAIDs. Patients with associated conditions like stroke, ischemic heart disease, and other physical comorbidity were excluded. They were categorized as 20, 50, and 70% improvement, if four of the five criteria occur. The Wilcoxon signed rank test and discriminant function analysis were done to identify the order of importance of measures on influencing the outcome. The ESR followed by patient improvement scale showed the least changes, while HAQ showed the highest changes. Discriminate function analysis has been carried out to see which factors influenced in grouping them for responses with post hoc analyses of finding the order of importance of these factors in classifying the response. Pain scale, ESR, HAQ score, patient improvement scale, and tender score were in the decreasing value of importance. The pain scale, HAQ, and ESR, which are more objective and discriminate measures, are useful as measures in RA.
Introduction: Cervical epithelial cell abnormalities (ECA) can result in cervical cancer which is the most common cause of cancer related death especially in developing countries. The aim of the present study is to find the association of CD4 count and Cervical epithelial abnormality in HIV positive women. Materials and Methods: A study of association between cervical epithelial abnormality and CD4 count in HIV positive women was taken up in a Care and Support Hospital in collaboration with the Department of Pathology, Government Medical College, Ananthapuramu. Based on the observations, periodic cervical screening in HIV positive women is emphasized. Results: 3.03% of women showed presence of cervical epithelial abnormality among HIV positive women. More number of HSIL (50%) followed by LSIL (28.2%), ASCUS (20.16%) and Carcinoma Cervix (1.6%). Conclusion: Present study also emphasizes that patients with low CD4 count are at high risk of developing precancerous lesions of cervix. Hence periodic biannual cervical screening is required for HIV positive women whose CD4 count is below 200, to bring down the incidence of cervical malignancy and premalignant conditions.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.