Treatment‘s side effects in MDR tuberculosis patients
I. G. Stoica (Bucharest, Romania)
Source: Annual Congress 2005 - Biological and treatment aspects of tuberculosis
Session: Biological and treatment aspects of tuberculosis
Session type: Poster Discussion
Number: 2905
Disease area: Respiratory infections
Abstract Aim: to find and to evaluate the side effects (SE) that occur to the patients who receive treatment for MDR tuberculosis. Study: 1 year (2004) prospective, accomplished by clinical and biological examination and questionnaires. 398 patients have been hospitalized in this period of time. 52 cases of these, were drug resistant tuberculosis; 81% were male (mean age 58, smokers 92%), 19% - female (mean age: 43, smokers 72%). Patients with resistance to at least one drug have been examined, 63% of these had MDR. The patients‘ treatment was conducted by using individualized treatment regimens (ITR) with 2nd -line anti-TB drugs (Amikacin, Kanamycin, Fluoroquinolones, Cycloserin, Prothionamid). ITR included 3rd -line drugs (Amoxicillin/Clavulanic acid, Clarithromycin) to the patients who had MDR resistant to 4 or more anti-TB drugs. We‘ve performed clinical and biological investigation and we‘ve asked the patients to fill up questionnaires. Results: SE were recorded for n=32(62%) patients. These were: aplastic anemia and leukopenia (n=3), renal failure (n=2), Stevens-Johnson syndrome (n=3), hearing disturbances to loss (n=7), nausea and vomiting (n=11), diarrhea (n=5),dizziness(n=8) and other (n=9). Patients have presented 1 or more SE, which were more common among women than men, older than younger (age adjusted). Discontinuance of treatment, curative or symptomatic medication were administrated. Conclusion: Treatment‘s SE in MDR tuberculosis patients occurred more commonly among women and among older patients. Is very important to know the SE, in order to prevent or cure, but mostly to prevent discontinuance of treatment.
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I. G. Stoica (Bucharest, Romania). Treatment‘s side effects in MDR tuberculosis patients. Eur Respir J 2005; 26: Suppl. 49, 2905
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