Raja Iqbal Mulya Harahap, Juandika Juandika, Dety Mulyanti
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摘要

介绍。结核病(TB)是已知最古老的人类疾病之一,由结核分枝杆菌引起。耐多药结核病(MDR-TB)是结核分枝杆菌对利福平和烟碱肼(INH)产生最低耐药性的阶段或状况。广泛耐药结核病(XDR-TB)是一种耐多药结核病,具有结核分枝杆菌对一种氟喹诺酮类药物和一种二线注射OAT(卷曲霉素、卡那霉素和阿米卡星)的免疫特征。本研究的目的是找出耐多药结核病/广泛耐药患者在一个治疗周期内实验室费用变化的描述。方法。纳入标准是诊断为耐多药结核病/广泛耐药并进行实验室检查的患者。本研究的设计是利用耐多药部门耐多药结核病/广泛耐药患者的医疗记录进行横断面回顾性分析。结果。共有30名耐多药结核研究对象和2名广泛耐药结核研究对象接受实验室检查。耐多药结核/XDR实验室平均值比较(p = 0.018)。讨论。在一个治疗周期内,耐多药结核病/广泛耐药实验室检查的总费用有显著差异。结论。耐多药结核病/广泛耐药患者的实验室检查需要相当大的费用,这是由于OAT的副作用需要患者临床监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PERBANDINGAN BIAYA PEMERIKSAAN LABORATORIUM PADA PASIEN TUBERKULOSIS MULTIDRUG RESISTANCE (TB-MDR) DENGAN TUBERKULOSIS EXTENSIVE DRUG RESISTANCE (TB-XDR): STUDI PADA RUMAH SAKIT TERSIER DI BANDUNG
Introduction. Tuberculosis (TB) is one of the oldest diseases known to attack humans, caused by the bacterium Mycobacterium tuberculosis. Multi-drug-resistant TB (MDR-TB) is a stage or condition in which Mycobacterium tuberculosis becomes minimally resistant to rifampicin administration and also insonicotinylhydrazine (INH). Extensive-drug-resistant TB (XDR-TB) is an MDR-TB with Mycobacterium tuberculosis immune characteristics against one of the fluoroquinolone class drugs and one of the second-line injection OAT (capreomycin, kanamycin, and amikacin). The aim of this study was to find out the description of variation in laboratory costs of MDR-TB/XDR patients on one treatment cycle. Method. The inclusion criteria were patients who had been diagnosed with MDR-TB/XDR and performed laboratory tests. The design of this study was a cross-sectional retrospective analytics using medical records of MDR-TB/XDR patients in MDR division. Results. There were 30 MDR-TB research subjects and 2 XDR-TB research subjects examined for laboratory examination. Comparison of laboratory mean of MDR-TB/XDR (p = 0,018). Discussion. There was a significant difference in the total cost of MDR-TB/XDR laboratory examinations in one treatment cycle. Conclusion. Laboratory examination of MDR-TB/XDR patients requires considerable cost, this is due to the side effects of OAT that require patient clinical monitoring.    
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