全球多中心三级医院耐多药结核病患者德拉马尼、氧氟沙星、左氧氟沙星和贝达喹啉流行处方模式的合理药物治疗研究

Moumita Hazra
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引用次数: 0

摘要

背景:Delamanid是一种硝基二氢咪唑唑类抗菌细胞壁甲氧基霉菌酸和酮酵母酸生物合成抑制剂,对结核分枝杆菌和堪萨斯分枝杆菌的活性复制、休眠和细胞内结核以及药敏和耐药菌株均有抑制作用,可降低疏水性,促进细菌更好地渗透药物。Delamanid促进细胞内产生杀灭微生物的氮氧化中间体,包括一氧化氮,甚至对休眠的结核分枝杆菌有毒。氧氟沙星外消旋混合物与氧氟沙星s或左旋异构体左氧氟沙星对结核分枝杆菌、MAC、福氏分枝杆菌等非典型分枝杆菌均有杀菌作用,对DNA旋切酶、DNA拓扑异构酶IV及IL-1α、IL-6、IL-8均有抑制作用。贝达喹啉是一种新型的二芳基喹啉,抑制结核分枝杆菌三磷酸腺苷合成酶,破坏分枝杆菌的能量代谢和复制。贝达喹啉最初的抑菌作用在5-7天后产生杀菌作用。目的是对全球多中心三级保健医院多重耐药结核病患者中delamanid、氧氟沙星、左氧氟沙星和贝达喹啉的普遍处方模式进行合理的药物治疗研究。方法:对我院100例耐多药结核病患者的临床处方进行多中心回顾性、观察性和分析性研究。在24-48周的时间里,这些患者服用了抗结核药物,如delamanid 100毫克,氧氟沙星400毫克,每天两次,左氧氟沙星750毫克,贝达喹啉400毫克,每天一次,随后每周服用200毫克,每周服用三次,作为耐多药结核病治疗方案的一部分。没有。记录每种药物的处方数,并以百分比统计得出相应的处方率。结果:处方最多的是德拉马尼(32张,占32%),其次是氧氟沙星(29张,占29%)、左氧氟沙星(24张,占24%)和贝达喹啉(15张,占15%)。100%的处方内容、用药剂量、疗程、用药说明、用药频次、药品名称、剂型的填写是否完整。结论:德拉马尼处方频次次之为氧氟沙星、左氧氟沙星、贝达喹啉。处方含量分析100%完整。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rational pharmacotherapeutic study of the prevalent prescription patterns of delamanid, ofloxacin, levofloxacin, and bedaquiline among the multi-drug resistant tuberculosis patients in global multi-centre tertiary care hospitals
Background: Delamanid, a nitro-dihydro-imidazooxazole, is a bactericidal cell wall methoxy-mycolic and ketomycolic acids biosynthesis inhibitor in actively replicating, dormant, and intracellular tuberculosis, and both drugsusceptible and drug-resistant strains of M. tuberculosis and M. kansasii, decreasing hydrophobicity and facilitating better bacterial drug penetration. Delamanid promotes intracellular generation of microbiocidal nitrogen oxidative intermediaries including nitric oxide, toxic even to dormant M. tuberculosis. Ofloxacin, the racemic mixture and levofloxacin, the S-or levorotatory isomer of ofloxacin, are bactericidal to M. tuberculosis, MAC, M. fortuitum, and other atypical mycobacteria, with inhibitory effect on DNA gyrase, DNA topoisomerase IV and IL-1α, IL-6, IL-8. Bedaquiline, a novel diarylquinoline, inhibits mycobacterial adenosine triphosphate synthase of M. tuberculosis, disrupting mycobacterial energy metabolism and replication. Bedaquiline’s initial bacteriostatic action is followed by a bactericidal effect after 5-7 days. The objective was to perform a rational pharmacotherapeutic study of the prevalent prescription patterns of delamanid, ofloxacin, levofloxacin, and bedaquiline, among the multi-drug resistant tuberculosis patients, in global multi-centre tertiary care hospitals. Methods: A multi-centre, retrospective, observational and analytical study of clinical prescriptions of 100 multi-drug resistant tuberculosis patients in hospitals, were performed. For 24-48 weeks, these patients had been prescribed antitubercular drugs, like delamanid 100 mg and ofloxacin 400 mg twice daily, levofloxacin 750 mg and bedaquiline 400 mg once daily followed by 200 mg thrice weekly, as part of MDR-TB treatment regimens. The no. of prescriptions for each drug were recorded, and the corresponding prescription rates were statistically derived in percentages. Results: Delamanid was most commonly prescribed (32 prescriptions, 32%), followed by ofloxacin (29 prescriptions, 29%), levofloxacin (24 prescriptions, 24%), and bedaquiline (15 prescriptions, 15%). The completeness of the prescription contents, the dose of drug, the duration of treatment, the instructions of medication, the frequency of drug intake, the name of the drug and the dosage form of the drug were observed in 100% of prescriptions. Conclusions: Prescription frequency of delamanid was followed by ofloxacin, levofloxacin and bedaquiline. Prescription content analyses showed 100% completeness.
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