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每日半剂量利奈唑胺治疗难治性耐多药结核病患者的疗效及耐受性

Efficacy and tolerability of daily-half dose linezolid in patients with intractable multidrug-resistant tuberculosis.

作者信息

Park I-Nae, Hong Sang-Bum, Oh Yeon-Mok, Kim Mi-Na, Lim Chae-Man, Lee Sang Do, Koh Younsuck, Kim Woo Sung, Kim Dong Soon, Kim Won Dong, Shim Tae Sun

机构信息

Division of Pulmonary & Critical Care Medicine, University of Ulsan College of Medicine, Asan Medical Center, 388-1 Pungnap-dong, Songpa-gu, Seoul, Korea.

出版信息

J Antimicrob Chemother. 2006 Sep;58(3):701-4. doi: 10.1093/jac/dkl298. Epub 2006 Jul 19.

Abstract

OBJECTIVES

Although linezolid has good in vitro activity against Mycobacterium tuberculosis, its long-term use in the treatment of multidrug-resistant tuberculosis (MDR-TB) may be limited by its cost and serious adverse reactions. We therefore evaluated the efficacy and tolerability of a reduced dose of linezolid, in combination with other anti-TB drugs, in patients with intractable or extensive MDR-TB.

METHODS

MDR-TB patients unresponsive to at least three cycles of treatment were treated with daily-half doses of linezolid (600 mg once per day) plus at least four companion drugs.

RESULTS

As of March 2006, eight patients, all HIV-negative, had been treated with linezolid for 3-18 months. Cultures became negative in all patients in an average of 82 days. Four patients developed peripheral neuropathy, two developed optic neuropathy and one developed anaemia. Although optic neuropathy resolved after cessation of linezolid therapy, peripheral neuropathy continued. One patient completed 18 months of linezolid therapy. Two patients, who have taken linezolid for 15-17 months, are still on treatment and remain in culture conversion. Three patients stopped linezolid after 7-9 months, two because of side effects and one for economic reasons, but remain on treatment with other second-line drugs with culture conversion. Two patients died from severe respiratory failure, but both previously had shown culture conversion.

CONCLUSIONS

Although daily-half doses of linezolid were effective in patients with intractable or extensive MDR-TB, this dosage regimen did not reduce long-term use-related side effects, such as peripheral and optic neuropathy.

摘要

目的

虽然利奈唑胺对结核分枝杆菌具有良好的体外活性,但其在多药耐药结核病(MDR-TB)治疗中的长期使用可能会受到成本和严重不良反应的限制。因此,我们评估了低剂量利奈唑胺联合其他抗结核药物治疗难治性或广泛耐药MDR-TB患者的疗效和耐受性。

方法

对至少三个疗程治疗无反应的MDR-TB患者,采用利奈唑胺每日半量(600mg,每日1次)加至少四种辅助药物进行治疗。

结果

截至2006年3月,8例均为HIV阴性的患者接受了利奈唑胺治疗3至18个月。所有患者的培养物平均在82天内转阴。4例患者出现周围神经病变,2例出现视神经病变,1例出现贫血。虽然视神经病变在利奈唑胺治疗停止后有所缓解,但周围神经病变仍持续存在。1例患者完成了18个月的利奈唑胺治疗。2例服用利奈唑胺15至17个月的患者仍在接受治疗,培养物仍在转阴。3例患者在7至9个月后停止使用利奈唑胺,2例因副作用,1例因经济原因,但仍继续使用其他二线药物治疗,培养物转阴。2例患者死于严重呼吸衰竭,但两者之前均已出现培养物转阴。

结论

虽然利奈唑胺每日半量对难治性或广泛耐药MDR-TB患者有效,但这种给药方案并未减少与长期使用相关的副作用,如周围神经病变和视神经病变。

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