1例结核分枝杆菌感染患者口服不能耐受,静脉注射含泰地唑胺治疗成功。

Haruka Karaushi, Masafumi Seki, Yutaka Miyawaki, Noriyuki Watanabe, Fumitaka Kamoshita, Kotaro Mitsutake
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引用次数: 0

摘要

背景结核分枝杆菌(M. tuberculosis)通常通过口服抗结核药物治疗,包括利福平、乙胺丁醇和吡嗪酰胺,但对于不能口服药物的患者,静脉注射和/或肌肉注射抗结核药物的治疗方案尚不清楚。病例报告一名77岁慢性肾衰竭患者行食管癌、胃癌切除及空肠重建手术后出现食管皮肤瘘,经美罗培南、替柯planin、米卡芬宁治疗蜂巢状组织炎及菌血症/念珠菌血症后,胸片示左上肺野腔、树芽状形成及胸腔积液。从他的痰中分离出结核分枝杆菌,并从重建的食管皮肤瘘中渗出液。虽然他不能口服抗真菌药物,但治疗开始时每隔一天静脉注射左氧氟沙星(LVFX)、异烟肼(INH)和利奈唑胺(LZD)。然而,他的血小板在治疗开始21天后下降,这被认为是LZD和/或INH的不良反应。将LZD改为tedizolid (TZD)后,除了每周两次从INH改为肌内链霉素外,血小板计数增加。静脉注射TZD可以继续,它维持了他的病情,没有加重血小板减少症和肾功能衰竭。治疗2个月后结核分枝杆菌消失,胸部x线异常影改善。结论:对于不能口服药物治疗的结核分枝杆菌患者,除静脉注射LVFX和肌肉注射SM外,静脉注射TZD可能是一种备选方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Mycobacterium tuberculosis-Infected Patient Who Could Not Tolerate Oral Intake Successfully Treated Using an Intravenous Tedizolid-Containing Regimen.

A Mycobacterium tuberculosis-Infected Patient Who Could Not Tolerate Oral Intake Successfully Treated Using an Intravenous Tedizolid-Containing Regimen.

A Mycobacterium tuberculosis-Infected Patient Who Could Not Tolerate Oral Intake Successfully Treated Using an Intravenous Tedizolid-Containing Regimen.

A Mycobacterium tuberculosis-Infected Patient Who Could Not Tolerate Oral Intake Successfully Treated Using an Intravenous Tedizolid-Containing Regimen.

BACKGROUND Mycobacterium tuberculosis (M. tuberculosis) is usually treated by oral antimycobacterial agents, including rifampicin, ethambutol, and pyrazinamide, but the treatment regimen with intravenous and/or intramuscular antimycobacterial agents for patients who cannot take medications orally remains unclear. CASE REPORT A 77-year-old man with chronic renal failure had an esophageal-skin fistula after he had surgeries for removal of esophageal and gastric cancers and reconstruction using jejunum, and he showed a cavity, tree-in-bud formation, and pleural effusions in his left upper lung fields on his chest X-ray after treatment of cellulitis and bacteremia/candidemia by meropenem, teicoplanin, and micafungin. M. tuberculosis was isolated from his sputum and exudate fluid from the reconstructed esophageal-skin fistula. Although he could not take antimycobacterial agents orally, treatment was started with intravenous agents combining levofloxacin (LVFX) every other day, isoniazid (INH), and linezolid (LZD). However, his platelets were decreased 21 days after treatment started, and it was thought to be an adverse effect of LZD and/or INH. After changing LZD to tedizolid (TZD), in addition to changing from INH to intramuscular streptomycin twice per week, his platelet counts increased. Intravenous TZD could be continued, and it maintained his condition without exacerbations of thrombocytopenia and renal failure. The M. tuberculosis disappeared, and the abnormal chest X-ray shadows were improved 2 months after the start of treatment. CONCLUSIONS Administration of intravenous TZD, in addition to intravenous LVFX and intramuscular SM in combination, might be a candidate regimen for M. tuberculosis patients who cannot take oral medications.

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