Division of Infectious Diseases, Kobe University Hospital, Japan.
Division of Infectious Diseases, Kobe University Hospital, Japan.
J Infect Chemother. 2022 Aug;28(8):1172-1176. doi: 10.1016/j.jiac.2022.03.020. Epub 2022 Apr 18.
Nocardiosis usually occurs in immunocompromised patients and causes infections in various organs, including the lungs, skin, and organs of the central nervous system. Herein, we report the case of a patient with minimal change nephrotic syndrome who had been on immunosuppressive drugs and developed pulmonary nocardiosis due to Nocardia nova complex and Pneumocystis pneumonia. For pulmonary nocardiosis, trimethoprim-sulfamethoxazole, linezolid, and clarithromycin were initiated sequentially, but were subsequently discontinued due to side effects; the treatment was completed with tedizolid. Tedizolid was used safely for 200 out of 286 days of antibiotic treatment, and clinical improvement was observed. Tedizolid is a bacteriostatic oxazolidine antibiotic that inhibits bacterial protein synthesis, the same mechanism as its predecessor, linezolid. Tedizolid is thought to cause less frequent myelosuppression than linezolid, at least for short-term use. In the future, tedizolid may be a promising alternative to linezolid in cases of nocardiosis that usually require long-term treatment.
奴卡氏菌病通常发生于免疫功能低下的患者,可引起肺部、皮肤和中枢神经系统等多种器官的感染。本文报告了一例微小病变肾病综合征患者,该患者因诺卡氏菌新复合群和卡氏肺孢子虫肺炎而接受免疫抑制药物治疗后发生肺部奴卡氏菌病。针对肺部奴卡氏菌病,先后使用了复方磺胺甲噁唑、利奈唑胺和克拉霉素治疗,但由于副作用而停药;最终使用替加环素完成了治疗。替加环素在 286 天的抗生素治疗中,有 200 天是安全使用的,并且观察到了临床改善。替加环素是一种抑菌性恶唑烷酮类抗生素,通过抑制细菌蛋白质合成发挥作用,其作用机制与前体药物利奈唑胺相同。替加环素引起骨髓抑制的频率似乎低于利奈唑胺,至少在短期使用时是这样。对于通常需要长期治疗的奴卡氏菌病,替加环素未来可能成为利奈唑胺的一种有前途的替代药物。