Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Department of Veterans Affairs, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Int J Antimicrob Agents. 2017 Apr;49(4):488-492. doi: 10.1016/j.ijantimicag.2016.11.032. Epub 2017 Feb 8.
Central nervous system (CNS) nocardiosis is a recognised opportunistic infection in immunocompromised patients. Treatment involves prolonged institution of antibiotics, making oral agents a convenient and desired option. Unfortunately, devising an effective, well-tolerated antimicrobial for the duration required to treat CNS nocardiosis is challenging owing to treatment intolerance and toxicities. This report highlights myelosuppression-sparing treatment with an oral tedizolid-based regimen following a complicated course with standard agents. A 68-year-old female from Florida (USA) with low-risk lambda light chain multiple myeloma complicated by persistently low CD4 counts, absolute neutrophil counts and IgG levels presented 18 months after diagnosis with fever, pneumonia, new-onset atrial fibrillation, right-sided hemiparesis, encephalopathy and slurred speech. Magnetic resonance imaging (MRI) showed numerous ring-enhancing lesions, and blood cultures were positive for Nocardia farcinica. The patient failed initial therapy with trimethoprim/sulfamethoxazole (SXT), linezolid and imipenem plus surgical debridement of the frontal lobe abscess. Intraoperative cultures were positive for N. farcinica. The treatment course was also complicated by steadily declining white blood cell and platelet counts despite receiving filgrastim. She was therefore placed on SXT and tedizolid for 6 months. Subsequent brain MRI showed complete resolution of the lesions and thus chemotherapy for multiple myeloma was re-initiated. In conclusion, tedizolid-based regimens may be an option for patients with myelosuppression requiring prolonged antibiotic therapy for CNS nocardiosis.
中枢神经系统(CNS)奴卡菌病是一种在免疫功能低下患者中公认的机会性感染。治疗需要长期使用抗生素,因此口服药物是一种方便且理想的选择。不幸的是,由于治疗不耐受和毒性,设计一种有效的、耐受性良好的抗生素来治疗 CNS 奴卡菌病是具有挑战性的。本报告强调了在经历了标准药物治疗的复杂过程后,采用口服替加环素为基础的方案来避免骨髓抑制。一位来自美国佛罗里达州的 68 岁女性,患有低危 lambda 轻链多发性骨髓瘤,伴有持续的低 CD4 计数、绝对中性粒细胞计数和 IgG 水平,在诊断后 18 个月出现发热、肺炎、新发心房颤动、右侧偏瘫、脑病和言语不清。磁共振成像(MRI)显示了许多环形增强病变,血液培养阳性为星形奴卡菌。该患者初始治疗使用磺胺甲噁唑/甲氧苄啶(SXT)、利奈唑胺和亚胺培南联合额叶脓肿手术清创失败。术中培养阳性为星形奴卡菌。尽管使用了非格司亭,但白细胞和血小板计数仍持续下降,导致治疗过程复杂。因此,她接受了 SXT 和替加环素治疗 6 个月。随后的脑部 MRI 显示病变完全消退,因此重新开始了多发性骨髓瘤的化疗。总之,对于需要长期抗生素治疗 CNS 奴卡菌病且伴有骨髓抑制的患者,替加环素为基础的方案可能是一种选择。