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在一项针对骨科感染患者的前瞻性观察研究中,长期使用利奈唑胺和万古霉素治疗的相似血液学效应。

Similar hematologic effects of long-term linezolid and vancomycin therapy in a prospective observational study of patients with orthopedic infections.

作者信息

Rao Nalini, Ziran Bruce H, Wagener Marilyn M, Santa Elizabeth R, Yu Victor L

机构信息

Division of Infectious Disease, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15232, USA.

出版信息

Clin Infect Dis. 2004 Apr 15;38(8):1058-64. doi: 10.1086/382356. Epub 2004 Mar 26.

DOI:10.1086/382356
PMID:15095207
Abstract

Linezolid is an alternative to vancomycin for the long-term treatment of gram-positive bacterial orthopedic infections because of its antibacterial spectrum and oral bioavailability, but duration-related myelosuppression could offset its advantages. To evaluate the hematologic effects of these agents, we prospectively studied 65 consecutive adults with gram-positive bacterial orthopedic infections requiring > or =2 weeks of vancomycin therapy (n=52) or linezolid therapy (n=20). Trends suggesting higher incidence of hematologic effects among the patients receiving vancomycin were not significant, regardless of whether the end point was lowest cell count during therapy or change from baseline. The only difference was a higher incidence of thrombocytopenia (<150x10(9) platelets/L) in the subset of the linezolid recipients who had received vancomycin within 2 weeks before starting linezolid therapy than in the linezolid recipients who had not received vancomycin (5 [71%] of 7 patients vs. 2 [15%] of 13; P=.02). All hematologic effects were reversible. In conclusion, hematologic effects were detectable through weekly monitoring and were reversible; therefore, concern about myelosuppression need not preclude linezolid use for orthopedic infections requiring long-term therapy.

摘要

由于利奈唑胺的抗菌谱和口服生物利用度,它是万古霉素用于长期治疗革兰氏阳性菌骨科感染的替代药物,但与疗程相关的骨髓抑制可能会抵消其优势。为评估这些药物的血液学影响,我们前瞻性地研究了65例连续的成年革兰氏阳性菌骨科感染患者,这些患者需要接受≥2周的万古霉素治疗(n = 52)或利奈唑胺治疗(n = 20)。无论终点是治疗期间的最低细胞计数还是相对于基线的变化,接受万古霉素治疗的患者血液学影响发生率较高的趋势均不显著。唯一的差异是,在开始利奈唑胺治疗前2周内接受过万古霉素治疗的利奈唑胺治疗组患者中,血小板减少症(血小板计数<150×10⁹/L)的发生率高于未接受过万古霉素治疗的利奈唑胺治疗组患者(7例患者中的5例[71%] vs. 13例患者中的2例[15%];P = 0.02)。所有血液学影响都是可逆的。总之,通过每周监测可检测到血液学影响且这些影响是可逆的;因此,对于需要长期治疗的骨科感染,不必因担心骨髓抑制而排除使用利奈唑胺。

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