Meissner H Cody, Townsend Timothy, Wenman Wanda, Kaplan Sheldon L, Morfin Maria Rayo, Edge-Padbury Barbara, Naberhuis-Stehouwer Sharon, Bruss Jon B
Pediatric Infectious Diseases, New England Medical Center, Tufts University School of Medicine, 750 Washington Street, NEMCH Box 321, Boston, MA 02111, USA.
Pediatr Infect Dis J. 2003 Sep;22(9 Suppl):S186-92. doi: 10.1097/01.inf.0000087021.20838.d9.
Linezolid is an effective and well-tolerated antibiotic for the treatment of Gram-positive infections, including hospital and community-acquired pneumonia and complicated and uncomplicated skin and skin structure infections. In adults linezolid treatment for >/=2 weeks has been associated with reversible hematopoietic suppression, primarily thrombocytopenia.
To evaluate the occurrence of hematologic effects in children with Gram-positive infections in an open label study of linezolid vs. vancomycin.
Detailed analyses of hematologic data, including reported hematologic adverse events, complete blood counts, reticulocyte index (RI) and iron studies (serum iron and transferrin saturation), were conducted in both groups at baseline and during and after treatment with the use of an intent-to-treat analysis.
Three hundred sixteen patients (median age, 1.65 yr) randomized 2:1 to linezolid (n = 215) or vancomycin (n = 101) were treated. Total treatment durations were similar in the vancomycin group (12.2 +/- 6.4 days; median, 11.0 days) and the linezolid group (11.3 +/- 5.0 days; median, 11.0 days) (P = 0.20). No significant differences were noted in drug-related hematologic events, such as thrombocytopenia (linezolid, 1.9% vs. vancomycin, 0%; P = 0.170), anemia (linezolid, 1.4% vs. vancomycin, 1.0%; P = 0.771) or neutropenia (linezolid, 0% vs. vancomycin, 0%). Hemoglobin values also were similar between treatment groups when assessed by shifts from baseline to lowest recorded value. Frequency of occurrence of any substantially abnormal value for hemoglobin (15.7% vs. 12.4%), platelets (12.9% vs. 13.4%) and neutrophils (5.9% vs. 4.3%) were similar in the linezolid and vancomycin groups. No clinically relevant changes in RI or iron studies were noted between treatment groups, and parallel increases in RI occurred with both linezolid and vancomycin.
No significant differences in hematologic profiles between linezolid and vancomycin occurred in this pediatric population.
利奈唑胺是一种有效且耐受性良好的抗生素,用于治疗革兰氏阳性菌感染,包括医院获得性肺炎和社区获得性肺炎以及复杂性和非复杂性皮肤及皮肤结构感染。在成人中,利奈唑胺治疗≥2周与可逆性造血抑制相关,主要是血小板减少。
在一项利奈唑胺与万古霉素的开放标签研究中,评估革兰氏阳性菌感染儿童血液学效应的发生情况。
使用意向性分析,在两组患者的基线、治疗期间及治疗后对血液学数据进行详细分析,包括报告的血液学不良事件、全血细胞计数、网织红细胞指数(RI)和铁代谢研究(血清铁和转铁蛋白饱和度)。
316例患者(中位年龄1.65岁)按2:1随机分为利奈唑胺组(n = 215)或万古霉素组(n = 101)并接受治疗。万古霉素组(12.2±6.4天;中位值11.0天)和利奈唑胺组(11.3±5.0天;中位值11.0天)的总治疗时长相似(P =0.20)。在药物相关的血液学事件方面未观察到显著差异,如血小板减少(利奈唑胺组为1.9%,万古霉素组为0%;P = 0.170)、贫血(利奈唑胺组为1.4%,万古霉素组为1.0%;P = 0.771)或中性粒细胞减少(利奈唑胺组为0%,万古霉素组为0%)。当根据从基线到最低记录值的变化评估时,治疗组之间的血红蛋白值也相似。利奈唑胺组和万古霉素组血红蛋白(15.7%对12.4%)、血小板(12.9%对13.4%)和中性粒细胞(5.9%对4.3%)出现任何显著异常值的频率相似。治疗组之间未观察到RI或铁代谢研究有临床相关变化,利奈唑胺和万古霉素治疗后RI均呈平行升高。
在该儿科人群中,利奈唑胺和万古霉素在血液学特征方面无显著差异。