Campo Marcela, Hachem Ray, Jiang Ying, Dvorak Tanya, Carrillo-Marquez Maria, Hulten Kristina, Chemaly Roy F, Raad Issam
From Department of Infectious Diseases (MC, RH, YJ, TD, RFC, IR), Infection Control and Employee Health, The University of Texas M. D. Anderson Cancer Center, Houston; and Texas Children's Hospital (MC-M, KH), Baylor College of Medicine, Houston, Texas.
Medicine (Baltimore). 2011 Sep;90(5):312-318. doi: 10.1097/MD.0b013e31822d8978.
The presence of Panton-Valentine leukocidin (PVL) gene in methicillin-resistant Staphylococcus aureus (MRSA) infections has been associated with high severity and mortality rates. In this study we evaluated the effect of PVL on outcome in cancer patients with MRSA infections.We retrospectively reviewed the records of 173 cancer patients diagnosed with MRSA pneumonia (n = 47), skin and soft tissue infections (n = 77), and bacteremia (n = 49) between September 2003 and September 2007 at M. D. Anderson Cancer Center. We obtained demographic and clinical data and tested isolates for the presence of PVL. The data were compared between patients with PVL (+) and those with PVL (-) strains. Statistical methods for comparison included Cochran-Mantel-Haenszel tests, 2-way nonparametric analysis of variance, chi-square or Fisher exact tests, and Wilcoxon rank sum tests. All tests were 2-sided with a significance level of 0.05.Seventy patients with PVL (+) strains and 103 patients with PVL (-) strains were included in our study. Fewer PVL (+) patients had pneumonia than did PVL (-) patients (14% vs. 36%, p = 0.002). PVL (-) patients were more likely to have concomitant infections (35% vs. 17%, p = 0.012). The 2 groups were similar in terms of fever, sepsis, vasopressor use, mechanical ventilation, antibiotics response, infection relapse, death, and death due to MRSA. In a skin and soft tissue subset analysis, PVL (+) patients were more likely to have solid tumors (73% vs. 47%, p = 0.02) and less likely to have fever (20% vs. 44%, p = 0.02) and sepsis (12% vs. 36%, p = 0.013). There were no differences in outcome between patients with pneumonia and bacteremia; however, most patients with pneumonia were PVL (-) (79% vs. 21%). Among the 73 patients who received vancomycin and the 20 who received linezolid, there was no difference in response to treatment, regardless of PVL status or neutropenia. In conclusion, the presence of the PVL gene had no negative effect on cancer patients with health care-associated MRSA.
耐甲氧西林金黄色葡萄球菌(MRSA)感染中存在杀白细胞素(PVL)基因与高严重程度和死亡率相关。在本研究中,我们评估了PVL对癌症患者MRSA感染结局的影响。我们回顾性分析了2003年9月至2007年9月期间在MD安德森癌症中心诊断为MRSA肺炎(n = 47)、皮肤和软组织感染(n = 77)以及菌血症(n = 49)的173例癌症患者的病历。我们获取了人口统计学和临床数据,并检测分离株中是否存在PVL。对PVL(+)患者和PVL(-)患者的数据进行比较。比较的统计方法包括 Cochr an-Mantel-Haenszel检验、双向非参数方差分析、卡方检验或 Fisher精确检验以及Wilcoxon秩和检验。所有检验均为双侧检验,显著性水平为0.05。我们的研究纳入了70例PVL(+)菌株患者和103例PVL(-)菌株患者。PVL(+)患者中患肺炎的人数少于PVL(-)患者(14%对36%,p = 0.002)。PVL(-)患者更易合并其他感染(35%对17%,p = 0.012)。两组在发热、脓毒症、血管活性药物使用、机械通气、抗生素反应、感染复发、死亡以及因MRSA导致的死亡方面相似。在皮肤和软组织亚组分析中,PVL(+)患者更易患实体瘤(73%对47%,p = 0.02),发热(20%对44%,p = 0.02)和脓毒症(12%对36%,p = 0.013)的可能性更低。肺炎患者和菌血症患者的结局无差异;然而,大多数肺炎患者为PVL(-)(79%对21%)。在接受万古霉素治疗的73例患者和接受利奈唑胺治疗的20例患者中,无论PVL状态或中性粒细胞减少情况如何,治疗反应均无差异。总之,PVL基因的存在对患有医疗保健相关MRSA的癌症患者没有负面影响。