Vergis E N, Hayden M K, Chow J W, Snydman D R, Zervos M J, Linden P K, Wagener M M, Schmitt B, Muder R R
Division of Infectious Diseases, University of Pittsburgh, Suite 3A, Falk Medical Building, 3601 Fifth Avenue, Pittsburgh, PA 15213, USA.
Ann Intern Med. 2001 Oct 2;135(7):484-92. doi: 10.7326/0003-4819-135-7-200110020-00007.
Enterococcus species are major nosocomial pathogens and are exhibiting vancomycin resistance with increasing frequency. Previous studies have not resolved whether vancomycin resistance is an independent risk factor for death in patients with invasive disease due to Enterococcus species or whether antibiotic therapy alters the outcome of enterococcal bacteremia.
To determine whether vancomycin resistance is an independent predictor of death in patients with enterococcal bacteremia and whether appropriate antimicrobial therapy influences outcome.
Prospective observational study.
Four academic medical centers and a community hospital.
All patients with enterococcal bacteremia.
Demographic characteristics; underlying disease; Acute Physiology and Chronic Health Evaluation (APACHE) II scores; antibiotic therapy, immunosuppression, and procedures before onset; and antibiotic therapy during the ensuing 6 weeks. The major end point was 14-day survival.
Of 398 episodes, 60% were caused by E. faecalis and 37% were caused by E. faecium. Thirty-seven percent of isolates exhibited resistance or intermediate susceptibility to vancomycin. Twenty-two percent of E. faecium isolates showed reduced susceptibility to quinupristin-dalfopristin. Previous vancomycin use (odds ratio [OR], 5.82 [95% CI, 3.20 to 10.58]; P < 0.001), previous corticosteroid use (OR, 2.43 [CI, 1.22 to 4.86]; P = 0.01), and total APACHE II score (OR, 1.06 per unit change [CI, 1.02 to 1.10 per unit change]; P = 0.003) were associated with vancomycin-resistant enterococcal bacteremia. The mortality rate was 19% at 14 days. Hematologic malignancy (OR, 3.83 [CI, 1.56 to 9.39]; P = 0.003), vancomycin resistance (OR, 2.10 [CI, 1.14 to 3.88]; P = 0.02), and APACHE II score (OR, 1.10 per unit change [CI, 1.05 to 1.14 per unit change]; P < 0.001) were associated with 14-day mortality. Among patients with monomicrobial enterococcal bacteremia, receipt of effective antimicrobial therapy within 48 hours independently predicted survival (OR for death, 0.21 [CI, 0.06 to 0.80]; P = 0.02).
Vancomycin resistance is an independent predictor of death from enterococcal bacteremia. Early, effective antimicrobial therapy is associated with a significant improvement in survival.
肠球菌属是主要的医院病原体,并且对万古霉素耐药的频率在不断增加。既往研究尚未明确万古霉素耐药是否是肠球菌属所致侵袭性疾病患者死亡的独立危险因素,以及抗生素治疗是否会改变肠球菌血症的结局。
确定万古霉素耐药是否是肠球菌血症患者死亡的独立预测因素,以及恰当的抗菌治疗是否会影响结局。
前瞻性观察性研究。
四家学术医疗中心和一家社区医院。
所有肠球菌血症患者。
人口统计学特征;基础疾病;急性生理与慢性健康状况评分系统(APACHE)Ⅱ评分;发病前的抗生素治疗、免疫抑制和操作;以及随后6周内的抗生素治疗。主要终点为14天生存率。
在398例病例中,60%由粪肠球菌引起,37%由屎肠球菌引起。37%的分离株对万古霉素耐药或中介敏感。22%的屎肠球菌分离株对奎奴普丁-达福普汀敏感性降低。既往使用万古霉素(比值比[OR],5.82[95%CI,3.20至10.58];P<0.001)、既往使用皮质类固醇(OR,2.43[CI,1.22至4.86];P=0.01)和APACHEⅡ总分(OR,每单位变化1.06[CI,每单位变化1.02至1.10];P=0.003)与万古霉素耐药肠球菌血症相关。14天死亡率为19%。血液系统恶性肿瘤(OR,3.83[CI,1.56至9.39];P=0.003)、万古霉素耐药(OR,2.10[CI,1.14至3.88];P=0.02)和APACHEⅡ评分(OR,每单位变化1.10[CI,每单位变化1.05至1.14];P<0.001)与14天死亡率相关。在单一微生物肠球菌血症患者中,48小时内接受有效的抗菌治疗可独立预测生存(死亡OR,0.21[CI,