Gallagher Jason C, Satlin Michael J, Elabor Abdulrahman, Saraiya Nidhi, McCreary Erin K, Molnar Esther, El-Beyrouty Claudine, Jones Bruce M, Dixit Deepali, Heil Emily L, Claeys Kimberly C, Hiles Jon, Vyas Nikunj M, Bland Christopher M, Suh Jin, Biason Kenneth, McCoy Dorothy, King Madeline A, Richards Lynette, Harrington Nicole, Guo Yi, Chaudhry Saira, Lu Xiaoning, Yu Daohai
Temple University, Department of Pharmacy Practice, Philadelphia, Pennsylvania.
Division of Infectious Diseases, Weill Cornell Medicine, New York, New York.
Open Forum Infect Dis. 2018 Oct 31;5(11):ofy280. doi: 10.1093/ofid/ofy280. eCollection 2018 Nov.
Multidrug-resistant infections remain common in hospitals worldwide. We investigated the outcomes associated with the use of ceftolozane-tazobactam for the treatment of these infections.
Data were collected retrospectively from 20 hospitals across the United States about adults who received ceftolozane-tazobactam for the treatment of multidrug-resistant infections of any source for at least 24 hours. The primary outcome was a composite of 30-day and inpatient mortality, and secondary outcomes were clinical success and microbiological cure. Multivariable regression analysis was conducted to determine factors associated with outcomes.
Two-hundred five patients were included in the study. Severe illness and high degrees of comorbidity were common, with median Acute Physiology and Chronic Health Evaluation (APACHE) II scores of 19 (interquartile range [IQR], 11-24) and median Charlson Comorbidity Indexes of 4 (IQR, 3-6). Delayed initiation of ceftolozane-tazobactam was common with therapy started a median of 9 days after culture collection. Fifty-nine percent of patients had pneumonia. On susceptibility testing, 125 of 139 (89.9%) isolates were susceptible to ceftolozane-tazobactam. Mortality occurred in 39 patients (19%); clinical success and microbiological cure were 151 (73.7%) and 145 (70.7%), respectively. On multivariable regression analysis, starting ceftolozane-tazobactam within 4 days of culture collection was associated with survival (adjusted odds ratio [OR], 5.55; 95% confidence interval [CI], 2.14-14.40), clinical success (adjusted OR, 2.93; 95% CI, 1.40-6.10), and microbiological cure (adjusted OR, 2.59; 95% CI, 1.24-5.38).
Ceftolozane-tazobactam appeared to be effective in the treatment of multidrug-resistant infections, particularly when initiated early after the onset of infection.
耐多药感染在全球医院中仍然很常见。我们调查了使用头孢他啶阿维巴坦治疗这些感染的相关结果。
回顾性收集美国20家医院中接受头孢他啶阿维巴坦治疗任何来源的耐多药感染至少24小时的成年患者的数据。主要结局是30天死亡率和住院死亡率的综合结果,次要结局是临床成功和微生物学治愈。进行多变量回归分析以确定与结局相关的因素。
205名患者纳入研究。严重疾病和高合并症发生率常见,急性生理与慢性健康状况评分系统(APACHE)Ⅱ评分中位数为19(四分位间距[IQR],11 - 24),查尔森合并症指数中位数为4(IQR,3 - 6)。头孢他啶阿维巴坦开始治疗延迟常见,中位时间为培养标本采集后9天开始治疗。59%的患者患有肺炎。药敏试验中,139株分离菌中的125株(89.9%)对头孢他啶阿维巴坦敏感。39例患者(19%)死亡;临床成功和微生物学治愈分别为151例(73.7%)和145例(70.7%)。多变量回归分析显示,在培养标本采集后4天内开始使用头孢他啶阿维巴坦与生存(调整优势比[OR],5.55;95%置信区间[CI],2.14 - 14.40)、临床成功(调整OR,2.93;95%CI,1.40 - 6.10)和微生物学治愈(调整OR,2.59;95%CI,1.24 - 5.38)相关。
头孢他啶阿维巴坦似乎对耐多药感染有效,尤其是在感染发生后早期开始使用时。