Legg Amy, Roberts Matthew A, Davies Jane, Cass Alan, Meagher Niamh, Sud Archana, Daitch Vered, Dishon Benattar Yael, Yahav Dafna, Paul Mical, Xinxin Chen, Ping Yeo He, Lye David, Lee Russel, Robinson J Owen, Foo Hong, Tramontana Adrian R, Bak Narin, Grenfell Adelaide, Rogers Benjamin, Li Ying, Joshi Neela, O'Sullivan Matthew, McKew Genevieve, Ghosh Niladri, Schneider Kellie, Holmes Natasha E, Dotel Ravindra, Chia Timothy, Archuleta Sophia, Smith Simon, Warner Morgyn S, Titin Christina, Kalimuddin Shirin, Roberts Jason A, Tong Steven Y C, Davis Joshua S
Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Herston Infectious Diseases Institute, Brisbane, Queensland, Australia.
Open Forum Infect Dis. 2023 Jul 3;10(7):ofad337. doi: 10.1093/ofid/ofad337. eCollection 2023 Jul.
The Combination Antibiotic Therapy for Methicillin-Resistant (CAMERA2) trial ceased recruitment in July 2018, noting that a higher proportion of patients in the intervention arm (combination therapy) developed acute kidney injury (AKI) compared to the standard therapy (monotherapy) arm. We analyzed the long-term outcomes of participants in CAMERA2 to understand the impact of combination antibiotic therapy and AKI.
Trial sites obtained additional follow-up data. The primary outcome was all-cause mortality, censored at death or the date of last known follow-up. Secondary outcomes included kidney failure or a reduction in kidney function (a 40% reduction in estimated glomerular filtration rate to <60 mL/minute/1.73 m). To determine independent predictors of mortality in this cohort, adjusted hazard ratios were calculated using a Cox proportional hazards regression model.
This post hoc analysis included extended follow-up data for 260 patients. Overall, 123 of 260 (47%) of participants died, with a median population survival estimate of 3.4 years (235 deaths per 1000 person-years). Fifty-five patients died within 90 days after CAMERA2 trial randomization; another 68 deaths occurred after day 90. Using univariable Cox proportional hazards regression, mortality was not associated with either the assigned treatment arm in CAMERA2 (hazard ratio [HR], 0.84 [95% confidence interval [CI], .59-1.19]; = .33) or experiencing an AKI (HR at 1 year, 1.04 [95% CI, .64-1.68]; = .88).
In this cohort of patients hospitalized with methicillin-resistant bacteremia, we found no association between either treatment arm of the CAMERA2 trial or AKI (using CAMERA2 trial definition) and longer-term mortality.
耐甲氧西林联合抗生素治疗(CAMERA2)试验于2018年7月停止招募,指出与标准治疗(单药治疗)组相比,干预组(联合治疗)中发生急性肾损伤(AKI)的患者比例更高。我们分析了CAMERA2试验参与者的长期结局,以了解联合抗生素治疗和AKI的影响。
试验地点获取了额外的随访数据。主要结局为全因死亡率,在死亡或最后一次已知随访日期进行截尾。次要结局包括肾衰竭或肾功能减退(估计肾小球滤过率降低40%至<60 ml/分钟/1.73 m²)。为了确定该队列中死亡率的独立预测因素,使用Cox比例风险回归模型计算调整后的风险比。
这项事后分析纳入了260例患者的延长随访数据。总体而言,260例参与者中有123例(47%)死亡,总体人群生存估计中位数为3.4年(每1000人年有235例死亡)。55例患者在CAMERA2试验随机分组后90天内死亡;另外68例死亡发生在90天之后。使用单变量Cox比例风险回归分析,死亡率与CAMERA2试验中指定的治疗组(风险比[HR],0.84[95%置信区间[CI],0.59 - 1.19];P = 0.33)或发生AKI(1年时的HR,1.04[95%CI,0.64 - 1.68];P = 0.88)均无关联。
在这组因耐甲氧西林菌血症住院的患者中,我们发现CAMERA2试验的任何一个治疗组或AKI(使用CAMERA2试验定义)与长期死亡率之间均无关联。