IDEAS 2.0 Center, Veterans Affairs (VA) Salt Lake City Health Care System, Salt Lake City, Utah2Division of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City.
Department of Pharmacotherapy, University of Utah College of Pharmacy, Salt Lake City.
JAMA Intern Med. 2017 Apr 1;177(4):546-553. doi: 10.1001/jamainternmed.2016.9045.
Metronidazole hydrochloride has historically been considered first-line therapy for patients with mild to moderate Clostridium difficile infection (CDI) but is inferior to vancomycin hydrochloride for clinical cure. The choice of therapy may likewise have substantial consequences on other downstream outcomes, such as recurrence and mortality, although these secondary outcomes have been less studied.
To evaluate the risk of recurrence and all-cause 30-day mortality among patients receiving metronidazole or vancomycin for the treatment of mild to moderate and severe CDI.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective, propensity-matched cohort study evaluated patients treated for CDI, defined as a positive laboratory test result for the presence of C difficile toxins or toxin genes in a stool sample, in the US Department of Veterans Affairs health care system from January 1, 2005, through December 31, 2012. Data analysis was performed from February 7, 2015, through November 22, 2016.
Treatment with vancomycin or metronidazole.
The outcomes of interest in this study were CDI recurrence and all-cause 30-day mortality. Recurrence was defined as a second positive laboratory test result within 8 weeks of the initial CDI diagnosis. All-cause 30-day mortality was defined as death from any cause within 30 days of the initial CDI diagnosis.
A total of 47 471 patients (mean [SD] age, 68.8 [13.3] years; 1947 women [4.1%] and 45 524 men [95.9%]) developed CDI, were treated with vancomycin or metronidazole, and met criteria for entry into the study. Of 47 147 eligible first treatment episodes, 2068 (4.4%) were with vancomycin. Those 2068 patients were matched to 8069 patients in the metronidazole group for a total of 10 137 included patients. Subcohorts were constructed that comprised 5452 patients with mild to moderate disease and 3130 patients with severe disease. There were no differences in the risk of recurrence between patients treated with vancomycin vs those treated with metronidazole in any of the disease severity cohorts. Among patients in the any severity cohort, those who were treated with vancomycin were less likely to die (adjusted relative risk, 0.86; 95% CI, 0.74 to 0.98; adjusted risk difference, -0.02; 95% CI, -0.03 to -0.01). No significant difference was found in the risk of mortality between treatment groups among patients with mild to moderate CDI, but vancomycin significantly reduced the risk of all-cause 30-day mortality among patients with severe CDI (adjusted relative risk, 0.79; 95% CI, 0.65 to 0.97; adjusted risk difference, -0.04; 95% CI, -0.07 to -0.01).
Recurrence rates were similar among patients treated with vancomycin and metronidazole. However, the risk of 30-day mortality was significantly reduced among patients who received vancomycin. Our findings may further justify the use of vancomycin as initial therapy for severe CDI.
盐酸甲硝锉一直被认为是轻度至中度艰难梭菌感染(CDI)患者的一线治疗药物,但在临床治愈率方面不如盐酸万古霉素。治疗选择可能同样对其他下游结果产生重大影响,例如复发和死亡率,尽管这些次要结果的研究较少。
评估接受甲硝锉或万古霉素治疗轻度至中度和重度 CDI 的患者的复发风险和全因 30 天死亡率。
设计、地点和参与者:这项回顾性、倾向匹配队列研究评估了在美国退伍军人事务部医疗保健系统中接受 CDI 治疗的患者,定义为粪便样本中存在艰难梭菌毒素或毒素基因的实验室检测结果阳性。数据分析于 2015 年 2 月 7 日至 2016 年 11 月 22 日进行。
接受万古霉素或甲硝锉治疗。
本研究的主要结果是 CDI 复发和全因 30 天死亡率。复发定义为初次 CDI 诊断后 8 周内第二次阳性实验室检测结果。全因 30 天死亡率定义为初次 CDI 诊断后 30 天内任何原因导致的死亡。
共有 47471 名患者(平均[标准差]年龄 68.8[13.3]岁;1947 名女性[4.1%]和 45524 名男性[95.9%])患有 CDI,接受了万古霉素或甲硝锉治疗,并符合进入研究的标准。在 47147 例合格的初次治疗发作中,2068 例(4.4%)使用万古霉素。这 2068 名患者与甲硝锉组的 8069 名患者相匹配,共有 10137 名患者纳入研究。构建了亚组,包括 5452 例轻度至中度疾病患者和 3130 例重度疾病患者。在任何严重程度的队列中,接受万古霉素治疗的患者与接受甲硝锉治疗的患者相比,复发风险没有差异。在任何严重程度的队列中,接受万古霉素治疗的患者死亡风险较低(校正相对风险 0.86;95%CI,0.74 至 0.98;校正风险差异-0.02;95%CI,-0.03 至-0.01)。在轻度至中度 CDI 患者中,治疗组之间的死亡率风险无显著差异,但万古霉素显著降低了重度 CDI 患者的全因 30 天死亡率风险(校正相对风险 0.79;95%CI,0.65 至 0.97;校正风险差异-0.04;95%CI,-0.07 至-0.01)。
接受万古霉素和甲硝锉治疗的患者复发率相似。然而,接受万古霉素治疗的患者 30 天死亡率显著降低。我们的发现可能进一步证明万古霉素作为重度 CDI 的初始治疗是合理的。