Risk Factors Associated with Severe Clostridioides difficile Infection in Patients with Cancer

被引:6
作者
Francisco, Denise Marie A. [1 ,8 ]
Zhang, Liangliang [2 ]
Jiang, Ying [3 ]
Olvera, Adilene [3 ]
Adachi, Javier [3 ]
Guevara, Eduardo Yepez [3 ]
Aitken, Samuel L. [4 ]
Garey, Kevin W. [5 ]
Peterson, Christine B. [2 ]
Do, Kim-Anh [2 ]
Dillon, Ryan [6 ]
Obi, Engels N. [6 ]
Jenq, Robert [7 ]
Okhuysen, Pablo C. [1 ,3 ]
机构
[1] Baylor Coll Med, Sect Infect Dis, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, 1515 Holcombe Blvd,Unit 1460, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Div Pharm, Houston, TX 77030 USA
[5] Univ Houston, Coll Pharm, Houston, TX 77030 USA
[6] Merck & Co Inc, Kenilworth, NJ USA
[7] Univ Texas MD Anderson Canc Ctr, Dept Genom Med, Houston, TX 77030 USA
[8] Univ Illinois, Coll Med, Peoria C-O 530 NE Glen Oak Ave, Peoria, IL 61637 USA
关键词
Clostridioides difficile; Metronidazole; Anaerobes; Microbiome; Cancer; HOSPITALIZED-PATIENTS; COLITIS; METRONIDAZOLE; EPIDEMIOLOGY; MORTALITY; HOST;
D O I
10.1007/s40121-022-00722-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction Antibiotic use is a risk factor for Clostridioides difficile infection (CDI). Few studies have correlated use of prior antibiotic classes with CDI, microbiome composition, and disease severity in patients with cancer. We hypothesized that previous antibiotic exposure and fecal microbiome composition at time of presentation are risk factors for severe CDI in patients with cancer. Methods This non-interventional, prospective, cohort study examined 200 patients with cancer who had their first episode or first recurrence of CDI. C. difficile was identified using nucleic acid amplification testing. Univariate analysis was used to determine significant risk factors for severe CDI. Fecal microbiome composition was determined by sequencing the V3/V4 region of 16 s rDNA encoding gene. Differential abundance analyses were used to single out significant microbial features which differed across severity levels. Results On univariate analysis, factors associated with severe CDI included the presence of toxin A/B in stools (odds ratio [OR] 2.14 [1.05-4.36] p = 0.04 and prior 90-day metronidazole use (OR 2.66 [1.09-6.50] p = 0.03). Although alpha and beta diversity was similar between disease severity groups and toxin A/B in stools, increased abundance of Bacteroides uniformis, Ruminococcaceae, and Citrobacter koseri were associated with protection from severe CDI (p < 0.05) and depletion of anaerobes was higher in patients with prior metronidazole exposure. Conclusion Use of metronidazole for non-CDI indications within 90 days prior to diagnosis and presence of toxin A/B in stools were associated with severe CDI. Findings provide valuable insights into risk factors for severe CDI in an underserved population with cancer that warrants further exploration.
引用
收藏
页码:209 / 225
页数:17
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