Reduced Vancomycin Susceptibility in Clostridioides difficile Is Associated With Lower Rates of Initial Cure and Sustained Clinical Response

被引:6
作者
Eubank, Taryn A. [1 ]
Dureja, Chetna [2 ]
Garey, Kevin W. [1 ]
Hurdle, Julian G. [2 ,4 ]
Gonzales-Luna, Anne J. [1 ,3 ]
机构
[1] Univ Houston, Coll Pharm, Dept Pharm Practice & Translat Res, Houston, TX USA
[2] Texas A&M Hlth Sci Ctr, Inst Biosci & Technol, Ctr Infect & Inflammatory Dis, Houston, TX USA
[3] Univ Houston, Coll Pharm, Dept Pharm Practice & Translat Res, 4349 Martin Luther King Blvd, Houston, TX 77204 USA
[4] Texas A&M Hlth Sci Ctr, Inst Biosci & Technol, 2121 West Holcombe Blvd, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
vancomycin; Clostridioides difficile; antimicrobial resistance; anaerobes; susceptibility testing; INFECTIOUS-DISEASES SOCIETY; HEALTH-CARE EPIDEMIOLOGY; UNITED-STATES; AMERICA IDSA; DOUBLE-BLIND; FIDAXOMICIN; GUIDELINES; RESISTANCE; METRONIDAZOLE; SURVEILLANCE;
D O I
10.1093/cid/ciae087
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Epidemiologic studies have shown decreasing vancomycin susceptibility among clinical Clostridioides difficile isolates, but the impact on patient outcomes is unknown. We hypothesized that reduced vancomycin susceptibility would be associated with decreased rates of sustained clinical response (SCR). Methods. This multicenter cohort study included adults with C. difficile infection (CDI) treated with oral vancomycin between 2016 and 2021. Clostridioides difficile isolates underwent agar dilution vancomycin susceptibility testing, ribotyping, and Sanger sequencing of the vancomycin resistance vanR gene. Reduced susceptibility was defined as vancomycin minimum inhibitory concentration (MIC) >2 mu g/mL. The primary outcome was 30-day SCR; secondary outcomes were 14-day initial cure, 30-day recurrence, and 30-day mortality. Exploratory analysis assessed the association between the VanR Thr115Ala polymorphism, susceptibility, and outcomes. Results. A high proportion (34% [102/300]) of C. difficile isolates exhibited reduced vancomycin susceptibility (range, 0.5-16 mu g/mL; MIC50/90 = 2/4 mu g/mL). Ribotype 027 accounted for the highest proportion (77.4% [41/53]) of isolates with reduced vancomycin susceptibility. Overall, 83% (249) of patients achieved 30-day SCR. Reduced vancomycin susceptibility was associated with lower rates of 30-day SCR (76% [78/102]) than vancomycin-susceptible strains (86% [171/198]; P = .031). A significantly lower rate of 14-day initial cure was also observed among individuals infected with strains with reduced vancomycin susceptibility (89% vs 96%; P = .04). Reduced susceptibility remained an independent predictor of 30-day SCR in multivariable modeling (odds ratio, 0.52 [95% confidence interval, .28-.97]; P = .04). Conclusions. Reduced vancomycin susceptibility in C. difficile was associated with decreased odds of 30-day SCR and lower 14-day initial cure rates in the studied patient cohort.
引用
收藏
页码:15 / 21
页数:7
相关论文
共 51 条
  • [21] Gargis AS., 2022, CLIN INFECT DIS, V75, P1677
  • [22] Comparative Susceptibilities to Fidaxomicin (OPT-80) of Isolates Collected at Baseline, Recurrence, and Failure from Patients in Two Phase III Trials of Fidaxomicin against Clostridium difficile Infection
    Goldstein, Ellie J. C.
    Citron, Diane M.
    Sears, Pamela
    Babakhani, Farah
    Sambol, Susan P.
    Gerding, Dale N.
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (11) : 5194 - 5199
  • [23] Faecal pharmacokinetics of orally administered vancomycin in patients with suspected Clostridium difficile infection
    Gonzales, Milagros
    Pepin, Jacques
    Frost, Eric H.
    Carrier, Julie C.
    Sirard, Stephanie
    Fortier, Louis-Charles
    Valiquette, Louis
    [J]. BMC INFECTIOUS DISEASES, 2010, 10
  • [24] Reduced Susceptibility to Metronidazole Is Associated With Initial Clinical Failure in Clostridioides dificile Infection
    Gonzales-Luna, Anne J.
    Olaitan, Abiola O.
    Shen, Wan-Jou
    Deshpande, Aditi
    Carlson, Travis J.
    Dotson, Kierra M.
    Lancaster, Chris
    Begum, Khurshida
    Alam, M. Jahangir
    Hurdle, Julian G.
    Garey, Kevin W.
    [J]. OPEN FORUM INFECTIOUS DISEASES, 2021, 8 (08):
  • [25] Houston, We Have a Problem: Reports of Clostridioides difficile Isolates With Reduced Vancomycin Susceptibility
    Greentree, David Henry
    Rice, Louis B.
    Donskey, Curtis J.
    [J]. CLINICAL INFECTIOUS DISEASES, 2022, 75 (09) : 1661 - 1664
  • [26] Guery B, 2018, LANCET INFECT DIS, V18, P296, DOI [10.1016/S1473-3099(17)30751-X, 10.1016/s1473-3099(17)30751-x]
  • [27] Trends in US Burden of Clostridioides difficile Infection and Outcomes
    Guh, Alice Y.
    Mu, Yi
    Winston, Lisa G.
    Johnston, Helen
    Olson, Danyel
    Farley, Monica M.
    Wilson, Lucy E.
    Holzbauer, Stacy M.
    Phipps, Erin C.
    Dumyati, Ghinwa K.
    Beldavs, Zintars G.
    Kainer, Marion A.
    Karlsson, Maria
    Gerding, Dale N.
    McDonald, L. Clifford
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2020, 382 (14) : 1320 - 1330
  • [28] The Roles of Clostridium difficile and Norovirus Among Gastroenteritis-Associated Deaths in the United States, 1999-2007
    Hall, Aron J.
    Curns, Aaron T.
    McDonald, L. Clifford
    Parashar, Umesh D.
    Lopman, Ben A.
    [J]. CLINICAL INFECTIOUS DISEASES, 2012, 55 (02) : 216 - 223
  • [29] Detection and Investigation of Eagle Effect Resistance to Vancomycin in Clostridium difficile With an ATP-Bioluminescence Assay
    Jarrad, Angie M.
    Blaskovich, Mark A. T.
    Prasetyoputri, Anggia
    Karoli, Tomislav
    Hansford, Karl A.
    Cooper, Matthew A.
    [J]. FRONTIERS IN MICROBIOLOGY, 2018, 9
  • [30] Johnson S, 2021, CLIN INFECT DIS, V73, P755, DOI 10.1093/cid/ciab718