4.7 Article

Use of Rifamycin Drugs and Development of Infection by Rifamycin-Resistant Strains of Clostridium difficile

期刊

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
卷 57, 期 6, 页码 2690-2693

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.00548-13

关键词

-

资金

  1. The University of Texas School of Public Health
  2. Public Health Service [DK56338]
  3. Salix Pharmaceuticals

向作者/读者索取更多资源

The relationship between rifamycin drug use and the development of resistant strains of Clostridium difficile was studied at a large university hospital in Houston, TX, between May 2007 and September 2011. In 49 of 283 (17.3%) patients with C. difficile infection (CDI), a rifamycin-resistant strain of C. difficile was identified that compares to a rate of 8% using the same definitions in 2006-2007 (P = 0.59). The 49 patients infected by a resistant organism were matched by date of admission to 98 control patients with CDI from whom a rifamycin-susceptible C. difficile strain was isolated. Cases and controls did not differ according to demographic and clinical characteristics and showed similar but low rates of prior rifamycin use. Similar rates of rifamycin resistance were seen in cases of hospital-acquired CDI (38/112 [34%]) versus community-acquired CDI (7/20 [35%]). At a university hospital in which rifaximin was commonly used, infection by rifamycin-resistant strains of C. difficile was not shown to relate to prior use of a rifamycin drug or to acquiring the infection in the hospital, although the rate of overall resistance appeared to be rising.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Microbiology

Colitis caused by Clostridioides difficile infection in a domestic dog: A case report

K. Rainha, Debora Lins, R. F. Ferreira, C. L. Costa, B. Penna, B. T. Endres, K. W. Garey, R. M. C. P. Domingues, E. O. Ferreira

Summary: Clostridioides difficile has been identified as one of the primary causes of nosocomial diarrhea and pseudomembranous colitis in humans and other mammals after the use of broad-spectrum antibiotics. A case of C. difficile infection (CDI) in a 13-year-old male dog is described in Rio de Janeiro, Brazil.

ANAEROBE (2022)

Article Immunology

Emergence of Clinical Clostridioides difficile Isolates With Decreased Susceptibility to Vancomycin

Charles Darkoh, Kadiatou Keita, Chioma Odo, Micah Oyaro, Eric L. Brown, Cesar A. Arias, Blake M. Hanson, Herbert L. DuPont

Summary: A study found that vancomycin nonsusceptible strains of Clostridioides difficile are circulating in patient populations, posing a serious challenge to treatment as vancomycin is a first-line antibiotic for CDI. Routine susceptibility testing may be necessary.

CLINICAL INFECTIOUS DISEASES (2022)

Article Immunology

Efficacy, Safety, Pharmacokinetics, and Microbiome Changes of Ibezapolstat in Adults with Clostridioides difficile Infection: A Phase 2a Multicenter Clinical Trial

Kevin W. Garey, Jacob McPherson, An Q. Dinh, Chenlin Hu, Jinhee Jo, Weiqun Wang, Chris K. Lancaster, Anne J. Gonzales-Luna, Caroline Loveall, Khurshida Begum, M. Jahangir Alam, Michael H. Silverman, Blake Hanson

Summary: This study validates the effectiveness of ibezapolstat in treating adult patients with Clostridioides difficileinfection. The results show sustained clinical cure and beneficial effects on the microbiome and bile acids.

CLINICAL INFECTIOUS DISEASES (2022)

Article Infectious Diseases

Genetic Mechanisms of Vancomycin Resistance in Clostridioides difficile: A Systematic Review

Taryn A. Eubank, Anne J. Gonzales-Luna, Julian G. Hurdle, Kevin W. Garey

Summary: Antimicrobial resistance in Clostridioides difficile infection poses a major threat to global health. While oral vancomycin is commonly used to treat CDI, there is a lack of susceptibility testing in clinical labs, making it challenging to detect and monitor resistance. This systematic review explores the gene determinants and mechanisms of vancomycin resistance in C. difficile and highlights the need for further research to understand their clinical impact.

ANTIBIOTICS-BASEL (2022)

Article Infectious Diseases

Durable reduction of Clostridioides difficile infection recurrence and microbiome restoration after treatment with RBX2660: results from an open-label phase 2 clinical trial

Robert Orenstein, Erik R. Dubberke, Sahil Khanna, Christine H. Lee, David Yoho, Stuart Johnson, Gail Hecht, Herbert L. DuPont, Dale N. Gerding, Ken F. Blount, Sarah Mische, Adam Harvey

Summary: In this Phase 2 trial, RBX2660 was found to be safe and effective in reducing the recurrence of rCDI compared to a historical control group. Microbiome changes in participants treated with RBX2660 were consistent with protective changes against C. difficile recurrence.

BMC INFECTIOUS DISEASES (2022)

Article Microbiology

A Vancomycin HPLC Assay for Use in Gut Microbiome Research

Chenlin Hu, Nicholas D. Beyda, Kevin W. Garey

Summary: The human microbiome project has revolutionized our understanding of the interaction between commensal microbes and human health. In this study, a simple and fast HPLC method was validated for quantitative fecal vancomycin analysis and the reproducibility of results were tested, establishing sample condition standards for quantitative HPLC studies on vancomycin pharmacokinetics with the human microbiome.

MICROBIOLOGY SPECTRUM (2022)

Article Microbiology

Functional and Metagenomic Evaluation of Ibezapolstat for Early Evaluation of Anti-Recurrence Effects in Clostridioides difficile Infection

Jacob McPherson, Chenlin Hu, Khurshida Begum, Weiqun Wang, Chris Lancaster, Anne J. Gonzales-Luna, Caroline Loveall, Michael H. Silverman, M. Jahangir Alam, Kevin W. Garey

Summary: This study used a functional and metagenomic approach to predict the potential anti-CDI recurrence effect of ibezapolstat. The results from the clinical study showed that ibezapolstat demonstrated beneficial changes in microbiome and bile acid concentrations, suggesting a lower risk of CDI recurrence compared to vancomycin.

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2022)

Letter Immunology

Untitled Reply

Charles Darkoh, Herbert L. DuPont, Cesar A. Arias, Micah Oyaro, Eric L. Brown, Blake M. Hanson

CLINICAL INFECTIOUS DISEASES (2022)

Article Infectious Diseases

Development of the invasive candidiasis discharge [I Can discharge] model: a mixed methods analysis

Jinhee Jo, Truc T. Tran, Nicholas D. Beyda, Debora Simmons, Joshua A. Hendrickson, Masaad Saeed Almutairi, Faris S. Alnezary, Anne J. Gonzales-Luna, Edward J. Septimus, Kevin W. Garey

Summary: This study aimed to assess the use of echinocandin at hospital discharge and develop a transition of care model for patients with invasive candidiasis (IC). The study found a significant use of echinocandin at discharge, with almost half of the discharged patients receiving outpatient echinocandin therapy. Osteomyelitis, other deep-seated infection, and non-home discharge location were independent predictors for outpatient echinocandin use. The developed discharge model may assist in facilitating smoother and earlier hospital discharges.

EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES (2022)

Review Microbiology

Nonmammalian models to study Clostridioides difficile infection; a systematic review

Chenlin Hu, Kevin W. Garey

Summary: Clostridioide difficile is the leading cause of diarrhea disease worldwide and is considered an urgent threat pathogen by CDC. Mammalian models are commonly used to study C. difficile infection, but alternative nonmammalian models, such as great wax worm, nematode, fruit fly, and zebrafish, have been explored due to cost, throughput capacity, and ethical concerns. This review provides a comprehensive summary of the use of nonmammalian models in studying CDI, including its infection mechanism, pathogenicity, colonization, host immunity, and therapy. The translational outcomes and strengths and weaknesses of each nonmammalian model are discussed.

ANAEROBE (2023)

Review Microbiology

Intestinal IgA-Coated Bacteria in Healthy- and Altered-Microbiomes (Dysbiosis) and Predictive Value in Successful Fecal Microbiota Transplantation

Herbert L. L. DuPont, Zhi-Dong Jiang, Ashley S. S. Alexander, Andrew W. W. DuPont, Eric L. L. Brown

Summary: IgA-coated bacteria in the gut provide important homeostatic functions and their impairment is associated with dysbiosis. Fecal microbiota transplantation has been successful in engrafting healthy microbiota and metabolites, with IgA-coated bacteria being transferred to recipients. The evaluation of the IgA-biome should be included in FMT studies, using metagenomic methods to better identify and compare microbiota data.

MICROORGANISMS (2023)

Article Pharmacology & Pharmacy

Micafungin pharmacodynamics predict clinical outcomes in hospitalized patients with candidemia caused by certain Candida species

Ahmed Zaki, Anne J. Gonzales-Luna, Nicholas D. Beyda, Todd Lasco, Kevin W. Garey

Summary: This study evaluated the clinical outcomes of micafungin based on population-predicted pharmacokinetic/pharmacodynamic factors and susceptibility. MIC and AUC/MIC breakpoints derived from CART analysis predicted patient mortality and treatment failure for certain Candida species. These results support further PK/PD studies to optimize echinocandin dosing and improve patient outcomes.

PHARMACOTHERAPY (2023)

Article Neurosciences

IgA-Biome Profiles Correlate with Clinical Parkinson's Disease Subtypes

Eric L. Brown, Heather T. Essigmann, Kristi L. Hoffman, Ashley S. Alexander, Michael Newmark, Zhi-Dong Jiang, Jessika Suescun, Mya C. Schiess, Craig L. Hanis, Herbert L. DuPont

Summary: Parkinson's disease is a heterogeneous neurodegenerative disorder with distinct gut microbiome patterns. This study characterized the IgA-Biome of individuals with different clinical subtypes of Parkinson's disease and identified unique bacterial profiles associated with these subtypes.

JOURNAL OF PARKINSONS DISEASE (2023)

Review Gastroenterology & Hepatology

Gut microbiota changes associated with Clostridioides difficile infection and its various treatment strategies

Anne J. Gonzales-Luna, Travis J. Carlson, Kevin W. Garey

Summary: Human gut microbiota play a critical role in the development and recovery of Clostridioides difficile infection (CDI). Antibiotics, although necessary for CDI treatment, can further disrupt the gut microbiota, leading to dysbiosis and complicating recovery. Various microbiota-based treatment approaches, such as fecal microbiota transplantation (FMT) and newly approved live biotherapeutic products, have been developed to address disease- and treatment-associated dysbiosis and improve cure rates. This review aims to discuss the changes in the gut microbiome associated with CDI and the effectiveness of different microbiota-based treatments.

GUT MICROBES (2023)

Article Immunology

Effect of Fecal Microbiota, Live-Jslm (REBYOTA [RBL]) on Health-Related Quality of Life in Patients With Recurrent Clostridioides difficile Infection: Results From the PUNCH CD3 Clinical Trial

Kevin W. Garey, Erik R. Dubberke, Amy Guo, Adam Harvey, Min Yang, Viviana Garcia-Horton, Mirko Fillbrunn, Hongjue Wang, Glenn S. Tillotson, Lindy L. Bancke, Paul Feuerstadt

Summary: In this study, the disease-specific health-related quality of life (HRQL) in patients with rCDI treated with fecal microbiota was evaluated. The results demonstrated that patients treated with RBL had more improvements in the mental domain compared to those receiving placebo.

OPEN FORUM INFECTIOUS DISEASES (2023)

暂无数据