Emerging therapies in the treatment of Clostridium difficile -: Associated disease

被引:20
作者
Jodlowski, Tomasz Z.
Oehler, Richard
Kam, Linda W.
Melnychuk, Igor
机构
[1] James A Haley Vet Hosp, Dept 119, Tampa, FL 33612 USA
[2] Univ S Florida, Coll Med, Div Infect Dis, Tampa, FL USA
[3] St Johns Univ, Jamaica, NY 11439 USA
[4] Jacobi Med Ctr, Bronx, NY USA
关键词
Clostridium difficile; intravenous immunoglobulin; nitazoxanide; rifaximin; tinidazole; tolevamer; vaccine;
D O I
10.1345/aph.1H340
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To describe emergent therapies, such as rifaximin, nitazoxanide, intravenous immunoglobulin (IVIG), tinidazole, tolevamer, and the possible use of a vaccine, in Clostridium difficile-associated disease (CDAD), one of the most common causes of diarrhea in hospitalized adults in North America. DATA SOURCES: A literature search was performed using MEDLINE (1996-October 2006), PubMed (1996-October 2006), abstracts from Infectious Diseases Society of America (September 2006) and International Conference on Antimicrobial Agents and Chemotherapy (September 2006), Internet (October 2006), Genzyme product Web site (October 2006), and Romark Laboratories Web site (October 2006) using the terms Clostridium difficile, rifaximin, nitazoxanide, intravenous immunoglobulin, tolevamer, vaccine, and tinidazole. STUDY SELECTION AND DATA EXTRACTION: Data presented in this article were selected based on clinical relevance and power of the studies. In vivo and in vitro studies supporting the use of drugs available for treatment of refractory CDAD were reviewed. Some of the information on new and emerging modalities was also included, although there were limited published data available. DATA SYNTHESIS: Clinical trials evaluating the use of nitazoxanide and tolevamer for the treatment of CDAD have been published. Tinidazole use is based on structural similarities to metronidazole; however, clinical trials have not been conducted and the cost of this agent may be a limiting factor. The use of rifaximin and IVIG will require randomized clinical trials to establish their place in therapy. Limited information in the literature suggests that a vaccine may be effective for CDAD prevention. CONCLUSIONS: CDAD is a debilitating disease with increasing treatment failure rates and recurrences using standard therapies. Clinicians need to look at other options to expand the available treatment arsenal in addition to placing a greater emphasis on prevention.
引用
收藏
页码:2164 / 2169
页数:6
相关论文
共 37 条
[1]   Clostridium difficile vaccine and serum immunoglobulin G antibody response to toxin A [J].
Aboudola, S ;
Kotloff, KL ;
Kyne, L ;
Warny, M ;
Kelly, EC ;
Sougioultzis, S ;
Giannasca, PJ ;
Monath, TP ;
Kelly, CP .
INFECTION AND IMMUNITY, 2003, 71 (03) :1608-1610
[2]   Treatment of Clostridium difficile-associated disease:: old therapies and new strategies [J].
Aslam, S ;
Hamill, R ;
Musher, DM .
LANCET INFECTIOUS DISEASES, 2005, 5 (09) :549-557
[3]   New drugs for Clostridium difficile infection [J].
Bartlett, John G. .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (04) :428-431
[4]  
Boero M B E, 1990, Microbiol Med, V5, P74
[5]   Toxin binding of tolevamer, a polyanionic drug that protects against antibiotic-associated diarrhea [J].
Braunlin, W ;
Xu, QW ;
Hook, P ;
Fitzpatrick, R ;
Klinger, JD ;
Burrier, R ;
Kurtz, CB .
BIOPHYSICAL JOURNAL, 2004, 87 (01) :534-539
[6]   Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease [J].
Dial, S ;
Delaney, JAC ;
Barkun, AN ;
Suissa, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 294 (23) :2989-2995
[7]   Risk of Clostridium difficile diarrhea among hospital inpatients prescribed proton pump inhibitors:: cohort and case-control studies [J].
Dial, S ;
Alrasadi, K ;
Manoukian, C ;
Huang, A ;
Menzies, D .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2004, 171 (01) :33-38
[8]   In vitro evaluation of activities of nitazoxanide and tizoxanide against anaerobes and aerobic organisms [J].
Dubreuil, L ;
Houcke, I ;
Mouton, Y ;
Rossignol, JF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (10) :2266-2270
[9]  
FETEKY R, 1997, AM J GASTROENTEROL, V92, P739
[10]   Nitazoxanide: A new thiazolide antiparasitic agent [J].
Fox, LM ;
Saravolatz, LD .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (08) :1173-1180