2010, Number 1
<< Back Next >>
Rev Biomed 2010; 21 (1)
Anaerobic etiology of nosocomial antibiotic associated diarrhea in elderly patients
Rodríguez-Cavallini E, Gamboa-Coronado MM, Camacho-Mora Z, Herrera ML
Language: Spanish
References: 31
Page: 13-20
PDF size: 80.46 Kb.
ABSTRACT
Introduction. C. difficile and C. perfringens are important etiological agents of antibiotic associated diarrhea in adults and children worldwide, including Costa Rica. We intend to expand on previous research by including hospitalized patients over 60 years, to evaluate their additional factors and more severe illnesses.
Materials and Methods. Over an 18 month period 51 samples of diarrheic feces were screened and cultured for C. difficile and C. perfringens enterotoxins. Every isolate was evaluated for toxin production and antibiotic susceptibility.
Results. C. difficile toxin A was detected in 12 samples (24%) and C. perfringens enterotoxin in 10 (20%). C. difficile was isolated from 6 samples (12%) and C. perfringens from 16 (31%). All C. difficile isolates and only two C. perfringens were toxigenic, but both agents were isolated from two samples. Every C. difficile isolate was sensitive to beta-lactam, chloramphenicol and metronidazole, but most were resistant to clindamycin. A high percentage of C. perfringens strains showed resistance to beta lactam antibiotics, chloramphenicol and metronidazole and like C. difficile, also clindamycin.
Conclusions. According to toxin detection in feces, C. difficile and C. perfringens were the etiological agents in 44% of the diarrhea cases, reinforcing the need to consider both agents for diagnosis of diarrhea in hospitalized elderly patients. Clindamycin resistance shown by many isolates should be noted, since it has been implicated as a risk factor for the development of diarrhea. Metronidazole may not be the best choice, since 25% of C. perfringens strains were also resistant to this drug.
REFERENCES
Zheng L, Keller SF, Lyerly DM, Carman RJ, Genheirmer CW, Gleaves CA, et al. Multicenter evaluation of a new screening test that detects Clostridium difficile in fecal specimens. J Clin Microbiol 2004; 42: 3837-3840.
Razavi B, Apisarnthanarak A, Mundy LM. Clostridium difficile: Emergence of Hypervirulence and Fluoroquinolone Resistance. Infection 2007; 35:300-3007.
Pareja Sierra P, Hornillos Calvo M. Factores epidemiológicos, clínicos y analíticos asociados a diarrea por Clostridium difficile en población anciana hospitalizada. Estudio de casos y controles. Rev Esp Geriatr Gerontol 2007; 42:257-262.
Muñoz C. Diarrea Asociada a Antibióticos. Gastr Latinoam 2007; 18:188-192.
Garey KW, Dao-Tran TK, Jiang ZD, Price MP, Gentry LO, DuPont HL. A clinical risk index for Clostridium difficile infection in hospitalized patients receiving broad spectrum antibiotics. J Hops Infec 2008; 70:142-147.
Asha NJ, Tompkins D, Wilcox MH. Comparative Analysis of Prevalence, Risk Factors, and Molecular Epidemiology of Antibiotic-Associated Diarrhea Due to Clostridium difficile, Clostridium perfringens, and Staphylococcus aureus. J Clin Microbiol 2006; 44: 2785-2791.
Verdoorn BP, Orenstein R, Rosenblatt JE, Sloan LM, Schleck CD, Harmsen WS, et al. High prevalence of tcdC deletion-carring Clostridium difficile and lackof association with disease severity. Diag Microbiol Infect Dis 2010; 66:24-28.
Abrahao C, Carman R, Han H, Liesenfeld O. Similar Frequency of detection of Clostridium perfringens and Clostridium difficile toxins in Patients with Antibiotic-Associated Diarrhea. Eur J Clin Microbiol Infect Dis 2001; 20:676-677.
Modi N, Wilcox MH. Evidence for antibiotic induced Clostridium perfringens diarrhea. J Clin Pathol 2001; 54:748-751
Pituch H, Obuch-Woszczatyński P, Wultańska D, van Belkum A, Meisel-Mikołajczk F, Luczak M. Laboratory diagnosis of antibiotic-associated diarrhea: a Polish pilot study into the clinical relevance of Clostridium difficile and Clostridium perfringens toxins. Diagn Microbiol Infect Dis 2007; 58:71-75.
Cohen SH, Shetab R, Tang-Feldman YJ, Sarma P, Silva JJr, Prindiville TP. Prevalence of enterotoxigenic Bacteroides fragilis in hospital-acquired diarrhea. Diag Microbiol Infect Dis 2006; 55:251-254.
Zumbado-Salas R, Gamboa-Coronado MM, Rodríguez-Cavallini E, Chaves-Olarte E. Short Report: Clostridium difficile en adult patients with nosocomial diarrhea in a Costa Rican hospital . Am J Trop Med Hyg 2008; 79: 164-165.
Ruiz-Corella M, Altamirano-Silva P, Rodríguez-Cavallini E, Gamboa-Coronado MM. Clostridium perfringens y Clostridium difficile como agentes etiológicos de diarrea nosocomial asociada a antibióticos en niños costarricenses. Rev Biomed 2007; 18:81-87.
Camacho N, Espinoza C, Rodríguez C, Rodríguez E. Isolates of Clostridium perfringens recovered from Costa Rican patients with antibiotic-associated diarrhoea are mostly enterotoxin-negative and susceptible to the first-choice antimicrobials. J Med Microbiol 2008; 57: 343-347
Pareja Sierra P, Hornillos Calvo M. Diarrea asociada a Clostridium difficile en el paciente anciano. Rev Clin Esp 2007; 207: 86-90.
Jousimies-Somer HR, Summanen P, Citron DM, Baron EL, Wexler HM, Finegold S. Anaerobic Bacteriology Manual. 6th ed. Star Publishing Company. California; 2002.
Asha NJ, Wilcox MH. Laboratory diagnosis of Clostridium perfringens antibiotic-associated diarrhea. J Med Microbiol 2002; 51: 891-894.
Durai R. Epidemiology, Pathogenesis, and Management of Clostridium difficile Infection. Dig Dis Sci 2007; 52: 2958-2962.
Legaria MC, Lumelsky G, Rosetti S. Clostridium difficile-associated diarrhea from a general hospital in Argentina. Anaerobe 2003; 9:113-116.
Cánovas Domínguez C. Diarrea nosocomial por Clostridium difficile en mayores de 80 años. Rev Esp Geriatr Gerontol 2005; 40:70-77.
Brett MM, Rodhouse JC, Donovan TJ, Tebbutt GM, Hutchinson DN. Detection of Clostridium perfringens and its enterotoxin in cases of sporadic diarrhoea. J Clin Pathol 1992; 45:609-611.
Shetab R, Cohen SH, Prindiville T, Tang YJ, Cantrell M, Rahmani D, Silva JJr. Detection of Bacteroides fragilis Enterotoxin Gen by PCR. J Clin Microbiol 1998; 36: 1729-1732.
Meisel-Mikołajczyk F, Leszczyński P, van Belkum A, Pituch H, Obuch-Woszczayński P, Rouyan GH S. Enterotoxin-producing Bacteroides fragilis (ETBF) Strains in Stool Samples Submitted for Testing of Clostridium difficile and its Toxins. Anaerobe 1999; 5: 217-219.
Cáceres M, Zhang G, Weintraub A, Nord C. Prevalence and Antimicrobial Susceptibility of Enterotoxigenic Bacteroides fragilis in Children with diarrohea in Nicaragua. Anaerobe 2000; 6:143-148.
Krzyzanowssky F, Avila-Campos MJ. Detection of non-enterotoxigenic and enterotoxigenic Bacteroides fragilis in stool samples from children in São Paulo, Brazil. Rev Inst Med Trop S Paulo 2003; 45: 225-227.
Durmaz B, Dalgalar M, Durmaz R. Prevalence of Enterotoxigenic Bacteroides fragilis in patients with diarrhea: A controlled study. Anaerobe 2005; 11:318-321.
Alves Ferreira CE, Nakano V, Avila-Campos MJ. Cytotoxicity and antimicrobial susceptibility of Clostridium difficile isolated from hospitalized children with acute diarrhea. Anaerobe 2004; 10: 171-177.
Citron DM, Kwok YY, Appleman MD. In Vitro Activity of oritavancin (LY333328), vancomycin, clindamycin and metronidazole against Clostridium perfringens, Propionibacterium acnes, and anaerobic Gram-positive cocci. Anaerobe 2005; 11:93-95.
Wexler HM, Molitoris D, Finegold SM. In Vitro Activities of MK-826 (L-749,345) against 363 Strains of Anaerobic Bacteria. Antimicrob Agents Chemother 2000; 44:2222-2224.
Bishara J, Bloch Y, Garty M, Behor J, Samra Z. Antimicrobial resistance of Clostridium difficile isolates in a tertiary medical center, Israel. Diag Microbiol Infect Dis 2006; 54:141-144.
Quesada-Gómez C, Rodríguez C, Gamboa Coronado MM, Rodríguez-Cavallini E, Du T, Mulvey MR, et al. The emergence of Clostridium difficile NAP1 in Latin America. J Clin Microbiol 2010; 48:669-670.