Halsey Jennifer
West Allis Memorial Hospital, 8901 West Lincoln Avenue, West Allis, WI 53227, USA.
Am J Health Syst Pharm. 2008 Apr 15;65(8):705-15. doi: 10.2146/ajhp070077.
Current and future treatment modalities for Clostridium difficile-associated disease (CDAD) are reviewed.
C. difficile, an anaerobic, spore-forming, gram-positive [corrected] rod, is the enteric pathogen most frequently identified in patients with antibiotic-associated, nosocomially acquired diarrhea. Infection can lead to severe gastrointestinal illness which can develop into pseudomembranous colitis. Recent outbreaks in North America involved more virulent C. difficile strains, more severe infections, and more complicated treatment courses. Because of the potential for increased toxin-associated damage due to increased toxin exposure time, CDAD treatment often involves cessation of the inciting antibiotic, C. difficile-targeted antibiotic therapy, electrolyte normalization, fluid replacement, and antimotility agent avoidance. First-line therapy for CDAD is treatment with the antibiotic metronidazole. Vancomycin is often used in more severe cases and for treatment-resistant organisms. Treatment regimens may also include probiotics, bile-acid sequestrants, and, in limited cases, intravenous immunoglobulin (IVIG). Alternative treatments for refractory and persistent CDAD include intracolonic vancomycin, nitazoxanide, rifaximin, IVIG, and probiotics. Several target proteins have been proposed for C. difficile vaccine production, including the flagellar cap protein FliD, flagellin FLiC, a cell wall protein (Cwp) (comprising amino- and carboxyl-terminal domains), a protease Cwp 84, and toxins A and B. Rarely, pseudomembranous colitis, a severe complication of CDAD, must be treated through surgical intervention.
CDAD is a major concern for health care systems and clinicians. New diagnostic tests with increased sensitivity for detecting CDAD with a short turnaround time are necessary for early treatment and prevention. Continued research for more effective treatments and vaccine development for CDAD is also needed.
综述艰难梭菌相关性疾病(CDAD)当前及未来的治疗方式。
艰难梭菌是一种厌氧、产芽孢、革兰氏阳性[已修正]杆菌,是抗生素相关性医院获得性腹泻患者中最常鉴定出的肠道病原体。感染可导致严重的胃肠道疾病,进而发展为假膜性结肠炎。北美近期的疫情涉及更具毒性的艰难梭菌菌株、更严重的感染以及更复杂的治疗过程。由于毒素暴露时间增加可能导致毒素相关损伤加重,CDAD治疗通常包括停用引发感染的抗生素、针对艰难梭菌的抗生素治疗、电解质正常化、补液以及避免使用抗动力剂。CDAD的一线治疗是使用甲硝唑抗生素。万古霉素常用于更严重的病例以及对治疗耐药的病原体。治疗方案还可能包括益生菌、胆汁酸螯合剂,在有限的情况下,还包括静脉注射免疫球蛋白(IVIG)。难治性和持续性CDAD的替代治疗包括结肠内万古霉素、硝唑尼特、利福昔明、IVIG和益生菌。已提出几种用于艰难梭菌疫苗生产的靶蛋白,包括鞭毛帽蛋白FliD、鞭毛蛋白FLiC、一种细胞壁蛋白(Cwp)(由氨基端和羧基端结构域组成)、蛋白酶Cwp 84以及毒素A和B。罕见情况下,假膜性结肠炎作为CDAD的一种严重并发症,必须通过手术干预进行治疗。
CDAD是医疗保健系统和临床医生主要关注的问题。需要新的诊断测试,以提高检测CDAD的灵敏度并缩短周转时间,以便早期治疗和预防。还需要继续开展针对CDAD更有效治疗方法和疫苗研发的研究。