Bailey Jason M, Erramouspe John
College of Pharmacy, Idaho State University, Pocatello, ID 83209-8333, USA.
Ann Pharmacother. 2004 Apr;38(4):634-40. doi: 10.1345/aph.1D451. Epub 2004 Feb 27.
To review the pharmacology, pharmacokinetics, adverse effects, drug interactions, dosing recommendations, and clinical efficacy of nitazoxanide, a new antiprotozoal/anthelmintic/antibacterial agent.
A MEDLINE search (1966-February 2004) of both human and animal research data published in the English language was conducted.
All primary and review articles pertaining to the MEDLINE search were reviewed for inclusion. Emphasis was placed on randomized, double-blind, placebo-controlled trials.
Nitazoxanide is approved for the treatment of giardiasis and cryptosporidiosis (first drug approved for the latter indication) in immune-competent children <12 years of age. Most studies in immune-competent patients have reported clinical and parasitologic response rates close to 80% and 70%, respectively, for both indications. Response rates have been lower in immune-compromised patients.
Nitazoxanide should be available for patients unable to tolerate or adhere to first-line therapy employed for these intestinal protozoa.
综述硝唑尼特(一种新型抗原生动物/抗蠕虫/抗菌药物)的药理学、药代动力学、不良反应、药物相互作用、给药建议及临床疗效。
对1966年至2004年2月期间以英文发表的人体和动物研究数据进行了MEDLINE检索。
对所有与MEDLINE检索相关的原始文章和综述文章进行评估以确定是否纳入。重点关注随机、双盲、安慰剂对照试验。
硝唑尼特已被批准用于治疗12岁以下免疫功能正常儿童的贾第虫病和隐孢子虫病(首个获批用于后一适应症的药物)。大多数针对免疫功能正常患者的研究报告称,这两种适应症的临床和寄生虫学缓解率分别接近80%和70%。免疫功能低下患者的缓解率较低。
对于无法耐受或坚持使用针对这些肠道原生动物的一线治疗方案的患者,硝唑尼特应可供使用。