Peters D H, Clissold S P
Adis International Limited, Auckland, New Zealand.
Drugs. 1992 Jul;44(1):117-64. doi: 10.2165/00003495-199244010-00009.
Clarithromycin is an acid-stable orally administered macrolide antimicrobial drug, structurally related to erythromycin. It has a broad spectrum of antimicrobial activity, similar to that of erythromycin and inhibits a range of Gram-positive and Gram-negative organisms, atypical pathogens and some anaerobes. Significantly, clarithromycin demonstrates greater in vitro activity than erythromycin against certain pathogens including Bacteroides melaninogenicus, Chlamydia pneumoniae, Chlamydia trachomatis, Mycobacterium chelonae subspecies--chelonae and--abscessus, Mycobacterium leprae, Mycobacterium marinum, Mycobacterium avium complex, Legionella spp. and, when combined with its 14-hydroxy metabolite, against Haemophilus influenzae. However, bacterial strains resistant to erythromycin are also generally resistant to clarithromycin. The antimicrobial activity of clarithromycin appears to be enhanced by the formation in vivo of the microbiologically active 14-hydroxy metabolite. In combination, additive or synergistic activity against a variety of pathogens including Haemophilus influenzae, Moraxella catarrhalis, Legionella species (principally Legionella pneumophila) and various staphylococci and streptococci has been demonstrated. Clarithromycin has a superior pharmacokinetic profile to that of erythromycin, allowing the benefits of twice daily administration with the potential for increased compliance among outpatients where a more frequent regimen for erythromycin might otherwise be indicated. The clinical efficacy of clarithromycin has been confirmed in the treatment of infections of the lower and upper respiratory tracts (including those associated with atypical pathogens), skin/soft tissues, and in paediatrics. Clarithromycin was as effective as erythromycin and other appropriate drugs including beta-lactams (penicillins and cephalosporins) in some of the above infections. A most promising indication for clarithromycin appears to be in the treatment of immunocompromised patients infected with M. avium complex, M. chelonae sp. and Toxoplasma sp. Small initial trials in this setting reveal clarithromycin alone or in combination with other antimicrobials to be effective in the eradication or amelioration of these infections. Noncomparative studies have provided preliminary evidence for the effectiveness of clarithromycin in the treatment of infections of the urogenital tract, oromaxillofacial and ophthalmic areas. However, the promising in vitro and preliminary in vivo activity of clarithromycin against Mycobacterium leprae and Helicobacter pylori warrant further clinical trials to assess its efficacy in patients with these infections. Despite the improved pharmacokinetic profile and in vitro antimicrobial activity of clarithromycin over erythromycin, comparative studies of patients with community-acquired infections reveal the 2 drugs to be of equivalent efficacy. However, clarithromycin demonstrates greater tolerability, principally by inducing fewer gastrointestinal disturbances.(ABSTRACT TRUNCATED AT 400 WORDS)
克拉霉素是一种酸稳定的口服大环内酯类抗菌药物,在结构上与红霉素相关。它具有广泛的抗菌活性,与红霉素相似,可抑制多种革兰氏阳性菌和革兰氏阴性菌、非典型病原体及一些厌氧菌。值得注意的是,克拉霉素在体外对某些病原体的活性比红霉素更强,这些病原体包括产黑色素拟杆菌、肺炎衣原体、沙眼衣原体、龟分枝杆菌龟分枝杆菌亚种和脓肿亚种、麻风分枝杆菌、海分枝杆菌、鸟分枝杆菌复合体、军团菌属,并且当其与14 - 羟基代谢物联合使用时,对流感嗜血杆菌也有活性。然而,对红霉素耐药的细菌菌株通常对克拉霉素也耐药。克拉霉素的抗菌活性似乎因体内形成具有微生物活性的14 - 羟基代谢物而增强。联合使用时,已证明对多种病原体具有相加或协同活性,这些病原体包括流感嗜血杆菌、卡他莫拉菌、军团菌属(主要是嗜肺军团菌)以及各种葡萄球菌和链球菌。克拉霉素具有比红霉素更优的药代动力学特征,允许每日给药两次,这对于门诊患者可能更易依从,否则红霉素可能需要更频繁的给药方案。克拉霉素的临床疗效已在治疗上下呼吸道感染(包括与非典型病原体相关的感染)、皮肤/软组织感染以及儿科感染中得到证实。在上述一些感染中,克拉霉素与红霉素及其他合适药物(包括β - 内酰胺类药物(青霉素和头孢菌素))疗效相当。克拉霉素最有前景的适应证似乎是用于治疗感染鸟分枝杆菌复合体、龟分枝杆菌属和弓形虫属的免疫功能低下患者。在这种情况下的小型初步试验表明,单独使用克拉霉素或与其他抗菌药物联合使用对根除或改善这些感染有效。非对照研究为克拉霉素治疗泌尿生殖道、口腔颌面和眼部感染的有效性提供了初步证据。然而,克拉霉素对麻风分枝杆菌和幽门螺杆菌有前景的体外和初步体内活性,需要进一步的临床试验来评估其在这些感染患者中的疗效。尽管克拉霉素的药代动力学特征和体外抗菌活性优于红霉素,但对社区获得性感染患者的比较研究表明这两种药物疗效相当。然而,克拉霉素耐受性更好,主要是因为引起的胃肠道不适较少。(摘要截选至400字)