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新型氟喹诺酮类抗菌药物的耐受性比较

Comparative tolerability of the newer fluoroquinolone antibacterials.

作者信息

Ball P, Mandell L, Niki Y, Tillotson G

机构信息

School of Biomedical Sciences, University of St Andrews, Fife, Scotland.

出版信息

Drug Saf. 1999 Nov;21(5):407-21. doi: 10.2165/00002018-199921050-00005.

Abstract

The most common adverse effects of the fluoroquinolones involve the gastrointestinal tract, skin and CNS, and are mainly mild and reversible. Of the gastrointestinal events, nausea and vomiting are the most common. Mild hepatic reactions are a class effect, usually presenting as mild transaminase level increases without clinical symptoms. However, postmarketing surveillance has revealed significant hepatotoxicity with trovafloxacin. It is not currently known whether the severe reactions to trovafloxacin are specific to that agent or simply represent an extreme of an emerging class effect. The enormous worldwide usage of, and extensive published adverse effect data on the other fluoroquinolones and naphthyridones suggests the former. In perspective, rare but serious hepatotoxicity has been reported with other fluoroquinolones and the overall incidence of trovafloxacin hepatotoxicity is not dissimilar to that reported with flucloxacillin and amoxicillin-clavulanic acid. CNS reactions vary in severity and include dizziness, convulsions (notably with lomefloxacin) and psychoses. Fluoroquinolones differ in their pro-convulsive activity, relating to their differing potential as gamma-aminobutyric acid antagonists and binding to the N-methyl-D-aspartate receptor. The basis for the increased seizure potential following the coadministration of nonsteroidal anti-inflammatory drugs with certain fluoroquinolones is not fully understood. Fluoroquinolone phototoxicity, caused by the generation of toxic free oxygen species under exposure to UVA radiation, is significantly more common with 8-halogenated compounds. Certain patient groups, e.g. patients with cystic fibrosis, are predisposed to this adverse effect. Murine photocarcinogenicity has been demonstrated with lomefloxacin, but no such effects have been reported in humans. Prolongation of the QTc interval is also a class effect, although cardiac arrhythmias have only been linked with sparfloxacin. Among the newer fluoroquinolones, clinically significant cardiac events are rare or absent but possible interactions in patients receiving other drugs capable of causi ng QT prolongation should be anticipated. Tendinitis and rupture, usually of the Achilles tendon, are rare, class-effects of fluoroquinolones, most frequently reported with pefloxacin. Predisposing factors include aging, corticosteroid use, renal disease, haemodialysis and transplantation. Use of fluoroquinolones in paediatric patients remains contentious. However, accruing human data suggest that restrictions on paediatric use imposed because of fluoroquinolone-induced cartilage damage in juvenile animals, may soon be relaxed. Data from over 1700 children in the UK failed to disclose arthropathy and extensive paediatric use of norfloxacin in Japan and ciprofloxacin in developing countries has been free of articular effects.

摘要

氟喹诺酮类药物最常见的不良反应累及胃肠道、皮肤和中枢神经系统,且大多轻微且可逆。在胃肠道不良反应中,恶心和呕吐最为常见。轻度肝脏反应是该类药物的共性,通常表现为转氨酶水平轻度升高但无临床症状。然而,上市后监测发现曲伐沙星具有显著的肝毒性。目前尚不清楚曲伐沙星的严重反应是该药物所特有的,还是仅仅代表了一种新出现的类效应的极端情况。全球范围内对其他氟喹诺酮类药物和萘啶酮类药物的大量使用以及广泛公布的不良反应数据表明是前者。从整体来看,其他氟喹诺酮类药物也有罕见但严重的肝毒性报道,曲伐沙星肝毒性的总体发生率与氟氯西林和阿莫西林 - 克拉维酸报道的发生率并无不同。中枢神经系统反应严重程度各异,包括头晕、惊厥(尤其是洛美沙星)和精神错乱。氟喹诺酮类药物的致惊厥活性不同,这与其作为γ-氨基丁酸拮抗剂的不同潜力以及与N-甲基-D-天冬氨酸受体的结合有关。非甾体抗炎药与某些氟喹诺酮类药物合用时癫痫发作风险增加的原因尚未完全明确。氟喹诺酮类药物的光毒性是由于在紫外线A辐射下产生有毒的活性氧所致,8-卤代化合物引起的光毒性明显更为常见。某些患者群体,如囊性纤维化患者,易发生这种不良反应。洛美沙星已在小鼠中证实有光致癌性,但人类中尚未有此类报道。QTc间期延长也是该类药物的共性,尽管心律失常仅与司帕沙星有关。在新型氟喹诺酮类药物中,临床上显著的心脏事件很少见或不存在,但对于正在接受其他可能导致QT间期延长药物治疗的患者,应预期可能存在相互作用。肌腱炎和肌腱断裂,通常是跟腱,是氟喹诺酮类药物罕见的类效应,最常报道于培氟沙星。易感因素包括年龄增长、使用皮质类固醇、肾脏疾病、血液透析和移植。氟喹诺酮类药物在儿科患者中的使用仍存在争议。然而,越来越多的人体数据表明,因氟喹诺酮类药物在幼年动物中导致软骨损伤而对儿科使用施加的限制可能很快会放宽。英国1700多名儿童的数据未发现关节病,日本诺氟沙星在儿科的广泛使用以及发展中国家环丙沙星的使用均未出现关节方面的影响。

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