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环丙沙星、氧氟沙星、左氧氟沙星、加替沙星和莫西沙星相关的尖端扭转型室速发生率。

Rates of torsades de pointes associated with ciprofloxacin, ofloxacin, levofloxacin, gatifloxacin, and moxifloxacin.

作者信息

Frothingham R

机构信息

Infectious Diseases Section, Veterans Affairs Medical Center, Durham, North Carolina 27705, USA.

出版信息

Pharmacotherapy. 2001 Dec;21(12):1468-72. doi: 10.1592/phco.21.20.1468.34482.

Abstract

STUDY OBJECTIVE

To compare the rates of torsades de pointes associated with ciprofloxacin, ofloxacin, levofloxacin, gatifloxacin, and moxifloxacin administration.

DESIGN

Retrospective database analysis.

INTERVENTION

Evaluation of reported rates of torsades de pointes in patients who received these quinolones between January 1, 1996, and May 2, 2001.

MEASUREMENTS AND MAIN RESULTS

In the United States, 25 cases of torsades de pointes associated with these quinolones (ciprofloxacin 2, ofloxacin 2, levofloxacin 13, gatifloxacin 8, moxifloxacin 0) were identified. Ciprofloxacin was associated with a significantly lower rate of torsades de pointes (0.3 cases/10 million prescriptions, 95% confidence interval [CI] 0.0-1.1) than levofloxacin (5.4/10 million, 95% CI 2.9-9.3, p<0.001) or gatifloxacin (27/10 million, 95% CI 12-53, p<0.001 for comparison with ciprofloxacin or levofloxacin). When the analysis was limited to the first 16 months after initial U.S. approval of the agent, the rates for levofloxacin (16/10 million) and gatifloxacin (27/10 million) were similar (p>0.5).

CONCLUSION

Levofloxacin should be administered with caution in patients with risk factors for QT prolongation. Gatifloxacin should be avoided in the same patient population, and the recommended dosage of 400 mg/day should not be exceeded.

摘要

研究目的

比较环丙沙星、氧氟沙星、左氧氟沙星、加替沙星和莫西沙星给药后发生尖端扭转型室速的发生率。

设计

回顾性数据库分析。

干预措施

评估1996年1月1日至2001年5月2日期间接受这些喹诺酮类药物治疗的患者中报告的尖端扭转型室速发生率。

测量指标及主要结果

在美国,共识别出25例与这些喹诺酮类药物相关的尖端扭转型室速病例(环丙沙星2例、氧氟沙星2例、左氧氟沙星13例、加替沙星8例、莫西沙星0例)。环丙沙星发生尖端扭转型室速的发生率(0.3例/1000万处方,95%置信区间[CI]0.0 - 1.1)显著低于左氧氟沙星(5.4/1000万,95%CI 2.9 - 9.3,p<0.001)或加替沙星(27/1000万,与环丙沙星或左氧氟沙星比较,95%CI 12 - 53,p<0.001)。当分析仅限于美国首次批准该药物后的前16个月时,左氧氟沙星(16/1000万)和加替沙星(27/1000万)的发生率相似(p>0.5)。

结论

对于有QT间期延长危险因素的患者,应谨慎使用左氧氟沙星。在同一患者群体中应避免使用加替沙星,且不应超过推荐剂量400毫克/天。

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