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头孢呋辛酯与多西环素治疗早期莱姆病伴游走性红斑患者的比较。

Comparison of cefuroxime axetil and doxycycline in treatment of patients with early Lyme disease associated with erythema migrans.

作者信息

Luger S W, Paparone P, Wormser G P, Nadelman R B, Grunwaldt E, Gomez G, Wisniewski M, Collins J J

机构信息

Lyme Disease Center for South Jersey, Absecon, New Jersey, USA.

出版信息

Antimicrob Agents Chemother. 1995 Mar;39(3):661-7. doi: 10.1128/AAC.39.3.661.

Abstract

A randomized, multicenter, investigator-blinded clinical trial was undertaken in order to compare the efficacies of cefuroxime axetil and doxycycline in the treatment of patients with Lyme disease associated with erythema migrans. A total of 232 patients with physician-documented erythema migrans were treated orally for 20 days with either cefuroxime axetil, 500 mg twice daily (119 patients), or doxycycline, 100 mg three times daily (113 patients), and clinical evaluations were conducted during treatment (8 to 12 days) and at 1 to 5 days and 1, 3, 6, 9, and 12 months posttreatment. Patients were assessed as to the resolution of erythema migrans and of the signs and symptoms related to early Lyme disease as well as to the prevention of late Lyme disease. A satisfactory clinical outcome (success or improvement) was achieved in 90 of 100 (90%) evaluable patients treated with cefuroxime axetil and in 89 of 94 (95%) patients treated with doxycycline (difference, -5%; 95% confidence interval, -12 to 3%). Patients with paresthesia, arthralgia, or irritability at enrollment were at higher risk for an unsatisfactory clinical outcome at 1 month posttreatment. Of the patients with satisfactory outcomes at 1 month posttreatment who were evaluable at 1 year posttreatment, a satisfactory outcome was achieved in 62 of 65 (95%) and in 53 of 53 (100%) patients treated with cefuroxime axetil and doxycycline, respectively (difference, -5%; 95% confidence interval, -10 to 4%). Twenty-eight percent of patients treated with doxycycline and 17% of those treated with cefuroxime axetil had one or more drug-related adverse events (P = 0.041). Doxycycline was associated with more photosensitivity reactions (6% compared with 0% for patients treated with cefuroxime axetil; P=0.006), and cefuroxime axetil was associated with more cases of diarrhea (5% compared with 0% for patients treated with doxycycline; P=0.030). Jarisch-Herxheimer reactions occurred in 12% of the patients in each treatment group. In summary, cefuroxime axetil is well tolerated and appears to be equally as effective as doxycycline in the treatment of early Lyme disease and in preventing the subsequent development of late Lyme disease.

摘要

为比较头孢呋辛酯和多西环素治疗莱姆病合并游走性红斑患者的疗效,进行了一项随机、多中心、研究者设盲的临床试验。共有232例经医生记录有游走性红斑的患者,分别口服头孢呋辛酯(500mg,每日2次,共119例)或多西环素(100mg,每日3次,共113例),疗程20天。在治疗期间(8至12天)以及治疗后1至5天、1、3、6、9和12个月进行临床评估。评估患者游走性红斑的消退情况、与早期莱姆病相关的体征和症状以及晚期莱姆病的预防情况。接受头孢呋辛酯治疗的100例可评估患者中有90例(90%)获得了满意的临床结局(成功或改善),接受多西环素治疗的94例患者中有89例(95%)获得了满意的临床结局(差异为-5%;95%置信区间为-12%至3%)。入组时伴有感觉异常、关节痛或易怒的患者在治疗后1个月出现不满意临床结局的风险较高。在治疗后随访1年可评估的治疗后1个月有满意结局的患者中,接受头孢呋辛酯和多西环素治疗的患者分别有65例中的62例(95%)和53例中的53例(100%)获得了满意结局(差异为-5%;95%置信区间为-10%至4%)。接受多西环素治疗的患者中有28%、接受头孢呋辛酯治疗的患者中有17%发生了1种或更多种药物相关不良事件(P=0.041)。多西环素与更多的光敏反应相关(接受头孢呋辛酯治疗的患者为0%;P=0.006),头孢呋辛酯与更多的腹泻病例相关(接受多西环素治疗的患者为0%;P=0.030)。每个治疗组中均有12% 的患者发生了雅-赫反应。总之,头孢呋辛酯耐受性良好,在治疗早期莱姆病以及预防晚期莱姆病后续发展方面似乎与多西环素同样有效。

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