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加巴喷丁与伐昔洛韦联合治疗急性带状疱疹患者后带状疱疹后神经痛的发生率:开放标签研究

Incidence of postherpetic neuralgia after combination treatment with gabapentin and valacyclovir in patients with acute herpes zoster: open-label study.

作者信息

Lapolla Whitney, Digiorgio Catherine, Haitz Kassie, Magel George, Mendoza Natalia, Grady James, Lu Wenzhe, Tyring Stephen

机构信息

Center for Clinical Studies, 451 N Texas Ave, Webster, TX 77598, USA.

出版信息

Arch Dermatol. 2011 Aug;147(8):901-7. doi: 10.1001/archdermatol.2011.81. Epub 2011 Apr 11.

Abstract

OBJECTIVE

To evaluate the efficacy of treatment with gabapentin plus valacyclovir hydrochloride for the prevention of postherpetic neuralgia in patients with acute herpes zoster.

DESIGN

Uncontrolled, open-label study.

SETTING

A private dermatology clinic.

PARTICIPANTS

Consecutive immunocompetent adults (age, ≥ 50 years) who presented with herpes zoster within 72 hours of vesicle formation with moderate to severe pain (≥ 4 on the 10-point Likert scale) were recruited for study participation. Intervention The patients received 1000 mg of valacylovir hydrochloride 3 times a day for 7 days plus gabapentin at an initial dose of 300 mg/d, titrated up to a maximum of 3600 mg/d, side effects permitting.

MAIN OUTCOME MEASURES

Proportion of patients with zoster pain (pain > 0) at 3, 4, and 6 months as well as average pain severity, the proportion of patients with sleep disturbance, and quality-of-life measures (determined by the Medical Outcome Study Short Form 36-Item Health Survey).

RESULTS

A total of 133 patients (mean age, 64.6 years) were enrolled in the study. The overall incidence of zoster pain at 6 months was 9.8%.

CONCLUSION

The combination of gabapentin and valacyclovir administered acutely in patients with herpes zoster reduces the incidence of postherpetic neuralgia. Trial Registration clinicaltrials.gov Identifier: NCT01250561.

摘要

目的

评估加巴喷丁联合盐酸伐昔洛韦治疗预防急性带状疱疹患者发生带状疱疹后神经痛的疗效。

设计

非对照、开放标签研究。

地点

一家私立皮肤科诊所。

参与者

连续纳入年龄≥50岁、在水疱形成72小时内出现带状疱疹且伴有中度至重度疼痛(10分李克特量表评分≥4分)的免疫功能正常的成年人参与研究。干预措施:患者接受盐酸伐昔洛韦1000mg,每日3次,共7天,加巴喷丁初始剂量为300mg/d,根据副作用情况逐渐滴定至最大剂量3600mg/d。

主要观察指标

3个月、4个月和6个月时带状疱疹疼痛(疼痛>0)患者的比例、平均疼痛严重程度、睡眠障碍患者的比例以及生活质量指标(由医学结局研究简明健康调查36项量表确定)。

结果

共有133例患者(平均年龄64.6岁)纳入研究。6个月时带状疱疹疼痛的总体发生率为9.8%。

结论

带状疱疹患者急性使用加巴喷丁和伐昔洛韦联合治疗可降低带状疱疹后神经痛的发生率。试验注册:clinicaltrials.gov标识符:NCT01250561。

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