• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

GPO-VIR(司他夫定+拉米夫定+奈韦拉平)在初治成年HIV患者中的疗效及不良反应。

The efficacy and adverse effects of GPO-VIR (stavudine+lamivudine+nevirapine) in treatment-naïve adult HIV patients.

作者信息

Tin Ei Ei, Bowonwatanuwong Chureeratana, Desakorn Varunee, Wilairatana Polrat, Krudsood Srivicha, Pitisuttithum Punnee

机构信息

Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

出版信息

Southeast Asian J Trop Med Public Health. 2005 Mar;36(2):362-9.

PMID:15916042
Abstract

A descriptive, combined retrospective and prospective study was conducted at the Anonymous Clinic, Chon Buri Hospital, Chon Buri Province, Thailand from November 10, 2003 to January 4, 2004. A total of 83 adult HIV-treatment-naïve patients undergoing treatment with GPO-VIR (stavudine, lamivudine, and nevirapine) for at least one year were studied. The objectives of the study were to assess the efficacy of GPO-VIR by evaluating body weight changes, CD4 T-cell count changes, the occurrence of opportunistic infections, and long-term side effects, such as lipodystrophy, during treatment. Of 83 studied patients, approximately half (52.3%) of them had a body weight increase > 10% of pre-treatment body weight after 12 months treatment. After taking GPO-VIR, CD4 T-cell counts increased rapidly, by a median of 78 x 10(6) cells/l during the first three months. 39.5% of the patients attained median CD4 counts > 200 x 10(6) cells/I, and 11.6% achieved > 500 x 10(6) cells/l after 2 years of treatment. The occurrence of opportunistic infections was significantly lower after treatment with GPO-VIR (p = 0.001). Subjective assessment of lipodystrophy by physicians and patients showed that 16.8% had symptoms of lipodystrophy within 2 years of GPO-VIR treatment. There was a significant association between older age group (40-49 years) and occurrence of lipodystrophy (p = 0.043). GPO-VIR is an inexpensive and effective antiretroviral drug regimen for initiating treatment of naïve patients, but careful assessment for lipodystrophy is necessary, especially after one year of treatment.

摘要

2003年11月10日至2004年1月4日,在泰国春武里府春武里医院的匿名诊所进行了一项描述性、回顾性与前瞻性相结合的研究。共研究了83例初治成人HIV患者,这些患者接受GPO-VIR(司他夫定、拉米夫定和奈韦拉平)治疗至少一年。该研究的目的是通过评估体重变化、CD4 T细胞计数变化、机会性感染的发生情况以及治疗期间的长期副作用(如脂肪代谢障碍)来评估GPO-VIR的疗效。在83例研究患者中,约一半(52.3%)在治疗12个月后体重增加超过治疗前体重的10%。服用GPO-VIR后,CD4 T细胞计数迅速增加,在前三个月中值增加了78×10⁶个细胞/升。39.5%的患者在治疗2年后CD4计数中值>200×10⁶个细胞/升,11.6%的患者达到>500×10⁶个细胞/升。接受GPO-VIR治疗后,机会性感染的发生率显著降低(p = 0.001)。医生和患者对脂肪代谢障碍的主观评估显示,在接受GPO-VIR治疗的2年内,16.8%的患者有脂肪代谢障碍症状。年龄较大的组(40 - 49岁)与脂肪代谢障碍的发生之间存在显著关联(p = 0.043)。GPO-VIR是一种用于初治患者开始治疗的廉价且有效的抗逆转录病毒药物方案,但需要仔细评估脂肪代谢障碍,尤其是在治疗一年后。

相似文献

1
The efficacy and adverse effects of GPO-VIR (stavudine+lamivudine+nevirapine) in treatment-naïve adult HIV patients.GPO-VIR(司他夫定+拉米夫定+奈韦拉平)在初治成年HIV患者中的疗效及不良反应。
Southeast Asian J Trop Med Public Health. 2005 Mar;36(2):362-9.
2
Efficacy and safety of generic fixed-dose combination of stavudine, lamivudine and nevirapine (GPO-vir) in advanced HIV infection.司他夫定、拉米夫定和奈韦拉平通用固定剂量复方制剂(GPO-vir)治疗晚期HIV感染的疗效与安全性
J Med Assoc Thai. 2006 Sep;89(9):1472-8.
3
Baseline CD4 cell counts and outcomes among adult treatment naive HIV patients after taking fixed dose combination GPO-VIR-S and GPO-VIR-Z in Thailand.泰国成年初治HIV患者服用固定剂量复方制剂GPO-VIR-S和GPO-VIR-Z后的基线CD4细胞计数及治疗结果
Southeast Asian J Trop Med Public Health. 2013 Mar;44(2):232-43.
4
Efficacy of a generic fixed-dose combination of stavudine, lamivudine and nevirapine (GPO-VIR) in Thai HIV-infected patients.司他夫定、拉米夫定和奈韦拉平通用固定剂量组合(GPO-VIR)对泰国HIV感染患者的疗效。
J Med Assoc Thai. 2007 Feb;90(2):237-43.
5
Effectiveness of fixed-dose combination stavudine, lamivudine and nevirapine (GPO-VIR) for treatment of naïve HIV patients in Thailand: a 3-year follow-up.固定剂量组合司他夫定、拉米夫定和奈韦拉平(GPO-VIR)治疗泰国初治HIV患者的疗效:3年随访
Southeast Asian J Trop Med Public Health. 2011 Nov;42(6):1414-22.
6
Plasma nevirapine levels and 24-week efficacy of a fixed-dose combination of stavudine, lamivudine and nevirapine (GPO-VIR) among Thai HIV-infected patients.泰国HIV感染患者中司他夫定、拉米夫定和奈韦拉平固定剂量复方制剂(GPO-VIR)的血浆奈韦拉平水平及24周疗效
J Med Assoc Thai. 2007 Feb;90(2):244-50.
7
Weight and body shape changes in a treatment-naive population after 6 months of nevirapine-based generic highly active antiretroviral therapy in South India.在印度南部,初治人群接受基于奈韦拉平的通用型高效抗逆转录病毒疗法6个月后的体重和体型变化。
Clin Infect Dis. 2007 Jan 15;44(2):295-300. doi: 10.1086/510491. Epub 2006 Dec 11.
8
Safety and efficacy of a simplified fixed-dose combination of stavudine, lamivudine and nevirapine (GPO-VIR) for the treatment of advanced HIV-infected patients: a 24-week study.司他夫定、拉米夫定和奈韦拉平简化固定剂量组合(GPO-VIR)治疗晚期HIV感染患者的安全性和有效性:一项为期24周的研究。
J Med Assoc Thai. 2004 Jul;87(7):760-7.
9
Effect of highly active antiretroviral therapy on CD4 count and weight in AIDS patients seen at the UITH, Ilorin.高效抗逆转录病毒疗法对伊洛林大学教学医院收治的艾滋病患者CD4细胞计数和体重的影响。
Niger J Clin Pract. 2008 Dec;11(4):312-5.
10
[Clinical safety of a generic fixed-dose combination of stavudine/lamivudine/névirapine (Triomune). Study of 297 cases in Togo].司他夫定/拉米夫定/奈韦拉平(三协唯)通用固定剂量复方制剂的临床安全性。多哥297例病例研究
Bull Soc Pathol Exot. 2008 Dec;101(5):404-6.

引用本文的文献

1
HIV/AIDS and lipodystrophy: implications for clinical management in resource-limited settings.艾滋病毒/艾滋病与脂肪代谢障碍:资源有限环境下对临床管理的影响
J Int AIDS Soc. 2015 Jan 15;18(1):19033. doi: 10.7448/IAS.18.1.19033. eCollection 2015.
2
Effectiveness and metabolic complications after 96 weeks of a generic fixed-dose combination of stavudine, lamivudine, and nevirapine among antiretroviral-naive advanced HIV-infected patients in Thailand: A prospective study.泰国未接受过抗逆转录病毒治疗的晚期HIV感染初治患者使用司他夫定、拉米夫定和奈韦拉平通用固定剂量组合96周后的疗效及代谢并发症:一项前瞻性研究
Curr Ther Res Clin Exp. 2008 Feb;69(1):90-100. doi: 10.1016/j.curtheres.2008.02.007.
3
Rapid CD4 decline after interruption of non-nucleoside reverse transcriptase inhibitor-based antiretroviral therapy in a resource-limited setting.
在资源有限的环境中,中断基于非核苷类逆转录酶抑制剂的抗逆转录病毒治疗后CD4快速下降。
AIDS Res Ther. 2007 Nov 21;4:26. doi: 10.1186/1742-6405-4-26.
4
Safety and efficacy of a generic fixed-dose combination of stavudine, lamivudine and nevirapine antiretroviral therapy between HIV-infected patients with baseline CD4 <50 versus CD4 > or = 50 cells/mm3.基线CD4<50个细胞/立方毫米与CD4≥50个细胞/立方毫米的HIV感染患者之间,司他夫定、拉米夫定和奈韦拉平抗逆转录病毒疗法通用固定剂量组合的安全性和疗效。
AIDS Res Ther. 2007 Mar 13;4:6. doi: 10.1186/1742-6405-4-6.
5
Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole.同时接受基于奈韦拉平的抗逆转录病毒疗法和氟康唑治疗的HIV感染患者的血浆奈韦拉平水平、不良事件及抗逆转录病毒疗法的疗效
BMC Infect Dis. 2007 Mar 12;7:14. doi: 10.1186/1471-2334-7-14.