• 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

相似文献

1
Virologic suppression and CD4+ cell count recovery after initiation of raltegravir or efavirenz-containing HIV treatment regimens.拉替拉韦或依非韦伦为基础的 HIV 治疗方案起始后病毒学抑制和 CD4+ 细胞计数恢复。
AIDS. 2018 Jan 14;32(2):261-266. doi: 10.1097/QAD.0000000000001668.
2
Incident AIDS or Death After Initiation of Human Immunodeficiency Virus Treatment Regimens Including Raltegravir or Efavirenz Among Adults in the United States.美国成年人开始使用包括拉替拉韦或依非韦伦在内的人类免疫缺陷病毒治疗方案后的艾滋病发病或死亡情况。
Clin Infect Dis. 2017 Jun 1;64(11):1591-1596. doi: 10.1093/cid/cix199.
3
Long-term treatment with raltegravir or efavirenz combined with tenofovir/emtricitabine for treatment-naive human immunodeficiency virus-1-infected patients: 156-week results from STARTMRK.初治人类免疫缺陷病毒 1 型感染者接受拉替拉韦或依非韦伦联合替诺福韦/恩曲他滨治疗:STARTMRK 的 156 周结果。
Clin Infect Dis. 2011 Oct;53(8):807-16. doi: 10.1093/cid/cir510.
4
Body composition and metabolic outcomes after 96 weeks of treatment with ritonavir-boosted lopinavir plus either nucleoside or nucleotide reverse transcriptase inhibitors or raltegravir in patients with HIV with virological failure of a standard first-line antiretroviral therapy regimen: a substudy of the randomised, open-label, non-inferiority SECOND-LINE study.在标准一线抗逆转录病毒治疗方案失败的 HIV 患者中,经过 96 周利托那韦增强洛匹那韦加核苷或核苷酸逆转录酶抑制剂或拉替拉韦治疗后的身体成分和代谢结果:一项随机、开放标签、非劣效性 SECOND-LINE 研究的子研究。
Lancet HIV. 2017 Jan;4(1):e13-e20. doi: 10.1016/S2352-3018(16)30189-8. Epub 2016 Nov 1.
5
Raltegravir versus Efavirenz regimens in treatment-naive HIV-1-infected patients: 96-week efficacy, durability, subgroup, safety, and metabolic analyses.拉替拉韦与依非韦伦方案治疗初治 HIV-1 感染患者:96 周疗效、持久性、亚组、安全性和代谢分析。
J Acquir Immune Defic Syndr. 2010 Sep;55(1):39-48. doi: 10.1097/QAI.0b013e3181da1287.
6
Efavirenz versus nevirapine-based initial treatment of HIV infection: clinical and virological outcomes in Southern African adults.依非韦伦与基于奈韦拉平的HIV感染初始治疗:南部非洲成年人的临床和病毒学结果
AIDS. 2008 Oct 18;22(16):2117-25. doi: 10.1097/QAD.0b013e328310407e.
7
[Efectiveness and safety of switching to raltegravir-based regimen in dyslipidemic HIV-infected patients receiving antiretroviral therapy at Arriaran Foundation].[在阿里亚兰基金会接受抗逆转录病毒治疗的血脂异常HIV感染患者中换用基于拉替拉韦方案的有效性和安全性]
Rev Chilena Infectol. 2019 Aug;36(4):490-495. doi: 10.4067/S0716-10182019000400490.
8
Once-daily highly active antiretroviral therapy for HIV-infected children: safety and efficacy of an efavirenz-containing regimen.对感染HIV的儿童进行每日一次的高效抗逆转录病毒治疗:含依非韦伦方案的安全性和疗效。
Pediatrics. 2007 Mar;119(3):e705-15. doi: 10.1542/peds.2006-1367. Epub 2007 Feb 16.
9
Adherence, virological and immunological outcomes for HIV-infected veterans starting combination antiretroviral therapies.开始联合抗逆转录病毒治疗的HIV感染退伍军人的依从性、病毒学和免疫学结果。
AIDS. 2007 Jul 31;21(12):1579-89. doi: 10.1097/QAD.0b013e3281532b31.
10
Intensification of a triple-nucleoside regimen with tenofovir or efavirenz in HIV-1-infected patients with virological suppression.在病毒学抑制的HIV-1感染患者中,用替诺福韦或依非韦伦强化三联核苷治疗方案。
AIDS. 2007 Apr 23;21(7):813-23. doi: 10.1097/QAD.0b013e32805e8753.

引用本文的文献

1
Assessing advances in three decades of clinical antiretroviral therapy on the HIV-1 reservoir.评估三十年来临床抗逆转录病毒疗法在HIV-1储存库方面取得的进展。
J Clin Invest. 2024 Nov 29;135(2):e183952. doi: 10.1172/JCI183952.
2
Characteristics and influencing factors of immunological non-responders in HIV-1-infected patients receiving antiretroviral therapy: a cross-sectional study in Guangxi.广西地区接受抗反转录病毒治疗的 HIV-1 感染者免疫无应答者的特征及其影响因素:一项横断面研究。
Sci Rep. 2024 Nov 12;14(1):27739. doi: 10.1038/s41598-024-79449-1.
3
Multilevel Resilience and HIV Virologic Suppression Among African American/Black Adults in the Southeastern United States.美国东南部非洲裔/黑人成年人的多层次韧性和 HIV 病毒抑制
J Racial Ethn Health Disparities. 2024 Feb;11(1):313-325. doi: 10.1007/s40615-023-01520-w. Epub 2023 Apr 12.
4
Analysis of the Influencing Factors of Immunological Nonresponders in Wuhan, China.中国武汉免疫无应答者的影响因素分析
Can J Infect Dis Med Microbiol. 2022 Aug 8;2022:5638396. doi: 10.1155/2022/5638396. eCollection 2022.
5
Determinants of long-term survival in late HIV presenters: The prospective PISCIS cohort study.晚期HIV感染者长期生存的决定因素:前瞻性PISCIS队列研究。
EClinicalMedicine. 2022 Aug 3;52:101600. doi: 10.1016/j.eclinm.2022.101600. eCollection 2022 Oct.
6
Current and Past Immunodeficiency Are Associated With Higher Hospitalization Rates Among Persons on Virologically Suppressive Antiretroviral Therapy for up to 11 Years.当前和既往免疫缺陷与接受抗病毒治疗长达 11 年的病毒学抑制的患者较高的住院率相关。
J Infect Dis. 2021 Aug 16;224(4):657-666. doi: 10.1093/infdis/jiaa786. Epub 2020 Dec 26.
7
Incomplete immune reconstitution in HIV/AIDS patients on antiretroviral therapy: Challenges of immunological non-responders.在接受抗逆转录病毒治疗的 HIV/AIDS 患者中不完全免疫重建:免疫无应答者面临的挑战。
J Leukoc Biol. 2020 Apr;107(4):597-612. doi: 10.1002/JLB.4MR1019-189R. Epub 2020 Jan 22.

本文引用的文献

1
Transportability of Trial Results Using Inverse Odds of Sampling Weights.使用抽样权重的逆概率进行试验结果的可转移性
Am J Epidemiol. 2017 Oct 15;186(8):1010-1014. doi: 10.1093/aje/kwx164.
2
Effect of HIV-infection and cumulative viral load on age-related decline in grip strength.HIV感染及累积病毒载量对握力随年龄下降的影响。
AIDS. 2016 Nov 13;30(17):2645-2652. doi: 10.1097/QAD.0000000000001245.
3
Unanticipated Effects of New Drug Availability on Antiretroviral Durability: Implications for Comparative Effectiveness Research.新药可及性对抗逆转录病毒药物耐久性的意外影响:对比较效果研究的启示
Open Forum Infect Dis. 2016 Jun 16;3(2):ofw109. doi: 10.1093/ofid/ofw109. eCollection 2016 Apr.
4
A longitudinal, HIV care continuum: 10-year restricted mean time in each care continuum stage after enrollment in care, by history of IDU.一个纵向的艾滋病病毒照护连续过程:根据注射吸毒史,入组照护后在每个照护连续阶段的10年受限平均时间。
AIDS. 2016 Sep 10;30(14):2227-34. doi: 10.1097/QAD.0000000000001183.
5
The effect of antiretroviral therapy on all-cause mortality, generalized to persons diagnosed with HIV in the USA, 2009-11.抗逆转录病毒疗法对全因死亡率的影响,推广至2009 - 2011年在美国被诊断为艾滋病毒的人群。
Int J Epidemiol. 2016 Feb;45(1):140-50. doi: 10.1093/ije/dyv352. Epub 2016 Jan 15.
6
Invited commentary: every good randomization deserves observation.特邀评论:每一次良好的随机分组都值得观察。
Am J Epidemiol. 2015 Nov 15;182(10):857-60. doi: 10.1093/aje/kwv200. Epub 2015 Oct 19.
7
Long-term immunologic and virologic responses on raltegravir-containing regimens among ART-experienced participants in the HIV Outpatient Study.在HIV门诊研究中,接受过抗逆转录病毒治疗的参与者使用含雷特格韦方案后的长期免疫和病毒学反应。
HIV Clin Trials. 2015 Aug;16(4):139-46. doi: 10.1179/1528433614Z.0000000019. Epub 2015 Jul 1.
8
Time above 1500 copies: a viral load measure for assessing transmission risk of HIV-positive patients in care.高于1500拷贝的时间:一种用于评估接受治疗的HIV阳性患者传播风险的病毒载量指标。
AIDS. 2015 May 15;29(8):947-54. doi: 10.1097/QAD.0000000000000640.
9
Illustration of a measure to combine viral suppression and viral rebound in studies of HIV therapy.图中展示了一项研究 HIV 疗法中病毒抑制和病毒反弹的措施。
J Acquir Immune Defic Syndr. 2015 Feb 1;68(2):241-4. doi: 10.1097/QAI.0000000000000423.
10
Dolutegravir, the Second-Generation of Integrase Strand Transfer Inhibitors (INSTIs) for the Treatment of HIV.多替拉韦,第二代整合酶链转移抑制剂(INSTIs),用于治疗 HIV。
Infect Dis Ther. 2014 Dec;3(2):83-102. doi: 10.1007/s40121-014-0029-7. Epub 2014 Jun 24.

拉替拉韦或依非韦伦为基础的 HIV 治疗方案起始后病毒学抑制和 CD4+ 细胞计数恢复。

Virologic suppression and CD4+ cell count recovery after initiation of raltegravir or efavirenz-containing HIV treatment regimens.

机构信息

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina.

Division of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia.

出版信息

AIDS. 2018 Jan 14;32(2):261-266. doi: 10.1097/QAD.0000000000001668.

DOI:10.1097/QAD.0000000000001668
PMID:29112076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5736462/
Abstract

OBJECTIVE

To explore the effectiveness of raltegravir-based antiretroviral therapy (ART) on treatment response among ART-naive patients seeking routine clinical care.

DESIGN

Cohort study of adults enrolled in HIV care in the United States.

METHODS

We compared virologic suppression and CD4 cell count recovery over a 2.5 year period after initiation of an ART regimen containing raltegravir or efavirenz using observational data from a US clinical cohort, generalized to the US population of people with diagnosed HIV. We accounted for nonrandom treatment assignment, informative censoring, and nonrandom selection from the US target population using inverse probability weights.

RESULTS

Of the 2843 patients included in the study, 2476 initiated the efavirenz-containing regimen and 367 initiated the raltegravir-containing regimen. In the weighted intent-to-treat analysis, patients spent an average of 74 (95% confidence interval: 41, 106) additional days alive with a suppressed viral load on the raltegravir regimen than on the efavirenz regimen over the 2.5-year study period. CD4 cell count recovery was also superior under the raltegravir regimen.

CONCLUSION

Patients receiving raltegravir spent more time alive and suppressed than patients receiving efavirenz, but the probability of viral suppression by 2.5 years after treatment was similar between groups. Optimizing the amount of time spent in a state of viral suppression is important to improve survival among people living with HIV and to reduce onward transmission.

摘要

目的

探索在接受常规临床护理的初治患者中,基于拉替拉韦的抗逆转录病毒疗法(ART)对治疗反应的效果。

设计

在美国接受 HIV 护理的成年人队列研究。

方法

我们使用来自美国临床队列的观察数据,比较了在开始包含拉替拉韦或依非韦伦的 ART 方案后 2.5 年内病毒学抑制和 CD4 细胞计数恢复情况,该队列数据推广至美国所有确诊 HIV 人群。我们使用逆概率加权法考虑了非随机治疗分配、信息性删失和从美国目标人群中进行的非随机选择。

结果

在纳入的 2843 例患者中,2476 例患者开始接受依非韦伦方案,367 例患者开始接受拉替拉韦方案。在加权意向治疗分析中,与依非韦伦方案相比,在 2.5 年的研究期间,接受拉替拉韦方案的患者平均多存活 74 天(95%置信区间:41,106),且病毒载量得到抑制。拉替拉韦方案也能更好地恢复 CD4 细胞计数。

结论

与接受依非韦伦的患者相比,接受拉替拉韦的患者存活时间更长且病毒得到抑制,但治疗后 2.5 年病毒抑制的概率在两组间相似。优化病毒抑制状态的持续时间对于改善 HIV 感染者的生存和减少病毒传播至关重要。