• 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

一项奥昔哌汀(利他林)控释片(专注达)在 ADHD 成年患者中替代即时释放型哌甲酯的随机、单盲、交叉研究。

A randomized, single-blind, substitution study of OROS methylphenidate (Concerta) in ADHD adults receiving immediate release methylphenidate.

机构信息

Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

出版信息

J Atten Disord. 2011 May;15(4):286-94. doi: 10.1177/1087054710367880. Epub 2010 May 21.

DOI:10.1177/1087054710367880
PMID:20495161
Abstract

OBJECTIVE

The main aim of this study was to examine the efficacy, tolerability, and compliance of an extended-release formulation of methylphenidate (OROS-MPH) in adults with ADHD receiving immediate-release methylphenidate (IR-MPH).

METHOD

Participants were outpatient adults with ADHD who were stable on IR-MPH-administered TID. Participants were randomized (4:1) to equipotent doses of OROS-MPH or to continue IR-MPH and were assessed weekly for 6 weeks with the Adult ADHD Investigator System Symptom Report Scale (AISRS).

RESULTS

Randomization of 53 IR-MPH responders to IR- or OROS-MPH had no effect on AISRS score at endpoint (11.2 ± 6.9 vs. 10.7 ± 5.1, p = .8). Participants stabilized on IR-MPH and switched to OROS-MPH remained satisfied over 71% of the time. However, the IR-MPH group missed more doses (7.3 ± 6.8 vs. 3.3 ± 4.2, p = .02) than the OROS-MPH group.

CONCLUSION

Findings showed that adults with ADHD can be successfully switched from an effective regimen of IR-MPH TID to once-daily OROS-MPH. Results also demonstrated better compliance with OROS-MPH than with IR-MPH treatment.

摘要

目的

本研究的主要目的是检验长效哌甲酯(OROS-MPH)在接受即时释放型哌甲酯(IR-MPH)治疗的 ADHD 成年患者中的疗效、耐受性和顺应性。

方法

参与者为门诊 ADHD 成年患者,他们在接受 IR-MPH TID 治疗时病情稳定。参与者随机(4:1)接受等效剂量的 OROS-MPH 或继续接受 IR-MPH 治疗,并在 6 周内每周接受成人 ADHD 研究者系统症状报告量表(AISRS)评估。

结果

53 名对 IR-MPH 有反应的患者随机分组接受 IR-MPH 或 OROS-MPH 治疗,对终点时 AISRS 评分无影响(11.2 ± 6.9 与 10.7 ± 5.1,p =.8)。在稳定接受 IR-MPH 治疗并换用 OROS-MPH 的患者中,有超过 71%的时间保持满意。然而,IR-MPH 组漏服的剂量(7.3 ± 6.8 与 3.3 ± 4.2,p =.02)多于 OROS-MPH 组。

结论

研究结果表明,ADHD 成年患者可以成功地从有效的 IR-MPH TID 方案转换为每日一次的 OROS-MPH。结果还表明,与 IR-MPH 治疗相比,患者对 OROS-MPH 的依从性更好。

相似文献

1
A randomized, single-blind, substitution study of OROS methylphenidate (Concerta) in ADHD adults receiving immediate release methylphenidate.一项奥昔哌汀(利他林)控释片(专注达)在 ADHD 成年患者中替代即时释放型哌甲酯的随机、单盲、交叉研究。
J Atten Disord. 2011 May;15(4):286-94. doi: 10.1177/1087054710367880. Epub 2010 May 21.
2
Efficacy and safety of OROS methylphenidate in adults with attention-deficit/hyperactivity disorder: a randomized, placebo-controlled, double-blind, parallel group, dose-escalation study.OROS 哌甲酯治疗成人注意力缺陷/多动障碍的疗效与安全性:一项随机、安慰剂对照、双盲、平行组、剂量递增研究。
J Clin Psychopharmacol. 2009 Jun;29(3):239-47. doi: 10.1097/JCP.0b013e3181a390ce.
3
A randomized, controlled effectiveness trial of OROS-methylphenidate compared to usual care with immediate-release methylphenidate in attention deficit-hyperactivity disorder.一项关于控释型哌甲酯与速释型哌甲酯常规治疗相比治疗注意力缺陷多动障碍的随机对照疗效试验。
Can J Clin Pharmacol. 2006 Winter;13(1):e50-62. Epub 2006 Jan 23.
4
Better efficacy for the osmotic release oral system methylphenidate among poor adherents to immediate-release methylphenidate in the three ADHD subtypes.在三种注意缺陷多动障碍(ADHD)亚型中,对于速释型哌甲酯依从性差的患者,渗透型口服系统哌甲酯疗效更佳。
Psychiatry Clin Neurosci. 2009 Apr;63(2):167-75. doi: 10.1111/j.1440-1819.2009.01937.x.
5
Impact of methylphenidate delivery profiles on driving performance of adolescents with attention-deficit/hyperactivity disorder: a pilot study.哌甲酯给药方式对注意力缺陷多动障碍青少年驾驶性能的影响:一项初步研究。
J Am Acad Child Adolesc Psychiatry. 2004 Mar;43(3):269-75. doi: 10.1097/00004583-200403000-00007.
6
A randomized, placebo-controlled trial of OROS methylphenidate in adults with attention-deficit/hyperactivity disorder.一项针对患有注意力缺陷/多动障碍的成年人的盐酸哌甲酯控释片随机安慰剂对照试验。
Biol Psychiatry. 2006 May 1;59(9):829-35. doi: 10.1016/j.biopsych.2005.09.011. Epub 2005 Dec 20.
7
Efficacy and safety of dexmethylphenidate extended-release capsules in adults with attention-deficit/hyperactivity disorder.右旋哌甲酯缓释胶囊治疗成人注意力缺陷/多动障碍的疗效与安全性
Biol Psychiatry. 2007 Jun 15;61(12):1380-7. doi: 10.1016/j.biopsych.2006.07.032. Epub 2006 Nov 29.
8
Randomized, controlled trial of oros methylphenidate once a day in children with attention-deficit/hyperactivity disorder.一日一次口服哌醋甲酯治疗儿童注意力缺陷/多动障碍的随机对照试验
Pediatrics. 2001 Oct;108(4):883-92. doi: 10.1542/peds.108.4.883.
9
A randomized, 3-phase, 34-week, double-blind, long-term efficacy study of osmotic-release oral system-methylphenidate in adults with attention-deficit/hyperactivity disorder.一项为期 34 周、随机、3 期、双盲、长效疗效研究,评估奥昔哌汀控释片在成人注意缺陷多动障碍中的疗效。
J Clin Psychopharmacol. 2010 Oct;30(5):549-53. doi: 10.1097/JCP.0b013e3181ee84a7.
10
Tolerability and effects of OROS® MPH (Concerta ®) on functioning, severity of disease and quality of life in children and adolescents with ADHD: results from a prospective, non-interventional trial.OROS® 甲基苯丙胺(专注达®)对注意缺陷多动障碍儿童和青少年的功能、疾病严重程度及生活质量的耐受性和影响:一项前瞻性非干预性试验的结果
Atten Defic Hyperact Disord. 2009 Dec;1(2):175-86. doi: 10.1007/s12402-009-0010-6. Epub 2009 Aug 6.

引用本文的文献

1
Immediate-release methylphenidate for attention deficit hyperactivity disorder (ADHD) in adults.即刻释放型哌甲酯治疗成人注意缺陷多动障碍(ADHD)。
Cochrane Database Syst Rev. 2021 Jan 18;1(1):CD013011. doi: 10.1002/14651858.CD013011.pub2.
2
Economic Burden Associated With Extended-Release vs Immediate-Release Drug Formulations Among Medicare Part D and Medicaid Beneficiaries.医疗保险处方药部分和医疗补助受益人与延长释放与即刻释放药物制剂相关的经济负担。
JAMA Netw Open. 2020 Feb 5;3(2):e200181. doi: 10.1001/jamanetworkopen.2020.0181.
3
Changing patterns of alpha agonist medication use in children and adolescents 2009-2011.
2009 - 2011年儿童和青少年使用α激动剂药物的模式变化
J Child Adolesc Psychopharmacol. 2015 May;25(4):362-7. doi: 10.1089/cap.2014.0122. Epub 2015 Apr 28.
4
A review of OROS methylphenidate (Concerta(®)) in the treatment of attention-deficit/hyperactivity disorder.奥昔哌汀(专注达(®))治疗注意缺陷多动障碍的研究综述。
CNS Drugs. 2014 Nov;28(11):1005-33. doi: 10.1007/s40263-014-0175-1.
5
Effect of extended-release dexmethylphenidate and mixed amphetamine salts on sleep: a double-blind, randomized, crossover study in youth with attention-deficit hyperactivity disorder.缓释右美沙芬和混合苯丙胺盐对睡眠的影响:一项针对注意力缺陷多动障碍青少年的双盲、随机、交叉研究。
CNS Drugs. 2014 Sep;28(9):825-33. doi: 10.1007/s40263-014-0181-3.
6
Long-acting stimulants for treatment of attention-deficit/hyperactivity disorder: a focus on extended-release formulations and the prodrug lisdexamfetamine dimesylate to address continuing clinical challenges.用于治疗注意力缺陷/多动障碍的长效兴奋剂:聚焦于缓释制剂和前体药物二甲磺酸赖右苯丙胺以应对持续的临床挑战。
Atten Defic Hyperact Disord. 2013 Sep;5(3):249-65. doi: 10.1007/s12402-013-0106-x. Epub 2013 Apr 6.
7
An update on the pharmacotherapy of attention-deficit/hyperactivity disorder in adults.成人注意缺陷多动障碍的药物治疗进展。
Expert Rev Neurother. 2011 Oct;11(10):1443-65. doi: 10.1586/ern.11.137.
8
Adult attention-deficit/hyperactivity disorder treatment and cardiovascular implications.成人注意缺陷/多动障碍的治疗与心血管影响。
Curr Psychiatry Rep. 2011 Oct;13(5):357-63. doi: 10.1007/s11920-011-0213-3.