Suppr超能文献

MG 复合量表:重症肌无力的有效且可靠的结局测量指标。

The MG Composite: A valid and reliable outcome measure for myasthenia gravis.

机构信息

University of Virginia, Department of Neurology, PO Box 800394, Charlottesville, VA 22908, USA.

出版信息

Neurology. 2010 May 4;74(18):1434-40. doi: 10.1212/WNL.0b013e3181dc1b1e.

Abstract

OBJECTIVE

To study the concurrent and construct validity and test-retest reliability in the practice setting of an outcome measure for myasthenia gravis (MG).

METHODS

Eleven centers participated in the validation study of the Myasthenia Gravis Composite (MGC) scale. Patients with MG were evaluated at 2 consecutive visits. Concurrent and construct validities of the MGC were assessed by evaluating MGC scores in the context of other MG-specific outcome measures. We used numerous potential indicators of clinical improvement to assess the sensitivity and specificity of the MGC for detecting clinical improvement. Test-retest reliability was performed on patients at the University of Virginia.

RESULTS

A total of 175 patients with MG were enrolled at 11 sites from July 1, 2008, to January 31, 2009. A total of 151 patients were seen in follow-up. Total MGC scores showed excellent concurrent validity with other MG-specific scales. Analyses of sensitivities and specificities of the MGC revealed that a 3-point improvement in total MGC score was optimal for signifying clinical improvement. A 3-point improvement in the MGC also appears to represent a meaningful improvement to most patients, as indicated by improved 15-item myasthenia gravis quality of life scale (MG-QOL15) scores. The psychometric properties were no better for an individualized subscore made up of the 2 functional domains that the patient identified as most important to treat. The test-retest reliability coefficient of the MGC was 98%, with a lower 95% confidence interval of 97%, indicating excellent test-retest reliability.

CONCLUSIONS

The Myasthenia Gravis Composite is a reliable and valid instrument for measuring clinical status of patients with myasthenia gravis in the practice setting and in clinical trials.

摘要

目的

研究在重症肌无力(MG)治疗实践环境下,一种肌无力综合评分(MGC)的同时效性、结构效度和重测信度。

方法

11 个中心参与了 MGC 量表的验证研究。MG 患者在 2 次连续就诊时进行评估。通过评估 MGC 评分与其他 MG 特定结局测量指标的关系,评估 MGC 的同时效性和结构效度。我们使用了许多潜在的临床改善指标来评估 MGC 检测临床改善的敏感性和特异性。在弗吉尼亚大学,对患者进行了重测信度评估。

结果

2008 年 7 月 1 日至 2009 年 1 月 31 日,11 个地点共纳入了 175 例 MG 患者。共 151 例患者接受了随访。MGC 总分与其他特定 MG 的量表具有极好的同时效性。MGC 的敏感性和特异性分析表明,MGC 总分提高 3 分是临床改善的最佳标志。MGC 提高 3 分似乎也代表了大多数患者的有意义改善,正如 15 项肌无力生活质量量表(MG-QOL15)评分的改善所表明的那样。对于由患者认为对治疗最重要的 2 个功能领域组成的个性化子评分,其心理测量特性并没有更好。MGC 的重测信度系数为 98%,95%置信区间下限为 97%,表明重测信度极好。

结论

在实践环境和临床试验中,重症肌无力综合评分是一种可靠且有效的工具,用于测量重症肌无力患者的临床状况。

相似文献

1
The MG Composite: A valid and reliable outcome measure for myasthenia gravis.
Neurology. 2010 May 4;74(18):1434-40. doi: 10.1212/WNL.0b013e3181dc1b1e.
2
The MG composite: an outcome measure for myasthenia gravis for use in clinical trials and everyday practice.
Ann N Y Acad Sci. 2012 Dec;1274:99-106. doi: 10.1111/j.1749-6632.2012.06812.x.
3
Developing outcome measures of disease activity in pediatric myasthenia.
Muscle Nerve. 2021 May;63(5):751-757. doi: 10.1002/mus.27208. Epub 2021 Feb 28.
4
Validation of the 15-item myasthenia gravis quality of life questionnaire (MG-QOL15) Persian version.
Muscle Nerve. 2016 Jun;54(1):65-70. doi: 10.1002/mus.25002. Epub 2016 Feb 26.
5
Translation and validation of the arabic version of the myasthenia gravis activities of daily living scale.
Muscle Nerve. 2019 May;59(5):583-586. doi: 10.1002/mus.26435. Epub 2019 Feb 12.
7
Reliability and Validity of Turkish Myasthenia Gravis-Activities of Daily Living Scale.
OTJR (Thorofare N J). 2021 Apr;41(2):101-107. doi: 10.1177/1539449220961077. Epub 2020 Oct 3.
8
10
Validation of the Italian version of the Myasthenia Gravis Impairment Index (MGII).
Neurol Sci. 2022 Mar;43(3):2059-2064. doi: 10.1007/s10072-021-05585-5. Epub 2021 Sep 9.

引用本文的文献

1
FcRn inhibitors for myasthenia gravis.
Cochrane Database Syst Rev. 2025 Aug 22;8(8):CD016097. doi: 10.1002/14651858.CD016097.
3
Complement inhibitors for myasthenia gravis in adults.
Cochrane Database Syst Rev. 2025 Jul 8;7(7):CD016098. doi: 10.1002/14651858.CD016098.
4
Rituximab for myasthenia gravis.
Cochrane Database Syst Rev. 2025 Jul 3;7(7):CD014574. doi: 10.1002/14651858.CD014574.pub2.
5
Bridging the Heterogeneity of Myasthenia Gravis Severity Scores for Digital Twin Development.
medRxiv. 2025 Jun 13:2025.06.13.25329566. doi: 10.1101/2025.06.13.25329566.
6
Immunomodulators and immunosuppressants for myasthenia gravis: a network meta-analysis.
Cochrane Database Syst Rev. 2025 Jun 4;6(6):CD016208. doi: 10.1002/14651858.CD016208.
7
Ravulizumab for generalized Myasthenia Gravis: a multicenter real-life experience.
J Neurol. 2025 May 14;272(6):396. doi: 10.1007/s00415-025-13127-8.
9
Handling rescue therapy in myasthenia gravis clinical trials: why it matters and why you should care.
Ann Clin Transl Neurol. 2025 May;12(5):888-897. doi: 10.1002/acn3.52309. Epub 2025 Apr 16.

本文引用的文献

1
Construction of an efficient evaluative instrument for myasthenia gravis: the MG composite.
Muscle Nerve. 2008 Dec;38(6):1553-62. doi: 10.1002/mus.21185.
2
Disease-specific measure of quality of life for myasthenia gravis.
Muscle Nerve. 2008 Aug;38(2):947-56. doi: 10.1002/mus.21016.
4
A trial of mycophenolate mofetil with prednisone as initial immunotherapy in myasthenia gravis.
Neurology. 2008 Aug 5;71(6):394-9. doi: 10.1212/01.wnl.0000312373.67493.7f. Epub 2008 Apr 23.
5
An international, phase III, randomized trial of mycophenolate mofetil in myasthenia gravis.
Neurology. 2008 Aug 5;71(6):400-6. doi: 10.1212/01.wnl.0000312374.95186.cc. Epub 2008 Apr 23.
6
Lifetime course of myasthenia gravis.
Muscle Nerve. 2008 Feb;37(2):141-9. doi: 10.1002/mus.20950.
7
MRI and clinical studies of facial and bulbar muscle involvement in MuSK antibody-associated myasthenia gravis.
Brain. 2006 Jun;129(Pt 6):1481-92. doi: 10.1093/brain/awl095. Epub 2006 May 3.
8
Clinical evaluation and management of myasthenia gravis.
Muscle Nerve. 2004 Apr;29(4):484-505. doi: 10.1002/mus.20030.
9
Standards of measurements in myasthenia gravis.
Ann N Y Acad Sci. 2003 Sep;998:445-52. doi: 10.1196/annals.1254.058.
10
A simple manual muscle test for myasthenia gravis: validation and comparison with the QMG score.
Ann N Y Acad Sci. 2003 Sep;998:440-4. doi: 10.1196/annals.1254.057.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验