期刊文献+

重症肌无力患者生活质量的研究进展 被引量:6

原文传递
导出
摘要 重症肌无力是乙酰胆碱受体致敏而累及神经-肌肉接头处突触后膜上乙酰胆碱受体的一种自身免疫性神经肌肉疾病,造成肌肉无力、易疲劳。重症肌无力是一种慢性疾病,病程长,病情重,迁延难愈,反复发作,对患者的生理、心理、工作、学习或生活以及家庭的经济、周围的人际关系均造成不同程度的影响,从而影响患者的生活质量。
出处 《中国实用护理杂志》 2015年第5期388-390,共3页 Chinese Journal of Practical Nursing
  • 相关文献

参考文献32

  • 1Deymeer F,Gungor-Tuncer 0,Yilmaz V,et al.Clinical comparison ofanti - MuSK vs anti - ACHR - positive and seronegative myastheniagravis[J]. Neurology,2007,68:609-611.
  • 2陈灏珠.实用内科学[M].北京:人民卫生出版社,2002.1843.
  • 3栗江霞,钱静文.1例重症肌无力危象病人的急救护理[J].护理研究(下半月),2005,19(4):748-748. 被引量:4
  • 4王彦,姚景鹏.生活质量——一种新型的健康测量工具[J].中华护理杂志,2001,36(5):375-377. 被引量:40
  • 5Spitzer WO. State of science 1986 :quality of life and function status astarget variables forresearch[j]. Chron Dis, 1987’40(6) :465-471.
  • 6黄泂,冯慧宇,郑民缨.SF-36量表测定重症肌无力患者生活质量分析[J].中国实用神经疾病杂志,2010,13(24):24-26. 被引量:7
  • 7Busch C,Machens A,Pichlmeier U,et al. Long term outcome andquality of life after thymectomy for myasthenia gravis[j ].Ann Surg,1996,224(2):225.
  • 8Jaretzki A,Barohn RJ,Emstoff RM,et al. Myasthenia gravis:rec -ommendations for clinical research standards :task Force of the Med-ical Scientific Advisory Board of the Myasthenia Gravis Foundation ofAmerica[ J ] .Neurology,2000,55:16-23.
  • 9Simmons Z,Bremer BA,Robbins RA,et al.Quality of life in ALS de -pends on factors other than strength and physical flmction[J]. Neurology,2000,55(3):388-392.
  • 10吕宏梅,张岩波.患者报告结局(PRO)在临床疗效评价体系中的应用与思考[J].医学与哲学(B),2011,32(12):1-3. 被引量:19

二级参考文献105

共引文献775

同被引文献82

  • 1薛志强,王如文,蒋耀光,马铮,赵云平,谭群友.成人重症肌无力胸腺切除术后远期生活质量评价[J].第三军医大学学报,2004,26(9):817-819. 被引量:9
  • 2万崇华,陈明清,张灿珍,汤学良,孟琼,张晓磬.癌症患者生命质量测定量表EORTC QLQ-C30中文版评介[J].实用肿瘤杂志,2005,20(4):353-355. 被引量:1312
  • 3Johnson M, Cowin LS, Wilson I, et al. Professional identity and nursing:Contemporary theoretical developments and future research challenges [ J ]. International nursing review, 2012,59(4) :562 - 569.
  • 4Akimova T, Beier UH, Wang L, et al. Helios expression is a marker of T cell activation and proliferation [ J ]. PLo S One,2011,6(9) :118 - 120.
  • 5Baillie L, Bromley B, Walker M, et al. Implementing service improvement projects within pre -registration nursing education:A multi - method case study evaluation [ J ]. Nurse education in practice,2014,14 ( 1 ) :62 - 68.
  • 6McPherson CJ,Wilson KG. Feeling like a burden :exploring the perspectives of patients at the end of life[J]. Social Science Medicine, 2007,64 (2) : 417-427.
  • 7Motl RW,Snook M,McAuley E,et al. Symptoms,self-efficacy, and physical activity among individual with multiple sclerosis[J]. Res Nurs Health,2006,29(6):597-606.
  • 8Casella F,Alcala MJ,Prieto L,et al. Assessment of the influ- ence of disease activity on the quality of life of patients with inflammatory bowel disease using a short questionnaire[J]. Am J Gastrcenterol, 2004,99 (3) : 457-461.
  • 9Cousinea N,McDowell I. Measuring chronic patients' feelings of being a burden to their caregivers:development and prelimi- nary validation of a scale[J]. Med Care ,2003,41 ( ! ) : 110-118.
  • 10Lorig KR,Sobe| DS,Ritter PL,et al. Effect of a self-manage- ment program on patients with chronic disease[J].Eff Clin Pract, 2001,4(6) :256-262.

引证文献6

二级引证文献54

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部