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Evaluation of Knowledge of Patients with Hemophilia Regarding Their Diseases and Treatment in Iran.

作者信息

Karimi Mehran, Zarei Tahereh, Haghpanah Sezaneh, Zahedi Zohreh

机构信息

Shiraz University of Medical Sciences, Hematology Research Center, Shiraz, Iran, Phone: 00987136473239, E-mail:

出版信息

Turk J Haematol. 2016 Dec 1;33(4):355-356. doi: 10.4274/tjh.2016.0041. Epub 2016 Jun 17.

DOI:10.4274/tjh.2016.0041
PMID:27312959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5204196/
Abstract
摘要

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Hemophilia in the developing world: transforming lives through international collaboration.发展中世界的血友病：通过国际合作改变生活。
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引用本文的文献

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A survey of characteristics and current educational needs of hemophilia treatment centers within Asia Pacific.亚太地区血友病治疗中心的特征与当前教育需求调查。
Res Pract Thromb Haemost. 2018 May 24;2(3):508-517. doi: 10.1002/rth2.12108. eCollection 2018 Jul.

本文引用的文献

1
Haemophilia A: patients' knowledge level of treatment and sources of treatment-related information.甲型血友病：患者的治疗知识水平及治疗相关信息来源
Haemophilia. 2009 Jan;15(1):73-7. doi: 10.1111/j.1365-2516.2008.01875.x. Epub 2008 Sep 8.
2
Knowledge, attitudes, and behaviors of youths in the US hemophilia population: results of a national survey.美国血友病患者群体中青少年的知识、态度和行为：一项全国性调查结果
Am J Public Health. 2006 Sep;96(9):1618-22. doi: 10.2105/AJPH.2005.075234. Epub 2006 Jul 27.
3
Compliance with treatment and understanding of own disease in patients with severe and moderate haemophilia.中重度血友病患者的治疗依从性及对自身疾病的了解情况
Haemophilia. 2006 Jan;12(1):47-51. doi: 10.1111/j.1365-2516.2006.01192.x.
4
Home management of haemophilia.血友病的家庭管理
Haemophilia. 2004 Mar;10(2):118-33. doi: 10.1046/j.1365-2516.2003.00853.x.
5
Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis.血友病的定义。国际血栓与止血协会科学与标准化委员会第八因子和第九因子科学小组委员会的建议。
Thromb Haemost. 2001 Mar;85(3):560.
6
Mortality among males with hemophilia: relations with source of medical care. The Hemophilia Surveillance System Project Investigators.血友病男性患者的死亡率：与医疗保健来源的关系。血友病监测系统项目研究人员。
Blood. 2000 Jul 15;96(2):437-42.
7
The benefits of comprehensive care of hemophilia: a five-year study of outcomes.血友病综合护理的益处：一项为期五年的结局研究。
Am J Public Health. 1984 Jun;74(6):616-7. doi: 10.2105/ajph.74.6.616.