• 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

Factors in the long term adjustment of children and adolescents with sickle cell disease: conceptualizations and review of the literature.

作者信息

Telfair J

机构信息

School of Public Health, University of North Carolina, Chapel Hill 27599.

出版信息

J Health Soc Policy. 1994;5(3-4):69-96. doi: 10.1300/J045v05n03_06.

DOI:10.1300/J045v05n03_06
PMID:10138764
Abstract

This paper focuses on the psychological and social factors that influence the adjustment process of children and adolescents with chronic conditions, primarily sickle cell disease. A review of the literature will reveal that psychological variables, such as anxiety and depression affecting adjustment, are the most studied. However, it will be pointed out that social variables such as family, school, and peers, also play a major role in this process. Furthermore, in keeping with the approach of this special collection, these psychological issues will be discussed within a developmental context. Clinical teams and practitioners are encouraged to take a longitudinal-biopsychosocial approach in addressing the needs of these children and their families. By doing so, they will be able to meet the present and long term psychological, social, educational, as well as medical needs of children and adolescents with sickle cell disease and other chronic conditions, and their families. This approach will also allow professionals to recognize and utilize the strengths of this population in the promotion of their overall well-being.

摘要

相似文献

1
Factors in the long term adjustment of children and adolescents with sickle cell disease: conceptualizations and review of the literature.
J Health Soc Policy. 1994;5(3-4):69-96. doi: 10.1300/J045v05n03_06.
2
Adaptation and coping: a look at a sickle cell patient population over age 30--an integral phase of the life long developmental process.适应与应对:对30岁以上镰状细胞病患者群体的观察——终身发育过程中的一个重要阶段。
J Health Soc Policy. 1994;5(3-4):141-60. doi: 10.1300/J045v05n03_09.
3
Natural history of sickle cell disease and the effects on biopsychosocial development.镰状细胞病的自然病史及其对生物心理社会发展的影响。
J Health Soc Policy. 1994;5(3-4):7-18. doi: 10.1300/J045v05n03_02.
4
Relationships in families of children and adolescents with sickle cell disease.患有镰状细胞病的儿童和青少年家庭中的关系。
J Health Soc Policy. 1994;5(3-4):161-83. doi: 10.1300/J045v05n03_10.
5
Empirically derived guidelines for assessing the psychosocial needs of children and adolescents with sickle cell.
Soc Work Health Care. 2002;36(1):29-44. doi: 10.1300/J010v36n01_03.
6
A longitudinal examination predicting emergency room use in children with sickle cell disease and their caregivers.一项预测镰状细胞病患儿及其照料者急诊室使用情况的纵向研究。
J Pediatr Psychol. 2006 Mar;31(2):163-73. doi: 10.1093/jpepsy/jsj002. Epub 2005 Mar 3.
7
Behavioral assessment of sickle cell disease pain.
J Health Soc Policy. 1994;5(3-4):19-38. doi: 10.1300/J045v05n03_03.
8
Evaluation of the psychological problems in children with sickle cell anemia and their families.镰状细胞贫血患儿及其家庭的心理问题评估。
Pediatr Hematol Oncol. 2011 May;28(4):321-8. doi: 10.3109/08880018.2010.540735. Epub 2011 Feb 23.
9
Family pediatrics: report of the Task Force on the Family.家庭儿科学:家庭问题特别工作组报告
Pediatrics. 2003 Jun;111(6 Pt 2):1541-71.
10
A prospective study of the role of coping and family functioning in health outcomes for adolescents with sickle cell disease.一项关于应对方式和家庭功能在镰状细胞病青少年健康结局中作用的前瞻性研究。
J Pediatr Hematol Oncol. 2007 Nov;29(11):752-60. doi: 10.1097/MPH.0b013e318157fdac.

引用本文的文献

1
Prevalence, patterns, correlates, and academic implications of sports betting and problem gambling among Nigerian undergraduates.尼日利亚大学生体育博彩与问题赌博的患病率、模式、相关因素及学术影响
Discov Ment Health. 2025 Aug 29;5(1):134. doi: 10.1007/s44192-025-00214-5.
2
Depression and Anxiety as Moderators of the Pain-Social Functioning Relationship in Youth with Sickle Cell Disease.抑郁和焦虑作为镰状细胞病青少年疼痛与社会功能关系的调节因素
J Pain Res. 2020 Apr 8;13:729-736. doi: 10.2147/JPR.S238115. eCollection 2020.
3
Anxiety and depression in children and adolescents with sickle cell disease.
镰状细胞病患儿及青少年的焦虑与抑郁
Curr Psychiatry Rep. 2007 Apr;9(2):114-21. doi: 10.1007/s11920-007-0080-0.