• 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

科威特镰状细胞病患儿住院情况十年回顾。

Ten-year review of hospital admissions among children with sickle cell disease in Kuwait.

作者信息

Akar Najwa Ali, Adekile Adekunle

机构信息

Department of Pediatrics, Mubarak Al-Kabeer Hospital, Kuwait University, Kuwait.

出版信息

Med Princ Pract. 2008;17(5):404-8. doi: 10.1159/000141506. Epub 2008 Aug 6.

DOI:10.1159/000141506
PMID:18685282
Abstract

OBJECTIVE

This study was designed to document the common causes and patterns of hospitalization among sickle cell disease (SCD) patients in Kuwait.

SUBJECTS AND METHODS

The case files of all SCD patients admitted to the hospital between 1995 and 2004 were studied. Their personal data, hemoglobin genotype, diagnosis on admission, complete blood count, treatment received, length of stay and outcome were documented.

RESULTS

Fifty SCD patients aged from 10 months to 14.8 years (mean: 8.7 +/- 2.8 years) had 351 admissions over the 10-year period accounting for 0.6% of all admissions to the pediatric wards. The 50 patients were made up of 18 Hb SS, 28 S beta(0)thal and 4 Hb SD patients. Common causes of admission were vaso-occlusive crisis: 222 (63.2%), acute splenic sequestration crisis: 32 (9.1%), hemolytic crisis: 31 (8.8%) and acute chest syndrome: 23 (6.6%). Stroke was seen in only 1 patient, and bacteriologically proven (Salmonella) acute osteomyelitis in 1 patient. There were no deaths during the study period.

CONCLUSIONS

Vaso-occlusive crisis was the commonest cause of hospitalization among our SCD patients. Efforts should be intensified to give advice on preventive measures. The use of hydroxyurea should be encouraged in patients with frequent severe pain crises.

摘要

目的

本研究旨在记录科威特镰状细胞病(SCD)患者住院的常见原因及模式。

对象与方法

对1995年至2004年间入院的所有SCD患者的病历进行研究。记录他们的个人资料、血红蛋白基因型、入院诊断、全血细胞计数、接受的治疗、住院时间及结局。

结果

50例年龄从10个月至14.8岁(平均:8.7±2.8岁)的SCD患者在10年期间共入院351次,占儿科病房所有入院病例的0.6%。这50例患者包括18例Hb SS型、28例Sβ⁰地中海贫血型和4例Hb SD型患者。常见的入院原因有:血管阻塞性危机:222次(63.2%),急性脾滞留危机:32次(9.1%),溶血危机:31次(8.8%),急性胸综合征:23次(6.6%)。仅1例患者发生中风,1例患者经细菌学证实(沙门氏菌)患有急性骨髓炎。研究期间无死亡病例。

结论

血管阻塞性危机是我们研究中SCD患者住院的最常见原因。应加大力度提供预防措施建议。对于频繁发生严重疼痛危机的患者,应鼓励使用羟基脲。

相似文献

1
Ten-year review of hospital admissions among children with sickle cell disease in Kuwait.科威特镰状细胞病患儿住院情况十年回顾。
Med Princ Pract. 2008;17(5):404-8. doi: 10.1159/000141506. Epub 2008 Aug 6.
2
Clinical analysis of mortality in hospitalized Zambian children with sickle cell anaemia.赞比亚住院镰状细胞贫血患儿死亡率的临床分析
East Afr Med J. 1994 Jun;71(6):388-91.
3
[The use of hydroxyurea in severe forms of sickle cell disease: study of 47 Tunisian paediatric cases].[羟基脲在镰状细胞病严重形式中的应用:47例突尼斯儿科病例研究]
Arch Pediatr. 2008 Jan;15(1):24-8. doi: 10.1016/j.arcped.2007.09.013. Epub 2007 Dec 31.
4
Hydroxyurea in sickle cell disease patients from Eastern Saudi Arabia.沙特阿拉伯东部镰状细胞病患者使用羟基脲的情况。
Saudi Med J. 2002 Mar;23(3):277-81.
5
Types of crises in sickle cell disease patients presenting at the haematology day care unit (HDCU), University College Hospital (UCH), Ibadan.在伊巴丹大学学院医院血液科日间护理病房(HDCU)就诊的镰状细胞病患者所出现的危机类型。
West Afr J Med. 2006 Oct-Dec;25(4):284-8.
6
Hydroxyurea therapy: improving the lives of patients with sickle cell disease.羟基脲疗法:改善镰状细胞病患者的生活
Pediatr Nurs. 2006 Nov-Dec;32(6):541-3.
7
Is morphine exposure associated with acute chest syndrome in children with vaso-occlusive crisis of sickle cell disease? A 6-year case-crossover study.吗啡暴露与镰状细胞病血管闭塞性危象患儿的急性胸部综合征有关吗?一项为期6年的病例交叉研究。
Clin Ther. 2007 Dec;29(12):2738-43. doi: 10.1016/j.clinthera.2007.12.016.
8
A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia.一项针对镰状细胞贫血幼儿的羟基脲两年期试点试验。
J Pediatr. 2001 Dec;139(6):790-6. doi: 10.1067/mpd.2001.119590.
9
Hospitalisations for sickle-cell disease in an Australian paediatric population.澳大利亚儿科人群中镰状细胞病的住院情况。
J Paediatr Child Health. 2013 Jan;49(1):68-71. doi: 10.1111/jpc.12018. Epub 2012 Dec 2.
10
Primary hyperparathyroidism mimicking vaso-occlusive crises in sickle cell disease.镰状细胞病中模仿血管闭塞危象的原发性甲状旁腺功能亢进症。
Pediatrics. 2006 Aug;118(2):e537-9. doi: 10.1542/peds.2006-0337.

引用本文的文献

1
Longitudinal assessment of transcranial Doppler imaging in children with sickle cell disease without neurological symptoms.镰状细胞病患儿无神经系统症状的经颅多普勒超声成像的纵向评估。
BMC Pediatr. 2024 Oct 28;24(1):684. doi: 10.1186/s12887-024-05155-6.
2
Orofacial anatomical and occlusal changes in patients with sickle cell disease in Kuwait.科威特镰状细胞病患者的口面部解剖结构和咬合变化
Saudi Dent J. 2023 May;35(4):330-336. doi: 10.1016/j.sdentj.2023.03.005. Epub 2023 Mar 15.
3
Repeat transcranial Doppler ultrasound imaging in Kuwaiti children with sickle cell disease after a 10-year interval: A prospective, cohort study.
科威特镰状细胞病患儿间隔10年后的重复经颅多普勒超声成像:一项前瞻性队列研究。
Health Sci Rep. 2023 Mar 27;6(3):e1159. doi: 10.1002/hsr2.1159. eCollection 2023 Mar.
4
Paediatric sickle cell disease at a tertiary hospital in Malawi: a retrospective cross-sectional study.马拉维一家三级医院的儿科镰状细胞病:一项回顾性横断面研究。
BMJ Paediatr Open. 2021 Sep 8;5(1):e001097. doi: 10.1136/bmjpo-2021-001097. eCollection 2021.
5
Analysis of Causes of Hospitalization Among Children with Sickle Cell Disease in a Group of Private Hospitals in Jeddah, Saudi Arabia.沙特阿拉伯吉达市一组私立医院中镰状细胞病患儿的住院原因分析。
J Blood Med. 2021 Aug 11;12:733-740. doi: 10.2147/JBM.S318824. eCollection 2021.
6
Prevalence of Stroke in Asian Patients with Sickle Cell Anemia: A Systematic Review and Meta-Analysis.亚洲镰状细胞贫血患者中风的患病率:系统评价与荟萃分析
Neurol Res Int. 2021 Jun 3;2021:9961610. doi: 10.1155/2021/9961610. eCollection 2021.
7
Haematological Profile of Children With Sickle Cell Anaemia in Steady State.镰状细胞贫血症患儿稳定期的血液学特征
Cureus. 2020 Oct 18;12(10):e11011. doi: 10.7759/cureus.11011.
8
The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease.《镰状细胞病中胎儿血红蛋白表达的遗传和临床意义》
Med Princ Pract. 2021;30(3):201-211. doi: 10.1159/000511342. Epub 2020 Sep 4.
9
Evaluation of von Willebrand factor and ADAMTS-13 antigen and activity levels in sickle cell disease patients in Kuwait.科威特镰状细胞病患者血管性血友病因子及ADAMTS-13抗原和活性水平的评估
J Thromb Thrombolysis. 2017 Jan;43(1):117-123. doi: 10.1007/s11239-016-1418-4.
10
Hospitalization Events among Children and Adolescents with Sickle Cell Disease in Basra, Iraq.伊拉克巴士拉镰状细胞病儿童和青少年的住院事件
Anemia. 2015;2015:195469. doi: 10.1155/2015/195469. Epub 2015 Oct 26.