• 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

多囊肾病中的隐匿性颅内动脉瘤。何时需要进行脑血管造影?

Occult intracranial aneurysms in polycystic kidney disease. When is cerebral arteriography indicated?

作者信息

Levey A S, Pauker S G, Kassirer J P

出版信息

N Engl J Med. 1983 Apr 28;308(17):986-94. doi: 10.1056/NEJM198304283081702.

DOI:10.1056/NEJM198304283081702
PMID:6835317
Abstract

Patients with polycystic kidney disease are at increased risk of subarachnoid hemorrhage from rupture of intracranial aneurysms. We used decision analysis to assess whether or not patients with polycystic kidney disease should undergo routine cerebral arteriography for intracranial aneurysms and prophylactic surgery, if an aneurysm is detected. We incorporated published data on the prevalence of intracranial aneurysms in patients with polycystic kidney disease, the annual rate of aneurysmal rupture, the risk of grave complications of rupture, and the likelihood of grave complications of arteriography and prophylactic surgery. Outcomes were assessed as years of survival, and benefit was calculated as the gain in survival. Our analysis shows that arteriography should not be carried out routinely because its benefit exceeds one year only if the prevalence of aneurysm exceeds 30 per cent, if the surgical complication rate is 1 per cent or less, and if the patient is under 25 years of age. If newer noninvasive tests, such as digital-subtraction angiography, prove to identify reliably patients who are highly likely to have a cerebral aneurysm, routine screening with these tests will be warranted in patients with polycystic kidney disease.

摘要

多囊肾病患者因颅内动脉瘤破裂而发生蛛网膜下腔出血的风险增加。我们采用决策分析来评估多囊肾病患者是否应接受常规脑动脉造影以检测颅内动脉瘤,以及如果检测到动脉瘤是否应进行预防性手术。我们纳入了已发表的关于多囊肾病患者颅内动脉瘤患病率、动脉瘤年破裂率、破裂严重并发症风险以及动脉造影和预防性手术严重并发症可能性的数据。结果以生存年数评估,益处以生存获益计算。我们的分析表明,不应常规进行动脉造影,因为仅当动脉瘤患病率超过30%、手术并发症率为1%或更低且患者年龄在25岁以下时,其益处才超过一年。如果更新的非侵入性检查,如数字减影血管造影,被证明能可靠地识别出极有可能患有脑动脉瘤的患者,那么对多囊肾病患者进行这些检查的常规筛查将是必要的。

相似文献

1
Occult intracranial aneurysms in polycystic kidney disease. When is cerebral arteriography indicated?多囊肾病中的隐匿性颅内动脉瘤。何时需要进行脑血管造影?
N Engl J Med. 1983 Apr 28;308(17):986-94. doi: 10.1056/NEJM198304283081702.
2
Intracranial aneurysms in autosomal dominant polycystic kidney disease.
N Engl J Med. 1992 Sep 24;327(13):916-20. doi: 10.1056/NEJM199209243271303.
3
Patients with polycystic kidney disease would benefit from routine magnetic resonance angiographic screening for intracerebral aneurysms: a decision analysis.多囊肾病患者将从针对颅内动脉瘤的常规磁共振血管造影筛查中获益:一项决策分析。
Neurosurgery. 1996 Mar;38(3):506-15; discussion 515-6. doi: 10.1097/00006123-199603000-00018.
4
[Bilateral distal anterior cerebral artery aneurysms associated with polycystic kidney and liver disease; a case report].[双侧大脑前动脉远端动脉瘤合并多囊肾和肝病;病例报告]
No Shinkei Geka. 1992 Aug;20(8):905-8.
5
Presymptomatic Screening for Intracranial Aneurysms in Patients with Autosomal Dominant Polycystic Kidney Disease.常染色体显性多囊肾病患者颅内动脉瘤的无症状筛查。
Clin J Am Soc Nephrol. 2019 Aug 7;14(8):1151-1160. doi: 10.2215/CJN.14691218. Epub 2019 Jul 30.
6
Polycystic kidney disease and intracranial aneurysms. Early angiographic diagnosis and early operation for the unruptured aneurysm.
J Neurosurg. 1983 Apr;58(4):488-91. doi: 10.3171/jns.1983.58.4.0488.
7
[A case of polycystic kidney associated with new growth of cerebral aneurysm after aneurysmal operation].
No Shinkei Geka. 1994 Sep;22(9):877-80.
8
The association between polycystic kidney disease and cerebral aneurysms.
Can J Neurol Sci. 1991 Nov;18(4):505-9. doi: 10.1017/s0317167100032248.
9
Screening for intracranial aneurysms in autosomal dominant polycystic kidney disease is cost-effective.在常染色体显性多囊肾病中筛查颅内动脉瘤具有成本效益。
Kidney Int. 2018 Mar;93(3):716-726. doi: 10.1016/j.kint.2017.08.016. Epub 2017 Oct 20.
10
[The association of polycystic kidneys with intracranial aneurysms (author's transl)].多囊肾与颅内动脉瘤的关联(作者译)
No To Shinkei. 1980 Mar;32(3):321-5.

引用本文的文献

1
Should we screen for intracranial aneurysms in children with autosomal dominant polycystic kidney disease?我们是否应该在常染色体显性多囊肾病患儿中筛查颅内动脉瘤?
Pediatr Nephrol. 2023 Jan;38(1):77-85. doi: 10.1007/s00467-022-05432-5. Epub 2022 Feb 2.
2
Cerebral Aneurysms in Autosomal Dominant Polycystic Kidney Disease: A Comparison of Management Approaches.常染色体显性多囊肾病相关的颅内动脉瘤:管理方法的比较。
Neurosurgery. 2019 Jun 1;84(6):E352-E361. doi: 10.1093/neuros/nyy336.
3
Current management of autosomal dominant polycystic kidney disease.
常染色体显性多囊肾病的当前管理
World J Nephrol. 2015 Sep 6;4(4):468-79. doi: 10.5527/wjn.v4.i4.468.
4
Genetic testing, life insurance, and adverse selection.基因检测、人寿保险与逆向选择。
Philos Trans R Soc Lond B Biol Sci. 1997 Aug 29;352(1357):1063-6. doi: 10.1098/rstb.1997.0086.
5
What, if any, is the appropriate neurological work-up for a child with autosomal dominant polycystic kidney disease and a family history of intra-cranial aneurysm?对于患有常染色体显性多囊肾病且有颅内动脉瘤家族史的儿童,合适的神经学检查是什么(若有的话)?
Pediatr Nephrol. 1995 Apr;9(2):158. doi: 10.1007/BF00860730.
6
Subarachnoid haemorrhage in identical twins.同卵双胞胎中的蛛网膜下腔出血
J Neurol Neurosurg Psychiatry. 1984 Jan;47(1):81-3. doi: 10.1136/jnnp.47.1.81.
7
Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis.多囊肾。遗传学、病理解剖学、临床表现及产前诊断。
Hum Genet. 1984;68(2):104-35. doi: 10.1007/BF00279301.
8
Unruptured intracranial aneurysms in polycystic kidney disease.多囊肾病中的未破裂颅内动脉瘤
Acta Neurochir (Wien). 1986;79(2-4):94-9. doi: 10.1007/BF01407451.
9
Dominant and recessive polycystic kidney disease in children: evaluation of clinical features and laboratory data.儿童显性和隐性多囊肾病:临床特征与实验室数据评估
Pediatr Nephrol. 1988 Jul;2(3):296-302. doi: 10.1007/BF00858681.
10
Adult polycystic kidney disease and intracranial aneurysms.成人多囊肾病与颅内动脉瘤。
Br Med J (Clin Res Ed). 1987 Aug 29;295(6597):526. doi: 10.1136/bmj.295.6597.526.