• 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

相似文献

1
Babies with spina bifida treated without surgery: parents' views on home versus hospital care.未接受手术治疗的脊柱裂患儿:父母对家庭护理与医院护理的看法。
BMJ. 1988 Nov 12;297(6658):1230-3. doi: 10.1136/bmj.297.6658.1230.
2
Love and loss. Conversations with parents of babies with spinal bifida managed without surgery, 1971-1981.爱与失去。与1971年至1981年期间未接受手术治疗的脊柱裂患儿家长的对话。
Dev Med Child Neurol Suppl. 1990 Aug;61:1-58.
3
Parents' perspective on symptoms, quality of life, characteristics of death and end-of-life decisions for children dying from cancer.父母对患癌濒死儿童的症状、生活质量、死亡特征及临终决策的看法。
Klin Padiatr. 2008 May-Jun;220(3):166-74. doi: 10.1055/s-2008-1065347.
4
Parents' Experiences and Wishes at End of Life in Children with Spinal Muscular Atrophy Types I and II.I型和II型脊髓性肌萎缩症患儿临终时父母的经历与愿望
J Pediatr. 2016 Aug;175:201-5. doi: 10.1016/j.jpeds.2016.04.062. Epub 2016 May 27.
5
'A bed in the middle of nowhere': parents' meanings of place of death for adults with cystic fibrosis.“荒郊野岭中的一张床”:父母对于成年囊性纤维化患者死亡地点的理解
Soc Sci Med. 2009 Oct;69(7):1056-62. doi: 10.1016/j.socscimed.2009.07.007. Epub 2009 Aug 18.
6
A comparison study of parental adaptation following a child's death at home or in the hospital.
Pediatrics. 1983 Jan;71(1):107-12.
7
What do parents think about enrolling their premature babies in several research studies?父母对于让他们的早产宝宝参加多项研究有什么看法?
Arch Dis Child Fetal Neonatal Ed. 2005 May;90(3):F225-8. doi: 10.1136/adc.2004.061986.
8
Parental experiences of their infant's hospitalization for cardiac surgery.父母对其婴儿心脏手术住院经历的体验。
Child Care Health Dev. 2015 Nov;41(6):1057-65. doi: 10.1111/cch.12230. Epub 2015 Feb 4.
9
Assessing the quality of bereavement care after perinatal death: development and piloting of a questionnaire to assess parents' experiences.评估围产期死亡后的丧亲照护质量:一份评估父母经历的问卷的编制与试行
J Obstet Gynaecol. 2017 Oct;37(7):931-936. doi: 10.1080/01443615.2017.1316710. Epub 2017 Jun 21.
10
Desperately seeking parenthood: neonatal nurses reflect on parental anguish.拼命寻求为人父母之路:新生儿护士对父母痛苦的反思。
J Clin Nurs. 2015 Jul;24(13-14):1885-94. doi: 10.1111/jocn.12811. Epub 2015 May 4.

引用本文的文献

1
Deliberate termination of life of newborns with spina bifida, a critical reappraisal.对患有脊柱裂新生儿故意终止生命的批判性重新评估。
Childs Nerv Syst. 2008 Jan;24(1):13-28; discussion 29-56. doi: 10.1007/s00381-007-0478-3. Epub 2007 Oct 10.
2
Dutch doctor convicted of murdering disabled infant.荷兰医生被判谋杀残疾婴儿罪。
BMJ. 1995 Jun 17;310(6994):1603. doi: 10.1136/bmj.310.6994.1603a.

本文引用的文献

1
Results of treatment of myelomeningocele. An analysis of 524 unselected cases, with special reference to possible selection for treatment.
Dev Med Child Neurol. 1971 Jun;13(3):279-303.
2
Adjustment to the death of a sibling.对兄弟姐妹死亡的调适。
Arch Dis Child. 1986 Mar;61(3):278-83. doi: 10.1136/adc.61.3.278.
3
The adaptation of parents to the birth of an infant with a congenital malformation: a hypothetical model.父母对患有先天性畸形婴儿出生的适应:一个假设模型。
Pediatrics. 1975 Nov;56(5):710-7.

未接受手术治疗的脊柱裂患儿:父母对家庭护理与医院护理的看法。

Babies with spina bifida treated without surgery: parents' views on home versus hospital care.

作者信息

Delight E, Goodall J

机构信息

Association for Spina Bifida and Hydrocephalus, London.

出版信息

BMJ. 1988 Nov 12;297(6658):1230-3. doi: 10.1136/bmj.297.6658.1230.

DOI:10.1136/bmj.297.6658.1230
PMID:2462949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1834693/
Abstract

From 1971 to 1981, 98 babies born with meningomyelocoele at the North Staffordshire Hospital Centre's district maternity hospital, were thought not suitable for surgery. Sixty three survived for more than one week. Over the period the hospital's policy changed: initially all such babies were kept in hospital, but later parents were given the choice of taking their baby home for palliative and terminal care. In an attempt to determine parents' views on the care of their baby the parents of 44 of the babies who survived to one week were traced in 1985-6, five to 14 years later; 80 of them were asked how they felt about the lives and deaths of their babies. Eighteen babies had been taken home, and they had lived longer than the 26 who had been cared for in hospital. Parents whose baby had remained in hospital were sadder than those who had taken their baby home when they looked back at their experiences, and they also considered that their baby's life had been of poor quality. Most of those who had taken their baby home had a more positive view of their child's life. The figures suggest that the bereavement process after a baby's death is longer than has been thought, but despite residual sadness just over half of the parents interviewed thought that something positive had come out of their experience.

摘要

1971年至1981年间,北斯塔福德郡医院中心地区妇产医院出生的98名患有脊髓脊膜膨出的婴儿被认为不适合手术。其中63名存活超过一周。在此期间,医院的政策发生了变化:最初所有此类婴儿都留在医院,但后来父母可以选择带孩子回家接受姑息治疗和临终关怀。为了确定父母对其婴儿护理的看法,1985年至1986年,即五到十四年后,追踪了44名存活一周的婴儿的父母;其中80人被问及他们对自己孩子生死的感受。18名婴儿被带回家,他们的存活时间比在医院接受护理的26名婴儿更长。回顾自己的经历时,孩子留在医院的父母比带孩子回家的父母更悲伤,他们也认为自己孩子的生活质量很差。大多数带孩子回家的父母对孩子的生活有更积极的看法。这些数据表明,婴儿死亡后的丧亲过程比人们想象的要长,但尽管仍有悲伤情绪,超过一半接受采访的父母认为他们的经历有积极的一面。