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本文引用的文献

1
Parents' perspectives on physician-parent communication near the time of a child's death in the pediatric intensive care unit.父母对儿科重症监护病房中孩子临终前医患沟通的看法。
Pediatr Crit Care Med. 2008 Jan;9(1):2-7. doi: 10.1097/01.PCC.0000298644.13882.88.
2
Understanding of prognosis and goals of care among couples whose child died of cancer.对孩子死于癌症的夫妇的预后及护理目标的理解。
J Clin Oncol. 2008 Mar 10;26(8):1310-5. doi: 10.1200/JCO.2007.13.4056.
3
Supportive and palliative care needs of families of children who die from cancer: an Australian study.死于癌症儿童家庭的支持性和姑息治疗需求:一项澳大利亚的研究。
Palliat Med. 2008 Jan;22(1):59-69. doi: 10.1177/0269216307084608.
4
Hope and prognostic disclosure.希望与预后告知
J Clin Oncol. 2007 Dec 10;25(35):5636-42. doi: 10.1200/JCO.2007.12.6110.
5
Sustaining hope when communicating with terminally ill patients and their families: a systematic review.与绝症患者及其家属沟通时维持希望:一项系统综述
Psychooncology. 2008 Jul;17(7):641-59. doi: 10.1002/pon.1288.
6
Psychosocial and spiritual needs of children living with a life-limiting illness.患有危及生命疾病的儿童的心理社会和精神需求。
Pediatr Clin North Am. 2007 Oct;54(5):609-29, ix-x. doi: 10.1016/j.pcl.2007.08.002.
7
Parents' intellectual and emotional awareness of their child's impending death to cancer: a population-based long-term follow-up study.父母对其患癌子女即将死亡的智力和情感认知:一项基于人群的长期随访研究。
Lancet Oncol. 2007 Aug;8(8):706-14. doi: 10.1016/S1470-2045(07)70209-7.
8
The role of support staff in pediatric palliative care: their perceptions, training, and available resources.辅助人员在儿科姑息治疗中的作用:他们的认知、培训及可用资源。
J Palliat Care. 2007 Spring;23(1):44-50.
9
Living in a world without closure: reality for parents who have experienced the death of a child.生活在一个没有终结的世界:经历过孩子死亡的父母的现实。
J Palliat Care. 2006 Summer;22(2):75-82.
10
Matters of spirituality at the end of life in the pediatric intensive care unit.儿科重症监护病房临终时的灵性问题。
Pediatrics. 2006 Sep;118(3):e719-29. doi: 10.1542/peds.2005-2298.

通过对那些为子女做出第一阶段、临终护理和复苏决定的父母进行访谈所定义的“努力成为好父母”。

"Trying to be a good parent" as defined by interviews with parents who made phase I, terminal care, and resuscitation decisions for their children.

作者信息

Hinds Pamela S, Oakes Linda L, Hicks Judy, Powell Brent, Srivastava Deo Kumar, Spunt Sheri L, Harper Joann, Baker Justin N, West Nancy K, Furman Wayne L

机构信息

School of Medicine, Department of Pediatrics, George Washington University, Washington, DC, USA.

出版信息

J Clin Oncol. 2009 Dec 10;27(35):5979-85. doi: 10.1200/JCO.2008.20.0204. Epub 2009 Oct 5.

DOI:10.1200/JCO.2008.20.0204
PMID:19805693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2793041/
Abstract

PURPOSE

When a child's cancer progresses beyond current treatment capability, the parents are likely to participate in noncurative treatment decision making. One factor that helps parents to make these decisions and remain satisfied with them afterward is deciding as they believe a good parent would decide. Because being a good parent to a child with incurable cancer has not been formally defined, we conducted a descriptive study to develop such a definition.

METHODS

In face-to-face interviews, 62 parents who had made one of three decisions (enrollment on a phase I study, do not resuscitate status, or terminal care) for 58 patients responded to two open-ended questions about the definition of a good parent and about how clinicians could help them fulfill this role. For semantic content analysis of the interviews, a rater panel trained in this method independently coded all responses. Inter-rater reliability was excellent.

RESULTS

Among the aspects of the definition qualitatively identified were making informed, unselfish decisions in the child's best interest, remaining at the child's side, showing the child that he is cherished, teaching the child to make good decisions, advocating for the child with the staff, and promoting the child's health. We also identified 15 clinician strategies that help parents be a part of making these decisions on behalf of a child with advanced cancer.

CONCLUSION

The definition and the strategies may be used to guide clinicians in helping parents fulfill the good parent role and take comfort afterward in having acted as a good parent.

摘要

目的

当儿童癌症进展到超出当前治疗能力时,父母很可能会参与到非治愈性治疗的决策中。有助于父母做出这些决策并在之后对决策感到满意的一个因素是按照他们认为好父母会做的那样去做决定。由于对于身患绝症的孩子而言,成为一名好父母尚未有正式的定义,我们开展了一项描述性研究来给出这样一个定义。

方法

在面对面访谈中,62位为58名患者做出三项决策之一(参加一项I期研究、选择不进行心肺复苏或接受临终关怀)的父母,回答了两个开放式问题,一个是关于好父母的定义,另一个是关于临床医生如何帮助他们履行这一角色。对于访谈的语义内容分析,一个接受过该方法培训的评分小组对所有回答进行了独立编码。评分者间信度极佳。

结果

在定性确定的定义方面包括:为了孩子的最大利益做出明智、无私的决定,陪伴在孩子身边,让孩子知道自己被珍视,教导孩子做出正确的决定,向医护人员为孩子争取权益,以及促进孩子的健康。我们还确定了15种临床医生策略,这些策略有助于父母代表患有晚期癌症的孩子参与这些决策。

结论

该定义和策略可用于指导临床医生帮助父母履行好父母的角色,并在之后因自己作为好父母的行为而感到安心。