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向亲属捐赠骨髓的经历。

The experience of donating bone marrow to a relative.

作者信息

Christopher K A

机构信息

College of Nursing, University of Massachusetts, Dartmouth, USA.

出版信息

Oncol Nurs Forum. 2000 May;27(4):693-700.

Abstract

PURPOSE/OBJECTIVES: To describe and understand the experience of donating bone marrow to a relative.

DESIGN

Exploratory, descriptive, and qualitative.

SETTING

An urban comprehensive cancer center.

SAMPLE

Twelve donors were interviewed--eight women and four men. The average age was 47, and the average length of time since donation was nine months. At the time of the interview, seven recipients were living and five had died.

METHODS

Open-ended, face-to-face, or telephone interviews were conducted within one year of bone marrow donation using an interview guide.

MAIN RESEARCH VARIABLES

Psychosocial consequences of donating bone marrow to a relative.

FINDINGS

The main theme was Doing What It Takes When a Family Member Has Cancer. This goal guided the decision-making process, psychological responses, and family relationships once transplantation was necessary. Six subthemes emerged: Dealing With the Donation Procedure, Informational Needs, Psychological Impact of the Donor Role, Managing Family Relationships, Monitoring One's Own Health Before Donation, and Adjusting to the Transplant Recipient's Medical Condition.

CONCLUSIONS

Subjects expressed little or no reluctance to donate bone marrow, and all would repeat the experience. Subjects felt deep personal satisfaction and gratitude for an opportunity to donate. Stressful aspects of the experience related to unanticipated pain after the procedure, negative transplant outcomes, and relationships with the bone marrow recipients' family.

IMPLICATIONS FOR NURSING PRACTICE

Predonation assessment should identify donors' need for information as well as types and sources of information, how donors and families have coped with previous crises, and discussions of potential negative transplantation outcomes and impact on donors. Donors' coping and adjustment should be monitored throughout the transplantation process, particularly when coping problems or potential problems are identified or with negative transplantation outcomes. Formal donor support programs should be considered.

摘要

目的/目标:描述并了解为亲属捐献骨髓的经历。

设计

探索性、描述性和定性研究。

地点

一家城市综合癌症中心。

样本

对12名捐献者进行了访谈,其中8名女性,4名男性。平均年龄为47岁,距捐献的平均时间为9个月。在访谈时,7名接受者还活着,5名已经去世。

方法

在骨髓捐献后一年内,使用访谈指南进行开放式面对面或电话访谈。

主要研究变量

为亲属捐献骨髓的心理社会后果。

研究结果

主要主题是“当家庭成员患癌症时竭尽全力”。一旦有必要进行移植,这个目标就指导了决策过程、心理反应和家庭关系。出现了六个子主题:应对捐献程序、信息需求、捐献者角色的心理影响、处理家庭关系、捐献前监测自身健康以及适应移植接受者的医疗状况。

结论

受试者表示很少或根本不愿意捐献骨髓,所有人都愿意再次经历这一过程。受试者对有机会捐献深感个人满足和感激。经历中压力较大的方面与术后意外疼痛、移植结果不佳以及与骨髓接受者家庭的关系有关。

对护理实践的启示

捐献前评估应确定捐献者对信息的需求以及信息的类型和来源、捐献者及其家人如何应对以前的危机,以及讨论潜在的负面移植结果及其对捐献者的影响。在整个移植过程中应监测捐献者的应对和适应情况,特别是当发现应对问题或潜在问题或出现负面移植结果时。应考虑建立正式的捐献者支持项目。

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