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识别并消除非裔美国家庭和非非裔美国家庭在关于前瞻性活体肾移植讨论方面的障碍。

Identifying and addressing barriers to African American and non-African American families' discussions about preemptive living related kidney transplantation.

作者信息

Boulware L Ebony, Hill-Briggs Felicia, Kraus Edward S, Melancon J Keith, Senga Mikiko, Evans Kira E, Troll Misty U, Ephraim Patti, Jaar Bernard G, Myers Donna I, McGuire Raquel, Falcone Brenda, Bonhage Bobbie, Powe Neil R

机构信息

Division of General Internal Medicine and Welch Center for Prevention, Epidemiology and Clinical Research, 2024 E. Monument Street, Suite 2-600, Baltimore, MD 21287, USA.

出版信息

Prog Transplant. 2011 Jun;21(2):97-104; quiz 105. doi: 10.1177/152692481102100203.

Abstract

CONTEXT

Ethnic/racial minority and nonminority families' perceived barriers to discussing preemptive living related kidney transplantation (LRKT) and their views on the potential value of health care professionals trained to address barriers are unknown. OBJECTIVE, SETTING, AND PARTICIPANTS: To collect pilot data for evaluating perceived barriers to preemptive LRKT and to inform the development of a culturally sensitive intervention to improve families' consideration of LRKT. In 4 structured group interviews of African American and non-African American patients (2 groups) with progressing chronic kidney disease and their family members (2 groups), participants' perceived barriers to initiating LRKT discussions and their views regarding the value of social workers to support discussions were explored.

RESULTS

Patients' barriers included concerns about their (1) ability to initiate discussions, (2) discussions being misinterpreted as donation requests, (3) potential burdening of family members, (4) uncertainty about when to initiate discussions, and (5) inducing guilt or coercing family members. Family members' barriers included (1) feeling overwhelmed by patients' illness, (2) patients' denial about their illness, (3) caregiver stress, and (4) uncertainty about their own health or the health of other family members who might donate or need a kidney in the future. Participants reported that social workers could facilitate difficult or awkward discussions and help families understand the LRKT process, address financial concerns, and cope emotionally. Themes were similar between African Americans and non-African Americans.

CONCLUSIONS

Families identified several barriers to discussing preemptive LRKT that could be addressed by social workers. Further research must be done to determine whether social workers need to tailor interventions to address families' cultural differences.

摘要

背景

少数族裔和非少数族裔家庭在讨论先发式活体肾移植(LRKT)时所感知到的障碍,以及他们对接受过解决这些障碍培训的医疗保健专业人员潜在价值的看法尚不清楚。目的、地点和参与者:收集试点数据,以评估先发式LRKT的感知障碍,并为制定一项具有文化敏感性的干预措施提供信息,以改善家庭对LRKT的考虑。在对患有进展性慢性肾病的非裔美国患者和非非裔美国患者(两组)及其家庭成员(两组)进行的4次结构化小组访谈中,探讨了参与者在发起LRKT讨论时所感知到的障碍,以及他们对社会工作者支持讨论的价值的看法。

结果

患者的障碍包括担心他们(1)发起讨论的能力,(2)讨论被误解为捐赠请求,(3)可能给家庭成员带来负担,(4)不确定何时发起讨论,以及(5)引起内疚或强迫家庭成员。家庭成员的障碍包括(1)被患者的疾病压得喘不过气来,(2)患者对自己疾病的否认,(3)照顾者的压力,以及(4)对自己的健康或未来可能捐赠或需要肾脏的其他家庭成员的健康不确定。参与者报告说,社会工作者可以促进困难或尴尬的讨论,并帮助家庭了解LRKT过程,解决财务问题,并在情感上应对。非裔美国人和非非裔美国人之间的主题相似。

结论

家庭确定了讨论先发式LRKT的几个障碍,社会工作者可以解决这些障碍。必须进行进一步的研究,以确定社会工作者是否需要调整干预措施以解决家庭的文化差异。

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