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本文引用的文献

1
Kidney disease mortality--Michigan, 1989-2005.1989 - 2005年密歇根州的肾病死亡率
MMWR Morb Mortal Wkly Rep. 2007 Mar 16;56(10):225-7.
2
Good for harvest, bad for planting.利于收割,不利于播种。
Health Aff (Millwood). 2007 Jan-Feb;26(1):232-7. doi: 10.1377/hlthaff.26.1.232.
3
Review: a gentle introduction to imputation of missing values.综述:缺失值插补的简要介绍
J Clin Epidemiol. 2006 Oct;59(10):1087-91. doi: 10.1016/j.jclinepi.2006.01.014. Epub 2006 Jul 11.
4
Rates of completion of the medical evaluation for renal transplantation.肾移植医学评估的完成率。
Am J Kidney Dis. 2005 Oct;46(4):734-45. doi: 10.1053/j.ajkd.2005.06.011.
5
Using navigators to improve care of underserved patients: current practices and approaches.利用导航工具改善对服务不足患者的护理:当前的实践与方法。
Cancer. 2005 Aug 15;104(4):848-55. doi: 10.1002/cncr.21214.
6
The impact of social support on end-stage renal disease.社会支持对终末期肾病的影响。
Semin Dial. 2005 Mar-Apr;18(2):98-102. doi: 10.1111/j.1525-139X.2005.18203.x.
7
Self-care among chronically ill African Americans: culture, health disparities, and health insurance status.慢性病缠身的非裔美国人的自我保健:文化、健康差异与健康保险状况。
Am J Public Health. 2004 Dec;94(12):2066-73. doi: 10.2105/ajph.94.12.2066.
8
Differences in health-related quality of life and treatment preferences among black and white patients with end-stage renal disease.晚期肾病黑人和白人患者在健康相关生活质量及治疗偏好上的差异。
Qual Life Res. 2004 Aug;13(6):1129-37. doi: 10.1023/B:QURE.0000031350.56924.cc.
9
Update in renal transplantation.肾移植的进展
Arch Intern Med. 2004 Jul 12;164(13):1373-88. doi: 10.1001/archinte.164.13.1373.
10
Physicians' beliefs about racial differences in referral for renal transplantation.医生对肾移植转诊中种族差异的看法。
Am J Kidney Dis. 2004 Feb;43(2):350-7. doi: 10.1053/j.ajkd.2003.10.022.

促进肾移植的可及性:社会支持网络在完成移植前评估中的作用。

Promoting access to renal transplantation: the role of social support networks in completing pre-transplant evaluations.

机构信息

Division of General Medicine and Primary Care, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

J Gen Intern Med. 2008 Aug;23(8):1187-93. doi: 10.1007/s11606-008-0628-7. Epub 2008 May 14.

DOI:10.1007/s11606-008-0628-7
PMID:18478302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2517970/
Abstract

BACKGROUND

Completing pre-transplant evaluations may be a greater barrier to renal transplantation for blacks with end-stage renal disease (ESRD) than for whites.

OBJECTIVE

To determine whether social support networks facilitate completing the pre-transplant evaluation and reduce racial disparities in this aspect of care.

DESIGN, SETTING, AND PARTICIPANTS: We surveyed 742 black and white ESRD patients in four regional networks 9 months after they initiated dialysis in 1996 and 1997. Patients reported instrumental support networks (number of friends or family to help with daily activities), emotional support networks (number of friends or family available for counsel on personal problems) and dialysis center support (support from dialysis center staff and patients). The completion of pre-transplant evaluations, including preoperative risk stratification and testing, was determined by medical record reviews.

OUTCOME MEASUREMENT

Complete renal pre-transplant evaluations.

RESULTS

Compared to patients with low levels of instrumental support, those with high levels were more likely to have complete evaluations (25% versus 46%, respectively, p < .001). In adjusted analyses, high levels of instrumental support were associated with higher rates of complete evaluations among black women (p < .05), white women (p < .05), and white men (p < .05), but not black men. Among black men, but not other groups, private insurance was a significant predictor of complete evaluations.

CONCLUSIONS

Instrumental support networks may facilitate completing renal pre-transplant evaluations. Clinical interventions that supplement instrumental support should be evaluated to improve access to renal transplantation. Access to supplemental insurance may also promote complete evaluations for black patients.

摘要

背景

对于终末期肾病(ESRD)的黑人患者来说,完成移植前评估可能比白人患者面临更大的障碍。

目的

确定社会支持网络是否有助于完成移植前评估,并减少这方面护理的种族差异。

设计、地点和参与者:我们在 1996 年和 1997 年对四个区域网络中的 742 名黑人和白人 ESRD 患者进行了调查,这些患者在开始透析后 9 个月接受了调查。患者报告了工具性支持网络(帮助进行日常活动的朋友或家人的数量)、情感支持网络(可在个人问题上提供咨询的朋友或家人的数量)和透析中心支持(透析中心工作人员和患者的支持)。通过病历回顾确定了移植前评估的完成情况,包括术前风险分层和检测。

结果测量

完成完整的肾脏移植前评估。

结果

与工具性支持水平较低的患者相比,高水平的患者更有可能完成评估(分别为 25%和 46%,p<0.001)。在调整分析中,高水平的工具性支持与黑人女性(p<0.05)、白人女性(p<0.05)和白人男性(p<0.05)完成完整评估的比率较高相关,但与黑人男性无关。在黑人男性中,但在其他群体中,私人保险是完成评估的一个重要预测因素。

结论

工具性支持网络可能有助于完成肾脏移植前评估。应评估补充工具性支持的临床干预措施,以改善接受肾脏移植的机会。补充保险的获得也可能促进黑人患者的完整评估。