将 CF 基金会患者登记处与移植受者科学登记处数据库连接起来。

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM
Elizabeth A Cromwell, Yoon Son Ahn, Patrick J Johnson, Kathleen J Ramos, A Jay Freeman, Albert Faro, Jon J Snyder
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引用次数: 0

摘要

背景:囊性纤维化基金会患者登记处(CFFPR)保存了在囊性纤维化基金会认可的护理中心接受治疗的囊性纤维化(CF)患者的临床数据,包括实体器官移植史。移植受者科学登记(SRTR)数据库收集了与器官移植相关的全国性数据,为评估实体器官移植候选者和受者结果的研究提供支持:使用一种比较姓名、社会保障号最后四位数字、出生日期和死亡日期的算法将 CFFPR 中的个人与 SRTR 记录进行匹配。我们按器官和上市或移植年份总结了两个数据源之间移植状态的一致程度,以此评估匹配质量。我们总结了 CFFPR 报告的移植前一年肺移植和肝移植的特征:共有 7594 名参与 CFFPR 的个人与 SRTR 记录相匹配,其中约 75% 在 SRTR 中至少有一项移植记录。超过 97% 的匹配人群向 SRTR 报告了 CF 诊断。在 SRTR 中,共有 5,253 人被确认为肺移植受者,499 人被确认为肝移植受者。肺移植和肝移植的临床特征与CF患者的移植流行病学一致:这两个数据源的链接是成功的,它们之间的高度一致支持将匹配人群作为研究 CF 移植的有效资源,特别是利用移植前特征(在 CFFPR 中收集)和详细的移植数据(在 SRTR 中收集)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Linkage of the CF Foundation Patient Registry with the Scientific Registry of Transplant Recipients database.

Background: The Cystic Fibrosis Foundation Patient Registry (CFFPR) maintains clinical data, including history of solid organ transplant, on people with cystic fibrosis (CF) who obtain care at CF Foundation-accredited care centers. The Scientific Registry of Transplant Recipients (SRTR) database is a collection of national data related to organ transplantation that supports research to evaluate solid organ transplant candidate and recipient outcomes.

Methods: Individuals in the CFFPR were matched to SRTR records using an algorithm that compared names, last four digits of social security numbers, date of birth and date of death. We evaluated match quality by summarizing the extent to which transplant status agreed between the two data sources by organ and year of listing or transplant. We summarized CFFPR-reported characteristics for lung and liver transplants in the year prior to transplant.

Results: A total of 7,594 individuals who participated in the CFFPR matched SRTR records with approximately 75% having at least one transplant record in SRTR. Over 97% of the matched population had a CF diagnosis reported to SRTR. In total, 5,253 people were identified as lung transplant recipients and 499 as liver transplant recipients in SRTR. Clinical characteristics for lung and liver transplants were consistent with the epidemiology of transplantation for people with CF.

Conclusions: Linkage of the two data sources was successful, with high agreement between them supporting the use of the matched population as a valid resource to study transplantation in CF, particularly leveraging pre-transplant characteristics (collected in CFFPR) with detailed transplant data (collected in SRTR).

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来源期刊
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis 医学-呼吸系统
CiteScore
10.10
自引率
13.50%
发文量
1361
审稿时长
50 days
期刊介绍: The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
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