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瑞典肾脏登记处:一个针对所有阶段慢性肾脏病的全国性登记处。

The Swedish Renal Registry: a nationwide registry for chronic kidney disease of all stages.

作者信息

Faucon Anne-Laure, Rydell Helena, Stendahl Maria, Welander Gunilla, Lundgren Torbjörn, Prûtz Karl-Göran, Schön Staffan, Bonnevier Ursa, Kåveryd Hult Aline, Hedman Håkan, Fondelius Frida, Segelmark Mårten, Evans Marie

机构信息

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Department of Clinical Epidemiology, Centre for Research in Epidemiology and Population Health, INSERM U1018, Paris-Saclay University, France.

出版信息

Clin Kidney J. 2025 Aug 6;18(9):sfaf238. doi: 10.1093/ckj/sfaf238. eCollection 2025 Sep.

Abstract

BACKGROUND

National registries that capture patients with chronic kidney disease (CKD) across all stages are scarce. We present here the Swedish Renal Registry (SRR), a nationwide prospective register covering the whole spectrum of CKD.

METHODS

Created in 1991, SRR enrolls CKD patients referred to adult nephrologist care (non-dialysis CKD [ND-CKD], kidney transplantation, maintenance dialysis), with an overall coverage of nearly all nephrology clinics in Sweden. SRR encompasses several interconnected databases in which longitudinal clinical, biological, kidney-related, patient-reported data, as well as provider-level information are collected. This report presents the design of the registry, as well as patients characteristics and temporal trends between 2008 and 2021.

RESULTS

A total of 45 590 new ND-CKD patients [72 years, 16 656 (36%) women, eGFR 26 ml/min per 1.73 m²], and 8829 incident kidney transplant recipients (51 years, 35% women) were enrolled in SRR between 2008 and 2021. SRR also included 16 034 new patients [68 years, 5420 (34%) women] on maintenance dialysis [70% hemodialysis (HD), 30% peritoneal dialysis (PD)]. Between 2015 and 2021, 4753 patients [59 years, 1884 (40%) women, eGFR 37 ml/min per 1.73 m²] had a registered kidney biopsy. We observed a decrease in HD incidence (69% to 60%, for trend <.01) and an increase in PD incidence (26% to 32%,  < .01) and pre-emptive transplantation (4.7% to 7.5%,  < .01). The prevalence of comorbidities is high in all CKD stages and increase as eGFR declines. While nephroangiosclerosis and diabetic kidney disease are the most common etiologies, glomerulonephritis are the most frequent diagnoses in biopsied and transplanted patients.

CONCLUSION

The SRR is a nationwide register which aims to contribute to address gaps in our understanding of CKD, to identify important challenges and health priorities, evaluate real-life clinical management and analyze international variations, improve health outcomes, improve quality of life, and reduce the burden of CKD.

摘要

背景

能够全面记录各阶段慢性肾脏病(CKD)患者情况的全国性登记系统十分稀少。我们在此介绍瑞典肾脏登记系统(SRR),这是一个覆盖CKD全谱的全国性前瞻性登记系统。

方法

SRR创建于1991年,纳入了转诊至成人肾脏病专科治疗的CKD患者(非透析CKD [ND-CKD]、肾移植、维持性透析),几乎涵盖了瑞典所有的肾脏病诊所。SRR包含多个相互关联的数据库,收集了纵向临床、生物学、肾脏相关、患者报告的数据以及医疗机构层面的信息。本报告介绍了该登记系统的设计,以及2008年至2021年间患者的特征和时间趋势。

结果

2008年至2021年间,共有45590例新的ND-CKD患者(72岁,16656例[36%]为女性,估算肾小球滤过率[eGFR]为26 ml/min/1.73 m²)和8829例新发肾移植受者(51岁,35%为女性)纳入SRR。SRR还包括16034例接受维持性透析的新患者(68岁,5420例[34%]为女性)[70%为血液透析(HD),30%为腹膜透析(PD)]。2015年至2021年间,4753例患者(59岁,1884例[40%]为女性,eGFR为37 ml/min/1.73 m²)进行了肾脏活检登记。我们观察到HD发病率下降(从69%降至60%,趋势P<0.01),PD发病率上升(从26%升至32%,P<0.01)以及抢先移植率上升(从4.7%升至7.5%,P<0.01)。所有CKD阶段的合并症患病率都很高,且随着eGFR下降而增加。虽然肾血管硬化和糖尿病肾病是最常见的病因,但肾小球肾炎是活检和移植患者中最常见的诊断。

结论

SRR是一个全国性登记系统,旨在填补我们对CKD认识的空白,识别重要挑战和健康优先事项,评估实际临床管理并分析国际差异,改善健康结局,提高生活质量,减轻CKD负担。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5b3/12421726/ce92589a5ae0/sfaf238gra.jpg

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