Department of Pediatrics B, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Ramat-Gan, Israel.
Department of Pediatric Nephrology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Clin J Am Soc Nephrol. 2023 Mar 1;18(3):363-373. doi: 10.2215/CJN.0000000000000063. Epub 2023 Jan 20.
Childhood kidney failure is a rare condition with worldwide clinical variability. We used a nationwide multicenter analysis to study the pretransplant course of the entire Israeli pediatric kidney failure population over 30 years.
In this nationwide, population-based, historical cohort study, we analyzed medical and demographic data of all children treated with KRT and reported to the Israeli kidney failure registry in 1990-2020. Statistical analysis was performed with incidence rate corrected for age, ethnicity, and calendar year, using the appropriate age-related general population as denominator.
During the last 30 years, childhood incidence of kidney failure decreased. Average incidence in 2015-2019 was 9.1 cases per million age-related population (pmarp). Arab and Druze children exhibited higher kidney failure incidence rates than Jewish children (18.4 versus 7.0 cases pmarp for minorities versus Jews). The most common kidney failure etiologies among Arab and Jewish children were congenital anomalies of the kidney and urinary tract (approximately 27%), followed by cystic kidney diseases among Arab children (13%) and glomerulonephritis among Jewish children (16%). The most common etiology among Druze children was primary hyperoxaluria type 1 (33%). Israel's national health insurance provides access to primary health care to all citizens. Accordingly, waiting time for deceased-donor transplantation was equal between all ethnicities. Living-donor kidney transplantation rates among minority populations remained low in comparison with Jews over the entire study period. Although all patient groups demonstrated improvement in survival, overall survival rates were mainly etiology dependent.
In Israel, Arab and Druze children had a higher incidence of kidney failure, a unique etiological distribution, and a lower rate of living-donor kidney transplantations compared with Jewish children.
儿童肾衰竭是一种罕见的疾病,具有全球临床变异性。我们使用一项全国性多中心分析,研究了 30 多年来整个以色列儿科肾衰竭患者的移植前病程。
在这项全国性、基于人群的历史队列研究中,我们分析了在 1990 年至 2020 年期间向以色列肾衰竭登记处报告的所有接受 KRT 治疗的儿童的医疗和人口统计学数据。使用适当的年龄相关普通人群作为分母,对经过年龄、种族和日历年份校正的发病率进行了统计分析。
在过去的 30 年中,儿童肾衰竭的发病率有所下降。2015-2019 年的平均发病率为每百万年龄相关人群 9.1 例(pmarp)。阿拉伯和德鲁兹儿童的肾衰竭发病率高于犹太儿童(少数民族为 18.4 例 pmarp,犹太人为 7.0 例 pmarp)。阿拉伯和犹太儿童中最常见的肾衰竭病因是肾脏和泌尿道先天性异常(约 27%),其次是阿拉伯儿童的囊性肾病(13%)和犹太儿童的肾小球肾炎(16%)。德鲁兹儿童最常见的病因是 1 型原发性高草酸尿症(33%)。以色列的国家健康保险为所有公民提供初级保健服务。因此,在所有种族中,等待接受已故供体移植的时间是相等的。在整个研究期间,少数民族的活体供肾移植率仍低于犹太人。尽管所有患者群体的生存率都有所提高,但总体生存率主要取决于病因。
在以色列,与犹太儿童相比,阿拉伯和德鲁兹儿童肾衰竭的发病率更高,病因分布独特,活体供肾移植率较低。