Pediatric Nephrology, Dialysis and Transplantation Unit, Department of Woman's and Child's Health, University-Hospital of Padova, Via Giustiniani 3, 35128, Padua, Italy.
ESPN/ERA-EDTA Registry and ERA-EDTA Registry, Amsterdam, the Netherlands.
Eur J Pediatr. 2018 Jan;177(1):117-124. doi: 10.1007/s00431-017-3040-7. Epub 2017 Nov 16.
Data concerning outcomes of children on hemodialysis (HD) and peritoneal dialysis (PD) are scarce and frequently derived from single-center experiences. We sought to compare survival and transplantation rates in a large cohort of PD and HD patients. We extracted all patients initiating dialysis under 16 years of age between 2004 and 2013 from the Italian Registry of Pediatric Chronic Dialysis. Patients on PD were propensity-matched to those on HD based on gender, age, primary cause of ESRD, and the number of co-morbidities. Stratified Cox proportional hazard models were used to compare outcomes by dialysis modality. Three hundred ten patients were matched from 452 incident patients. In the unmatched cohort, PD patients were younger, more likely to be diagnosed with CAKUT, and had a higher urine output than HD patients. In the propensity-matched cohort, covariates were balanced between the two groups. At 2 years, the cumulative hazard ratio for death was similar (CHR 0.95, 95% CI 0.17-5.20) for HD relative to PD patients; and at 5 years, the CHR was lower for HD patients (0.22 95% CI 0.16-0.29). The cumulative incidence of transplantation at 3 years after dialysis initiation was 60.9% in HD patients and 59.7% in PD patients, with a CHR of 1.03 (95% CI 0.73-1.45).
Pediatric PD and HD patients have distinct characteristics. After controlling for treatment-selection biases, children selected to start on PD or HD exhibit a similar mortality risk during the first 2 years on treatment, after which this risk increases in PD children. What is Known: • Few studies have compared hard outcomes in children on maintenance dialysis. • Children started on different dialysis modalities have distinct characteristics that impact on survival. What is New: • After controlling for treatment-selection biases, children selected to start dialysis on PD or HD exhibit a similar mortality risk during the first 2 years on treatment, after which this risk appears to be increased in PD children. • An "integrative care" approach should be used in children on PD, switching them to HD when PD-related morbidity tends to increase.
关于儿童血液透析(HD)和腹膜透析(PD)的结果数据很少,并且经常来自单中心经验。我们旨在比较大量 PD 和 HD 患者的生存率和移植率。我们从意大利儿科慢性透析登记处中提取了 2004 年至 2013 年间所有 16 岁以下开始透析的患者。根据性别,年龄,ESRD 的主要病因和合并症的数量,对 PD 患者进行倾向匹配,以匹配 HD 患者。使用分层 Cox 比例风险模型比较了两种透析方式的结果。从 452 例新发病例中匹配了 310 例患者。在未匹配的队列中,PD 患者年龄较小,更可能被诊断为 CAKUT,并且尿排量高于 HD 患者。在倾向匹配的队列中,两组之间的协变量是平衡的。在 2 年时,HD 患者相对于 PD 患者的死亡累积风险比(CHR 0.95,95%CI 0.17-5.20)相似;而在 5 年时,HD 患者的 CHR 较低(0.22,95%CI 0.16-0.29)。起始透析后 3 年时,HD 患者的移植累积发生率为 60.9%,PD 患者为 59.7%,CHR 为 1.03(95%CI 0.73-1.45)。
儿科 PD 和 HD 患者具有不同的特征。在控制治疗选择偏倚后,选择开始 PD 或 HD 治疗的儿童在治疗的前 2 年内具有相似的死亡率风险,此后 PD 儿童的风险增加。
•关于维持性透析儿童的硬结局的研究很少。•开始使用不同透析方式的儿童具有不同的特征,这会影响生存。
•在控制治疗选择偏倚后,选择开始 PD 或 HD 治疗的儿童在治疗的前 2 年内具有相似的死亡率风险,此后 PD 儿童的风险似乎增加。•应在 PD 儿童中采用“综合护理”方法,当 PD 相关发病率趋于增加时,将其切换为 HD。