Deger İbrahim, Çelik Muhittin, Taş İbrahim, Samancı Serhat
Department of Pediatric, Division of Neonatology, Dicle University School of Medicine, Diyarbakir, Turkey.
Department of Pediatric, Division of Neonatology, Gaziantep University School of Medicine, Gaziantep, Turkey.
Ther Apher Dial. 2022 Jun;26(3):658-666. doi: 10.1111/1744-9987.13816. Epub 2022 Feb 24.
Herein, we aimed to discuss our experience in 16 newborn patients with Maple syrup urine disease (MSUD) who were treated with urgent renal replacement therapy (RRT).
The patients underwent continuous veno-venous hemodiafiltration (CVVHDF) or peritoneal dialysis (PD) as renal replacement therapy.
Eleven (68.75%) patients underwent CVVHDF and five (31.25%) underwent peritoneal dialysis. The median leucine reduction rate per hour was 2.56% (1.75-7.6) in the CVVHDF group, 0.78% (0.54-1.83) in the PD group, and was significantly higher in the CVVHDF group (p = 0.001). Posttreatment plasma leucine levels were found to be 198 (20-721) μmol/L in the CVVHDF group and 600 (250-967) μmol/L in the PD group, and CVVHDF was found to be significantly lower (p = 0.08). Complications such as hypotension, electrolyte imbalance, and filter obstruction occurred in the CVVHDF group.
This study showed that CVVHDF is more effective than PD for rapidly eliminating elevated leucine levels caused by MSUD in the newborn and it is not associated with increased complication rates.
在此,我们旨在探讨16例接受紧急肾脏替代治疗(RRT)的枫糖尿症(MSUD)新生儿患者的治疗经验。
患者接受持续静脉-静脉血液透析滤过(CVVHDF)或腹膜透析(PD)作为肾脏替代治疗。
11例(68.75%)患者接受了CVVHDF,5例(31.25%)接受了腹膜透析。CVVHDF组每小时亮氨酸降低率中位数为2.56%(1.75 - 7.6),PD组为0.78%(0.54 - 1.83),CVVHDF组显著更高(p = 0.001)。发现CVVHDF组治疗后血浆亮氨酸水平为198(20 - 721)μmol/L,PD组为600(250 - 967)μmol/L,CVVHDF组显著更低(p = 0.08)。CVVHDF组出现了低血压、电解质失衡和滤器阻塞等并发症。
本研究表明,CVVHDF在快速消除新生儿MSUD所致升高的亮氨酸水平方面比PD更有效,且不伴有更高的并发症发生率。