Authors
Lingling Liu, Yanqing Jie, Xiaojing Tang, Suhua Shi, Anna Lorenzin, Zhiguo Mao, Lin Li, Haoran Liu, Xiaoyan Zheng, Xiaohong Xing, Bing Dai, Jing Chen
Published in
Blood purification. Pages 1-23. Jul 10, 2026. Epub Jul 10, 2026.
Abstract
Conventional priming for Hemoadsorption Combined with Hemodialysis (HAHD) is complex, time-consuming, and resource-intensive. We aimed to develop and validate a standardized, efficient, and safe tandem priming protocol by systematically evaluating its operational efficiency, circuit cleanliness, clinical efficacy and clinical safety.
A two-stage "in vitro screening-clinical validation" design was utilized, using the HA130 hemoadsorption cartridge (Jafron, China) throughout all experiments and clinical sessions. The in vitro phase compared four novel tandem priming methods (varying slow-prime flow rates and fast-flush volumes) against a traditional separate-priming method to identify an optimal protocol based on efficiency and cleanliness. This protocol was then validated in a single-center, single-blind randomized controlled trial involving 53 maintenance hemodialysis patients randomized to the optimized tandem method (n = 29) or the traditional method (n = 24). The primary safety outcome was circuit clotting; the primary efficacy outcome was in solute clearance.
In vitro, all tandem methods were significantly faster (26.05-34.89 min vs. 55.40 min, P < 0.001) and consumed fewer resources while meeting all cleanliness standards. After preliminary safety screening excluded a faster flow rate (100 mL/min), the 50 mL/min slow-prime with 2000 mL fast-flush protocol was selected. In the clinical trial, the incidence of Grade I cartridge clotting was low and statistically comparable between the tandem (3.45%) and traditional (4.17%) groups (P > 0.05). Solute reduction values for urea, creatinine, and β2-microglobulin were not significantly different, demonstrating comparable therapeutic efficacy.
The novel tandem priming protocol is a highly efficient, resource-sparing, and safe alternative to traditional methods. It maintains therapeutic efficacy and circuit patency, offering a valuable, standardized solution for clinical practice.
PMID:
42430289
Bibliographic data and abstract were imported from PubMed on 11 Jul 2026.
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