Organ support & nutrition

The effects of hemoadsorption in patients with sepsis-associated persistent severe AKI who require CRRT: A prospective, randomized controlled pilot study

Ann Intensive CarePublished Randomised controlled trial

Authors' conclusion

In this pilot trial, hemoadsorption therapy did not significantly reduce 30-day mortality across the entire cohort. However, a post hoc exploratory subgroup analysis suggested a potential association with improved survival in patients with elevated urinary CCL14 levels.

Study context

Population
Patients with sepsis-associated persistent severe AKI (S-PAKI) requiring CRRT
Participants
76 patients
Comparison
CVVH + hemoadsorption vs conventional CVVH
  • CVVH + HAn = 38
  • CVVHn = 38reference
Primary endpoint
All-cause mortality
Follow-up
30 days
Methodological detailsprospective, single-centre, pilot
  • Prospective
  • Single-centre
  • Pilot

Primary result

As reported in the abstract

P = 0.159

Secondary outcomes

30-day mortality, CCL14 >1.3 ng/ml (post hoc exploratory subgroup)

Lower mortality risk with CVVH + HA vs CVVH
  • Post hoc exploratory subgroup analysis

APACHE II and Sequential Organ Failure Assessment (SOFA) scores, cytokine clearance, hemodynamic status

Hemoadsorption significantly decreased APACHE II and SOFA scores, enhanced cytokine clearance and improved hemodynamic status

Renal functional prognosis; duration of mechanical ventilation, RRT, ICU stay and hospital stay among survivors

No significant improvement or shortening with hemoadsorption

Original publication

The effects of hemoadsorption in patients with sepsis-associated persistent severe AKI who require CRRT: A prospective, randomized controlled pilot study. Ann Intensive Care. Published 22 September 2026. doi:10.1016/j.aicoj.2026.100167

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.