Relapsing and Progressive Complications of Severe Hypertriglyceridemia: Effective Long-Term Treatment with Double

Clemens Grupp1,2, Johannes Beckermann3, Eric Köster4

  • 1Department of Nephrology, Academic Teaching Hospital Bamberg, Bamberg, Germany.

Blood Purification
|March 20, 2020
PubMed

Insights

Double filtration plasmapheresis (DFPP) effectively prevents recurrent pancreatitis and cardiovascular events in severe hypertriglyceridemia (HTG) patients. This safe treatment stabilizes patients refractory to standard therapies, reducing complications significantly.

Area of Science:

  • Cardiology
  • Gastroenterology
  • Medical Technology

Background:

  • Severe hypertriglyceridemia (HTG) poses significant risks, including acute pancreatitis (AP) and atherosclerotic cardiovascular disease (ASCVD).
  • Double filtration plasmapheresis (DFPP) shows promise for acute HTG management, but long-term efficacy data are limited.

Purpose of the Study:

  • To assess the efficacy and safety of regular DFPP in preventing recurrent HTG-associated complications.
  • To evaluate DFPP in patients with severe HTG refractory to conventional treatments.

Main Methods:

  • A retrospective multicenter study involving patients with severe, drug- and diet-refractory HTG undergoing regular DFPP.
  • Comparison of complication rates before and during DFPP treatment.

Main Results:

  • Ten patients with severe HTG (median TG 5,487 mg/dL) were observed for a mean of 3.9 years pre-DFPP and 3.8 years post-DFPP.
  • The annual rate of HTG-associated complications decreased from 1.4 to 0 (p < 0.005), a 77% reduction.
  • DFPP was safe, well-tolerated, and effective in eliminating triglyceride-rich lipoproteins, with 60% of patients experiencing no AP or ASCVD progression.

Conclusions:

  • Regular, long-term DFPP stabilizes patients with severe HTG and associated complications who are resistant to standard therapies.
  • DFPP offers a safe and effective therapeutic option for managing refractory hypertriglyceridemia and preventing severe adverse events.
Abstract

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