LIPOSORBER® is indicated for use in clinically diagnosed Familial Hypercholesterolemic patients with either documented Coronary Artery Disease (CAD)* or Peripheral Artery Disease (PAD) †, if:
- LDL-C ≥ 100mg/dL or Lp(a) ≥ 60 mg/dL and LDL-C ≥ 100mg/dL and diet and maximum tolerable combination lipid-lowering drug therapies have failed to achieve the establish therapeutic targets per profesional guidelines.
Please take our quiz or ask your doctor to confirm if you are a candidate for LIPOSORBER® treatment.
During the procedure, the plasma is separated from the whole blood and the bad LDL cholesterol and Lp(a) are removed from the plasma. Then the plasma and blood are recombined, warmed and returned back to you.
The LIPOSORBER® consists of disposable components and an automated computer machine that controls and monitors you each step of the way.
In order for LIPOSORBER® treatment to maintain a lower level of Lp(a) and LDL cholesterol in the blood, patients should repeat the procedure regularly. In general, individuals with LDL cholesterol levels starting above 300 mg/dl after diet and maximum tolerated drug therapy should be treated once per week, and individuals with LDL cholesterol levels starting at 200 mg/dl will usually be treated once every two weeks. LIPOSORBER® treatment is regarded as a lifelong therapy. Patients must continue their diet and cholesterol-lowering medications after starting the LIPOSORBER® treatment. Patients should consult with their treating physician for a personalized procedure recommendation.
Find out more about the treatment
There are more than 50 locations across the United States and Canada that offer LIPOSORBER® treatment with new facilities added regularly.
The most common adverse events are hypotension (0.8%), nausea/vomiting (0.5%), and flushing/blotching (0.4%). Other adverse reactions include angina/chest pain, shortness of breath, fainting, lightheadedness and anemia.1
Angiotensin converting enzyme [ACEI(s)] inhibitors are contraindicated with LIPOSORBER due to possible bradykinin reaction. ACEI(s) should be replaced with angiotensin II receptor blockers (ARBs) or any other antihypertensive agent as determined by your prescribing doctor.1
For complete safety information, including adverse events and additional contraindications, please visit: https://www.accessdata.fda.gov/cdrh_docs/pdf17/H170002D.pdf