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Multidisciplinary Approach to Managing FCS

Video content above is prompted by the following:

What is the importance of a multidisciplinary approach to managing FCS?

What kind of professionals typically comprise a multidisciplinary care team for a patient with FCS?

How should specialists engage with each other along the spectrum of the disease course–from early to advanced stages?

What is a typical referral pattern for patients with FCS across specialties? When should patients be referred?


Treatment of Familial Chylomicronemia Syndrome: A Multidisciplinary Approach

HCPLive® Peer Exchange panel discussions feature authoritative insights, opinions, and perspectives on important issues facing today's care professionals.

Peer Exchange

Familial chylomicronemia syndrome (FCS) is a rare genetic disorder characterized by extremely high triglyceride levels, leading to recurrent pancreatitis and other complications. Delayed diagnosis and treatment can exacerbate cardiovascular and metabolic consequences, including increased risk of atherosclerosis, cardiovascular disease, and metabolic syndrome. Long-term health risks involve persistent hypertriglyceridemia, which can cause chronic pancreatitis, diabetes, and liver disease. Early intervention is crucial to mitigate these risks, improve patient outcomes, and enhance quality of life by managing triglyceride levels and preventing severe complications.

Panelists discuss the importance of a multidisciplinary approach to managing familial chylomicronemia syndrome (FCS), outlining the key professionals involved in the care team, and how specialists should engage with one another throughout the disease course, from early to advanced stages, including typical referral patterns and optimal timing for patient referrals.