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ACUTE PANCREATITIS DUE TO PROTEASE INHIBITOR CONTAINING REGIMEN TREATED WITH
PLASMAPHERESIS
JP Routy1, S Bruce1, MR Boulassel1, GRH Smith1, DW Blank2, BM Gilfix2
1Immunodeficiency Service; 2Division of Clinical Biochemistry, McGill University
Health Centre, Montreal, Quebec
Objective: Lipid changes are a well-recognized side effect of long-term
treatment with protease inhibitors (PIs). Here we report a case of severe hypertriglyceridemia
complicated by acute pancreatitis treated by plasmapheresis in an HIV-1 patient
treated with a boosted PI regimen containing ritonavir and indinavir.
Case presentation: A 35-year-old HIV-1 positive male was in remission
from a high-grade non-Hodgkin lymphoma after the completion of six cycles of
CHOP. Over the past 3 years, he was successfully treated with a combination
of d4T (40 mg b.i.d.), 3TC (150 mg b.i.d.) and indinavir (800 mg t.i.d.). In
response to an increase of his HIV RNA plasma level, which was detectable for
the first time (5040 copies/mL with CD4=101x106/L), ritonavir (400 mg b.i.d.)
was added to the same therapy regimen with a dose reduction of indinavir (400
mg b.i.d.). Three weeks later, the patient developed nausea, severe abdominal
pain, a distended abdomen and presented abnormal laboratory test values: total
cholesterol (27.1 mmol/L, reference value 3.8-5.2), lipase (864 U/L, reference
value 8-57), amylase (238 U/L, reference value 20-130) and triglycerides (62.9
mmol/L, reference value 0.0-2.3). A CT scan of the abdomen confirmed the presence
of stage C acute pancreatitis. Anti-HIV medication was immediately held, and
plasmapheresis was performed. Symptoms were alleviated after the first plasmapheresis
and the laboratory values returned to their normal ranges. The patient fully
recovered after one week of treatment with dT4, 3TC and indinavir (800 mg t.i.d.)
regimens.
Conclusion: This is the first case reporting acute pancreatitis due to
ritonavir-indinavir related hypertriglyceridemia treated by plasmapheresis.
This case stresses the importance of closely monitoring total cholesterol and
triglyceride levels during the first month of therapy in patients initiating
ritonavir containing regimens. This case also illustrates the use of plasmapheresis
to treat acute pancreatitis in the setting of ritonavir-induced hypertriglyceridemia.