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Letters to Editor
29 (
3
); 217-219
doi:
10.4103/ijn.IJN_241_17

Severe Hypertriglyceridemia-induced Acute Pancreatitis: Successful Management by Plasmapheresis

Department of Nephrology, Nizams Institute of Medical Sciences, Hyderabad, Telangana, India
Address for correspondence: Dr. S. Raju, Department of Nephrology, Nizams Institute of Medical Sciences, Punjagutta, Hyderabad - 500 082, Telangana, India. E-mail: sreebhushan@hotmail.com
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Disclaimer:
This article was originally published by Wolters Kluwer - Medknow and was migrated to Scientific Scholar after the change of Publisher.

Sir,

This presentation illustrates case of a 44-year-old female with uncontrolled Type II diabetes mellitus for 6 years, who presented to the emergency room with upper abdominal pain and vomiting of 3 days’ duration. Clinical examination revealed stable vitals with epigastric tenderness and guarding per abdomen. Random blood sugar was 494 mg/dl and urine ketones were negative. She was started on insulin infusion and other supportive management. The blood was highly lipemic [Figure 1] with serum triglyceride (TG) level of 6800 mg/dl, total cholesterol of 613 mg/dl, low-density lipoprotein cholesterol of 137 mg/dl, and high-density lipoprotein cholesterol of 53 mg/dl. Serum amylase was 871 U/L, lipase was 796 U/L, and renal and liver function tests were normal. Her ultrasound abdomen showed bulky pancreas with fat stranding. Contrast-enhanced computed tomography (CT) abdomen was suggestive of acute pancreatitis (AP) with modified CT severity score of >6. She had no history of alcohol use, drug intake, gallstones or pancreatitis. The patient was managed as severe hypertriglyceridemia (SHTG)-induced AP (revised Atlanta classification 2012). She was kept nil per oral, given intravenous fluids along with other supportive management. However, abdominal pain persisted with persistently high TG levels, for which she was started on plasmapheresis. Her TG after plasmapheresis decreased to 1158 mg/dl and 761 mg/dl after the 1st and 2nd session, respectively. She reported clinical improvement after two sessions of plasmapheresis. She was started on oral statins and fenofibrate. Insulin infusion was switched over to intermittent short-acting insulin. She was discharged in a stable condition on statins, fibrate, and insulin. On follow-up, her serum TG decreased to 289 mg/dl after 2 weeks [Figure 2].

Figure 1
Image showing highly lipemic serum
Figure 2
Graphical representation of serum triglyceride levels after plasmapheresis

Hypertriglyceridemia is classified as mild (150–199 mg/dl), moderate (200–999 mg/dl), severe (1000–1999 mg/dl), and very severe (>2000 mg/dl). SHTG with serum TG concentrations >1000 mg/dl is a risk factor for AP.[1] The exact pathophysiology of hypertriglyceridemia-induced AP is not clear. A proposed mechanism is hydrolysis of TG by pancreatic lipase, leading to accumulation of high concentrations free fatty acids and chylomicrons which can produce acinar cell injury and capillary plugging causing ischemia and acidosis activating trypsinogen and AP.[2] Conventional management of hypertriglyceridemia includes dietary fat restriction and pharmacotherapy which are time-consuming. Furthermore, in the patients with severe AP (SAP), urgent lowering of TG is necessary to prevent disease complications and oral pharmacological therapy may not always be feasible.[3]

Plasmapheresis is an effective therapeutic option for hypertriglyceridemia-induced SAP with rapid reduction of serum TG and can be considered early in the management. There are few case studies reports published in the literature.[4567] The absolute indications of plasmapheresis in patients with hypertriglyceridemia are (a) patient refractory to nutritional and pharmacological approaches, (b) serum TG exceed 1000 mg/dl, (c) worsening inflammation and organ dysfunction.[8] The relative indications include (a) serum lipase 3 times the upper limit of normal, (b) severe hypocalcemia, and (c) lactic acidosis. Our patient had TG >1000 with AP refractory to treatment with lipase >3 times.

The beneficial effect of plasmapheresis is believed to be because of rapid decrease in TG levels; however, removal of excessive proteases from the plasma which are key enzymes in inflammation and replacement of consumed protease inhibitors might be an additional benefit.[3] Two sessions of plasmapheresis costs about 35,000 in our center and it is a rather expensive treatment option and not available in all centers. This might therefore limit its use.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

Acknowledgment

We are very much thankful to Dr. Alekhya for helping us in the preparation of this manuscript.

References

  1. , , . Treatment options for severe hypertriglyceridemia (SHTG): The role of apheresis. Clin Res Cardiol Suppl. 2012;7:31-5.
    [Google Scholar]
  2. , . Pathogenesis, differentiation and management of hypertriglyceridemia. Adv Intern Med. 1969;15:117-54.
    [Google Scholar]
  3. , , , , . Factors affecting outcome in acute hypertriglyceridemic pancreatitis treated with plasma exchange: An observational cohort study. PLoS One. 2014;9:e102748.
    [Google Scholar]
  4. , , , , , . Plasmapheresis as treatment for hyperlipidemic pancreatitis. Eur J Intern Med. 2014;25:160-3.
    [Google Scholar]
  5. , , , , . Plasmapheresis in the treatment of hypertriglyceridemia-induced pancreatitis: A community hospital's experience. J Clin Apher. 2010;25:229-34.
    [Google Scholar]
  6. , , , , , , . Plasmapheresis in the treatment of hypertriglyceridemia. Orv Hetil. 2014;155:1203-6.
    [Google Scholar]
  7. , , , , , , . Plasmapheresis in the management of acute severe hyperlipidemic pancreatitis: Report of 5 cases. Pancreatology. 2005;5:201-4.
    [Google Scholar]
  8. , , , , , . Severe hypertriglyceridemia induced pancreatitis in pregnancy. Case Rep Obstet Gynecol. 2014;2014:485493.
    [Google Scholar]
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