High-volume hemofiltration plus hemoperfusion for hyperlipidemic severe acute pancreatitis: a controlled pilot study

original articleHigh-volume hemofiltration plus hemoperfusion for hyperlipidemic severe acute pancreatitis: a controlled pilot study Shiren Sun, Lijie He, Ming Bai, Hongbao Liu, Yangping Li, Li Li, Yan Yu, Meilan Shou, Rui Jing, Liyuan Zhao, Chen Huang, and Hanmin Wang Shiren Sun Search for more papers by this author , Lijie He Search for more papers by this author , Ming Bai Search for more papers by this author , Hongbao Liu Search for more papers by this author , Yangping Li Search for more papers by this author , Li Li Search for more papers by this author , Yan Yu Search for more papers by this author , Meilan Shou Search for more papers by this author , Rui Jing Search for more papers by this author , Liyuan Zhao Search for more papers by this author , Chen Huang Search for more papers by this author , and Hanmin Wang Search for more papers by this author Published Online::1 Oct 2015https://doi.org/10.5144/0256-4947.2015.352SectionsPDF ToolsAdd to favoritesDownload citationTrack citations ShareShare onFacebookTwitterLinked InRedditEmail AboutAbstractBACKGROUND AND OBJECTIVES: The evidence for high-volume hemofiltration plus hemoperfusion (HVHF&HP) for hyperlipidemic severe acute pancreatitis (HL-SAP) is anecdotal. The purpose of our study was to evaluate the efficacy of HVHF&HP for HL-SAP in a prospective controlled study.DESIGN AND SETTING: Prospective controlled pilot study between May 2010 and May 2013 in a hospital intensive care unit.PATIENTS AND METHODS: HL-SAP patients chose conventional treatment alone (the control group) or conventional treatment combined with the experimental protocol (the HVHF&HP group) and were prospectively followed in our hospital. APACHE II score, SOFA score, ICU and hospital stay duration, and serum biomarkers were considered endpoints.RESULTS: Ten HL-SAP patients accepted conventional treatment alone (the control group) and 10 patients underwent HVHF&HP combined with conventional treatment (the HVHF&HP group). The APACHE II score, SOFA score, systolic blood pressure, diastolic blood pressure, heart rate, serum amylase, and serum creatinine were significantly reduced after the HVHF&HP treatment. The changes in these variables were significantly different between the HVHF&HP and control group at 48 hours after the initiation of treatment. Patients in the HVHF&HP group had a significantly shorter ICU stay (P=.015). The reduction in serum triglyceride and cholesterol in the HVHF&HP group after 2, 6, 12, 24, and 48 hours was greater than the control group. All of the tested serum cytokines were significantly decreased after HVHF&HP treatment (P<.05). However, in patients who underwent conventional treatment alone, there was no significant change in the serum cytokines.CONCLUSION: This study suggests that the addition of HVHF&HP to conventional treatment for HL-SAP patients may be superior to conventional treatment alone for the improvement of serum biomarkers and clinical outcomes.IntroductionSevere acute pancreatitis (SAP) is a life-threatening condition which may cause systematic inflammatory response syndrome (SIRS), sepsis, and even multiple organ dysfunction syndromes (MODS). Cholelithiasis, alcohol abuse, and hyperlipidemia are the main causes of acute pancreatitis. The morbidity of SAP secondary to hyperlipidemia (HL-SAP) has apparently increased in recent years. SAP occurred in 12–38% of hyperlipidemic patients.1,2The main treatment for HL-SAP is to decrease the serum triglyceride level and prevent a systemic inflammatory response.3 Although serum triglyceride can be decreased by plasmapheresis, it is not widely used in clinical practice because of the limited availability of plasma donors especially in developing countries.4–6 Continuous veno-venous hemofiltration (CVVH), especially high-volume hemofiltration (HVHF), has been widely used for treating SAP because it can effectively remove the excessive inflammatory mediators from the system circulation and help maintain homeostasis. However, CVVH does not allow large molecules such as triglycerides to pass through the hemofilter. Hemoperfusion (HP) is another blood purification modality which can absorb large pathogenic molecules from the circulation by adsorbent materials installed in the HP cartridge. HP is more effective in removing middle and large molecules and toxins bonded with proteins than CVVH. In 2011, Tang et al successfully treated a pregnant woman with hyperlipidemic pancreatitis by using CVVH and HP.7 However, to the best of our knowledge, the evidence for using HVHF&HP for HLSAP is limited to anecdotal descriptions. Therefore, we evaluated the efficacy of HVHF&HP combined with conventional treatment versus conventional treatment alone for HL-SAP in a prospective controlled study.PATIENTS AND METHODSThis was a prospective controlled study conducted between May 2010 and May 2013. HL-SAP patients admitted to our intensive care unit (ICU) who underwent experimental HVHF&HP treatment based on conventional treatment and HL-SAP patients who underwent conventional treatment alone were prospectively followed. Exclusion criteria were the following: i) flare-up of chronic pancreatitis, ii) previous exploratory laparotomy during the current episode of pancreatitis, iii) pancreatitis caused by abdominal surgery, iv) CVVH treatment prior to admission, v) patients had other indications for CVVH, such as hyperkalemia, acute kidney failure, and so on. The protocol of the present study complied with the protocol and principles of the Declaration of Helsinki and was approved by the ethic committee of our hospital. Written informed consent was obtained from all patients or their legal guardians.A diagnosis of HL-SAP was made according to the Atlanta criteria8 and the guidelines for the management of acute pancreatitis issued by the World Congress of Gastroenterology.9 SIRS and MODS were diagnosed using the criteria of the American College of Chest Physicians (ACCP) and the Society of Critical Care Medicine (SCCM), respectively.10All patients received standard conventional treatment, including aggressive fluid resuscitation, oxygen supplementation, gastrointestinal decompression, insulin and/or heparin treatment, oral antihyperlipidemic drug therapy, dietary interventions, nutritional support, prophylactic antibiotics, and drainage of peripancreatic abscesses.8–12In addition to the standard conventional treatment, patients in the HVHF&HP group underwent two cycles of HVHF&HP treatment. Each cycle included 24 hours of HVHF and 2 hours of HP. The HVHF&HP treatment was initiated in the first 48 hours after the ICU admission. At first, a double lumen catheter was inserted into the internal jugular to establish vascular access. Secondly, HVHF was performed with a Diapact CRRT machine (B. Braun, http://www.bbraun.com/cps/rde/xchg/bbraun-com). The blood flow rates ranged from 250 to 300 mL/min. The substitution fluid was infused at a rate of 70 mL/kg/h in a pre-diluted manner (before the hemofilter). An AN69 hemofilter (1.6 m2 surface area, 35-KD limit; Baxter Healthcare Corp. Deerfield, IL, USA, http://www.baxter.com/) was used and changed every 24 hours or at the occurrence of filter dysfunction. The anticoagulant was low molecular weight heparin or no anticoagulant when there was any contraindication for anticoagulant treatment. Two hours of HP was carried out every 24 hours using a synthetic resin cartridge (HA-330; Zhuhai Lizhu Group, Biological Material Co, Ltd., China) installed before the hemofilter.Body temperature, breathing rate, blood pressure, heart rate, central venous pressure, PaO2 and FiO2 were tested and recorded every 6 hours. Biochemical parameters including platelet count, serum creatinine, base excess, and blood calcium were tested and recorded every 24 hours. Acute Physiology and Chronic Health Evaluation II (APACHE II) scores and Sequential Organ Failure Assessment (SOFA) scores were calculated to evaluate the severity of the disease at 2-, 6-, 12-, 24-, and 48-hour after the treatment. Blood and effluent samples were taken before the initiation of treatment (0 h) and at 2-, 6-, 12-, 24-, and 48-hour. IL-1, IL-2, IL- 6, IL-8, IL-10, and TNF-α concentrations were tested by using quantitative colormetrics sandwich ELISA kits (Shanghai Senxiong Science and Technology Company, China). All measurements were performed according to the protocols provided by the manufacturers. Every sample was tested twice and the mean cytokine concentration was calculated and used in the analyses. The researcher who performed the tests was blinded to the patients’ treatment and baseline data.Statistical analysisContinuous variables are expressed as the mean and standard deviation. The differences in continuous variables between the control and HVHF&HP groups were estimated by the Mann-Whitney U test. The Wilcoxon matched-pairs test was used to evaluate the internal group differences for continuous variables. For discontinuous variables, the chi-square and Fisher’s exact tests were used to evaluate the differences between groups. All of the statistical analyses were performed using the statistical package SPSS (version 12.0; SPSS Inc., Chicago, IL, USA). P values <.05 were considered to be statistically significant.RESULTSThe mean (SD) age were 40.3 (7.6) years and 43.2 (7.0) years for the patients in the HVHF&HP and the control group, respectively (Table 1). APACHE II scores were 13.33 ( 1.68) for the treatment group and 14.0 (0.4) for the control group. There were no significant differences in baseline characteristics between the two groups before treatment (Table 1).Table 1 Baseline characteristics of the in the HVH&HP group and the control group.VariablesControl (n=10)HVHF&HP (n=10)P valueMale, n (%)8 (80%)7 (70%).99Age (years)40.25 (1.63)43.2 (1.03).30APACHE II13.33 (1.68)14.00 (0.37).23SOFA10.67 (1.35)10.00 (0.36).15ARDS, n (%)6 (60%)7 (70%).99Mechanical ventilation, n (%)7 (70%)7 (70%).99Vasopressor, n (%)8 (80%)9 (90%).99DIC, n (%)1 (10%)1 (10%).99Serum creatinine (μmol/L)209.67 (67.79)205.8 (19.56).86BUN (mmol/L)11.93 (2.51)11.66 (0.80).75PH7.12 (0.16)7.10 (0.01).70HCO3 (mmol/L)12.00 (0.94)14.10 (0.89).22BE (mmol/L)−9.87 (0.44)−10.82 (0.84).21WBC (109/L)19.95 (0.29)22.74 (0.35).34Hemoglobin (g/L)140.50 (11.55)143.67 (3.05).41Albumin (g/L)34.60 (2.36)31.97 (0.76).21Serum amylase (IU/L)1284.50 (143.54)1455.30 (135.00).43SBP (mm Hg)149.00 (0.47)153.57 (2.30).33DBP (mm Hg)79.50 (3.06)82.33 (1.00).51Heart rate (bpm)134.00 (5.46)134.38 (2.23).84ARDS, Acute respiratory distress syndrome ; APACHE II, Acute Physiology and Chronic Health Evaluation II score; BE, base excess; BUN, blood urea nitrogen; DBP, diastolic blood pressure; DIC, Disseminated intravascular coagulation; SBP, systolic blood pressure; SOFA, Sequential Organ Failure Assessment score; WBC, white blood cell.Change in clinical featuresOnly one patient in the control group died during the ICU stay and the causes of death were ARDS and cardiogenic shock. The two groups were not significantly different in ICU mortality rate (P=.99). After 48 hours, the average APACHE II score of the HVHF&HP group decreased from 14.00 (0.37) to 5.44 (0.46) (P<.05). However, the reduction of the APACHE II score of the control group was not significant (0-hour: 13.33 [1.68], 48-hour: 12.00 [2.87], P>.05, Table 2). The two groups were significantly different in the change in APACHE II score at 6, 12, 24, and 48 hours after the start of the treatment (Table 2). The change in SOFA score after 48 hours treatment was significant for the HVHF&HP group (baseline: 10.00 [0.36], after 48 hours treatment: 4.07 [0.38], P<.05), but was not significant for the control group (0-hour: 10.67 [1.35], 48-hour: 8.98 [0.63], P≥.05, Table 2). The differences in the change of SOFA score between groups were significant at 6, 12, 24, and 48 hours.Table 2 Changes in clinical laboratory variables in the HVH&HP group vs the control group.Time pointsAPACHE IISOFASBP (mm Hg)DBP (mm Hg)Heart rate (bpm)Serum amylase (IU/L)Serum creatinine (μmol/L)ControlHVHF & HPControlHVHF & HPControlHVHF & HPControlHVHF & HPControlHVHF & HPControlHVHF & HPControlHVHF & HP0 hr13.33 (1.68)14.00 (0.37)10.67 (1.35)10.00 (0.36)149.00 (0.47)153.57 (2.30)79.50 (3.06)82.33 (1.00)134.00 (5.46)134.38 (2.23)1284.50 (143.54)1455.30 (135.00)209.67 (67.79)205.8 (19.56)2 hrs12.93 (1.28)13.08 (0.46)10.17 (1.31)6.71 (0.38)149.95 (0.62)134.76 (2.68)a,b81.50 (2.64)80.03 (1.07)133.00 (5.64)134.31 (2.74)901.90 (115.29)555.30 (121.00)a,b208.91 (79.32)190.18 (16.67)b6 hrs12.00 (1.76)10.25 (0.32)a,b10.00 (0.94)4.88 (0.28)a,b145.75 (3.17)134.43 (1.60)a,b86.00 (1.53)a77.00 (0.67)b131.00 (1.17)122.00 (1.24)a,b830.75 (83.44)484.38 (78.30)a,b207.0 (62.0)174.8 (15.25)a,b12 hrs12.00 (1.76)9.00 (0.33)a,b10.50 (0.71)3.88 (0.17)a,b147.00 (5.82)135.00 (2.17)a,b83.00 (3.95)76.33 (0.47)a,b131.75 (5.10)131.75 (5.10853.75 (70.29)359.88 (34.40a,b208.0 (46.53)169.7 (15.14)a,b24 hrs12.00 (1.76)6.33 (0.36)a,b9.67 (0.51)4.00 (0.27)a,b148.33 (2.83)129.00 (1.20)a,b80.33 (1.18)76.291 (0.92)a129.25 (7.07)94.38 (0.82)a,b813.25 (55.33)a260.78 (27.79)a,b211.0 (52.54)146.5 (14.34)a,b48 hrs12.00 (2.87)5.44 (0.46)a,b8.98 (0.63)4.07 (0.38)a,b149.47 (3.72)127.11 (2.32)a,b82.45 (2.42)70.21 (0.28)a,b125.45 (7.18)82.49 (0.71)a,b924.52 (57.67)213.87 (29.99a,b209.90 (11.24)125.5 (12.42)a,bAPACHE II, Acute Physiology and Chronic Health Evaluation II score; DBP, diastolic blood pressure; SOFA, Sequential Organ Failure Assessment score; Hr, hour; SBP, systolic blood pressure;aIdentifies these variables differ significantly from their baseline value;bIdentifies these variables differ significantly from the control group.Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were significantly improved in the patients who underwent HVHF&HP treatment, but were not significantly changed in the patients who underwent conventional treatment alone (P<.05, Table 2). Mean heart rates in the HVHF&HP group decreased from 134.38 (2.23) to 82.49 (0.71) (P<.05). Serum amylase and creatinine levels gradually decreased during HVHF&HP treatment. Changes in SBP, DBP, heart rate, serum amylase level, and serum creatinine level at 48 hours were significantly different between the two groups (Table 2).Patients who underwent HVHF&HP plus conventional treatment had a significantly shorter ICU stay duration (10.1 [3.8] days versus 16.0 [5.0] days, P=.015) than patients underwent conventional treatment alone. The HVHF&HP group tended to have a shorter period of hospitalization (17.4 [3.9] days versus 22.6 [6.6 ] days, P=.105), compared with the control group.All patients were followed for up to 6 months, and no recurrence of pancreatitis or death was observed during the 6 months follow-up. No adverse event was observed during HVHF&HP treatment. The means of the total medical cost were RMB 62 000 and 50 000 for the HVHF&HP and control groups, respectively.Change in serum lipid levelThe serum lipid levels were significantly reduced after 48 hours of HVHF&HP treatment. The mean serum triglyceride (TG) level was reduced to 10.62 (1.78) mmol/L at 2 hours (P<.05) and 2.92 (1.03) mmol/L at 48 hours (P<.05) in the HVHF&HP group. The mean serum cholesterol (CHO) level in the HVHF&HP group was reduced from 11.68 (1.37) mmol/L to 6.9 (1.02) mmol/L at 2 hours (P<.05) and 4.10 (1.00) mmol/L at 48 hours (P<.05). However, the mean serum TG (0 hour: 27.53 [1.68] mmol/L, 48 hours: 19.39 [2.01] mmol/L, P≥.05) and CHO (0 hour: 11.20 [1.64] mmol/L, 48 hours: 10.10 [1.10] mmol/L, P≥.05) levels in the control group were not significantly reduced after 48 hours of conventional treatment alone (Figure 1). The changes in the TG and CHO levels were significantly different between groups at 2, 6, 12, 24, and 48 hours (Figure 1).Figure 1 Serum CHO and TG levels at 0-, 2-, 6-, 12-, 24-, 48-hour after the initiation of treatment. *Variables differed significantly from their baseline value; ‡Variables differed significantly from the control group.Download FigureChange of cytokinesAfter 2 hours of HVHF&HP treatment, the serum concentrations of all of the tested cytokines (including IL-1, IL-2, IL-6, IL-8, IL-10, and TNF-α) were significantly decreased (Figure 2). The serum concentrations of all of the tested cytokines were decreased to nearly normal after 48 hours of HVHF&HP treatment (Figure 2). We also found out that the serum levels of IL-1, IL-2, IL-6, IL-8, IL-10, and TNF-α in the effluent displacement liquid were increased gradually after 6, 12, and 24 hours of HVHF treatment (Figure 3). However, in the control group, serum IL-1, IL-2, IL- 6, IL-8, IL-10, and TNF-α levels were not significantly decreased after 48 hours of conventional treatment alone, with a mean baseline value of 0.35 (0.02) ng/mL, 10.59 (0.72) ng/mL, 0.40 (0.04) ng/mL, 0.78 (0.03) ng/mL, 150.70 (13.63) ng/mL, and 78.11 (8.99) fmol/mL, respectively, and a mean 48-hour value of 0.310 (0.02) ng/mL, 10.94 (0.83) ng/mL, 0.47 (0.02) ng/mL, 0.68 (0.06) ng/mL, 140.87 (12.21) ng/mL, and 91.80 (6.21) fmol/mL (P>.05, Figure 2), respectively. The changes in all of the cytokines after 48 hours of treatment were significantly different in the two groups (P<.05, Figure 2).Figure 2 Serum IL-1, IL-2, IL-6, IL-8, IL-10, and TNF-a level at 0-, 2-, 6-, 12-, 24-, 48-hour after the initiation of treatment. *Variables differed significantly from their baseline value; ‡Variables differed significantly from the control group.Download FigureFigure 3 IL-1, IL-2, IL-6, IL-8, IL-10, and TNF-a levels of the effluent displacement liquid increased after 6, 12, 24, and 48 hours of HVHF&HP treatment.Download FigureDISCUSSIONThe incidence of AP caused by hyperlipidemia has shown a rising trend in the past decade. In 1995, Fortson et al reported on 577 AP patients from four centers and showed that the incidence of hyperlipidemic AP during 1982 and 1994 was 1.3%~3.8%.13 In 2003, the incidence of HL-SAP was reported to be 12%~38% and 12.3% by Mao et al14 and Chang et al,15 respectively.The pathogenesis of hyperlipidemia-induced pancreatitis is not well understood. Previous studies have elucidated the following possible mechanisms. First, free fatty acids (FFAs), one of the products of triglyceride metabolism, cause direct damage to pancreatic acinar cells. Second, an increase in circulating FFA induces acidosis, which accelerates the activation of trypsinogen. Third, hyperlipidemia increases blood viscosity and FFAs damages the capillary endothelium, both of which lead to microcirculatory disturbances in the pancreas. Moreover, triglycerides play an important role in the occurrence and development of AP, which can further aggravate pancreatic necrosis and cause severe pancreatitis.14,16 Serum triglyceride levels of 11.3–22.6 mmol/L have been associated with incidences of pancreatitis as high as 21%.2,16 Early and rapid reduction of serum triglyceride to <5.65 mmol/L could prevent further development of pancreatitis.17, 18How can we effectively and rapidly reduce triglycerides and thereby prevent the resultant damage to the pancreas? Several studies have proven that plasma replacement can swiftly reduce triglyceride and alleviate AP symptoms.15,19,20 Therefore, plasma replacement has become an effective alternate for pancreatitis. However, plasma replacement is expensive and the use of plasma replacement is limited by many factors, including hospital plasma supply and plasma allocation time. Therefore, it is used sparingly in clinical practice. HP is an important hemopurification technique, and the adsorbent materials installed in the HP cartridge can effectively clear the hydrophobic substances that commonly bond to the serum proteins and lipids. Direct lipoprotein adsorption without initial plasma separation is the primary HP technique for extracorporeal CHO and TG elimination, and can improve the patient symptoms impressively. Tasaki et al and Bosch et al showed that direct HP was an effective and safe method for the clearance of serum lipoprotein (a) (Lp[a]) and triglyceride. 21,22 In 2011, Tang et al successfully managed a pregnant woman with hyperlipidemic pancreatitis by the early use of CVVH and HP.7 In our present study, HVHF&HP was successfully used in 10 HL-SAP patients. The results indicate that blood lipids level (TG and CHO) significantly decreased after every HP session, and the serum amylase concentration significantly decreased after the second HP session. Rapid elimination of the blood lipids was associated with dramatic alleviation of patient symptoms and reduction of the APACHE II and SOFA score.Based on the pathogenesis of SAP, the pancreatic autophagy theory appears to be insufficient to fully explain the occurrence and development of SAP. In 1988, Rinderknecht et al proposed the theory of “excessive activation of leukocyte”.23 Recently, the “second strike theory”, i.e., the productions of inflammatory cytokines, and the “cascade reaction”, are considered as the primary causes for progression of pancreatitis to multiple-organ failure and death. Continuous HF, especially HVHF, has proved to be effective in the clearance of inflammatory mediators, reconstitution of the immune system, stabilization of the internal environment, preservation of organ function, and a reduction in mortality rate.24–26 However, HVHF is not effective in the clearance of large molecules. Mao et al found that coupled plasma filtration adsorption (CPFA) was better than HVHF in increasing the anti-inflammatory to pro-inflammatory mediator ratios, improving the antigen presentation ability, and restoring leukocyte responsiveness.27 Accordingly, we hypothesized that the combination of HVHF with HP would eliminate blood lipids and serum inflammatory cytokines and preserve the homeostasis and fluid-electrolyte balance. Two cycles of HVHF&HP treatment were performed for the patients in the HVHF&HP group. Significant reductions of TG, CHO, IL-1, IL-2, IL-6, IL-8, IL-10, and TNF-α were observed after the treatment, compared with either the baseline values or the control group. The reductions in these serum biomarkers were consistent with the improvement of patient physical status. IL- 1, IL-2, IL-6, IL-8, IL-10, and TNF-α were reported to be the main inducers of hepatic synthesis of acute-phase protein response. The level of these cytokines was reported to directly relate to the degree of various types of organ damage in AP patients. Therefore, most likely, both the clearance of blood lipids by HP and the clearance of serum inflammatory cytokines by HVHF contributed to the improvement of the APACHE II and SOFA score and the reduction of ICU duration of stay in the HVHF&HP group.LIMITATIONSThe present study was performed in a single center with a small sample size. The application of the conclusions to other centers should be with caution. Additionally, the present study was not designed to evaluate the mortality difference between the two groups. The efficacy of the combination of HVHF&HP with conventional treatment on patient survival has not been well assessed. Therefore, we are designing an RCT with large sample size to evaluate the efficacy of HVHF&HP on long-term survival of HL-ASP patients. Further trials on this subject from other centers are needed as well.CONCLUSIONIn conclusion, the combination of HVHF&HP with conventional treatment for HL-SAP patients could effectively decrease the level of serum cytokines and improve patient physical status. Further studies are needed to evaluate the efficacy of HVHF&HP on patient mortality.Conflict of interestNo conflict of interest is declared.ARTICLE REFERENCES:1. Iskandar SB, Olive KE. "Plasmapheresis as an adjuvant therapy for hypertriglyceridemia-induced pancreatitis" . Am J Med Sci. 2004; 328:290-4. Google Scholar2. Yadav D, Pitchumoni CS. "Issues in hyperlipidemic pancreatitis" . J Clin Gastroenterol. 2003; 36:54-62. Google Scholar3. Kyriakidis AV, Raitsiou B, Sakagianni A, et al. "Management of acute severe hyperlipidemic pancreatitis" . Digestion. 2006; 73:259-64. Google Scholar4. Hen K, Bogdanski P, Pupek-Musialik D. Successful treatment of severe hypertriglyceridemia with plasmapheresis--case reportPol Merkur Lekarski. 2009; 26:62-4. Google Scholar5. Saravanan P, Blumenthal S, Anderson C, et al. "Plasma exchange for dramatic gestational hyperlipidemic pancreatitis" . J Clin Gastroenterol. 1996; 22:295-8. Google Scholar6. Kadikoylu G, Yavasoglu I, Bolaman Z. "Plasma exchange in severe hypertriglyceridemia a clinical study" . Transfus Apher Sci. 2006; 34:253-7. Google Scholar7. Tang Y, Zhang L, Fu P, et al. "Hemoperfusion plus continuous veno-venous hemofiltration in a pregnant woman with severe acute pancreatitis: a case report" . Int Urol Nephrol. 2012; 44:987-90. Google Scholar8. Bradley EL. "A clinically based classification system for acute pancreatitis" . Summary of the International Symposium on Acute PancreatitisAtlanta, GaSeptember 11 through 13, 1992Arch Surg. 1993; 128:586-90. Google Scholar9. Toouli J, Brooke-Smith M, Bassi C, et al. "Guidelines for the management of acute pancreatitis" . J Gastroenterol Hepatol. 2002; 17(Suppl):S15-39. Google Scholar10. Bone RC, Balk RA, Cerra FB, et al. "Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/ SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine" . Chest. 1992; 101:1644-55. Google Scholar11. Tsuang W, Navaneethan U, Ruiz L, et al. "Hypertriglyceridemic pancreatitis: presentation and management" . Am J Gastroenterol. 2009; 104:984-91. Google Scholar12. van Santvoort HC, Besselink MG, Bakker OJ, et al. "A step-up approach or open necrosectomy for necrotizing pancreatitis" . N Engl J Med. 2010; 362:1491-502. Google Scholar13. Fortson MR, Freedman SN, Webster PD. "Clinical assessment of hyperlipidemic pancreatitis" . Am J Gastroenterol. 1995; 90:2134-9. Google Scholar14. Mao EQ, Tang YQ, Zhang SD. "Formalized therapeutic guideline for hyperlipidemic severe acute pancreatitis" . World J Gastroenterol. 2003; 9:2622-6. Google Scholar15. Chang MC, Su CH, Sun MS, et al. "Etiology of acute pancreatitis--a multi-center study in Taiwan" . Hepatogastroenterology. 2003; 50:1655-7. Google Scholar16. Murphy MJ, Sheng X, MacDonald TM, et al. "Hypertriglyceridemia and acute pancreatitis" . JAMA Intern Med. 2013; 173:162-4. Google Scholar17. Bush ZM, Kosmiski LA. "Acute pancreatitis in HIV-infected patients: are etiologies changing since the introduction of protease inhibitor therapy?" Pancreas. 2003; 27:e1-5. Google Scholar18. Nair S, Yadav D, Pitchumoni CS. "Association of diabetic ketoacidosis and acute pancreatitis: observations in 100 consecutive episodes of DKA" . Am J Gastroenterol. 2000; 95:2795-800. Google Scholar19. Al-Humoud H, Alhumoud E, Al-Hilali N. "Therapeutic plasma exchange for acute hyperlipidemic pancreatitis: a case series" . Ther Apher Dial. 2008; 12:202-4. Google Scholar20. Dominguez-Munoz JE, Junemann F, Malfertheiner P. "Hyperlipidemia in acute pancreatitis. Cause or epiphenomenon?" Int J Pancreatol. 1995; 18:101-6. Google Scholar21. Tasaki H, Yamashita K, Saito Y, et al. "Lowdensity lipoprotein apheresis therapy with a direct hemoperfusion column: a Japanese multicenter clinical trial" . Ther Apher Dial. 2006; 10:32-41. Google Scholar22. Bosch T, Keller C. "Clinical effects of direct adsorption of lipoprotein apheresis: beyond cholesterol reduction" . Ther Apher Dial. 2003; 7:341-4. Google Scholar23. Rinderknecht H, Adham NF, Renner IG, et al. "A possible zymogen self-destruct mechanism preventing pancreatic autodigestion" . Int J Pancreatol. 1988; 3:33-44. Google Scholar24. Kobe Y, Oda S, Matsuda K, et al. "Direct hemoperfusion with a cytokine-adsorbing device for the treatment of persistent or severe hypercytokinemia: a pilot study" . Blood Purif. 2007; 25:446-53. Google Scholar25. Saotome T, Endo Y, Sasaki T, et al. "A case of severe acute pancreatitis treated with CTR-001 direct hemoperfusion for cytokine apheresis" . Ther Apher Dial. 2005; 9:367-71. Google Scholar26. Ronco C, Tetta C, Mariano F, et al. "Interpreting the mechanisms of continuous renal replacement therapy in sepsis: the peak concentration hypothesis" . Artif Organs. 2003; 27:792-801. Google Scholar27. Mao HJ, Yu S, Yu XB, et al. "Effects of coupled plasma filtration adsorption on immune function of patients with multiple organ dysfunction syndrome" . Int J Artif Organs. 2009; 32:31-8. Google Scholar Previous article Next article FiguresReferencesRelatedDetails Volume 35, Issue 5September-October 2015 Metrics History Published online1 October 2015 InformationCopyright © 2015, Annals of Saudi MedicineThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.PDF download