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<str<strong>on</strong>g>ABSTRACTS</str<strong>on</strong>g> FROM 17 TH INTERNATIONAL CONFERENCE ON <strong>CRRT</strong>,<br />

SAN DIEGO, FEB 14-17, 2012<br />

62. Treatment of hyperlipidemia in<br />

resistant nephrotic syndrome: the<br />

effect of combined therapy using<br />

double filtrati<strong>on</strong> plasmapheresis<br />

and oral statins<br />

Dehua G<strong>on</strong>g, Daxi Ji, D<strong>on</strong>gd<strong>on</strong>g Zhu,<br />

Lihua Zhang, Bin Xu, Zhih<strong>on</strong>g Liu<br />

Research Institute of Nephrology<br />

Objective: by a case-c<strong>on</strong>trolled design,<br />

to compare the effects of treatment <strong>on</strong><br />

hyperlipidemia in resistant nephrotic<br />

syndrome by combined therapy using<br />

double filtrati<strong>on</strong> plasmapheresis(DFPP)<br />

and oral statins or oral statins <strong>on</strong>ly.<br />

Methods: Eight inpatients were enrolled<br />

and received 1 sessi<strong>on</strong> of DFPP for<br />

severe hyperlipidemia due to resistant<br />

nephrotic syndrome(NS). Oral<br />

Atorvastatin(2mg/d) were c<strong>on</strong>tinuously<br />

given to these patients 1 week prior to<br />

start of DFPP until the end of<br />

followup(Combinati<strong>on</strong> group). In the<br />

same period 12 outpatients with severe<br />

hyperlididemia due to resistant NS were<br />

enrolled to take oral Atorvastatin<br />

(2mg/d)( statins group). In additi<strong>on</strong> to<br />

treatment of hyperlipidemia, standard<br />

cares for primary renal disease were also<br />

given to all patients. For 1-m<strong>on</strong>th<br />

follow-up period, the changes of plasma<br />

c<strong>on</strong>centrati<strong>on</strong> of lipids and albumin as<br />

well as urinary proteins were m<strong>on</strong>itored.<br />

Results: There were no significant<br />

changes of serum albumin c<strong>on</strong>centrati<strong>on</strong><br />

and urinary proteins after 1 m<strong>on</strong>th in<br />

both groups. In the combinati<strong>on</strong> group,<br />

baseline values for serum albumin, total<br />

cholesterol, triglycerides, LDL-C and<br />

fibrogen were 18.7±5.g/L, 15.2±7.4<br />

mmol/L, 5.5±5.21mmol/L,<br />

9.±4.2mmol/L and 426±5mg/L,<br />

respectively. The reducti<strong>on</strong> rate after<br />

single sessi<strong>on</strong> of DFPP for these<br />

parameters were -11.3±13.4, 85.8±7.2,<br />

8.1±6.2, 86.9±11.4, and 54.7±14.3%,<br />

respectively. At 2 weeks and 4 weeks<br />

after DFPP, the c<strong>on</strong>centrati<strong>on</strong>s of plasma<br />

total cholesterol were as 41.8±13.4%<br />

and 7.2±21.% of baseline, while the<br />

c<strong>on</strong>centrati<strong>on</strong> of triglycerides were as<br />

68.6±45.5% and 125.8±48.8% of<br />

baseline. In the statins group, the<br />

baseline value of plasma albumin, total<br />

cholesterol and triglycerides were<br />

23.6±3.9g/L, 15.4±5.mmol/L and<br />

5.2±3.3mmol/L, respectively. At 2<br />

weeks and 4 weeks follow-up, the<br />

c<strong>on</strong>centrati<strong>on</strong>s of plasma total<br />

cholesterol were as 81.2±21.1% and<br />

81.±16.7% of baseline, while the<br />

c<strong>on</strong>centrati<strong>on</strong> of triglycerides were as<br />

85.3±43.1% and 18.4±55.6% of<br />

baseline. The difference of plasma total<br />

cholesterol levels between two groups at<br />

the 2 weeks follow-up was significant<br />

(P

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