ABSTRACTS from 16th International COnference on ... - CRRT Online
ABSTRACTS from 16th International COnference on ... - CRRT Online
ABSTRACTS from 16th International COnference on ... - CRRT Online
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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