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Netherlands Journal

NJCC Volume 10, Oktober 2006

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netherlands journal of critical care<br />

Table 1: Characteristics of HES products<br />

HES 70/0,5 HES 130/0,4 HES 200/0,5 HES 200/0,5 HES 200/0,62 HES 450/0,7<br />

Concentration in % 6 6 6 10 6 6<br />

Volume Effect in % 80 100 100 140 100 100<br />

Effect duration in hours 1-2 2-3 3-4 3-4 5-6 5-6<br />

Mean mol. weight in kD 70 130 200 200 200 450<br />

Degree of substitution 0,5 0,4 0,5 0,5 0,62 0,7<br />

C2/C6 ration 4:1 9:1 6:1 6:1 9:1 4,5:1<br />

Table 2: Fluids for true hypovolemia<br />

Author/Trial name Number of patients Design Kind of fluid used Renal outcome Evidence<br />

London MJ et al. 94 RCT 10% HES vs. 5% albumin no difference level I<br />

Stockwell MA et al. 475 RCT albumin vs. polygelin no difference level I<br />

Vogt NH et al. 41 RCT HES vs. albumin no difference level II<br />

Beyer R 46 RCT HES vs.3% gelatine no difference level II<br />

Kumle B et al. 60 RCT LMW HES vs. MMW HES vs. Gelatine no difference level II<br />

Allison KP et al. 45 RCT HES vs. Gelatine HES better level II<br />

Boldt J et al 20 RCT HES 130/0,4 vs. HES 200/0,5 no difference level II<br />

Dehne MJ et al. 60 RCT lactated ringer vs. 3 different HES no difference level II<br />

Sedrakyan A et al. 19578 retrospective albumin vs. non-protein colloids albumin renders survival benefit level III<br />

Winkelmayer W. et al 238 retrospective HES 670/0.75 vs. no HES reduced GFR level III<br />

Neff TA et al. 31 RCT HES 130/0,4 vs. HES 200/0,5 + albumin no difference level III<br />

filtration as well as osmotic nephrosis (osmotic tubular damage) if<br />

insufficient free water accompanies administration.Four types of<br />

colloids are used: albumin, gelatins and hydroxy-ethyl starch.<br />

Human albumin (HA)<br />

Human albumin (HA) is the natural colloid present in human circulation<br />

and therefore may appear to be the ideal substitution in<br />

hypo-oncotic hypovolaemia. Furthermore albumin decreases inflammatory<br />

cytokine expression after haemorrhagic shock [14;15] and is<br />

necessary for delivery of furosemide to the thick ascending limb of<br />

Henle for effective diuresis [16]. However, albumin is expensive, and<br />

due to its relative small size (69 kD) its intravascular effect may be<br />

reduced in states of endothelial damage and capillary leakage. Albumin<br />

is derived from pooled plasma and potentially carries the risk of<br />

infection. Despite earlier concerns about safety a recent large multicentre<br />

RCT using 4% albumin did not show any difference in either<br />

outcome parameter including renal function when compared to normal<br />

saline [17].<br />

Gelatins<br />

Gelatins usually have an average molecular weight around 30 kD<br />

which is even smaller than albumin. Thus, its intravascular volume<br />

effect is even shorter at around 2 hours. The advantage of this substance<br />

is absence of adverse effects on renal function [18;19]. Problems<br />

associated with gelatin, however, are the possibility of prion<br />

transmission, their capacity to release histamine and their negative<br />

influence on the coagulation system [20;21].<br />

Dextrans<br />

Dextrans are single chain polysaccharides with a size comparable<br />

to albumin (40 , 60 or 70 kD) and a reasonably high volume effect.<br />

However, main disadvantages include anaphylactic reactions and serious<br />

interference with coagulation system at doses higher than 1.5<br />

g/kg/day [22;23]. Additionally, case reports on the occurrence of ARF<br />

after dextran administration have been published [24;25].<br />

Hydroxyethyl starch (HES)<br />

Hydroxyethyl starches (HES) are highly polymerised sugar molecules.<br />

They are characterised by their molecular weight, grade of<br />

substitution, concentration and C2/C6 ratio. Their volume effect is<br />

significantly longer than that of albumin especially when larger size<br />

HES are used (Table 1). Degradation occurs by hydrolytic cleavage<br />

which results in smaller molecules which will finally be eliminated<br />

by the reticular endothelial system or filtered and eliminated by the<br />

kidney. In this way these degradation products may be reabsorbed<br />

and contribute to osmotic nephrosis and probably to medullary hypoxia<br />

[26;27]. Another problem associated with administration of<br />

HES is pruritus [28].<br />

Recently there was a review of fourteen studies investigating the<br />

use of various colloids on renal function [29]. Although no statistical<br />

analysis was performed in this study owing to the heterogeneity of<br />

the studies selected, the authors stated that rapidly degradable HES<br />

preparations (degree of substitution (DS) 0.4 or 0.5) appear to have<br />

less risk for impairing renal function than HES with a high DS (0.62<br />

or 0.7).<br />

Whereas albumin appears to be safe [17], recent data indicate<br />

possible impairment of renal function by HES [19]. This is further<br />

supported by a cohort study in patients undergoing coronary artery<br />

bypass graft surgery (CABG and demonstrating moderate reduction<br />

of glomerular filtration rate (GFR) after administration of HES [30]<br />

Clinical situations in which renal protection/renal<br />

recovery by volume expansion appears feasible and<br />

supported by clinical studies<br />

We performed a systematic MEDLINE search for randomised controlled<br />

trials (RCT) addressing the use of different types of hydration<br />

regimens to prevent deterioration of renal function in adult patients<br />

at risk for ARF.<br />

• The following clinical conditions were considered: major surgery,<br />

sepsis, shock, use of potentially nephrotoxic drugs, radiocontrast<br />

media and renal transplantation.<br />

• The following terms and text words were used: kidney failure,<br />

acute, kidney failure, acute/prevention and control, renal, cardiac<br />

surgery, sepsis, contrast, shock, liver cirrhosis, normal saline,<br />

hydroyethyl starch, colloids, crystalloids, gelatine, human albumin.<br />

neth j crit care • volume 10 • no 5 • october 2006<br />

549

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