Target intelligence / Profile preview

Hydroxyethyl starch polymer (HES)

Target
HES
Molecular classification
Other (synthetic polymer), Colloid volume expander
01

Overview

Hydroxyethyl starch polymers (HES) are synthetic derivatives of amylopectin (branched polysaccharides) chemically modified with hydroxyethyl groups primarily at positions C2, C3, and C6 of the glucose units, which increase molecular resistance to enzymatic degradation and enhance their ability to act as plasma volume expanders. In clinical practice, HES solutions are used intravenously to restore and maintain intravascular oncotic pressure, especially in the setting of hypovolemia due to acute blood loss or low plasma protein states. By sustaining colloid osmotic pressure, HES helps keep fluid within the vascular space. However, HES solutions can produce significant adverse effects including coagulopathy (by interfering with clotting factors and platelet function), renal dysfunction, tissue persistence over years, and increased mortality in critically ill populations. These effects are dose-dependent and influenced by the molecular weight, degree of hydroxyethylation, and solution concentration. HES is not a receptor, enzyme, nor an endogenous molecular target, but a drug formulation designed to manipulate a physiological parameter (oncotic pressure).

Other names
HetastarchTetrastarchPentastarchVoluvenElohesHaes-Steril
02

Mechanism of action

Hydroxyethyl starch polymers exert osmotic pressure in the intravascular compartment by increasing plasma colloid concentration, thereby promoting fluid retention within blood vessels, and sustaining blood volume following fluid loss; they also impact coagulation, partly by interfering with platelet function (e.g., fibrinogen receptor GPIIb/IIIa binding)

03

Biological functions

Volume expansionmaintenance/restoration of intravascular volumeincreasing colloid osmotic pressurereducing capillary leakage
04

Disease associations

Hypovolemiashock (especially due to trauma or surgery)perioperative hemodynamic supporthypoproteinemia
05

Safety considerations

Increased risk of kidney injury (acute kidney injury)Increased risk of death in critically ill patientsImpaired coagulation (e.g., reduced factor VIII, von Willebrand factor, impaired platelet aggregation)Tissue accumulation and long-term persistenceAllergic reactionsDose-dependent side effects; recommended not to exceed maximum daily dose or use beyond 24 hours
06

Interacting drugs

Digoxin (may decrease excretion rate, raising serum levels)

1 more in the full profile.

07

Biomarkers

Plasma colloid osmotic pressureplasma albuminimmunoglobulins (IgG, IgM)fibrinogencoagulation screen parameters (PT, APTT, platelet count)

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