Literature DB >> 6190620

Hetastarch: an overview of the colloid and its metabolism.

J D Hulse, A Yacobi.   

Abstract

Hetastarch, ethoxylated amylopectin, has found clinical utility as a plasma volume expansion agent, a sedimenting agent during pheresis, and a pump priming fluid. Hetastarch is a complex mixture of derivatized amylopectin molecules of various molecular sizes. The derivatization causes resistance to enzymatic hydrolysis, therefore, allowing hetastarch sufficient vascular residence time to be an effective vascular osmotic agent. This has led to its use as a volume expander and to its consequent use as a pump priming fluid. The metabolism of hetastarch proceeds through alpha-amylase hydrolysis of glycosidic bonds, yielding molecules small enough for renal clearance, but does not result in complete hydrolysis. Hence, glucose is not a significant product of hetastarch metabolism. Metabolism proceeds at such a rate that volume expansion is seen for 24-36 hours with a maximum effect (100-172 percent of the infused volume) occurring shortly after infusion. Ninety percent of the dose is eliminated with a half-life of about 17 days.

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Year:  1983        PMID: 6190620     DOI: 10.1177/106002808301700503

Source DB:  PubMed          Journal:  Drug Intell Clin Pharm        ISSN: 0012-6578


  14 in total

Review 1.  Pharmacokinetics of hydroxyethyl starch.

Authors:  Cornelius Jungheinrich; Thomas A Neff
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

2.  Pharmacodynamics and organ storage of hydroxyethyl starch in acute hemodilution in pigs: influence of molecular weight and degree of substitution.

Authors:  Christoph Eisenbach; Alexander H Schönfeld; Norbert Vogt; Moritz N Wente; Jens Encke; Wolfgang Stremmel; Eike Martin; Ernst Pfenninger; Markus A Weigand
Journal:  Intensive Care Med       Date:  2007-06-07       Impact factor: 17.440

Review 3.  Intravenous volume replacement: which fluid and why?

Authors:  L Huskisson
Journal:  Arch Dis Child       Date:  1992-05       Impact factor: 3.791

4.  [Ascites as a complication of hepatic storage of hydroxyethyl starch in long-term dialysis].

Authors:  U Pfeifer; J Kult; H Förster
Journal:  Klin Wochenschr       Date:  1984-09-17

5.  Ultrasound assessment of ex vivo lung tissue properties using a fluid-filled negative pressure bath.

Authors:  Sarah Duenwald-Kuehl; Melissa L Bates; Sonia Y Cortes; Marlowe W Eldridge; Ray Vanderby
Journal:  J Biomech Eng       Date:  2014-07       Impact factor: 2.097

6.  Hydroxyethylstarch deposits in human skin--a model for pruritus?

Authors:  W Jurecka; Z Szépfalusi; E Parth; W Schimetta; W Gebhart; O Scheiner; D Kraft
Journal:  Arch Dermatol Res       Date:  1993       Impact factor: 3.017

7.  Mechanisms of postoperative prolonged plasma volume expansion with low molecular weight hydroxethy starch (HES 200/0.62, 6%).

Authors:  A C Degrémont; M Ismaïl; M Arthaud; B Oulare; O Mundler; M Paris; J F Baron
Journal:  Intensive Care Med       Date:  1995-07       Impact factor: 17.440

8.  Human monocytes and keratinocytes in culture ingest hydroxyethylstarch.

Authors:  Z Szépfalusi; E Parth; W Jurecka; T A Luger; D Kraft
Journal:  Arch Dermatol Res       Date:  1993       Impact factor: 3.017

Review 9.  Use of plasma volume expanders in myocardial revascularisation.

Authors:  J H Lacy; C B Wright
Journal:  Drugs       Date:  1992-11       Impact factor: 9.546

10.  Effect of isovolaemic haemodilution on visual outcome in branch retinal vein occlusion.

Authors:  H C Chen; J Wiek; A Gupta; A Luckie; E M Kohner
Journal:  Br J Ophthalmol       Date:  1998-02       Impact factor: 4.638

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