Pentastarch 6% / Sodium chloride 0.9% infusion 500ml bags
Pentastarch is an artificial colloid (hydroxyethyl starch derivative).
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2 branded products available
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Supply & safety information
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary.
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing all 13 studies.
Reviews & meta-analyses: 1 · Randomised trials: 3 · 1988–2024
Showing all 13 studies, sorted by most relevant.
L. Wilkins
Stroke, 1989
- Acute Disease
- Cardiac Output
- Cerebrovascular Disorders
Martin J. London, J. S. Ho, J. Triedman, et al.
The Journal of thoracic and cardiovascular surgery, 1989
- Plasma Substitutes
- Albumins
- Clinical Trials as Topic
M. London, M. Franks, E. Verrier, et al.
The Journal of thoracic and cardiovascular surgery, 1992
- Cardiopulmonary Bypass
- Ringer's Lactate
- Blood Coagulation
F. Brunkhorst, C. Engel, F. Bloos, et al.
The New England journal of medicine, 2008
- Fluid Therapy
- Ringer's Solution
- Combined Modality Therapy
N. Khardori
Yearbook of Medicine, 2008
R. Strauss, C. Stansfield, R. Henriksen, et al.
Transfusion, 1988
- Blood Coagulation
- Blood Specimen Collection
- Factor VIII
J. Rioux, M. Lessard, Bruno J. De Bórtoli, et al.
Critical Care Medicine, 2009
- Cardiac Surgical Procedures
- Hydroxyethyl Starch Derivatives
- Plasma Substitutes
Kang DO, Nam HS, Kim S, et al.
2023
- Coronary Vessels
- Tomography, Optical Coherence
- Feasibility Studies
Intracoronary optical coherence tomography (OCT) requires injection of flushing media for image acquisition. Alternative flushing media needs to be investigated to reduce the risk of contrast-induced renal dysfunction. We investigated the feasibility and safety of pentastarch (hydroxyethyl starch) for clinical OCT imaging. We prospectively enrolled 43 patients with 70 coronary lesions (46-stented; 24-native). Total 81 OCT pullback pairs were obtained by manual injection of iodine contrast, followed by pentastarch. Each pullback was assessed frame-by-frame using an automated customized lumen contour/stent strut segmentation algorithm. Paired images were compared for the clear image segments (CIS), blood-flushing capability, and quantitative morphometric measurements. Overall image quality, as assessed by the proportion of CIS, was comparable between the contrast- and pentastarch-flushed images (97.1% vs. 96.5%; p = 0.160). The pixel-based blood-flushing capability was similar between the groups (0.951 [0.947-0.953] vs. 0.950 [0.948-0.952], p = 0.125). Quantitative two- and three-dimensional morphometric measurements of the paired images correlated well (p < 0.001) with excellent inter-measurement variability. All patients safely underwent OCT imaging using pentastarch without resulting in clinically relevant complications or renal deterioration. Non-contrast OCT imaging using pentastarch is clinically safe and technically feasible with excellent image quality and could be a promising alternative strategy for patients at high risk of renal impairment.
Abstract licence: CC BY
E. Rackow, C. Mecher, M. Astiz, et al.
Critical Care Medicine, 1989
- Albumins
- Bacterial Infections
- Blood Circulation
Rasika Dhawan Setia, Mitu Dogra, Sanjeev Kumar Sharma, et al.
Global Journal of Transfusion Medicine, 2024
A BSTRACT Background and Objectives: Dimethylsulfoxide(DMSO) is gold standard for cryopreservation of hematopoietic progenitor cells (HPC) to reconstitute hematopoiesis in autologous stem cell transplants (auto-HSCT). Higher DMSO-related adverse effects (AEs) are reported in pediatric patients due to lower body weight with the recommended maximal dose of 1g/kg bodyweight. This study compares adding Hhydroxyethyl starch Vs Pentastarch to DMSO in order to reduce the DMSO related adverse effects. Adding a non-permeating cryoprotectant like Hydroxyethyl starch (HES) lowers DMSO concentration. HES is known to cause pruritus and nephrotoxicity. Pentastarch has lower molecular weight hence faster renal elimination with fewer reported AEs. Adding a non-permeating cryoprotectant like Hydroxyethyl starch (HES) lowers DMSO concentration. Methods: This study is a single-centre retrospective-comparative analysis from October 2022 to February 2024, comparing cryopreservation outcomes using standard cryoprotectant-DMSO+ HES+albumin solution (CPS-1) with pentastarch+albumin+DMSO solution (CPS-2). During the study period, 20 pediatric patients who underwent auto-HSCT requiring cryopreserved HPC-A were included. Results: Average CD34+ recovery with CPS-1 and CPS-2 were 86.58±13.42 and 87.5±13.2% (P-value=0.879). Median time to neutrophil engraftment was comparable (10 days) and no significant difference in platelet engraftment was observed, median 13.5 and 15 days with CPS-1 and CPS-2. Post-cryopreservation product volume was lesser with CPS-2 compared to CPS-1 (271±34.77ml and 78±24.7; P< 0.0001). Mean DMSO volume in CPS-2 was significantly lower than in CPS-1 (7.5±2.63ml and 13.55±1.83ml; P<0.0001). AEs were lesser with CPS-2 than CPS-1 (P = 0.178), and most patients with AEs were <25kg. Reducing volume of DMSO infusion with CPS-2 decreased AEs without impairing hematopoietic function of the HPC graft. Conclusion: Pentastarch containing freezing solution appears to be suitable for pediatric auto-HSCT cases, especially with body weight<25kgs offering additional advantage in case of patients with renal impairment.
Abstract licence: CC BY-NC-SA
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
2.5 hours
Mechanism
Not available
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Half-life
2.5 hours
Metabolism
Elimination
10%
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Pentastarch
DrugBank citations
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q21011237), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.