Optimising insulin aspart practices in a neonatal intensive care unit: a clinical and pharmaco-technical study.


Journal

European journal of pediatrics
ISSN: 1432-1076
Titre abrégé: Eur J Pediatr
Pays: Germany
ID NLM: 7603873

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 01 02 2021
accepted: 21 03 2021
revised: 16 03 2021
pubmed: 19 4 2021
medline: 11 8 2021
entrez: 18 4 2021
Statut: ppublish

Résumé

Neonatal hyperglycaemia is frequent and requires insulin therapy. To resolve the difficulties encountered by paediatricians in stabilising glycaemia, the preparation and administration of insulin aspart were assessed and optimised. After high-performance liquid chromatography (HPLC-UV) assessment of insulin aspart preparations made according to the old protocol, a new protocol was drawn up. Dosage reliability of solutions prepared by paediatric nurses was evaluated by HPLC-UV. This new protocol was also tested in a Y-infusion situation and the need to saturate infusion tubes assessed. Wide deviations in insulin aspart concentrations were found between theoretical concentrations and preparations made according to the old protocol. Glycated insulin aspart was found in the majority of these preparations. The new protocol significantly reduced the variability of data and relative deviations around the target value. It also eliminated the formation of glycated insulin even in the case of co-infusion of parenteral nutrition and confirmed the need to saturate infusion tubes.Conclusion: The revision of the insulin therapy protocol reduced the variability of insulin concentration in preparations and avoided the administration of glycated derivatives potentially toxic for neonates. What is Known: • Insulin preparation in NICUs is a risky task because it is a two-step preparation • Diluted in dextrose, insulin aspart is unstable, with formation of potentially toxic glycated derivatives What is New: • This work proposes a new insulin therapy protocol validated by HPLC-UV for NICU allowing suppression of the formation of glycated insulin, to significantly reduce deviations from theoretical concentrations and to limit adsorption phenomena • This protocol is validated in case of co-infusion of parenteral nutrition.

Identifiants

pubmed: 33866404
doi: 10.1007/s00431-021-04041-y
pii: 10.1007/s00431-021-04041-y
doi:

Substances chimiques

Blood Glucose 0
Hypoglycemic Agents 0
Insulin 0
Insulin Aspart D933668QVX

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2985-2992

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

Mitanchez-Mokhtari D, Walter-Nicolet E, Farges C, Egrot F, Tréluyer JM, Hubert P (2004) Modalités d’administration de l’insuline par voie intraveineuse chez le nouveau-né prématuré. Arch Pediatr 11:1054–1059. https://doi.org/10.1016/j.arcped.2004.03.027
doi: 10.1016/j.arcped.2004.03.027 pubmed: 15350994
Préta L-H, Henry H, Masse M, Barthélémy C, Carta N, Foulon C, Goossens JF, Kouach M, Lannoy D, Storme L, Décaudin B, Genay S, Odou P (2020) Instability of insulin aspart diluted in dextrose. Diabetes Care 43:e77–e78. https://doi.org/10.2337/dc19-2462
doi: 10.2337/dc19-2462 pubmed: 32381586
Hunter SJ, Boyd AC, O’Harte FPM et al (2003) Demonstration of glycated insulin in human diabetic plasma and decreased biological activity assessed by euglycemic-hyperinsulinemic clamp technique in humans. Diabetes 52:492–498. https://doi.org/10.2337/diabetes.52.2.492
doi: 10.2337/diabetes.52.2.492 pubmed: 12540626
McKillop AM, Lindsay JR, Au S et al (2006) Meal-dependent regulation of circulating glycated insulin in type 2 diabetic subjects. Horm Metab Res 38:94–97. https://doi.org/10.1055/s-2006-925125
doi: 10.1055/s-2006-925125 pubmed: 16523409
Shahriyary L, Riazi G, Lornejad MR, Ghezlou M, Bigdeli B, Delavari B, Mamashli F, Abbasi S, Davoodi J, Saboury AA (2018) Effect of glycated insulin on the blood-brain barrier permeability: an in vitro study. Arch Biochem Biophys 647:54–66. https://doi.org/10.1016/j.abb.2018.02.004
doi: 10.1016/j.abb.2018.02.004 pubmed: 29444458
Masse M, Maton M, Genay S, Blanchemain N, Barthélémy C, Décaudin B, Odou P (2018) In vitro assessment of the influence of intravenous extension set materials on insulin aspart drug delivery. PLoS One 13:e0201623. https://doi.org/10.1371/journal.pone.0201623
doi: 10.1371/journal.pone.0201623 pubmed: 30114258 pmcid: 6095494
https://www.equator-network.org/reporting-guidelines/squire/ (2015) Revised Standards for Quality Improvement Reporting Excellence (SQUIRE 2.0). Accessed 9 Mar 2021
Préta L-H (2019) Révision et optimisation des pratiques de préparation et d’administration de l’insuline asparte en réanimation néonatale. Université de Lille. https://pepite-depot.univ-lille2.fr/nuxeo/site/esupversions/af81991f-5604-4cfc-84ed-05307bdec563 . Accessed 9 Mar 2021
Goodacre S (2015) Uncontrolled before-after studies: discouraged by Cochrane and the EMJ. Emerg Med J 32:507–508. https://doi.org/10.1136/emermed-2015-204761
doi: 10.1136/emermed-2015-204761 pubmed: 25820301
Ainscough LP, Ford JL, Morecroft CW, Peak M, Turner MA, Nunn AJ, Roberts M (2018) Accuracy of intravenous and enteral preparations involving small volumes for paediatric use: a review. Eur J Hosp Pharm 25:66–71. https://doi.org/10.1136/ejhpharm-2016-001117
doi: 10.1136/ejhpharm-2016-001117 pubmed: 31156991
Abdel-Wahab YH, O’Harte FP, Boyd AC et al (1997) Glycation of insulin results in reduced biological activity in mice. Acta Diabetol 34:265–270. https://doi.org/10.1007/s005920050086
doi: 10.1007/s005920050086 pubmed: 9451470
Boyd AC, Abdel-Wahab YH, McKillop AM et al (2000) Impaired ability of glycated insulin to regulate plasma glucose and stimulate glucose transport and metabolism in mouse abdominal muscle. Biochim Biophys Acta 1523:128–134. https://doi.org/10.1016/s0304-4165(00)00113-6
doi: 10.1016/s0304-4165(00)00113-6 pubmed: 11099867
Foinard A, Décaudin B, Simon N, Barthélémy C, Storme L, Odou P (2014) Vancomycin syringe study shows significant reduction in dosing variability after introducing a revised protocol. Acta Paediatr 103:e93–e94. https://doi.org/10.1111/apa.12484
doi: 10.1111/apa.12484 pubmed: 24164676
Knopp JL, Chase JG (2020) Clinical recommendations for managing the impact of insulin adsorptive loss in hospital and diabetes care. J Diabetes Sci Technol 1932296820915875. https://doi.org/10.1177/1932296820915875
Knopp JL, Bishop K, Lerios T, Chase JG (2019) Capacity of infusion lines for insulin adsorption: effect of flow rate on total adsorption. J Diabetes Sci Technol 1932296819876924:109–120. https://doi.org/10.1177/1932296819876924
doi: 10.1177/1932296819876924
Eibensteiner F, Laml-Wallner G, Thanhaeuser M, Ristl R, Ely S, Jilma B, Berger A, Haiden N (2020) ELBW infants receive inadvertent sodium load above the recommended intake. Pediatr Res 88:412–420. https://doi.org/10.1038/s41390-020-0867-9
doi: 10.1038/s41390-020-0867-9 pubmed: 32272484

Auteurs

Laure-Hélène Préta (LH)

ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, F-59000, Lille, France. lh.preta@gmail.com.
Institut de Pharmacie, CHU Lille, F-59000, Lille, France. lh.preta@gmail.com.

Stéphanie Genay (S)

ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, F-59000, Lille, France.
Institut de Pharmacie, CHU Lille, F-59000, Lille, France.

Cécile Malat (C)

Institut de Pharmacie, CHU Lille, F-59000, Lille, France.

Natacha Carta (N)

ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, F-59000, Lille, France.

Mohamed Riadh Boukhris (MR)

Hôpital Jeanne de Flandre, Département de néonatologie, CHU Lille, F-59000, Lille, France.

Julie Verspieren (J)

Hôpital Jeanne de Flandre, Département de néonatologie, CHU Lille, F-59000, Lille, France.

Pascal Odou (P)

ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, F-59000, Lille, France.
Institut de Pharmacie, CHU Lille, F-59000, Lille, France.

Laurent Storme (L)

Hôpital Jeanne de Flandre, Département de néonatologie, CHU Lille, F-59000, Lille, France.
ULR 4489 - Environnement Périnatal et Santé, University of Lille, F-59000, Lille, France.

Bertrand Décaudin (B)

ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, F-59000, Lille, France.
Institut de Pharmacie, CHU Lille, F-59000, Lille, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH