Central venous catheter-associated thrombosis in children with congenital hyperinsulinism


Journal

Endocrinology, diabetes & metabolism case reports
ISSN: 2052-0573
Titre abrégé: Endocrinol Diabetes Metab Case Rep
Pays: England
ID NLM: 101618943

Informations de publication

Date de publication:
09 07 2019
Historique:
entrez: 3 8 2019
pubmed: 3 8 2019
medline: 3 8 2019
Statut: epublish

Résumé

Congenital hyperinsulinism (CHI) is an important cause of severe hypoglycaemia in infancy. To correct hypoglycaemia, high concentrations of dextrose are often required through a central venous catheter (CVC) with consequent risk of thrombosis. We describe a series of six cases of CHI due to varying aetiologies from our centre requiring CVC for the management of hypoglycaemia, who developed thrombosis in association with CVC. We subsequently analysed the incidence and risk factors for CVC-associated thrombosis, as well as the outcomes of enoxaparin prophylaxis. The six cases occurred over a 3-year period; we identified an additional 27 patients with CHI who required CVC insertion during this period (n = 33 total), and a separate cohort of patients with CHI and CVC who received enoxaparin prophylaxis (n = 7). The incidence of CVC-associated thrombosis was 18% (6/33) over the 3 years, a rate of 4.2 thromboses/1000 CVC days. There was no difference in the frequency of genetic mutations or focal CHI in those that developed thromboses. However, compound heterozygous/homozygous potassium ATP channel mutations correlated with thrombosis (R2 = 0.40, P = 0.001). No difference was observed in CVC duration, high concentration dextrose or glucagon infused through the CVC. In patients receiving enoxaparin prophylaxis, none developed thrombosis or bleeding complications. The characteristics of these patients did not differ significantly from those with thrombosis not on prophylaxis. We therefore conclude that CVC-associated thrombosis can occur in a significant proportion (18%) of patients with CHI, particularly in severe CHI, for which anticoagulant prophylaxis may be indicated. CVC insertion is one of the most significant risk factors for thrombosis in the paediatric population. Risk factors for CVC-associated thrombosis include increased duration of CVC placement, malpositioning and infusion of blood products. To our knowledge, this is the first study to evaluate CVC-associated thrombosis in patients with congenital hyperinsulinism (CHI). The incidence of CVC-associated thrombosis development is significant (18%) in CHI patients and higher compared to other neonates with CVC. CHI severity may be a risk factor for thrombosis development. Although effective prophylaxis for CVC-associated thrombosis in infancy is yet to be established, our preliminary experience suggests the safety and efficacy of enoxoaparin prophylaxis in this population and requires on-going evaluation.

Identifiants

pubmed: 31373474
doi: 10.1530/EDM-19-0032
pmc: PMC8115433
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

This is an Open Access article distributed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. 2019

Références

Semin Thromb Hemost. 2016 Oct;42(7):752-759
pubmed: 27637010
J Clin Endocrinol Metab. 2016 Mar;101(3):815-26
pubmed: 26908106
Clin Endocrinol (Oxf). 2013 Jun;78(6):803-13
pubmed: 23347463
Hosp Pediatr. 2015 Feb;5(2):59-66
pubmed: 25646197
J Pediatr. 2001 Feb;138(2):255-9
pubmed: 11174625
Blood Coagul Fibrinolysis. 2014 Mar;25(2):97-106
pubmed: 24477225
J Pediatr. 1998 Dec;133(6):770-6
pubmed: 9842042

Auteurs

Daphne Yau (D)

Departments of Paediatric Endocrinology, Royal Manchester Children’s Hospital, Manchester, UK

Maria Salomon-Estebanez (M)

Departments of Paediatric Endocrinology, Royal Manchester Children’s Hospital, Manchester, UK

Amish Chinoy (A)

Departments of Paediatric Endocrinology, Royal Manchester Children’s Hospital, Manchester, UK

John Grainger (J)

Departments of Paediatric Haematology, Royal Manchester Children’s Hospital, Manchester, UK

Ross Craigie (RJ)

Departments of Paediatric Surgery, Royal Manchester Children’s Hospital, Manchester, UK

Raja Padidela (R)

Departments of Paediatric Endocrinology, Royal Manchester Children’s Hospital, Manchester, UK

Mars Skae (M)

Departments of Paediatric Endocrinology, Royal Manchester Children’s Hospital, Manchester, UK

Mark Dunne (MJ)

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK

Philip Murray (PG)

Departments of Paediatric Endocrinology, Royal Manchester Children’s Hospital, Manchester, UK

Indraneel Banerjee (I)

Departments of Paediatric Endocrinology, Royal Manchester Children’s Hospital, Manchester, UK

Classifications MeSH