System of Criteria for Treatment Evaluation of Acromegaly in Bulgaria.
Acromegaly
Growth Hormone
Insulin-like Growth Factor-1
case study
clinical informatics
endocrine disease
evaluation
treatment
Journal
Studies in health technology and informatics
ISSN: 1879-8365
Titre abrégé: Stud Health Technol Inform
Pays: Netherlands
ID NLM: 9214582
Informations de publication
Date de publication:
26 Jun 2020
26 Jun 2020
Historique:
entrez:
2
7
2020
pubmed:
2
7
2020
medline:
29
8
2020
Statut:
ppublish
Résumé
Acromegaly is a rare endocrine disorder caused by excessive and longstanding secretion of growth hormone (GH) by the pituitary somatotroph and resulting from this overproduction of insulin-like growth factor-1 hormone (IGF-1) by the liver. There are few registers and rather limited clinical data about acromegaly treatment. The analysis of acromegaly data is rarely subject to a system of criteria for evaluating acromegaly treatment. The novelty of this paper is that it presents a real- life practice case study about the implementation results of such a system in Bulgaria. The case study analysis illustrates a clinical information approach to manage thousands of records in the Bulgarian Acromegaly Database. The here reported results provide evidence about the difficulties in maintaining both GH and IGF-1 levels inside their reference values in acromegaly treatment. Ongoing research extends the evaluation results by enabling semantic interoperability between acromegaly databases based on openEHR specification.
Identifiants
pubmed: 32604690
pii: SHTI200583
doi: 10.3233/SHTI200583
doi:
Substances chimiques
Human Growth Hormone
12629-01-5
Types de publication
Journal Article
Langues
eng