Cargando…

MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China)

Objective: To review the clinical symptoms and biochemical parameters associated with diabetic ketoacidosis (DKA) in children newly diagnosed with type 1 diabetes (T1D) in our single medical centre over 10 years. Methods: Participants were children aged <16 years diagnosed with T1D between 1 Janu...

Descripción completa

Detalles Bibliográficos
Autores principales: Peng, Wei, Jin, Binghan, Yuan, Jinna, Dong, Guanping, Lin, Hu, Huang, Ke, Wu, Wei, Derraik, José G B, Fu, Junfen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208188/
http://dx.doi.org/10.1210/jendso/bvaa046.1645
_version_ 1783530786351218688
author Peng, Wei
Jin, Binghan
Yuan, Jinna
Dong, Guanping
Lin, Hu
Huang, Ke
Wu, Wei
Derraik, José G B
Fu, Junfen
author_facet Peng, Wei
Jin, Binghan
Yuan, Jinna
Dong, Guanping
Lin, Hu
Huang, Ke
Wu, Wei
Derraik, José G B
Fu, Junfen
author_sort Peng, Wei
collection PubMed
description Objective: To review the clinical symptoms and biochemical parameters associated with diabetic ketoacidosis (DKA) in children newly diagnosed with type 1 diabetes (T1D) in our single medical centre over 10 years. Methods: Participants were children aged <16 years diagnosed with T1D between 1 January 2009 and 31 December 2018 at the Children’s Hospital, at Zhejiang University School of Medicine (Hangzhou, China). DKA occurrence was assessed by blood gases using pH and bicarbonate. The severity of DKA was categorized according to ISPAD 2014 guidelines, as mild, moderate, or severe. The child’s history prior to diagnosis was recorded, and patients underwent a number of clinical assessments, including anthropometry, biochemical parameters, and OGTT. The demographic and clinical characteristics of children with and without DKA were compared. Results: 681 patients (314 boys and 367 girls) were diagnosed with T1D over the study period. 341 (50.1%) had DKA at diagnosis, with yearly rates ranging from 45.0% to 56.8%. Eight cases had missing data on severity, but 120 had mild (36.0%), 100 moderate (30.0%), and 113 severe (33.9%) DKA. Children with DKA were younger than those without DKA (7.2 vs 8.2 years, respectively; p=0.001), and were more likely to report vomiting (13.2% vs 1.5%; p<0.001), loss of appetite (3.2% vs 0.9%; p=0.031), fatigue (39.3% vs 5.6%; p<0.001), and abdominal pain (9.1% vs 1.5%; p<0.001) prior to T1D diagnosis. The classical symptoms of diabetes were similar in children with and without DKA, such as polyuria (86.8% vs 90.3%, respectively; p=0.153), polydipsia (90.6% vs 91.5%; p=0.696), polyphagia (26.4% vs 30.3%; p=0.259), and weight loss (50.7% vs 50.6%; p=0.970). Children with DKA had higher blood lipids and fasting insulin levels at presentation, but displayed similar HbA1c levels. Conclusions: We report a high incidence of DKA at our centre (50%) among children diagnosed with T1D. As most children displayed classical symptoms of diabetes, it is important to increase community awareness of the disease to ensure an early diagnosis and lower the risk of children presenting with DKA.
format Online
Article
Text
id pubmed-7208188
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-72081882020-05-13 MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China) Peng, Wei Jin, Binghan Yuan, Jinna Dong, Guanping Lin, Hu Huang, Ke Wu, Wei Derraik, José G B Fu, Junfen J Endocr Soc Pediatric Endocrinology Objective: To review the clinical symptoms and biochemical parameters associated with diabetic ketoacidosis (DKA) in children newly diagnosed with type 1 diabetes (T1D) in our single medical centre over 10 years. Methods: Participants were children aged <16 years diagnosed with T1D between 1 January 2009 and 31 December 2018 at the Children’s Hospital, at Zhejiang University School of Medicine (Hangzhou, China). DKA occurrence was assessed by blood gases using pH and bicarbonate. The severity of DKA was categorized according to ISPAD 2014 guidelines, as mild, moderate, or severe. The child’s history prior to diagnosis was recorded, and patients underwent a number of clinical assessments, including anthropometry, biochemical parameters, and OGTT. The demographic and clinical characteristics of children with and without DKA were compared. Results: 681 patients (314 boys and 367 girls) were diagnosed with T1D over the study period. 341 (50.1%) had DKA at diagnosis, with yearly rates ranging from 45.0% to 56.8%. Eight cases had missing data on severity, but 120 had mild (36.0%), 100 moderate (30.0%), and 113 severe (33.9%) DKA. Children with DKA were younger than those without DKA (7.2 vs 8.2 years, respectively; p=0.001), and were more likely to report vomiting (13.2% vs 1.5%; p<0.001), loss of appetite (3.2% vs 0.9%; p=0.031), fatigue (39.3% vs 5.6%; p<0.001), and abdominal pain (9.1% vs 1.5%; p<0.001) prior to T1D diagnosis. The classical symptoms of diabetes were similar in children with and without DKA, such as polyuria (86.8% vs 90.3%, respectively; p=0.153), polydipsia (90.6% vs 91.5%; p=0.696), polyphagia (26.4% vs 30.3%; p=0.259), and weight loss (50.7% vs 50.6%; p=0.970). Children with DKA had higher blood lipids and fasting insulin levels at presentation, but displayed similar HbA1c levels. Conclusions: We report a high incidence of DKA at our centre (50%) among children diagnosed with T1D. As most children displayed classical symptoms of diabetes, it is important to increase community awareness of the disease to ensure an early diagnosis and lower the risk of children presenting with DKA. Oxford University Press 2020-05-08 /pmc/articles/PMC7208188/ http://dx.doi.org/10.1210/jendso/bvaa046.1645 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Pediatric Endocrinology
Peng, Wei
Jin, Binghan
Yuan, Jinna
Dong, Guanping
Lin, Hu
Huang, Ke
Wu, Wei
Derraik, José G B
Fu, Junfen
MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China)
title MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China)
title_full MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China)
title_fullStr MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China)
title_full_unstemmed MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China)
title_short MON-107 Diabetic Ketoacidosis at Type 1 Diabetes Diagnosis in Children from a Large Centre (Hangzhou, China)
title_sort mon-107 diabetic ketoacidosis at type 1 diabetes diagnosis in children from a large centre (hangzhou, china)
topic Pediatric Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208188/
http://dx.doi.org/10.1210/jendso/bvaa046.1645
work_keys_str_mv AT pengwei mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT jinbinghan mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT yuanjinna mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT dongguanping mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT linhu mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT huangke mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT wuwei mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT derraikjosegb mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina
AT fujunfen mon107diabeticketoacidosisattype1diabetesdiagnosisinchildrenfromalargecentrehangzhouchina