高血糖高渗状态的儿科管理挑战:韩国 2 型糖尿病青少年病例系列。

IF 2.8 Q3 ENDOCRINOLOGY & METABOLISM Annals of Pediatric Endocrinology & Metabolism Pub Date : 2023-03-01 Epub Date: 2022-01-17 DOI:10.6065/apem.2142108.054
Sumin Lee, Sukdong Yoo, Ju Young Yoon, Chong Kun Cheon, Young A Kim
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引用次数: 0

摘要

高血糖高渗状态(HHS)被认为是 2 型糖尿病(DM)最致命的并发症。最近,随着肥胖症和 2 型糖尿病在儿童患者中的流行,描述小儿高血糖高渗状态的病例报告数量也在增加。在这项研究中,我们调查了 9 名患有肥胖症和 2 型糖尿病的青少年 HHS 患者的特征和预后。几乎所有患者都表现出 HHS 和糖尿病酮症酸中毒(DKA)的混合临床特征,包括高渗性和酮症酸中毒等特征。这些特征给明确诊断带来了困难;9 名患者中有 5 人被初步诊断为 DKA,并接受了相应的治疗。与其他患者相比,被初步诊断为 HHS 的患者接受了更有力、更适当的液体补充。没有患者死亡,但有 3 名患者出现了并发症,如心律失常、需要肾脏替代治疗的急性肾损伤、横纹肌溶解症和急性胰腺炎。高渗透压导致严重脱水被认为是影响 HHS 患者预后的一个重要因素。因此,早期识别高渗对于适当诊断和充分补液至关重要,以便在治疗早期恢复灌注,从而改善这种罕见但严重的儿科新发疾病的患者预后。
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Pediatric management challenges of hyperglycemic hyperosmolar state: case series of Korean adolescents with type 2 diabetes.

The hyperglycemic hyperosmolar state (HHS) is considered the most fatal complication of type 2 diabetes mellitus (DM). The number of case reports describing pediatric HHS has increased recently in parallel with obesity and the prevalence of type 2 DM in pediatric patients. In this study, we investigated the patient characteristics and outcomes of HHS in 9 adolescents with obesity and type 2 DM. Almost all patients exhibited mixed clinical features of HHS and diabetic ketoacidosis (DKA), including characteristics such as hyperosmolality and ketoacidosis. These features made definitive diagnosis difficult; 5 out of 9 patients were initially diagnosed with DKA and were treated accordingly. Patients who were initially diagnosed with HHS received a more vigorous and appropriate fluid replacement than other patients did. No patients died, although 3 exhibited complications, such as arrhythmia, acute kidney injury requiring renal replacement therapy, rhabdomyolysis, and acute pancreatitis. Hyperosmolality with consequent severe dehydration is considered a significant factor contributing to the outcomes of patients with HHS. Therefore, early recognition of hyperosmolality is crucial for an appropriate diagnosis and adequate fluid rehydration to restore perfusion in the early period of treatment to improve patient outcomes for this rare but serious emerging condition in pediatric patients.

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来源期刊
CiteScore
4.00
自引率
18.20%
发文量
59
审稿时长
24 weeks
期刊介绍: The Annals of Pediatric Endocrinology & Metabolism Journal is the official publication of the Korean Society of Pediatric Endocrinology. Its formal abbreviated title is “Ann Pediatr Endocrinol Metab”. It is a peer-reviewed open access journal of medicine published in English. The journal was launched in 1996 under the title of ‘Journal of Korean Society of Pediatric Endocrinology’ until 2011 (pISSN 1226-2242). Since 2012, the title is now changed to ‘Annals of Pediatric Endocrinology & Metabolism’. The Journal is published four times per year on the last day of March, June, September, and December. It is widely distributed for free to members of the Korean Society of Pediatric Endocrinology, medical schools, libraries, and academic institutions. The journal is indexed/tracked/covered by web sites of PubMed Central, PubMed, Emerging Sources Citation Index (ESCI), Scopus, EBSCO, EMBASE, KoreaMed, KoMCI, KCI, Science Central, DOI/CrossRef, Directory of Open Access Journals(DOAJ), and Google Scholar. The aims of Annals of Pediatric Endocrinology & Metabolism are to contribute to the advancements in the fields of pediatric endocrinology & metabolism through the scientific reviews and interchange of all of pediatric endocrinology and metabolism. It aims to reflect the latest clinical, translational, and basic research trends from worldwide valuable achievements. In addition, genome research, epidemiology, public education and clinical practice guidelines in each country are welcomed for publication. The Journal particularly focuses on research conducted with Asian-Pacific children whose genetic and environmental backgrounds are different from those of the Western. Area of specific interest include the following : Growth, puberty, glucose metabolism including diabetes mellitus, obesity, nutrition, disorders of sexual development, pituitary, thyroid, parathyroid, adrenal cortex, bone or other endocrine and metabolic disorders from infancy through adolescence.
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