Bińczyk Wiktoria, Dróżdż Olgierd, Siudek Bartosz, Głuszczyk Agnieszka Michalina, Plizga Jakub Igor, Grajnert Filip Jan
Department and Clinic of Diabetology and Internal Medicine, University Teaching Hospital, Wroclaw, Poland.
A. Falkiewicz Specialist Hospital, Wroclaw, Poland.
Eur J Case Rep Intern Med. 2024 May 13;11(6):004567. doi: 10.12890/2024_004567. eCollection 2024.
Euglycemic diabetic ketoacidosis (euDKA) is a rare but severe metabolic complication of diabetes mellitus characterised by elevated anion gap metabolic acidosis despite normal or mildly elevated blood glucose levels. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have emerged as effective antidiabetic medications, yet their use is associated with an increased risk of euDKA, especially when coupled with insulin dose reduction. We present the case of a 50-year-old male with a 20-year history of diabetes mellitus, initially managed with insulin and metformin, who developed euDKA following the introduction of empagliflozin and sitagliptin alongside a reduction in insulin therapy. Despite normoglycaemia the patient exhibited symptoms of ketoacidosis, including chronic fatigue, polydipsia, and polyuria. Diagnostic workup revealed metabolic acidosis, elevated inflammatory markers, acute kidney injury and ketonuria. Subsequent specialised laboratory tests confirmed type 1 diabetes mellitus (T1DM) with the presence of anti-glutamic acid decarboxylase (anti-GAD) antibodies and the absence of C-peptide secretion. Management involved fluid therapy, intravenous insulin and glucose administration. This case underscores the diagnostic challenges of euDKA and emphasises the importance of differentiating between T1DM and T2DM, as management strategies vary significantly. Patient education on insulin therapy and injection techniques is crucial to prevent complications such as improper insulin delivery and dose reduction, which can precipitate euDKA. In conclusion, clinicians should be vigilant for euDKA in patients on SGLT2 inhibitors, particularly when insulin dose reduction is involved. Comprehensive patient education and accurate differentiation between diabetes types are essential for timely diagnosis and optimal management, thereby reducing the risk of severe complications.
The reduction in insulin doses combined with the introduction of an SGLT2 inhibitor in a patient with type 1 diabetes may lead to the development of a dangerous health complication known as euglycemic diabetic ketoacidosis.In cases of diagnostic uncertainty regarding the differentiation of diabetes types, measuring the levels of C-peptide and anti-GAD antibodies can be helpful.Abnormal glycaemic results in a patient using insulin may result from improper administration. During follow-up visits, it is worthwhile to check the subcutaneous tissue for lipodystrophy and also remind the patient about the necessity of rotating insulin injection sites.
正常血糖性糖尿病酮症酸中毒(euDKA)是糖尿病一种罕见但严重的代谢并发症,其特征是尽管血糖水平正常或轻度升高,但阴离子间隙代谢性酸中毒仍会升高。钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)已成为有效的抗糖尿病药物,但其使用与euDKA风险增加有关,尤其是与胰岛素剂量减少同时使用时。我们报告一例50岁男性,有20年糖尿病病史,最初用胰岛素和二甲双胍治疗,在引入恩格列净和西格列汀并减少胰岛素治疗后发生了euDKA。尽管血糖正常,但患者出现了酮症酸中毒症状,包括慢性疲劳、多饮和多尿。诊断检查发现代谢性酸中毒、炎症标志物升高、急性肾损伤和酮尿。随后的专门实验室检查证实为1型糖尿病(T1DM),存在抗谷氨酸脱羧酶(抗GAD)抗体且无C肽分泌。治疗包括液体疗法、静脉注射胰岛素和葡萄糖。该病例强调了euDKA的诊断挑战,并强调了区分T1DM和T2DM的重要性,因为管理策略差异很大。对患者进行胰岛素治疗和注射技术的教育对于预防诸如胰岛素给药不当和剂量减少等并发症至关重要,这些并发症可能引发euDKA。总之,临床医生应对使用SGLT2抑制剂的患者警惕euDKA,尤其是在涉及胰岛素剂量减少时。全面的患者教育和准确区分糖尿病类型对于及时诊断和优化管理至关重要,从而降低严重并发症的风险。
1型糖尿病患者胰岛素剂量减少并引入SGLT2抑制剂可能导致发生一种称为正常血糖性糖尿病酮症酸中毒的危险健康并发症。在糖尿病类型鉴别诊断存在不确定性的情况下,检测C肽和抗GAD抗体水平可能会有所帮助。使用胰岛素的患者血糖结果异常可能是由于给药不当。在随访期间,检查皮下组织是否有脂肪营养不良并提醒患者轮换胰岛素注射部位的必要性是值得的。