Severe tolvaptan-associated hyperglycemia: a case report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Huihuan Sun, Ping Yang, Lijuan Chen, Ying Zhang, Shudong Liu, Wenxiu Sun
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引用次数: 0

Abstract

Background: Tolvaptan-associated hyperglycemia has rarely been described in literature.

Case presentation: A 95-year-old East Asian (Chinese) male patient with hyponatremia started on tolvaptan treatment at a dosage of 15 mg per day. The patient had a serum sodium concentration of 124.5 mmol/L at baseline; this concentration increased to 138.3 mmol/L over the ensuing 5 months of treatment. Moreover, the patient's fasting blood glucose dramatically increased from 6.3 to 17.2 mmol/L with tolvaptan treatment, and his glycated hemoglobin A1c increased from 5.8% to 9.4%. Tolvaptan was withdrawn owing to hyperglycemia, and insulin pump treatment was started. The serum sodium concentration decreased to 123 mmol/L after tolvaptan withdrawal. The higher levels of blood glucose, insulin, and C-peptide did not return to their previous levels for 5 months after the withdrawal of tolvaptan.

Conclusion: We reported a rare case of tolvaptan-associated chronic severe hyperglycemia with a Naranjo probability scale score of 6. Our findings increase clinical knowledge and indicate the need for proactive blood glucose monitoring during prolonged tolvaptan use in clinical practice.

重度托伐他坦相关高血糖1例报告。
背景:托伐普坦相关的高血糖在文献中很少被描述。病例介绍:一名95岁的东亚(中国)男性低钠血症患者开始接受托伐普坦治疗,剂量为每天15mg。患者基线血钠浓度为124.5 mmol/L;在随后的5个月的处理中,该浓度增加到138.3 mmol/L。此外,患者的空腹血糖由6.3 mmol/L急剧上升至17.2 mmol/L,糖化血红蛋白由5.8%上升至9.4%。因高血糖停用托伐普坦,并开始胰岛素泵治疗。停药后血清钠浓度降至123 mmol/L。停用托伐普坦后5个月,血糖、胰岛素和c肽水平均未恢复到原来的水平。结论:我们报告了一例罕见的托伐普坦相关的慢性严重高血糖症,其纳兰霍概率量表评分为6分。我们的研究结果增加了临床知识,并表明在临床实践中长期使用托伐普坦期间需要主动监测血糖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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