Polydipsia Secondary to Quetiapine Use: A Case Report

A. Trevizol, I. Sato, Q. Cordeiro, P. Shiozawa
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引用次数: 0

Abstract

Polydipsia is characterized by excessive water drinking. It has been related to psychiatric conditions such as schizophrenia, cognitive impairments, and neurological disorders such as brain tumors. Excessive drinking may lead to hyponatremia, nausea, vomiting, delirium, ataxia, seizures, coma, and even death. Here, we present a case of polydipsia secondary to quetiapine use in a patient with schizophrenia. JVO, 20 years old, male, single, diagnosed with schizophrenia according to the DSM-IV criteria for about six years ago. The patient was under pharmacological treatment with quetiapine in increasing doses, reaching 800 mg/day. One week later, he presented at the psychiatric emergency room with nausea, vomiting, confusion, and disorientation. Psychiatric symptoms included blunt affect, auditory hallucinations (voices commenting on patient’s actions and conversing with one another), and persecutory delusions. In fact, the patient was persecutory with near relatives and daily activit ies were l imited by his psychotic behaviors. Increased water intake was observed and diuresis reached approximately 12 liters/ day. Complementary tests showed hyponatrenia with a serum sodium level of 105 mmol/L (135145 mmol/L). All other laboratory tests and neuroimaging studies were within normal range. Other possible etiologies of polydipsia, such as diabetes mellitus, diabetes insipidus, syndrome of inappropriate antidiuretic hormone secretion (SIADH), and thyroid or adrenal dysfunctions were excluded. Psychogenic polydipsia was a possible differential diagnosis, however we could observe a strong temporal association between polydipsia symptoms intensity and quetiapine u s e . F u r t h e r m o r e , w i t h q u e t i a p i n e discontinuation, clinical remission of polydipsia symptoms with normalization of complementary laboratory tests were obtained. The patient has never manifested such behavior before quetiapine use. Initial treatment was 1,000 ml intravenous infusion of sodium chloride 0.9% and water intake restriction to one liter per 24 hours. Quetiapine was replaced by risperidone. Patient showed improvement with normalization of serum sodium levels and presented with clinical improvement during the next three days. In polydipsia the excessive drinking of water reduces plasma osmolarity. Considering the use of antipsychotic drugs inducing polydipsia, it has been previously hypothesized that the use of neuroleptics may increase vasopressin (ADH) secretion, therefore inducing water retention. Another theoretical mechanism could be based on possible anticolinergic effects inherent to antipsychotics that would induce sensation of thirst. Regarding the specific use of quetiapine, there has been only one case in medical literature reporting quetiapine inducing hyponatremia. However, the metabolic imbalance was due to syndrome of inappropriate secretion of antidiuretic hormone rather than secondary to polydipsia. In this present case, we report and highlight DOI: 10.5455/bcp.20151019014403
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喹硫平引起的烦渴1例报告
烦渴的特点是饮水过量。它与精神疾病如精神分裂症、认知障碍和神经系统疾病如脑肿瘤有关。过量饮酒可导致低钠血症、恶心、呕吐、谵妄、共济失调、癫痫发作、昏迷,甚至死亡。在这里,我们提出一个病例多饮继发奎硫平使用精神分裂症患者。JVO, 20岁,男性,单身,六年前根据DSM-IV诊断为精神分裂症。患者正在接受喹硫平的药物治疗,剂量逐渐增加,达到800mg /天。一周后,他出现在精神科急诊室,表现为恶心、呕吐、精神错乱和定向障碍。精神症状包括钝感、幻听(对患者行为的评论和彼此交谈的声音)和受迫害妄想。事实上,患者受到近亲属的迫害,日常活动受到精神病行为的限制。观察到饮水量增加,利尿达到约12升/天。补充试验显示低钠血症,血清钠水平为105 mmol/L (135145 mmol/L)。所有其他实验室检查和神经影像学检查均在正常范围内。排除其他可能的多饮原因,如糖尿病、尿崩症、抗利尿激素分泌不当综合征(SIADH)、甲状腺或肾上腺功能障碍。心因性烦渴是一种可能的鉴别诊断,但我们可以观察到烦渴症状强度与喹硫平剂量之间存在较强的时间相关性。经停药治疗后,多饮症状临床缓解,辅助实验室检查正常化。患者在使用喹硫平前从未出现过此类行为。初始治疗为静脉输注0.9%氯化钠1000毫升,饮水限制为每24小时1升。用利培酮代替喹硫平。患者血清钠水平恢复正常,并在随后3天出现临床改善。在烦渴时,过量饮水会降低血浆渗透压。考虑到抗精神病药物的使用会导致烦渴,以前的假设是,使用抗精神病药物可能会增加抗利尿激素(ADH)的分泌,从而导致水潴留。另一种理论机制可能是基于抗精神病药物固有的抗共碱能作用,这种作用会引起口渴的感觉。关于喹硫平的具体使用,医学文献中仅有一例报道喹硫平诱发低钠血症。然而,代谢失衡是由于抗利尿激素分泌不当综合征,而不是继发于烦渴。在本例中,我们报告并突出显示DOI: 10.5455/bcp.20151019014403
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