甲状腺功能亢进症儿童的围手术期护理

Joseph Bonanno, T. Grannell, Gregory S Maves, Joseph D. Tobias
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引用次数: 0

摘要

在儿童患者中,甲状腺功能亢进症通常是由自身免疫性疾病--巴塞杜氏病(GD)引起的。甲状腺激素(三碘甲状腺原氨酸和甲状腺素)水平过高会导致易怒、情绪不稳定、紧张、震颤、心悸、心动过速和心律失常。甲状腺功能亢进症患者如果需要手术治疗,由于有可能发展成甲状腺风暴(TS),发病率和死亡率的风险都会增加。一名3岁1个月大的患儿既往有GD病史,在出现类似血清病的疾病后,由于不能耐受甲巯咪唑的药物控制,因此前来接受全甲状腺切除术。手术前,他的甲亢症状加重,出现发热、心动过速、全身乏力和高血压。随后,他出现了TS,被送进了儿科重症监护室,治疗包括氢化可的松、碘化钾以及使用艾司洛尔和普萘洛尔进行β肾上腺素能阻断。手术前的甲状腺检查结果有所改善,成功完成了全甲状腺切除术。他在门诊接受了缓慢减量的皮质类固醇治疗,并于住院第9天出院回家。出院后,他的甲亢症状和体征消失,并开始接受口服左甲状腺素替代治疗。他术后和出院后的其余病程均无异常。在过去的 20 年中,只有两篇关于围手术期小儿 TS 的病例报告发表过。我们的病例提醒人们注意儿童 TS 的体征,并概述了儿科患者的治疗方案,尤其是那些不能耐受甲巯咪唑或丙基硫氧嘧啶等一线药物疗法的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perioperative Care of a Child With Hyperthyroidism
In pediatric-aged patients, hyperthyroidism generally results from the autoimmune disorder, Graves’ disease (GD). Excessive levels of thyroid hormones (triiodothyronine and thyroxine) result in irritability, emotional lability, nervousness, tremors, palpitations, tachycardia, and arrhythmias. The risk of morbidity and mortality is increased when surgical intervention is required in patients with hyperthyroidism due to the potential for the development of thyroid storm (TS). A 3-year, 1-month-old child with a past medical history of GD presented for total thyroidectomy when pharmacologic control with methimazole was not feasible due to intolerance following development of a serum sickness-like illness. Prior to surgery, his thyrotoxicosis symptoms worsened with fever, tachycardia, diaphoresis, and hypertension. He subsequently developed TS and was admitted to the pediatric intensive care unit where management included hydrocortisone, potassium iodide, and β-adrenergic blockade with esmolol and propranolol. Thyroid studies improved prior to surgery, and a total thyroidectomy was successfully completed. Corticosteroid therapy was slowly tapered as an outpatient, and he was discharged home on hospital day 9. Following discharge, his signs and symptoms of thyrotoxicosis resolved, and he was started on oral levothyroxine replacement therapy. The remainder of his postoperative and post-discharge course were unremarkable. Only two case reports of perioperative pediatric TS have been published in the past 20 years. Our case serves as an important reminder of the signs of TS in children and to outline the treatment options in a pediatric patient, especially in those unable to tolerate first-line pharmacologic therapies such as methimazole or propylthiouracil.
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