Central diabetes insipidus from a patient's perspective: management, psychological co-morbidities, and renaming of the condition: results from an international web-based survey.

The lancet. Diabetes & endocrinology Pub Date : 2022-10-01 Epub Date: 2022-08-22 DOI:10.1016/S2213-8587(22)00219-4
Cihan Atila, Paul Benjamin Loughrey, Aoife Garrahy, Bettina Winzeler, Julie Refardt, Patricia Gildroy, Malak Hamza, Aparna Pal, Joseph G Verbalis, Christopher J Thompson, Lars G Hemkens, Steven J Hunter, Mark Sherlock, Miles J Levy, Niki Karavitaki, John Newell-Price, John A H Wass, Mirjam Christ-Crain
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引用次数: 8

Abstract

Background: Central diabetes insipidus is a rare neuroendocrine condition. Data on treatment-associated side-effects, psychological comorbidities, and incorrect management are scarce. The aim of this study was to investigate patients' perspectives on their disease.

Methods: This study used a cross-sectional, web-based, anonymous survey, developed by endocrinologists and patient representatives, to collect the opinions of patients with central diabetes insipidus on management and complications of their disease, psychological comorbidities, degree of knowledge and awareness of the condition among health-care professionals, and renaming the disease to avoid confusion with diabetes mellitus (diabetes).

Findings: Between Aug 23, 2021, and Feb 7, 2022, 1034 patients with central diabetes insipidus participated in the survey. 91 (9%) participants were children and adolescents (37 [41%] girls and 54 [59%] boys; median age 10 years [IQR 6-15]) and 943 (91%) were adults (757 [80%] women and 186 [20%] men]; median age 44 years [34-54]). 488 (47%) participants had isolated posterior pituitary dysfunction and 546 (53%) had combined anterior and posterior pituitary dysfunction. Main aetiologies were idiopathic (315 [30%] of 1034 participants) and tumours and cysts (pre-surgical 217 [21%]; post-surgical 254 [25%]). 260 (26%; 95% CI [0·23-0·29]) of 994 patients on desmopressin therapy had hyponatraemia leading to hospitalisation. Patients who routinely omitted or delayed desmopressin to allow intermittent aquaresis had a significantly lower prevalence of hyponatraemia compared with those not aware of this approach (odds ratio 0·55 [95% CI 0·39-0·77]; p=0·0006). Of patients who had to be hospitalised for any medical reason, 71 (13%; 95% CI 0·10-0·16) of 535 patients did not receive desmopressin while in a fasting state (nil by mouth) without intravenous fluid replacement and reported symptoms of dehydration. 660 (64%; 0·61-0·67) participants reported lower quality of life, and 369 (36%; 0·33-0·39) had psychological changes subjectively associated with their central diabetes insipidus. 823 (80%; 0·77-0·82) participants encountered a situation where central diabetes insipidus was confused with diabetes mellitus (diabetes) by health-care professionals. 884 (85%; 0·83-0·88) participants supported renaming the disease; the most favoured alternative names were vasopressin deficiency and arginine vasopressin deficiency.

Interpretation: This is the largest survey of patients with central diabetes insipidus, reporting a high prevalence of treatment-associated side-effects, mismanagement during hospitalisation, psychological comorbidities, and a clear support for renaming the disease. Our data are the first to indicate the value of routinely omitting or delaying desmopressin.

Funding: Swiss National Science Foundation, Swiss Academy of Medical Sciences, and G&J Bangerter-Rhyner-Foundation.

从患者的角度看中枢性尿崩症:管理、心理合并症和病情重命名:一项国际网络调查的结果
背景:中枢性尿崩症是一种罕见的神经内分泌疾病。关于治疗相关副作用、心理合并症和不正确处理的数据很少。本研究的目的是调查患者对其疾病的看法。方法:本研究采用由内分泌科医生和患者代表开展的横断面、网络、匿名调查,收集中心性尿囊症患者对其疾病的处理和并发症、心理合并症、卫生保健专业人员对该病的了解程度和认知度的意见,并重新命名疾病以避免与糖尿病(糖尿病)混淆。结果:在2021年8月23日至2022年2月7日期间,1034例中枢性尿崩症患者参与了调查。91例(9%)参与者为儿童和青少年(女孩37例[41%],男孩54例[59%];中位年龄为10岁[IQR 6-15]),成人943例(91%),其中女性757例(80%),男性186例(20%);中位年龄44岁[34-54])。488例(47%)参与者有孤立性垂体后叶功能障碍,546例(53%)参与者有合并垂体前、后叶功能障碍。主要病因为特发性(315例(30%))、肿瘤和囊肿(术前217例(21%);术后254[25%])。260 (26%;994例接受去氨加压素治疗的患者因低钠血症住院,95% CI[0.23 - 0.29]。常规省略或延迟去氨加压素以允许间歇性停水的患者与不知道这种方法的患者相比,低钠血症的患病率显着降低(优势比0.55 [95% CI 0.39 - 0.77];p = 0·0006)。在因任何医疗原因不得不住院的患者中,71例(13%;535例患者中95% CI 0.10 - 0.16)在空腹状态(口服零)未接受去氨加压素治疗,没有静脉补液,并报告有脱水症状。660 (64%;0.61 - 0.67名参与者报告生活质量较低,369名(36%;0.33 - 0.39)主观上有与中枢性尿崩症相关的心理变化。823 (80%;0.77 - 0.82)参与者遇到中枢性尿崩症与糖尿病(糖尿病)混淆的情况。884 (85%;0.83 ~ 0.88)的参与者支持重命名疾病;最受欢迎的替代名称是抗利尿激素缺乏症和精氨酸抗利尿激素缺乏症。解释:这是对中枢性尿崩症患者进行的最大规模的调查,报告了治疗相关副作用、住院期间管理不善、心理合并症的高患病率,并明确支持重命名该疾病。我们的数据首次表明常规省略或延迟去氨加压素的价值。资助:瑞士国家科学基金会、瑞士医学科学院和G&J bangerter - rhyner基金会。
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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