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Burden of illness in patients with chronic hypoparathyroidism not adequately controlled with conventional therapy: a Belgium and the Netherlands survey.慢性甲状旁腺功能减退症患者在常规治疗下病情控制不佳的疾病负担:一项比利时和荷兰的调查。
J Endocrinol Invest. 2021 Jul;44(7):1437-1446. doi: 10.1007/s40618-020-01442-y. Epub 2020 Oct 30.
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The effects of patient and disease-related factors on the quality of life in patients with hypoparathyroidism.甲状旁腺功能减退症患者生活质量的患者和疾病相关因素的影响。
Arch Osteoporos. 2020 May 19;15(1):75. doi: 10.1007/s11657-020-00759-8.
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Burden of illness in not adequately controlled chronic hypoparathyroidism: Findings from a 13-country patient and caregiver survey.慢性甲状旁腺功能减退症未得到充分控制的疾病负担:来自 13 个国家的患者和照护者调查结果。
Clin Endocrinol (Oxf). 2020 Feb;92(2):159-168. doi: 10.1111/cen.14128. Epub 2019 Dec 11.
4
Defining the Characteristics of Chronic Hypoparathyroidism Not Adequately Controlled on Conventional Therapy: Consensus Findings of Three European Delphi Panels.定义常规治疗未能充分控制的慢性甲状旁腺功能减退症的特征:三个欧洲德尔菲小组的共识结果。
Adv Ther. 2019 Nov;36(11):3007-3016. doi: 10.1007/s12325-019-01102-5. Epub 2019 Oct 5.
5
Safety and Efficacy of 5 Years of Treatment With Recombinant Human Parathyroid Hormone in Adults With Hypoparathyroidism.甲状旁腺功能减退症成人患者接受重组人生长激素治疗 5 年的安全性和疗效。
J Clin Endocrinol Metab. 2019 Nov 1;104(11):5136-5147. doi: 10.1210/jc.2019-01010.
6
Therapy of Hypoparathyroidism With rhPTH(1-84): A Prospective, 8-Year Investigation of Efficacy and Safety.rhPTH(1-84)治疗甲状旁腺功能减退症:疗效和安全性的前瞻性 8 年研究。
J Clin Endocrinol Metab. 2019 Nov 1;104(11):5601-5610. doi: 10.1210/jc.2019-00893.
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Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism.慢性甲状旁腺功能减退症患者报告结局测量指标的制定。
Adv Ther. 2019 Aug;36(8):1999-2009. doi: 10.1007/s12325-019-00999-2. Epub 2019 Jun 10.
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Clinical burden and healthcare resource utilization among patients with chronic hypoparathyroidism, overall and by adequately vs not adequately controlled disease: a multi-country chart review.慢性甲状旁腺功能减退症患者的临床负担和医疗资源利用情况:一项多国图表回顾,按疾病控制充分与不充分进行划分。
J Med Econ. 2019 Nov;22(11):1141-1152. doi: 10.1080/13696998.2019.1624081. Epub 2019 Jun 17.
9
Psychometric evaluation of the hypoparathyroidism symptom diary.甲状旁腺功能减退症状日记的心理测量评估
Patient Relat Outcome Meas. 2019 Jan 29;10:25-36. doi: 10.2147/PROM.S179310. eCollection 2019.
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Standards of care for hypoparathyroidism in adults: a Canadian and International Consensus.成人甲状旁腺功能减退症的护理标准:加拿大与国际共识
Eur J Endocrinol. 2019 Mar;180(3):P1-P22. doi: 10.1530/EJE-18-0609.

PARADIGHM(医师推进甲状旁腺功能减退症知识)登记研究:慢性甲状旁腺功能减退症患者的研究方案和中期基线患者特征。

The PARADIGHM (physicians advancing disease knowledge in hypoparathyroidism) registry for patients with chronic hypoparathyroidism: study protocol and interim baseline patient characteristics.

机构信息

Centre for Endocrinology, Diabetes and Metabolism (CEDAM), Queen Elizabeth Hospital Edgbaston, 3rd Floor, Heritage Building, Birmingham, B15 2TH, UK.

Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Palle Juul-Jensens Boulevard 99, 8200, Aarhus N, Denmark.

出版信息

BMC Endocr Disord. 2021 Nov 20;21(1):232. doi: 10.1186/s12902-021-00888-2.

DOI:
10.1186/s12902-021-00888-2
PMID:34801015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8606089/
Abstract

BACKGROUND

The PARADIGHM registry of adult and pediatric patients with chronic hypoparathyroidism evaluates the long-term safety and effectiveness of treatment with recombinant human parathyroid hormone, rhPTH(1-84), and describes the clinical disease course under conditions of routine clinical practice. In this first report, we detail the registry protocol and describe the baseline characteristics of two adult patient cohorts from an interim database analysis. One cohort after study entry were prescribed rhPTH(1-84), and the other cohort received conventional therapy of calcium and active vitamin D.

METHODS

An observational study of patients with chronic hypoparathyroidism in North America and Europe, collecting data for ≥10 years per patient. Main outcome measures were baseline patient demographics, clinical characteristics, medications, and disease outcome variables of symptoms, biochemical parameters, and health assessments. Baseline is the enrollment assessment for all variables except biochemical measurements in patients treated with rhPTH(1-84); those measurements were the most recent value before the first rhPTH(1-84) dose. Exclusion criteria applied to the analysis of specified outcomes included pediatric patients, patients who initiated rhPTH(1-84) prior to enrollment, and those who received rhPTH(1-34). Clinically implausible biochemical outlier data were excluded.

RESULTS

As of 30 June 2019, data of 737 patients were analyzed from 64 centers; 587 (80%) were women, mean ± SD age 49.1±16.45 years. At enrollment, symptoms reported for patients later prescribed rhPTH(1-84) (n=60) and those who received conventional therapy (n=571), respectively, included fatigue (51.7%, 40.1%), paresthesia (51.7%, 29.6%), muscle twitching (48.3%, 21.9%), and muscle cramping (41.7%, 33.8%). Mean serum total calcium, serum phosphate, creatinine, and estimated glomerular filtration rate were similar between cohorts. Health-related quality of life (HRQoL) 36-item Short Form Health Survey questionnaire scores for those later prescribed rhPTH(1-84) were generally lower than those for patients in the conventional therapy cohort.

CONCLUSIONS

At enrollment, based on symptoms and HRQoL, a greater percentage of patients subsequently prescribed rhPTH(1-84) appeared to have an increased burden of disease than those who received conventional therapy despite having normal biochemistry measurements. PARADIGHM will provide valuable real-world insights on the clinical course of hypoparathyroidism in patients treated with rhPTH(1-84) or conventional therapy in routine clinical practice.

TRIAL REGISTRATION

EUPAS16927, NCT01922440.

摘要

背景

成人和儿科慢性甲状旁腺功能减退症患者的 PARADIGHM 登记处评估了重组人甲状旁腺激素 rhPTH(1-84)的长期安全性和有效性,并描述了在常规临床实践条件下的临床疾病过程。在第一份报告中,我们详细介绍了登记处方案,并描述了来自中期数据库分析的两个成年患者队列的基线特征。一组患者在研究入组后接受 rhPTH(1-84)治疗,另一组患者接受钙和活性维生素 D 的常规治疗。

方法

这是一项在北美和欧洲进行的慢性甲状旁腺功能减退症患者的观察性研究,每位患者的数据收集时间≥ 10 年。主要终点是基线患者人口统计学、临床特征、药物和疾病结局变量,包括症状、生化参数和健康评估。rhPTH(1-84)治疗患者的所有变量的基线是入组评估,除了生化测量值,这些测量值是接受 rhPTH(1-84)之前的最近值。排除了特定结局分析中应用的排除标准,包括儿科患者、在入组前开始 rhPTH(1-84)治疗的患者以及接受 rhPTH(1-34)治疗的患者。排除了生化异常值的临床不合理数据。

结果

截至 2019 年 6 月 30 日,对来自 64 个中心的 737 名患者进行了数据分析;587 名(80%)为女性,平均年龄 49.1±16.45 岁。在登记时,随后接受 rhPTH(1-84)治疗的患者(n=60)和接受常规治疗的患者(n=571)报告的症状分别包括疲劳(51.7%,40.1%)、感觉异常(51.7%,29.6%)、肌肉抽搐(48.3%,21.9%)和肌肉痉挛(41.7%,33.8%)。两组间血清总钙、血清磷酸盐、肌酐和估算肾小球滤过率均相似。rhPTH(1-84)治疗组的健康相关生活质量(HRQoL)36 项简明健康调查问卷评分普遍低于常规治疗组患者。

结论

基于症状和 HRQoL,与接受常规治疗的患者相比,随后接受 rhPTH(1-84)治疗的患者在登记时似乎有更多的疾病负担,尽管他们的生化指标正常。PARADIGHM 将为 rhPTH(1-84)治疗或常规治疗的患者在常规临床实践中的甲状旁腺功能减退症临床病程提供有价值的真实世界见解。

试验注册

EUPAS16927,NCT01922440。