Análisis retrospectivo multicéntrico del tiosulfato sódico como tratamiento de la calcifilaxis no urémica

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Laura Cardona-Roca , Laura Borràs Trias , Rosario Bueno Uceda , Adrià Siles , Adrián Vilariño Seijas , Nuria Rudi Sola , Carlos Seguí-Solanes
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引用次数: 0

Abstract

Objectives

To describe the results obtained in terms of effectiveness and safety of intravenous sodium thiosulfate in patients diagnosed with non-uremic calciphylaxis, to identify and analyse possible etiological factors of the disease, and to determine the associated morbidity and mortality.

Method

A multicenter and retrospective study was conducted with patients diagnosed with non-uremic calciphylaxis who received intravenous sodium thiosulfate between 2013 and 2023. Effectiveness was evaluated based on the status of the ulcers at the end of treatment, and safety was assessed according to the main reported adverse effects and the need for dosage adjustment.

Results

A total of 33 patients from three university hospitals were evaluated (93.9% Caucasian, 78.8% women, mean age 80 [SD 8.1] years) with non-uremic calciphylaxis confirmed by skin biopsy. The localization pattern was 90.9% distal. The following complementary therapeutic measures were undertaken: topical wound care, removal of precipitating factors (mainly vitamin D supplements and vitamin K antagonists), medications to reduce calcification (bisphosphonates, cinacalcet), and techniques to promote ulcer healing. The main associated factors for developing calciphylaxis were: non-uremic chronic kidney disease (81.8%), vitamin D supplementation (72.7%), and hypoalbuminemia (66.7%). The most commonly used sodium thiosulfate dosage was 25 g (n = 26) three times per week (n = 28) intravenously, with a median treatment duration of 11.4 (IQR 5.7-18) weeks. A complete resolution or improvement of the ulcers was achieved in 78.8% of the cases. Adverse effects were observed in 96.7% of patients, with the most common being metabolic acidosis (n = 19) and nausea and/or vomiting (n = 18). Dosage adjustments due to toxicity were necessary in 9% of cases. The significant morbidity rate was 69.7% (n = 23). The main complications were: 57.6% ulcer superinfection and 24.3% poor pain control. The overall mortality rate was 66.7%; 42.4% within the first 6 months after diagnosis and 39.4% secondary to non-uremic calciphylaxis.

Conclusions

Sodium thiosulfate shows a potential benefit in the treatment of ulcers due to non-uremic calciphylaxis, with a similar safety profile to that reported for uremic calciphylaxis, considering the high morbidity and mortality associated with the condition. Further studies are needed to determine its efficacy and assess the specific contribution of the different treatments used.
硫代硫酸钠治疗非尿毒症性钙化反应的多中心回顾性分析。
目的:描述在诊断为非尿毒症性钙化反应的患者中静脉注射硫代硫酸钠的有效性和安全性方面获得的结果,确定和分析该疾病的可能病因,并确定相关的发病率和死亡率。方法:对2013年至2023年间静脉注射硫代硫酸钠的非尿毒症性钙化反应患者进行多中心回顾性研究。根据治疗结束时溃疡的状况来评估有效性,根据报告的主要不良反应和剂量调整的需要来评估安全性。结果:来自三所大学医院的33例患者(93.9%为白人,78.8%为女性,平均年龄80 [SD 8.1]岁)经皮肤活检证实为非尿毒症性钙化反应。定位模式为90.9%远端。采取了以下补充治疗措施:局部伤口护理,去除沉淀因素(主要是维生素D补充剂和维生素K拮抗剂),减少钙化的药物(双膦酸盐,cinacalcet)和促进溃疡愈合的技术。发生钙化反应的主要相关因素是:非尿毒症慢性肾病(81.8%)、维生素D补充(72.7%)和低白蛋白血症(66.7%)。最常用的硫代硫酸钠剂量为25 g (n = 26),静脉滴注,每周3次(n = 28),中位治疗时间为11.4周(IQR为5.7-18)。78.8%的病例溃疡完全缓解或改善。96.7%的患者出现不良反应,最常见的是代谢性酸中毒(n = 19)和恶心和/或呕吐(n = 18)。9%的病例由于毒性需要调整剂量。显著发病率为69.7% (n = 23)。主要并发症为:溃疡重复感染57.6%,疼痛控制不良24.3%。总死亡率为66.7%;42.4%在诊断后的前6个月内,39.4%继发于非尿毒症性钙化反应。结论:考虑到与尿毒症相关的高发病率和死亡率,硫代硫酸钠在治疗非尿毒症性钙化反应引起的溃疡方面显示出潜在的益处,其安全性与报道的尿毒症性钙化反应相似。需要进一步的研究来确定其疗效并评估所使用的不同治疗方法的具体贡献。
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来源期刊
FARMACIA HOSPITALARIA
FARMACIA HOSPITALARIA PHARMACOLOGY & PHARMACY-
CiteScore
1.90
自引率
21.40%
发文量
46
审稿时长
37 days
期刊介绍: Una gran revista para acceder a los mejores artículos originales y revisiones de la farmacoterapia actual. Además, es Órgano de expresión científica de la Sociedad Española de Farmacia Hospitalaria, y está indexada en Index Medicus/Medline, EMBASE/Excerpta Médica, Alert, Internacional Pharmaceutical Abstracts y SCOPUS.
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