Service de Pharmacie-Stérilisation, Hôpitaux universitaires de Strasbourg, Strasbourg, France.
Service de Néphrologie, Hôpitaux universitaires de Strasbourg, Strasbourg, France.
RMD Open. 2024 Jan 31;10(1):e003872. doi: 10.1136/rmdopen-2023-003872.
Colchicine, commonly used in gout flare, is contraindicated in severe chronic kidney disease (CKD) (estimated glomerular filtration rate <30 mL/min). However, in this context, there are few alternatives, and colchicine use persists. We evaluated the tolerance of colchicine and its efficacy in patients with severe CKD.
All prescriptions of colchicine for managing crystal-induced arthritis flare (gout or calcium pyrophosphate deposition (CPPD) disease) in a hospitalised patient with severe CKD were screened from September 2020 to September 2021. After patient consent and treatment information, clinical and biological safety and efficacy data were prospectively collected from day 1 (D1) to D11.
We included 54 patients (median age 75 years (IQR 67-83)) with 62 colchicine prescriptions (cases). Twelve (22%) patients were on dialysis. The main reason for hospitalisation was heart failure (31.5%), acute renal failure (22.2%), infection (18.5%) or an acute joint episode (9.3%). In total, 59.3% of patients had diabetes. The prescriptions concerned 58 cases of gout flares, 1 case of CPPD and 3 cases of both. Initial colchicine dosages were ≤0.5 mg/day in 47/62 (75.8%) cases; no dosage exceeded 1 mg/day (median duration of 6 days (IQR 3-11)). Colchicine was well tolerated in 47/61 (77%) cases. No serious adverse event was reported. Colchicine was considered completely effective by the medical team in 48/58 (83%) of cases.
The use of colchicine, at reduced doses, was mostly effective to treat crystal-induced arthritis flare in 54 patients with severe CKD and was well tolerated, without any serious adverse events.
秋水仙碱常用于痛风发作,在严重慢性肾脏病(CKD)(估计肾小球滤过率 <30mL/min)时禁用。然而,在这种情况下,替代药物很少,秋水仙碱的使用仍然存在。我们评估了严重 CKD 患者使用秋水仙碱的耐受性及其疗效。
从 2020 年 9 月至 2021 年 9 月,对一家医院中患有严重 CKD 的晶体诱导关节炎发作(痛风或焦磷酸钙沉积(CPPD)病)的住院患者的所有秋水仙碱处方进行筛选。在获得患者同意和治疗信息后,从第 1 天(D1)至第 11 天(D11)前瞻性收集临床和生物学安全性及疗效数据。
我们纳入了 54 名患者(中位年龄 75 岁(IQR 67-83))和 62 份秋水仙碱处方(病例)。12 名(22%)患者正在接受透析。住院的主要原因是心力衰竭(31.5%)、急性肾衰竭(22.2%)、感染(18.5%)或急性关节发作(9.3%)。共有 59.3%的患者患有糖尿病。处方涉及 58 例痛风发作、1 例 CPPD 和 3 例同时发生痛风和 CPPD。初始秋水仙碱剂量为≤0.5mg/天的有 47/62(75.8%)例;没有剂量超过 1mg/天(中位数持续时间 6 天(IQR 3-11))。61 例(77%)中 47 例秋水仙碱耐受良好。没有报告严重不良事件。医疗团队认为 48/58(83%)例的秋水仙碱完全有效。
在 54 名严重 CKD 患者中,以较低剂量使用秋水仙碱治疗晶体诱导的关节炎发作,大多数是有效的,且耐受性良好,无严重不良事件。