Garg Amit X, Cuerden Meaghan, Cata Juan, Chan Matthew T V, Devereaux P J, Fleischmann Edith, Grande Ascensión Martín, Kabon Barbara, Landoni Giovanni, Maziak Donna E, McLean Sean, Parikh Chirag, Popova Ekaterine, Reimer Cara, Trujillo Reyes Juan Carlos, Roshanov Pavel, Sessler Daniel I, Srinathan Sadeesh, Sontrop Jessica M, Gonzalez Tallada Anna, Wang Michael Ke, Wells Jennifer R, Conen David
London Health Sciences Centre, ON, Canada.
MD Anderson Cancer Center, Houston, TX, USA.
Can J Kidney Health Dis. 2023 Jul 11;10:20543581231185427. doi: 10.1177/20543581231185427. eCollection 2023.
Inflammation during and after surgery can lead to organ damage including acute kidney injury. Colchicine, an established inexpensive anti-inflammatory medication, may help to protect the organs from pro-inflammatory damage. This protocol describes a kidney substudy of the colchicine for the prevention of perioperative atrial fibrillation (COP-AF) study, which is testing the effect of colchicine versus placebo on the risk of atrial fibrillation and myocardial injury among patients undergoing thoracic surgery.
Our kidney substudy of COP-AF will determine whether colchicine reduces the risk of perioperative acute kidney injury compared with a placebo. We will also examine whether colchicine has a larger absolute benefit in patients with pre-existing chronic kidney disease, the most prominent risk factor for acute kidney injury.
Randomized, superiority clinical trial conducted in 40 centers in 11 countries from 2018 to 2023.
Patients (~3200) aged 55 years and older having major thoracic surgery.
Patients are randomized 1:1 to receive oral colchicine (0.5 mg tablet) or a matching placebo, given twice daily starting 2 to 4 hours before surgery for a total of 10 days. Patients, health care providers, data collectors, and outcome adjudicators will be blinded to the randomized treatment allocation.
Serum creatinine concentrations will be measured before surgery and on postoperative days 1, 2, and 3 (or until hospital discharge). The primary outcome of the substudy is perioperative acute kidney injury, defined as an increase (from the prerandomization value) in serum creatinine concentration of either ≥26.5 μmol/L (≥0.3 mg/dL) within 48 hours of surgery or ≥50% within 7 days of surgery. The primary analysis (intention-to-treat) will examine the relative risk of acute kidney injury in patients allocated to receive colchicine versus placebo. We will repeat the primary analysis using alternative definitions of acute kidney injury and examine effect modification by pre-existing chronic kidney disease, defined as a prerandomization estimated glomerular filtration rate (eGFR) <60 mL/min per 1.73 m.
The substudy will be underpowered to detect small effects on more severe forms of acute kidney injury treated with dialysis.
Substudy results will be reported in 2024.
This substudy will estimate the effect of colchicine on the risk of perioperative acute kidney injury in older adults undergoing major thoracic surgery.
NCT03310125.
手术期间及术后的炎症可导致包括急性肾损伤在内的器官损伤。秋水仙碱是一种公认的廉价抗炎药物,可能有助于保护器官免受促炎损伤。本方案描述了秋水仙碱预防围手术期房颤(COP-AF)研究的肾脏子研究,该研究正在测试秋水仙碱与安慰剂对胸外科手术患者房颤风险和心肌损伤的影响。
我们对COP-AF的肾脏子研究将确定秋水仙碱与安慰剂相比是否能降低围手术期急性肾损伤的风险。我们还将研究秋水仙碱在已有慢性肾病(急性肾损伤最突出的危险因素)患者中是否具有更大的绝对获益。
2018年至2023年在11个国家的40个中心进行的随机、优效性临床试验。
年龄在55岁及以上接受胸外科大手术的患者(约3,200名)。
患者按1:1随机分组,接受口服秋水仙碱(0.5毫克片剂)或匹配的安慰剂,于手术前2至4小时开始每日两次给药,共10天。患者、医护人员、数据收集者和结果判定者将对随机治疗分配情况不知情。
在手术前以及术后第1、2和3天(或直至出院)测量血清肌酐浓度。子研究的主要结局是围手术期急性肾损伤,定义为手术48小时内血清肌酐浓度较随机分组前值升高≥26.5 μmol/L(≥0.3 mg/dL)或手术7天内升高≥50%。主要分析(意向性分析)将检查分配接受秋水仙碱与安慰剂的患者发生急性肾损伤的相对风险。我们将使用急性肾损伤的替代定义重复主要分析,并研究已有慢性肾病(定义为随机分组前估计肾小球滤过率(eGFR)<60 mL/min/1.73 m²)对疗效的修正作用。
该子研究检测对更严重形式的需透析治疗的急性肾损伤的微小影响的效能不足。
子研究结果将于2024年报告。
本项子研究将评估秋水仙碱对接受胸外科大手术的老年人围手术期急性肾损伤风险的影响。
NCT03310125。