Department of cardiovascular surgery.
Department of critical care medicine, Shanxi Cardiovascular Hospital, Shanxi.
Medicine (Baltimore). 2021 Feb 19;100(7):e24661. doi: 10.1097/MD.0000000000024661.
: We performed this randomized controlled study protocol to investigate the efficacy and adverse effects of furosemide vs torasemide in patients with heart failure (HF).
: The present study was authorized by the local research ethics committee of Shanxi Cardiovascular Hospital (no. 48736645) and informed consent was obtained from all patients. Patients were enrolled in a consecutive prospective manner on a voluntary basis. Patients who were aged 18 years and older with HF who were eligible to enroll in this randomized trial. All patients had evidence of left ventricular systolic dysfunction, confirmed by echocardiographic or nuclear imaging. The exclusion criteria were left ventricular diastolic dysfunction only, or receipt of medical or pharmaceutical care in other health systems. The primary efficacy end point was the change in procollagen type I carboxyterminal peptide (PICP) serum levels between baseline and final visit. Secondary efficacy variables included parameters related to the clinical course of HF, such as body weight, presence of edema, signs and symptoms of HF, electrocardiogram and echocardiographic evaluation, amino-terminal pro brain-type natriuretic peptide (NT-proBNP) serum levels measured by ELISA method, systolic blood pressure (SBP), diastolic blood pressure (DBP), heart rate, and renal function.
: One hundred patients who met the inclusion criteria were included in our study, Table 1 showed the effects of furosemide and torsemide on measures of clinical outcomes.
: Fluid overload is the primary cause of hospitalization among patients with HF. Preventing circulatory congestion requires careful control of dietary sodium and chronic administration of loop diuretics. Torasemide and furosemide are representatives of loop diuretics with an identical diuretic mechanism, but different pharmacokinetic properties and additional effects. There is a need for reliable conclusion regarding the comparison of furosemide and torasemide in patients with HF. Several limitation should be noted: 1. the small number of participants did not enable assessment of the impact of torasemide and furosemide in different clinically relevant subgroups that is, elderly, patients with chronic kidney disease, dilated cardiomyopathy; 2. short-term follow up might lead to underestimation of the complications; 3. methodological weakness in study design may affect the results. Future high quality studies were still required.
我们进行了这项随机对照研究方案,以研究心力衰竭(HF)患者中呋塞米与托拉塞米的疗效和不良反应。
本研究得到了山西心血管病医院当地研究伦理委员会的授权(编号 48736645),并获得了所有患者的知情同意。患者以自愿的方式连续前瞻性入组。年龄在 18 岁及以上、符合本随机试验入组条件的 HF 患者。所有患者均有左心室收缩功能障碍的证据,通过超声心动图或核成像证实。排除标准为仅有左心室舒张功能障碍,或在其他医疗系统接受药物或药物治疗。主要疗效终点是基线和最终访视时血清 I 型前胶原羧基末端肽(PICP)水平的变化。次要疗效变量包括与 HF 临床病程相关的参数,如体重、水肿存在、HF 的体征和症状、心电图和超声心动图评估、用 ELISA 法测量的氨基末端脑利钠肽前体(NT-proBNP)血清水平、收缩压(SBP)、舒张压(DBP)、心率和肾功能。
符合纳入标准的 100 例患者纳入本研究,表 1 显示了呋塞米和托拉塞米对临床结局测量指标的影响。
液体超负荷是 HF 患者住院的主要原因。预防循环充血需要仔细控制饮食中的钠和慢性给予袢利尿剂。托拉塞米和呋塞米是具有相同利尿机制但药代动力学特性和其他作用不同的袢利尿剂的代表。需要有可靠的结论来比较 HF 患者中呋塞米和托拉塞米的疗效。有几个限制应注意:1. 参与者人数少,无法评估托拉塞米和呋塞米在不同临床相关亚组中的影响,即老年患者、慢性肾脏病患者、扩张型心肌病患者;2. 短期随访可能导致并发症低估;3. 研究设计中的方法学弱点可能影响结果。仍需要进行高质量的未来研究。