Marzoa-Rivas R, Crespo-Leiro M G, Paniagua-Marin M J, Llinares-García D, Muñiz-Garcia J, Aldama-López G, Piñón-Esteban P, Campo-Pérez R, Castro-Beiras A
Area del Corazón, belong to Red Investigación Cardiovascular RECAVA (Instituto de Salud Carlos III), Spain.
Transplant Proc. 2005 Nov;37(9):4071-3. doi: 10.1016/j.transproceed.2005.09.163.
Statins are used as first-line drugs against hypercholesterolemia after heart transplantation. Randomized clinical trials have shown that they reduce cholesterol levels, and the incidence of rejection and coronary vasculopathy. Adverse effects have been related to the use of certain statins, high statin dosages, comorbidities, and coadministration with cyclosporine. However, estimation of the risk of adverse effects for a given patient is difficult. The aims of this study were to determine the incidence of various kinds of adverse effect of statins; to evaluate certain potential risk factors; and to assess the efficacy of early response to signs of adverse effects.
Between April 1991 and December 2003, we retrospectively evaluated 336 heart transplant patients (including 55 women) with regard to the occurrence of possible adverse effects of statins (rhabdomyolysis, myalgia, hepatotoxicity, high CK without muscle symptoms, and others). Resolution on reduction of dosage or discontinuance and/or change of statin were deemed to constitute confirmation of cause. Relations were sought between adverse effects and age, sex, immunosuppressive therapy, kidney failure, body mass index (BMI), arterial hypertension, and diabetes mellitus.
Possible adverse events of statins were suffered by 60 patients, all of them men. The causal role of statins was confirmed in 41 (12.2% of all 336): hepatotoxicity was suffered by 13, high CK without muscle ache or weakness by 18, rhabdomyolysis by 5, myalgia by 3, and other effects by 2. The incidence of confirmed statin-related complications was higher among patients with BMI >29 kg/m(2) than among those with lower BMI (P = .055). None of the patients with confirmed statin-related complications needed dialysis, none died, and permanent suspension of statin treatment was only necessary in 13 cases (3.9% of the 336).
Some 10% to 20% of HT patients appear to suffer adverse side effects of initial statin therapy. However, early detection of such effects through diligent clinical and analytical monitoring allows the therapy to be modified in time to minimize the appearance of severe complications. In only a minority of cases permanent suspension of statin therapy is necessary.
他汀类药物被用作心脏移植后抗高胆固醇血症的一线药物。随机临床试验表明,它们可降低胆固醇水平、排斥反应发生率和冠状动脉病变发生率。不良反应与某些他汀类药物的使用、高剂量他汀类药物、合并症以及与环孢素的联合使用有关。然而,估计特定患者发生不良反应的风险很困难。本研究的目的是确定他汀类药物各种不良反应的发生率;评估某些潜在风险因素;并评估对不良反应迹象的早期反应的疗效。
在1991年4月至2003年12月期间,我们回顾性评估了336例心脏移植患者(包括55名女性)他汀类药物可能的不良反应(横纹肌溶解、肌痛、肝毒性、无肌肉症状的高肌酸激酶以及其他不良反应)的发生情况。通过减少剂量或停药和/或更换他汀类药物后症状缓解被视为病因确诊。研究了不良反应与年龄、性别、免疫抑制治疗、肾衰竭、体重指数(BMI)、动脉高血压和糖尿病之间的关系。
60例患者出现了他汀类药物可能的不良事件,均为男性。41例(占全部336例的12.2%)他汀类药物的因果关系得到确诊:13例出现肝毒性,18例出现无肌肉疼痛或无力的高肌酸激酶,5例出现横纹肌溶解,3例出现肌痛,2例出现其他不良反应。BMI>29 kg/m²的患者中确诊的他汀类药物相关并发症的发生率高于BMI较低的患者(P = 0.055)。确诊为他汀类药物相关并发症的患者均无需透析,无一例死亡,仅13例(336例中的3.9%)需要永久停用他汀类药物治疗。
约10%至20%的心脏移植患者似乎会出现初始他汀类药物治疗的不良副作用。然而,通过认真的临床和分析监测早期发现此类影响,可及时调整治疗方案,以尽量减少严重并发症的出现。仅在少数情况下需要永久停用他汀类药物治疗。