Palmer A J, Valentine W J, Ray J A
CORE - Center for Outcomes Research, A Unit of IMS Health, Allschwil, Switzerland.
Int J Clin Pract. 2007 Oct;61(10):1626-33. doi: 10.1111/j.1742-1241.2007.01343.x.
The objective of the study was to determine the impact of irbesartan treatment on life expectancy (LE), costs and progression to end-stage renal disease (ESRD) in hypertensive type 2 diabetes patients. A peer-reviewed and published Markov model was used to simulate progression from microalbuminuria to overt nephropathy, doubling of serum creatinine, ESRD and all-cause mortality in hypertensive patients with type 2 diabetes. Three treatment strategies were evaluated: (i) 'control' regimen of conventional antihypertensive therapy (excluding angiotensin-converting enzyme inhibitors, angiotensin-2-receptor antagonists and dihydropyridine calcium-channel blockers), (ii) 'early irbesartan' 300 mg daily and (iii) 'late irbesartan' 300 mg daily (started when overt nephropathy developed). Transition probabilities determining nephropathy progression were taken from the Irbesartan in Reduction of Microalbuminuria-2 study, Irbesartan in Diabetic Nephropathy Trial and other published sources. Outcomes were projected over 25 years. The mean +/- SD cumulative incidence of ESRD was reduced by 8.8% +/- 0.6 and 12.4% +/- 0.7 in patients treated with early irbesartan compared with late irbesartan and control respectively. Early irbesartan treatment improved undiscounted LE by 1.38 +/- 0.08 years (discounted: 0.81 +/- 0.04 years) compared with late irbesartan and 1.41 +/- 0.08 years (discounted: 0.83 +/- 0.04 years) compared with control. Early irbesartan treatment was projected to save (mean +/- SD) pounds 2310 +/- 327 and pounds 3801 +/- 327 over patient lifetimes compared with late irbesartan and control respectively. Irbesartan treatment is predicted to improve survival and reduce costs in hypertensive patients with type 2 diabetes and microalbuminuria compared with 'control'. Early irbesartan treatment is more effective than late irbesartan. Irbesartan is a valuable treatment option in this patient group in a UK setting.
该研究的目的是确定厄贝沙坦治疗对高血压2型糖尿病患者的预期寿命(LE)、成本以及终末期肾病(ESRD)进展的影响。采用经同行评审并发表的马尔可夫模型,模拟高血压2型糖尿病患者从微量白蛋白尿进展为显性肾病、血清肌酐翻倍、ESRD以及全因死亡率的情况。评估了三种治疗策略:(i)传统抗高血压治疗的“对照”方案(不包括血管紧张素转换酶抑制剂、血管紧张素2受体拮抗剂和二氢吡啶类钙通道阻滞剂),(ii)每日300毫克的“早期厄贝沙坦”,以及(iii)每日300毫克的“晚期厄贝沙坦”(在显性肾病出现时开始)。确定肾病进展的转移概率取自厄贝沙坦减少微量白蛋白尿-2研究、厄贝沙坦糖尿病肾病试验及其他已发表的资料。对25年的结果进行了预测。与晚期厄贝沙坦和对照组相比,早期接受厄贝沙坦治疗的患者ESRD的平均±标准差累积发病率分别降低了8.8%±0.6和12.4%±0.7。与晚期厄贝沙坦相比,早期厄贝沙坦治疗使未贴现的LE提高了1.38±0.08年(贴现后:0.81±0.04年);与对照组相比,提高了1.41±0.08年(贴现后:0.83±0.04年)。预计早期厄贝沙坦治疗在患者的一生中分别比晚期厄贝沙坦和对照组节省(平均±标准差)2310±327英镑和3801±327英镑。与“对照”相比,预计厄贝沙坦治疗可提高2型糖尿病合并微量白蛋白尿的高血压患者的生存率并降低成本。早期厄贝沙坦治疗比晚期厄贝沙坦更有效。在英国的环境下,厄贝沙坦是该患者群体中一种有价值的治疗选择。