Young M, Plosker G L
Adis International Limited, Auckland, New Zealand.
Pharmacoeconomics. 2001;19(6):679-703. doi: 10.2165/00019053-200119060-00006.
Torasemide is a loop diuretic used for the treatment of hypertension and for oedema in chronic heart failure (CHF), renal failure and cirrhosis. The efficacy of torasemide in reducing salt and water retention in CHF has been established in double-blind comparative studies against furosemide. Torasemide has been shown to be at least as effective as furosemide in terms of total volume of urine excreted and also has a longer duration of action. The efficacy of torasemide (in terms of improved CHF symptoms and reduced pulmonary congestion, oedema and bodyweight) has been shown in randomised controlled trials and confirmed in large postmarketing studies. In addition, data from postmarketing studies have shown that patients receiving torasemide had significantly reduced hospital admission rates compared with patients receiving furosemide. Pharmacoeconomic assessments of torasemide have focused on its effect in reducing hospitalisation. Hospitalisation costs due to CHF decreased by 86% during the 11.2-month period of torasemide treatment, compared with the 6-month period prior to treatment, in a US retrospective study assessing medical and pharmacy claims data. Overall, average monthly costs for patients decreased by 56.6% after 5.1 months (from $US1,897.28 to $US823.70 per patient per month; PPPM), and by 76% after 11.2 months (from $US1,944.76 to $US470.76 PPPM) of torasemide treatment. In the furosemide group, average monthly costs for patients increased moderately from $US227.28 to $US261.18 PPPM after 12 months. Direct comparison of the torasemide and furosemide study groups was not possible because the group receiving torasemide had much higher healthcare resource use at baseline. Compared with furosemide, torasemide was associated with reduced rates of hospital admissions for CHF and/or cardiovascular causes in 3 studies, a retrospective analysis conducted in Germany, a prospective US study of patients enrolled from hospital admissions and a decision-analysis model. As a result, the direct costs of treatment for CHF or cardiovascular diseases for patients treated with torasemide were less than those with furosemide. However, in the US study, there was no statistically significant difference in hospital admissions for all causes and/or in overall direct medical costs, although the study was not powered to show this. In another US study of managed care patients with New York Heart Association (NYHA) class II or III CHF, no difference in clinical or economic outcomes was observed between patients taking torasemide or furosemide; despite the higher acquisition costs for torasemide, total costs were similar for both groups. Torasemide was found to be more cost effective than furosemide in terms of cost per patient with improved functional (NYHA) class of CHF severity in a retrospective German analysis, although this measure is not ideal. This study also evaluated indirect costs (for loss of productivity of employed patients) and resultssuggest torasemide has a favourable effect in reducing days off work compared with furosemide, although the population of employed patients in the study was very small. Torasemide has been shown to improve some measures of quality of life in 2 studies. It was associated with higher quality-of-life scores than furosemide in a 6-month study, but the differences were only significant at month 4. In another study, torasemide significantly improved fatigue, but full study details are yet to be published.
Despite the higher acquisition cost of torasemide over furosemide, pharmacoeconomic analyses have shown that torasemide is likely to reduce overall treatment costs of CHF by reducing hospital admissions and readmissions. Torasemide has generally shown clinical and economic advantages over furosemide, although more long term data are needed to confirm these results and to further investigate effects on quality of life. There are limitations to the currently available pharmacoeconomic data, but present data support the use of torasemide as a first-line option for diuretic therapy in patients with CHF presenting with oedema and especially in those patients not achieving relief of symptoms with furosemide.
托拉塞米是一种袢利尿剂,用于治疗高血压以及慢性心力衰竭(CHF)、肾衰竭和肝硬化引起的水肿。在针对呋塞米的双盲对照研究中,已证实托拉塞米在CHF中减少盐和水潴留的疗效。就总尿量而言,托拉塞米已被证明至少与呋塞米一样有效,且作用持续时间更长。托拉塞米的疗效(在改善CHF症状、减轻肺淤血、水肿和体重方面)已在随机对照试验中得到证实,并在大型上市后研究中得到确认。此外,上市后研究数据表明,与接受呋塞米治疗的患者相比,接受托拉塞米治疗的患者住院率显著降低。托拉塞米的药物经济学评估主要集中在其对减少住院的影响上。在美国一项评估医疗和药房索赔数据的回顾性研究中,与治疗前6个月相比,在托拉塞米治疗的11.2个月期间,CHF导致的住院费用下降了86%。总体而言,患者的平均每月费用在托拉塞米治疗5.1个月后下降了56.6%(从每位患者每月1897.28美元降至823.70美元;按购买力平价计算),在治疗11.2个月后下降了76%(从1944.76美元降至470.76美元按购买力平价计算)。在呋塞米组中,患者的平均每月费用在12个月后从227.28美元适度增加至261.18美元按购买力平价计算。由于接受托拉塞米治疗的组在基线时医疗资源使用量高得多,因此无法对托拉塞米和呋塞米研究组进行直接比较。与呋塞米相比,在3项研究中,托拉塞米与CHF和/或心血管疾病导致的住院率降低相关,这3项研究分别是在德国进行的回顾性分析、美国一项对因住院入院患者进行的前瞻性研究以及一个决策分析模型。因此,接受托拉塞米治疗的患者CHF或心血管疾病的直接治疗成本低于接受呋塞米治疗的患者。然而,在美国的研究中,所有原因导致的住院率和/或总体直接医疗成本没有统计学上的显著差异,尽管该研究没有足够的效力来显示这一点。在美国另一项针对纽约心脏协会(NYHA)II级或III级CHF的管理式医疗患者的研究中,服用托拉塞米或呋塞米的患者在临床或经济结果方面没有差异;尽管托拉塞米的购置成本较高,但两组的总成本相似。在德国一项回顾性分析中,就每位CHF严重程度功能(NYHA)分级改善的患者成本而言,托拉塞米被发现比呋塞米更具成本效益,尽管这一衡量标准并不理想。该研究还评估了间接成本(在职患者的生产力损失),结果表明与呋塞米相比,托拉塞米在减少工作日方面有有利影响,尽管该研究中的在职患者群体非常小。在2项研究中,托拉塞米已被证明可改善一些生活质量指标。在一项为期6个月的研究中,它与比呋塞米更高的生活质量评分相关,但差异仅在第4个月显著。在另一项研究中,托拉塞米显著改善了疲劳,但完整的研究细节尚未发表。
尽管托拉塞米的购置成本高于呋塞米,但药物经济学分析表明,托拉塞米可能通过减少住院和再住院来降低CHF的总体治疗成本。托拉塞米总体上已显示出优于呋塞米的临床和经济优势,尽管需要更多长期数据来证实这些结果并进一步研究对生活质量的影响。目前可用的药物经济学数据存在局限性,但现有数据支持将托拉塞米作为有水肿的CHF患者利尿剂治疗的一线选择,特别是对于那些使用呋塞米不能缓解症状的患者。