College of Pharmacy, Korea University Sejong Campus 2511 Sejong-ro, Sejong City 339-770, Korea.
College of Pharmacy, Ajou University, 206 Worldcup-ro, Yeongtong-gu, Suwon-si, Gyeonggi-do 443-749, Korea.
Cost Eff Resour Alloc. 2014 Sep 10;12:19. doi: 10.1186/1478-7547-12-19. eCollection 2014.
Iron-deficiency anemia (IDA) is prevalent in patients with advanced chronic heart failure (CHF). It affects the patients' overall physical condition and is suggested as a strong outcome predictor in CHF. Recent clinical trials suggested that intravenous iron supplementation improves CHF functional status and quality of life. The aim of this study was to assess the cost-effectiveness of ferric carboxymaltose(FCM) in CHF patients with IDA.
Ferric carboxymaltose, an intravenous iron preparation, was compared with placebo. The target population comprised CHF patients with IDA in hospital and outpatient care settings. We conducted this study from the Korean healthcare payers' perspective with a time horizon of 24 weeks. One clinical trial provided the clinical outcomes of ferric carboxymaltose therapy. The improvement rates of the New York Heart Association (NYHA) functional class in the placebo and ferric carboxymaltose groups were used to estimate effectiveness in the base-case model. We also conducted a scenario 2 analysis using quality of life investigated in the clinical trial. A panel survey was conducted to obtain the ratio of healthcare resource use based on NYHA class in Korea. Cost-effectiveness was expressed as incremental cost (US dollars) per quality-adjusted life-year (QALY) gained.
In the base-case analysis, the incremental cost-effectiveness ratio (ICER) of ferric carboxymaltose compared with placebo was $22,192 (₩25,010,451) per QALY gained. The sensitivity analysis showed robust results, with the ICERs of ferric carboxymaltose ranging from $5,156 to $29,796 per QALY gained. In the scenario 2 analysis, ICER decreased to $12,598 (₩14,198,501) per QALY gained.
Iron repletion with ferric carboxymaltose for IDA in CHF patients was cost-effective compared with placebo.
缺铁性贫血(IDA)在晚期慢性心力衰竭(CHF)患者中很常见。它影响患者的整体身体状况,并被认为是 CHF 的强有力预后预测指标。最近的临床试验表明,静脉内铁补充剂可改善 CHF 功能状态和生活质量。本研究旨在评估羧基麦芽糖铁(FCM)在 CHF 伴 IDA 患者中的成本效益。
羧基麦芽糖铁是一种静脉内铁制剂,与安慰剂进行比较。目标人群包括住院和门诊治疗环境中的 CHF 伴 IDA 患者。我们从韩国医疗保健支付者的角度进行了这项研究,时间范围为 24 周。一项临床试验提供了铁羧基麦芽糖治疗的临床结局。安慰剂和铁羧基麦芽糖组纽约心脏协会(NYHA)功能分级的改善率用于估计基础模型中的疗效。我们还使用临床试验中调查的生活质量进行了方案 2 分析。进行了小组调查,以根据韩国的 NYHA 分级获得医疗资源使用比例。成本效益表示为每获得一个质量调整生命年(QALY)的增量成本(美元)。
在基础分析中,与安慰剂相比,铁羧基麦芽糖的增量成本效益比(ICER)为每获得一个 QALY 增加 22,192 美元(₩25,010,451)。敏感性分析显示结果稳健,铁羧基麦芽糖的 ICER 范围为每获得一个 QALY 增加 5,156 美元至 29,796 美元。在方案 2 分析中,ICER 降至每获得一个 QALY 增加 12,598 美元(₩14,198,501)。
与安慰剂相比,CHF 伴 IDA 患者用铁羧基麦芽糖进行铁补充是具有成本效益的。