Rodríguez González-Moro Jose Miguel, Menéndez Rosario, Campins Magda, Lwoff Nadia, Oyagüez Itziar, Echave María, Rejas Javier, Antoñanzas Fernando
Department of Pneumology, Hospital Universitario Gregorio Marañón, Madrid, Spain.
Department of Pneumology, Hospital Universitario La Fe, Valencia, Spain.
Clin Drug Investig. 2016 Jan;36(1):41-53. doi: 10.1007/s40261-015-0345-z.
Patients with chronic obstructive pulmonary disease (COPD) are at elevated risk of pneumococcal infection. A 13-valent pneumococcal conjugate vaccine (PCV13) was approved for protection against invasive disease and pneumonia caused by Streptococcus pneumoniae in adults. This study estimated the incremental cost-effectiveness ratio (ICER) of vaccinating COPD patients ≥50 years old with PCV13 compared with current vaccination policy (CVP) with 23-valent pneumococcal polysaccharide vaccine.
A Markov model accounting for the risks and costs for all-cause non-bacteremic pneumonia (NBP) and invasive pneumococcal disease (IPD) was developed. All parameters, such as disease incidence and costs (€; 2015 values), were based on published data. The perspective of the analysis was that of the Spanish National Healthcare System, and the horizon of evaluation was lifetime in the base case. Vaccine effectiveness considered waning effect over time. Outcomes and costs were both discounted by 3% annually.
Over a lifetime horizon and for a 629,747 COPD total population, PCV13 would prevent 2224 cases of inpatient NBP, 3134 cases of outpatient NBP, and 210 IPD extra cases in comparison with CVP. Additionally, 398 related deaths would be averted. The ICER was €1518 per quality-adjusted life-year (QALY) gained for PCV13 versus CVP. PCV13 was found to be cost effective versus CVP from a 5-year modelling horizon (1302 inpatient NBP and 1835 outpatient NBP cases together with 182 deaths would be prevented [ICER €25,573/QALY]). Univariate and probabilistic sensitivity analyses confirmed the robustness of the model.
At the commonly accepted willingness-to-pay threshold of €30,000/QALY gained, PCV13 vaccination in COPD patients aged ≥50 years was a cost-effective strategy compared with CVP from 5 years to lifetime horizon in Spain.
慢性阻塞性肺疾病(COPD)患者发生肺炎球菌感染的风险较高。13价肺炎球菌结合疫苗(PCV13)已被批准用于预防成人由肺炎链球菌引起的侵袭性疾病和肺炎。本研究估计了与使用23价肺炎球菌多糖疫苗的现行疫苗接种政策(CVP)相比,为≥50岁的COPD患者接种PCV13的增量成本效益比(ICER)。
建立了一个马尔可夫模型,该模型考虑了全因非菌血症性肺炎(NBP)和侵袭性肺炎球菌疾病(IPD)的风险和成本。所有参数,如疾病发病率和成本(欧元;2015年数值),均基于已发表的数据。分析的视角是西班牙国家医疗保健系统,基础病例的评估期限为终身。疫苗效力考虑了随时间推移的衰减效应。结果和成本均按每年3%进行贴现。
在终身期限内,对于629,747名COPD患者的总体人群,与CVP相比,PCV13可预防2224例住院NBP、3134例门诊NBP和210例额外的IPD病例。此外,可避免398例相关死亡。PCV13与CVP相比,每获得一个质量调整生命年(QALY)的ICER为1518欧元。从5年的建模期限来看,发现PCV13相对于CVP具有成本效益(可预防1302例住院NBP和1835例门诊NBP病例以及182例死亡[ICER 25,573欧元/QALY])。单因素和概率敏感性分析证实了模型的稳健性。
在普遍接受的每获得一个QALY支付意愿阈值为30,000欧元的情况下,在西班牙,对于≥50岁的COPD患者,与CVP相比,接种PCV13从5年到终身期限都是一种具有成本效益的策略。