University of Louisville, Louisville, Kentucky, USA.
Symmetron Ltd, London, UK.
Open Heart. 2021 Feb;8(1). doi: 10.1136/openhrt-2020-001263.
Early use of insertable cardiac monitor (ICM) is recommended for patients with unexplained syncope following initial clinical workup, due to its superior ability to establish symptom-rhythm correlation compared with conventional testing (CONV). However, ICMs incur higher upfront costs, and the impact of additional diagnoses and resulting treatment on downstream costs and outcomes is unclear. We aimed to evaluate the cost-effectiveness of ICM compared with CONV for the diagnosis of arrhythmia in patients with unexplained syncope, from a US payer perspective.
A Markov model was developed to estimate lifetime costs and benefits of arrhythmia diagnosis with ICM versus CONV, considering all related diagnostic and arrhythmia-related treatment costs and consequences. Cohort characteristics and costs were informed by original claims database analyses. Risks of mortality, syncopal recurrence, injury due to syncope and quality of life consequences from syncopal events were identified from the literature.
ICM was less costly and more effective than CONV. Most of the observed US$4532 cost savings were attributed to reduced downstream diagnostic testing. For every 1000 patients, ICM was projected to yield an additional 253 arrhythmia diagnoses and lead to treatment in an additional 168 patients. The ICM strategy resulted in overall improved outcomes (0.30 quality-adjusted life years gained), due to a reduction in syncope recurrence and injury resulting from arrhythmia treatment. The results were robust to changes in the base case parameters but sensitive to the model time horizon, underlying probability of syncope recurrence and prevalence of arrhythmias.
Our model projected that early ICM for the diagnosis of unexplained syncope reduced long-term costs, and led to an improvement in overall clinical outcomes by shortening time to arrhythmia treatment. The cost of ICM was outweighed by savings arising from fewer downstream diagnostic episodes, and the increased cost of treatment was counterbalanced by fewer syncope-related event costs.
对于初始临床检查后不明原因晕厥的患者,建议早期使用可植入式心脏监测仪(ICM),因为与常规检查(CONV)相比,它能更好地建立症状与节律的相关性。然而,ICM 的前期成本更高,并且额外诊断和由此产生的治疗对下游成本和结果的影响尚不清楚。我们旨在从美国支付者的角度评估 ICM 与 CONV 相比在诊断不明原因晕厥患者心律失常方面的成本效益。
我们开发了一个马尔可夫模型,以评估 ICM 与 CONV 诊断心律失常的终生成本和效益,同时考虑了所有相关的诊断和心律失常治疗成本和后果。队列特征和成本来自原始索赔数据库分析。死亡率、晕厥复发、晕厥相关伤害以及晕厥事件对生活质量的影响风险来自文献。
ICM 比 CONV 更具成本效益。观察到的 4532 美元成本节约大部分归因于下游诊断测试减少。在 1000 名患者中,ICM 预计将额外诊断出 253 例心律失常,并额外治疗 168 例患者。由于心律失常治疗后晕厥复发和损伤减少,ICM 策略导致整体结局改善(增加 0.30 个质量调整生命年)。结果对基础病例参数的变化具有稳健性,但对模型时间范围、潜在晕厥复发概率和心律失常患病率敏感。
我们的模型预测,早期 ICM 用于诊断不明原因晕厥可降低长期成本,并通过缩短心律失常治疗时间改善整体临床结局。ICM 的成本被较少的下游诊断发作节省所抵消,而治疗成本的增加被减少的晕厥相关事件成本所平衡。