Cai Qian, Batista Alberto E, Börsum Jakob, Zhang Qiaoyi, Isheden Gabriel, Kunovszki Peter, Gandhi Kavita, Heerlein Kristin, Brauner Susanna
Janssen Global Services, Titusville, New Jersey, USA.
SDS Life Science AB, Uppsala, Sweden.
Neuroepidemiology. 2024;58(6):460-469. doi: 10.1159/000538640. Epub 2024 Apr 23.
Healthcare costs and societal impact of myasthenia gravis (MG), a potentially life-threatening rare, chronic neuromuscular disease, are sparsely studied. We assessed healthcare resource utilization (HCRU) and associated costs among patients with newly diagnosed (ND) and preexisting (PE) MG in Sweden.
This observational, retrospective cohort study used data from four linkable Swedish nationwide population-based registries. Adult MG patients receiving pharmacological treatment for MG and having ≥24-month follow-up during the period January 1, 2010, to December 31, 2017, were included.
A total of 1,275 patients were included in the analysis, of which 554 patients were categorized into the ND MG group and 721 into the PE MG group. Mean (±SD) age was 61.3 (±17.4) years, and 52.3% were female. In the first year post-diagnosis, ND patients had significantly higher utilization of acetylcholinesterase inhibitors (96.0% vs. 83.9%), corticosteroids (59.6% vs. 45.8%), thymectomy (12.1% vs. 0.7%), and plasma exchange (3.8% vs. 0.6%); had higher all-cause (70.9% vs. 35.8%) and MG-related (62.5% vs. 18.4%) hospitalization rates with 11 more hospitalization days (all p < 0.01) and an increased risk of hospitalization (odds ratio [95% CI] = 4.4 [3.43, 5.64]) than PE MG. In year 1 post-diagnosis, ND MG patients incurred EUR 7,302 (p < 0.01) higher total all-cause costs than PE MG, of which 84% were estimated to be MG-related and the majority (86%) were related to inpatient care. These results remained significant also after controlling for baseline demographics and comorbidities (p < 0.01). In year 2 post-diagnosis, the all-cause medical costs decreased by ∼55% for ND MG from year 1 and were comparable with PE MG.
In this population-based study, MG patients required significantly more healthcare resources in year 1 post-diagnosis than PE MG primarily due to more pharmacological treatments, thymectomies, and associated hospitalizations. These findings highlight the need to better understand potential factors including disease characteristics associated with increased health resource use and costs and need for more efficacious treatments early in the disease course.
重症肌无力(MG)是一种潜在危及生命的罕见慢性神经肌肉疾病,对其医疗成本和社会影响的研究较少。我们评估了瑞典新诊断(ND)和既往已确诊(PE)MG患者的医疗资源利用(HCRU)及相关成本。
这项观察性回顾性队列研究使用了来自瑞典四个可关联的全国性人群登记处的数据。纳入了在2010年1月1日至2017年12月31日期间接受MG药物治疗且随访时间≥24个月的成年MG患者。
共有1275例患者纳入分析,其中554例患者被归类为ND MG组,721例为PE MG组。平均(±标准差)年龄为61.3(±17.4)岁,52.3%为女性。在诊断后的第一年,ND患者乙酰胆碱酯酶抑制剂的使用率显著更高(96.0%对83.9%)、皮质类固醇(59.6%对45.8%)、胸腺切除术(12.1%对0.7%)和血浆置换(3.8%对0.6%);全因住院率(70.9%对35.8%)和MG相关住院率(62.5%对18.4%)更高,住院天数多11天(所有p<0.01),住院风险增加(比值比[95%置信区间]=4.4[3.43,5.64]),高于PE MG。在诊断后的第1年,ND MG患者的全因总成本比PE MG高7302欧元(p<0.01),其中84%估计与MG相关且大部分(86%)与住院治疗有关。在控制了基线人口统计学和合并症后,这些结果仍然显著(p<0.01)。在诊断后的第2年,ND MG的全因医疗成本比第1年下降了约55%,与PE MG相当。
在这项基于人群的研究中,MG患者在诊断后的第1年比PE MG需要显著更多的医疗资源,主要是由于更多的药物治疗、胸腺切除术和相关住院治疗。这些发现凸显了需要更好地了解包括与健康资源使用和成本增加相关的疾病特征等潜在因素,以及在疾病进程早期对更有效治疗的需求。