O'Byrne Michael L, Faerber Jennifer A, Katcoff Hannah, Frank David B, Davidson Alex, Giglia Therese M, Avitabile Catherine M
Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Pulm Circ. 2020 Oct 27;10(3):2045894020933083. doi: 10.1177/2045894020933083. eCollection 2020 Jul-Sep.
Despite progress in pharmacotherapy in pediatric pulmonary hypertension, real-world patterns of directed pulmonary hypertension therapy have not been studied in the current era. A retrospective observational study of children (≤18 years) with pulmonary hypertension was performed using data from the MarketScan® Commercial and Medicaid claims databases. Associations between etiology of pulmonary hypertension and pharmaceutical regimen were evaluated, as were the associations between subject social and geographic characteristics (insurance-type, race, and/or census region) and regimen. Annualized costs of single- and multi-class regimens were calculated. In total, 873 subjects were studied, of which 94% received phosphodiesterase-5 inhibitors, 31% endothelin receptor antagonist, 9% prostacyclin analogs, and 7% calcium channel blockers. Monotherapy was used in 72% of subjects. Phosphodiesterase-5 inhibitors monotherapy was the most common regimen (93%). Subjects with idiopathic pulmonary hypertension, congenital heart disease, and unclassified pulmonary hypertension receive more than one agent and were more likely to receive both endothelin receptor antagonist and prostacyclin analogs than other forms of pulmonary hypertension. Compared to recipients of public insurance, subjects with commercial insurance were more likely to receive more intense therapy ( = 0.003), which was confirmed in multivariable analysis (OR: 1.4, = 0.03). Receipt of commercial insurance was also associated with increased annual costs across all subjects ( < 0.001) and for the most common specific regimens. The majority of children with pulmonary hypertension receive phosphodiesterase monotherapy, followed by phosphodiesterase-endothelin receptor antagonist two drug regimens, and finally the addition of prostacyclin analogs for three-drug therapy. However, even after adjustment for measurable confounders, commercial insurance was associated with higher intensity care and higher costs (even within specific classes of pulmonary vasodilators). The effect of these associations on clinical outcome cannot be discerned from the current data set, but patterns of treatment deserve further attention.
尽管小儿肺动脉高压的药物治疗取得了进展,但当前时代尚未对定向肺动脉高压治疗的实际模式进行研究。利用MarketScan®商业和医疗补助索赔数据库中的数据,对患有肺动脉高压的儿童(≤18岁)进行了一项回顾性观察研究。评估了肺动脉高压病因与药物治疗方案之间的关联,以及受试者的社会和地理特征(保险类型、种族和/或人口普查区域)与治疗方案之间的关联。计算了单类和多类治疗方案的年化成本。总共研究了873名受试者,其中94%接受磷酸二酯酶-5抑制剂治疗,31%接受内皮素受体拮抗剂治疗,9%接受前列环素类似物治疗,7%接受钙通道阻滞剂治疗。72%的受试者采用单药治疗。磷酸二酯酶-5抑制剂单药治疗是最常见的治疗方案(93%)。特发性肺动脉高压、先天性心脏病和未分类肺动脉高压的受试者接受不止一种药物治疗,并且比其他形式的肺动脉高压更有可能同时接受内皮素受体拮抗剂和前列环素类似物治疗。与接受公共保险的受试者相比,拥有商业保险的受试者更有可能接受更强化的治疗(P = 0.003),这在多变量分析中得到了证实(OR:1.4,P = 0.03)。拥有商业保险还与所有受试者(P < 0.001)以及最常见的特定治疗方案的年度成本增加相关。大多数患有肺动脉高压的儿童接受磷酸二酯酶单药治疗,其次是磷酸二酯酶-内皮素受体拮抗剂两药治疗方案,最后是添加前列环素类似物进行三药治疗。然而,即使在对可测量的混杂因素进行调整之后,商业保险仍与更高强度的治疗和更高的成本相关(即使在特定类别的肺血管扩张剂中)。从当前数据集中无法看出这些关联对临床结局的影响,但治疗模式值得进一步关注。