Matsugi Emi, Takashima Shigeki, Doteguchi Shuhei, Kobayashi Tomomi, Okayasu Motohiro
Medical Affairs, Mallinckrodt Pharmaceuticals, 1-12-32 Akasaka, Minato-ku, Tokyo, 107-6030, Japan.
Pharmacovigilance, Mallinckrodt Pharmaceuticals, Tokyo, Japan.
Gen Thorac Cardiovasc Surg. 2024 May;72(5):311-323. doi: 10.1007/s11748-023-01971-2. Epub 2023 Sep 15.
To evaluate the real-world safety and effectiveness of inhaled nitric oxide (INOflo for Inhalation 800 ppm) for perioperative pulmonary hypertension associated with cardiac surgery in Japan.
This was a prospective, non-interventional, all-case, post-marketing study of pediatric and adult patients who received perioperative INOflo with cardiac surgery from November 2015-December 2020. Safety and effectiveness were monitored from INOflo initiation to 48 h after treatment completion or withdrawal. Safety outcomes included adverse drug reactions, blood methemoglobin concentrations, and inspired nitrogen dioxide concentrations over time. Effectiveness outcomes included changes in central venous pressure among pediatrics, mean pulmonary arterial pressure among adults, and the partial pressure of arterial oxygen/fraction of inspired oxygen ratio (PaO/FiO) in both populations.
The safety analysis population included 2,817 Japanese patients registered from 253 clinical sites (pediatrics, n = 1375; adults, n = 1442). INOflo was generally well tolerated; 15 and 20 adverse drug reactions were reported in 14 pediatrics (1.0%) and 18 adults (1.2%), respectively. No clinically significant elevations in blood methemoglobin and inspired nitrogen dioxide concentrations were observed. INOflo treatment was associated with significant reductions in both central venous pressure among pediatrics and mean pulmonary arterial pressure among adults, and significant improvements in PaO/FiO among pediatrics and adults with PaO/FiO ≤ 200 at baseline.
Perioperative INOflo treatment was a safe and effective strategy to improve hemodynamics and oxygenation in patients with pulmonary hypertension during cardiac surgery. These data support the use of INOflo for this indication in Japanese clinical practice.
评估吸入一氧化氮(吸入用一氧化氮800 ppm)在日本用于心脏手术围手术期肺动脉高压的真实世界安全性和有效性。
这是一项前瞻性、非干预性、全病例、上市后研究,研究对象为2015年11月至2020年12月接受心脏手术围手术期吸入用一氧化氮的儿科和成年患者。从开始使用吸入用一氧化氮至治疗结束或停药后48小时监测安全性和有效性。安全性指标包括药物不良反应、血液中高铁血红蛋白浓度以及随时间变化的吸入二氧化氮浓度。有效性指标包括儿科患者中心静脉压的变化、成年患者平均肺动脉压的变化以及两组患者动脉血氧分压/吸入氧分数比(PaO/FiO)的变化。
安全性分析人群包括来自253个临床地点登记的2817例日本患者(儿科,n = 1375;成年,n = 1442)。吸入用一氧化氮总体耐受性良好;分别有14例儿科患者(1.0%)和18例成年患者(1.2%)报告了15例和20例药物不良反应。未观察到血液中高铁血红蛋白和吸入二氧化氮浓度出现具有临床意义的升高。吸入用一氧化氮治疗与儿科患者中心静脉压和成年患者平均肺动脉压的显著降低相关,并且使基线时PaO/FiO≤200的儿科和成年患者的PaO/FiO有显著改善。
围手术期吸入用一氧化氮治疗是改善心脏手术期间肺动脉高压患者血流动力学和氧合的安全有效策略。这些数据支持在日本临床实践中使用吸入用一氧化氮治疗这一适应症。