Satsuma Yukari, Ikesue Hiroaki, Kusuda Kaori, Maeda Mami, Muroi Nobuyuki, Mori Ryobu, Kogo Mariko, Hirabayashi Ryosuke, Nagata Kazuma, Nakagawa Atsushi, Tachikawa Ryo, Tomii Keisuke, Hashida Tohru
Department of Pharmacy, Kobe City Medical Center General Hospital, Kobe, Japan.
Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
Front Pharmacol. 2020 Nov 26;11:529654. doi: 10.3389/fphar.2020.529654. eCollection 2020.
Pirfenidone is an anti-fibrotic agent used to treat patients with idiopathic pulmonary fibrosis (IPF). Managing adverse drug events and ensuring compliance with pirfenidone treatment for a prolonged period are important to reduce the rate of disease progression. To maximize the benefits of pirfenidone treatment, we established and evaluated an ambulatory care pharmacy practice, a model of pharmacist-physician collaborative management, for patients receiving pirfenidone. We conducted a retrospective chart review of 76 consecutive patients treated with pirfenidone in the Kobe City Medical Center General Hospital, Japan, between January 2012 and January 2019. The first group (61 patients) received pirfenidone treatment as conventional management, whereas the second group (15 patients) started pirfenidone based on collaborative pharmacist-physician management. The drug discontinuation rate and time to drug discontinuation were compared between the groups. To analyze factors associated with pirfenidone discontinuation, we used a multivariate Cox regression analysis to evaluate the baseline characteristics of patients, including those receiving the collaborative management. Clinical outcomes were compared using a propensity score matched analysis. In the collaborative management group, pharmacists made 56 suggestions, including suggestions for supportive care (51 suggestions), to the physicians. Among these suggestions, 52 were accepted by the physicians. The discontinuation rates at 3 [6.7% (1/15) vs. 26.2% (16/61)] and 6 [9.1% (1/11) vs. 36.1% (22/61)] months were lower in the collaborative management group than in the conventional management group. Multivariate analysis revealed that collaborative management [hazard ratio (HR) 0.34, 95% CI 0.08-0.96, = 0.041] and predicted baseline forced vital capacity <60% (HR 2.13, 95% CI 1.17-3.85, = 0.015) were significantly associated with pirfenidone discontinuation. The time to drug discontinuation was also significantly longer in the collaborative management group than in the conventional management group ( = 0.034, log-rank test). Propensity score matched analysis confirmed a significant correlation between collaborative management and drug discontinuation time (HR 0.20, 95% CI 0.03-0.84, = 0.027). We established an ambulatory care pharmacy practice for out-patients with IPF receiving pirfenidone. The results suggest that collaborative management may help prevent pirfenidone discontinuation compared with conventional management.
吡非尼酮是一种用于治疗特发性肺纤维化(IPF)患者的抗纤维化药物。管理药物不良事件并确保患者长期坚持吡非尼酮治疗对于降低疾病进展速率至关重要。为了使吡非尼酮治疗的益处最大化,我们为接受吡非尼酮治疗的患者建立并评估了一种门诊护理药房实践模式,即药师 - 医师协作管理模式。我们对2012年1月至2019年1月期间在日本神户市立医疗中心总医院连续接受吡非尼酮治疗的76例患者进行了回顾性病历审查。第一组(61例患者)接受吡非尼酮常规治疗管理,而第二组(15例患者)基于药师 - 医师协作管理开始使用吡非尼酮。比较两组之间的停药率和停药时间。为了分析与吡非尼酮停药相关的因素,我们使用多变量Cox回归分析来评估患者的基线特征,包括接受协作管理的患者。使用倾向得分匹配分析比较临床结局。在协作管理组中,药师向医师提出了56条建议,包括支持性护理建议(51条建议)。其中,52条建议被医师接受。协作管理组在3个月[6.7%(1/15)对26.2%(16/61)]和6个月[9.1%(1/11)对36.1%(22/61)]时的停药率低于常规管理组。多变量分析显示,协作管理[风险比(HR)0.34,95%置信区间0.08 - 0.96,P = 0.041]和预测基线用力肺活量<60%(HR 2.13,95%置信区间1.17 - 3.85,P = 0.015)与吡非尼酮停药显著相关。协作管理组的停药时间也显著长于常规管理组(P = 0.034,对数秩检验)。倾向得分匹配分析证实协作管理与停药时间之间存在显著相关性(HR 0.20,95%置信区间0.03 - 0.84,P = 0.027)。我们为接受吡非尼酮治疗的IPF门诊患者建立了门诊护理药房实践模式。结果表明,与常规管理相比,协作管理可能有助于预防吡非尼酮停药。