Dipartimento Universitario di Promozione Della Salute, Materno Infantile, Medicina Interna e Specialistica di Eccellenza "G. D'Alessandro" (PROMISE), Division of Respiratory Medicine, "Paolo Giaccone" University Hospital, University of Palermo; Palermo; Italy.
Dipartimento Universitario di Promozione Della Salute, Materno Infantile, Medicina Interna e Specialistica di Eccellenza "G. D'Alessandro" (PROMISE), Division of Respiratory Medicine, "Paolo Giaccone" University Hospital, University of Palermo; Palermo; Italy.
Pulm Pharmacol Ther. 2021 Aug;69:102038. doi: 10.1016/j.pupt.2021.102038. Epub 2021 Jun 24.
The SARS-CoV-2 pandemic has changed the health-care systems around the world in a remarkable way. We describe the strategies adopted to cope with the limitations imposed by the pandemic to the access to health care by patients diagnosed with idiopathic Pulmonary Fibrosis (IPF).
We conducted a retrospective observational analysis including IPF patients under antifibrotic drugs (nintedanib and pirfenidone) that accessed to the Outpatient clinic of the University of Palermo, Italy. Patients received a phone number and an email address in case of any urgency and a virtual meeting was settled up monthly.
40 patients (M/F: 30/10) were followed up, 33 under nintedanib treatment, 7 under pirfenidone. Among patients under nintedanib, 1 patient reported high fever (T max 39 °C) and purulent sputum with no sign of infections, 1 had hemoptysis that was spontaneously resolved. 2 patients accessed to the emergency department for the worsening of dyspnea; 5 patients had diarrhea that resolved with symptomatic drugs in few days. 3 patients had an increase of alkaline phosphatase levels, leading to the withdrawal of the antifibrotic drug for 15 days, and subsequent normalization of the plasmatic levels. Among patients under pirfenidone, one subject had an increase of ferritin serum levels with no symptoms. The remaining subjects were in stable clinical conditions. None of the patients reported hospitalization or exacerbations, and did not experience antifibrotic withdrawal.
We were able to demonstrate that by implementing alternative ways to monitor the disease, patients did not incur in increased rates of acute exacerbations or higher frequency of side effects and antifibrotic treatment withdrawal.
SARS-CoV-2 大流行以显著的方式改变了全球的医疗体系。我们描述了为应对大流行对特发性肺纤维化 (IPF) 患者获得医疗保健的限制而采用的策略。
我们进行了一项回顾性观察分析,纳入了在意大利巴勒莫大学接受抗纤维化药物(尼达尼布和吡非尼酮)治疗的 IPF 患者。患者获得了一个电话号码和电子邮件地址,以备有任何紧急情况,并每月安排一次虚拟会议。
共随访了 40 名患者(男/女:30/10),其中 33 名患者接受尼达尼布治疗,7 名患者接受吡非尼酮治疗。在接受尼达尼布治疗的患者中,1 名患者报告高热(T max 39°C)和脓性痰,无感染迹象,1 名患者出现咯血,自行缓解。2 名患者因呼吸困难加重而就诊于急诊部;5 名患者出现腹泻,数天内用对症药物缓解。3 名患者碱性磷酸酶水平升高,导致抗纤维化药物停药 15 天,随后血浆水平恢复正常。在接受吡非尼酮治疗的患者中,1 名患者血清铁蛋白水平升高,但无症状。其余患者临床状况稳定。没有患者报告住院或恶化,也没有经历抗纤维化药物停药。
我们能够证明,通过实施替代监测疾病的方法,患者没有增加急性加重的发生率或更高的副作用和抗纤维化药物停药频率。