特发性肺纤维化治疗和随访的真实数据:单中心研究。

IF 0.7 Q4 RESPIRATORY SYSTEM Tuberkuloz ve Toraks-Tuberculosis and Thorax Pub Date : 2023-12-01 DOI:10.5578/tt.20239603
Fatih Üzer, Sena Akanlar, Aykut Çilli
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引用次数: 0

摘要

导言本研究旨在评估单中心特发性肺纤维化(IPF)患者的实际治疗和随访数据:研究对象包括 2014 年 1 月 1 日至 2022 年 12 月 31 日期间在阿克登尼兹大学接受随访的被诊断为 IPF 的连续患者。患者信息来自医院自动化系统:研究共纳入 227 名患者,平均年龄为 72.0 ± 8.2 岁。167名患者(73.6%)接受了吡非尼酮治疗,60名患者(26.4%)接受了宁替尼治疗。79.3%的病例(180 例)通过放射学检查结果确诊为 IPF。抗纤维化治疗的平均持续时间为 26.3 ± 19.9 个月。49.8%的患者在治疗过程中入院,其中因呼吸系统原因入院的占大多数(33.6%)。26.6%的患者在治疗期间发现病情恶化。126名患者(55.5%)至少出现了一种副作用,其中大部分为轻度至中度副作用(79人,34.8%)。在接受抗纤维化治疗的患者中,21.6%的患者出现了疾病进展。22.9%的患者需要减少剂量,平均减量时间为29个月。24.2%的患者改用其他药物进行抗纤维化治疗。两组患者的基线用力肺活量(FVC)水平差异无统计学意义(P= 0.314),而宁替尼组患者的一氧化碳肺弥散容量(DLCO)水平更高(P= 0.024),六分钟步行距离更短(P= 0.049):本研究对我院随访的 IPF 患者进行了评估,观察到大多数患者为老年男性,经常因呼吸系统原因住院,两种抗纤维化药物的耐受性良好,副作用相似。
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Real-life data in the treatment and follow-up of idiopathic pulmonary fibrosis: A single-center study.

Introduction: The aim of this study was to evaluate the real-life treatment and follow-up data of patients with idiopathic pulmonary fibrosis (IPF) in a singlecenter setting.

Materials and methods: The study included consecutive patients diagnosed with IPF who were followed up at the Akdeniz University, between January 1, 2014 and December 31, 2022. Patient information was obtained from the hospital automation system.

Result: A total of 227 patients with a mean age of 72.0 ± 8.2 years were included in the study. One hundred sixty-seven patients (73.6%) received pirfenidone while 60 patients (26.4%) received nintedanib treatment. Radiological findings were used to diagnose IPF in 79.3% (n= 180) of cases. Mean duration of antifibrotic treatment was 26.3 ± 19.9 months. Of the patients, 49.8% experienced hospital admissions during the treatment course, with respiratory reasons accounting for a majority of these admissions (33.6%). Disease exacerbation was detected in 26.6% of the patients during the treatment period. At least one side effect was observed in 126 patients (55.5%), with a significant portion of these side effects being mild to moderate (n= 79, 34.8%). Disease progression was observed in 21.6% of the patients under antifibrotic treatment. Dose reduction was necessary in 22.9% of the patients, with an average duration of dose reduction of 29 months. Antifibrotic treatment was switched to another medication in 24.2% of the patients. There were no statistically significant differences in baseline forced vital capacity (FVC) levels between the two groups (p= 0.314) while the diffusing capacity of the lungs for carbon monoxide (DLCO) level was higher in the nintedanib group (p= 0.024), and the six-minute walk distance was shorter (p= 0.049).

Conclusions: In this study evaluating patients with IPF under follow-up in our hospital, it was observed that the majority of patients consisted of elderly male individuals, frequent hospitalizations were due to respiratory reasons, and both antifibrotic medications were well tolerated with a similar side effect profile.

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