41例特发性肺纤维化患者的抗纤维治疗经验

IF 0.1 Q4 RESPIRATORY SYSTEM Eurasian Journal of Pulmonology Pub Date : 2020-09-01 DOI:10.4103/ejop.ejop_102_19
Berna Akıncı Özyürek, D. Yenibertiz, A. G. Kaya, Sertaç Büyükyaylacı Özden, Y. Erdoğan
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引用次数: 0

摘要

引言:近年来用于治疗特发性肺纤维化(IPF)的抗纤维化药物(吡非尼酮和宁替达尼)可以减缓肺功能测试的恶化和疾病的进展,还可以降低急性加重和住院的频率。在这项研究中,我们旨在评估自2013年以来我们在临床上使用的抗纤维化治疗的结果。材料和方法:本研究纳入了2013年8月1日至2019年2月1日在我院第八诊所诊断为IPF的41名患者。患者的信息是从患者档案中获得的。采用描述性统计方法、Kolmogorov–Smirnov检验和Wilcoxon检验对数据进行分析。结果:38例患者为男性,3例为女性。平均年龄65.6±7.0岁。34例患者经临床和放射学诊断,7例经病理学诊断。抗纤维化药物最长使用时间为5.5年的2例,最短使用时间为6个月的2例。根据上次就诊的数据,34名患者使用吡非尼酮,7名患者使用宁替达尼。基线6分钟步行测试结果与第6个月、第1年、第2年、第3年和第4年的结果之间没有显著差异。与基线(基线:63%,第6个月:57%,第1年:43%)相比,第6月和第1年的肺部一氧化碳(DLCO)扩散能力显著降低(P 0.05)在文献中,我们发现抗纤维化药物可以减缓疾病的进展,降低病情恶化的风险,并且与以前的治疗相比,在副作用方面更容易耐受。
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Antifibrotic treatment in patients with idiopathic pulmonary fibrosis: Our experience in 41 cases
INTRODUCTION: It has been shown that antifibrotic agents (pirfenidone and nintedanib), used in the treatment of idiopathic pulmonary fibrosis (IPF) in recent years, decelerate the worsening of pulmonary function tests and the progression of the disease and also reduce the frequency of acute exacerbations and hospitalizations. In this study, we aimed to evaluate the results of antifibrotic treatment that we have been using since 2013 in our clinic. MATERIALS AND METHODS: Forty-one patients diagnosed as IPF between August 1, 2013, and February 1, 2019, in the eighth clinic of our hospital were included in this study. The information of the patients was obtained from the patient files. Data were analyzed by descriptive statistical methods, Kolmogorov–Smirnov test, and Wilcoxon test. RESULTS: Thirty-eight patients were male and three patients were female. The mean age was 65.6 ± 7.0 years. The diagnosis of 34 patients was made clinically and radiologically, and 7 patients were diagnosed pathologically. The longest usage time of antifibrotic drugs was 5.5 years in 2 patients, and the minimum usage time was 6 months in 2 patients. Thirty-four patients were using pirfenidone and seven patients were using nintedanib according to the data of their last visit. There was no significant difference between the baseline 6-min walk test results and the 6th-month, 1st-year, 2nd-year, 3rd-year, and 4th-year results. A significant decrease was determined in diffusing capacity of the lungs for carbon monoxide (DLCO) test results of the 6th month and 1st year compared to baseline (baseline: 63%, 6th month: 57%, and 1st year: 43%) (P 0.05). A significant decrease was determined in forced vital capacity (FVC) results of the 2nd year compared to baseline (68% and 59%, respectively) (P 0.05). CONCLUSION: Similar to the literature, we have experienced that antifibrotic drugs decelerate the progression of the disease, reduce the risk of developing exacerbations, and are more tolerable in terms of side effect profile compared to the previous treatments.
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来源期刊
Eurasian Journal of Pulmonology
Eurasian Journal of Pulmonology RESPIRATORY SYSTEM-
自引率
0.00%
发文量
9
审稿时长
16 weeks
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