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Acute exacerbation of idiopathic pulmonary fibrosis: outcome and prognostic factors.

机译:特发性肺纤维化急性加重:预后和预后因素。

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Background: Acute exacerbation is a substantial cause of death in patients with idiopathic pulmonary fibrosis with poorly described prognostic factors. Objectives: To review the features associated with acute exacerbation of idiopathic pulmonary fibrosis and assess its prognostic factors. Methods: Thirty-seven occurrences of acute exacerbation of idiopathic pulmonary fibrosis were retrospectively reviewed in the medical records of 27 patients. Clinical presentation, radiographic studies, pulmonary function tests, laboratory data, treatment, and outcome were analyzed. Results: Acute exacerbation of idiopathic pulmonary fibrosis occurred more frequently between December and May (75.7%) than between June and November (24.3%) (p = 0.01). In-hospital mortality was 27% and median survival was 4.2 months (range 0.2-36.6). Significant differences between nonsurvivors and survivors included the time elapsed between their admission and the initiation of treatment for acute exacerbation (6 vs. 3.1 days, p = 0.04), lactate dehydrogenase levels at admission (801 vs. 544.6 IU/l, p = 0.002), impairment of the prior forced vital capacity (51.2 vs. 65%, p = 0.01) and diffusing capacity for carbon monoxide (21.7 vs. 34%, p = 0.01). Furthermore, the evolution of gas exchange in the first 10 days after the initiation of treatment was associated with in-hospital and long-term mortality. Conclusions: Acute exacerbations of idiopathic pulmonary fibrosis are more frequent during winter and spring. The time between admission and initiation of treatment is a new reported prognostic factor that should be investigated further. This finding highlights the need for a fast diagnostic approach that should probably be standardized. Early gas exchange modifications reflect the response to treatment and predict the prognosis.
机译:背景:急性加重是特发性肺纤维化患者的主要死因,其预后因素较差。目的:回顾与特发性肺纤维化急性加重相关的特征,并评估其预后因素。方法:回顾性分析27例患者中37例特发性肺纤维化急性加重病情。分析了临床表现,影像学检查,肺功能检查,实验室数据,治疗和结果。结果:特发性肺纤维化的急性加重在12月至5月之间(75.7%)比6月至11月之间(24.3%)的发生率更高(p = 0.01)。住院死亡率为27%,中位生存期为4.2个月(范围0.2-36.6)。非幸存者与幸存者之间的显着差异包括入院与开始急性加重治疗之间的时间间隔(6天对3.1天,p = 0.04),入院时乳酸脱氢酶水平(801对544.6 IU / l,p = 0.002) ),先前的强制肺活量受损(51.2对65%,p = 0.01)和一氧化碳扩散能力(21.7对34%,p = 0.01)。此外,开始治疗后的头10天发生气体交换与医院内和长期死亡率有关。结论:特发性肺纤维化急性加重在冬季和春季。入院与开始治疗之间的时间是新报告的预后因素,应进一步研究。这一发现强调了对可能应该标准化的快速诊断方法的需求。早期气体交换的修改反映了对治疗的反应并预测了预后。

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