Published online Aug 6, 2024. doi: 10.12998/wjcc.v12.i22.4913
Revised: May 10, 2024
Accepted: June 7, 2024
Published online: August 6, 2024
Processing time: 120 Days and 16.1 Hours
Idiopathic pulmonary fibrosis (IPF) is classified under fibrotic interstitial pneu
To assess the effects of pirfenidone in the early treatment of IPF on lung function in patients.
A retrospective analysis was performed on 113 patients with IPF who were trea
The observation group exhibited significantly higher rates than the control group after therapy, with a clear distinction (P < 0.05). After treatment, the observation group experienced significantly fewer adverse reactions than the control group, with a noticeable difference (P < 0.05). When analyzing the symptom severity scores between the two groups of patients after treatment, the observation group had significantly lower scores than the control group, with a distinct difference (P < 0.05). When comparing the pulmonary function index levels between the two groups of patients after therapy, the observation group displayed significantly higher levels than the control group, with a noticeable difference (P < 0.05). Evaluating the inflammatory marker data (C-reactive protein, interleukin-2 [IL-2], and IL-8) between the two groups of patients after therapy, the observation group exhibited significantly lower levels than the control group, with significant disparities (P < 0.05). Comparison of the 6-min walking distance data between the two groups of patients after treatment showed that the observation group achieved significantly greater distances than the control group, with a marked difference (P < 0.05).
Prompt initiation of pirfenidone treatment in individuals diagnosed with IPF can enhance pulmonary function, elevate inflammatory factor levels, and increase the distance covered in the 6-min walk test. This intervention is conducive to effectively decreasing the occurrence of adverse reactions in patients.
Core Tip: This study assessed the effects of pirfenidone in the early treatment of idiopathic pulmonary fibrosis (IPF). A retrospective analysis was conducted on 113 patients with IPF, who were divided into control and observation groups. The control group received routine therapy in combination with methylprednisolone tablets, while the observation group received routine therapy along with pirfenidone. The results showed that the prompt initiation of pirfenidone treatment in individuals diagnosed with IPF can enhance pulmonary function, elevate inflammatory factor levels, and increase the distance covered in the 6-min walk test. This intervention is conducive to effectively decreasing the occurrence of adverse reactions.
