Literature DB >> 36105040

Clinical efficacy and quality of life effect of acetylcysteine plus pirfenidone in patients with pulmonary fibrosis.

Rong Zhang1, Zhanshuai Song1, Yan Guan2, Juan Zhang1, Jianfang Zou1, Yingxin Sun3, Hua Shao1.   

Abstract

OBJECTIVE: To study the clinical efficacy of acetylcysteine combined with pirfenidone in patients with pulmonary fibrosis (PF).
METHODS: A total of 114 PF patients admitted from January 2018 to January 2019 were retrospectively analyzed. Among them, 64 patients treated with acetylcysteine combined with pirfenidone were classified into a research group, and the other 50 treated with acetylcysteine combined with budesonide were assigned into a control group. The clinical efficacy and total effectiveness rate of the two groups were compared after 6 months of therapy. The quality of life (QoL) in the two groups before and after treatment was evaluatedusing Asthma Therapy Assessment Questionnaire for idiopathic pulmonary fibrosis patients (ATAQ-IPF). The 2-year survival of the two groups was compared. Additionally, the incidence of adverse reactions was compared between the two groups. The changes in forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), inflammatory factors, and PF markers were compared between the two groups before and after therapy.
RESULTS: There were no significant differences in clinical efficacy or total effectiveness rate (all P > 0.05), serum IL-4, INFγ or IL-6 expression (all P > 0.05), as well as FEV1 and FVC levels (all P > 0.05) after therapy between two groups. After therapy, the research group showed significantly lower PCIII and HA levels, lower ATAQ-IPF scores, and lower total incidence of adverse reactions than the control group (all P < 0.05). In addition, a higher 2-year survival rate was observed in the research group than in the control group (P=0.025).
CONCLUSION: Acetylcysteine combined with pirfenidone can reduce adverse reactions and improve the QoL and survival time of patients. AJTR
Copyright © 2022.

Entities:  

Keywords:  Acetylcysteine; budesonide; pifenidone; prognosis; pulmonary fibrosis

Year:  2022        PMID: 36105040      PMCID: PMC9452344     

Source DB:  PubMed          Journal:  Am J Transl Res        ISSN: 1943-8141            Impact factor:   3.940


  26 in total

1.  Pirfenidone in patients with unclassifiable progressive fibrosing interstitial lung disease: a double-blind, randomised, placebo-controlled, phase 2 trial.

Authors:  Toby M Maher; Tamera J Corte; Aryeh Fischer; Michael Kreuter; David J Lederer; Maria Molina-Molina; Judit Axmann; Klaus-Uwe Kirchgaessler; Katerina Samara; Frank Gilberg; Vincent Cottin
Journal:  Lancet Respir Med       Date:  2019-09-29       Impact factor: 30.700

2.  Pirfenidone in idiopathic pulmonary fibrosis.

Authors:  H Taniguchi; M Ebina; Y Kondoh; T Ogura; A Azuma; M Suga; Y Taguchi; H Takahashi; K Nakata; A Sato; M Takeuchi; G Raghu; S Kudoh; T Nukiwa
Journal:  Eur Respir J       Date:  2009-12-08       Impact factor: 16.671

Review 3.  Idiopathic pulmonary fibrosis.

Authors:  Antoni Xaubet; Julio Ancochea; María Molina-Molina
Journal:  Med Clin (Barc)       Date:  2016-12-18       Impact factor: 1.725

4.  Idiopathic Pulmonary Fibrosis: Epidemiology, Diagnosis andOutcomes.

Authors:  Yosafe Wakwaya; Kevin K Brown
Journal:  Am J Med Sci       Date:  2019-02-15       Impact factor: 2.378

Review 5.  Clinical trials of N-acetylcysteine in psychiatry and neurology: A systematic review.

Authors:  John Slattery; Nihit Kumar; Leanna Delhey; Michael Berk; Olivia Dean; Charles Spielholz; Richard Frye
Journal:  Neurosci Biobehav Rev       Date:  2015-05-06       Impact factor: 8.989

Review 6.  Pirfenidone safety and adverse event management in idiopathic pulmonary fibrosis.

Authors:  Lisa H Lancaster; Joao A de Andrade; Joseph D Zibrak; Maria L Padilla; Carlo Albera; Steven D Nathan; Marlies S Wijsenbeek; John L Stauffer; Klaus-Uwe Kirchgaessler; Ulrich Costabel
Journal:  Eur Respir Rev       Date:  2017-12-06

7.  Pulmonary delivery of liposomal dry powder inhaler formulation for effective treatment of idiopathic pulmonary fibrosis.

Authors:  S Chennakesavulu; A Mishra; A Sudheer; C Sowmya; C Suryaprakash Reddy; E Bhargav
Journal:  Asian J Pharm Sci       Date:  2017-08-18       Impact factor: 6.598

Review 8.  Idiopathic pulmonary fibrosis beyond the lung: understanding disease mechanisms to improve diagnosis and management.

Authors:  Fabrizio Luppi; Meena Kalluri; Paola Faverio; Michael Kreuter; Giovanni Ferrara
Journal:  Respir Res       Date:  2021-04-17

Review 9.  Time for a change: is idiopathic pulmonary fibrosis still idiopathic and only fibrotic?

Authors:  Paul J Wolters; Timothy S Blackwell; Oliver Eickelberg; James E Loyd; Naftali Kaminski; Gisli Jenkins; Toby M Maher; Maria Molina-Molina; Paul W Noble; Ganesh Raghu; Luca Richeldi; Marvin I Schwarz; Moises Selman; Wim A Wuyts; David A Schwartz
Journal:  Lancet Respir Med       Date:  2018-02       Impact factor: 30.700

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.