PMID- 29705620 OWN - NLM STAT- MEDLINE DCOM- 20190207 LR - 20220409 IS - 1522-9629 (Electronic) IS - 1094-5539 (Linking) VI - 51 DP - 2018 Aug TI - Impact of doxofylline in COPD: A pairwise meta-analysis. PG - 1-9 LID - S1094-5539(18)30094-4 [pii] LID - 10.1016/j.pupt.2018.04.010 [doi] AB - Doxofylline is an effective bronchodilator for relieving airway obstruction in patients with asthma or chronic obstructive pulmonary disease (COPD), and displays a better safety profile with respect to theophylline. Herein, we performed a pairwise meta-analysis of the currently available data to provide consistent and homogeneous findings on the impact of this xanthine in COPD patients. Results obtained from 820 patients were selected from 20 clinical trials. Meta-regression was performed to examine the source of heterogeneity between-studies and identify potential confounder covariates. The quality of the evidence was assessed by the GRADE system. Doxofylline induced a significant (P < 0.001) increase in forced expiratory volume in 1 s (FEV(1)) of 8.20% (95%CI 4.00-12.41; I(2) 93%) and 317 ml (95%CI 19-439; I(2) 87%) compared with baseline. The total administered dose of doxofylline significantly (P < 0.001) interacted with the size of the effect estimates detected for FEV(1). Doxofylline induced a significant (P < 0.001), although moderate, increase in adverse events (AEs) frequency (proportion 0.03, 95%CI 0.02-0.04; I(2) 88%), but only epigastralgia, nausea, dyspepsia and headache were statistically significant (P < 0.05). The GRADE analysis indicated high quality of evidence (++++) for the impact of doxofylline on FEV(1), and moderate quality of evidence (+++) for the safety profile in COPD patients. Doxofylline is an effective and safe medicine when administered to patients with COPD and can be considered as an alternative to theophylline. CI - Copyright (c) 2018 The Authors. Published by Elsevier Ltd.. All rights reserved. FAU - Cazzola, Mario AU - Cazzola M AD - Unit of Respiratory Medicine, Department of Experimental Medicine and Surgery, University of Rome "Tor Vergata", Rome, Italy. FAU - Calzetta, Luigino AU - Calzetta L AD - Unit of Respiratory Medicine, Department of Experimental Medicine and Surgery, University of Rome "Tor Vergata", Rome, Italy. Electronic address: luigino.calzetta@uniroma2.it. FAU - Rogliani, Paola AU - Rogliani P AD - Unit of Respiratory Medicine, Department of Experimental Medicine and Surgery, University of Rome "Tor Vergata", Rome, Italy. FAU - Page, Clive AU - Page C AD - Sackler Institute of Pulmonary Pharmacology, Institute of Pharmaceutical Science, King's College London, London, UK. FAU - Matera, Maria Gabriella AU - Matera MG AD - Unit of Pharmacology, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy. LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20180426 PL - England TA - Pulm Pharmacol Ther JT - Pulmonary pharmacology & therapeutics JID - 9715279 RN - 0 (Bronchodilator Agents) RN - C137DTR5RG (Theophylline) RN - MPM23GMO7Z (doxofylline) SB - IM MH - Bronchodilator Agents/*administration & dosage/adverse effects/pharmacology MH - Forced Expiratory Volume MH - Humans MH - Pulmonary Disease, Chronic Obstructive/*drug therapy/physiopathology MH - Theophylline/administration & dosage/adverse effects/*analogs & derivatives/pharmacology MH - Treatment Outcome OTO - NOTNLM OT - Chronic obstructive pulmonary disease OT - Doxofylline OT - Lung function OT - Pairwise meta-analysis OT - Safety EDAT- 2018/05/01 06:00 MHDA- 2019/02/08 06:00 CRDT- 2018/04/30 06:00 PHST- 2018/04/16 00:00 [received] PHST- 2018/04/24 00:00 [accepted] PHST- 2018/05/01 06:00 [pubmed] PHST- 2019/02/08 06:00 [medline] PHST- 2018/04/30 06:00 [entrez] AID - S1094-5539(18)30094-4 [pii] AID - 10.1016/j.pupt.2018.04.010 [doi] PST - ppublish SO - Pulm Pharmacol Ther. 2018 Aug;51:1-9. doi: 10.1016/j.pupt.2018.04.010. Epub 2018 Apr 26.