| Literature DB >> 29725530 |
Takashi Makino1, Hajime Otsuka1, Yoshinobu Hata1, Satoshi Koezuka1, Yoko Azuma1, Kazutoshi Isobe2, Keishi Sugino2, Satoru Ebihara3, Sakae Homma2, Akira Iyoda1.
Abstract
Bronchodilators are essential for the perioperative management of patients with chronic obstructive pulmonary disease (COPD) undergoing surgery for lung cancer. The objective of the present study was to examine whether the usage of a long-acting β2-agonist (LABA) with a long-acting muscarinic antagonist (LAMA) could optimize preoperative lung function and reduce the risk for postoperative pulmonary complications. Thirty-two consecutive patients with moderate-to-severe COPD who underwent a lobectomy for lung cancer and received preoperative LAMA (n=19) or LAMA/LABA (n=13) therapy between January 2005 and December 2015 were enrolled in this retrospective study. The improvement of preoperative pulmonary function and the postoperative morbidity were compared between the patients with preoperative LAMA, and LAMA/LABA therapy. Increases in the forced expiratory volume in one second (FEV1) were significantly larger in the LAMA/LABA group than in the LAMA group (0.26±0.05 l vs. 0.07±0.05 l; P=0.0145). More patients in the LAMA/LABA group than in the LAMA group showed a marked improvement of >10% in %FEV1 after bronchodilators (85 vs. 32%; P=0.0046). The incidence of postoperative pneumonia was significantly lower in the LAMA/LABA group than in the LAMA group (0 vs. 26%; P=0.044). In conclusion, the present study showed that preoperative LAMA/LABA therapy was associated with larger improvements in preoperative pulmonary function and less postoperative pneumonia than LAMA therapy. These results may lead to greater improvements in FEV1 and less postoperative pneumonia by encouraging preoperative LAMA/LABA therapy in this patient population.Entities:
Keywords: bronchodilator; chronic obstructive pulmonary disease; long-acting muscarinic antagonist; long-acting β2-agonist; lung cancer; surgery
Year: 2018 PMID: 29725530 PMCID: PMC5920355 DOI: 10.3892/mco.2018.1595
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450