BMJ Open Respiratory Research (Aug 2024)

Dynamic chest radiographic evaluation of the effects of tiotropium/olodaterol combination therapy in chronic obstructive pulmonary disease: the EMBODY study protocol for an open-label, prospective, single-centre, non-controlled, comparative study

  • Kentaro Okamoto,
  • Hajime Yokota,
  • Kazuyuki Matsushita,
  • Takashi Uno,
  • Koichiro Tatsumi,
  • Akira Nishiyama,
  • Yoshihito Ozawa,
  • Takuji Suzuki,
  • Jun Ikari,
  • Megumi Katsumata,
  • Akira Urano,
  • Takuro Imamoto,
  • Yuri Suzuki,
  • Kojiro Ono,
  • Eriko Abe,
  • Tomoko Kamata,
  • Shota Fujii,
  • Kenichiro Okumura,
  • Joji Ota,
  • Eiko Suzuki,
  • Naoko Kawata,
  • Yoshitada Masuda,
  • Seiichiro Sakao

DOI
https://doi.org/10.1136/bmjresp-2024-002374
Journal volume & issue
Vol. 11, no. 1

Abstract

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Introduction To date, there is limited evidence on the effects of bronchodilators on respiratory dynamics in chronic obstructive pulmonary disease (COPD). Dynamic chest radiography (DCR) is a novel radiographic modality that provides real-time, objective and quantifiable kinetic data, including changes in the lung area (Rs), tracheal diameter, diaphragmatic kinetics and pulmonary ventilation during respiration, at a lower radiation dose than that used by fluoroscopic or CT imaging. However, the therapeutic effect of dual bronchodilators on respiratory kinetics, such as chest wall dynamics and respiratory muscle function, has not yet been prospectively evaluated using DCR.Aim This study aims to evaluate the effects of bronchodilator therapy on respiratory kinetics in patients with COPD using DCR.Methods and analysis This is an open-label, prospective, single-centre, non-controlled, comparative study. A total of 35 patients with COPD, aged 40–85 years, with a forced expiratory volume in the first second of 30–80%, will be enrolled. After a 2–4 weeks washout period, patients will receive tiotropium/olodaterol therapy for 6 weeks. Treatment effects will be evaluated based on DCR findings, pulmonary function test results and patient-related outcomes obtained before and after treatment. The primary endpoint is the change in Rs after therapy. The secondary endpoints include differences in other DCR parameters (diaphragmatic kinetics, tracheal diameter change and maximum pixel value change rate), pulmonary function test results and patient-related outcomes between pre-therapy and post-therapy values. All adverse events will be reported.Ethics and dissemination Ethical approval for this study was obtained from the Ethics Committee of Chiba University Hospital. The results of this trial will be published in a peer-reviewed journal.Trial registration number jRCTs032210543.