首页> 外文期刊>European journal of cardio-thoracic surgery: Official journal of the European Association for Cardio-thoracic Surgery >Short-term effects of inhalative tiotropium/formoterol/budenoside versus tiotropium/formoterol in patients with newly diagnosed chronic obstructive pulmonary disease requiring surgery for lung cancer: a prospective randomized trial.
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Short-term effects of inhalative tiotropium/formoterol/budenoside versus tiotropium/formoterol in patients with newly diagnosed chronic obstructive pulmonary disease requiring surgery for lung cancer: a prospective randomized trial.

机译:吸入噻托溴铵/福莫特罗/丁二糖苷与噻托溴铵/福莫特罗在新诊断为需要手术的慢性阻塞性肺疾病患者中的近期疗效:一项前瞻性随机试验。

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OBJECTIVE: A new diagnosis of chronic obstructive pulmonary disease (COPD) is often made during the evaluation of patients requiring a surgical intervention for lung cancer. Based on initial impaired lung function, these untreated patients are often considered not fit for lung surgery. There is limited information on the short-term effectiveness of preoperative pharmacologic treatment strategies in patients with newly diagnosed COPD before lung surgery. METHODS: A prospective randomized study was conducted comparing 1-week-treatment periods of tiotropium/formoterol/budenoside (GR1) with tiotropium/formoterol (GR2) in conjunction with smoking cessation and chest physiotherapy. No patients had been previously treated for COPD. The primary end point was body plethysmography (forced expiratory volume in 1s (FEV1), forced vital capacity (FVC), and airway resistance (RAW)) at the end of each treatment period. Secondary end points were improvement of >/= 10% in FEV1 (% predicted) and improvement of the severity of COPD after the 1-week treatment, as well as the rate of pulmonary complications after surgery. RESULTS: A total of 46 patients were randomized in GR1 (n=24) and GR2 (n=22). Both groups were comparable with regard to age, height, weight, smoking history, baseline body plethysmography (FVC, FEV1, and RAW), and the severity of COPD according to the Global Initiative for Obstructive Lung Disease (GOLD) staging, respectively. However, the short-term effects of the treatment with regard to FEV1 (2.0 l vs 1.7 l; p=0.031) and increase of FEV1 (0.31 l vs 0.10 l; p=0.02) were better in GR1. More patients in GR1 had an improvement of >/= 10% in FEV1 (p=0.004) and improvement of the severity of COPD (p=0.012) after the 1-week treatment. Fewer pulmonary complications (11.1% vs 42.9%, p=0.04) were observed in GR1 after surgery. CONCLUSIONS: Both therapies resulted in an improvement of lung function. There is benefit from adding inhalative budenoside to tiotropium and formoterol in terms of an improvement in FEV1 and the severity of COPD. These beneficial results might lead to less pulmonary complications in the postoperative period.
机译:目的:在评估需要外科手术治疗肺癌的患者时,常常会做出新的慢性阻塞性肺疾病(COPD)诊断。基于最初的肺功能受损,这些未经治疗的患者通常被认为不适合进行肺部手术。对于肺手术前新诊断为COPD的患者,术前药物治疗策略的短期有效性的信息有限。方法:一项前瞻性随机研究比较了噻托溴铵/福莫特罗/丁腺苷(GR1)与噻托溴铵/福莫特罗(GR2)联合戒烟和胸部物理治疗的1周治疗期。之前没有患者接受过COPD治疗。主要终点是每次治疗期结束时的人体体积描记法(1s呼气量(FEV1),强制肺活量(FVC)和气道阻力(RAW))。次要终点是治疗1周后FEV1的改善> / = 10%(预测的百分比)和COPD严重程度的改善以及肺部并发症的发生率。结果:总共46例患者被随机分为GR1(n = 24)和GR2(n = 22)。根据全球阻塞性肺疾病倡议(GOLD)分期,两组的年龄,身高,体重,吸烟史,基线人体体积描记法(FVC,FEV1和RAW)以及COPD的严重程度均具有可比性。但是,在GR1中,治疗对FEV1的短期效果(2.0 l vs 1.7 l; p = 0.031)和FEV1的增加(0.31 l vs 0.10 l; p = 0.02)更好。经过1周的治疗后,更多GR1患者的FEV1改善> / = 10%(p = 0.004),COPD严重程度改善(p = 0.012)。术后GR1的肺部并发症较少(11.1%vs 42.9%,p = 0.04)。结论:两种疗法均能改善肺功能。就改善FEV1和COPD的严重性而言,将吸入性布地那苷添加到噻托溴铵和福莫特罗中是有好处的。这些有益的结果可能会减少术后的肺部并发症。

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