Klooster Karin, Slebos Dirk-Jan, Zoumot Zaid, Davey Claire, Shah Pallav L, Hopkinson Nicholas S
Department of Pulmonary Diseases, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Respiratory and Critical Care Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates.
BMJ Open Respir Res. 2017 Nov 2;4(1):e000214. doi: 10.1136/bmjresp-2017-000214. eCollection 2017.
Endobronchial valve placement has potential as a treatment for patients with chronic obstructive pulmonary disease (COPD). However, a robust evidence base will be needed to convince commissioners of healthcare that it is a high-value treatment. We sought to develop the evidence base by performing an individual patient-level analysis of randomised controlled trials in people with heterogeneous emphysema and an absence of collateral ventilation.
A literature search (PROSPERO register CRD42016048127) identified two trials meeting these criteria, the BelieVeR-HIFi and STELVIO studies. Anonymised individual patient data were obtained from investigators and analysed. The primary outcome measure was a comparison of change in forced expiratory volume in 1 s (FEV) from baseline between the treatment and control groups. Secondary end points were change from baseline in 6 min walk distance (6MWD), Medical Research Council dyspnoea score and St George's Respiratory Questionnaire (SGRQ).
114 individuals were treated with 3-month to 6-month follow-up data available for 101 individuals. FEV improved by 23.1 (±28.3)% in patients treated with valves with a mean (95% CI) difference in response between groups of 17.8 (26.5, 9.2)% (p<0.0001). Relative to controls valve placement was associated with a fall in residual volume of 0.64 (0.43, 0.86) L (p<0.0001), a 9.5 (3.5, 15.6) unit fall in SGRQ (p=0.0022) and a 64.2 (94.0, 34.5) m increase in 6MWD. There were three deaths in the treatment arm and the pneumothorax rate was 15%.
These data strengthen the evidence that endobronchial valve treatment can produce clinically meaningful improvements in appropriately selected COPD patients.
支气管内瓣膜置入术有潜力用于治疗慢性阻塞性肺疾病(COPD)患者。然而,需要强有力的证据基础来说服医疗保健专员相信这是一种高价值的治疗方法。我们试图通过对患有异质性肺气肿且无侧支通气的患者进行随机对照试验的个体患者水平分析来建立证据基础。
文献检索(PROSPERO登记号CRD42016048127)确定了两项符合这些标准的试验,即BelieVeR-HIFi和STELVIO研究。从研究者处获得匿名的个体患者数据并进行分析。主要结局指标是治疗组和对照组之间1秒用力呼气量(FEV)相对于基线的变化比较。次要终点是6分钟步行距离(6MWD)、医学研究委员会呼吸困难评分和圣乔治呼吸问卷(SGRQ)相对于基线的变化。
114例患者接受了治疗,101例患者有3个月至6个月的随访数据。接受瓣膜治疗的患者FEV改善了23.1(±28.3)%,两组之间的平均(95%CI)反应差异为17.8(26.5,9.2)%(p<0.0001)。相对于对照组,瓣膜置入与残气量下降0.64(0.43,0.86)L(p<0.0001)、SGRQ下降9.5(3.5,15.6)单位(p=0.0022)以及6MWD增加64.2(94.0,34.5)m相关。治疗组有3例死亡,气胸发生率为15%。
这些数据强化了支气管内瓣膜治疗可在适当选择的COPD患者中产生具有临床意义改善的证据。