Service de Pneumologie, INSERM U903, Hôpital Universitaire de Reims, Reims, France.
Service de Pneumologie, Hôpital Universitaire Bichat, Paris, France.
JAMA. 2016 Jan 12;315(2):175-84. doi: 10.1001/jama.2015.17821.
Therapeutic options for severe emphysema are limited. Lung volume reduction using nitinol coils is a bronchoscopic intervention inducing regional parenchymal volume reduction and restoring lung recoil.
To evaluate the efficacy, safety, cost, and cost-effectiveness of nitinol coils in treatment of severe emphysema.
DESIGN, SETTING, AND PARTICIPANTS: Multicenter 1:1 randomized superiority trial comparing coils with usual care at 10 university hospitals in France. Enrollment of patients with emphysema occurred from March to October 2013, with 12-month follow-up (last follow-up, December 2014).
Patients randomized to usual care (n = 50) received rehabilitation and bronchodilators with or without inhaled corticosteroids and oxygen; those randomized to bilateral coil treatment (n = 50) received usual care plus additional therapy in which approximately 10 coils per lobe were placed in 2 bilateral lobes in 2 procedures.
The primary outcome was improvement of at least 54 m in the 6-minute walk test at 6 months (1-sided hypothesis test). Secondary outcomes included changes at 6 and 12 months in the 6-minute walk test, lung function, quality of life as assessed by St George's Respiratory Questionnaire (range, 0-100; 0 being the best and 100 being the worst quality of life; minimal clinically important difference, ≥4), morbidity, mortality, total cost, and cost-effectiveness.
Among 100 patients, 71 men and 29 women (mean age, 62 years) were included. At 6 months, improvement of at least 54 m was observed in 18 patients (36%) in the coil group and 9 patients (18%) in the usual care group, for a between-group difference of 18% (1-sided 95% CI, 4% to ∞; P = .03). Mean between-group differences at 6 and 12 months in the coil and usual care groups were +0.09 L (95% CI, 0.05 L to ∞) (P = .001) and +0.08 L (95% CI, 0.03 L to ∞) (P = .002) for forced expiratory volume in the first second, +21 m (95% CI, -4 m to ∞) (P = .06) and +21 m (95% CI, -5 m to ∞) (P = .12) for 6-minute walk distance, and -13.4 points (95% CI, -8 points to ∞) and -10.6 points (95% CI, -5.8 points to ∞) for St George's Respiratory Questionnaire (1-sided P < .001 for both). Within 12 months, 4 deaths occurred in the coil group and 3 in the usual care group. The mean total 1-year per-patient cost difference between groups was $47,908 (95% CI, $47,879-$48,073) (P < .001); the incremental cost-effectiveness ratio was $782,598 per additional quality-adjusted life-year.
In this preliminary study of patients with severe emphysema followed up for 6 months, bronchoscopic treatment with nitinol coils compared with usual care resulted in improved exercise capacity with high short-term costs. Further investigation is needed to assess durability of benefit and long-term cost implications.
clinicaltrials.gov Identifier: NCT01822795.
严重肺气肿的治疗选择有限。使用镍钛诺线圈进行肺减容术是一种支气管镜介入治疗,可诱导区域性实质体积减少并恢复肺回弹。
评估镍钛诺线圈治疗严重肺气肿的疗效、安全性、成本和成本效益。
设计、地点和参与者:多中心 1:1 随机优势试验,在法国的 10 所大学医院比较线圈与常规护理。2013 年 3 月至 10 月期间招募肺气肿患者,随访 12 个月(最后随访,2014 年 12 月)。
随机分配至常规护理组的患者(n = 50)接受康复和支气管扩张剂治疗,可加用或不加用吸入性皮质类固醇和氧气;随机分配至双侧线圈治疗组的患者(n = 50)接受常规护理,加用附加治疗,每叶约放置 10 个线圈,分 2 次双侧 2 个肺叶进行治疗。
主要结局是在 6 个月时 6 分钟步行试验至少改善 54 m(单侧假设检验)。次要结局包括 6 个月和 12 个月时的 6 分钟步行试验、肺功能、圣乔治呼吸问卷(范围 0-100;0 为最佳,100 为最差的生活质量;最小临床重要差异,≥4)、发病率、死亡率、总费用和成本效益。
在 100 名患者中,71 名男性和 29 名女性(平均年龄 62 岁)入选。在 6 个月时,线圈组中有 18 名患者(36%)和常规护理组中有 9 名患者(18%)至少改善了 54 m,组间差异为 18%(单侧 95%置信区间,4%至∞;P = .03)。在 6 个月和 12 个月时,线圈组和常规护理组之间的平均组间差异分别为 0.09 L(95%置信区间,0.05 L 至 ∞)(P = .001)和 0.08 L(95%置信区间,0.03 L 至 ∞)(P = .002),用力呼气量第一秒增加 21 m(95%置信区间,-4 m 至 ∞)(P = .06)和 6 分钟步行距离增加 21 m(95%置信区间,-5 m 至 ∞)(P = .12),圣乔治呼吸问卷评分降低 13.4 分(95%置信区间,-8 分至 ∞)和 10.6 分(95%置信区间,-5.8 分至 ∞)(单侧 P < .001)。在 12 个月内,线圈组中有 4 例死亡,常规护理组中有 3 例死亡。两组患者 1 年总人均成本差异为 47908 美元(95%置信区间,47879-48073 美元)(P < .001);增量成本效益比为每增加 1 个质量调整生命年需 782598 美元。
在这项对随访 6 个月的严重肺气肿患者的初步研究中,与常规护理相比,镍钛诺线圈支气管镜治疗可改善运动能力,但短期成本较高。需要进一步研究以评估疗效的持久性和长期成本影响。
clinicaltrials.gov 标识符:NCT01822795。