Weaver Lindell K, Churchill Susan, Wilson Steffanie H, Hebert Donald, Deru Kayla, Lindblad Anne S
Division of Hyperbaric Medicine, Intermountain Medical Center, Murray, Utah and Intermountain LDS Hospital, Salt Lake City, Utah U.S.
Department of Medicine, University of Utah School of Medicine, Salt Lake City, Utah U.S.
Undersea Hyperb Med. 2019;46(3):341-352.
Global outcomes can strengthen inferences from clinical trials. We evaluate global outcomes for persistent post-concussive symptoms (PCS) after mild traumatic brain injury (mTBI) in two clinical trials of hyperbaric oxygen (HBO2) in United States service members.
During study design, outcomes of symptom, cognitive, and functional impairments planned for a trial of HBO2 for PCS (HOPPS) were weighted and grouped into different domains to formulate the composite outcome total score. The composite outcome was compared between the intervention groups in HOPPS and those in a subsequent HBO2 trial (BIMA) for validation. Additionally, two post hoc global outcome measures were explored, including one composed of components that demonstrated favorable characteristics in both studies and another via components used in another TBI randomized trial (COBRIT).
In total, 143 active-duty or veteran military personnel were randomized across the two studies. Composite total scores improved from baseline for HBO2 (mean ± SD -2.9±9.0) and sham (-2.9±6.6) groups in HOPPS but did not differ significantly between groups (p=0.33). In BIMA, 13-week changes from baseline favored the HBO2 group (-3.6±6.4) versus sham (-0.3±5.2; p=0.02). No between-group differences were found when COBRIT composite scoring was applied to BIMA. Overall, HBO2 effects were maximized when the post hoc global measure derived from both studies was applied to the data.
Composite total scores in HOPPS and BIMA were consistent with primary study results. The global measures considered may offer utility as endpoints to achieve maximal HBO2 effect in future trials of the mTBI population.
clinicaltrials.gov Identifiers NCT01611194 (BIMA) and NCT01306968 (HOPPS).
整体结果可增强临床试验的推断力。我们在美国现役军人的两项高压氧(HBO2)临床试验中,评估了轻度创伤性脑损伤(mTBI)后持续性脑震荡后症状(PCS)的整体结果。
在研究设计过程中,对一项针对PCS的HBO2试验(HOPPS)计划的症状、认知和功能障碍结果进行加权,并分组到不同领域,以制定综合结果总分。将HOPPS中的干预组与随后一项HBO2试验(BIMA)中的干预组的综合结果进行比较以作验证。此外,还探索了两种事后整体结果测量方法,一种由在两项研究中均显示出良好特征的成分组成,另一种则通过另一项TBI随机试验(COBRIT)中使用的成分组成。
两项研究共纳入143名现役或退伍军人并进行随机分组。在HOPPS中,HBO2组(均值±标准差 -2.9±9.0)和假手术组(-2.9±6.6)的综合总分较基线均有改善,但两组间无显著差异(p = 0.33)。在BIMA中,从基线开始的13周变化显示HBO2组(-3.6±6.4)优于假手术组(-0.3±5.2;p = 0.02)。将COBRIT综合评分应用于BIMA时,未发现组间差异。总体而言,当将源自两项研究的事后整体测量方法应用于数据时,HBO2的效果达到最大化。
HOPPS和BIMA中的综合总分与主要研究结果一致。所考虑的整体测量方法可能作为未来mTBI人群试验中实现最大HBO2效果的终点指标。
clinicaltrials.gov标识符NCT01611194(BIMA)和NCT01306968(HOPPS)。