Dryden Donna M, Spooner Carol H, Stickland Michael K, Vandermeer Ben, Tjosvold Lisa, Bialy Liza, Wong Kai, Rowe Brian H
Evid Rep Technol Assess (Full Rep). 2010 Jan(189):1-154, v-vi.
The objectives are: (1) To assess diagnostic test characteristics of six alternative index tests compared with the selected reference standard-a standardized exercise challenge test (ECT) in patients with suspected exercise-induced bronchoconstriction or asthma (EIB/EIA); (2) to determine the efficacy of a single prophylactic dose of four pharmacologic and one nonpharmacologic interventions vs. placebo to attenuate EIB/EIA in patients with diagnosed EIB/EIA; and (3) to determine if regular daily treatment with short-acting or long-acting beta-agonists (SABA or LABA) causes patients with EIA to develop tachyphylaxis when additional prophylactic doses are used pre-exercise.
A systematic and comprehensive literature search was conducted in 14 electronic databases (Diagnosis) and the Cochrane Airways Register (Therapy).
Study selection, quality assessment, and data extraction were conducted independently by two reviewers. The primary outcome was the maximum percent fall in the post-exercise forced expiratory volume in 1 second (percent fall FEV1). The diagnostic threshold for a positive ECT was a percent fall FEV1 of 10% or more. Sensitivity (SN) and specificity (SP) were calculated. For therapy, mean differences (MD) in the percent fall FEV1 and 95% confidence intervals (CI) (random effects model) were calculated. A positive MD indicates the intervention works better than the control.
For the diagnostic reviews, 5,318 citations yielded 28 relevant studies; for the therapy reviews, 1,634 citations yielded 109 relevant RCTs. Diagnostic test results versus ECT: self-reported history (2 studies) SN=36-8 percent; SP=85-86 percent; sport specific challenges (5 studies) SN=0-100 percent, SP=0-100 percent; eucapnic voluntary hyperpnea (7 studies) SN=25-90 percent, SP=0-71 percent; free running asthma screening test (3 studies) SN=60-67 percent, SP=47-67 percent; mannitol (3 studies) SN=58-96 percent, SP=65-78 percent. All SN and SP calculations indicated substantial heterogeneity that could not be explained by sensitivity or subgroup analyses. Therapy results: SABA offered greater protection than mast cell stabilizers (MCS) (12 studies); MD=6.8 (95 percent CI: 4.5, 9.2) but combining them offered no additional benefit; SABA versus MCS plus SABA (5 studies) MD=1.3 (95 percent CI: -6.3, 8.9). Leukotriene receptor antagonists (LTRA), MCS, ipratropium bromide, and interval warmup routines provided statistically significant attenuation of EIA when compared with placebo; inhaled corticosteroids (ICS) and other warmup routines did not. Single-dose intervention versus placebo results are: LTRA (9 studies) MD=8.9 (95 percent CI: 6.9, 11.0); MCS (nedocromil sodium) (17 studies) MD=15.6 (95 percent CI: 13.2, 18.2); interval warmup versus no warmup (4 studies) MD=10.6 (95 percent CI: 6.5, 14.7); ICS (4 studies) MD=5.0 (95 percent CI: 0.0, 9.9); continuous low intensity warmup versus no warmup (3 studies) MD=12.6 (95 percent CI: -1.5, 26.7); continuous high intensity warmup versus no warmup (2 studies) MD=9.8 (95 percent CI: -6.4, 26.0). After daily LABA (salmeterol) use for 3 to 4 weeks (4 studies), the percent fall FEV1 following an ECT at 2 and 4 weeks was greater than at day 1 in the LABA arm indicating that tachyphylaxis to prophylactic LABA use occurred. Daily SABA use for 1 week (1 study) also indicated development of tachyphylaxis. However, both LABA and SABA continued to have an attenuating effect on EIA.
Given the small number of studies comparing EIB/EIA diagnostic tests, the heterogeneity of the study populations, and the varied study methodologies, there is no clear evidence that any of the index tests are a suitable replacement for a standardized ECT to diagnose EIB/EIA in the general population. All bronchodilator agents and most anti-inflammatory agents when used as pretreatment are somewhat effective in attenuating the percent fall FEV1 associated with EIA.
目标如下:(1)评估六种替代指标测试与选定参考标准——疑似运动诱发性支气管收缩或哮喘(EIB/EIA)患者的标准化运动激发试验(ECT)相比的诊断测试特征;(2)确定四种药物干预和一种非药物干预的单次预防性剂量与安慰剂相比,对已确诊EIB/EIA患者减轻EIB/EIA的疗效;(3)确定当运动前使用额外的预防性剂量时,每日规律使用短效或长效β受体激动剂(SABA或LABA)是否会使EIA患者产生快速耐受。
在14个电子数据库(诊断)和Cochrane气道注册库(治疗)中进行了系统全面的文献检索。
由两名审阅者独立进行研究选择、质量评估和数据提取。主要结局是运动后第1秒用力呼气量的最大下降百分比(FEV1下降百分比)。ECT阳性的诊断阈值为FEV1下降百分比≥10%。计算敏感性(SN)和特异性(SP)。对于治疗,计算FEV1下降百分比的平均差值(MD)和95%置信区间(CI)(随机效应模型)。MD为正值表明干预措施比对照更有效。
对于诊断性综述,5318条引文产生了28项相关研究;对于治疗性综述,1634条引文产生了109项相关随机对照试验。与ECT相比的诊断测试结果:自我报告病史(2项研究)SN = 36% - 8%;SP = 85% - 86%;特定运动激发试验(5项研究)SN = 0% - 100%,SP = 0% - 100%;等二氧化碳分压自主过度通气(7项研究)SN = 25% - 90%,SP = 0% - 71%;自由跑步哮喘筛查试验(3项研究)SN = 60% - 67%,SP = 47% - 67%;甘露醇(3项研究)SN = 58% - 96%,SP = 65% - 78%。所有SN和SP计算均显示存在显著异质性,无法通过敏感性分析或亚组分析解释。治疗结果:SABA比肥大细胞稳定剂(MCS)提供了更好的保护(12项研究);MD = 6.8(95%CI:4.5,9.2),但联合使用它们没有额外益处;SABA与MCS加SABA相比(5项研究)MD = 1.3(95%CI: - 6.3,8.9)。与安慰剂相比,白三烯受体拮抗剂(LTRA)、MCS、异丙托溴铵和间歇热身常规措施对EIA有统计学显著的减轻作用;吸入性糖皮质激素(ICS)和其他热身常规措施则没有。单剂量干预与安慰剂的结果如下:LTRA(9项研究)MD = 8.9(95%CI:6.9,11.0);MCS(奈多罗米钠)(17项研究)MD = 15.6(95%CI:13.2,18.2);间歇热身与无热身相比(4项研究)MD = 10.6(95%CI:6.5,14.7);ICS(4项研究)MD = 5.0(95%CI:0.0,9.9);持续低强度热身与无热身相比(3项研究)MD = 12.6(95%CI: - 1.5,26.7);持续高强度热身与无热身相比(2项研究)MD = 9.8(95%CI: - 6.4,26.0)。每日使用LABA(沙美特罗)3至4周后(4项研究),LABA组在第2周和第4周进行ECT后的FEV1下降百分比大于第1天,表明对预防性LABA使用产生了快速耐受。每日使用SABA 1周(1项研究)也表明出现了快速耐受。然而,LABA和SABA对EIA仍有减轻作用。
鉴于比较EIB/EIA诊断测试的研究数量较少、研究人群的异质性以及多样的研究方法,没有明确证据表明任何一种指标测试可作为标准化ECT在普通人群中诊断EIB/EIA的合适替代方法。所有支气管扩张剂和大多数抗炎药作为预处理使用时,在减轻与EIA相关的FEV1下降百分比方面都有一定效果。