Rank Matthew A, Gionfriddo Michael R, Pongdee Thanai, Volcheck Gerald W, Li James T, Hagan Christina R, Erwin Patricia J, Hagan John B
Division of Allergy, Asthma, and Clinical Immunology, Mayo Clinic, Scottsdale, Arizona, USA.
Allergy Asthma Proc. 2015 May-Jun;36(3):200-5. doi: 10.2500/aap.2015.36.3839.
The risks of using leukotriene receptor antagonists (LTRA) as part of a strategy for stepping down inhaled corticosteroid (ICS) are not well known.
To estimate the risk of asthma exacerbation in individuals with stable asthma who start LTRA when stopping ICS or reducing ICS dose.
We identified articles from a systematic review of English and non-English articles by using a number of data bases. We included randomized controlled trials with a stable asthma run-in period of 4 weeks or more and a follow-up period of at least 3 months. We included studies of individuals with stable asthma who stopped ICS and substituted LTRA (versus continuing ICS) and who reduced ICS while starting LTRA (versus placebo).
The search strategy identified 1132 potential articles, of which 52 were reviewed at the full-text level, and four met criteria for inclusion. The single article that met the inclusion criteria for substitution of LTRA for ICS as a step-down strategy found a statistically increased risk of treatment failure of 30.3% for substituting LTRA compared with 20.2% for continuing ICS. The three articles that met the inclusion criteria for comparing LTRA versus placebo in patients with stable asthma who reduce ICS found a modestly decreased risk ratio that favored LTRA of 0.57 (95% confidence interval, 0.36-0.90; I(2) = 0%) in studies that only included individuals >15 years old.
Only one study addressed the risk of substitution of LTRA for ICS in stable asthma, which limited any strong conclusions about this step-down strategy.
作为减少吸入性糖皮质激素(ICS)使用策略的一部分,使用白三烯受体拮抗剂(LTRA)的风险尚不清楚。
评估在稳定期哮喘患者停用ICS或降低ICS剂量时开始使用LTRA后哮喘加重的风险。
我们通过多个数据库对英文和非英文文章进行系统综述来识别文章。我们纳入了稳定期哮喘导入期为4周或更长时间且随访期至少3个月的随机对照试验。我们纳入了对稳定期哮喘患者停用ICS并换用LTRA(与继续使用ICS相比)以及在开始使用LTRA时降低ICS剂量(与安慰剂相比)的研究。
检索策略识别出1132篇潜在文章,其中52篇进行了全文评审,4篇符合纳入标准。作为减量策略,唯一一篇符合将LTRA替代ICS纳入标准的文章发现,与继续使用ICS的20.2%相比,替代LTRA的治疗失败风险在统计学上增加了30.3%。在对降低ICS剂量的稳定期哮喘患者比较LTRA与安慰剂的三篇符合纳入标准的文章中,在仅纳入15岁以上个体的研究中发现风险比适度降低,LTRA更具优势,为0.57(95%置信区间,0.36 - 0.90;I² = 0%)。
仅有一项研究探讨了在稳定期哮喘中用LTRA替代ICS的风险,这限制了对该减量策略得出任何有力结论。