Cazzola Mario, Hanania Nicola A
Antonio Cardarelli Hospital, Department of Respiratory Medicine, Unit of Pneumology and Allergology, Naples, Italy.
Int J Chron Obstruct Pulmon Dis. 2006;1(4):345-54. doi: 10.2147/copd.2006.1.4.345.
Acute exacerbations of COPD can complicate the course of the disease in patients with severe airway obstruction. Reduction of exacerbations is an important clinical outcome in evaluating new therapies in COPD. Combination therapies with long-acting beta-agonists and inhaled corticosteroids have now been approved for use. Three 1-year randomized clinical trials, which studied the effect of combining a long-acting beta2-agonist with an inhaled corticosteroid in COPD, documented that exacerbation frequency was lower with therapy than placebo. Combination therapy had a similar effect to its monocomponents in the trial evaluating salmeterol/fluticasone combination. However, when patients with more severe COPD were studied using a combination of budesonide and formoterol, a clear improvement was seen in the overall exacerbation rates compared with the use of a long-acting beta2-agonist alone.
慢性阻塞性肺疾病(COPD)急性加重可使严重气道阻塞患者的病程复杂化。减少急性加重是评估COPD新疗法的一项重要临床指标。长效β受体激动剂与吸入性糖皮质激素的联合疗法现已获批使用。三项为期1年的随机临床试验研究了长效β受体激动剂与吸入性糖皮质激素联合应用于COPD的效果,结果表明,与安慰剂相比,联合治疗组的急性加重频率更低。在评估沙美特罗/氟替卡松联合用药的试验中,联合治疗与其单一成分治疗效果相似。然而,当使用布地奈德和福莫特罗联合治疗更严重的COPD患者时,与单独使用长效β2受体激动剂相比,总体急性加重率有明显改善。