慢性阻塞性肺疾病:对复发症状患者有用的药物。

Q4 Medicine
Prescrire International Pub Date : 2016-11-01
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引用次数: 0

摘要

慢性阻塞性肺疾病(COPD)是一种呼吸系统疾病,其特征是由于烟草烟雾等刺激物引起的气流基本上不可逆的变化。慢性阻塞性肺病患者经历急性加重。严重的疾病可能发展为慢性呼吸衰竭。我们使用标准处方方法学回顾了COPD基本药物的文献。关于治疗轻度慢性阻塞性肺病的临床资料很少。没有复发症状的患者不需要定期服药。消除接触香烟烟雾和其他刺激物(如工作场所刺激物)是已知改善慢性阻塞性肺病结果的唯一措施。吸入短效β -2激动剂的评价主要基于短期试验。这些药物已被证明能改善呼吸困难。沙美特罗和福莫特罗是两种长效β -2激动剂,在有症状的患者中得到了广泛的评价。与未治疗相比,这些药物可减少呼吸困难和急性加重,每100名中重度COPD患者治疗7个月可避免约2例住院。吲哚卡特罗和罗替他罗没有更好的损益平衡。吸入β -2激动剂偶尔会引起心血管疾病。在数千名参与临床试验的慢性阻塞性肺病患者中,没有报告出现额外的死亡率。几乎没有证据表明异丙托品,一种吸入短效抗毒蕈碱支气管扩张剂,可以改善COPD症状。不能排除使用异丙托梅治疗的COPD患者死亡率增加的风险。Tiotroplum是一种吸入性长效抗uscarinic支气管扩张剂,已被广泛评估用于COPD。噻托罗梅对慢性阻塞性肺病有对症疗效,可减轻呼吸困难和急性加重。在包括12000多名患者的7项随机试验中,Tiotroplum与长效β -2激动剂相比没有明显的优势。glycopyronium和aclidinium是另外两种吸入性长效抗蛇毒素,似乎并不更有效。Tiotroplum与其他吸入抗毒蕈碱药物一样,具有抗毒蕈碱的不良反应,包括心脏、视力和口腔疾病。Glycopyronium可能具有较高的严重心血管影响风险。抗毒蕈碱联合吸入β -2激动剂可改善7% - 10%患者的症状。在每年有1 -2次COPD加重的患者中,在长效β -2激动剂的基础上加入吸入性皮质激素(百氯美松、布地奈德或氟替卡松)可在3 - 4年治疗期间预防1次加重。吸入皮质类固醇可引起肺炎、念珠菌病、呼吸困难和肾上腺功能不全。氟替卡松似乎比其他吸入性皮质类固醇有更多的副作用。茶碱对慢性阻塞性肺病症状的疗效尚不确定。该药治疗指标狭窄,有严重不良反应的危险。它不应用于慢性阻塞性肺病。长期使用罗氟司特或口服皮质类固醇治疗COPD存在不利的利弊平衡。在实践中,2016年,慢性阻塞性肺病的第一项措施是消除接触刺激物,通常是烟草。用于慢性阻塞性肺病的药物只有适度的、主要是对症的疗效。治疗应适应症状和发作频率:应首先尝试短效β -2激动剂,然后用吸入性长效支气管扩张剂或噻托溴铵替代,如果其作用太短暂的话。如果症状持续或恶化频繁,可增加吸入性皮质类固醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic obstructive pulmonary disease: Useful medications for patients with recurrent symptoms.

Chronic obstructive pulmonary disease (COPD) is a respiratory disorder characterised by largely irreversible changes in air flow due to irritants such as tobacco smoke. Patients with COPD experience acute exacerbations. Severe disease may progress to chronic respiratory failure. We reviewed the literature on basic medications available for COPD, using the standard Prescrire methodology. There are few clinical data on treatment of mild COPD. Regular medication is not necessary for patients who do not have recurrent symptoms. Eliminating exposure to cigarette smoke and other irritants such as workplace irritants, is the only measure known to improve the outcome of COPD. Evaluation of inhaled short-acting beta-2 agonists is based mainly on short-term trials. These drugs have been shown to improve dyspnoea. Salmeterol and formoterol, two long-acting beta-2 agonists, have been extensively evaluated in symptomatic patients. Compared with no treatment, these drugs reduce breathlessness and acute exacerbations, preventing about two hospital admissions per 100 patients with moderate to severe COPD treated for 7 months. Indacaterol and olodateroldo not have a better harm-benefit balance. Inhaled beta-2 agonists occasionally provoke cardiovascular disorders. No excess mortality has been reported among the thousands of COPD patients included in clinical trials. There Is little evidence that ipratropium, an inhaled short-acting anti-muscarinic bronchodilator, improves COPD symptoms. A risk of Increased mortality among COPD patients treated with ipratroplum cannot be ruled out. Tiotroplum, an inhaled long-acting antimuscarinic bronchodilator, has been extensively evaluated In COPD. Tiotroplum has symptomatic efficacy in COPD, reducing dyspnoea and acute exacerbations. Tiotroplum had no tangible advantages over long-acting beta-2 agonists in seven randomised trials including more than 12 000 patients. Glycopyrronium and aclidinium, two other Inhaled long-acting antimuscarinics, do not appear to be more effective. Tiotroplum, like other inhaled anti-muscarinics, has antimuscarinic adverse effects including cardiac, visual and buccal disorders. Glycopyronium may carry a higher risk of serious cardiovascular effects. Combination of an antimuscarinic with an inhaled beta-2 agonist improves symptoms in 7% to 10% of patients. In patients with one or two COPD exacerbations per year, adding an Inhaled corticosterold (beclometa- sone, budesonide or fluticasone) to a long-acting beta-2 agonist prevents about 1 exacerbation during 3 to 4 years of treatment. Inhaled corticosteroids can cause pneumonia, candidiasis, dysphonia and adrenal Insufficiency. Fluticasone seems to have more adverse effects than other inhaled corticosterolds. Theophylline has uncertain efficacy on symptoms of COPD. This drug has a narrow therapeutic index and carries a risk of serious adverse effects. It should not be used in COPD. Long-term treatment with roflumilast or oral corticosteroids has an unfavourable harm-benefit balance in COPD. In practice, in 2016, the first measure in COPD is to eliminate exposure to the irritant, most often tobacco. Drugs used in COPD have only modest, mainly symptomatic efficacy. Treatment should be adapted to symptoms and the frequency of exacerbations: a short-acting beta-2 agonist should be tried first, then replaced by an inhaled long-acting bronchodilator, or possibly tiotropium, when its effect is too short-lived. An inhaled corticosteroid can be added if symptoms persist or exacerbations are frequent.

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Prescrire International
Prescrire International Medicine-Pharmacology (medical)
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