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稳定期慢性阻塞性肺疾病的诊断与药物治疗:芬兰指南

Diagnosis and pharmacotherapy of stable chronic obstructive pulmonary disease: the finnish guidelines.

作者信息

Kankaanranta Hannu, Harju Terttu, Kilpeläinen Maritta, Mazur Witold, Lehto Juho T, Katajisto Milla, Peisa Timo, Meinander Tuula, Lehtimäki Lauri

机构信息

Department of Respiratory Medicine, Seinäjoki Central Hospital, Seinäjoki, Finland; Department of Respiratory Medicine, University of Tampere, Tampere, Finland.

出版信息

Basic Clin Pharmacol Toxicol. 2015 Apr;116(4):291-307. doi: 10.1111/bcpt.12366. Epub 2015 Jan 22.

Abstract

The Finnish Medical Society Duodecim initiated and managed the update of the Finnish national guideline for chronic obstructive pulmonary disease (COPD). The Finnish COPD guideline was revised to acknowledge the progress in diagnosis and management of COPD. This Finnish COPD guideline in English language is a part of the original guideline and focuses on the diagnosis, assessment and pharmacotherapy of stable COPD. It is intended to be used mainly in primary health care but not forgetting respiratory specialists and other healthcare workers. The new recommendations and statements are based on the best evidence available from the medical literature, other published national guidelines and the GOLD (Global Initiative for Chronic Obstructive Lung Disease) report. This guideline introduces the diagnostic approach, differential diagnostics towards asthma, assessment and treatment strategy to control symptoms and to prevent exacerbations. The pharmacotherapy is based on the symptoms and a clinical phenotype of the individual patient. The guideline defines three clinically relevant phenotypes including the low and high exacerbation risk phenotypes and the neglected asthma-COPD overlap syndrome (ACOS). These clinical phenotypes can help clinicians to identify patients that respond to specific pharmacological interventions. For the low exacerbation risk phenotype, pharmacotherapy with short-acting β2 -agonists (salbutamol, terbutaline) or anticholinergics (ipratropium) or their combination (fenoterol-ipratropium) is recommended in patients with less symptoms. If short-acting bronchodilators are not enough to control symptoms, a long-acting β2 -agonist (formoterol, indacaterol, olodaterol or salmeterol) or a long-acting anticholinergic (muscarinic receptor antagonists; aclidinium, glycopyrronium, tiotropium, umeclidinium) or their combination is recommended. For the high exacerbation risk phenotype, pharmacotherapy with a long-acting anticholinergic or a fixed combination of an inhaled glucocorticoid and a long-acting β2 -agonist (budesonide-formoterol, beclomethasone dipropionate-formoterol, fluticasone propionate-salmeterol or fluticasone furoate-vilanterol) is recommended as a first choice. Other treatment options for this phenotype include combination of long-acting bronchodilators given from separate inhalers or as a fixed combination (glycopyrronium-indacaterol or umeclidinium-vilanterol) or a triple combination of an inhaled glucocorticoid, a long-acting β2 -agonist and a long-acting anticholinergic. If the patient has severe-to-very severe COPD (FEV1  < 50% predicted), chronic bronchitis and frequent exacerbations despite long-acting bronchodilators, the pharmacotherapy may include also roflumilast. ACOS is a phenotype of COPD in which there are features that comply with both asthma and COPD. Patients belonging to this phenotype have usually been excluded from studies evaluating the effects of drugs both in asthma and in COPD. Thus, evidence-based recommendation of treatment cannot be given. The treatment should cover both diseases. Generally, the therapy should include at least inhaled glucocorticoids (beclomethasone dipropionate, budesonide, ciclesonide, fluticasone furoate, fluticasone propionate or mometasone) combined with a long-acting bronchodilator (β2 -agonist or anticholinergic or both).

摘要

芬兰医学协会十二门徒会发起并管理了芬兰慢性阻塞性肺疾病(COPD)国家指南的更新。芬兰COPD指南进行了修订,以认可COPD诊断和管理方面的进展。这份英文的芬兰COPD指南是原始指南的一部分,重点关注稳定期COPD的诊断、评估和药物治疗。它主要 intended to be used mainly in primary health care but not forgetting respiratory specialists and other healthcare workers. 新的建议和声明基于医学文献、其他已发表的国家指南以及慢性阻塞性肺疾病全球倡议(GOLD)报告中可得的最佳证据。本指南介绍了诊断方法、与哮喘的鉴别诊断、控制症状和预防急性加重的评估及治疗策略。药物治疗基于个体患者的症状和临床表型。该指南定义了三种具有临床相关性的表型,包括低急性加重风险表型和高急性加重风险表型以及被忽视的哮喘-慢性阻塞性肺疾病重叠综合征(ACOS)。这些临床表型可帮助临床医生识别对特定药物干预有反应的患者。对于低急性加重风险表型,症状较轻的患者建议使用短效β2受体激动剂(沙丁胺醇、特布他林)或抗胆碱能药物(异丙托溴铵)或它们的联合制剂(非诺特罗-异丙托溴铵)进行药物治疗。如果短效支气管扩张剂不足以控制症状,则建议使用长效β2受体激动剂(福莫特罗、茚达特罗、奥达特罗或沙美特罗)或长效抗胆碱能药物(毒蕈碱受体拮抗剂;阿地溴铵、格隆溴铵、噻托溴铵、乌美溴铵)或它们的联合制剂。对于高急性加重风险表型,建议首选长效抗胆碱能药物或吸入性糖皮质激素与长效β2受体激动剂的固定复方制剂(布地奈德-福莫特罗、二丙酸倍氯米松-福莫特罗、丙酸氟替卡松-沙美特罗或糠酸氟替卡松-维兰特罗)进行药物治疗。该表型的其他治疗选择包括从单独吸入器给药的长效支气管扩张剂联合制剂或固定复方制剂(格隆溴铵-茚达特罗或乌美溴铵-维兰特罗)或吸入性糖皮质激素、长效β2受体激动剂和长效抗胆碱能药物的三联复方制剂。如果患者患有重度至极重度COPD(FEV1<预测值的50%)、慢性支气管炎且尽管使用了长效支气管扩张剂仍频繁急性加重,则药物治疗可能还包括罗氟司特。ACOS是COPD的一种表型,其具有符合哮喘和COPD两者的特征。属于该表型的患者通常在评估哮喘和COPD药物疗效的研究中被排除。因此,无法给出基于证据的治疗建议。治疗应涵盖两种疾病。一般来说,治疗应至少包括吸入性糖皮质激素(二丙酸倍氯米松、布地奈德、环索奈德、糠酸氟替卡松、丙酸氟替卡松或莫米松)与长效支气管扩张剂(β2受体激动剂或抗胆碱能药物或两者)联合使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f0/4409821/eafe7d3ce317/bcpt0116-0291-f1.jpg

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