2025 非结核分枝杆菌肺病与支气管扩张症复合病的诊断与治疗专家共识
编写组专家名单:
顾问:唐神结(首都医科大学附属北京胸科医院);瞿介明(上海交通大学医学院附属瑞金医院);李亮(首都医科大学附属北京胸科医院);曹彬(中日友好医院)
总负责:沙巍、徐金富
执笔人:孙勤、王鹏、沙巍(同济大学附属上海市肺科医院);徐金富(复旦大学附属华东医院)
咨询讨论专家(按单位拼音字母排序):王华(安徽省胸科医院);沈宁(北京大学第三医院);彭丽(重庆医科大学附属第一医院);裴异(长沙市中心医院);邵凌云(复旦大学附属华山医院);揭志军(复旦大学附属上海市第五人民医院);宋元林(复旦大学附属中山医院);刘旭晖(复旦大学医学院附属公共卫生临床中心);陈品儒(广州市胸科医院);白冲、黄怡(海军军医大学第一附属医院);魏明(华中科技大学同济医学院附属武汉金银潭医院);王琳(解放军第九〇五医院);梁建琴(解放军总医院第八医学中心);苏欣(南京大学医学院附属鼓楼医院);张侠(南京市第二医院);任涛(上海交通大学医学院附属第六人民医院);秦慧(上海交通大学医学院附属仁济医院);程齐俭(上海交通大学医学院附属瑞金医院北院);陈雪融、张培泽(深圳市第三人民医院);初乃惠、丁卫民、段鸿飞、聂文娟(首都医科大学附属北京胸科医院);贺建清(四川大学华西医院);吴妹英(苏州市第五人民医院);高永华、顾瑾、李冰、刘一典、梁硕、陆海雯、毛贝、史祥、孙勤、王鹏、姚岚、郑旭彬(同济大学附属上海市肺科医院);何贵清(温州市中心医院);徐凯进、周华(浙江大学医学院附属第一医院);蔡青山(浙江大学医学院附属杭州市胸科医院);崔晓敬(中日友好医院)
证据评价组专家:张嵬(复旦大学);蒋泓、徐飚、赵琦(复旦大学公 共卫生学院) 利益冲突 所有作者声明无利益冲突
参 考 文 献
[1] 中华医学会结核病学分会 . 非结核分枝杆菌病诊断与治疗指 南 (2020 年版 )[J]. 中华结核和呼吸杂志 , 2020, 43(11): 918‑946. DOI: 10.3760/cma.j.cn112147‑20200508‑00570. [2] Daley CL, Iaccarino JM, Lange C, et al. Treatment of nontuberculous mycobacterial pulmonary disease: an official ATS/ERS/ESCMID/IDSA clinical practice guideline [J]. Eur Respir J, 2020, 56(1): 2000535. DOI: 10.1183/13993003.00535-2020. [3] Hill AT, Sullivan AL, Chalmers JD, et al. British Thoracic Society Guideline for bronchiectasis in adults[J]. Thorax, 2019, 74(Suppl 1): 1‑69. DOI: 10.1136/ thoraxjnl‑2018‑212463. [4] 支气管扩张症专家共识撰写协作组 , 中华医学会呼吸病学 分会感染学组 . 中国成人支气管扩张症诊断与治疗专家共 识 [J]. 中华结核和呼吸杂志 , 2021, 44(4):311‑321. DOI: 10.3760/cma.j.cn112147‑20200617‑00717. [5] 周玉民 , 王辰 , 姚婉贞 , 等 . 我国 7 省市城区 40 岁及以上居 民支气管扩张症的患病情况及危险因素调查 [J]. 中华内科 杂志 , 2013, 52(5): 379‑382. DOI: 10.3760/cma. j. issn.0578‑1426.2013.05.006. [6] 王宇 . 全国第五次结核病流行病学抽样调查调查资料汇编 [M]. 北京 : 军事医学科学出版社 , 2011. [7] Tan Y, Deng Y, Yan X, et al. Nontuberculous mycobacterial pulmonary disease and associated risk factors in China: A prospective surveillance study[J]. J Infect, 2021, 83(1): 46‑53. DOI: 10.1016/j.jinf.2021.05.019. [8] Liu CF, Song YM, He WC, et al. Nontuberculous mycobacteria in China: incidence and antimicrobial resistance spectrum from a nationwide survey[J]. Infect Dis Poverty, 2021, 10(1): 59. DOI: 10.1186/ s40249‑021‑00844‑1. [9] Mirsaeidi M, Hadid W, Ericsoussi B, et al. Non‑tuberculous mycobacterial disease is common in patients with non‑cystic fibrosis bronchiectasis[J]. Int J Infect Dis, 2013, 17(11):e1000‑1004. DOI: 10.1016/j.ijid.2013.03.018. [10] Kim HJ, Yim JJ. Bronchiectasis and Nontuberculous Mycobacteria: It Is Not Over till It Is Over[J]. Respiration, 2021, 100(12):1149‑1150. DOI: 10.1159/000518329. [11] Quint JK, Millett ER, Joshi M, et al. Changes in the incidence, prevalence and mortality of bronchiectasis in the UK from 2004 to 2013: a population‑based cohort study[J]. Eur Respir J, 2016, 47(1): 186‑193. DOI: 10.1183/13993003.01033-2015. [12] Weycker D, Hansen GL, Seifer FD. Prevalence and incidence of noncystic fibrosis bronchiectasis among US adults in 2013[J]. Chron Respir Dis, 2017, 14(4):377‑384. DOI: 10.1177/1479972317709649. [13] Winthrop KL, Marras TK, Adjemian J, et al. Incidence and Prevalence of Nontuberculous Mycobacterial Lung Disease in a Large U. S. Managed Care Health Plan, 2008‑2015[J]. Ann Am Thorac Soc, 2020, 17(2):178‑185. DOI: 10.1513/AnnalsATS.201804‑236OC. [14] Chaisson RE, Benson CA, Dube MP, et al. Clarithromycin disease. A randomized, double‑blind, dose‑ranging study in patients with AIDS. AIDS Clinical Trials Group Protocol 157 Study Team[J]. Ann Intern Med, 1994, 121(12): 905‑911. DOI: 10.7326/0003‑4819‑121‑12‑199412150‑00001. [15] Polverino E, Goeminne PC, McDonnell MJ, et al. European Respiratory Society guidelines for the management of adult bronchiectasis[J]. Eur Respir J, 2017, 50(3): 1700629 [pii]. DOI: 10.1183/13993003.00629-2017. [16] Aliberti S, Hill AT, Mantero M, et al. Quality standards for the management of bronchiectasis in Italy: a national audit[J]. Eur Respir J, 2016, 48(1): 244‑248. DOI: 10.1183/13993003.00232-2016. [17] O′Donnell AE. Bronchiectasis‑A Clinical Review[J]. N Engl J Med, 2022, 387(6): 533‑545. DOI: 10.1056/ NEJMra2202819. [18] Aksamit TR, O′Donnell AE, Barker A, et al. Adult Patients With Bronchiectasis: A First Look at the US Bronchiectasis Research Registry[J]. Chest, 2017, 151(5): 982‑992. DOI: 10.1016/j.chest.2016.10.055. [19] Lonni S, Chalmers JD, Goeminne PC, et al. Etiology of Non‑Cystic Fibrosis Bronchiectasis in Adults and Its Correlation to Disease Severity[J]. Ann Am Thorac Soc, 2015, 12(12): 1764‑1770. DOI: 10.1513/ AnnalsATS.201507‑472OC. [20] Chandrasekaran R, Mac Aogáin M, Chalmers JD, et al. Geographic variation in the aetiology, epidemiology and microbiology of bronchiectasis[J]. BMC Pulm Med, 2018, 18(1):83. DOI: 10.1186/s12890‑018‑0638‑0. [21] Qi Q, Wang W, Li T, et al. Aetiology and clinical characteristics of patients with bronchiectasis in a Chinese Han population: A prospective study[J]. Respirology, 2015, 20(6): 917‑924. DOI: 10.1111/ resp.12574. [22] Guan WJ, Gao YH, Xu G, et al. Aetiology of bronchiectasis in Guangzhou, southern China[J]. Respirology, 2015, 20(5):739‑748. DOI: 10.1111/resp.12528. [23] 葛亚如 , 史琦 , 阎玥 , 等 . 成人非囊性纤维化支气管扩张的 病因及诊断 [J]. 中日友好医院学报 , 2018, 32(5):307‑310. DOI: 10.3969/j.issn.1001‑0025.2018.05.015. [24] 田欣伦 , 吴翔 , 徐凯峰 , 等 . 成人支气管扩张患者的病因及 临床特点分析 [J]. 中国呼吸与危重监护杂志 , 2013, 12(6): 576‑580. DOI: 10.7507/1671‑6205.20130137. [25] Gao YH, Guan WJ, Liu SX, et al. Aetiology of bronchiectasis in adults: A systematic literature review[J]. Respirology, 2016, 21(8):1376‑1383. DOI: 10.1111/resp.12832. [26] Chai YH, Xu JF. How does Pseudomonas aeruginosa affect the progression of bronchiectasis? [J]. Clin Microbiol Infect, 2020, 26(3): 313‑318. DOI: 10.1016/j. cmi.2019.07.010. [27] 徐金富 , 柴燕华 . 支气管扩张症患者下呼吸道分离出铜绿假 单胞菌的临床意义和对策 [J]. 中华结核和呼吸杂志 , 2019, 42(7): 506‑509. DOI: 10.3760/cma.j.issn.1001‑0939.2109.07.009. [28] Lin JL, Xu JF, Qu JM. Bronchiectasis in China[J]. Ann Am Thorac Soc, 2016, 13(5): 609‑616. DOI: 10.1513/ AnnalsATS.201511‑740PS. [29] Mirsaeidi M, Machado RF, Garcia JG, et al. Nontuberculous mycobacterial disease mortality in the United States, 1999‑2010: a population‑based comparative study[J]. PLoS One, 2014, 9(3): e91879. DOI: 10.1371/journal. pone.0091879. [30] Renna M, Schaffner C, Brown K, et al. Azithromycin blocks autophagy and may predispose cystic fibrosis patients to mycobacterial infection[J]. J Clin Invest, 2011, 121(9): 3554‑3563. DOI: 10.1172/JCI46095. [31] Shteinberg M, Stein N, Adir Y, et al. Prevalence, risk factors and prognosis of nontuberculous mycobacterial infection among people with bronchiectasis: a population survey[J]. Eur Respir J, 2018, 51(5): 1702469 [pii]. DOI: 10.1183/13993003.02469-2017. [32] Bonaiti G, Pesci A, Marruchella A, et al. Nontuberculous Mycobacteria in Noncystic Fibrosis Bronchiectasis[J]. Biomed Res Int, 2015, 2015: 197950. DOI: 10.1155/2015/197950. [33] Zhu YN, Xie JQ, He XW, et al. Prevalence and Clinical Characteristics of Nontuberculous Mycobacteria in Patients with Bronchiectasis: A Systematic Review and Meta‑Analysis[J]. Respiration, 2021, 100(12): 1218‑1229. DOI: 10.1159/000518328. [34] Yin H, Gu X, Wang Y, et al. Clinical characteristics of patients with bronchiectasis with nontuberculous mycobacterial disease in Mainland China: a single center cross‑sectional study[J]. BMC Infect Dis, 2021, 21(1): 1216. DOI: 10.1186/s12879‑021‑06917‑8. [35] Garcia B, Wilmskoetter J, Grady A, et al. Chest Computed Tomography Features of Nontuberculous Mycobacterial Pulmonary Disease Versus Asymptomatic Colonization: A Cross‑sectional Cohort Study[J]. J Thorac Imaging, 2022, 37(3):140‑145. DOI: 10.1097/RTI.0000000000000610. [36] Kwak N, Lee JH, Kim HJ, et al. New‑onset nontuberculous mycobacterial pulmonary disease in bronchiectasis: tracking the clinical and radiographic changes[J]. BMC Pulm Med, 2020, 20(1): 293. DOI: 10.1186/ s12890‑020‑01331‑3. [37] Wei W, Cao J, Wu XC, et al. Diagnostic performance of metagenomic next‑generation sequencing in non‑tuberculous mycobacterial pulmonary disease when applied to clinical practice[J]. Infection, 2023, 51(2): 397‑405. DOI: 10.1007/s15010‑022‑01890‑z. [38] Yao L, Gui X, Wu X, et al. Rapid Identification of Nontuberculous Mycobacterium Species from Respiratory Specimens Using Nucleotide MALDI‑TOF MS [J]. Microorganisms, 2023, 11(8): 1975. DOI: 10.3390/ microorganisms11081975. [39] 中国人民解放军总医院第八医学中心结核病医学部 《中 国防痨杂志》编辑委员会 , 中国医疗保健国际交流促进会 结核病防治分会 . 核酸基质辅助激光解吸电离飞行时间质 谱技术在结核病和非结核分枝杆菌病诊断中的临床应用 专家共识 [J]. 中国防痨杂志 , 2023, 45(6):543‑558. DOI: 10.19982/j.issn.1000‑6621.20230113. [40] 高通量测序共识专家组 . 高通量测序技术在分枝杆菌病诊断 中的应用专家共识 [J]. 中华传染病杂志 , 2023, 41(3):175‑182. DOI: 10.3760/cma.j.cn311365‑20221203‑00492. [41] Fan LC, Lin JL, Yang JW, et al. Macrolides protect against Pseudomonas aeruginosa infection via inhibition of inflammasomes[J]. Am J Physiol Lung Cell Mol Physiol, 2017, 313(4): L677‑L686. DOI: 10.1152/ ajplung.00123.2017. [42] Fan LC, Xu JF. Advantages and drawbacks of long‑term macrolide use in the treatment of non‑cystic fibrosis bronchiectasis[J]. J Thorac Dis, 2014, 6(7):867‑871. DOI: 10.3978/j.issn.2072‑1439.2014.07.24.
[43]
范莉超, 徐金富. 大环内酯类药物维持治疗对支气管扩张
症的应用价值 [J]. 中华结核和呼吸杂志 , 2014, 37(1): 48‑50. DOI: 10.3760/cma.j.issn.1001‑0939.2014.01.014. [44] 席秀红 , 毕晶 , 李涛 , 等 . 成人非囊性纤维化性支气管扩张 的诊治进展 [J]. 国际呼吸杂志 , 2014, 34(12):953‑957. DOI: 10.3760/cma.j.issn.1673‑436X.2014.12.017. [45] Fan LC, Lu HW, Wei P, et al. Effects of long‑term use of macrolides in patients with non‑cystic fibrosis bronchiectasis: a meta‑analysis of randomized controlled trials[J]. BMC Infect Dis, 2015, 15: 160. DOI: 10.1186/ s12879‑015‑0872‑5. [46] Haworth CS, Banks J, Capstick T, et al. British Thoracic Society guidelines for the management of non‑tuberculous mycobacterial pulmonary disease (NTM‑PD) [J]. Thorax, 2017, 72(Suppl 2): ii1‑ii64. DOI: 10.1136/thoraxjnl‑2017‑210927. [47] Pasipanodya JG, Ogbonna D, Deshpande D, et al. Meta‑analyses and the evidence base for microbial outcomes in the treatment of pulmonary Mycobacterium avium‑intracellulare complex disease[J]. J Antimicrob Chemother, 2017, 72(suppl_2): i3‑i19. DOI: 10.1093/ jac/dkx311. [48] Kwak N, Park J, Kim E, et al. Treatment Outcomes of Mycobacterium avium Complex Lung Disease: A Systematic Review and Meta‑analysis[J]. Clin Infect Dis, 2017, 65(7):1077‑1084. DOI: 10.1093/cid/cix517. [49] Diel R, Nienhaus A, Ringshausen FC, et al. Microbiologic Outcome of Interventions Against Mycobacterium avium Complex Pulmonary Disease: A Systematic Review[J]. Chest, 2018, 153(4): 888‑921. DOI: 10.1016/j. chest.2018.01.024. [50] Griffith DE, Brown‑Elliott BA, Langsjoen B, et al. Clinical and molecular analysis of macrolide resistance in Mycobacterium avium complex lung disease[J]. Am J Respir Crit Care Med, 2006, 174(8): 928‑934. DOI: 10.1164/rccm.200603‑450OC. [51] Kadota T, Matsui H, Hirose T, et al. Analysis of drug treatment outcome in clarithromycin‑resistant Mycobacterium avium complex lung disease[J]. BMC Infect Dis, 2016, 16: 31. DOI: 10.1186/ s12879‑016‑1384‑7. [52] Morimoto K, Namkoong H, Hasegawa N, et al. Macrolide‑Resistant Mycobacterium avium Complex Lung Disease: Analysis of 102 Consecutive Cases[J]. Ann Am Thorac Soc, 2016, 13(11): 1904‑1911. DOI: 10.1513/ AnnalsATS.201604‑246OC. [53] Moon SM, Park HY, Kim SY, et al. Clinical Characteristics, Treatment Outcomes, and Resistance Mutations Associated with Macrolide‑Resistant Mycobacterium avium Complex Lung Disease[J]. Antimicrob Agents Chemother, 2016, 60(11): 6758‑6765. DOI: 10.1128/ AAC.01240‑16. [54] Pierce M, Crampton S, Henry D, et al. A randomized trial of clarithromycin as prophylaxis against disseminated Mycobacterium avium complex infection in patients with advanced acquired immunodeficiency syndrome[J]. N Engl J Med, 1996, 335(6): 384‑391. DOI: 10.1056/ NEJM199608083350603. [55] Griffith DE, Aksamit T, Brown‑Elliott BA, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases[J]. Am J Respir Crit Care Med, 2007, 175(4): 367‑416. DOI: 10.1164/rccm.200604‑571ST. [56] Hwang JA, Kim S, Jo KW, et al. Natural history of Mycobacterium avium complex lung disease in untreated patients with stable course[J]. Eur Respir J, 2017, 49(3): 1600537 [pii]. DOI: 10.1183/13993003.00537-2016. [57] Davies G, Wells AU, Doffman S, et al. The effect of Pseudomonas aeruginosa on pulmonary function in patients with bronchiectasis[J]. Eur Respir J, 2006, 28(5): 974‑979. DOI: 10.1183/09031936.06.00074605. [58] Martínez‑García MA, Soler‑Cataluña JJ, Perpiñá‑Tordera M, et al. Factors associated with lung function decline in adult patients with stable non‑cystic fibrosis bronchiectasis[J]. Chest, 2007, 132(5): 1565‑1572. DOI: 10.1378/chest.07‑0490. [59] Araújo D, Shteinberg M, Aliberti S, et al. The independent contribution of Pseudomonas aeruginosa infection to long‑term clinical outcomes in bronchiectasis[J]. Eur Respir J, 2018, 51(2): 1701953 [pii]. DOI: 10.1183/13993003.01953-2017. [60] Tiew PY, Mac Aogáin M, Ter SK, et al. Respiratory Mycoses in COPD and Bronchiectasis[J]. Mycopathologia, 2021, 186(5):623‑638. DOI: 10.1007/s11046‑021‑00539‑z. [61] Mac Aogáin M, Narayana JK, Tiew PY, et al. Integrative microbiomics in bronchiectasis exacerbations[J]. Nat Med, 2021, 27(4): 688‑699. DOI: 10.1038/ s41591‑021‑01289‑7. [62] Budden KF, Shukla SD, Rehman SF, et al. Functional effects of the microbiota in chronic respiratory disease[J]. Lancet Respir Med, 2019, 7(10): 907‑920. DOI: 10.1016/ S2213‑2600(18)30510‑1. [63] Tiew PY, Jaggi TK, Chan L, et al. The airway microbiome in COPD, bronchiectasis and bronchiectasis‑COPD overlap [J]. Clin Respir J, 2021, 15(2): 123‑133. DOI: 10.1111/ crj.13294. [64] Tiew PY, Thng KX, Chotirmall SH. Clinical Aspergillus Signatures in COPD and Bronchiectasis[J]. J Fungi (Basel), 2022, 8(5):480. DOI: 10.3390/jof8050480. [65] Cheng LP, Chen SH, Lou H, et al. Factors Associated with Treatment Outcome in Patients with Nontuberculous Mycobacterial Pulmonary Disease: A Large Population‑Based Retrospective Cohort Study in Shanghai [J]. Trop Med Infect Dis, 2022, 7(2): 27. DOI: 10.3390/ tropicalmed7020027. [66] Cheng LP, Zhang Q, Lou H, et al. Effectiveness and safety of regimens containing linezolid for treatment of Mycobacterium abscessus pulmonary Disease[J]. Ann Clin Microbiol Antimicrob, 2023, 22(1): 106. DOI: 10.1186/ s12941‑023‑00655‑2. [67] Nasiri MJ, Ebrahimi G, Arefzadeh S, et al. Antibiotic therapy success rate in pulmonary Mycobacterium avium complex: a systematic review and meta‑analysis[J]. Expert Rev Anti Infect Ther, 2020, 18(3): 263‑273. DOI: 10.1080/14787210.2020.1720650. [68] Park Y, Lee EH, Jung I, et al. Clinical characteristics and treatment outcomes of patients with macrolide‑resistant Mycobacterium avium complex pulmonary disease: a systematic review and meta‑analysis[J]. Respir Res, 2019, 20(1):286. DOI: 10.1186/s12931‑019‑1258‑9. [69] Pasipanodya JG, Ogbonna D, Ferro BE, et al. Systematic Review and Meta‑analyses of the Effect of Chemotherapy
on Pulmonary Mycobacterium abscessus Outcomes and
2017, 61(11): e01206‑01217. DOI: 10.1128/ AAC.01206‑17. [70] Lee BY, Kim S, Hong Y, et al. Risk factors for recurrence after successful treatment of Mycobacterium avium complex lung disease[J]. Antimicrob Agents Chemother, 2015, 59(6):2972‑2977. DOI: 10.1128/AAC.04577‑14. [71] Basavaraj A, Segal L, Samuels J, et al. Effects of Chest Physical Therapy in Patients with Non‑Tuberculous Mycobacteria[J]. Int J Respir Pulm Med, 2017, 4(1): 065 [pii]. DOI: 10.23937/2378‑3516/1410065. [72] Chalmers JD, Chotirmall SH. Bronchiectasis: new therapies and new perspectives[J]. Lancet Respir Med, 2018, 6(9): 715‑726. DOI: 10.1016/S2213‑2600(18) 30053‑5. [73] Nathavitharana RR, Strnad L, Lederer PA, et al. Top Questions in the Diagnosis and Treatment of Pulmonary M. abscessus Disease[J]. Open Forum Infect Dis, 2019, 6(7):ofz221. DOI: 10.1093/ofid/ofz221. [74] Faverio P, De Giacomi F, Bodini BD, et al. Nontuberculous mycobacterial pulmonary disease: an integrated approach beyond antibiotics[J]. ERJ Open Res, 2021, 7(2): 00574‑02020 [pii]. DOI: 10.1183/23120541.00574-2020. [75] O′Brien C, Guest PJ, Hill SL, et al. Physiological and radiological characterisation of patients diagnosed with chronic obstructive pulmonary disease in primary care[J]. Thorax, 2000, 55(8): 635‑642. DOI: 10.1136/ thorax.55.8.635. [76] Patel IS, Vlahos I, Wilkinson TM, et al. Bronchiectasis, exacerbation indices, and inflammation in chronic obstructive pulmonary disease[J]. Am J Respir Crit Care Med, 2004, 170(4): 400‑407. DOI: 10.1164/ rccm.200305‑648OC. [77] Gatheral T, Kumar N, Sansom B, et al. COPD‑related bronchiectasis; independent impact on disease course and outcomes[J]. COPD, 2014, 11(6): 605‑614. DOI: 10.3109/15412555.2014.922174. [78] Martínez‑García MA, de la Rosa Carrillo D, Soler‑Cataluña JJ, et al. Prognostic value of bronchiectasis in patients with moderate‑to‑severe chronic obstructive pulmonary disease[J]. Am J Respir Crit Care Med, 2013, 187(8): 823‑831. DOI: 10.1164/rccm.201208‑1518OC. [79] Mao B, Yang JW, Lu HW, et al. Asthma and bronchiectasis exacerbation[J]. Eur Respir J, 2016, 47(6): 1680‑1686. DOI: 10.1183/13993003.01862-2015. [80] 中华医学会呼吸病学分会哮喘学组 . 支气管哮喘防治指南 (2020 年版 )[J]. 中华结核和呼吸杂志 , 2020, 43(12):1023‑1048. DOI: 10.3760/cma.j.cn112147‑20200618‑00721. [81] 中国系统性红斑狼疮研究协作组专家组 . 糖皮质激素在系 统性红斑狼疮患者合理应用的专家共识 [J]. 中华内科杂志 , 2014, 53(6): 502‑504. DOI: 10.3760/cma. j. issn.0578‑1426.2014.06.023. [82] 中华医学会风湿病学分会 . 2018 中国类风湿关节炎诊疗 指南 [J]. 中华内科杂志 , 2018, 57(4): 242‑251. DOI: 10.3760/cma.j.issn.0578‑1426.2018.04.004. [83] 中国人民解放军总医院第八医学中心结核病医学部 / 全军 结核病研究所 / 全军结核病防治重点实验室 / 结核病诊疗 新技术北京市重点实验室 《中国防痨杂志》编辑委员会 . 糖皮质激素在结核病治疗中的合理应用专家共识 [J]. 中国 防痨杂志 , 2022, 44(1): 28‑37. DOI: 10.19982/j. issn.1000‑6621.20210683. [84] Yu JA, Pomerantz M, Bishop A, et al. Lady Windermere revisited: treatment with thoracoscopic lobectomy/segmentectomy for right middle lobe and lingular bronchiectasis associated with non‑tuberculous mycobacterial disease[J]. Eur J Cardiothorac Surg, 2011, 40(3):671‑675. DOI: 10.1016/j.ejcts.2010.12.028. [85] Corpe RF. Surgical management of pulmonary disease due to Mycobacterium avium‑intracellulare[J]. Rev Infect Dis, 1981, 3(5): 1064‑1067. DOI: 10.1093/clinids/ 3.5.1064. [86] Koh WJ, Kim YH, Kwon OJ, et al. Surgical treatment of pulmonary diseases due to nontuberculous mycobacteria [J]. J Korean Med Sci, 2008, 23(3):397‑401. DOI: 10.3346/ jkms.2008.23.3.397. [87] Law SW. Surgical treatment of atypical Mycobacterial disease; a survey of experience in veterans administration hospitals[J]. Dis Chest, 1965, 47:296‑303. DOI: 10.1378/chest.47.3.296. [88] Mitchell JD, Bishop A, Cafaro A, et al. Anatomic lung resection for nontuberculous mycobacterial disease[J]. Ann Thorac Surg, 2008, 85(6): 1887‑1892; discussion 1892‑1893. DOI: 10.1016/j.athoracsur.2008.02.041. [89] Moran JF, Alexander LG, Staub EW, et al. Long‑term results of pulmonary resection for atypical mycobacterial disease[J]. Ann Thorac Surg, 1983, 35(6): 597‑604. DOI: 10.1016/s0003‑4975(10)61069‑7. [90] Muangsombut J, Hankins JR, Miller JE, et al. Surgical treatment of pulmonary infections caused by atypical mycobacteria[J]. Am Surg, 1975, 41(1):37‑40. [91] Nelson KG, Griffith DE, Brown BA, et al. Results of operation in Mycobacterium avium‑intracellulare lung disease[J]. Ann Thorac Surg, 1998, 66(2): 325‑330. DOI: 10.1016/s0003‑4975(98)00401‑9. [92] Ono N, Satoh K, Yokomise H, et al. Surgical management of Mycobacterium avium complex disease[J]. Thorac Cardiovasc Surg, 1997, 45(6): 311‑313. DOI: 10.1055/ s‑2007‑1013756. [93] Parrot RG, Grosset JH. Post‑surgical outcome of 57 patients with Mycobacterium xenopi pulmonary infection [J]. Tubercle, 1988, 69(1): 47‑55. DOI: 10.1016/0041‑3879(88)90040‑2. [94] Shiraishi Y, Fukushima K, Komatsu H, et al. Early pulmonary resection for localized Mycobacterium avium complex disease[J]. Ann Thorac Surg, 1998, 66(1): 183‑186. DOI: 10.1016/s0003‑4975(98)00373‑7. [95] Shiraishi Y, Nakajima Y, Takasuna K, et al. Surgery for Mycobacterium avium complex lung disease in the clarithromycin era[J]. Eur J Cardiothorac Surg, 2002, 21(2):314‑318. DOI: 10.1016/s1010‑7940(01)01122‑8. [96] Shiraishi Y, Katsuragi N, Kita H, et al. Different morbidity after pneumonectomy: multidrug‑resistant tuberculosis versus non‑tuberculous mycobacterial infection[J]. Interact Cardiovasc Thorac Surg, 2010, 11(4): 429‑432. DOI: 10.1510/icvts.2010.236372. [97] Tsunezuka Y, Sato H, Hiranuma C. Surgical outcome of mycobacterium other than mycobacterium tuberculosis pulmonary disease[J]. Thorac Cardiovasc Surg, 2000, 48(5):290‑293. DOI: 10.1055/s‑2000‑7884. [98] van Ingen J, Verhagen AF, Dekhuijzen PN, et al. Surgical treatment of non‑tuberculous mycobacterial lung disease: strike in time[J]. Int J Tuberc Lung Dis, 2010, 14(1): [99] Watanabe M, Hasegawa N, Ishizaka A, et al. Early pulmonary resection for Mycobacterium avium complex lung disease treated with macrolides and quinolones[J]. Ann Thorac Surg, 2006, 81(6):2026‑2030. DOI: 10.1016/j. athoracsur.2006.01.031. [100] Zvetina JR, Neville WE, Maben HC, et al. Surgical treatment of pulmonary disease due to Mycobacterium kansasii[J]. Ann Thorac Surg, 1971, 11(6): 551‑556. DOI: 10.1016/s0003‑4975(10)65071‑0. [101] Shiraishi Y, Katsuragi N, Kita H, et al. Adjuvant surgical treatment of nontuberculous mycobacterial lung disease [J]. Ann Thorac Surg, 2013, 96(1):287‑291. DOI: 10.1016/ j.athoracsur.2013.03.008. [102] Wang GS, Wang Z, Yang L, et al. Thoracoscopic management for bronchiectasis with non‑tuberculous mycobacterial infection[J]. Chin Med J (Engl), 2008, 121(24):2539‑2543. [103] Mitchell JD. Surgical Treatment of Pulmonary Nontuberculous Mycobacterial Infections[J]. Thorac Surg Clin, 2019, 29(1): 77‑83. DOI: 10.1016/j. thorsurg.2018.09.011. [104] Choi Y, Jhun BW, Kim J, et al. Clinical Characteristics and Outcomes of Surgically Resected Solitary Pulmonary Nodules Due to Nontuberculous Mycobacterial Infections [J]. J Clin Med, 2019, 8(11): 1898. DOI: 10.3390/ jcm8111898. [105] Yamada K, Seki Y, Nakagawa T, et al. Outcomes and risk factors after adjuvant surgical treatments for Mycobacterium avium complex lung disease[J]. Gen Thorac Cardiovasc Surg, 2019, 67(4): 363‑369. DOI: 10.1007/s11748‑018‑1029‑4. [106] Griffith DE, Adjemian J, Brown‑Elliott BA, et al. Semiquantitative Culture Analysis during Therapy for Mycobacterium avium Complex Lung Disease[J]. Am J Respir Crit Care Med, 2015, 192(6): 754‑760. DOI: 10.1164/rccm.201503‑0444OC. [107] van Ingen J, Aksamit T, Andrejak C, et al. Treatment outcome definitions in nontuberculous mycobacterial pulmonary disease: an NTM‑NET consensus statement[J]. Eur Respir J, 2018, 51(3): 1800170. DOI: 10.1183/13993003.00170 - 2018. [108] Wallace RJ Jr, Brown‑Elliott BA, McNulty S, et al. Macrolide/Azalide therapy for nodular/bronchiectatic mycobacterium avium complex lung disease[J]. Chest, 2014, 146(2):276‑282. DOI: 10.1378/chest.13‑2538. [109] Zo S, Kim H, Kwon OJ, et al. Antibiotic Maintenance and Redevelopment of Nontuberculous Mycobacteria Pulmonary Disease after Treatment of Mycobacterium avium Complex Pulmonary Disease[J]. Microbiol Spectr, 2022, 10(4): e0108822. DOI: 10.1128/ spectrum.01088‑22. [110] Wallace RJ Jr, Zhang Y, Brown‑Elliott BA, et al. Repeat positive cultures in Mycobacterium intracellulare lung disease after macrolide therapy represent new infections in patients with nodular bronchiectasis[J]. J Infect Dis, 2002, 186(2):266‑273. DOI: 10.1086/341207. [111] Field SK, Fisher D, Cowie RL. Mycobacterium avium complex pulmonary disease in patients without HIV infection[J]. Chest, 2004, 126(2):566‑581. DOI: 10.1378/ chest.126.2.566. [112] Xu HB, Jiang RH, Li L. Treatment outcomes for Mycobacterium avium complex: a systematic review and meta‑analysis[J]. Eur J Clin Microbiol Infect Dis, 2014, 33(3):347‑358. DOI: 10.1007/s10096‑013‑1962‑1. [113] Suska K, Amati F, Sotgiu G, et al. Nontuberculous mycobacteria infection and pulmonary disease in bronchiectasis[J]. ERJ Open Res, 2022, 8(4):00060‑02022 [pii]. DOI: 10.1183/23120541.00060-2022. [114] Dawson DJ. Potential pathogens among strains of mycobacteria isolated from house‑dusts[J]. Med J Aust, 1971, 1(13): 679‑681. DOI: 10.5694/j. 1326‑5377.1971. tb87787.x. [115] Torvinen E, Torkko P, Rintala AN. Real‑time PCR detection of environmental mycobacteria in house dust[J]. J Microbiol Methods, 2010, 82(1): 78‑84. DOI: 10.1016/j. mimet.2010.04.007. [116] De Groote MA, Pace NR, Fulton K, et al. Relationships between Mycobacterium isolates from patients with pulmonary mycobacterial infection and potting soils[J]. Appl Environ Microbiol, 2006, 72(12): 7602‑7606. DOI: 10.1128/AEM.00930‑06. [117] Iivanainen E, Martikainen P, Raisanen M, et al. Mycobacteria in coniferous forest soils[J]. FEMS Microbiol Ecol, 1997, 23: 325‑332. DOI: 10.1016/S0168‑6496(97) 00040‑844. [118] Falkinham JO 3rd, Iseman MD, de Haas P, et al. Mycobacterium avium in a shower linked to pulmonary disease[J]. J Water Health, 2008, 6(2): 209‑213. DOI: 10.2166/wh.2008.032. [119] Feazel LM, Baumgartner LK, Peterson KL, et al. Opportunistic pathogens enriched in showerhead biofilms [J]. Proc Natl Acad Sci U S A, 2009, 106(38):16393‑16399. DOI: 10.1073/pnas.0908446106. [120] Thomson R, Tolson C, Carter R, et al. Isolation of nontuberculous mycobacteria (NTM) from household water and shower aerosols in patients with pulmonary disease caused by NTM[J]. J Clin Microbiol, 2013, 51(9): 3006‑3011. DOI: 10.1128/JCM.00899‑13. [121] Slosárek M, Kubín M, Jaresová M. Water‑borne household infections due to Mycobacterium xenopi[J]. Cent Eur J Public Health, 1993, 1(2):78‑80. [122] Donohue MJ, Mistry JH, Donohue JM, et al. Increased Frequency of Nontuberculous Mycobacteria Detection at Potable Water Taps within the United States[J]. Environ Sci Technol, 2015, 49(10):6127‑6133. DOI: 10.1021/acs. est.5b00496. [123] Iivanainen E, Northrup J, Arbeit RD, et al. Isolation of mycobacteria from indoor swimming pools in Finland[J]. APMIS, 1999, 107(2): 193‑200. DOI: 10.1111/ j.1699‑0463.1999.tb01544.x. [124] Mangione EJ, Huitt G, Lenaway D, et al. Nontuberculous mycobacterial disease following hot tub exposure[J]. Emerg Infect Dis, 2001, 7(6): 1039‑1042. DOI: 10.3201/ eid0706.010623. [125] Falkinham JO 3rd. Ecology of nontuberculous mycobacteria‑‑where do human infections come from?[J]. Semin Respir Crit Care Med, 2013, 34(1): 95‑102. DOI: 10.1055/s‑0033‑1333568. [126] Morimoto K, Yoshiyama T, Kurashima A, et al. Nutritional indicators are correlated with the radiological severity score in patients with Mycobacterium avium complex pulmonary disease: a cross‑sectional study[J]. Intern Med, 2014, 53(5): 397‑401. DOI: 10.2169/ internalmedicine.53.1277. [127] Faverio P, Stainer A, Bonaiti G, et al. Characterizing Non‑Tuberculous Mycobacteria Infection in Bronchiectasis[J]. Int J Mol Sci, 2016, 17(11): 1913. DOI: 10.3390/ijms17111913. [128] Fujita K, Ito Y, Oguma T, et al. Association between Mycobacterium avium complex lung disease and serum vitamin D status, antimicrobial peptide levels, and bone mineral density[J]. Medicine (Baltimore), 2018, 97(38): e12463. DOI: 10.1097/MD.0000000000012463. [129] Chan ED, Iseman MD. Slender, older women appear to be more susceptible to nontuberculous mycobacterial lung disease[J]. Gend Med, 2010, 7(1): 5‑18. DOI: 10.1016/j. genm.2010.01.005. [130] Ikegame S, Maki S, Wakamatsu K, et al. Nutritional assessment in patients with pulmonary nontuberculous mycobacteriosis[J]. Intern Med, 2011, 50(21):2541‑2546. DOI: 10.2169/internalmedicine.50.5853. [131] Gochi M, Takayanagi N, Kanauchi T, et al. Retrospective study of the predictors of mortality and radiographic deterioration in 782 patients with nodular/bronchiectatic Mycobacterium avium complex lung disease[J]. BMJ Open, 2015, 5(8): e008058. DOI: 10.1136/bmjopen‑2015‑008058. [132] Hayashi M, Takayanagi N, Kanauchi T, et al. Prognostic factors of 634 HIV‑negative patients with Mycobacterium avium complex lung disease[J]. Am J Respir Crit Care Med, 2012, 185(5): 575‑583. DOI: 10.1164/ rccm.201107‑1203OC. [133] Kim RD, Greenberg DE, Ehrmantraut ME, et al. Pulmonary nontuberculous mycobacterial disease: prospective study of a distinct preexisting syndrome[J]. Am J Respir Crit Care Med, 2008, 178(10): 1066‑1074. DOI: 10.1164/ rccm.200805‑686OC. [134] Nishiyama O, Kondoh Y, Kimura T, et al. Effects of pulmonary rehabilitation in patients with idiopathic pulmonary fibrosis[J]. Respirology, 2008, 13(3):394‑399. DOI: 10.1111/j.1440‑1843.2007.01205.x. [135] O′Neill K, O′Donnell AE, Bradley JM. Airway clearance, mucoactive therapies and pulmonary rehabilitation in bronchiectasis[J]. Respirology, 2019, 24(3):227‑237. DOI: 10.1111/resp.13459. [136] Severiche‑Bueno D, Gamboa E, Reyes LF, et al. Hot topics and current controversies in non‑cystic fibrosis bronchiectasis[J]. Breathe (Sheff), 2019, 15(4): 286‑295. DOI: 10.1183/20734735.0261-2019.
| 证据质量 | 具体描述 | 研究类型 | 表达字母 |
|---|---|---|---|
| 蕾 | 非常确信真实的效应值接近效应估计值 | 高质量的随机对照试验(RCT);系统评价/Meta分析 | |
| 对效应估计值有中等程度的信心;真实值有可能接近估计有研究缺陷的RCT;低质量的系统评价/Meta分析;高质量 的观察性研究 | B | ||
| 天 | 对效应估计值的确信程度有限;真实值可能与估计值大不非随机对照病例研究;其他观察性研究 同 | ||
| 极 | 对效应估计值没有信心;真实值很可能与估计值大不相同病例报道;专家意见 |
| 推荐强度 | 具体描述 | 表达数字 |
|---|---|---|
| 支持使用某项干预措施的强推荐 | 评价者确信干预措施利大于弊 | |
| 支持使用某项干预措施的弱推荐 | 利不确定或无论高低质量的证据均显示利相当 | |
| 反对使用某项干预措施的弱推荐 | 利不确定或无论高低质量的证据均显示利相当 | |
| 反对使用某项干预措施的强推荐 | 评价者确信干预措施大于利 |
| 病因 | 临床表现 | 检查及评估方法 |
|---|---|---|
| 既往下呼吸道感染 | ||
| 婴幼儿和儿童时期下呼吸道感染是支气管扩张症 最常见的病因,如麻疹、百日咳、肺结核、肺炎 (细菌、病毒、支原体)。其中铜绿假单胞菌的感 染或定植与支扩病情发生发展的关系尤为密切 | 下呼吸道感染症状 | 需详细询问患者的病史和合并症,尤其是幼年下呼 吸道感染病史 |
| 原发性:低免疫球蛋白血症 | ||
| 继发性:长期服用免疫抑制药物、HIV感染 | ||
| 气道阻塞或误吸 | 病史询问、HIV抗体和病毒载量、全血细胞计数、外 周血淋巴细胞亚群计数 | |
| 支气管哮喘症状 | 病史询问,有无误吸史。影像学检查、局灶性疾病 的支气管镜检查 | |
| 变应性支气管肺曲霉病 | 曲霉特异性IgE,血清总IgE水平 肺功能检查 | |
| 慢阻肺病或支气管哮喘 遗传因素 | 咳、痰、喘 | |
| 囊性纤维化 | 发病早,鼻窦炎、胰腺炎或吸收 汗液氯化物检测,囊性纤维化跨膜传导调节蛋白 (CFTR)基因突变 | |
| 原发性纤毛运动障碍 | 发病早,鼻窦炎,慢性扁桃体炎,鼻呼出气一氧化碳(FeNO)浓度检测、基因检测、纤 毛功能评估 | |
| αl-抗胰蛋白酶缺乏症 | 肺气肿 | αl-抗胰蛋白酶水平与表型 |
| 先天支气管病变:巨大气管-支气管症、软骨塌陷等 | CT检查 | |
| 自身免疫性疾病 | ||
| 类风湿性关节炎 | 晨僵等 | 类风湿因子 |
| 干燥综合征 | 口干、鼻干、眼干等 | 抗环瓜氨酸肽 |
| 硬皮病 | 面具脸等 | 抗核抗体 |
| 炎症性肠病 | 腹泻、便血 | 肠镜黏膜活检 |
| 项目 | 大容 |
|---|---|
| 临床表现具有呼吸系统症状和(或)全身性症状 | |
| 影像学经胸部影像学检查发现空洞性阴影、多灶性支气管扩张以及多发性小结节病变 | |
| 并且排除其他肺部疾病 | |
| 微生物学在确保标本无外源性污染的前提下,符合以下条件之一者可诊断为NTM肺病 | |
| 1.2份分开送检的痰标本NTM培养阳性并鉴定为同一致病菌,和(或)NTM分子生物学检测均为同一致病菌; 2.支气管冲洗液或支气管肺泡灌洗液NTM培养和(或)分子生物学检测1次阳性; | |
| 3.经支气管镜或其他途径肺活组织检查发现分枝杆菌病组织病理学特征性改变(肉芽肿性炎症或抗酸染色阳性),并且NTM培 养和(或)分子生物学检测阳性; | |
| 4.经支气管镜或其他途径肺活组织检查发现分枝杆菌病组织病理学特征性改变(肉芽肿性炎症或抗酸染色阳性),并且1次及 以上的痰标本、支气管冲洗液或支气管肺泡灌洗液中NTM培养和(或)分子生物学检测阳性。 |
推荐意见与 GRADE 证据分级
| # | 推荐意见 | 证据等级 | 出处 |
|---|---|---|---|
| 1 | 不同病因的支扩治疗策略和预后有所不同。因此,发现NTM‑PD 患者合并支扩时,建议对支扩病因学进行排查,有助于NTM‑PD 与支扩复合病患者的诊治和预后判断(1B)。 | 1B | |
| 2 | 支扩病因学的检查及评估方法,包括:1)询问病史和临床症状;2) 痰细菌、真菌、分枝杆菌培养等;检测血细胞计数、血清免疫球蛋白 $(\mathrm{{logG}\,\mathrm{{logM}\,\mathrm{{lgA})}}}$ )水平,曲霉特异性IgE、血清总IgE水平;检测肺功能;3)怀疑合并遗传或自身免疫性疾病时,进一步行相关的特殊检查。详见表3(1B)。 | 1B | |
| 3 | 具有以下4 种情况的支扩患者,建议重点排查是否合并NTM 感染:1)新诊断;2)临 | — | |
| 4 | 推荐的送检标本包括:(1)痰、诱导痰、支气管肺泡灌洗液等呼吸道标本;2)肺部穿刺及活检等病理标本。推荐的检测方法:抗酸染色涂片、分枝杆菌培养(固体或液体培养基)、菌种鉴定和药物敏感试验(1A);质谱、高通量测序等具有诊断效率快、可鉴定至菌种水平的优势,但不作为常规检测,建议参照相关指南或共识中的临床应用指征酌情开展高通量测序或质谱分析等分子检测以协助NTM‑PD的诊断(2B)。 | 1A | |
| 5 | 拟对支扩患者长期使用大环内酯类药物前,需明确其有无NTM‑PD 或既往有无NTM‑PD 病史,尤其是鸟分枝杆菌肺病。若存在上述情况,不建议长期、小剂量、单独使用大环内酯类药物治疗支扩(2C)。 | 2C | |
| 6 | 对于痰抗酸染色涂片阳性和(或)影像学有空洞样病灶改变的支扩合并NTM‑PD 患者,建议启动抗NTM治疗(2B)。 | 2B | |
| 7 | NTM‑PD 与支扩复合病患者,抗NTM 治疗期间,支扩感染病情加重,推荐在加用抗菌药物治疗前,完善痰及呼吸道分泌物的病原学检测,包括细菌、真菌培养及药敏检测(1A)。病原学结果出来前,建议维持原NTM 治疗,经验性加用抗菌药物治疗;抗菌药物的选择参考既往药敏结果,对既往无病原学培养结果的中重度支扩患者,建议常规覆盖铜绿假单胞菌(1B)。除细菌之外,病毒、真菌等其他病原体也可能与病情急性加重有关,应注意鉴别诊断(2C)。 | 1A | |
| 8 | 抗NTM 治疗失败、或无法耐受正规抗NTM 治疗方案的患者,考虑治疗重点应集中在支扩的治疗和管理(2C)。 | 2C | |
| 9 | NTM‑PD 与支扩复合病的患者,不考虑常规使用激素控制症状。如患者存在阻塞性通气功能障碍,优先推荐吸入性支气管舒张剂。合并哮喘、系统性红斑狼疮、类风湿性关节炎等需要使用激素控制病情的疾病时,参照各相关疾病诊治指南或共识谨慎使用激素(2C)。 | 2C | |
| 10 | 手术治疗需慎重,内科抗分枝杆菌治疗有效的情况下不推荐外科手术(1A)。建议应在经验丰富的、多学科专家评估后开展手术治疗(1B)。 | 1A | |
| 11 | 对于肺内病灶集中且局限,患者心肺功能能够耐受手术,无手术禁忌证,并且符合下列3 种情况或之一的复合病患者,建议外科手术治疗:1)多次药敏结果显示NTM 菌株对大环内酯类耐药,正规抗分枝杆菌药物治疗失败;或者感染大环内酯类耐药的脓肿分枝杆菌,经内科治疗效果不佳的患者;2)经药物治疗后虽症状缓解,病情好转,但发生难治性咯血甚至可能危及生命者的患者;(3)反复NTM 感染影响日常生活和工作的患者(1B)。 | 1B | |
| 12 | NTM‑PD 与支扩复合病患者,术后建议继续抗NTM 治疗,直至患者痰分枝杆菌培养转阴至少1年后停药(1B)。 | 1B | |
| 13 | 疗效与转归判定建议同时兼顾“NTM‑PD 的预后判定标准”和“支扩症状指标”(1B);判定可分为3 个等级:(1)治疗成功:符合NTM‑PD 判定标准 $\textcircled{\scriptsize{1}}$ \~ $\textcircled{4}$ 中任何1条,同时支扩病情稳定;2)好转:符合NTM‑PD 判定标准 $\textcircled{1}$ \~④中任何1 条,或支扩病情稳定;(3)治疗失败:符合NTM‑PD 判定标准 ${\widehat{\mathcal{S}}})\cdot$ \~ $\textcircled{2}$ 中任何1条,和(或)支扩反复急性加重(2D)。 | 1B | |
| 14 | 治疗成功的NTM‑PD 与支扩复合病患者,日常生活中,建议减少NTM 的环境暴露,评估生活方式和习惯(1B);对于体重指数低和(或)有体重减轻史的患者,可考虑进行营养评估和干预(2D);对于全身免疫功能低下或长期使用免疫抑制剂/激素的患者,应在专业医师指导下,在不影响原有疾病治疗的前提下,尽可能减少免疫抑制剂/激素的剂量或使用时间,同时建议定期复查胸部CT和痰分枝杆菌培养(2D)。 | 1B |
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引用 / 出处
中华医学会结核病学分会 中华医学会呼吸病学分会. 2025 非结核分枝杆菌肺病与支气管扩张症复合病的诊断与治疗专家共识[S/OL]. 2025.