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结缔组织病肺间质改变的诊治进展

结缔组织病肺间质改变的诊治进展. 北京协和医院风湿免疫科 张 烜. 间质性肺病( interstitial lung disease,ILD). CTD 的常见疾病 可以是 CTD 的首发症状 是预后不良的原因之一 是肺动脉高压( pulmonary hypertension,PAH) 的原因之一. 影响肺功能. respiratory muscle dysfunction recurrent aspiration (esophageal dysmotility) thromboembolic events

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结缔组织病肺间质改变的诊治进展

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  1. 结缔组织病肺间质改变的诊治进展 北京协和医院风湿免疫科 张 烜

  2. 间质性肺病(interstitial lung disease,ILD) • CTD的常见疾病 • 可以是CTD的首发症状 • 是预后不良的原因之一 • 是肺动脉高压(pulmonary hypertension,PAH)的原因之一

  3. 影响肺功能 • respiratory muscle dysfunction • recurrent aspiration (esophagealdysmotility) • thromboembolic events • Inflammationof the cricoarytenoid joints or • development ofbronchiectasis.

  4. ILD的发生率 • 15%的CTD合并ILD • 70% SSc合并肺部病变,2年内可发展为ILD,组织病理77.5%SSc伴ILD • 10%DM/PM合并ILD • 胸片显示3.7%RA合并ILD • SLE,SS,MCTD Clin Chest Med 2004;25:549 ~ 559 Am J Respir Crit Care Med 2002;165:1581 ~ 6 Ann Rheum Dis 2003 ; 62 : 897 ~ 900

  5. CTD中ILD的特点 CTD中的ILD发生率、严重度及病死率的比较1) 注:1)指5年之内因呼吸衰竭死亡 2)国外无对比数据 3)均为DM患者 张烜,董怡,张奉春.中华风湿病学杂志, 1999;3:247

  6. 分型的目的 自然病程、对激素反应、预后 CTD-UIP是否等同特发UIP?

  7. ILD病理和影像学特点

  8. Curr Opin Rheumtol 2004;16:186 ~ 191

  9. HRCT - non-specific interstitial pneumonia Systemic sclerosis DM/PM

  10. HRCT - usual interstitial pneumonia Systemic sclerosis RA DM/PM

  11. UIP-HRCT特点 • patchy pattern of peripheral “honeycombing” • more prominent in the bases of the lungs, • traction bronchiectasis • absence ofprominent ground-glass opacity.

  12. HRCT - chronic lymphocytic interstitial pneumonia Sjogren’s syndrome RA Drug induced

  13. HRCT obliterative bronchiolitis RA SLE Scleroderma PM/DM

  14. HRCT organizing pneumonia Gold SSZ MTX Sjogren’s syndrom RA

  15. HRCT a patient with RA 33% of with RA associated parenchymal lung disease 31 IPF Radiography: 2-6% 29 HRCT: 10% - 47% 35-8 HRCT: 50% with broncioectases and bronchiolectasis

  16. SLE - Chronic interstitial pneumonia • Radiographic - 6–24% • HRCT – 24/34 abnormal • 11/34 CIP • Fenlon HM, Doran M, Sant SM, et al. Am J Roentgenol 1996;166:301–7. • Estes D, Christian CL. Medicine • (Baltimore) 1971;50:85–95. • Raynaud’s phenomenon, swollen fingers, sclerodactyly, telangiectasia, dyspnoea, nailfold capillary abnormalities • May be efficacious: • Corticosteroids • Immunosuppressive agents

  17. 与ILD的相关因素 • 与病种有关 • 在RA中与RF的滴度有关 • DM/PM与抗Jo-1抗体有关 • 抗RNP抗体 Clin Exp Allergy 2003;33:226 ~ 232 Arthritis Rheum 2002;47:614 ~ 622

  18. 预后 • 病理分型还是CTD

  19. 治疗 • ILD 治疗的中心问题是GC和免疫抑制的指征 GC是最常用药,众多病人无反应 预后取决于分型 GC+CTX疗效好于单用GC Am J Respir Crit Care Med 1996;154:400 Arthritis Rheum 1994;37:1290 Semin Arthritis Rheum 2003;32:273

  20. 治疗 • ILD 治疗的中心问题是GC和免疫抑制的指征 GC是最常用药,众多病人无反应 预后取决于分型 GC+CTX疗效好于单用GC Am J Respir Crit Care Med 1996;154:400 Arthritis Rheum 1994;37:1290 Semin Arthritis Rheum 2003;32:273

  21. 治疗RA-ILD CTX,cyclosporine ,azathioprine, hydroxychloroquine have all been reported to be useful in the management of RA-associated ILD refractory to corticosteroids.

  22. 治疗RA-ILDTNFa? • In a preliminary study, infliximab also led to stabilization or improvement in symptoms, lung function, and radiologyscores in five RA-ILD . RCT trial needed • 非UIP--recommend corticosteroids UIP--recommend TNFa screen for secondary PH. • Bosentan?

  23. 治疗SSc-ILD prognosis better --77.5% respond to IS histopathologic subset severity of disease at presentation increased level of plasma homocysteine PH BAL eosinophil and neutrophil levels? TGFbeta,MMP

  24. 治疗SSc-ILD-ACR2006报道 美国DenverFischer A对27例肺活检的SSc患者(14例NSIP,8例UIP)分析表明:尽管都予同样的激素和免疫抑制剂治疗,SSc-NSIP中位生存时间为15.3年,而UIP为3年。

  25. the first positive results of a PCT

  26. 治疗SSc-ILD-NEJM报道 DBRPCT 美国13个中心,158例患者 口服CTX或安慰剂1年,随访2年 PEP--FVC

  27. 治疗SSc-ILD-NEJM报道 • Of 158 patients, 145 completed at least six months of treatment and were includedin the analysis. • The mean absolute difference in adjusted 12-month FVC% predictedbetween the CTX and placebo groups was 2.53% (95%CI 0.28 to 4.79%), favoring CTX (P<0.03).

  28. 治疗SSc-ILD-NEJM报道 • There were also treatment-related differences in physiological and symptom outcomes,and the difference in FVC was maintained at 24 months. • There was a greaterfrequency of adverse events in the CTX group, but the difference not significant.

  29. 治疗SSc-ILD-NEJM报道 在治疗1年时,HRCT纤维化严重病人在安慰剂组FVC下降明显,而在CTX组纤维化对FVC影响不明显 (P = 0.009) 对SSc中已有纤维化说明存在相对早期活动性肺泡炎,如不治疗,病情容易进展。

  30. 治疗SSc-ILD-NEJM结论 • One year of oral CTX in symptomatic SSc-ILD had a significant but modest beneficial effect onlung function, dyspnea, thickening of the skin, and the health-related quality of life. • The effects on lung function weremaintained through the 24 ms of the study.

  31. 治疗SSc-ILD-NEJM问题 no significant treatment-related difference was noted in the DLco

  32. 治疗ILD-排除感染 • mimic ILD or develop as a complication of immunosuppressivetherapy. • Pneumocystis carinii pneumonia. SLE, myositis,WG—chronic corticosteroids, MTX, inhibitors of TNFa all patients with CTD on chronic immunosuppression (>8 ws) should be considered for P. carinii prophylaxis?

  33. 治疗ILD-排除感染 CMV感染

  34. 治疗ILD-MTX? • acute hypersensitivity pneumonitis and pulmonary fibrosis • May predispose to P. carinii independently of corticosteroid use • prefer to avoid using MTX in patients with ILD • recent studies suggest that low-dose MTX is associated with a very low risk of pulmonary toxicity, suggesting that patients should not be automatically discontinued from the MTX, provided that the ILD does not progress

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