Derleme
BibTex RIS Kaynak Göster

SEVERE ASTHMA

Yıl 2018, Cilt: 19 Sayı: 4, 157 - 163, 26.10.2018
https://doi.org/10.18229/kocatepetip.475027

Öz

Asthma is a common inflammatory disease that has wide

clinical characteristics of the airway of the lungs. Asthma

symptoms can be prevented by avoiding triggers like

allergens and by the effective inhaled treatment. The

majority of asthma patients can be treated effectively

by current medications. Difficult asthma is a distinct

entity of asthma, comprising approximately %5-10 of

asthmatic patients. Despite the high effective treatment,

the patients with asthma have disease that is poorly

controlled. Severe asthmatics account for up to half of

the cost for asthma. It will include asthma uncontrolled

by new standard therapy, steroid dependent, steroid

resistant asthma patients. Asthma related deaths

are seen especially in severe asthma group. Asthma

is a heterogeneous disease, consisting of different

phenotypes. It requires multidisciplinary approach for

treatment management. Severe asthma may suddenly

develop in early time in disease or overtime. There was an

evidence that severe asthma related to genetic factors,

environmental factors, age, inflammation, duration of

disease The genetic and environmental factors may

play a role in severe asthma management. Phenotypetargeted

therapy has an important role in severe asthma,

but it is associated with high treatment costs. At first

diagnosis of asthma must be confirmed COPD and vocal

cord dysfunction is needed to be particular interest in

differential diagnosis. Triggering factors such as smoking,

atopy, work place condition and aspirin hypersensitivity

should be evaluated. Comorbidities that may affect

asthma should be considered. This review examines

the definition of asthma, its differential diagnosis,

phenotypes and available treatment options.

Kaynakça

  • 1. Global Initiative for Asthma (GINA). Global strategy for asthma management and prevention. Revised 2017 available from http://www.ginasthma.org
  • 2. Bavbek S, Misirligil Z; Study Group. A breath for health: an exploratory study in severe asthma patients in Turkey. Allergy 2008;63(9): 1218-27.
  • 3. Chung KF , Wenzel SE, Brozek JL, et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur Respir J 2014;43(2):343-73.
  • 4. Bousquet J, Jeffery PK, Busse WW, et al. Asthma. From bronchoconstriction to airways inflammation and remodeling. Am J Respir Crit Care Med 2000;161:1720-45.
  • 5. Miller AL, Lukacs NW. Chemokine receptors: understanding their role in asthmatic disease. Immunol Allergy Clin North Am 2004;24:667-83, vii.
  • 6. Simpson JL, Scott RJ, Boyle MJ, et al. Differential proteolytic enzyme activity in eosinophillic and neutrophillic asthma. Am J Respir Crit Care Med 2005;172:559-65.
  • 7. Hastie AT, Moore WC, Meyers DA, et al. Analyses of asthma severity phenotypes and inflammatory proteins in subjects stratified by sputum granulocytes. J Allergy Clin Immunol 2010; 125: 1028–1036
  • 8. Kharitonov SA. Exhaled nitric oxide and carbon monoxide in asthma. Eur Respir Rev 1999;68:212-18.
  • 9. Turktas H, Oguzulgen K, Kokturk N, et al. Correlation of exhaled nitric oxide levels and airway inflammation markers in stable asthmatic patients. J Asthma 2003;40:425-30.
  • 10. Vignola AM, Mirabella F, Costanzo G, et al. Airway remodeling in asthma. Chest 2003;123(3 Suppl):417S-22S
  • 11. Robinson DS, Campbell DA, Durham SR, et al. Systematic assessment of difficult-to-treat asthma. Eur Respir J 2003; 22: 478–483.
  • 12. Aaron SD, Vandemheen KL, Boulet LP, et al. Overdiagnosis of asthma in obese and nonobese adults. CMAJ 2008; 179: 1121–1131.
  • 13. Moore WC, Bleecker ER, Curran-Everett D, et al. Characterization of the severe asthma phenotype by the National Heart, Lung, and Blood Institute’s Severe Asthma Research Program. J Allergy Clin Immunol 2007; 119:405–413.
  • 14. The ENFUMOSA cross-sectional Europe an multicentre study of the clinical phenotype of chronic severe asthma. European Network for Understanding Mechanisms of Severe Asthma. Eur Respir J 2003;22(3):470-7.
  • 15. Ten Brinke A, Grootendorst DC, Schmidt JT, et al. Chronic sinusitis in severe asthma is related to sputum eosinophilia. J Allergy Clin Immunol 2002; 109: 621–626.
  • 16. Chaudhuri R, Livingston E, McMahon AD, et al. Effects of smoking cessation on lung function and airway inflammation in smokers with asthma. Am J Respir Crit Care Med 2006; 174: 127–133
  • 17. Good JT Jr, Kolakowski CA, Groshong SD, et al. Refractory asthma: importance of bronchoscopy to identify phenotypes and direct therapy. Chest 2012; 141: 599–606.
  • 18. Mastronarde JG, Anthonisen NR, Castro M, et al. Efficacy of esomeprazole for treatment of poorly controlled asthma. N Engl J Med 2009; 360: 1487–1499.
  • 19. Holguin F, Bleecker ER, Busse WW, et al. Obesity and asthma: an association modified by age of asthma onset. J Allergy Clin Immunol 2011;127(6):148693
  • 20. Peters-Golden M, Swern A, Bird SS, et al. Influence of body mass index on the response to asthma controller agents. Eur Respir J 2006; 27: 495–503
  • 21. Vamos M, Kolbe J. Psychological factors in severe chronic asthma. Aust NZ J Psychiatry 1999; 33: 538–544
  • 22. Moore WC, Meyers DA, Wenzel SE, et al. Identification of asthma phenotypes using cluster analysis in the Severe Asthma Research Program. Am J Respir Crit Care Med 2010; 181: 315– 323. 163
  • 23. Haldar P, Pavord ID, Shaw DE, et al. Cluster analysis and clinical asthma phenotypes. Am J Respir Crit Care Med 2008; 178: 218–224.
  • 24. Sutherland ER, Goleva E, Strand M, et al. Body mass and glucocorticoid response in asthma. Am J Respir Crit Care Med 2008; 178: 682–687.
  • 25. Berry M, Morgan A, Shaw DE, et al. Pathological features and inhaled corticosteroid response of eosinophilic and noneosinophilic asthma. Thorax 2007; 62: 1043–1049
  • 26. Rabe KF, Atienza T, Magyar P, et al. Effect of budesonide in combination with formoterol for reliever therapy in asthma exacerbations: a randomised controlled, double-blind study. Lancet 2006;368(9537):74453.
  • 27. Scicchitano R, Aalbers R, Ukena D, et al. Efficacy and safety of budesonide/formoterol single inhaler therapy versus a higher dose of budesonide in moderate to severe asthma. Curr Med Res Opin 2004;20(9):140318.
  • 28. ten Brinke A, Zwinderman AH, Sterk PJ, et al. ‘‘Refractory’’ eosinophilic airway inflammation in severe asthma: effect of parenteral corticosteroids. Am J Respir Crit Care Med 2004; 170: 601–605.
  • 29. Ogirala RG, Aldrich TK, Prezant DJ, et al. High-dose intramuscular triamcinolone in severe, chronic, life-threatening asthma. N Engl J Med 1991; 324: 585–589
  • 30. Ducharme FM, Lasserson TJ, Cates CJ. Longacting beta2agonists versus antileukotrienes as add-on therapy to inhaled corticosteroids for chronic asthma. Cochrane Database Syst Rev 2006(4):CD003137.
  • 31. Evans DJ, Taylor DA, Zetterstrom O, et al. A comparison of lowdose inhaled budesonide plus theophylline and highdose inhaled budesonide for moderate asthma. N Engl J Med1997;337(20):14128
  • 32. Spears M, Donnelly I, Jolly L, et al. Effect of lowdose theophylline plus beclometasone on lung function in smokers with asthma: a pilot study. Eur Respir J 2009;33(5):10107.
  • 33. Barnes PJ. Theophylline. Am J Respir Crti Care Med 2013:188;9016
  • 34. Kerstjens HA, Engel M, Dahl R, et al. Tiotropium in asthma poorly controlled with standard combination therapy. N Engl J Med 2012;367(13):1198207.
  • 35. Bousquet J, Siergiejko Z, Swiebocka E, et al. Persistency of response to omalizumab therapy in severe allergic (Ig- Emediated) asthma. Allergy 2011;66(5):6718.
  • 36. Bousquet J, Cabrera P, Berkman N, et al. The effect of treatment with omalizumab, an anti-IgE antibody, on asthma exacerbations and emergency medical visits in patients with severe persistent asthma. Allergy 2005;60(3):3028.
  • 37. Schumann C, Kropf C, Wibmer T, et al. Omalizumab in patients with severe asthma: the XCLUSIVE study. Clin Respir J 2012;6(4):21527.
  • 38. Reiter J, Demirel N, Mendy A, et al. Macrolides for the longterm management of asthma a metaanalysis of randomized clinical trials. Allergy 2013;68(8):10409.
  • 39. Brusselle GG, Vanderstichele C, Jordens P, et al. Azithromycin for prevention of exacerbations in severe asthma (AZISAST): a multicentre randomised double-blind placebo-controlled trial. Thorax 2013 Apr;68(4):3229.
  • 40. Berry MA, Hargadon B, Shelley M, et al. Evidence of a role of tumor necrosis factoralpha in refractory asthma. N Engl J Med 2006;354(7):697708.
  • 41. Morjaria JB, Chauhan AJ, Babu KS, et al. The role of a soluble TNFalpha receptor fusion protein (etanercept) in corticosteroid refractory asthma: a double blind, randomised, placebo controlled trial. Thorax 2008;63(7):58491.
  • 42. Holgate ST, Noonan M, Chanez P, et al. Efficacy and safety of etanercept in moderatetosevere asthma: a randomised, controlled trial. Eur Respir J 2011;37(6):13529
  • 43. Castro M , Rubin AS , Laviolette M, et al ; AIR2 Trial Study Group. Effectiveness and safety of bronchial thermoplasty in the treatment of severe asthma: a multicenter, randomized, double-blind, sham-controlled clinical trial . Am J Respir Crit Care Med . 2010 ; 181 ( 2 ): 116 - 124
  • 44. Pavord ID, Korn S, Howarth P, et al. Mepolizumab for severe eosinophilic asthma (DREAM): a multicentre, double-blind, placebo-controlled trial. Lancet 2012;380(9842):651-9.
  • 45. Corren J, Lemanske RF, Hanania NA, et al. Lebrikizumab treatment in adults with asthma. N Engl J Med 2011;365(12):1088-98.
  • 46. Rodrigo GJ, Castro-Rodríguez JA What is the role of tiotropium in asthma?: a systematic review with meta-analysis. Chest. 2015 Feb;147(2):388-39
  • 47. Castro, M, Zangrilli, J, Wechsler, ME. Reslizumab for inadequately controlled asthma with elevated blood eosinophil counts: results from two multicentre, parallel, double-blind, randomised, placebo-controlled, phase 3 trials. Lancet Respir Med 2015; 3: 355–366

ZOR ASTIM

Yıl 2018, Cilt: 19 Sayı: 4, 157 - 163, 26.10.2018
https://doi.org/10.18229/kocatepetip.475027

Öz

Astım havayolu inflamasyonu ile seyreden çeşitli klinik
özelliklere sahip bir hastalıktır. Dünyada yaklaşık 300
milyon insanı etkileyen bir inflamatuvar hastalıktır. Astım
semptomları alerjenler gibi risk faktörlerinden kaçınarak
ve etkili inhaler tedavi ile kontrol altına alınmaktadır.
Astımlı hastaların büyük bir çoğunluğu uygun tedavi
ile kontrol altına alınmaktadır. Astımlı hastaların %
5-10’unu oluşturan zor astım klinisyenler için tanımı
ve tedavisi hala zor bir grubu oluşturmaktadır. İş gücü
kaybı ve ekonomik maliyet açısından yüksektir. Uygun
tedaviye rağmen bazı olguların kontrolü zorlaşmaktadır.
Standart tedavi ile kontrol edilemeyen, steroide bağımlı
veya dirençli astım olgularını içermektedir. Astıma bağlı
ölümlerin çoğu ağır olan veya stabil olmayan grupta
görülmektedir. Heterojen bir hastalık olan astımda farklı
fenotipler vardır ve net olarak anlaşılmamıştır. Tedavi
yönetimi için multidisipliner yaklaşım gerekmektedir. Ağır
astım hastalığın ilk yıllarında veya yıllar sonra gelişebilir.
Ağır astımda fenotipe özgü tedaviler günümüzde önem
kazanmıştır ve tedavi maliyeti yüksektir. Genetik, çevresel
faktörler, yaş ve hastalık süresinin ağır astımda rolü
olduğuna dair kanıtlar vardır. Özellikle genetik ve çevresel
faktörler ağır astımda önemli rol oynamaktadır. Ağır astım
olduğu düşünülen hastalar dikkatle değerlendirilmelidir.
Birçok hastalık astımı taklit edebilir. Bu hastalarda
öncelikle astım tanısı doğrulanmalıdır. KOAH ve vokal
kord disfonksiyonu ayırıcı tanıda özellikle dikkat edilmesi
gerekli hastalıklardır. İkinci olarak hastanın tedaviye
uyumu gözden geçirilmelidir. Ardından sigara içimi,
atopik durum, çalışma ortamı ve aspirin aşırı duyarlılığı
gibi faktörler araştırılmalıdır. Aynı zamanda ek hastalıklar
gibi astım kontrolünü etkileyebilen durumlar gözden
geçirilmelidir. Astımı zorlaştıran durumlar tek tek
araştırılmalıdır. Bu derlemede ağır astım tanımı, ayırıcı
tanıların dışlanması, fenotipleri ve tedavi yaklaşımları ele alınmıştır.

Kaynakça

  • 1. Global Initiative for Asthma (GINA). Global strategy for asthma management and prevention. Revised 2017 available from http://www.ginasthma.org
  • 2. Bavbek S, Misirligil Z; Study Group. A breath for health: an exploratory study in severe asthma patients in Turkey. Allergy 2008;63(9): 1218-27.
  • 3. Chung KF , Wenzel SE, Brozek JL, et al. International ERS/ATS guidelines on definition, evaluation and treatment of severe asthma. Eur Respir J 2014;43(2):343-73.
  • 4. Bousquet J, Jeffery PK, Busse WW, et al. Asthma. From bronchoconstriction to airways inflammation and remodeling. Am J Respir Crit Care Med 2000;161:1720-45.
  • 5. Miller AL, Lukacs NW. Chemokine receptors: understanding their role in asthmatic disease. Immunol Allergy Clin North Am 2004;24:667-83, vii.
  • 6. Simpson JL, Scott RJ, Boyle MJ, et al. Differential proteolytic enzyme activity in eosinophillic and neutrophillic asthma. Am J Respir Crit Care Med 2005;172:559-65.
  • 7. Hastie AT, Moore WC, Meyers DA, et al. Analyses of asthma severity phenotypes and inflammatory proteins in subjects stratified by sputum granulocytes. J Allergy Clin Immunol 2010; 125: 1028–1036
  • 8. Kharitonov SA. Exhaled nitric oxide and carbon monoxide in asthma. Eur Respir Rev 1999;68:212-18.
  • 9. Turktas H, Oguzulgen K, Kokturk N, et al. Correlation of exhaled nitric oxide levels and airway inflammation markers in stable asthmatic patients. J Asthma 2003;40:425-30.
  • 10. Vignola AM, Mirabella F, Costanzo G, et al. Airway remodeling in asthma. Chest 2003;123(3 Suppl):417S-22S
  • 11. Robinson DS, Campbell DA, Durham SR, et al. Systematic assessment of difficult-to-treat asthma. Eur Respir J 2003; 22: 478–483.
  • 12. Aaron SD, Vandemheen KL, Boulet LP, et al. Overdiagnosis of asthma in obese and nonobese adults. CMAJ 2008; 179: 1121–1131.
  • 13. Moore WC, Bleecker ER, Curran-Everett D, et al. Characterization of the severe asthma phenotype by the National Heart, Lung, and Blood Institute’s Severe Asthma Research Program. J Allergy Clin Immunol 2007; 119:405–413.
  • 14. The ENFUMOSA cross-sectional Europe an multicentre study of the clinical phenotype of chronic severe asthma. European Network for Understanding Mechanisms of Severe Asthma. Eur Respir J 2003;22(3):470-7.
  • 15. Ten Brinke A, Grootendorst DC, Schmidt JT, et al. Chronic sinusitis in severe asthma is related to sputum eosinophilia. J Allergy Clin Immunol 2002; 109: 621–626.
  • 16. Chaudhuri R, Livingston E, McMahon AD, et al. Effects of smoking cessation on lung function and airway inflammation in smokers with asthma. Am J Respir Crit Care Med 2006; 174: 127–133
  • 17. Good JT Jr, Kolakowski CA, Groshong SD, et al. Refractory asthma: importance of bronchoscopy to identify phenotypes and direct therapy. Chest 2012; 141: 599–606.
  • 18. Mastronarde JG, Anthonisen NR, Castro M, et al. Efficacy of esomeprazole for treatment of poorly controlled asthma. N Engl J Med 2009; 360: 1487–1499.
  • 19. Holguin F, Bleecker ER, Busse WW, et al. Obesity and asthma: an association modified by age of asthma onset. J Allergy Clin Immunol 2011;127(6):148693
  • 20. Peters-Golden M, Swern A, Bird SS, et al. Influence of body mass index on the response to asthma controller agents. Eur Respir J 2006; 27: 495–503
  • 21. Vamos M, Kolbe J. Psychological factors in severe chronic asthma. Aust NZ J Psychiatry 1999; 33: 538–544
  • 22. Moore WC, Meyers DA, Wenzel SE, et al. Identification of asthma phenotypes using cluster analysis in the Severe Asthma Research Program. Am J Respir Crit Care Med 2010; 181: 315– 323. 163
  • 23. Haldar P, Pavord ID, Shaw DE, et al. Cluster analysis and clinical asthma phenotypes. Am J Respir Crit Care Med 2008; 178: 218–224.
  • 24. Sutherland ER, Goleva E, Strand M, et al. Body mass and glucocorticoid response in asthma. Am J Respir Crit Care Med 2008; 178: 682–687.
  • 25. Berry M, Morgan A, Shaw DE, et al. Pathological features and inhaled corticosteroid response of eosinophilic and noneosinophilic asthma. Thorax 2007; 62: 1043–1049
  • 26. Rabe KF, Atienza T, Magyar P, et al. Effect of budesonide in combination with formoterol for reliever therapy in asthma exacerbations: a randomised controlled, double-blind study. Lancet 2006;368(9537):74453.
  • 27. Scicchitano R, Aalbers R, Ukena D, et al. Efficacy and safety of budesonide/formoterol single inhaler therapy versus a higher dose of budesonide in moderate to severe asthma. Curr Med Res Opin 2004;20(9):140318.
  • 28. ten Brinke A, Zwinderman AH, Sterk PJ, et al. ‘‘Refractory’’ eosinophilic airway inflammation in severe asthma: effect of parenteral corticosteroids. Am J Respir Crit Care Med 2004; 170: 601–605.
  • 29. Ogirala RG, Aldrich TK, Prezant DJ, et al. High-dose intramuscular triamcinolone in severe, chronic, life-threatening asthma. N Engl J Med 1991; 324: 585–589
  • 30. Ducharme FM, Lasserson TJ, Cates CJ. Longacting beta2agonists versus antileukotrienes as add-on therapy to inhaled corticosteroids for chronic asthma. Cochrane Database Syst Rev 2006(4):CD003137.
  • 31. Evans DJ, Taylor DA, Zetterstrom O, et al. A comparison of lowdose inhaled budesonide plus theophylline and highdose inhaled budesonide for moderate asthma. N Engl J Med1997;337(20):14128
  • 32. Spears M, Donnelly I, Jolly L, et al. Effect of lowdose theophylline plus beclometasone on lung function in smokers with asthma: a pilot study. Eur Respir J 2009;33(5):10107.
  • 33. Barnes PJ. Theophylline. Am J Respir Crti Care Med 2013:188;9016
  • 34. Kerstjens HA, Engel M, Dahl R, et al. Tiotropium in asthma poorly controlled with standard combination therapy. N Engl J Med 2012;367(13):1198207.
  • 35. Bousquet J, Siergiejko Z, Swiebocka E, et al. Persistency of response to omalizumab therapy in severe allergic (Ig- Emediated) asthma. Allergy 2011;66(5):6718.
  • 36. Bousquet J, Cabrera P, Berkman N, et al. The effect of treatment with omalizumab, an anti-IgE antibody, on asthma exacerbations and emergency medical visits in patients with severe persistent asthma. Allergy 2005;60(3):3028.
  • 37. Schumann C, Kropf C, Wibmer T, et al. Omalizumab in patients with severe asthma: the XCLUSIVE study. Clin Respir J 2012;6(4):21527.
  • 38. Reiter J, Demirel N, Mendy A, et al. Macrolides for the longterm management of asthma a metaanalysis of randomized clinical trials. Allergy 2013;68(8):10409.
  • 39. Brusselle GG, Vanderstichele C, Jordens P, et al. Azithromycin for prevention of exacerbations in severe asthma (AZISAST): a multicentre randomised double-blind placebo-controlled trial. Thorax 2013 Apr;68(4):3229.
  • 40. Berry MA, Hargadon B, Shelley M, et al. Evidence of a role of tumor necrosis factoralpha in refractory asthma. N Engl J Med 2006;354(7):697708.
  • 41. Morjaria JB, Chauhan AJ, Babu KS, et al. The role of a soluble TNFalpha receptor fusion protein (etanercept) in corticosteroid refractory asthma: a double blind, randomised, placebo controlled trial. Thorax 2008;63(7):58491.
  • 42. Holgate ST, Noonan M, Chanez P, et al. Efficacy and safety of etanercept in moderatetosevere asthma: a randomised, controlled trial. Eur Respir J 2011;37(6):13529
  • 43. Castro M , Rubin AS , Laviolette M, et al ; AIR2 Trial Study Group. Effectiveness and safety of bronchial thermoplasty in the treatment of severe asthma: a multicenter, randomized, double-blind, sham-controlled clinical trial . Am J Respir Crit Care Med . 2010 ; 181 ( 2 ): 116 - 124
  • 44. Pavord ID, Korn S, Howarth P, et al. Mepolizumab for severe eosinophilic asthma (DREAM): a multicentre, double-blind, placebo-controlled trial. Lancet 2012;380(9842):651-9.
  • 45. Corren J, Lemanske RF, Hanania NA, et al. Lebrikizumab treatment in adults with asthma. N Engl J Med 2011;365(12):1088-98.
  • 46. Rodrigo GJ, Castro-Rodríguez JA What is the role of tiotropium in asthma?: a systematic review with meta-analysis. Chest. 2015 Feb;147(2):388-39
  • 47. Castro, M, Zangrilli, J, Wechsler, ME. Reslizumab for inadequately controlled asthma with elevated blood eosinophil counts: results from two multicentre, parallel, double-blind, randomised, placebo-controlled, phase 3 trials. Lancet Respir Med 2015; 3: 355–366
Toplam 47 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Derlemeler
Yazarlar

Seda Beyhan Sağmen

Berrin Ceyhan Bu kişi benim

Yayımlanma Tarihi 26 Ekim 2018
Kabul Tarihi 1 Şubat 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 19 Sayı: 4

Kaynak Göster

APA Sağmen, S. B., & Ceyhan, B. (2018). SEVERE ASTHMA. Kocatepe Tıp Dergisi, 19(4), 157-163. https://doi.org/10.18229/kocatepetip.475027
AMA Sağmen SB, Ceyhan B. SEVERE ASTHMA. KTD. Ekim 2018;19(4):157-163. doi:10.18229/kocatepetip.475027
Chicago Sağmen, Seda Beyhan, ve Berrin Ceyhan. “SEVERE ASTHMA”. Kocatepe Tıp Dergisi 19, sy. 4 (Ekim 2018): 157-63. https://doi.org/10.18229/kocatepetip.475027.
EndNote Sağmen SB, Ceyhan B (01 Ekim 2018) SEVERE ASTHMA. Kocatepe Tıp Dergisi 19 4 157–163.
IEEE S. B. Sağmen ve B. Ceyhan, “SEVERE ASTHMA”, KTD, c. 19, sy. 4, ss. 157–163, 2018, doi: 10.18229/kocatepetip.475027.
ISNAD Sağmen, Seda Beyhan - Ceyhan, Berrin. “SEVERE ASTHMA”. Kocatepe Tıp Dergisi 19/4 (Ekim 2018), 157-163. https://doi.org/10.18229/kocatepetip.475027.
JAMA Sağmen SB, Ceyhan B. SEVERE ASTHMA. KTD. 2018;19:157–163.
MLA Sağmen, Seda Beyhan ve Berrin Ceyhan. “SEVERE ASTHMA”. Kocatepe Tıp Dergisi, c. 19, sy. 4, 2018, ss. 157-63, doi:10.18229/kocatepetip.475027.
Vancouver Sağmen SB, Ceyhan B. SEVERE ASTHMA. KTD. 2018;19(4):157-63.

88x31.png
Bu Dergi Creative Commons Atıf-GayriTicari-AynıLisanslaPaylaş 4.0 Uluslararası Lisansı ile lisanslanmıştır.