Evaluation of high-resolution computed tomography findings and associated factors in hypersensitivity pneumonitis

Evaluation of HRCT findings in hypersensitivity pneumonitis

Authors

Keywords:

hypersensitivity pneumonitis, non-fibrotic hypersensitivity pneumonitis, fibrotic hypersensitivity pneumonitis, high-resolution computed tomography

Abstract

Background/Aim: Hypersensitivity pneumonitis (HP) is a lung disease from inhaling diverse environmental and occupational organic substances, such as fungi, bacteria, birds, and occasionally nonorganic materials. An immune response triggers this condition. A high-resolution chest computed tomography (HRCT) scan is typically performed as part of the initial diagnostic assessment. This study assesses HRCT findings in HP patients and examines associated factors between fibrotic and non-fibrotic patient groups.

Methods: This retrospective cross-sectional study encompassed all HP patients monitored between 2010 and 2022. The analysis included data from 117 patients. HRCT findings from the patients were categorized based on fibrosis presence, leading to the division of patients into fibrotic and non-fibrotic groups. Comparative analyses were conducted between these groups.

Results: Among the 117 subjects analyzed, 59 (50.4%) were male, and 58 (49.6%) were female. The mean age at diagnosis was 52.1 (13.6) years, ranging from 20 to 81. The non-fibrotic HP group comprised 70 (59.8%) patients, while the fibrotic HP group comprised 47 (40.2%). The most prevalent HRCT findings were ground-glass opacity (90.6%), mosaic attenuation (87.2%), and traction bronchiectasis (50.4%). Statistically significant disparities were observed between non-fibrotic and fibrotic HP groups in terms of HRCT findings: ground-glass opacity, irregular linear opacities, reticulation, traction bronchiectasis, honeycombing, and fibrosis (P=0.024, P<0.001). In contrast, the lymphocyte ratio in bronchoalveolar lavage fluid was 28.78 (16.2) in the non-fibrotic HP group and 14.66 (10.3) in the fibrotic HP group. The fibrotic HP group exhibited a statistically significant lower lymphocyte ratio in bronchoalveolar lavage fluid (P<0.001).

Conclusion: HRCT findings are pivotal in HP diagnosis and classification. Computed tomography also assists in delineating the HP classification. This study identified ground-glass opacity and mosaic attenuation as the most prevalent HRCT findings in HP patients. Investigating the connection between fibrosis and prognosis is vital for determining patient outcomes, as fibrosis appears to be the principal determinant.

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References

Fernández Pérez ER, Travis WD, Lynch DA, Brown KK, Johannson KA, Selman M, et al. Diagnosis and Evaluation of Hypersensitivity Pneumonitis: CHEST Guideline and Expert Panel Report. Chest. 2021 Aug;160(2):e97-e156. doi: 10.1016/j.chest.2021.03.066. Epub 2021 April 20. PMID: 33861992.

Barnes H, Jones K, Blanc P. The hidden history of hypersensitivity pneumonitis. Eur Respir J. 2022 Jan 20;59(1):2100252. doi: 10.1183/13993003.00252-2021. PMID: 34083405.

Salisbury ML, Myers JL, Belloli EA, Kazerooni EA, Martinez FJ, Flaherty KR. Diagnosis and Treatment of Fibrotic Hypersensitivity Pneumonia. Where We Stand and Where We Need to Go. Am J Respir Crit Care Med. 2017 Sep 15;196(6):690-9. doi: 10.1164/rccm.201608-1675PP. PMID: 28002680; PMCID: PMC5620675.

Richerson HB, Bernstein IL, Fink JN, Hunninghake GW, Novey HS, Reed CE, et al. Guidelines for the clinical evaluation of hypersensitivity pneumonitis. Report of the Subcommittee on Hypersensitivity Pneumonitis. J Allergy Clin Immunol. 1989 Nov;84(5 Pt 2):839-44. doi: 10.1016/0091-6749(89)90349-7. PMID: 2809034.

Raghu G, Remy-Jardin M, Ryerson CJ, Myers JL, Kreuter M, Vasakova M, et al. Diagnosis of Hypersensitivity Pneumonitis in Adults. An Official ATS/JRS/ALAT Clinical Practice Guideline. Am J Respir Crit Care Med. 2020 Aug 1;202(3):e36-e69. doi: 10.1164/rccm.202005-2032ST. Erratum in: Am J Respir Crit Care Med. 2021 Jan 1;203(1):150-1. Erratum in: Am J Respir Crit Care Med. 2022 Aug 15;206(4):518. PMID: 32706311; PMCID: PMC7397797.

Kouranos V, Jacob J, Nicholson A, Renzoni E. Fibrotic Hypersensitivity Pneumonitis: Key Issues in Diagnosis and Management. J Clin Med. 2017 June 15;6(6):62. doi: 10.3390/jcm6060062. PMID: 28617305; PMCID: PMC5483872.

Chelala L, Adegunsoye A, Cody BA, Husain AN, Chung JH. Updated Imaging Classification of Hypersensitivity Pneumonitis. Radiol Clin North Am. 2022 Nov;60(6):901-13. doi: 10.1016/j.rcl.2022.06.013. Epub 2022 September 7. PMID: 36202477.

Shobeirian F, Mehrian P, Doroudinia A. Hypersensitivity Pneumonitis High-resolution Computed Tomography Findings, and Their Correlation with the Etiology and the Disease Duration. Prague medical report. 2020;121(3):133-41. doi: 10.14712/23362936.2020.12. PMID: 33030142.

Walsh SL, Sverzellati N, Devaraj A, Wells AU, Hansell DM. Chronic hypersensitivity pneumonitis: high resolution computed tomography patterns and pulmonary function indices as prognostic determinants. Eur Radiol. 2012 Aug;22(8):1672-9. doi: 10.1007/s00330-012-2427-0. Epub 2012 April 1. PMID: 22466512.

Dabiri M, Jehangir M, Khoshpouri P, Chalian H. Hypersensitivity Pneumonitis: A Pictorial Review Based on the New ATS/JRS/ALAT Clinical Practice Guideline for Radiologists and Pulmonologists. Diagnostics (Basel). 2022 Nov 20;12(11):2874. doi: 10.3390/diagnostics12112874. PMID: 36428934; PMCID: PMC9689332.

Barnett J, Molyneaux PL, Rawal B, Abdullah R, Hare SS, Vancheeswaran R, Desai SR, et al. Variable utility of mosaic attenuation to distinguish fibrotic hypersensitivity pneumonitis from idiopathic pulmonary fibrosis. Eur Respir J. 2019;54:1900531. doi: 10.1183/13993003.00531-2019. PMID: 31164428.

Nishida T, Kawate E, Ishiguro T, Kanauchi T, Shimizu Y, Takayanagi N. Antigen avoidance and outcome of non-fibrotic and fibrotic hypersensitivity pneumonitis. ERJ Open Res. 2021 Feb 7;8(1):00474-2021. doi: 10.1183/23120541.00474-2021. PMID: 35141326; PMCID: PMC8819255.

Fernández Pérez ER, Swigris JJ, Forssén AV, Tourin O, Solomon JJ, Huie TJ, et al. Identifying an inciting antigen is associated with improved survival in patients with chronic hypersensitivity pneumonitis. Chest. 2013 Nov;144(5):1644-51. doi: 10.1378/chest.12-2685. PMID: 23828161; PMCID: PMC4694094.

Salisbury ML, Gu T, Murray S, Gross BH, Chughtai A, Sayyouh M, et al. Hypersensitivity Pneumonitis: Radiologic Phenotypes Are Associated With Distinct Survival Time and Pulmonary Function Trajectory. Chest. 2019 Apr;155(4):699-711. doi: 10.1016/j.chest.2018.08.1076. Epub 2018 September 19. PMID: 30243979; PMCID: PMC6514431.

De Sadeleer LJ, Hermans F, De Dycker E, Yserbyt J, Verschakelen JA, Verbeken EK, et al. Effects of Corticosteroid Treatment and Antigen Avoidance in a Large Hypersensitivity Pneumonitis Cohort: A Single-Centre Cohort Study. J Clin Med. 2018 December 21;8(1):14. doi: 10.3390/jcm8010014. PMID: 30577667; PMCID: PMC6352061.

Hanak V, Golbin JM, Hartman TE, Ryu JH. High-resolution CT findings of parenchymal fibrosis correlate with prognosis in hypersensitivity pneumonitis. Chest. 2008 Jul;134(1):133-8. doi: 10.1378/chest.07-3005. Epub 2008 April 10. PMID: 18403660.

Mooney JJ, Elicker BM, Urbania TH, Agarwal MR, Ryerson CJ, Nguyen MLT, et al. Radiographic fibrosis score predicts survival in hypersensitivity pneumonitis. Chest. 2013 Aug;144(2):586-92. doi: 10.1378/chest.12-2623. PMID: 23392130.

Wang LJ, Cai HR, Xiao YL, Wang Y, Cao MS. Clinical characteristics and outcomes of hypersensitivity pneumonitis: a population-based study in China. Chin Med J (Engl). 2019 June 5;132(11):1283-92. doi: 10.1097/CM9.0000000000000256. Erratum in: Chin Med J (Engl). 2021 Jan 11;134(3):378. PMID: 31021982; PMCID: PMC6629344.

Walters GI, Mokhlis JM, Moore VC, Robertson AS, Burge GA, Bhomra PS, et al. Characteristics of hypersensitivity pneumonitis diagnosed by interstitial and occupational lung disease multidisciplinary team consensus. Respir Med. 2019 Aug;155:19-25. doi: 10.1016/j.rmed.2019.06.026. Epub 2019 June 29. PMID: 31295673.

Warren CP. Extrinsic allergic alveolitis: a disease commoner in non-smokers. Thorax. 1977 Oct;32(5):567-9. doi: 10.1136/thx.32.5.567. PMID: 594937; PMCID: PMC470791.

Terho EO, Husman K, Vohlonen I. Prevalence and incidence of chronic bronchitis and farmer’s lung with respect to age, sex, atopy, and smoking. Eur J Respir Dis Suppl. 1987;152:19-28. PMID: 3499342.

Furuiye M, Miyake S, Miyazaki Y, Ohtani Y, Inase N, Umino T, et al. Effect of cigarette smoking on the development of murine chronic pigeon breeder’s lung. The difference between a short-term and a long-term exposure. J Med Dent Sci. 2007 Mar;54(1):87-95. PMID: 19845140.

Churg A, Sin DD, Everett D, Brown K, Cool C. Pathologic patterns and survival in chronic hypersensitivity pneumonitis. Am J Surg Pathol. 2009 Dec;33(12):1765-70. doi: 10.1097/PAS.0b013e3181bb2538. PMID: 19809277.

Kumar R, Spalgais S, Ranga V. Hypersensitivity pneumonitis: clinical, radiological and pathological profile of 103 patients from North India. Monaldi Arch Chest Dis. 2020 Aug 3;90(3). doi: 10.4081/monaldi.2020.1307. PMID: 32885932.

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Published

2023-08-14

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Research Article

How to Cite

1.
Koyuncu A, Ertürk H. Evaluation of high-resolution computed tomography findings and associated factors in hypersensitivity pneumonitis: Evaluation of HRCT findings in hypersensitivity pneumonitis. J Surg Med [Internet]. 2023 Aug. 14 [cited 2024 Jun. 30];7(8):458-62. Available from: https://jsurgmed.com/article/view/7855