Physicians' Perspectives and Practice Patterns in India on the Diagnosis and Treatment of Interstitial Lung Disease (IN-ILD Survey)

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dc.contributor.authorRajan, Sujeet Ken_US
dc.contributor.authorMeshram, Sushanten_US
dc.contributor.authorChhajed, Prashanten_US
dc.contributor.authorMehta, Monalien_US
dc.contributor.authorLopez, Meenaen_US
dc.contributor.authorGogtay, Jaideepen_US
dc.date.accessioned2024-12-07T11:59:03Z
dc.date.available2024-12-07T11:59:03Z
dc.date.issued2024-06
dc.description.abstractAim and background: Data on clinicians’ views and practice patterns regarding interstitial lung disease (ILD) management in India is currently lacking. The objective of this survey was to understand clinicians’ perspectives on the diagnosis and treatment of patients with ILDs. Materials and methods: This was a questionnaire-based survey conducted among clinicians attending continuing medical education programs on ILDs across India in February 2020. Data entry and statistical analysis were done for completed questionnaires and results are expressed in terms of percentages based on the number of responses obtained. Results: A total of 321 clinicians managing ILDs participated in this survey, of which 87.75% were pulmonologists. Chronic hypersensitivity pneumonitis was ranked as the most common ILD seen in clinical practice, followed by idiopathic pulmonary fibrosis (IPF), connective tissue-ILD, and sarcoidosis. In total 43% of respondents preferred a combination of clinical evaluation, high-resolution computed tomography, and serology for ILD diagnosis. In the case of a planned biopsy, transbronchial lung biopsy (50.17%) was most preferred for idiopathic interstitial pneumonia. For follow-up, spirometry (86.60%) and a 6-minute walk distance (78.19%) were the most commonly performed tests. Antifibrotics (63.42%) were the preferred treatment for IPF while steroids either alone or in combination with immunosuppressants were preferred for non-IPF ILDs. Only 50% of respondents opined that pirfenidone 1800 mg/day and above was tolerated by over 45% of their IPF patients. Conclusion: Management of ILD has improved significantly in India. Antifibrotic dosing remains suboptimal in IPF. In non-IPF ILDs, a significant number of clinicians now use alternative immunosuppressants to steroids.en_US
dc.identifier.affiliationsDepartment of Respiratory Medicine, Bombay Hospital Institute of Medical Sciences and Bhatia Hospital, Mumbai, Indiaen_US
dc.identifier.affiliationsDepartment of Respiratory Medicine, Government Medical College, Nagpur, Indiaen_US
dc.identifier.affiliationsDepartment of Research, Institute of Pulmonology, Medical Research and Development; Chhajed Lung Care and Sleep Centre, Mumbai, Indiaen_US
dc.identifier.affiliationsDepartment of Medical Affairs, Cipla Ltd, Mumbai, Indiaen_US
dc.identifier.affiliationsDepartment of Medical Affairs, Cipla Ltd, Mumbai, Indiaen_US
dc.identifier.affiliationsDepartment of Medical Affairs, Cipla Ltd, Mumbai, Indiaen_US
dc.identifier.citationRajan Sujeet K, Meshram Sushant, Chhajed Prashant, Mehta Monali, Lopez Meena, Gogtay Jaideep . Physicians' Perspectives and Practice Patterns in India on the Diagnosis and Treatment of Interstitial Lung Disease (IN-ILD Survey) . The Indian Journal of Chest Diseases and Allied Sciences. 2024 Jun; 66(2): 44-53en_US
dc.identifier.issn0377-9343
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/242316
dc.languageenen_US
dc.publisherJaypee Brothers Medical Publishers Pvt. Ltd.en_US
dc.relation.issuenumber2en_US
dc.relation.volume66en_US
dc.source.urihttps://doi.org/10.5005/jp-journals-11007-0116en_US
dc.subjectAntifibroticen_US
dc.subjectClinician surveyen_US
dc.subjectDiagnosisen_US
dc.subjectIdiopathic pulmonary fibrosisen_US
dc.subjectImmunosuppressanten_US
dc.subjectIndiaen_US
dc.subjectInterstitial lung diseaseen_US
dc.subjectPirfenidoneen_US
dc.titlePhysicians' Perspectives and Practice Patterns in India on the Diagnosis and Treatment of Interstitial Lung Disease (IN-ILD Survey)en_US
dc.typeJournal Articleen_US
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