Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/20290
Title: Therapeutic burden in interstitial lung disease: Lessons to learn.
Authors: Khor, Yet H;Glaspole, Ian;Goh, Nicole S L
Affiliation: School of Medicine, University of Melbourne, Melbourne, VIC, Australia
Department of Respiratory and Sleep Medicine, Austin Health, Heidelberg, Victoria, Australia
Institute for Breathing and Sleep, Melbourne, VIC, Australia
Department of Allergy, Immunology and Respiratory Medicine, Alfred Health, Melbourne, VIC, Australia
School of Medicine, Monash University, Melbourne, VIC, Australia
Issue Date: 20-Feb-2019
EDate: 2019-02-20
Citation: Respirology 2019; online first: 20 February
Abstract: Patients with interstitial lung disease (ILD) are often prescribed disease-targeted and symptomatic therapies, both of which can cause significant treatment burden due to polypharmacy and drug-disease interactions. This study aimed to evaluate medication regimen complexity before and after introduction of ILD-specific therapies. Potential drug-disease interactions were evaluated for patients who were prescribed prednisolone. In this study, 214 patients with ILD were assessed for demographic information, co-morbidities and medication use. Medication lists were reviewed prior to and after the introduction of ILD-specific therapies. Complexity of treatment regimen was examined using the validated Medication Regimen Complexity Index (MRCI). Of the 214 patients, 75 had idiopathic pulmonary fibrosis (IPF) while the rest had inflammatory ILD (chronic hypersensitivity pneumonitis: 45; connective tissue disease-related ILD: 41). Polypharmacy was common at baseline (IPF: 51%, inflammatory ILD: 63%). Following introduction of ILD-specific therapies, median total MRCI scores significantly increased from 8 (interquartile range (IQR) = 8-15) to 22.5 (17.5-27.5) and 14.5 (8.5-21) to 21.5 (16-30) for IPF and inflammatory ILD groups, respectively (P < 0.0001 for both). Complex dosing instructions contributed the most to total MRCI scores for ILD-specific therapies. Among patients receiving prednisolone (n = 113), 88% had ≥1 co-morbidity which may be impacted. Common co-morbidities included gastrointestinal diseases (56%), obesity (37%), osteoporosis (24%) and diabetes mellitus (18%). Polypharmacy and complex medication regimen are common in patients with ILD of different aetiologies. There is a high frequency of potential drug-disease interactions among patients who are prescribed systemic corticosteroids. These findings highlight the need for careful evaluation of the impact of therapeutic complexity and burden in patients with ILD.
URI: http://ahro.austin.org.au/austinjspui/handle/1/20290
DOI: 10.1111/resp.13480
ORCID: 0000-0002-5434-9342
0000-0002-5118-2890
0000-0003-2065-4346
PubMed URL: 30790404
Type: Journal Article
Subjects: anti-fibrotics
idiopathic pulmonary fibrosis
immunosuppressants
interstitial lung disease
medication regimen complexity
Appears in Collections:Journal articles

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