Interstitial lung disease: a review of classification, etiology, epidemiology, clinical diagnosis, pharmacological and non-pharmacological treatment

MA Althobiani, AM Russell, J Jacob, Y Ranjan… - Frontiers in …, 2024 - frontiersin.org
Interstitial lung diseases (ILDs) refer to a heterogeneous and complex group of conditions
characterized by inflammation, fibrosis, or both, in the interstitium of the lungs. This results in …

Palliative care in interstitial lung disease: living well

M Kreuter, E Bendstrup, AM Russell… - The lancet respiratory …, 2017 - thelancet.com
Progressive fibrotic interstitial lung diseases (ILDs) are characterised by major reductions in
quality of life and survival and have similarities to certain malignancies. However, palliative …

Telomere biology disorders

MLW Kam, TTT Nguyen, JYY Ngeow - NPJ genomic medicine, 2021 - nature.com
Telomere biology disorders (TBD) are a heterogeneous group of diseases arising from
germline mutations affecting genes involved in telomere maintenance. Telomeres are DNA …

The supportive care needs of people living with pulmonary fibrosis and their caregivers: a systematic review

JYT Lee, G Tikellis, TJ Corte, NS Goh… - European …, 2020 - publications.ersnet.org
Background People with pulmonary fibrosis often experience a protracted time to diagnosis,
high symptom burden and limited disease information. This review aimed to identify the …

Epidemiology and prognostic significance of cough in fibrotic interstitial lung disease

YH Khor, KA Johannson, V Marcoux… - American Journal of …, 2024 - atsjournals.org
Rationale: Cough is a key symptom in patients with fibrotic interstitial lung disease (ILD).
Objectives: This study evaluated the prevalence, longitudinal change, associations, and …

An examination and proposed definitions of family members' grief prior to the death of individuals with a life-limiting illness: A systematic review

J Singer, KE Roberts, E McLean, C Fadalla… - Palliative …, 2022 - journals.sagepub.com
Background: Research has extensively examined family members' grief prior to the death of
an individual with a life-limiting illness but several inconsistencies in its conceptualization of …

Gaps in care of patients living with pulmonary fibrosis: a joint patient and expert statement on the results of a Europe-wide survey

CC Moor, MS Wijsenbeek, E Balestro… - ERJ Open …, 2019 - publications.ersnet.org
Introduction Pulmonary fibrosis (PF) and its most common form, idiopathic pulmonary
fibrosis (IPF), are chronic, progressive diseases resulting in increasing loss of lung function …

Patient and caregiver shared experiences of pulmonary fibrosis (PF): a systematic literature review

M Wells, S Harding, G Dixon, K Buckley, AM Russell… - Respiratory …, 2024 - Elsevier
Pulmonary Fibrosis (PF) describes a group of lung diseases characterised by progressive
scarring (fibrosis). Symptoms worsen over time and include breathlessness, tiredness, and …

Understanding patient experience of chronic cough in interstitial lung disease

JMV Mann, AE Holland, NSL Goh… - ERJ Open …, 2023 - publications.ersnet.org
Rationale Chronic cough is a common symptom in patients with interstitial lung disease
(ILD), negatively contributing to health-related quality of life. Despite this, there is limited …

A sco** review of the unmet needs of patients diagnosed with idiopathic pulmonary fibrosis (IPF)

C Bramhill, D Langan, H Mulryan, J Eustace-Cook… - PLoS …, 2024 - journals.plos.org
Aims Patients diagnosed with idiopathic pulmonary fibrosis (IPF) have a high symptom
burden and numerous needs that remain largely unaddressed despite advances in …