Zobrazeno 1 - 10
of 32
pro vyhledávání: '"R K, Coker"'
Autor:
Miriam F. Moffatt, Chalmers G, R K Coker, Spenser L, Chris Barber, Melissa Wickremasinghe, Alex West, Dhruv Parekh, Nik Hirani, David R Thickett, Sara De Matteis, Dempsey O, Catherine J. Reynolds, Harrison K, R Sisodia, Alison Taylor, Sophie V. Fletcher, Pepperell J, Huzaifa Adamali, Walters G, Andrew M. Wilson, Helen Parfrey, Cosetta Minelli, Michael A Gibbons, Ian Forrest, Cherrie J, Gauri Saini, Babu S, Paul Cullinan, O’Hickey S, Paul Beirne, Nazia Chaudhuri
RationaleAsbestos is posited to cause otherwise ‘idiopathic’ pulmonary fibrosis (IPF); establishing this has important diagnostic and therapeutic implications.ObjectivesTo determine the association between occupational asbestos exposure and IPF;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c57cea8082278eb87d8560383085b27a
https://doi.org/10.1101/2021.03.09.21253224
https://doi.org/10.1101/2021.03.09.21253224
Publikováno v:
The nuts and bolts of ILD clinical management.
Introduction Idiopathic pulmonary fibrosis (IPF) often coexists with pulmonary hypertension (PH) and left heart disease (LHD). Estimates of PH prevalence vary, from 8–15% at initial assessment to 30–50% at transplant evaluation. PH conveys increa
Autor:
Mohini Parmar, Anna Bokobza, Yasmin Razak, Sarah L. Elkin, V Mak, Loong-Yuan Han, Ernie Wong, Toby Hyde, Kartik Kumar, Joanna L Brown, Katherine Groom, R K Coker
Publikováno v:
e92
e88
Future Healthc J
e88
Future Healthc J
Integration of primary and secondary care for the management of respiratory disease is a long-held ambition. Here, we describe how respiratory specialists at a large NHS trust, working with primary care clinicians in the area, set up a GP hotline and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f2a3f091b28e713461c33e0d8cb918
http://hdl.handle.net/10044/1/104159
http://hdl.handle.net/10044/1/104159
Autor:
Philip L. Molyneaux, Maria Molina-Molina, Felix Chua, Siva Mahendran, R K Coker, Pilar Rivera-Ortega, Maria Kokosi, George Margaritopoulos, Alice Packham, Alex West, Suresh Babu, Joanna C. Porter, Nazia Chaudhuri, Elisabeth Bendstrup, Michael Henry, Sharon Sturney, Ewen M Harrison, Tim Wallis, Athol U. Wells, Peter J. M. Openshaw, Louise E. Crowley, Laura Mackay, Elisabetta A. Renzoni, Glenn Hearson, Lisa G. Spencer, Iain A. Stewart, Killian Hurley, Ian Forrest, Diego Castillo Villegas, Sarah Agnew, Thomas M Drake, Simon P. Hart, Gauri Saini, Katherine M.A. O'Reilly, Huzaifa Adamali, Annemarie B Docherty, Jennifer K Quint, J Kenneth Baillie, Muhunthan Thillai, Rachel K. Hoyles, Katie Ward, Melissa Wickremasinghe, Michael A Gibbons, Malcolm G Semple, Davinder Dosanjh, Venerino Poletti, John M. Hutchinson, Helen Parfrey, R. Gisli Jenkins, David R Thickett, Aiden O’Brien, Lucy Howard, Emily Heiden, Michael Kreuter, Shaney L Barratt, Isaric C Investigators, Chris Barber, Anne-Marie Russell, Katherine Groom, S Jones, Stephen Bianchi, Christine A Fiddler, Giulia M. Stella, Anjali Crawshaw, Sarah Haney, Ling-Pei Ho, Helen Stone, William Chang, Peter M. George, Mark Jones, Felix Woodhead
RationaleThe impact of COVID-19 on patients with Interstitial Lung Disease (ILD) has not been established.ObjectivesTo assess outcomes following COVID-19 in patients with ILD versus those without in a contemporaneous age, sex and comorbidity matched
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8fd371c39f470ec88f1a4be1f856c2
M12 52 month follow up of patients with IPF receiving nintedanib via the compassionate use programme
Publikováno v:
Real world studies with antifibrotics in IPF.
Introduction In 2015 nintedanib became available on a compassionate use programme (CUP) to patients with idiopathic pulmonary fibrosis (IPF), after the 2014 publication of the INPULSIS trial1 and before receiving National Institute for Health and Car
Publikováno v:
A multi-faceted approach to ILD management.
Introduction and aims Patients with respiratory disease often report activity limitation that is not always adequately or efficiently described by existing physiological parameters or patient reported outcome measure (PROM) tools such as the MRC Dysp
Autor:
David Price, Mandy Ow, Jaco Voorham, Ronan Ryan, Andrew Wilson, Victoria Carter, Priyanka Raju, Rupert Jones, Sen Yang, Isha Chaudry, David R Thickett, R K Coker
Publikováno v:
Idiopathic interstitial pneumonias.
Publikováno v:
1.5 Diffuse Parenchymal Lung Disease.
Background: The National Institute for Health and Care Excellence (NICE) approved pirfenidone (PIR) in England & Wales for IPF in April 2013. Nintedanib (NIN) became available more recently on a named patient basis. We review our experience with both
Autor:
Ian Forrest, L. Richeldi, Toby M. Maher, Lisa Spencer, Ling-Pei Ho, Owen Dempsey, Helen Parfrey, Monica Spiteri, Sue Copley, Nazia Chaudhuri, William Chang, Michael A Gibbons, R K Coker
Publikováno v:
1.5 Diffuse Parenchymal Lung Disease.
Introduction: Sarcoidosis makes up a third of ILD cases seen in UK chest clinics. Primary care data suggest an incidence of 3 per 100,000 person years. In 2013 BTS set up a Sarcoidosis Registry: an ongoing longitudinal UK database with epidemiologica
Autor:
Sue Copley, R K Coker, Ian Forrest, L. Richeldi, Lisa Spencer, Helen Parfrey, Ling-Pei Ho, William Chang, Toby M. Maher, Monica Spiteri, Owen Dempsey, Nazia Chaudhuri, Michael A Gibbons
Publikováno v:
1.5 Diffuse Parenchymal Lung Disease.
Background: The BTS IPF Registry, launched Feb 2013, is the first UK national platform for the collection of demographic and outcome data on IPF patients. We present a summary of the data and initial conclusions regarding care provision. Methods: Phy