Search Results - "CONDLIFFE, R"

CT features of pulmonary arterial hypertension and its major subtypes: a systematic CT evaluation of 292 patients from the ASPIRE Registry by Rajaram, S, Swift, A J, Condliffe, R, Johns, C, Elliot, C A, Hill, C, Davies, C, Hurdman, J, Sabroe, I, Wild, J M, Kiely, D G

“…We evaluated the prevalence and prognostic value of CT-pulmonary angiographic (CTPA) measures in 292 treatment naive patients with pulmonary arterial…”
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Living with pulmonary hypertension: quality not just quantity by Condliffe, R

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ASPIRE registry: Assessing the Spectrum of Pulmonary hypertension Identified at a REferral centre by HURDMAN, J, CONDLIFFE, R, BILLINGS, C, LAWRIE, A, SABROE, I, AKIL, M, O'TOOLE, L, KIELY, D. G, ELLIOT, C. A, DAVIES, C, HILL, C, WILD, J. M, CAPENER, D, SEPHTON, P, HAMILTON, N, ARMSTRONG, I. J

“…Pulmonary hypertension (PH) is a heterogeneous condition. To date, no registry data exists reflecting the spectrum of disease across the five diagnostic groups…”
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Switching to riociguat versus maintenance therapy with phosphodiesterase-5 inhibitors in patients with pulmonary arterial hypertension (REPLACE): a multicentre, open-label, randomised controlled trial by Hoeper, Marius M, Al-Hiti, Hikmet, Benza, Raymond L, Chang, Sung-A, Corris, Paul A, Gibbs, J Simon R, Grünig, Ekkehard, Jansa, Pavel, Klinger, James R, Langleben, David, McLaughlin, Vallerie V, Meyer, Gisela M B, Ota-Arakaki, Jaquelina, Pulido, Tomás, Rosenkranz, Stephan, Vizza, Carmine Dario, Vonk-Noordegraaf, Anton, White, R James, Chang, Mikyung, Meier, Christian, Paraschin, Karen, Ghofrani, Hossein Ardeschir, Simonneau, Gérald, Olschewski, H, Delcroix, M, Andrade-Lima, M, de Amorim Corrêac, R, Meyer, G, De Souza, R, Al-Hiti, H, Jansa, P, Mellemkjær, S, Bauer, F, Montani, D, Simonneau, G, Drömann, D, Ghofrani, H-A, Grünig, E, Halank, M, Held, M, Hoeper, MM, Klose, H, Kneidinger, N, Leuchte, H, Opitz, C, Rosenkranz, S, Wirtz, H, Karvounis, H, Pitsiou, G, Orfanos, S, D'Alto, M, Ghio, S, Vitulo, P, Maki, H, Tatebe, S, de los Rios Ibarra, M, Pulido, T, Van Dijk, A, Vonk-Noordegraaf, A, Roleder, T, Castro, G, Loureiro, MJ, Robalo-Martins, S, Barberá, JA, Lázaro, M, Perez-Penate, GM, Román, A, Cheng, C-C, Hsu, H-H, Atahan, E, Mogulkoc Bishop, N, Okumus, NG, Onen, Z, Chang, H-J, Chang, S-A, Lee, J-S, Kim, H-K, Coghlan, JG, Corris, PA, Church, AC, Gibbs, JSR, Peacock, AJ, Wort, S, Allen, S, Awdish, R, Benza, RL, DeSouza, S, Feldman, J, Johri, S, Klinger, JR, Layish, D, McConnell, J, McLaughlin, VV, Migliore, C, Rahaghi, F, Rischard, F, Robbins, I, Satterwhite, L, Sulica, R, White, RJ

“…Riociguat and phosphodiesterase-5 inhibitors (PDE5i), approved for the treatment of pulmonary arterial hypertension (PAH), act on the same pathway via…”
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Prognostic and aetiological factors in chronic thromboembolic pulmonary hypertension by Condliffe, R, Kiely, D. G, Gibbs, J. S. R, Corris, P. A, Peacock, A. J, Jenkins, D. P, Goldsmith, K, Coghlan, J. G, Pepke-Zaba, J

“…Several prognostic variables have previously been identified in patients with chronic thromboembolic pulmonary hypertension (CTEPH). Specific medical…”
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Non-invasive methods for estimating mPAP in COPD using cardiovascular magnetic resonance imaging by Johns, C. S., Rajaram, S., Capener, D. A., Oram, C., Elliot, C., Condliffe, R., Kiely, D. G., Wild, J. M., Swift, A. J.

“…Purpose Pulmonary hypertension (PH) is associated with a poor outcome in chronic obstructive pulmonary disease (COPD) and is diagnosed invasively. We aimed to…”
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Improved survival in pregnancy and pulmonary hypertension using a multiprofessional approach by Kiely, DG, Condliffe, R, Webster, V, Mills, GH, Wrench, I, Gandhi, SV, Selby, K, Armstrong, IJ, Martin, L, Howarth, ES, Bu’Lock, FA, Stewart, P, Elliot, CA

“…Please cite this paper as: Kiely D, Condliffe R, Webster V, Mills G, Wrench I, Gandhi S, Selby K, Armstrong I, Martin L, Howarth E, Bu’Lock F, Stewart P,…”
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Critical care management of pulmonary hypertension by Condliffe, R, MD, Kiely, DG, MD

“…Abstract Patients with pulmonary hypertension (PH) can be extremely challenging to manage in the critical care setting. In this article we review the…”
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Management dilemmas in pulmonary arterial hypertension associated with congenital heart disease by Condliffe, R., Clift, P., Dimopoulos, K., Tulloh, R.M.R.

“…There are few randomised controlled data to guide management of patients with pulmonary arterial hypertension associated with congenital heart disease…”
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Central venous catheter-related blood stream infections in patients receiving intravenous iloprost for pulmonary hypertension by Sammut, D., Elliot, C. A., Kiely, D. G., Armstrong, I. J., Martin, L., Wilkinson, J., Sephton, P., Jones, J., Hamilton, N., Hurdman, J., McLellan, E., Sabroe, I., Condliffe, R.

“…Catheter-related blood stream infection (CR-BSI) in patients with pulmonary hypertension (PH) receiving intravenous iloprost via an indwelling central line has…”
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Macitentan for pulmonary arterial hypertension related to repaired congenital heart disease: real-world UK experience by Constantine, A, Condliffe, R, Clift, P, Jansen, K, Wort, S J, Moledina, S, Dimopoulos, K

“…Abstract Introduction Patients with pulmonary arterial hypertension (PAH) following congenital heart disease (CHD) repair are an emerging population at…”
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Paediatric pulmonary arterial hypertension following congenital heart defect repair: enhanced risk stratification and outcomes in a national cohort by Constantine, A, Dimopoulos, K, Condliffe, R, Clift, P, Jansen, K, Dhillon, R, Chaplin, G, Muthurangu, V, Moledina, S

“…Abstract Introduction Pulmonary arterial hypertension (PAH) is a common complication of congenital heart disease (CHD). PAH following CHD repair (repaired…”
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Improved Survival in Pregnancy and Pulmonary Hypertension Using a Multiprofessional Approach by Kiely, D.G, Condliffe, R, Webster, V, Mills, G.H, Wrench, I, Gandhi, S.V, Selby, K, Armstrong, I.J, Martin, L, Howarth, E.S, Buʼlock, F.A, Stewart, P, Elliot, C.A

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Pulmonary arterial hypertension associated with congenital heart disease in children: clinical characterisation, outcomes and changes in demographics over time by Constantine, A, Dimopoulos, K, Condliffe, R, Clift, P, Chaplin, G, Muthurangu, V, Haworth, S G, Moledina, S

“…Abstract Background/Introduction Pulmonary arterial hypertension (PAH) is a common complication of congenital heart disease (CHD) in children and is associated…”
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Multicentre study on pulmonary arterial hypertension therapies in fontan patients: underutilised or of limited use? by Constantine, A, Jenkins, P, Oliver, J, Chung, N, Jansen, K, Fitzsimmons, S, Walker, N, Papaioannou, V, Parry, H, Condliffe, R, Tulloh, R, Dimopoulos, K, Clift, P

“…Abstract Introduction The Fontan circulation is successful in abolishing cyanosis and chronic volume overload in congenital heart disease (CHD) patients with…”
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Inducible bronchus-associated lymphoid tissue and the pathogenesis of rheumatoid lung by Condliffe, R

“…[...]dense areas of collagen deposition and myofibroblast activity around the follicles were seen in the patients with highly organised iBALT…”
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Mining the Plasma Proteome for Insights into the Molecular Pathology of Pulmonary Arterial Hypertension by Harbaum, Lars, Rhodes, Christopher J, Wharton, John, Lawrie, Allan, Karnes, Jason H, Desai, Ankit A, Nichols, William C, Humbert, Marc, Montani, David, Girerd, Barbara, Sitbon, Olivier, Boehm, Mario, Novoyatleva, Tatyana, Schermuly, Ralph T, Ghofrani, H Ardeschir, Toshner, Mark, Kiely, David G, Howard, Luke S, Swietlik, Emilia M, Gräf, Stefan, Pietzner, Maik, Morrell, Nicholas W, Wilkins, Martin R

“…Pulmonary arterial hypertension (PAH) is characterized by structural remodeling of pulmonary arteries and arterioles. Underlying biological processes are…”
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Pulmonary hypertension: diagnosis and management by Kiely, David G, Elliot, Charlie A, Sabroe, Ian, Condliffe, Robin

“…SUMMARY POINTS Pulmonary hypertension has many causes so prognoses and treatments vary The condition is diagnosed by systematically evaluating the breathless…”
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543A machine-learning CMR approach to extract disease features and automate pulmonary arterial hypertension diagnosis by Swift, A J, Lu, H, Garg, P, Taylor, J, Metherall, P, Zhou, S, Johns, C, Condliffe, R A, Lawrie, A, Wild, J M, Kiely, D G

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A57 WHO GROUP III/IV PULMONARY HYPERTENSION: Reduced Gas Transfer (tlco) Predicts Poor Outcome In Patients With Pulmonary Hypertension And Heart Failure With Preserved Ejection Fraction by Hussain, N, Ramjug, S, Billings, C G, Hurdman, J, Elliot, C, Condliffe, R, Kiely, D

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