N. Keane
University College London Hospitals NHS Foundation Trust
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by N. Keane.
Nutrition and Cancer | 2018
N. Keane; Konstantinos C. Fragkos; P.S. Patel; Friderike Bertsch; Shameer J. Mehta; Simona Di Caro; F. Rahman
ABSTRACT We describe a cohort of Home Parenteral Nutrition (HPN) patients with advanced cancer in order to identify factors affecting prognosis. Demographic, anthropometric, biochemical and medical factors, Karnofsky Performance Status (KPS), Glasgow Prognostic Score (GPS), and PN requirements were recorded. Univariate and multivariate analyses were performed including Kaplan–Meier curves, Cox Regression, and correlation analyses. In total, 107 HPN patients (68 women, 39 men, mean age 57 yr) with advanced cancer were identified. The main indications for HPN were bowel obstruction (74.3%) and high output ostomies (14.3%). Cancer cachexia was present in 87.1% of patients. The hazard ratio (HR) for upper gastrointestinal and “other” cancers vs. gynaecological malignancy was 1.75 (p = 0.077) and 2.11 (p = 0.05), respectively. KPS score, GPS, PN volume, and PN potassium levels significantly predicted survival (HRKPS ≥50 vs <50 = 0.47; HRGPS = 2 vs. GPS = 0 = 3.19). In multivariate analysis, KPS and GPS remained significant predictors (p < 0.05), whilst PN volume reached borderline significance (p = 0.094). Survival was not significantly affected by the presence of metastatic disease, previous or concurrent surgery, chemo-radiotherapy, or indication for HPN (p > 0.05). Most patients passed away in their homes or hospice (77.9%). Performance status, prognostic scoring, and PN requirements may predict survival in patients with advanced cancer receiving HPN.
Gut | 2015
N. Keane; F Bertsch; P.S. Patel; Konstantinos C. Fragkos; I Barnova; Mark A. Samaan; S Morgan; La Smith; M Babbington; S Di Caro; F. Rahman
Introduction HPN support should be a nutritional management strategy in patients who cannot meet their nutritional requirements by oral or enteral routes and those who are eligible to receive therapy outside an acute-care setting.1However, use of HPN in incurable patients who cannot eat remains controversial and is only accounted for by approximately 8% of the UK HPN population.2We therefore aimed to describe the HPN palliativeoncology cohort at University College London Hospital (UCLH) and identify what factors determine their survival rates and performance status. Method Data was collected retrospectively and prospectively for palliative oncologypatients receiving HPNthrough hospital computer systems and databases stored by members of the Nutrition team at UCLH between 01/01/2006 to 31/12/2014 (censor date). Survival time was expressed in weeks, Kaplan Meier curves were plotted and performance status was obtained using Karnofsky score (KPS). Results A cohort of n = 65 (n = 12 active at analysis) palliative oncology patients (male 36.9%, median age 56 years) recieved HPN at UCLH from 2006–2014. Cancers of the following aetiologies comprised most of the cohort: upper gastrointestinal (n = 13, 20%); lower gastrointestinal (n = 15, 23%); and gynaecological (n = 24, 36.9%). The main indicator for HPN was bowel obstruction (n = 44). Overall mean/median survival was 22.4 and 10 weeks (range: 0.4 to 193.3), respectively (Figure 1). Survival also differed by malignancy (mean/median survival-weeks: upper gastrointestinal 10.3/6.4; lower gastrointestinal 24.8/10.7), gynaecological 28.1/8.3). Overall median KPS was 50. The correlation between KPS and survival from discharge to death was r = 0.315 (P < 0.05) in n = 48 patients. Abstract PTH-208 Figure 1 Survival of palliative oncology HPN patients (N = 65) Conclusion Our results show there is an indication for HPN in palliative oncology patients as it may increase survival period post hospital discharge however this may differ by underlying malignancy. In addition, HPN may improve performance status. Further research is required into patients’ quality of life to provide holistic as well as medical insights into HPN in this patient group. Disclosure of interest None Declared. References Staun M, et al. ESPEN guidelines on Parenteral nutrition: Home Parenteral Nutrtiion (HPN) in adult patients. Clin Nutr. 2009:467–479 BANS: Annual BANS Report, 2011; Artificial Nutrition Support in the UK 2000–2010. www.bapen.org.uk
Gut | 2017
Konstantinos C. Fragkos; Lucia Fini; N. Keane; H. Kwok; E. Paulon; J. Barragry; F O’Hanlon; Shameer J. Mehta; F. Rahman; S Di Caro
Digestive and Liver Disease | 2018
K.C. Fragkos; D. Thong; N. Keane; S. Mehta; F. Rahman; S. Di Caro
Digestive and Liver Disease | 2018
N. Keane; K.C. Fragkos; F. Rahman; S. Mehta; S. Di Caro
Clinical Nutrition | 2018
Felipe Pantoja; Konstantinos C. Fragkos; P.S. Patel; N. Keane; Mark A. Samaan; Ivana Barnova; Simona Di Caro; Shameer J. Mehta; F. Rahman
Clinical Nutrition | 2018
K.C. Fragkos; P.S. Patel; N. Keane; M. Assoku; A. Baptista; K. Murray; S. Obbard; T. Shepherd; J. Barragry; A. Nwaogu; J. Rogers; S. Ajibodu; M. MacRae; S. Mehta; S. Di Caro; F. Rahman
Clinical Nutrition | 2018
P.S. Patel; K.C. Fragkos; N. Keane; K. Murray; S. Obbard; S. Mehta; F. Rahman; S. Di Caro
Clinical Nutrition | 2018
K.C. Fragkos; K. Murray; S. Obbard; T. Shepherd; J. Barragry; A. Nwaogu; J. Rogers; S. Ajibodu; N. Keane; P.S. Patel; M. MacRae; S. Mehta; S. Di Caro; F. Rahman
Clinical Nutrition | 2018
K.C. Fragkos; H. Kwok; A. Bhakta; N. Keane; R. Chakraverty; K. Thomson; F. Rahman; S. Di Caro; S. Mehta
Collaboration
Dive into the N. Keane's collaboration.
University College London Hospitals NHS Foundation Trust
View shared research outputs