K. Hunt

发表

Rethinking the patient: using Burden of Treatment Theory to understand the changing dynamics of illness

Alison Richardson, Katie Gallacher, Victor M Montori, 2014, BMC Health Services Research.

EXPERTS 1—experiences of long-term life-limiting conditions among patients and carers: protocol for a qualitative meta-synthesis and conceptual modelling study

J. Glanville, C. Pope, C. May, 2015, BMJ Open.

Quality of life of colorectal cancer survivors in England: report on a national survey of colorectal cancer survivors using Patient Reported Outcome Measures (PROMs)

P. Kind, S. Vernon, P. Wright, 2015 .

Development and testing of a text-mining approach to analyse patients’ comments on their experiences of colorectal cancer care

M. Simon, M. Bracher, C. Foster, 2015, BMJ Quality & Safety.

Developing the methods and questionnaire (VOICES-SF) for a national retrospective mortality follow-back survey of palliative and end-of-life care in England

A. Richardson, A. Darlington, J. Addington-hall, 2017, BMJ Supportive & Palliative Care.

Inflammation in Aging Part 2: Implications for the Health of Older People and Recommendations for Nursing Practice

D. Voegeli, H. Roberts, K. Hunt, 2010, Biological research for nursing.

Burden of treatment in the light of the international classification of functioning, disability and health: a “best fit” framework synthesis

A. Marques, C. Jácome, S. Demain, 2017, Disability and rehabilitation.

Clinician Perspectives on How to Hold Earlier Discussions About Palliative and End-of-Life Care With Chronic Obstructive Pulmonary Disease Patients

N. Tavares, T. Wilkinson, K. Hunt, 2022, Journal of hospice and palliative nursing : JHPN : the official journal of the Hospice and Palliative Nurses Association.

Last months of life of people with intellectual disabilities: A UK population-based study of death and dying in intellectual disability community services.

T. Kroll, J. Shearn, M. McCarron, 2020, Journal of applied research in intellectual disabilities : JARID.

End-of-life care and preferences for place of death among the oldest old: results of a population-based survey using VOICES-Short Form.

J. Addington-hall, N. Shlomo, K. Hunt, 2014, Journal of palliative medicine.

Managing expectations: cognitive authority and experienced control in complex healthcare processes

C. May, K. Hunt, 2017, BMC Health Services Research.

International study of the place of death of people with cancer: a population-level comparison of 14 countries across 4 continents using death certificate data

B. Onwuteaka-Philipsen, L. Deliens, J. Teno, 2015, British Journal of Cancer.

Hidden lives and deaths: the last months of life of people with intellectual disabilities living in long-term, generic care settings in the UK.

S. Brearley, J. Shearn, M. McCarron, 2021, Journal of applied research in intellectual disabilities : JARID.

End-of-life care in intellectual disability: a retrospective cross-sectional study

T. Kroll, J. Shearn, M. McCarron, 2019, BMJ Supportive & Palliative Care.

Nursing care at end of life: a UK-based survey of the deaths of people living in care settings for people with intellectual disability

J. Shearn, R. Northway, K. Hunt, 2018, Journal of research in nursing : JRN.

Expecting the unexpected: measures, outcomes and dying trajectories for expected and unexpected death in adults with intellectual disabilities in social care settings in the UK.

J. Shearn, K. Lowe, E. Jones, 2020, Journal of applied research in intellectual disabilities : JARID.

The palliative care needs of adults with intellectual disabilities and their access to palliative care services: A systematic review

S. Brearley, I. Tuffrey‐Wijne, K. Sleeman, 2020, Palliative medicine.

Work of being an adult patient with chronic kidney disease: a systematic review of qualitative studies

C. May, M. Myall, Amanda Cummings, 2018, BMJ Open.

Inflammation in Aging Part 1: Physiology and Immunological Mechanisms

D. Voegeli, H. Roberts, K. Hunt, 2010, Biological research for nursing.

Palliative and end-of-life care conversations in COPD: a systematic literature review

N. Tavares, N. Jarrett, T. Wilkinson, 2017, ERJ Open Research.

Differences in place of death between lung cancer and COPD patients: a 14-country study using death certificate data

B. Onwuteaka-Philipsen, L. Deliens, J. Teno, 2017, npj Primary Care Respiratory Medicine.

End-of-life care and achieving preferences for place of death in England: Results of a population-based survey using the VOICES-SF questionnaire

J. Addington-hall, N. Shlomo, K. Hunt, 2014, Palliative medicine.

Patient-Centered Discussions About Disease Progression, Symptom, and Treatment Burden in Chronic Obstructive Pulmonary Disease Could Facilitate the Integration of End-of-Life Discussions in the Disease Trajectory: Patient, Clinician, and Literature Perspectives: A Multimethod Approach.

N. Tavares, T. Wilkinson, K. Hunt, 2022, Journal of palliative medicine.

The preferences of patients with chronic obstructive pulmonary disease are to discuss palliative care plans with familiar respiratory clinicians, but to delay conversations until their condition deteriorates: A study guided by interpretative phenomenological analysis

N. Tavares, N. Jarrett, T. Wilkinson, 2020, Palliative medicine.

Participant recruitment in sensitive surveys: a comparative trial of ‘opt in’ versus ‘opt out’ approaches

Natalie Shlomo, Julia Addington-Hall, J. Addington-hall, 2013, BMC Medical Research Methodology.

Cross-cultural adaptation and measurement properties of generic and cancer-related patient-reported outcome measures (PROMs) for use with cancer patients in Brazil: a systematic review

R. Wagland, K. Hunt, C. A. Albach, 2017, Quality of Life Research.

Development and initial validation of a new outcome measure for hospice and palliative care: the St Christopher's Index of Patient Priorities (SKIPP)

B. Monroe, J. Addington-hall, N. Sykes, 2013, BMJ Supportive & Palliative Care.

Reducing avoidable hospital admission in older people: health status, frailty and predicting risk of ill-defined conditions diagnoses in older people admitted with collapse.

D. Voegeli, H. Roberts, K. Hunt, 2013, Archives of gerontology and geriatrics.

Living With, Managing and Minimising Treatment Burden in Long Term Conditions: A Systematic Review of Qualitative Research

Alda Marques, Sara Demain, Carlos Areia, 2015, PloS one.

The nursing work of hospital-based clinical practice guideline implementation: an explanatory systematic review using Normalisation Process Theory.

C. May, K. Hunt, A. Sibley, 2014, International journal of nursing studies.

Prognostic disclosure and quality of life in palliative care: a systematic review

Sanhapan Wattanapisit, R. Wagland, K. Hunt, 2020, BMJ Supportive & Palliative Care.

Place of death for people with HIV: a population-level comparison of eleven countries across three continents using death certificate data

B. Onwuteaka-Philipsen, L. Deliens, J. Teno, 2018, BMC Infectious Diseases.

Quality of life of colorectal cancer survivors in England: report on a national survey of colorectal cancer survivors using Patient Reported Outcome Measures (PROMs)

P. Kind, S. Vernon, P. Wright, 2015 .

Rethinking the patient: using Burden of Treatment Theory to understand the changing dynamics of illness

F. Mair, D. Eton, V. Montori, 2014, BMC Health Services Research.

Inflammation in Aging Part 2: Implications for the Health of Older People and Recommendations for Nursing Practice

D. Voegeli, H. Roberts, K. Hunt, 2010, Biological research for nursing.