A5002688185- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Immunodeficiency and Autoimmune Disorders
- Genetic Syndromes and Imprinting
- Nutrition, Genetics, and Disease
- Nursing Roles and Practices
- Hip and Femur Fractures
- Medical Imaging and Pathology Studies
- Cystic Fibrosis Research Advances
- Gender Diversity and Inequality
- Dental Health and Care Utilization
- Grief, Bereavement, and Mental Health
- Physical Activity and Health
- Quality and Safety in Healthcare
- Obesity and Health Practices
- Homelessness and Social Issues
- Medical Malpractice and Liability Issues
- Musculoskeletal synovial abnormalities and treatments
- LGBTQ Health, Identity, and Policy
- Vitamin D Research Studies
- Employment and Welfare Studies
- Health Services Management and Policy
- Peripheral Nerve Disorders
- Nonprofit Sector and Volunteering
Queen's University Belfast
2019-2025
University of Ulster
2013-2021
Amersham Hospital
2000
Bensham Hospital
1970-1975
Royal Buckinghamshire Hospital
1973
Western Regional Hospital
1963
Background The National Institute for Health and Care Research call research partnerships was designed to build capacity in palliative end-of-life care ensure that the of is conducted areas greatest need where there are historically low levels research. Northern Ireland has high need, relatively underdeveloped services, comparatively Aims To Ireland, with a specific focus on less experienced sites, so strong applications could be submitted Part 2 Commissioned Call: building evidence base....
Abstract Background Many people living and working with rare diseases describe consistent difficulties accessing appropriate information support. In this study an evaluation of the awareness diseases, alongside related educational resources available for patients, their families healthcare professionals, was conducted in 2018–2019 using online survey semi-structured interviews disease collaborative groups (charities, voluntary community groups) active across Northern Ireland (NI). Methods...
This exploratory study aimed to gain an understanding of carer reported experiences derived specifically from persons caring for someone with a rare disease. The survey took place online on the SmartSurvey platform November 2019 January 2020. facilitated workshop in Bangor Carnegie Library, Northern Ireland. To be eligible participate respondents had adults Fifty-seven part, 15.8% male, 84.2% female. Thirty-two attendees were part workshop. While carers several positive aspects their role,...
Abstract Objective Many older patients, housebound or living in long‐term care facilities (LTCFs) have limited access to dental care. This descriptive qualitative study aimed understand general practitioners (GDPs) attitudes and perceived barriers undertaking Domiciliary Dental Care (DDC) for those patients Northern Ireland (NI). Methods Semi‐structured telephone interviews were conducted with a purposive sample of 12 GDPs Ireland. Interviews digitally recorded transcribed verbatim. An...
To explore university nursing students and academic staff's perceptions of what increased gender diversity might bring to the profession.
Abstract Objectives The impact of the current COVID-19 pandemic has been felt worldwide. Many vulnerable populations rely heavily on peer support provided by individual or collaborative groups. This study aimed to evaluate groups supporting patients with a rare disease(s). Anecdotally significantly changed way in which these operate and services they can provide. Data description A targeted survey was conducted online disease results highlight challenges are facing during this help identify...
Abstract Background Oral healthcare service provision for dependent older adults is often poor. For dental services to provide more responsive and equitable care, evidence-based approaches are needed. To facilitate future research, the development application of a core outcome set would be beneficial. The aim this study develop oral health research involving adults. Methods A multi-step process consensus methods including key stakeholders will undertaken. This involve identifying potentially...
Journal Article The Problem of the Ageing Population Get access J McMullan, M.D Formerly Deputy S.A.M.O. S.E. Metropolitan Regional Hospital Board Search for other works by this author on: Oxford Academic Google Scholar Postgraduate Medical Journal, Volume 39, Issue 453, July 1963, Pages 382–393, https://doi.org/10.1136/pgmj.39.453.382 Published: 01 1963
Background: The UK 100,000 Genomes Project was a transformational research project which facilitated whole genome sequencing (WGS) diagnostics for rare diseases. We evaluated experiences of introducing WGS in Northern Ireland, providing recommendations future projects. Methods: This formative evaluation included (1) an appraisal the logistics implementing and delivering WGS, (2) survey participant self-reported views experiences, (3) semi-structured interviews with healthcare staff as key...
Abstract In this paper we explore whether government policy acts as a barrier or facilitator to the work of nonprofits, and in what ways (if at all) different contexts influence place-based community-led nonprofit organizations working improve health wellbeing their communities. Employing ‘abductive’ analysis qualitative data collected through in-depth semi-structured interviews focus groups with 20 non-profit leaders located parts UK, found that can act both various times. There is often...
<b><i>Introduction:</i></b> Only 5% of rare diseases have an approved treatment available, therefore patients often utilise complementary and integrative medicines (CIMs) to help manage their condition. Limited high-quality evidence-based studies are available which support the effectiveness CIM, as it is difficult show that outcome a direct result CIM intervention not due bias. Patients healthcare professionals must weigh up evidence quality, safety, efficacy,...
Abstract Background General Practitioners (GPs) play an important role in healthcare delivery for people living with a rare disease and their families. Managing long-term multisystem diseases that often have no cure sub-optimal treatment options can be extremely challenging. Aim To gain understanding of GP’s perception experience diseases. Design Setting This is exploratory study GPs from Northern Ireland. Method An online survey was hosted within SmartSurvey, available 6 weeks early 2019,...
Abstract Background Many people living and working with rare diseases describe consistent difficulties accessing appropriate information support. In this study an evaluation of the awareness diseases, alongside related educational resources available for patients, their families healthcare professionals, was conducted in 2018-2019 using online survey semi-structured interviews disease collaborative groups (charities, voluntary community groups) active across Northern Ireland (NI). Results...
Background The uniqueness and complexity of rare diseases, together with a perceived lack understanding from health professionals, can make caring for someone disease extremely challenging. Carers are often forced to become ‘expert’ patients alongside people they care for. Due the demands placed upon carers it is essential that appropriate support available them ensure continue carry out this vital role. This exploratory study researched challenges face when looking after identify how could...
Setting: An online survey was hosted within Smart Survey, available for 6 weeks in early 2019, which queried: GPs career to date, interaction with rare disease patients, challenges faced, the exchange of information priorities future, support such patients and finally training. The contained open-ended closed-ended questions both qualitative (narrative) quantitative analyses were carried out.