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Featured researches published by Helen Busby.


web science | 1998

Estimating the burden of musculoskeletal disorders in the community: the comparative prevalence of symptoms at different anatomical sites, and the relation to social deprivation

Michelle Urwin; Deborah Symmons; Timothy C. Allison; Therese Brammah; Helen Busby; Morven Roxby; Alicia Simmons; Gareth Williams

BACKGROUND Epidemiologically-based rheumatology healthcare needs assessment requires an understanding of the incidence and prevalence of musculoskeletal disorders in the community, of the reasons why people consult in primary care, and of the proportion of people who would benefit from referral to secondary care and paramedical services. This paper reports the first phase of such a needs assessment exercise. SPECIFIC OBJECTIVE To estimate the relative frequency of musculoskeletal pain in different, and multiple, anatomical sites in the adult population. SETTING Three general practices in the former Tameside and Glossop Health Authority, Greater Manchester, UK, a predominantly urban area. DESIGN Population survey. METHODS An age and sex stratified sample of 6000 adults from the three practices was mailed a questionnaire that sought data on demographic factors, musculoskeletal symptoms (pain in the past month lasting for more than a week), and physical disability (using the modified Health Assessment Questionnaire- mHAQ). The areas of pain covered were neck, back, shoulder, elbow, hand, hip, knee, and multiple joints. The Carstairs index was used as a measure of social deprivation of the postcode sector in which the person lived. RESULTS The response rate after two reminders was 78.5%. Non-responders were more likely to live in areas of high social deprivation. People who lived in more deprived areas were also more likely to report musculoskeletal pain, especially backpain. After adjusting for social deprivation the rates of musculoskeletal pain did not differ between the practices and so their results were combined. After adjustment for social deprivation, the most common site of pain was back (23%; 95% CI 21, 25) followed by knee (19%; 95% CI 18, 21), and shoulder (16%; 95% CI 14, 17). The majority of subjects who reported pain had pain in more than one site. The prevalence of physical disability in the community rose with age. It was highest in those with multiple joint problems but was also high in those with isolated back or knee pain. CONCLUSION Musculoskeletal pain is common in the community. People who live in socially deprived areas have more musculoskeletal symptoms. Estimates of the overall burden of musculoskeletal pain that combine the results of site specific surveys will be too high, those that do not adjust for socioeconomic factors will be too low.


Science As Culture | 2006

Biobanks, national identity and imagined communities: The case of UK biobank

Helen Busby; Paul Martin

Recent years have seen the emergence of a number of large-scale national and regional genetic biobanks. Amongst these biobanks are those population collections that, as their name suggests, seek to...


Clinical Ethics | 2010

The meanings of consent to the donation of cord blood stem cells: perspectives from an interview-based study of a public cord blood bank in England.

Helen Busby

This paper explores the perspectives of women who have agreed that their umbilical cord blood may be collected for a public ‘cord blood bank’, for use in transplant medicine or research. Drawing on interview data from 27 mothers who agreed to the collection and use of their umbilical cord blood, these choices and the informed consent process are explored. It is shown that the needs of sick children requiring transplants are prominent in narrative accounts of cord blood banking, together with high expectations for future applications of stem cells. Given this dynamic, a concern arises that the complex and multiple uses of tissues and related data might be oversimplified in the consent process. In conclusion, the positive finding of a commitment to mutuality in cord blood banking among these women is underlined, and its implications for the wider debate on cord blood banking are discussed.


Sociology of Health and Illness | 2008

3. Bodies of knowledge: lay and biomedical understandings of musculoskeletal disorders

Helen Busby; Gareth Williams; Anne Rogers


Sociology of Health and Illness | 2006

Biobanks, bioethics and concepts of donated blood in the UK

Helen Busby


Health & Place | 2003

‘Everywhere and nowhere’: locating and understanding the ‘new’ public health ☆

Sara MacKian; Heather Elliott; Helen Busby; Jennie Popay


Primary Health Care Research & Development | 2004

Developing public health work in local health systems

Jennie Popay; Ute Kowarzik; Sara MacKian; Helen Busby; Heather Elliot


web science | 1999

Public health and primary care: a necessary relationship

Helen Busby; Heather Elliott; Jennie Popay Ba; Gareth Williams


Clinical Ethics | 2006

Consent, trust and ethics: reflections on the findings of an interview based study with people donating blood for genetic research for research within the NHS

Helen Busby


Archive | 2004

Reassessing the gift relationship : the meaning and ethics of blood donation for genetic research in the UK.

Helen Busby

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Anne Rogers

University of Southampton

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Michelle Urwin

University of Manchester

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