scholarly journals Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani women

2019 ◽  
Vol 27 (3) ◽  
pp. 130-137 ◽  
Author(s):  
Victoria G Woof ◽  
Helen Ruane ◽  
Fiona Ulph ◽  
David P French ◽  
Nadeem Qureshi ◽  
...  

Objectives Previous research has largely attempted to explore breast screening experiences of South Asian women by combining opinions from Pakistani, Bangladeshi, and Indian women. This research often fails to reach the most underserved sub-groups of this population, with socioeconomic status not routinely reported, and English fluency being a participation requirement. With uptake low amongst British-Pakistani women, this study explores the experiences these women encounter when accessing the NHS Breast Screening Programme. Methods 19 one-to-one semi-structured interviews were carried out with British-Pakistani women from East Lancashire, UK. 14 interviews were conducted via an interpreter. Results Data were analysed using thematic analysis. Three themes were identified: ‘Absence of autonomy in screening and healthcare access’ describes how currently the screening service does not facilitate confidentiality or independence. Access requires third-party intervention, with language barriers preventing self-expression. ‘Appraisal of information sources’ makes distinctions between community and NHS communication. Whereas community communication was invaluable, NHS materials were deemed inaccessible due to translation incongruences and incomprehensible terminology. ‘Personal suppositions of breast screening’ explores the subjective issues associated with disengagement, including, the cultural misalignment of the service, and perceiving screening as a symptomatic service. Conclusions British-Pakistani women face some unique challenges when accessing breast screening. To promote uptake, the service needs to address the translation of screening materials and optimize upon community networks to disseminate knowledge, including knowledge of the screening environment within the context of culture to promote informed choice about attendance.

2003 ◽  
Vol 10 (1) ◽  
pp. 22-26 ◽  
Author(s):  
T Marshall ◽  
P Adab

Objective: To illustrate visually the lifetime probabilities of the principal outcomes of the UK breast screening programme in a readily understandable format. Methods: We derived prognostic data from a modelling exercise using published effectiveness data and routine data sources. We calculated the probability that a woman will survive to the age of 75 if she chooses to participate fully in breast screening from age 50 to 64 and if she chooses not to participate. We also calculated her probability of being referred for assessment, undergoing fine-needle biopsy and undergoing open biopsy. We present these data in two alternative decision aid formats. These alternative formats illustrate visually the outcomes for 1000 women and 100 women choosing each alternative: breast screening or no breast screening. Results: A woman participating in breast screening from age 50 to 64 increases her chances of surviving to age 75 by 0.6%. She has a 21.8% probability of surviving to age 75 and being referred for assessment but no further investigation. She has a 5.7% probability of undergoing core biopsy and a 0.9% probability of undergoing open biopsy. This information can easily be presented visually. Conclusions: We can provide realistic estimates of the effects of the breast screening programme on mortality in a readily understandable format. If we wish women to make an informed choice about breast screening they must be given this information.


BMC Cancer ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Victoria G. Woof ◽  
Helen Ruane ◽  
David P. French ◽  
Fiona Ulph ◽  
Nadeem Qureshi ◽  
...  

1983 ◽  
Vol 34 (5) ◽  
pp. 529-542 ◽  
Author(s):  
G.W.H. Stamp ◽  
G.H. Whitehouse ◽  
I.W. McDicken ◽  
S.J. Leinster ◽  
W.D. George

2007 ◽  
Vol 14 (4) ◽  
pp. 200-204 ◽  
Author(s):  
R L Bennett ◽  
R G Blanks ◽  
J Patnick ◽  
S M Moss

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