{"id":49231,"date":"2020-12-15T14:29:06","date_gmt":"2020-12-15T13:29:06","guid":{"rendered":"https:\/\/blogs.bmj.com\/bmj\/?p=49231"},"modified":"2020-12-15T14:29:06","modified_gmt":"2020-12-15T13:29:06","slug":"patients-and-carers-views-must-be-involved-in-the-rollout-of-precision-medicine","status":"publish","type":"post","link":"https:\/\/blogs.bmj.com\/bmj\/2020\/12\/15\/patients-and-carers-views-must-be-involved-in-the-rollout-of-precision-medicine\/","title":{"rendered":"Patients and carers views must be involved in the rollout of precision medicine"},"content":{"rendered":"

The sequencing of the human genome has begun to enhance our understanding of the biological mechanisms underlying chronic diseases, for example asthma. The twentieth century model of asthma management is often that of a generic disease with grades of severity, treated by adding layer on layer of medicine. However, the discoveries that follow from the description of the human genome are influencing our thinking. They are enriching the established milieu with additional information about new individual pathways, urging us to move \u201c<\/span>from mostly one-size-fits-all treatment to genuinely personalized care.\u201d <\/span><\/i>[<\/span>1] We may soon have the power to decide whether or not we can let this novel information fine-tune the management of chronic diseases in wider populations.<\/span><\/p>\n

Or will we?\u00a0<\/span><\/p>\n

We are only empowered by information when we understand and realise it. Currently, there exists a gap between the information about genomics and chronic diseases that researchers know and share through articles in specialist journals, and the understanding of this information among patients and carers, the public, and many healthcare professionals. Unless this gap closes, doctors, nurses, patients and the public cannot make the right decisions about future patient care, and a small body of experts, with or without links to industry, may remain in the driving seat through sheer knowledge power, and this might not work in the best interests of the patients.\u00a0<\/span><\/p>\n

A recent systematic review of 21 studies demonstrates an overall interest in 9000 members of the public, including patients, almost exclusively from North America and Europe, to engage in a wider discussion on personalised medicine. [2] However, other than one study from Singapore, we could identify no evidence of a systematic exploration of the public\u2019s views on personalised medicine from Africa, South America and Asia, where over half the world\u2019s populations live, and where personalised medicine-related treatment approaches will inevitably influence the management of common diseases over the next decade.<\/span><\/p>\n

Historically, doctors may not have been efficient at seeking patient\u2019s views about new treatment choices, but views are shifting in the North, and we were pleased to note the breadth of studies seeking the views of the public regarding personalised medicine. Many of us in the developed world are actively seeking patient feedback regarding our day-to-day performance, while researchers are exploring opportunities for public engagement to discuss future medicine and inviting public involvement to strengthen clinical trial design.\u00a0<\/span><\/p>\n

How much of this is happening outside the developed world? The treatment choices are creeping in, often at different rates, depending on ability to pay. From the patient\u2019s point of view, there is arguably an even greater need to think about cost versus benefit. Our exploratory discussions last year with rural and urban populations in India revealed one clear message: people, particularly the young, are keen to engage in this process, but there is very little scope for discussion. Young women employed in rice fields spared their valuable morning time learning how a skin barrier defect might worsen their child\u2019s asthma or eczema and joined in the discussion on how this could be prevented through the use of emollients that are available in the local market. [3,4] Speaking in the local language (Bengali) and translating from English as necessary, we used models and pictures, communicating allergy advice. As doctors and researchers, we learnt that there are fewer cultural, educational and economic barriers to worldwide public participation in discussing the pros and cons of medical treatments than we currently perceive.\u00a0<\/span><\/p>\n

We know that the price of ignoring the views of patients and carers is high. We run the risk of mis-diagnosis, overdiagnosis and overtreatment, or in ignoring the public\u2019s views when developing research programmes. In Europe, a clear and articulate patient voice is guiding the development of these interventions. There are, however, major healthcare and societal costs if patients and carers are not involved worldwide in the roll out of personalised medicine over the forthcoming years.\u00a0<\/span><\/p>\n

Somnath Mukhopadhyay<\/strong> is Chair of Paediatrics at the Royal Alexandra Children\u2019s Hospital and the Brighton and Sussex Medical School, UK. He is a consultant in children\u2019s respiratory diseases and allergy<\/span><\/em><\/p>\n

Katy Fidler<\/strong> is Clinical Senior Lecturer in Paediatrics at the Royal Alexandra Children\u2019s Hospital and Brighton and Sussex Medical School, UK. She is a consultant in children\u2019s infectious diseases.<\/span><\/em><\/p>\n

Ciara Holden<\/strong> is a clinical academic fellow and specialist registrar in paediatrics at the Royal Alexandra Children\u2019s Hospital in Brighton, UK<\/span><\/em><\/p>\n

Christina Jones<\/strong> is a senior lecturer in Clinical Psychology at the University of Surrey, UK.<\/span><\/em><\/p>\n

All the members of this group have a strong interest in the development of new personalised \/ precision medicine-linked treatment strategies for children\u2019s allergy and asthma and other chronic diseases, with the aim of improving quality-of-life and reducing disease morbidity, and are currently performing exploratory research or randomised controlled trials to develop these strategies.<\/span><\/p>\n

Competing interests: None declared<\/span><\/i><\/p>\n

    \n
  1. NHS England \u2013 Full text of Simon Stevens\u2019 speech (2018). <\/span>www.england.nhs.uk\/2014\/04\/simon-stevens-speech\/<\/span><\/a><\/li>\n
  2. Holden C<\/span><\/a>, <\/span>Bignell L<\/span><\/a>, <\/span>Mukhopadhyay S<\/span><\/a>, <\/span>Jones C<\/span><\/a> The public perception of the facilitators and barriers to implementing personalized medicine: a systematic review Personalized Medicine 2019 Oct 8. doi: 10.2217\/pme-2018-0151. [Epub ahead of print].<\/span><\/li>\n
  3. Palmer CN, Irvine AD, Terron-Kwiatkowski A, Zhao Y, Liao H, Lee SP, Goudie DR, Sandilands A, Campbell LE, Smith FJ, O’Regan GM, Watson RM, Cecil JE, Bale SJ, Compton JG, DiGiovanna JJ, Fleckman P, Lewis-Jones S, Arseculeratne G, Sergeant A, Munro CS, El Houate B, McElreavey K, Halkjaer LB, Bisgaard H, Mukhopadhyay S, McLean WH. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nature Genetics 2006;38(4):441-446.<\/span><\/li>\n
  4. Soares P, Fidler K, Felton J, Tavendale R, H\u00f6vels A, Bremner SA, Palmer CNA, Mukhopadhyay S Individuals with filaggrin-related eczema and asthma have increased long-term medication and hospital admission costs. British Journal of Dermatology 2018;179(3):717-723.<\/span><\/li>\n
  5. Turner S, Francis B, Vijverberg S, Pino-Yanes M, Maitland-van der Zee AH, Basu K, Bignell L, Mukhopadhyay S, Tavendale R, Palmer C, Hawcutt D, Pirmohamed M, Burchard EG, Lipworth B; Pharmacogenomics in Childhood Asthma Consortium. Childhood asthma exacerbations and the Arg16 \u03b22-receptor polymorphism: A meta-analysis stratified by treatment. Journal of Allergy and Clinical Immunology 2016;138:107-113.<\/span><\/li>\n<\/ol>\n

     <\/p>\n

     <\/p>\n","protected":false},"excerpt":{"rendered":"

    The sequencing of the human genome has begun to enhance our understanding of the biological mechanisms underlying chronic diseases, for example asthma. The twentieth century model of asthma management is […]<\/p>\n

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