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  1. Article ; Online: Personalized Medicine, Disruptive Innovation, and "Trailblazer" Guidelines: Case Study and Theorization of an Unsuccessful Change Effort.

    Rushforth, Alex / Greenhalgh, Trisha

    The Milbank quarterly

    2020  Volume 98, Issue 2, Page(s) 581–617

    Abstract: Policy Points For complex reasons, the promise of "precision medicine" based on molecular pathways remains unrealized for many conditions. Clinical practice guidelines (theoretically, at least) can act as "trailblazers" to introduce tests and treatments ... ...

    Abstract Policy Points For complex reasons, the promise of "precision medicine" based on molecular pathways remains unrealized for many conditions. Clinical practice guidelines (theoretically, at least) can act as "trailblazers" to introduce tests and treatments that reflect precision medicine discoveries. We describe a detailed case study from the United Kingdom in which such an attempt was (so far) unsuccessful and show how this case provides generalizable lessons. Policymakers should be wary of using clinical practice guidelines as the sole, or even the primary, lever for introducing precision medicine.
    Context: Precision medicine, which addresses underlying molecular mechanisms of disease, depends on new technologies that measure specific biomarkers, leading (it is anticipated) to more accurate diagnosis, patient stratification, and tailored treatment. These technologies can be disruptive-that is, they make possible, and often require, radical changes to clinical practice and service organization-thereby improving quality, safety, or efficiency of care. Clinical practice guidelines may act as "trailblazers," introducing and legitimizing novel technologies and practices.
    Methods: We describe a case study of an attempt by academic researchers to radically change asthma management in the United Kingdom using a precision medicine biomarker (fractional exhaled nitric oxide, FeNO), measured using a portable breath device. We collected a wide-ranging data set that included more than 100 documents, 61 interviews, and 150 hours of ethnographic observation, and we analyzed it using technology-enhanced strong structuration theory (TESST).
    Findings: Our study describes a so-far unsuccessful attempt by academic respiratory medicine researchers to pave the way for a precision medicine approach to asthma using a government-endorsed national guideline. These researchers considered asthma management, especially in primary care, to be characterized by overdiagnosis and poor tailoring of treatment; engaged a national guideline development body in an effort to fix this problem; and ensured that the guideline required primary care clinicians to use FeNO technology for diagnosis and monitoring. However, clinicians working outside the tertiary referral centers did not accept, or agree to enact, the vision of precision medicine inscribed in the guideline-for multiple professional, operational, and economic reasons.
    Conclusions: "Trailblazer" guidelines, in which new technologies are recommended, may succeed as catalysts of change only in a limited way for interested individuals and groups. In the absence of a wider program of professionally led and adequately resourced change efforts, such guidelines will lack meaning, legitimacy, and authority among intended users and may be strongly resisted.
    MeSH term(s) Asthma/metabolism ; Asthma/therapy ; Biomarkers/metabolism ; Breath Tests ; Diffusion of Innovation ; Humans ; Nitric Oxide/metabolism ; Practice Guidelines as Topic ; Precision Medicine/methods ; United Kingdom
    Chemical Substances Biomarkers ; Nitric Oxide (31C4KY9ESH)
    Language English
    Publishing date 2020-05-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632829-5
    ISSN 1468-0009 ; 0887-378X
    ISSN (online) 1468-0009
    ISSN 0887-378X
    DOI 10.1111/1468-0009.12455
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: What’s in a slogan? Translational science and the rhetorical work of cancer researchers in a UK university

    Alex Rushforth

    Nordic Journal of Science and Technology Studies, Vol 4, Iss 1, Pp 32-

    2016  Volume 42

    Abstract: Translational science is currently proving a highly influential term in framing how biomedical research is promoted and evaluated in a great number of countries. Although there has been a steady trickle of scholarly literature on the topic, the ... ...

    Abstract Translational science is currently proving a highly influential term in framing how biomedical research is promoted and evaluated in a great number of countries. Although there has been a steady trickle of scholarly literature on the topic, the performative uses effects of the term in practices of academic researchers has been under-researched. Drawing on interviews with members of a cancer laboratory and research institute in a UK research university, the paper analyzes various uses and contexts in which the slogan is deployed. The findings demonstrate the multi-dimensional uses of the term across different levels of the organisation, acting at one level as a managerial function for formulating an ‘impact’ narrative, whilst also fulfilling researcher requirements to satisfy demands made of them in pursuing funding and positions. Analyzing how this specific slogan functions in this site evokes a wider set of considerations about the kinds of rhetoric invoked and increasingly expected of cancer scientists in academic settings.
    Keywords Translational science ; Academic researchers ; Cancer research ; Research governance ; General Works ; A
    Language English
    Publishing date 2016-07-01T00:00:00Z
    Publisher Nordic Journal of Science and Technology Studies
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: What’s in a slogan? Translational science and the rhetorical work of cancer researchers in a UK university

    Alex Rushforth

    Nordic Journal of Science and Technology Studies, Vol 4, Iss

    2016  Volume 1

    Abstract: Translational science is currently proving a highly influential term in framing how biomedical research is promoted and evaluated in a great number of countries. Although there has been a steady trickle of scholarly literature on the topic, the ... ...

    Abstract Translational science is currently proving a highly influential term in framing how biomedical research is promoted and evaluated in a great number of countries. Although there has been a steady trickle of scholarly literature on the topic, the performative uses effects of the term in practices of academic researchers has been under-researched. Drawing on interviews with members of a cancer laboratory and research institute in a UK research university, the paper analyzes various uses and contexts in which the slogan is deployed. The findings demonstrate the multi-dimensional uses of the term across different levels of the organisation, acting at one level as a managerial function for formulating an ‘impact’ narrative, whilst also fulfilling researcher requirements to satisfy demands made of them in pursuing funding and positions. Analyzing how this specific slogan functions in this site evokes a wider set of considerations about the kinds of rhetoric invoked and increasingly expected of cancer scientists in academic settings.
    Keywords Translational science ; Academic researchers ; Cancer research ; Research governance ; General Works ; A
    Language English
    Publishing date 2016-12-01T00:00:00Z
    Publisher Nordic Journal of Science and Technology Studies
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article: Enhanced Photon-Phonon Interaction in WSe

    Carr, Alex D / Ruppert, Claudia / Samusev, Anton K / Magnabosco, Giulia / Vogel, Nicolas / Linnik, Tetiana L / Rushforth, Andrew W / Bayer, Manfred / Scherbakov, Alexey V / Akimov, Andrey V

    ACS photonics

    2024  Volume 11, Issue 3, Page(s) 1147–1155

    Abstract: Acoustic nanocavities (ANCs) with resonance frequencies much above 1 GHz are prospective to be exploited in sensors and quantum operating devices. Nowadays, acoustic nanocavities fabricated from van der Waals (vdW) nanolayers allow them to exhibit ... ...

    Abstract Acoustic nanocavities (ANCs) with resonance frequencies much above 1 GHz are prospective to be exploited in sensors and quantum operating devices. Nowadays, acoustic nanocavities fabricated from van der Waals (vdW) nanolayers allow them to exhibit resonance frequencies of the breathing acoustic mode up to
    Language English
    Publishing date 2024-03-07
    Publishing country United States
    Document type Journal Article
    ISSN 2330-4022
    ISSN 2330-4022
    DOI 10.1021/acsphotonics.3c01601
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Changing media depictions of remote consulting in COVID-19: analysis of UK newspapers.

    Mroz, Gilly / Papoutsi, Chrysanthi / Rushforth, Alex / Greenhalgh, Trisha

    The British journal of general practice : the journal of the Royal College of General Practitioners

    2020  Volume 71, Issue 702, Page(s) e1–e9

    Abstract: Background: Remote consulting was introduced quickly into UK general practice in March 2020 as an emergency response to COVID-19. In July 2020, 'remote-first' became long-term government policy.: Aim: To explore how this change was portrayed in ... ...

    Abstract Background: Remote consulting was introduced quickly into UK general practice in March 2020 as an emergency response to COVID-19. In July 2020, 'remote-first' became long-term government policy.
    Aim: To explore how this change was portrayed in national newspapers and how depictions changed over time.
    Design and setting: Thematic analysis of newspaper articles referring to remote GP consultations from two time periods: 2 March-31 May 2020 (period 1) and 30 July-12 August 2020 (period 2).
    Method: Articles were identified through, and extracted from, LexisNexis Academic UK. A coding system of themes and narrative devices was developed and applied to the data. The analysis was developed iteratively, amending the coding structure as new data were added.
    Results: Remote consulting was widely covered in newspapers. Articles in period 1 depicted it positively, equating digital change with progress and linking novel technological solutions with improved efficiency and safety (for example, infection control) in a service that was overdue for modernisation. Articles in period 2 questioned the persistence of a remote-first service now that the pandemic was waning, emphasising, for example, missed diagnoses, challenges to the therapeutic relationship, and digital inequalities.
    Conclusion: As the first wave of the pandemic came and went, media depictions of remote consulting evolved from an 'efficiency and safety' narrative to a 'risks, inequalities, and lack of choice' narrative. To restore public trust in general practice, public communication should emphasise the wide menu of consulting options now available to patients and measures being taken to assure safety and avoid inequity.
    MeSH term(s) COVID-19/epidemiology ; General Practice ; Humans ; Information Dissemination ; Newspapers as Topic ; Pandemics ; Remote Consultation ; United Kingdom/epidemiology
    Language English
    Publishing date 2020-12-28
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1043148-2
    ISSN 1478-5242 ; 0035-8797 ; 0960-1643
    ISSN (online) 1478-5242
    ISSN 0035-8797 ; 0960-1643
    DOI 10.3399/BJGP.2020.0967
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Erratum: Developing services for long COVID: lessons from a study of wounded healers.

    Ladds, Emma / Rushforth, Alex / Wieringa, Sietse / Taylor, Sharon / Rayner, Clare / Husain, Laiba / Greenhalgh, Trisha

    Clinical medicine (London, England)

    2021  Volume 21, Issue 2, Page(s) 160

    Language English
    Publishing date 2021-03-26
    Publishing country England
    Document type Journal Article ; Published Erratum
    ZDB-ID 2048646-7
    ISSN 1473-4893 ; 1470-2118
    ISSN (online) 1473-4893
    ISSN 1470-2118
    DOI 10.7861/clinmed.err.21.2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Long Covid - The illness narratives.

    Rushforth, Alex / Ladds, Emma / Wieringa, Sietse / Taylor, Sharon / Husain, Laiba / Greenhalgh, Trisha

    Social science & medicine (1982)

    2021  Volume 286, Page(s) 114326

    Abstract: Callard and Perego depict long Covid as the first illness to be defined by patients who came together on social media. Responding to their call to address why patients were so effective in making long Covid visible and igniting action to improve its care, ...

    Abstract Callard and Perego depict long Covid as the first illness to be defined by patients who came together on social media. Responding to their call to address why patients were so effective in making long Covid visible and igniting action to improve its care, we use narrative inquiry - a field of research that investigates the place and power of stories and storytelling. We analyse a large dataset of narrative interviews and focus groups with 114 people with long Covid (45 of whom were healthcare professionals) from the United Kingdom, drawing on socio-narratology (Frank), therapeutic emplotment (Mattingly) and polyphonia (Bakhtin). We describe how storytelling devices including chronology, metaphor, characterisation, suspense and imagination were used to create persuasive accounts of a strange and frightening new condition that was beset with setbacks and overlooked or dismissed by health professionals. The most unique feature of long Covid narratives (in most but not all cases) was the absence, for various pandemic-related reasons, of a professional witness to them. Instead of sharing their narratives in therapeutic dialogue with their own clinician, people struggled with a fragmented inner monologue before finding an empathetic audience and other resonant narratives in the online community. Individually, the stories seemed to make little sense. Collectively, they provided a rich description of the diverse manifestations of a grave new illness, a shared account of rejection by the healthcare system, and a powerful call for action to fix the broken story. Evolving from individual narrative postings to collective narrative drama, long Covid communities challenged the prevailing model of Covid-19 as a short-lived respiratory illness which invariably delivers a classic triad of symptoms; undertook and published peer-reviewed research to substantiate its diverse and protracted manifestations; and gained positions as experts by experience on guideline development groups and policy taskforces.
    MeSH term(s) COVID-19/complications ; Communication ; Humans ; Narration ; SARS-CoV-2
    Language English
    Publishing date 2021-08-19
    Publishing country England
    Document type Journal Article ; Personal Narrative ; Research Support, Non-U.S. Gov't
    ZDB-ID 4766-1
    ISSN 1873-5347 ; 0037-7856 ; 0277-9536
    ISSN (online) 1873-5347
    ISSN 0037-7856 ; 0277-9536
    DOI 10.1016/j.socscimed.2021.114326
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Developing services for long COVID: lessons from a study of wounded healers.

    Ladds, Emma / Rushforth, Alex / Wieringa, Sietse / Taylor, Sharon / Rayner, Clare / Husain, Laiba / Greenhalgh, Trisha

    Clinical medicine (London, England)

    2021  Volume 21, Issue 1, Page(s) 59–65

    Abstract: Persistent symptoms lasting longer than 3 weeks are thought to affect 10-20% of patients following SARS-CoV-2 infection. No formal guidelines exist in the UK for treating patients with long COVID and services are sporadic and variable, although ... ...

    Abstract Persistent symptoms lasting longer than 3 weeks are thought to affect 10-20% of patients following SARS-CoV-2 infection. No formal guidelines exist in the UK for treating patients with long COVID and services are sporadic and variable, although additional funding is promised for their development.In this study, narrative interviews and focus groups are used to explore the lived experience of 43 healthcare professionals with long COVID. These individuals see the healthcare system from both professional and patient perspectives, thus represent an important wealth of expertise to inform service design.We present a set of co-designed quality standards, highlighting equity and ease of access, minimal patient care burden, clinical responsibility, a multidisciplinary and evidence-based approach, and patient involvement; and we apply these to propose a potential care pathway model that could be adapted and translated to improve care of patients long COVID.
    MeSH term(s) Adult ; COVID-19/diagnosis ; COVID-19/epidemiology ; COVID-19/therapy ; Delivery of Health Care/organization & administration ; Female ; Health Personnel/statistics & numerical data ; Humans ; Male ; Middle Aged ; Pandemics ; SARS-CoV-2
    Language English
    Publishing date 2021-01-20
    Publishing country England
    Document type Journal Article
    ZDB-ID 2048646-7
    ISSN 1473-4893 ; 1470-2118
    ISSN (online) 1473-4893
    ISSN 1470-2118
    DOI 10.7861/clinmed.2020-0962
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Persistent symptoms after Covid-19: qualitative study of 114 "long Covid" patients and draft quality principles for services.

    Ladds, Emma / Rushforth, Alex / Wieringa, Sietse / Taylor, Sharon / Rayner, Clare / Husain, Laiba / Greenhalgh, Trisha

    BMC health services research

    2020  Volume 20, Issue 1, Page(s) 1144

    Abstract: Background: Approximately 10% of patients with Covid-19 experience symptoms beyond 3-4 weeks. Patients call this "long Covid". We sought to document such patients' lived experience, including accessing and receiving healthcare and ideas for improving ... ...

    Abstract Background: Approximately 10% of patients with Covid-19 experience symptoms beyond 3-4 weeks. Patients call this "long Covid". We sought to document such patients' lived experience, including accessing and receiving healthcare and ideas for improving services.
    Methods: We held 55 individual interviews and 8 focus groups (n = 59) with people recruited from UK-based long Covid patient support groups, social media and snowballing. We restricted some focus groups to health professionals since they had already self-organised into online communities. Participants were invited to tell their stories and comment on others' stories. Data were audiotaped, transcribed, anonymised and coded using NVIVO. Analysis incorporated sociological theories of illness, healing, peer support, clinical relationships, access, and service redesign.
    Results: Of 114 participants aged 27-73 years, 80 were female. Eighty-four were White British, 13 Asian, 8 White Other, 5 Black, and 4 mixed ethnicity. Thirty-two were doctors and 19 other health professionals. Thirty-one had attended hospital, of whom 8 had been admitted. Analysis revealed a confusing illness with many, varied and often relapsing-remitting symptoms and uncertain prognosis; a heavy sense of loss and stigma; difficulty accessing and navigating services; difficulty being taken seriously and achieving a diagnosis; disjointed and siloed care (including inability to access specialist services); variation in standards (e.g. inconsistent criteria for seeing, investigating and referring patients); variable quality of the therapeutic relationship (some participants felt well supported while others felt "fobbed off"); and possible critical events (e.g. deterioration after being unable to access services). Emotionally significant aspects of participants' experiences informed ideas for improving services.
    Conclusion: Suggested quality principles for a long Covid service include ensuring access to care, reducing burden of illness, taking clinical responsibility and providing continuity of care, multi-disciplinary rehabilitation, evidence-based investigation and management, and further development of the knowledge base and clinical services.
    Trial registration: NCT04435041.
    MeSH term(s) Adult ; Aged ; COVID-19/complications ; COVID-19/therapy ; Female ; Focus Groups ; Health Personnel/psychology ; Health Personnel/statistics & numerical data ; Health Services Research ; Hospitalization/statistics & numerical data ; Humans ; Male ; Middle Aged ; Qualitative Research ; Quality of Health Care/organization & administration ; Time Factors ; United Kingdom
    Language English
    Publishing date 2020-12-20
    Publishing country England
    Document type Journal Article
    ISSN 1472-6963
    ISSN (online) 1472-6963
    DOI 10.1186/s12913-020-06001-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Persistent symptoms after Covid-19

    Emma Ladds / Alex Rushforth / Sietse Wieringa / Sharon Taylor / Clare Rayner / Laiba Husain / Trisha Greenhalgh

    BMC Health Services Research, Vol 20, Iss 1, Pp 1-

    qualitative study of 114 “long Covid” patients and draft quality principles for services

    2020  Volume 13

    Abstract: Abstract Background Approximately 10% of patients with Covid-19 experience symptoms beyond 3–4 weeks. Patients call this “long Covid”. We sought to document such patients’ lived experience, including accessing and receiving healthcare and ideas for ... ...

    Abstract Abstract Background Approximately 10% of patients with Covid-19 experience symptoms beyond 3–4 weeks. Patients call this “long Covid”. We sought to document such patients’ lived experience, including accessing and receiving healthcare and ideas for improving services. Methods We held 55 individual interviews and 8 focus groups (n = 59) with people recruited from UK-based long Covid patient support groups, social media and snowballing. We restricted some focus groups to health professionals since they had already self-organised into online communities. Participants were invited to tell their stories and comment on others’ stories. Data were audiotaped, transcribed, anonymised and coded using NVIVO. Analysis incorporated sociological theories of illness, healing, peer support, clinical relationships, access, and service redesign. Results Of 114 participants aged 27–73 years, 80 were female. Eighty-four were White British, 13 Asian, 8 White Other, 5 Black, and 4 mixed ethnicity. Thirty-two were doctors and 19 other health professionals. Thirty-one had attended hospital, of whom 8 had been admitted. Analysis revealed a confusing illness with many, varied and often relapsing-remitting symptoms and uncertain prognosis; a heavy sense of loss and stigma; difficulty accessing and navigating services; difficulty being taken seriously and achieving a diagnosis; disjointed and siloed care (including inability to access specialist services); variation in standards (e.g. inconsistent criteria for seeing, investigating and referring patients); variable quality of the therapeutic relationship (some participants felt well supported while others felt “fobbed off”); and possible critical events (e.g. deterioration after being unable to access services). Emotionally significant aspects of participants’ experiences informed ideas for improving services. Conclusion Suggested quality principles for a long Covid service include ensuring access to care, reducing burden of illness, taking clinical responsibility and providing continuity ...
    Keywords Post-acute Covid-19 ; Chronic Covid-19 ; Long Covid ; Qualitative study ; Quality standards ; Public aspects of medicine ; RA1-1270
    Subject code 360
    Language English
    Publishing date 2020-12-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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