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  1. Article ; Online: Exploring trial publication and research waste in COVID-19 randomised trials of hydroxychloroquine, corticosteroids, and vitamin D: a meta-epidemiological cohort study.

    Fincham, Lisa / Hohlfeld, Ameer / Clarke, Mike / Kredo, Tamara / McCaul, Michael

    BMC medical research methodology

    2024  Volume 24, Issue 1, Page(s) 19

    Abstract: Background: The global research response to the COVID-19 pandemic was impressive, but also led to an infodemic and considerable research waste. Registered, but unpublished trials added to this noise. We aimed to determine the proportion of registered ... ...

    Abstract Background: The global research response to the COVID-19 pandemic was impressive, but also led to an infodemic and considerable research waste. Registered, but unpublished trials added to this noise. We aimed to determine the proportion of registered randomised trials of common COVID-19 treatments that were published and to describe the characteristics of these trials to examine the association between trial characteristics, publication status and research waste.
    Methods: This meta-epidemiological cohort study used a sample of randomised trials of corticosteroids, hydroxychloroquine or vitamin D as treatments for COVID-19, registered between 1 November 2019 and 31 December 2021 and available via the WHO ICTRP portal. We searched for the trials' published results up to 20 October 2022. We extracted the trial characteristics, analysing with descriptive statistics. We performed univariate logistic regression to examine the association between trials' characteristics and publication status, followed by multiple logistic regression using significant characteristics to assess the association between trial characteristics and publication status.
    Results: We identified 357 eligible trials on ICTRP. Of these, 107 (30%) had published or made their results available publicly by 20 October 2022, while 250 (70%) had not been published or shared their results publicly. Multiple logistic regression analysis showed that a larger target sample size was a significant positive predictor of publication with target sample sizes above 300 almost tripling the odds of publication (aOR: 2.75, 95% CI: 1.35 to 5.62).
    Conclusions: Less than one third of registered trials made their results public and our findings identified that many trialists had not updated their trial registry entry with the trial status, results or both. Failure to share trial results publicly is a disservice to patients, clinicians and policy makers and adds to research waste.
    MeSH term(s) Humans ; Adrenal Cortex Hormones ; Cohort Studies ; COVID-19 ; COVID-19 Drug Treatment ; Hydroxychloroquine ; Pandemics ; Randomized Controlled Trials as Topic ; Vitamin D
    Chemical Substances Adrenal Cortex Hormones ; Hydroxychloroquine (4QWG6N8QKH) ; Vitamin D (1406-16-2)
    Language English
    Publishing date 2024-01-23
    Publishing country England
    Document type Journal Article ; Meta-Analysis
    ZDB-ID 2041362-2
    ISSN 1471-2288 ; 1471-2288
    ISSN (online) 1471-2288
    ISSN 1471-2288
    DOI 10.1186/s12874-023-02110-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Pharmacological interventions for periorificial (perioral) dermatitis in children and adults: a systematic review.

    Gray, N A / Tod, B / Rohwer, A / Fincham, L / Visser, W I / McCaul, M

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2021  Volume 36, Issue 3, Page(s) 380–390

    Abstract: The plethora of pharmacologic treatments used for periorificial dermatitis (POD) makes clinical decision-making challenging. The objectives of this review were to assess the efficacy and safety of pharmacological interventions for POD in children and ... ...

    Abstract The plethora of pharmacologic treatments used for periorificial dermatitis (POD) makes clinical decision-making challenging. The objectives of this review were to assess the efficacy and safety of pharmacological interventions for POD in children and adults. The search was performed on 2 February 2021 and included seven databases and trial registries, with no date or language restrictions Study selection, data extraction and risk of bias assessments were performed independently and in duplicate by two authors, in accordance with a prespecified protocol. Meta-analyses were performed and reported in accordance with PRISMA guidelines. Where meta-analysis was not possible, a narrative synthesis was performed and reported in accordance with SWiM guidelines. The certainty of evidence was assessed using the Grading of Recommendation, Assessment, Development and Evaluation approach. Eleven studies representing 733 participants were included. Oral tetracycline may improve physician-reported severity of POD from day 20 onwards (low certainty evidence). Adverse effects may include abdominal discomfort, facial dryness and pruritus. Pimecrolimus cream may improve physician-reported severity slightly after 4 weeks of treatment (MD -0.49, 95% CI -1.02 to 0.04, n = 164, low certainty evidence). Adverse effects may include erythema, herpes simplex virus infection, burning and pruritus. Azelaic acid gel may result in no change in either physician- or patient-reported severity after 6 weeks of treatment. The evidence is very uncertain about the effect of praziquantel ointment on physician-reported severity and skin-related quality of life after 4 weeks of treatment. The evidence is also very uncertain about the effect of topical clindamycin/benzoyl peroxide on physician-reported severity. The body of evidence to inform treatment of POD currently consists of low and very low certainty evidence for important outcomes. Well-designed trials are needed to further investigate treatment options. Data are required for children and from low-middle income countries to improve external validity. Future trials should also include adequate post-treatment follow-up and standardized outcome measures.
    MeSH term(s) Adult ; Child ; Dermatitis, Perioral ; Emollients/therapeutic use ; Humans ; Pruritus/drug therapy ; Quality of Life
    Chemical Substances Emollients
    Language English
    Publishing date 2021-12-02
    Publishing country England
    Document type Journal Article ; Review ; Systematic Review
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.17817
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Supportive care needs of men living with prostate cancer in England: a survey.

    Ream, E / Quennell, A / Fincham, L / Faithfull, S / Khoo, V / Wilson-Barnett, J / Richardson, A

    British journal of cancer

    2008  Volume 98, Issue 12, Page(s) 1903–1909

    Abstract: Men with prostate cancer have various treatment options depending upon their stage of disease, age and presence of comorbidity. However, these treatments typically induce side effects, which generate currently ill-defined supportive care needs. This ... ...

    Abstract Men with prostate cancer have various treatment options depending upon their stage of disease, age and presence of comorbidity. However, these treatments typically induce side effects, which generate currently ill-defined supportive care needs. This study examined the supportive care needs of men with prostate cancer within England. A postal questionnaire survey was conducted in six acute NHS Trusts. Seven hundred and forty-one men with prostate cancer participated. They had been diagnosed 3-24 months prior to the survey and had received various treatments. Men surveyed had specific and significant unmet supportive care needs. Areas of greatest need are related to psychological distress, sexuality-related issues and management of enduring lower urinary tract symptoms. High levels of psychological distress were reported, and those reporting psychological distress reported greater unmet supportive care needs. Unmet sexuality-related need was highest in younger men following radical prostatectomy. Lower urinary tract symptoms were almost universal in the sample. Perceived quality of life varied; men unsure of their remission status reported lowest quality of life. Psychological distress impacts significantly on perceived unmet need and is currently not being assessed or managed well in men living with prostate cancer in England.
    MeSH term(s) Aged ; England ; Health Services Needs and Demand ; Humans ; Male ; Middle Aged ; Prostatic Neoplasms/physiopathology ; Prostatic Neoplasms/psychology ; Prostatic Neoplasms/therapy ; Quality of Life ; State Medicine ; Stress, Psychological ; Surveys and Questionnaires ; United Kingdom ; Urinary Tract/physiopathology
    Language English
    Publishing date 2008-05-27
    Publishing country England
    Document type Journal Article
    ZDB-ID 80075-2
    ISSN 1532-1827 ; 0007-0920
    ISSN (online) 1532-1827
    ISSN 0007-0920
    DOI 10.1038/sj.bjc.6604406
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Working patterns and perceived contribution of prostate cancer clinical nurse specialists: a mixed method investigation.

    Ream, Emma / Wilson-Barnett, Jenifer / Faithfull, Sara / Fincham, Lorraine / Khoo, Vincent / Richardson, Alison

    International journal of nursing studies

    2009  Volume 46, Issue 10, Page(s) 1345–1354

    Abstract: Background: Prostate cancer is prevalent worldwide. In England, men living with this malignancy often report unmet psychological, informational, urological and sexual needs. Their experience of care is correspondingly lower than that of other patient ... ...

    Abstract Background: Prostate cancer is prevalent worldwide. In England, men living with this malignancy often report unmet psychological, informational, urological and sexual needs. Their experience of care is correspondingly lower than that of other patient groups with cancer. To address this, prostate cancer clinical nurse specialist posts were established across England and Scotland. Their intent was to support men with this form of cancer, enhance symptom management and improve quality of service provision.
    Objectives: The research sought to investigate prostate cancer clinical nurse specialists' roles, determine whom they targeted services at, and determine their work practices and perceived contribution.
    Design: A mixed method multi-site exploratory-descriptive design was employed.
    Settings: Data were collected across four acute NHS Trusts-one in the South of England, one in the Midlands, one in Northern England and one in Scotland, respectively.
    Participants: Participants included 4 prostate cancer clinical nurse specialists, 19 of their clinical colleagues and 40 men they provided care to.
    Methods: Data were collected through nurse specialists' completion of a Diary and Contact Sheets. Interviews were conducted concurrently with the nurses, stakeholders they worked alongside and patients on their caseload. Data were collected between November 2004 and January 2006.
    Results: There was great variation in the qualifications and experience of nurse specialists and in the services they provided. Services ranged from generic support and information provided across the disease trajectory to provision of services to meet specific care needs, e.g. providing nurse-led clinics for erectile dysfunction. Patients and members of the multidisciplinary team welcomed the introduction of nurse specialists but were aware they could become over burdened through their rapidly growing caseloads.
    Conclusions: Variability in services provided by the prostate cancer nurse specialists arose from differences in local demand for nursing services and the skills and experiences of those appointed. Such variability - whilst understandable - has implications for access and equity across patient groups. Further, it can compromise efforts to define clinical nurse specialists' contribution to care, can impede others' expectation of their role, and render their outcomes difficult to evaluate.
    MeSH term(s) Aged ; Aged, 80 and over ; Attitude of Health Personnel ; Attitude to Health ; Clinical Competence ; England/epidemiology ; Female ; Health Services Needs and Demand ; Humans ; Incidence ; Male ; Middle Aged ; Nurse Clinicians/education ; Nurse Clinicians/organization & administration ; Nurse Clinicians/psychology ; Nurse's Role/psychology ; Nursing Evaluation Research ; Nursing Methodology Research ; Oncology Nursing/education ; Oncology Nursing/organization & administration ; Professional Autonomy ; Prostatic Neoplasms/epidemiology ; Prostatic Neoplasms/nursing ; Prostatic Neoplasms/psychology ; Qualitative Research ; Research Design ; Scotland/epidemiology ; Surveys and Questionnaires ; Time and Motion Studies
    Language English
    Publishing date 2009-10
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80148-3
    ISSN 1873-491X ; 0020-7489
    ISSN (online) 1873-491X
    ISSN 0020-7489
    DOI 10.1016/j.ijnurstu.2009.03.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Supportive care: experiences of cancer patients.

    Fincham, Lorraine / Copp, Gina / Caldwell, Kay / Jones, Louise / Tookman, Adrian

    European journal of oncology nursing : the official journal of European Oncology Nursing Society

    2005  Volume 9, Issue 3, Page(s) 258–268

    Abstract: The aim of this study was to explore how cancer patients with progressive disease perceived and experienced supportive care at the different stages of their cancer journey and to compare this to the perceptions of health care professionals. It was a ... ...

    Abstract The aim of this study was to explore how cancer patients with progressive disease perceived and experienced supportive care at the different stages of their cancer journey and to compare this to the perceptions of health care professionals. It was a single centre study using qualitative data obtained from two focus group interviews in an independent centre for specialist palliative care. Eight patients attending the centre were interviewed in two focus groups to ascertain their views on the supportive care that they had experienced during the course of their illness, focusing on: time of diagnosis, acute treatment phase and palliative care phase. Themes that emerged from the analysis of the interview transcripts using the QSR NUD*IST (version 4) software package included the following: manner in which diagnosis was revealed, information made available to family and friends, patients' acceptance of cancer; service provision such as a named contact person, choices in treatment and care, problems of limited resources; feelings of being unsupported, and ways in which supportive care could be improved.
    MeSH term(s) Adult ; Aged ; Attitude to Health ; Choice Behavior ; Day Care, Medical/psychology ; Day Care, Medical/standards ; Disease Progression ; Family/psychology ; Female ; Focus Groups ; Friends/psychology ; Health Services Needs and Demand ; Humans ; Male ; Middle Aged ; Neoplasms/diagnosis ; Neoplasms/psychology ; Neoplasms/therapy ; Nursing Methodology Research ; Palliative Care/psychology ; Palliative Care/standards ; Patient Education as Topic/standards ; Power (Psychology) ; Professional-Patient Relations ; Qualitative Research ; Research Design/standards ; Social Support ; Surveys and Questionnaires ; Truth Disclosure
    Language English
    Publishing date 2005-09
    Publishing country Scotland
    Document type Journal Article
    ZDB-ID 2017117-1
    ISSN 1462-3889
    ISSN 1462-3889
    DOI 10.1016/j.ejon.2004.08.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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