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  1. AU=McCaughan Dorothy
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  1. Artikel ; Online: Incurable but treatable: Understanding, uncertainty and impact in chronic blood cancers-A qualitative study from the UK's Haematological Malignancy Research Network.

    Howell, Debra A / McCaughan, Dorothy / Smith, Alexandra G / Patmore, Russell / Roman, Eve

    PloS one

    2022  Band 17, Heft 2, Seite(n) e0263672

    Abstract: Objective: Most blood cancers are incurable and typically follow unpredictable remitting-relapsing pathways associated with varying need for treatment, which may be distressing for patients. Our objective was to conduct a qualitative study to explore ... ...

    Abstract Objective: Most blood cancers are incurable and typically follow unpredictable remitting-relapsing pathways associated with varying need for treatment, which may be distressing for patients. Our objective was to conduct a qualitative study to explore understanding among patients with such malignancies, including the explanations given by HCPs and the impact of uncertain trajectories, to generate evidence that could guide improvements in clinical practice.
    Methods: The study is set within a population-based patient cohort (the Haematological Malignancy Research Network), in which care is delivered across 14 hospitals according to national guidelines. In-depth interviews were conducted with 35 patients with chronic lymphocytic leukaemia, follicular lymphoma, marginal zone lymphoma or myeloma; and 10 accompanying relatives. Purposive sampling ensured selection of information-rich participants and the data were interrogated using reflective thematic analysis.
    Results: Rich data were collected and four themes (11 sub-themes) were identified: 1) Knowledge and understanding of chronic haematological malignancies; 2) Incurable but treatable; 3) Uncertainty about the future; and 4) Treatable (but still incurable): Impact on patients. Patients had rarely heard of blood cancer and many expressed difficulty understanding how an incurable malignancy that could not be removed, was treatable, often for long periods. While some were reassured that their cancer did not pose an immediate survival threat, others were particularly traumatised by the uncertain future it entailed, suffering ongoing emotional distress as a result, which could be more burdensome than any physical symptoms. Nonetheless, most interviewees understood that uncertain pathways were caused by the unpredictability of their disease trajectory, and not information being withheld.
    Conclusions: Many participants lacked knowledge about chronic haematological malignancies. HCPs acted to reassure patients about their diagnosis, and while this was appropriate and effective for some, it was less so for others, as the cancer-impact involved struggling to cope with ongoing uncertainty, distress and a shortened life-span.
    Mesh-Begriff(e) Aged ; Aged, 80 and over ; Family/psychology ; Female ; Health Knowledge, Attitudes, Practice ; Humans ; Interviews as Topic ; Leukemia, Lymphocytic, Chronic, B-Cell/psychology ; Leukemia, Lymphocytic, Chronic, B-Cell/therapy ; Lymphoma, B-Cell, Marginal Zone/psychology ; Lymphoma, B-Cell, Marginal Zone/therapy ; Lymphoma, Follicular/psychology ; Lymphoma, Follicular/therapy ; Male ; Middle Aged ; Multiple Myeloma/psychology ; Multiple Myeloma/therapy ; Practice Guidelines as Topic ; Qualitative Research ; Uncertainty
    Sprache Englisch
    Erscheinungsdatum 2022-02-10
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0263672
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Treatment decision making (TDM): a qualitative study exploring the perspectives of patients with chronic haematological cancers.

    McCaughan, Dorothy / Roman, Eve / Smith, Alexandra / Patmore, Russell / Howell, Debra

    BMJ open

    2022  Band 12, Heft 3, Seite(n) e050816

    Abstract: Objectives: Haematological malignancies are the fifth most common cancer in the UK, with chronic subtypes comprising around a third of all new diagnoses. These complex diseases have some similarities with other cancers, but often require different ... ...

    Abstract Objectives: Haematological malignancies are the fifth most common cancer in the UK, with chronic subtypes comprising around a third of all new diagnoses. These complex diseases have some similarities with other cancers, but often require different management. Surgical resection is not possible, and while some are curable with intensive chemotherapy, most indolent subtypes are managed with non-aggressive intermittent or continuous treatment, often over many years. Little is known about the views of patients with chronic haematological cancers regarding treatment decision making (TDM), a deficit our study aimed to address.
    Setting and design: Set within the Haematological Malignancy Research Network (HMRN: www.hmrn.org), an ongoing population-based cohort that provides infrastructure to support evidence-based research, HMRN data were augmented by qualitative information from in-depth interviews. Data were analysed for thematic content, combining inductive and deductive approaches. Interpretation involved seeking meaning, salience and connections within data.
    Participants: Thirty-five patients with four chronic subtypes: chronic lymphocytic leukaemia, follicular lymphoma, marginal zone lymphoma, and myeloma. Ten relatives were present and contributed to varying extents.
    Results: Five themes were discerned: (1) Preference for clinician recommendations; (2) Factors implicated in patient involvement in TDM; (3) Perceptions of proactive/non-proactive approaches to TDM; (4) Experiences of TDM at various points in the disease trajectory; (5) Support from others. Our principal finding relates to a strong preference among interviewees for treatment recommendations from haematologists, based on trust in their expertise and perceptions of empathetic patient-clinician relationships.
    Conclusion: Interviewees wanted to be involved in TDM to varying extents, contingent on complex, inter-related factors, that are dynamic and subject to change according to differing clinical and personal contexts. Patients may benefit from clinicians assessing their shifting preferences for involvement on multiple occasions. Strong preferences for acceptance of recommendations was associated with cancer complexity, trust in clinician expertise and positive perceptions of patient-clinician relationships.
    Mesh-Begriff(e) Decision Making ; Graft vs Host Disease ; Hematologic Neoplasms/therapy ; Humans ; Leukemia, Lymphocytic, Chronic, B-Cell ; Multiple Myeloma/therapy ; Qualitative Research
    Sprache Englisch
    Erscheinungsdatum 2022-03-29
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2021-050816
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Experiences and preferences for psychosocial support: a qualitative study exploring the views of patients with chronic haematological cancers.

    Sheridan, Rebecca / McCaughan, Dorothy / Hewison, Ann / Roman, Eve / Smith, Alexandra / Patmore, Russell / Howell, Debra

    BMJ open

    2023  Band 13, Heft 8, Seite(n) e070467

    Abstract: Objectives: Patients with chronic haematological cancers are often treated on a relapsing-remitting pathway, which may extend for many years. Such diagnoses are associated with uncertainties that often cause anxiety and distress, meaning patients (and ... ...

    Abstract Objectives: Patients with chronic haematological cancers are often treated on a relapsing-remitting pathway, which may extend for many years. Such diagnoses are associated with uncertainties that often cause anxiety and distress, meaning patients (and families) are susceptible to potentially prolonged emotional difficulties, across the cancer journey. Experiences and preferences regarding psychosocial needs and support over time are relatively unexplored, which this study aimed to address.
    Setting and design: Set within the UK's Haematological Malignancy Research Network (an ongoing population-based cohort that generates evidence to underpin improved clinical practice) a qualitative, exploratory study was conducted, using semistructured interviews. Reflexive thematic analysis was used to assess the interview data via an exploratory, inductive approach, underpinned by the research questions.
    Participants: Thirty-five patients were included with chronic lymphocytic leukaemia, follicular lymphoma, marginal zone lymphoma or myeloma; 10 of whom were interviewed alongside a relative.
    Results: Five themes were identified from the data: (1) accessing support, (2) individual coping behaviour affecting support preferences, (3) divergent and fluctuating thoughts on patient support forums, (4) the role, influence and needs of family and friends and (5) other sources of support and outstanding needs. Findings suggest that patients' individual attitudes towards support varied over time. This also influenced whether support was perceived to be available, and if it was then used.
    Conclusion: This study highlighted the variation in preferences towards psychosocial support among patients with chronic haematological cancers. As patients can live for many years with significant emotional difficulties, they may benefit from frequent monitoring of their psychosocial well-being, as well as signposting to holistic support, if this is needed.
    Mesh-Begriff(e) Humans ; Neoplasm Recurrence, Local ; Hematologic Neoplasms/therapy ; Leukemia, Lymphocytic, Chronic, B-Cell ; Multiple Myeloma ; Adaptation, Psychological
    Sprache Englisch
    Erscheinungsdatum 2023-08-18
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2022-070467
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Patient perspectives of 'Watch and Wait' for chronic haematological cancers: Findings from a qualitative study.

    McCaughan, Dorothy / Roman, Eve / Sheridan, Rebecca / Hewison, Ann / Smith, Alexandra G / Patmore, Russell / Howell, Debra A

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

    2023  Band 65, Seite(n) 102349

    Abstract: Purpose: Chronic blood cancers are incurable, and characterised by unpredictable, remitting-relapsing pathways. Management often involves periods of observation prior to treatment (if required), and post-treatment, in an approach known as 'Watch and ... ...

    Abstract Purpose: Chronic blood cancers are incurable, and characterised by unpredictable, remitting-relapsing pathways. Management often involves periods of observation prior to treatment (if required), and post-treatment, in an approach known as 'Watch and Wait'. This study aimed to explore patient experiences of 'Watch and Wait'.
    Methods: In-depth interviews with 35 patients (10 accompanied by relatives) with chronic lymphocytic leukaemia, follicular lymphoma, marginal zone lymphoma or myeloma. Data were analysed using descriptive qualitative techniques.
    Results: Patient views of Watch and Wait ranged along a continuum, from immediate acceptance, to concern about treatment deferral. Significant ongoing anxiety and distress were described by some, due to the uncertain pathways associated with Watch and Wait. Infrequent contact with clinical staff was said to exacerbate this, as there was limited opportunity to ask questions and seek reassurance. Patients indicated that the impact of their malignancy could be underestimated by clinicians; possibly due to them comparing chronic and acute subtypes. Most patients lacked knowledge of blood cancers. Support from clinicians was considered greater among treated patients, possibly due to increased contact, and many drew on relatives for aid. Most patients were satisfied with their time-allocation with haematology staff, although experiences could be improved by greater access to clinical nurse specialists, counselling services, and community-based facilities.
    Conclusion: Experiences varied. Anxiety about unpredictable futures could be more distressing than any physical symptoms and have a greater impact on quality of life. Ongoing assessment could facilitate identification of difficulties, and is particularly important among individuals without supportive networks.
    Mesh-Begriff(e) Humans ; Quality of Life ; Neoplasm Recurrence, Local/therapy ; Hematologic Neoplasms/diagnosis ; Hematologic Neoplasms/therapy ; Rectal Neoplasms/therapy
    Sprache Englisch
    Erscheinungsdatum 2023-05-13
    Erscheinungsland Scotland
    Dokumenttyp Journal Article
    ZDB-ID 2017117-1
    ISSN 1532-2122 ; 1462-3889
    ISSN (online) 1532-2122
    ISSN 1462-3889
    DOI 10.1016/j.ejon.2023.102349
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Chronic myeloid leukaemia: A qualitative interview study exploring disease impact from patient and practitioner perspectives.

    Hewison, Ann / Roman, Eve / Smith, Alexandra / McCaughan, Dorothy / Sheridan, Rebecca / Patmore, Russell / Atkin, Karl / Howell, Debra

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

    2023  Band 67, Seite(n) 102421

    Abstract: Purpose: Improvements in chronic myeloid leukaemia treatment mean it is now relevant to examine the experiences of living with this cancer over a lifetime. This qualitative study aimed to investigate the impact of chronic myeloid leukaemia, from patient ...

    Abstract Purpose: Improvements in chronic myeloid leukaemia treatment mean it is now relevant to examine the experiences of living with this cancer over a lifetime. This qualitative study aimed to investigate the impact of chronic myeloid leukaemia, from patient and healthcare practitioner perspectives.
    Methods: The research was set within the UK's Haematological Malignancy Research Network; a population-based cohort of patients newly diagnosed with blood cancer, treated at one of fourteen hospitals. Purposive sampling led to interviews with seventeen patients and thirteen health care practitioners. Data were analysed using thematic analysis.
    Results: Two analytical themes, "Significant impact of disease and treatment" and "Mediators of the impact of disease and treatment", and six sub-themes, were derived from patient interviews and supported with data from practitioners. Chronic myeloid leukaemia was described by patients as having significant widespread impact, which could be mediated by their knowledge, social support, and the quality of healthcare systems. Practitioners reflected patient accounts, but could underestimate the impact of this cancer. They generally viewed chronic myeloid leukaemia as less complex, severe and impactful than acute blood cancers; a message that reassured patients at diagnosis, but could later unintentionally contribute to difficulties discussing side effects and struggles to cope.
    Conclusion: Chronic myeloid leukaemia may significantly impact individuals, particularly as it is experienced over the lifetime. Greater understanding and discussion of the breadth and extent to which patients are affected, including potential mediators, could enhance clinical care.
    Mesh-Begriff(e) Humans ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Hematologic Neoplasms/therapy ; Hematology ; Qualitative Research
    Sprache Englisch
    Erscheinungsdatum 2023-09-17
    Erscheinungsland Scotland
    Dokumenttyp Journal Article
    ZDB-ID 2017117-1
    ISSN 1532-2122 ; 1462-3889
    ISSN (online) 1532-2122
    ISSN 1462-3889
    DOI 10.1016/j.ejon.2023.102421
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Incurable but treatable

    Debra A Howell / Dorothy McCaughan / Alexandra G Smith / Russell Patmore / Eve Roman

    PLoS ONE, Vol 17, Iss 2, p e

    Understanding, uncertainty and impact in chronic blood cancers-A qualitative study from the UK's Haematological Malignancy Research Network.

    2022  Band 0263672

    Abstract: Objective Most blood cancers are incurable and typically follow unpredictable remitting-relapsing pathways associated with varying need for treatment, which may be distressing for patients. Our objective was to conduct a qualitative study to explore ... ...

    Abstract Objective Most blood cancers are incurable and typically follow unpredictable remitting-relapsing pathways associated with varying need for treatment, which may be distressing for patients. Our objective was to conduct a qualitative study to explore understanding among patients with such malignancies, including the explanations given by HCPs and the impact of uncertain trajectories, to generate evidence that could guide improvements in clinical practice. Methods The study is set within a population-based patient cohort (the Haematological Malignancy Research Network), in which care is delivered across 14 hospitals according to national guidelines. In-depth interviews were conducted with 35 patients with chronic lymphocytic leukaemia, follicular lymphoma, marginal zone lymphoma or myeloma; and 10 accompanying relatives. Purposive sampling ensured selection of information-rich participants and the data were interrogated using reflective thematic analysis. Results Rich data were collected and four themes (11 sub-themes) were identified: 1) Knowledge and understanding of chronic haematological malignancies; 2) Incurable but treatable; 3) Uncertainty about the future; and 4) Treatable (but still incurable): Impact on patients. Patients had rarely heard of blood cancer and many expressed difficulty understanding how an incurable malignancy that could not be removed, was treatable, often for long periods. While some were reassured that their cancer did not pose an immediate survival threat, others were particularly traumatised by the uncertain future it entailed, suffering ongoing emotional distress as a result, which could be more burdensome than any physical symptoms. Nonetheless, most interviewees understood that uncertain pathways were caused by the unpredictability of their disease trajectory, and not information being withheld. Conclusions Many participants lacked knowledge about chronic haematological malignancies. HCPs acted to reassure patients about their diagnosis, and while this was appropriate and ...
    Schlagwörter Medicine ; R ; Science ; Q
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2022-01-01T00:00:00Z
    Verlag Public Library of Science (PLoS)
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  7. Artikel ; Online: Nurses' and surgeons' views and experiences of surgical wounds healing by secondary intention: A qualitative study.

    McCaughan, Dorothy / Sheard, Laura / Cullum, Nicky / Dumville, Jo / Chetter, Ian

    Journal of clinical nursing

    2020  Band 29, Heft 13-14, Seite(n) 2557–2571

    Abstract: Aims and objectives: To explore surgeons' and nurses' perspectives of managing surgical wounds healing by secondary intention.: Background: Every year, more than 10 million surgical operations are performed in the NHS in the UK. Most surgical wounds ... ...

    Abstract Aims and objectives: To explore surgeons' and nurses' perspectives of managing surgical wounds healing by secondary intention.
    Background: Every year, more than 10 million surgical operations are performed in the NHS in the UK. Most surgical wounds heal by primary intention, where the edges of the wound are brought together with staples, sutures, adhesive glue or clips. Sometimes wounds are deliberately left open to heal, from the base up, known as "healing by secondary intention." These wounds are often slow to heal, prone to infection and complex to manage.
    Design: A qualitative, descriptive approach, using semi-structured interviews.
    Methods: Interviews with five (general, vascular and plastic) surgeons and 7 nurses (3 tissue viability nurses, 2 district and 1 community nurse, and 1 hospital nurse) working in hospital and community care settings in two locations in the north of England. Data analysis followed the recommended sequential steps of "Framework" approach. Consolidated criteria for reporting qualitative research guided the study report.
    Results: Participants reported that the main types of wounds healing by secondary intention that they manage are extensive abdominal cavity wounds; open wounds relating to treatment for pilonidal sinus; large open wounds on the feet of patients with diabetes; and axilla and groin wounds, associated with removal of lymph nodes for cancer. Infection and prolonged time to healing were the main challenges. Negative pressure wound therapy was the most favoured treatment option.
    Conclusions: Negative pressure wound therapy was advocated by professionals despite a lack of research evidence indicating clinical or cost-effectiveness. Our findings underscore the need for rigorous evaluation of negative pressure wound therapy, and other wound care treatments, through studies that include economic evaluation.
    Relevance for clinical practice: Clinical decision-making in wound care could be optimised through further robust studies to inform practitioners about the cost-effectiveness of available treatments.
    Mesh-Begriff(e) Attitude of Health Personnel ; Female ; Humans ; Male ; Negative-Pressure Wound Therapy/economics ; Negative-Pressure Wound Therapy/standards ; Qualitative Research ; Surgical Wound/therapy ; Surgical Wound Infection/prevention & control ; Wound Healing
    Sprache Englisch
    Erscheinungsdatum 2020-04-23
    Erscheinungsland England
    Dokumenttyp Journal Article ; Multicenter Study
    ZDB-ID 1159483-4
    ISSN 1365-2702 ; 0962-1067 ; 1752-9816
    ISSN (online) 1365-2702
    ISSN 0962-1067 ; 1752-9816
    DOI 10.1111/jocn.15279
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Chromosome microarray characterisation of chromosome arm 12p loss associated with complex molecular karyotype and recurrent adverse cytogenetic markers in multiple myeloma.

    Hung, Dorothy / Lenton, Douglas / Eslick, Renee / Blennerhassett, Richard / Joshi, Maansi / McCaughan, Georgia / Day, Samantha / Wright, Dale

    Genes, chromosomes & cancer

    2021  Band 60, Heft 10, Seite(n) 668–677

    Abstract: Copy number loss within chromosome 12 short arm (12p) has gained attention as an adverse cytogenetic marker in multiple myeloma. The prognostic significance and characterisation of the common minimal deleted region remains controversial between various ... ...

    Abstract Copy number loss within chromosome 12 short arm (12p) has gained attention as an adverse cytogenetic marker in multiple myeloma. The prognostic significance and characterisation of the common minimal deleted region remains controversial between various studies with loss of CD27 proposed as the putative critical gene. We aimed to determine the frequency of 12p loss, its correlation with adverse cytogenetic markers further to define and characterise 12p deletions. Our study included a prospective cohort of 574 multiple myeloma patients referred for cytogenetic testing, including interphase fluorescence in situ hybridisation for IGH (14q32.33) translocations and chromosome microarray. Loss of 12p was detected in 54/574 (9.4%) patients and when compared with the non-12p loss group [520/574 (90.6%)], 12p loss patients demonstrated a statistically significant association with specific recurrent cytogenetic markers: complex molecular karyotypes (98.1% vs 45.2%), 1p loss (50.0% vs 20.2%), t(4;14) (20.4% vs 7.7%), 8p loss (37.0% vs 15.0%), 13/13q loss (70.4% vs 41.7%), and 17p loss (33.3% vs 6.5%). The size and location of 12p losses were heterogeneous with a common 0.88 Mb minimally deleted region that included ~9 genes from ETV6 to CDKN1B in 52/54 (~96.3%) patients but did not include CD27. Our findings support 12p loss being a secondary chromosome abnormality frequently co-occurring with adverse cytogenetic markers and complex molecular karyotypes indicative of chromosome instability.
    Mesh-Begriff(e) Abnormal Karyotype ; Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor/genetics ; Chromosome Aberrations ; Chromosome Deletion ; Chromosomes, Human, Pair 12/genetics ; Cytogenetics ; Female ; Follow-Up Studies ; Gene Expression Regulation, Neoplastic ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Middle Aged ; Multiple Myeloma/genetics ; Multiple Myeloma/pathology ; Prognosis ; Prospective Studies ; Translocation, Genetic
    Chemische Substanzen Biomarkers, Tumor
    Sprache Englisch
    Erscheinungsdatum 2021-06-07
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 1018988-9
    ISSN 1098-2264 ; 1045-2257
    ISSN (online) 1098-2264
    ISSN 1045-2257
    DOI 10.1002/gcc.22975
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: The effect of organisational culture on patient safety.

    Kaufman, Gerri / McCaughan, Dorothy

    Nursing standard (Royal College of Nursing (Great Britain) : 1987)

    2013  Band 27, Heft 43, Seite(n) 50–56

    Abstract: This article explores the links between organisational culture and patient safety. The key elements associated with a safety culture, most notably effective leadership, good teamwork, a culture of learning and fairness, and fostering patient-centred care, ...

    Abstract This article explores the links between organisational culture and patient safety. The key elements associated with a safety culture, most notably effective leadership, good teamwork, a culture of learning and fairness, and fostering patient-centred care, are discussed. The broader aspects of a systems approach to promoting quality and safety, with specific reference to clinical governance, human factors, and ergonomics principles and methods, are also briefly explored, particularly in light of the report of the public inquiry into care failings at Mid Staffordshire NHS Foundation Trust.
    Mesh-Begriff(e) Hospitals, Public/organization & administration ; Humans ; Leadership ; Organizational Culture ; Patient Safety/standards ; Patient-Centered Care/organization & administration ; Quality of Health Care/organization & administration ; Quality of Health Care/standards ; Safety Management/methods ; State Medicine/organization & administration ; United Kingdom
    Sprache Englisch
    Erscheinungsdatum 2013-06
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 645016-7
    ISSN 2047-9018 ; 0029-6570
    ISSN (online) 2047-9018
    ISSN 0029-6570
    DOI 10.7748/ns2013.06.27.43.50.e7280
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: Patient safety: threats and solutions.

    McCaughan, Dorothy / Kaufman, Gerri

    Nursing standard (Royal College of Nursing (Great Britain) : 1987)

    2013  Band 27, Heft 44, Seite(n) 48–55; quiz 56, 58

    Abstract: The recent landmark report into the care failings at Stafford Hospital has called for sweeping changes to end the NHS's neglect of patient safety (Francis 2013). The report calls for a 'fundamental change' in culture so that patients are always put first, ...

    Abstract The recent landmark report into the care failings at Stafford Hospital has called for sweeping changes to end the NHS's neglect of patient safety (Francis 2013). The report calls for a 'fundamental change' in culture so that patients are always put first, and it makes 290 recommendations covering a broad range of issues relating to patient care and safety in the NHS. This article explores issues surrounding patient safety, including the terminology associated with harm and error. The types of patient safety incidents that occur in different care environments are discussed. It offers insight into why patient safety incidents occur and describes some of the underlying factors. It also discusses preventive strategies and the role of patients and family members in enhancing safety.
    Mesh-Begriff(e) Education, Continuing ; Hospitals, Public ; Humans ; Models, Theoretical ; Patient Admission ; Patient Safety ; Primary Health Care ; Quality of Health Care ; United Kingdom
    Sprache Englisch
    Erscheinungsdatum 2013-08-03
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 645016-7
    ISSN 2047-9018 ; 0029-6570
    ISSN (online) 2047-9018
    ISSN 0029-6570
    DOI 10.7748/ns2013.07.27.44.48.e7580
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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