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  1. Book ; Online: Naval Leadership in the Atlantic World : The Age of Reform and Revolution, 1700 -1850

    Harding, Richard / Guiméra, Agustin

    2017  

    Keywords Naval forces & warfare ; History ; Frigate ; Horatio Nelson ; 1st Viscount Nelson ; Louis Guillouet ; comte d'Orvilliers ; Royal Navy ; Spain
    Size 1 Online-Ressource
    Publisher University of Westminster Press
    Publishing place London
    Document type Book ; Online
    Note English ; Open Access
    HBZ-ID HT021051487
    ISBN 9781911534099 ; 9781911534105 ; 1911534092 ; 1911534106
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  2. Book: The lung

    Harding, Richard / Pinkerton, Kent E.

    development, aging and the environment

    2015  

    Author's details ed. Richard Harding ; Kent E. Pinkerton
    Keywords Lunge ; Ontogenie ; Altern
    Subject Alterungsprozess ; Altwerden ; Seneszenz ; Alterung ; Entwicklung ; Ontogenese ; Entwicklungsgeschichte ; Individualentwicklung ; Pulmo
    Language English
    Size XV, 499, [8] S. : Ill., graph. Darst.
    Edition 2. ed.
    Publisher Elsevier Acad. Press
    Publishing place Amsterdam u.a.
    Publishing country Netherlands
    Document type Book
    HBZ-ID HT018476527
    ISBN 978-0-12-799941-8 ; 0-12-799941-8
    Database Catalogue ZB MED Medicine, Health

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    In stock of ZB MED Cologne/Königswinter

    Shelf markLoan statusLocation
    2014 A 4524 available for loan (reading room) Lesesaal EG

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  3. Book ; Online: Naval Leadership in the Atlantic World: The Age of Reform and Revolution, 1700-1850

    Harding, Richard / Guimerá, Augustin

    2017  

    Abstract: The naval leader has taken centre stage in traditional naval histories. However, while the historical narrative has been fairly consistent the development of various navies has been accompanied by assumptions, challenges and competing visions of the ... ...

    Abstract The naval leader has taken centre stage in traditional naval histories. However, while the historical narrative has been fairly consistent the development of various navies has been accompanied by assumptions, challenges and competing visions of the social characteristics of naval leaders and of their function. Whilst leadership has been a constant theme in historical studies, it has not been scrutinised as a phenomenon in its own right. This book examines the critical period in Europe between 1700 -1850, when political, economic and cultural shifts were bringing about a new understanding of the individual and of society. Bringing together context with a focus on naval leadership as a phenomenon is at the heart of this book, a unique collaborative venture between British, French and Spanish scholars. As globalisation develops in the twenty-first century the significance of navies looks set to increase. This volume of essays aims to place naval leadership in its historical context
    Keywords Sociology (General) ; Political institutions and public administration (General) ; History (General) ; Atlantischer Ozean ; Marine ; Führung ; Geschichte 1700-1850
    Subject Führen ; Führerschaft ; Personalführung ; Mitarbeiterführung ; Menschenführung ; Führungsverhalten ; Kriegsflotte ; Kriegsmarine ; Schlachtflotte ; Seestreitkräfte
    Size 1 electronic resource (212 p.)
    Publisher University of Westminster Press
    Document type Book ; Online
    Note English ; Open Access
    HBZ-ID HT020093699
    ISBN 9781911534082 ; 9781911534761 ; 9781911534099 ; 9781911534105 ; 1911534084 ; 1911534769 ; 1911534092 ; 1911534106
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  4. Article: Building evidence and capacity in global health palliative care.

    Harding, Richard

    Ecancermedicalscience

    2022  Volume 16, Page(s) 1378

    Abstract: To achieve universal health coverage goals, access to quality palliative care must be rapidly scaled up in low and middle-income countries. By 2060, people living with cancer at the end of life will be the major contributors to serious health-related ... ...

    Abstract To achieve universal health coverage goals, access to quality palliative care must be rapidly scaled up in low and middle-income countries. By 2060, people living with cancer at the end of life will be the major contributors to serious health-related suffering. Major developments have occurred in the science of palliative care research in low- and middle-income countries (LMIC), from the development and validation of outcome measures to the delivery of randomised controlled trials. While the evidence has demonstrated context-specific needs among patients and families facing life-limiting illness, there are also many commonalities. Specific areas of leadership in the field have emerged from LMIC in HIV palliative care and in care for children. These innovations offer enormous potential for adaptation in high income countries. International partnerships in research, founded on mutually beneficial learning and capacity building, are central to achieving universal health coverage goals.
    Language English
    Publishing date 2022-04-28
    Publishing country England
    Document type Journal Article
    ISSN 1754-6605
    ISSN 1754-6605
    DOI 10.3332/ecancer.2022.1378
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Book: The lung

    Harding, Richard

    development, aging and the environment

    2004  

    Author's details ed. Richard Harding
    Keywords Lunge ; Ontogenie ; Altern
    Subject Alterungsprozess ; Altwerden ; Seneszenz ; Alterung ; Entwicklung ; Ontogenese ; Entwicklungsgeschichte ; Individualentwicklung ; Pulmo
    Language English
    Size XIV, 403, [8] S. : Ill., graph. Darst.
    Publisher Elsevier
    Publishing place Amsterdam u.a.
    Publishing country Netherlands
    Document type Book
    HBZ-ID HT013840843
    ISBN 0-12-324751-9 ; 978-0-12-324751-3
    Database Catalogue ZB MED Medicine, Health

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    In stock of ZB MED Cologne/Königswinter

    Shelf markLoan statusLocation
    2003 A 4297 order for loan Magazin

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  6. Book: Fetal growth and development

    Harding, Richard

    2001  

    Author's details ed. by Richard Harding
    Keywords Mensch ; Embryonalentwicklung
    Subject Embryo ; Embryogenese ; Keimesentwicklung ; Menschen ; Homo sapiens
    Language English
    Size X, 284 S. : Ill., graph. Darst.
    Publisher Cambridge Univ. Press
    Publishing place Cambridge u.a.
    Publishing country Great Britain
    Document type Book
    HBZ-ID HT013069783
    ISBN 0-521-64543-3 ; 0-521-64237-X ; 978-0-521-64543-0 ; 978-0-521-64237-8
    Database Catalogue ZB MED Medicine, Health

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    In stock of ZB MED Cologne/Königswinter

    Shelf markLoan statusLocation
    2001 A 3104 order for loan Magazin

    Order via subito

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  7. Article ; Online: Palliative care as an essential component of the HIV care continuum.

    Harding, Richard

    The lancet. HIV

    2018  Volume 5, Issue 9, Page(s) e524–e530

    Abstract: Although antiretroviral therapy has reduced mortality among people with HIV, inadequate treatment coverage, ageing, and the increasing incidence of organ failure and malignancies mean that high-quality care should include care at the end of life. This ... ...

    Abstract Although antiretroviral therapy has reduced mortality among people with HIV, inadequate treatment coverage, ageing, and the increasing incidence of organ failure and malignancies mean that high-quality care should include care at the end of life. This Review summarises the epidemiology of HIV in relation to mortality, and the symptoms and concerns of people with AIDS and those living with HIV who have either related or unrelated advanced comorbidities. In response to the evidence of a need for palliative care, the principles and practice of palliative care are described, and the evidence for its effectiveness and cost-effectiveness is appraised. The core practices of palliative care offer a mechanism to enhance the person-centred nature of HIV care; I identify the gaps in this type of care, and present evidence for effective models of care to address these. I detail the policies that prompt governments and health systems to respond to the palliative care needs of their population. Finally, I conclude this Review with evidence-based recommendations to improve the delivery of, and access to, high-quality HIV care until the end of life, reducing unnecessary suffering while optimising person-centred outcomes.
    MeSH term(s) Continuity of Patient Care ; HIV Infections/epidemiology ; HIV Infections/mortality ; HIV Infections/therapy ; Humans ; Incidence ; Palliative Care/methods ; Survival Analysis
    Language English
    Publishing date 2018-07-17
    Publishing country Netherlands
    Document type Journal Article ; Review
    ISSN 2352-3018
    ISSN (online) 2352-3018
    DOI 10.1016/S2352-3018(18)30110-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Access to advanced cancer care services in the West Bank-occupied Palestinian territory.

    Mitwalli, Suzan / Hammoudeh, Weeam / Giacaman, Rita / Harding, Richard

    Frontiers in oncology

    2023  Volume 13, Page(s) 1120783

    Abstract: Introduction: Universal Health Coverage (UHC) identifies the provision of palliative care for people with advanced disease as an essential health service. Palliative care is also stipulated as a human right under existing covenants. Oncology services ... ...

    Abstract Introduction: Universal Health Coverage (UHC) identifies the provision of palliative care for people with advanced disease as an essential health service. Palliative care is also stipulated as a human right under existing covenants. Oncology services provided by the Palestinian Authority under Israeli military occupation are limited to surgery and chemotherapy treatment. Our study aimed to describe the experiences of patients with advanced-stage cancer in the West Bank in accessing oncology services and meeting their health care needs.
    Methodology: We conducted a qualitative study among adult patients diagnosed with advanced lung, colon, or breast cancer in three Palestinian governmental hospitals, and with oncologists. Thematic analysis was conducted on the verbatim interview transcripts.
    Results: The sample consisted of 22 Palestinian patients (10 men and 12 women) and 3 practicing oncologists. The findings reveal that cancer care is fragmented, with limited access to the services needed. Patients face referral delays in accessing treatment which worsen their health condition in some cases. Some patients reported difficulties in getting Israeli permits to access radiotherapy treatment in East-Jerusalem, and others experienced interruptions of their chemotherapy treatment sessions due to the unavailability of chemotherapy medications caused by Israeli-side delays. Other reported problems were related to the Palestinian health system and service delivery and quality, including fragmentation of services, infrastructure issues, and unavailability of medications. Advanced diagnostic services and palliative care are almost absent at Palestinian governmental hospitals, and patients need to seek these services in the private sector.
    Conclusion: The data demonstrate specific access restrictions to cancer care in the West Bank due to Israeli military occupation of Palestinian land. This affects all stages of the care pathway, from restricted diagnosis services, to limited treatment and then poor availability of palliative care. Cancer patients will continue to suffer if the root causes of these structural constraints are not addressed.
    Language English
    Publishing date 2023-03-16
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2023.1120783
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Response to 'Place of death in the population dying from diseases indicative of palliative care need: a cross-national population-level study in 14 countries'.

    Harding, Richard

    Journal of epidemiology and community health

    2016  Volume 70, Issue 1, Page(s) 9

    MeSH term(s) Death ; Humans ; Palliative Care ; Terminal Care
    Language English
    Publishing date 2016-01
    Publishing country England
    Document type Comment ; Journal Article
    ZDB-ID 391868-3
    ISSN 1470-2738 ; 0142-467X ; 0141-7681 ; 0143-005X
    ISSN (online) 1470-2738
    ISSN 0142-467X ; 0141-7681 ; 0143-005X
    DOI 10.1136/jech-2015-206362
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 186: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  10. Article ; Online: Lessons from a research partnership in southwest England to understand community palliative care needs in rural, coastal and low-income communities.

    Hansford, Lorraine / Wyatt, Katrina / Creanor, Siobhan / McCready, Sheena / Harding, Richard

    Public health research (Southampton, England)

    2024  , Page(s) 1–40

    Abstract: Background: The South West Peninsula (Cornwall, Devon, Somerset) has the highest proportion of over 65s (24.2%) and is the only English rural population with greater economic deprivation than in urban areas. Coastal populations have the worst health ... ...

    Abstract Background: The South West Peninsula (Cornwall, Devon, Somerset) has the highest proportion of over 65s (24.2%) and is the only English rural population with greater economic deprivation than in urban areas. Coastal populations have the worst health outcomes in England. Despite innovation among communities to support those with health and care needs in later life, recruitment to palliative care research in the region is low and there has been no evaluation of public health palliative care interventions.
    Objectives: A new South West Peninsula Palliative Care Research Partnership was funded for 15 months, bringing together four universities, the voluntary and community sector (including hospices) and local National Institute for Health and Care Research networks. The aim was to establish a sustainable multisectoral partnership that would identify community-based support needs for underserved rural and coastal populations by: • conducting a literature scoping review on interventions to enable community members to support the dying; • delivering a research capacity-building programme; • co-creating public and patient involvement capacity; • determining the resources and needs for communities to support dying well; • integrating findings to develop a framework of community-based support and identify future research questions; • establishing a sustainable research network infrastructure for the long-term design and delivery of palliative care research.
    Design: We convened partners to identify research needs and co-designed activities to meet our objectives. These included a scoping review; a capacity-building programme of training, seminars and a journal club; forming a patient and public involvement group; a multistranded community engagement programme using different creative approaches; four focus groups with members of the public and one with community workers; and producing three 'storytelling' audio recordings. Findings were presented to the partnership at a regional workshop.
    Results: The scoping review showed that community-engaged palliative care interventions can improve outcomes for individuals but provided little evidence about which approaches work for different communities. Five online seminars and a quarterly journal club to develop research capacity were regularly attended by 15 to 25 participants from across the partnership. While evaluating our engagement methods was beyond the partnership's scope, levels of participation suggested that creative methods of engagement show potential to help researchers and practitioners better understand the needs and priorities of underserved populations. Data showed that rural, coastal and low-income communities face challenges in accessing end-of-life care and support due to issues such as transport to and distance from services, erosion of neighbourhood networks, isolation from family and friends, 'patchiness' of palliative care services and a lack of care providers. Community organisations are well-placed to co-produce and facilitate methodologies for involving communities in palliative care research.
    Limitations: Although activities took place in diverse areas, it was not possible within the available resources to cover the entire large geographical region, particularly the most isolated rural areas.
    Conclusions: Partnerships bringing together voluntary and community sector organisations, palliative care providers, health and social care providers, individuals with experience and academics have potential to design future research and public health interventions that better understand local context, involving and supporting communities to address their needs at end of life.
    Funding: This article presents independent research funded by the National Institute for Health and Care Research (NIHR)
    Language English
    Publishing date 2024-02-28
    Publishing country England
    Document type Journal Article
    ISSN 2050-439X
    ISSN (online) 2050-439X
    DOI 10.3310/ATFA4287
    Database MEDical Literature Analysis and Retrieval System OnLINE

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