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  1. Article: Concern about our public image.

    Greene, Ann

    The Canadian nurse

    2008  Volume 104, Issue 7, Page(s) 4

    MeSH term(s) Canada ; Humans ; Nursing ; Philately ; Public Relations ; Stereotyping
    Language English
    Publishing date 2008-09
    Publishing country Canada
    Document type Letter
    ZDB-ID 603665-x
    ISSN 0008-4581 ; 1492-5494
    ISSN 0008-4581 ; 1492-5494
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: XBB.1.5 spike protein COVID-19 vaccine induces broadly neutralizing and cellular immune responses against EG.5.1 and emerging XBB variants.

    Patel, Nita / Trost, Jessica F / Guebre-Xabier, Mimi / Zhou, Haixia / Norton, Jim / Jiang, Desheng / Cai, Zhaohui / Zhu, Mingzhu / Marchese, Anthony M / Greene, Ann M / Mallory, Raburn M / Kalkeri, Raj / Dubovsky, Filip / Smith, Gale

    Scientific reports

    2023  Volume 13, Issue 1, Page(s) 19176

    Abstract: Monovalent SARS-CoV-2 Prototype (Wuhan-Hu-1) and bivalent (Prototype + BA.4/5) COVID-19 vaccines have demonstrated a waning of vaccine-mediated immunity highlighted by lower neutralizing antibody responses against SARS-CoV-2 Omicron XBB sub-variants. The ...

    Abstract Monovalent SARS-CoV-2 Prototype (Wuhan-Hu-1) and bivalent (Prototype + BA.4/5) COVID-19 vaccines have demonstrated a waning of vaccine-mediated immunity highlighted by lower neutralizing antibody responses against SARS-CoV-2 Omicron XBB sub-variants. The reduction of humoral immunity due to the rapid evolution of SARS-CoV-2 has signaled the need for an update to vaccine composition. A strain change for all authorized/approved vaccines to a monovalent composition with Omicron subvariant XBB.1.5 has been supported by the WHO, EMA, and FDA. Here, we demonstrate that immunization with a monovalent recombinant spike protein COVID-19 vaccine (Novavax, Inc.) based on the subvariant XBB.1.5 induces neutralizing antibodies against XBB.1.5, XBB.1.16, XBB.2.3, EG.5.1, and XBB.1.16.6 subvariants, promotes higher pseudovirus neutralizing antibody titers than bivalent (Prototype + XBB.1.5) vaccine, induces SARS-CoV-2 spike-specific Th1-biased CD4 + T-cell responses against XBB subvariants, and robustly boosts antibody responses in mice and nonhuman primates primed with a variety of monovalent and bivalent vaccines. Together, these data support updating the Novavax vaccine to a monovalent XBB.1.5 formulation for the 2023-2024 COVID-19 vaccination campaign.
    MeSH term(s) Animals ; Humans ; Mice ; COVID-19 Vaccines ; Spike Glycoprotein, Coronavirus ; COVID-19 ; SARS-CoV-2 ; Antibodies, Neutralizing ; Immunity, Cellular ; Antibodies, Viral
    Chemical Substances COVID-19 Vaccines ; spike protein, SARS-CoV-2 ; Spike Glycoprotein, Coronavirus ; Antibodies, Neutralizing ; Antibodies, Viral
    Language English
    Publishing date 2023-11-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-023-46025-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A Brighton Collaboration standardized template with key considerations for a benefit/risk assessment for the Novavax COVID-19 Vaccine (NVX-CoV2373), a recombinant spike protein vaccine with Matrix-M adjuvant to prevent disease caused by SARS-CoV-2 viruses.

    Wilkinson, Bethanie / Patel, Kinjal S / Smith, Katherine / Walker, Robert / Wang, Chengbin / Greene, Ann M / Smith, Gale / Smith, Emily R / Gurwith, Marc / Chen, Robert T

    Vaccine

    2023  Volume 41, Issue 45, Page(s) 6762–6773

    Abstract: Novavax, a global vaccine company, began evaluating NVX-CoV2373 in human studies in May 2020 and the pivotal placebo-controlled phase 3 studies started in November 2020; five clinical studies provided adult and adolescent clinical data for over 31,000 ... ...

    Abstract Novavax, a global vaccine company, began evaluating NVX-CoV2373 in human studies in May 2020 and the pivotal placebo-controlled phase 3 studies started in November 2020; five clinical studies provided adult and adolescent clinical data for over 31,000 participants who were administered NVX-CoV2373. This extensive data has demonstrated a well-tolerated response to NVX-CoV2373 and high vaccine efficacy against mild, moderate, or severe COVID-19 using a two-dose series (Dunkle et al., 2022) [1], (Heath et al., 2021) [2], (Keech et al., 2020) [3], (Mallory et al., 2022) [4]. The most common adverse events seen after administration with NVX-CoV2373 were injection site tenderness, injection site pain, fatigue, myalgia, headache, malaise, arthralgia, nausea, or vomiting. In addition, immunogenicity against variants of interest (VOI) and variants of concern (VOC) was established with high titers of ACE2 receptor-inhibiting and neutralizing antibodies in these studies (EMA, 2022) [5], (FDA, 2023) [6]. Further studies on correlates of protection determined that titers of anti-Spike IgG and neutralizing antibodies correlated with efficacy against symptomatic COVID-19 established in clinical trials (p < 0.001 for recombinant protein vaccine and p = 0.005 for mRNA vaccines for IgG levels) (Fong et al., 2022) [7]. Administration of a booster dose of the recombinant protein vaccine approximately 6 months following the primary two-dose series resulted in substantial increases in humoral antibodies against both the prototype strain and all evaluated variants, similar to or higher than the antibody levels observed in phase 3 studies that were associated with high vaccine efficacy (Dunkle et al., 2022) [1], (Mallory et al., 2022) [4]. These findings, together with the well tolerated safety profile, support use of the recombinant protein vaccine as primary series and booster regimens.
    MeSH term(s) Adolescent ; Adult ; Humans ; COVID-19 Vaccines/adverse effects ; SARS-CoV-2 ; Spike Glycoprotein, Coronavirus/genetics ; COVID-19/prevention & control ; Adjuvants, Immunologic ; Vaccines, Synthetic/adverse effects ; Vaccines, Synthetic/genetics ; Antibodies, Neutralizing ; Risk Assessment ; Immunoglobulin G ; Antibodies, Viral ; Immunogenicity, Vaccine
    Chemical Substances NVX-CoV2373 adjuvated lipid nanoparticle (2SCD8Q63PF) ; COVID-19 Vaccines ; Matrix-M ; spike protein, SARS-CoV-2 ; Spike Glycoprotein, Coronavirus ; Adjuvants, Immunologic ; Vaccines, Synthetic ; Antibodies, Neutralizing ; Immunoglobulin G ; Antibodies, Viral
    Language English
    Publishing date 2023-09-20
    Publishing country Netherlands
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, U.S. Gov't, P.H.S. ; Research Support, N.I.H., Extramural
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2023.07.040
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Book: Horses at work

    Greene, Ann Norton

    harnessing power in industrial America

    2008  

    Author's details Ann Norton Greene
    Keywords Draft horses/History ; Working animals/History
    Language English
    Size xiv, 322 p. :, ill. ;, 22 cm.
    Publisher Harvard University Press
    Publishing place Cambridge, Mass
    Document type Book
    ISBN 9780674031296 ; 0674031296
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: XBB.1.5 Spike Protein COVID-19 Vaccine Induces Broadly Neutralizing and Cellular Immune Responses Against EG.5.1 and Emerging XBB Variants

    Patel, Nita / Trost, Jessica F. / Guebre-Xabier, Mimi / Zhou, Haixia / Norton, Jim / Jiang, Desheng / Cai, Zhaohui / Zhu, Mingzhu / Marchese, Anthony M / Greene, Ann M / Mallory, Raburn M / Kalkeri, Raj / Dubovsky, Filip / Smith, Gale

    bioRxiv

    Abstract: Monovalent SARS-CoV-2 Prototype (Wuhan-Hu-1) and bivalent (Prototype + BA.4/5) COVID-19 vaccines have demonstrated a waning of vaccine-mediated immunity highlighted by lower neutralizing antibody responses against SARS-CoV-2 Omicron XBB sub-variants. The ...

    Abstract Monovalent SARS-CoV-2 Prototype (Wuhan-Hu-1) and bivalent (Prototype + BA.4/5) COVID-19 vaccines have demonstrated a waning of vaccine-mediated immunity highlighted by lower neutralizing antibody responses against SARS-CoV-2 Omicron XBB sub-variants. The reduction of humoral immunity due to the rapid evolution of SARS-CoV-2 has signaled the need for an update to vaccine composition. A strain change for all authorized/approved vaccines to a monovalent composition with Omicron subvariant XBB.1.5 has been supported by the WHO, EMA, and FDA. Here, we demonstrate that immunization with a monovalent recombinant spike protein COVID-19 vaccine (Novavax, Inc.) based on the subvariant XBB.1.5 induces cross-neutralizing antibodies against XBB.1.5, XBB.1.16, XBB.2.3, EG.5.1, and XBB.1.16.6 subvariants, promotes higher pseudovirus neutralizing antibody titers than bivalent (Prototype + XBB.1.5) vaccine, induces SARS-CoV-2 spike-specific Th1-biased CD4+ T-cell responses against XBB subvariants, and robustly boosts antibody responses in mice and nonhuman primates primed with a variety of monovalent and bivalent vaccines. Together, these data support updating the Novavax vaccine to a monovalent XBB.1.5 formulation for the 2023-2024 COVID-19 vaccination campaign.
    Keywords covid19
    Language English
    Publishing date 2023-08-31
    Publisher Cold Spring Harbor Laboratory
    Document type Article ; Online
    DOI 10.1101/2023.08.30.554497
    Database COVID19

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  6. Article: Achieving Excellence Through Contemporary and Relevant Psychiatric-Mental Health Nursing Standards of Practice.

    McInnis-Perry, Gloria / Greene, Ann / Mina, Elaine Santa

    Journal of psychosocial nursing and mental health services

    2015  Volume 53, Issue 9, Page(s) 32–37

    Abstract: Standards of practice (SOPs) comprise competency statements, which are grounded in current knowledge and research, and provide foundations for performance that support professional accountability. The nursing profession, and specifically the psychiatric- ... ...

    Abstract Standards of practice (SOPs) comprise competency statements, which are grounded in current knowledge and research, and provide foundations for performance that support professional accountability. The nursing profession, and specifically the psychiatric-mental health specialty of nursing practice in Canada, develops and revises practice standards regularly. The current article describes the collaborative, evidence-informed journey of the Canadian Federation of Mental Health Nurses during its fourth revision of the Canadian Psychiatric-Mental Health Nursing SOPs. An intraprofessional team of psychiatric-mental health nurses from the clinical, academic, research, and policy areas developed and nurtured collaborative processes that emphasize collegial and authentic relationships. Effective communication and a respectful learning environment supported the process for all members of the team. The current article provides recommendations for other professional organizations considering developing and/or revising SOPs.
    MeSH term(s) Canada ; Clinical Competence/standards ; Education, Nursing, Continuing ; Humans ; Nurse's Role ; Practice Guidelines as Topic ; Psychiatric Nursing/standards
    Language English
    Publishing date 2015-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 225817-1
    ISSN 1938-2413 ; 0279-3695
    ISSN (online) 1938-2413
    ISSN 0279-3695
    DOI 10.3928/02793695-20150821-02
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Immunogenicity and protection of a variant nanoparticle vaccine that confers broad neutralization against SARS-CoV-2 variants.

    Logue, James / Johnson, Robert M / Patel, Nita / Zhou, Bin / Maciejewski, Sonia / Foreman, Bryant / Zhou, Haixia / Portnoff, Alyse D / Tian, Jing-Hui / Rehman, Asma / McGrath, Marisa E / Haupt, Robert E / Weston, Stuart M / Baracco, Lauren / Hammond, Holly / Guebre-Xabier, Mimi / Dillen, Carly / Madhangi, M / Greene, Ann M /
    Massare, Michael J / Glenn, Greg M / Smith, Gale / Frieman, Matthew B

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 1130

    Abstract: SARS-CoV-2 variants have emerged with elevated transmission and a higher risk of infection for vaccinated individuals. We demonstrate that a recombinant prefusion-stabilized spike (rS) protein vaccine based on Beta/B.1.351 (rS-Beta) produces a robust ... ...

    Abstract SARS-CoV-2 variants have emerged with elevated transmission and a higher risk of infection for vaccinated individuals. We demonstrate that a recombinant prefusion-stabilized spike (rS) protein vaccine based on Beta/B.1.351 (rS-Beta) produces a robust anamnestic response in baboons against SARS-CoV-2 variants when given as a booster one year after immunization with NVX-CoV2373. Additionally, rS-Beta is highly immunogenic in mice and produces neutralizing antibodies against WA1/2020, Beta/B.1.351, and Omicron/BA.1. Mice vaccinated with two doses of Novavax prototype NVX-CoV2373 (rS-WU1) or rS-Beta alone, in combination, or heterologous prime-boost, are protected from challenge. Virus titer is undetectable in lungs in all vaccinated mice, and Th1-skewed cellular responses are observed. We tested sera from a panel of variant spike protein vaccines and find broad neutralization and inhibition of spike:ACE2 binding from the rS-Beta and rS-Delta vaccines against a variety of variants including Omicron. This study demonstrates that rS-Beta vaccine alone or in combination with rS-WU1 induces antibody-and cell-mediated responses that are protective against challenge with SARS-CoV-2 variants and offers broader neutralizing capacity than a rS-WU1 prime/boost regimen alone. Together, these nonhuman primate and murine data suggest a Beta variant booster dose could elicit a broad immune response to fight new and future SARS-CoV-2 variants.
    MeSH term(s) Animals ; Humans ; Mice ; Antibodies, Neutralizing ; COVID-19/prevention & control ; Nanoparticles ; Papio ; SARS-CoV-2/genetics ; Vaccines/chemistry ; Vaccines/immunology ; COVID-19 Vaccines/chemistry ; COVID-19 Vaccines/immunology
    Chemical Substances Antibodies, Neutralizing ; Vaccines ; COVID-19 Vaccines
    Language English
    Publishing date 2023-02-28
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-022-35606-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: A novel calcium-dependent mechanism of acquired resistance to IGF-1 receptor inhibition in prostate cancer cells.

    Fahrenholtz, Cale D / Greene, Ann M / Beltran, Pedro J / Burnstein, Kerry L

    Oncotarget

    2014  Volume 5, Issue 19, Page(s) 9007–9021

    Abstract: Inhibition of the mitogenic insulin-like growth factor receptor 1 (IGF-1R) signaling axis is a compelling treatment strategy for prostate cancer. Combining the IGF-1R inhibitor ganitumab (formerly AMG 479) with standard of care androgen-deprivation ... ...

    Abstract Inhibition of the mitogenic insulin-like growth factor receptor 1 (IGF-1R) signaling axis is a compelling treatment strategy for prostate cancer. Combining the IGF-1R inhibitor ganitumab (formerly AMG 479) with standard of care androgen-deprivation therapy greatly delays prostate cancer recurrence in xenograft models; however, a significant proportion of these tumors ultimately acquire resistance to ganitumab. Here we describe the development of a stable and reproducible ganitumab-resistant VCaP human prostate cancer cell derivative termed VCaP/GanR to investigate the mechanism of acquired resistance to IGF-1R inhibition. Unlike parental VCaP, VCaP/GanR did not undergo apoptosis following ganitumab treatment. VCaP/GanR did not express increased levels of IGF-1R, insulin receptor, or phospho-AKT compared to parental VCaP. VCaP/GanR exhibited increased levels of phospho-S6 indicative of increased mTOR activity. However, acquired resistance to ganitumab was not dependent on increased mTOR activity in VCaP/GanR. Phospho-proteomic arrays revealed alterations in several calcium-regulated signaling components in VCaP/GanR compared to VCaP. Reduction of intracellular calcium using cell-permeable calcium-specific chelators restored ganitumab sensitivity to VCaP/GanR through inhibition of cell-cycle progression. These data suggest a new mechanism of resistance to IGF-1R inhibition involving calcium-mediated proliferation effects. Such pathways should be considered in future clinical studies of IGF-1R inhibitors in prostate cancer.
    MeSH term(s) Antibodies, Monoclonal/pharmacology ; Antibodies, Monoclonal, Humanized ; Apoptosis/drug effects ; Calcium/metabolism ; Calcium Chelating Agents/pharmacology ; Calcium Signaling/drug effects ; Calcium Signaling/genetics ; Cell Cycle Checkpoints/drug effects ; Cell Line, Tumor ; Cell Proliferation ; Drug Resistance, Neoplasm ; Focal Adhesion Kinase 2/antagonists & inhibitors ; Focal Adhesion Kinase 2/metabolism ; Humans ; Male ; Neoplasm Recurrence, Local/drug therapy ; Neoplasm Recurrence, Local/prevention & control ; Phospholipase C gamma/antagonists & inhibitors ; Phospholipase C gamma/metabolism ; Phosphorylation ; Prostatic Neoplasms/drug therapy ; Proto-Oncogene Proteins c-akt/metabolism ; Receptor, IGF Type 1/antagonists & inhibitors ; Receptor, IGF Type 1/biosynthesis ; Receptor, Insulin/biosynthesis ; TOR Serine-Threonine Kinases/metabolism ; Xenograft Model Antitumor Assays
    Chemical Substances Antibodies, Monoclonal ; Antibodies, Monoclonal, Humanized ; Calcium Chelating Agents ; ganitumab (CK1441RCZ8) ; MTOR protein, human (EC 2.7.1.1) ; TOR Serine-Threonine Kinases (EC 2.7.1.1) ; Receptor, IGF Type 1 (EC 2.7.10.1) ; Receptor, Insulin (EC 2.7.10.1) ; Focal Adhesion Kinase 2 (EC 2.7.10.2) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1) ; Phospholipase C gamma (EC 3.1.4.3) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2014-10-26
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2560162-3
    ISSN 1949-2553 ; 1949-2553
    ISSN (online) 1949-2553
    ISSN 1949-2553
    DOI 10.18632/oncotarget.2346
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Patient, Family, and Community Advisory Councils in Health Care and Research: a Systematic Review.

    Oldfield, Benjamin J / Harrison, Marcus A / Genao, Inginia / Greene, Ann T / Pappas, Mary Ellen / Glover, Janis G / Rosenthal, Marjorie S

    Journal of general internal medicine

    2018  Volume 34, Issue 7, Page(s) 1292–1303

    Abstract: Background: Patient-centeredness is a characteristic of high-quality medical care and requires engaging community members in health systems' decision-making. One key patient engagement strategy is patient, family, and community advisory boards/councils ( ...

    Abstract Background: Patient-centeredness is a characteristic of high-quality medical care and requires engaging community members in health systems' decision-making. One key patient engagement strategy is patient, family, and community advisory boards/councils (PFACs), yet the evidence to guide PFACs is lacking. Systematic reviews on patient engagement may benefit from patient input, but feasibility is unclear.
    Methods: A team of physicians, researchers, and a PFAC member conducted a systematic review to examine the impact of PFACs on health systems and describe optimal strategies for PFAC conduct. We searched MEDLINE, Embase, PsycINFO, CINAHL, Scopus, and Social Science Citation Index from inception through September 2016, as well as pre-identified websites. Two reviewers independently screened and abstracted data from studies, then assessed randomized studies for risk of bias and observational studies for quality using standardized measures. We performed a realist synthesis-which asks what works, for whom, under what circumstances-of abstracted data via 12 monthly meetings between investigators and two feedback sessions with a hospital-based PFAC.
    Results: Eighteen articles describing 16 studies met study criteria. Randomized studies demonstrated moderate to high risk of bias and observational studies demonstrated poor to fair quality. Studies engaged patients at multiple levels of the health care system and suggested that in-person deliberation with health system leadership was most effective. Studies involving patient engagement in research focused on increasing study participation. PFAC recruitment was by nomination (n = 11) or not described (n = 5). No common measure of patient, family, or community engagement was identified. Realist synthesis was enriched by feedback from PFAC members.
    Discussion: PFACs engage communities through individual projects but evidence of their impact on outcomes is lacking. A paucity of randomized controlled trials or high-quality observational studies guide strategies for engagement through PFACs. Standardized measurement tools for engagement are needed. Strategies for PFAC recruitment should be investigated and reported. PFAC members can feasibly contribute to systematic reviews.
    Registration and funding source: A protocol for record eligibility was developed a priori and was registered in the PROSPERO database of systematic reviews (registration number CRD42016052817). The Department of Veterans Affairs' Office of Academic Affiliations, through the National Clinician Scholars Program, funded this study.
    MeSH term(s) Advisory Committees/organization & administration ; Community-Based Participatory Research/methods ; Humans ; Patient Participation ; Patient-Centered Care/organization & administration ; Professional-Family Relations ; Qualitative Research
    Language English
    Publishing date 2018-07-26
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Systematic Review
    ZDB-ID 639008-0
    ISSN 1525-1497 ; 0884-8734
    ISSN (online) 1525-1497
    ISSN 0884-8734
    DOI 10.1007/s11606-018-4565-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Building community resilience to prevent and mitigate community impact of gun violence: conceptual framework and intervention design.

    Wang, Emily A / Riley, Carley / Wood, George / Greene, Ann / Horton, Nadine / Williams, Maurice / Violano, Pina / Brase, Rachel Michele / Brinkley-Rubinstein, Lauren / Papachristos, Andrew V / Roy, Brita

    BMJ open

    2020  Volume 10, Issue 10, Page(s) e040277

    Abstract: Introduction: The USA has the highest rate of community gun violence of any developed democracy. There is an urgent need to develop feasible, scalable and community-led interventions that mitigate incident gun violence and its associated health impacts. ...

    Abstract Introduction: The USA has the highest rate of community gun violence of any developed democracy. There is an urgent need to develop feasible, scalable and community-led interventions that mitigate incident gun violence and its associated health impacts. Our community-academic research team received National Institutes of Health funding to design a community-led intervention that mitigates the health impacts of living in communities with high rates of gun violence.
    Methods and analysis: We adapted 'Building Resilience to Disasters', a conceptual framework for natural disaster preparedness, to guide actions of multiple sectors and the broader community to respond to the man-made disaster of gun violence. Using this framework, we will identify existing community assets to be building blocks of future community-led interventions. To identify existing community assets, we will conduct social network and spatial analyses of the gun violence episodes in our community and use these analyses to identify people and neighbourhood blocks that have been successful in avoiding gun violence. We will conduct qualitative interviews among a sample of individuals in the network that have avoided violence (n=45) and those living or working on blocks that have not been a location of victimisation (n=45) to identify existing assets. Lastly, we will use community-based system dynamics modelling processes to create a computer simulation of the community-level contributors and mitigators of the effects of gun violence that incorporates local population-based based data for calibration. We will engage a multistakeholder group and use themes from the qualitative interviews and the computer simulation to identify feasible community-led interventions.
    Ethics and dissemination: The Human Investigation Committee at Yale University School of Medicine (#2000022360) granted study approval. We will disseminate study findings through peer-reviewed publications and academic and community presentations. The qualitative interview guides, system dynamics model and group model building scripts will be shared broadly.
    MeSH term(s) Computer Simulation ; Disasters ; Gun Violence ; Humans ; Residence Characteristics ; Violence/prevention & control
    Language English
    Publishing date 2020-10-10
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; 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-2020-040277
    Database MEDical Literature Analysis and Retrieval System OnLINE

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