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American Academy of Nursing Expert Panel consensus statement on nursing's roles in ensuring universal palliative care access
Rosa, William E; Buck, Harleah G; Squires, Allison P; Kozachik, Sharon L; Huijer, Huda Abu-Saad; Bakitas, Marie; Boit, Juli McGowan; Bradley, Patricia K; Cacchione, Pamela Z; Chan, Garrett K; Crisp, Nigel; Dahlin, Constance; Daoust, Pat; Davidson, Patricia M; Davis, Sheila; Doumit, Myrna A A; Fink, Regina M; Herr, Keela A; Hinds, Pamela S; Hughes, Tonda L; Karanja, Viola; Kenny, Deborah J; King, Cynthia R; Klopper, Hester C; Knebel, Ann R; Kurth, Ann E; Madigan, Elizabeth A; Malloy, Pamela; Matzo, Marianne; Mazanec, Polly; Meghani, Salimah H; Monroe, Todd B; Moreland, Patricia J; Paice, Judith A; Phillips, J Craig; Rushton, Cynda H; Shamian, Judith; Shattell, Mona; Snethen, Julia A; Ulrich, Connie M; Wholihan, Dorothy; Wocial, Lucia D; Ferrell, Betty R
The purpose of this consensus paper was to convene leaders and scholars from eight Expert Panels of the American Academy of Nursing and provide recommendations to advance nursing's roles and responsibility to ensure universal access to palliative care. Part I of this consensus paper herein provides the rationale and background to support the policy, education, research, and clinical practice recommendations put forward in Part II. On behalf of the Academy, the evidence-based recommendations will guide nurses, policy makers, government representatives, professional associations, and interdisciplinary and community partners to integrate palliative nursing services across health and social care settings. The consensus paper's 43 authors represent eight countries (Australia, Canada, England, Kenya, Lebanon, Liberia, South Africa, United States of America) and extensive international health experience, thus providing a global context for the subject matter. The authors recommend greater investments in palliative nursing education and nurse-led research, nurse engagement in policy making, enhanced intersectoral partnerships with nursing, and an increased profile and visibility of palliative nurses worldwide. By enacting these recommendations, nurses working in all settings can assume leading roles in delivering high-quality palliative care globally, particularly for minoritized, marginalized, and other at-risk populations.
PMID: 34711419
ISSN: 1528-3968
CID: 5079782
Defining Telepresence as Experienced in Telehealth Encounters: A Dimensional Analysis
Groom, Lisa L; Brody, Abraham A; Squires, Allison P
PURPOSE/OBJECTIVE:Telehealth's uptake has increased substantially in recent years, with an especially large jump in 2020 due to the emergence of COVID-19. This article provides background on and explores "telepresence" in healthcare literature. Telepresence strongly impacts the patient experience, but it is poorly defined in current research. The aim was to conceptually define telepresence using qualitative methods. DESIGN/METHODS:Dimensional analysis was used to analyze telepresence in clinical literature and create a clearer definition of telepresence as a concept. Multiple databases were searched for articles related to telepresence. Thirteen international articles related to telepresence were selected for analysis. METHODS:Dimensional analysis allowed for multiple viewpoints to be explored within each distinct context and perspective. FINDINGS/RESULTS:Twenty-five dimensions were discovered within the articles, which were synthesized to seven core dimensions of telepresence: connection, technological mediation, experienced realism, trust, being supportive, collaboration, and emotional consequence. CONCLUSIONS:Telepresence is highly impactful on the patient's experience of telehealth care visits. The conceptual map produced by this dimensional analysis provides direction for clinicians to improve their ability to be present with patients during telehealth care. Potential implications include a starting point for future qualitative research, and the use of this dimensional analysis to inform clinical guidelines, improve clinician training, and assist in the development of new care models. CLINICAL RELEVANCE/CONCLUSIONS:A telepresence definition brings clarity to an ill-defined concept. COVID-19 magnifies the need for a better understanding of telepresence, which allows clinicians to improve telehealth encounters.
PMID: 34060218
ISSN: 1547-5069
CID: 4895052
Assessing the influence of patient language preference on 30 day hospital readmission risk from home health care: A retrospective analysis
Squires, Allison; Ma, Chenjuan; Miner, Sarah; Feldman, Penny; Jacobs, Elizabeth A; Jones, Simon A
BACKGROUND:In home health care, language barriers are understudied. Language barriers between patients and providers are known to affect a variety of patient outcomes. How a patient's language preference influences hospital readmission risk from home health care has yet to be determined. OBJECTIVE:To determine if home care patients' language preference is associated with their risk for hospital readmission from home health care within 30 days of hospital discharge. DESIGN/METHODS:Retrospective cross-sectional study of hospital readmissions from an urban home health care agency's administrative records and the national electronic home health care record for the United States, captured between 2010 and 2015. SETTING/METHODS:New York City, New York, USA. PARTICIPANTS/METHODS:The dataset comprised 90,221 post-hospitalization patients and 6.5 million home health care visits. METHODS:First, a Chi-square test was used to determine if there were significant differences in crude readmission rates based on language group. Inverse probability of treatment weighting was used to adjust for significant differences in known hospital readmission risk factors between to examine all-cause hospital readmission during a home health care stay. The final matched sample included 87,561 patients with a language preference of English, Spanish, Russian, Chinese, or Korean. English-speaking patients were considered the comparison group to the non-English speaking patients. A Marginal Structural Model was applied to estimate the impact of non-English language preference against English language preference on rehospitalization. The results of the marginal structural model were expressed as an odds ratio of likelihood of readmission to the hospital from home health care. RESULTS:Home health patients with a non-English language preference had a higher hospital readmission risk than English-speaking patients. Crude readmission rate for the limited English proficiency patients was 20.4% (95% CI, 19.9-21.0%) overall compared to 18.5% (95% CI, 18.7-19.2%) for English speakers (p < 0.001). Being a non-English-speaking patient was associated with an odds ratio of 1.011 (95% CI, 1.004-1.018) in increased hospital readmission rates from home health care (p = 0.001). There were also statistically significant differences in readmission rate by language group (p < 0.001), with Korean speakers having the lowest rate and Spanish speakers having the highest, when compared to English speakers. CONCLUSIONS:People with a non-English language preference have a higher readmission rate from home health care. Hospital and home healthcare agencies may need specialized care coordination services to reduce readmission risk for these patients. Tweetable abstract: A new US-based study finds that home care patients with language barriers are at higher risk for hospital readmission.
PMID: 34710627
ISSN: 1873-491x
CID: 5037332
Continuity of Nursing Care in Home Health: Impact on Rehospitalization Among Older Adults With Dementia
Ma, Chenjuan; McDonald, Margaret V; Feldman, Penny H; Miner, Sarah; Jones, Simon; Squires, Allison
BACKGROUND:Home health care (HHC) is a leading form of home and community-based services for persons with dementia (PWD). Nurses are the primary providers of HHC; however, little is known of nursing care delivery and quality. OBJECTIVE:The objective of this study was to examine the association between continuity of nursing care in HHC and rehospitalization among PWD. RESEARCH DESIGN/METHODS:This is a retrospective cohort study using multiple years (2010-2015) of HHC assessment, administrative, and human resources data from a large urban not-for-profit home health agency. SUBJECTS/METHODS:This study included 23,886 PWD receiving HHC following a hospitalization. MEASURES/METHODS:Continuity of nursing care was calculated using the Bice and Boxerman method, which considered the number of total visits, nurses, and visits from each nurse during an HHC episode. The outcome was all-cause rehospitalization during HHC. Risk-adjusted logistic regression was used for analysis. RESULTS:Approximately 24% of PWD were rehospitalized. The mean continuity of nursing care score was 0.56 (SD=0.33). Eight percent of PWD received each nursing visit from a different nurse (no continuity), and 26% received all visits from one nurse during an HHC episode (full continuity). Compared with those receiving high continuity of nursing care (third tertile), PWD receiving low (first tertile) or moderate (second tertile) continuity of nursing care had an adjusted odds ratio of 1.33 (95% confidence interval: 1.25-1.46) and 1.30 (95% confidence interval: 1.22-1.43), respectively, for being rehospitalized. CONCLUSIONS:Wide variations exist in continuity of nursing care to PWD. Consistency in nurse staff when providing HHC visits to PWD is critical for preventing rehospitalizations.
PMID: 34166269
ISSN: 1537-1948
CID: 4935792
Disparities in Breastfeeding Duration of New York City Latinx Mothers by Birth Region
Gerchow, Lauren; Squires, Allison; Jones, Simon
PMID: 33826404
ISSN: 1556-8342
CID: 4839722
Leading Policy and Practice Change During Unprecedented Times: The Nursing Health Services Research Response
Germack, Hayley; Cary, Michael; Gilmartin, Heather; Girouard, Shirley; Jones, Tammie M; Martin, Barbara J; Norful, Allison A; Anusiewicz, Colleen V; Riman, Kathryn A; Schlak, Amelia E; Squires, Allison; Estrada, Leah V; Gazarian, Priscilla; Gerchow, Lauren; Ghazal, Lauren V; Henderson, Marcus D; Mitha, Shazia; Mpundu, Gloria; Nikpour, Jacqueline; Royster, Monique; Thompson, Roy; Stolldorf, Deonni P
PMCID:8425338
PMID: 34513205
ISSN: 2155-8256
CID: 5079762
Infection Prevention and Control in Liberia 5 Years After Ebola: A Case Study
Ridge, Laura Jean; Stimpfel, Amy Witkoski; Klar, Robin Toft; Dickson, Victoria Vaughan; Squires, Allison Patricia
BACKGROUND/UNASSIGNED:Effective management of health emergencies is an important strategy to improve health worldwide. One way to manage health emergencies is to build and sustain national capacities. The Ebola epidemic of 2014 to 2015 resulted in greater infection prevention and control (IPC) capacity in Liberia, but few studies have investigated if and how that capacity was sustained. The purpose of this study was to examine the maintenance of IPC capacity in Liberia after Ebola. METHODS/UNASSIGNED:theoretical framework, which describes an organization's intangible occupational health resources. FINDINGS/UNASSIGNED:Thirty-seven nurses from 12 facilities participated. Ebola was a seminal event in the development of safety capital in Liberia, particularly regarding nurse knowledge of IPC and facilities' investments in safety. The safety capital developed during Ebola is still being applied at the individual and organizational levels. Tangible resources, including personal protective equipment, however, have been depleted. CONCLUSIONS/APPLICATION TO PRACTICE/UNASSIGNED:IPC capacity in Liberia had been sustained since Ebola but was threatened by under-investments in physical resources. Donor countries should prioritize sustained support, both financial and technical, in partnership with Liberian leaders. Occupational health nurses participating in disaster response should advocate for long-term investment by donor countries in personal protective equipment, access to water, and clinician training.
PMID: 33845686
ISSN: 2165-0969
CID: 4845782
A Scoping Review of the Evidence About the Nurses Improving Care for Healthsystem Elders (NICHE) Program
Squires, Allison; Murali, Komal Patel; Greenberg, Sherry A; Herrmann, Linda L; D'amico, Catherine O
BACKGROUND AND OBJECTIVES/OBJECTIVE:The Nurses Improving Care for Healthsystem Elders (NICHE) is a nurse-led education and consultation program designed to help health care organizations improve the quality of care for older adults. To conduct a scoping review of the evidence associated with the NICHE program to (a) understand how it influences patient outcomes through specialized care of the older adult and (b) provide an overview of implementation of the NICHE program across organizations as well as its impact on nursing professionals and the work environment. RESEARCH DESIGN AND METHODS/METHODS:Six databases were searched to identify NICHE-related articles between January 1992 and April 2019. After critical appraisal, 43 articles were included. RESULTS:Four thematic categories were identified including specialized older adult care, geriatric resource nurse (GRN) model, work environment, and NICHE program adoption and refinement. Specialized older adult care, a key feature of NICHE programs, resulted in improved quality of care, patient safety, lower complications, and decreased length of stay. The GRN model emphasizes specialized geriatric care education and consultation. Improvements in the geriatric nurse work environment as measured by perceptions of the practice environment, quality of care, and aging-sensitive care delivery have been reported. NICHE program adoption and refinement focuses on the methods used to improve care, implementation and adoption of the NICHE program, and measuring its impact. DISCUSSION AND IMPLICATIONS/UNASSIGNED:The evidence about the NICHE program in caring for older adults is promising but more studies examining patient outcomes and the impact on health care professionals are needed.
PMID: 31681955
ISSN: 1758-5341
CID: 4179192
Entrustable Professional Activities (EPAs) for Global Health
Steeb, David R; Brock, Tina P; Dascanio, Sarah A; Drain, Paul K; Squires, Allison; Thumm, Melissa; Tittle, Robin; Haines, Stuart T
PURPOSE/OBJECTIVE:As global health education and training shifts towards competency-based approaches, academic institutions and organizations must define appropriate assessment strategies for use across health professions. The authors of this study aim to develop entrustable professional activities (EPAs) for global health to apply across academic and workplace settings. METHOD/METHODS:In 2019, the authors invited 55 global health experts from medicine, nursing, pharmacy, and public health to participate in a multi-round, online Delphi process; 30 (55%) agreed. Experts averaged 17 years of global health experience, and 12 (40%) were from low-to-middle-income countries. In round one participants listed essential global health activities. The authors used in-vivo coding for round one responses to develop initial EPA statements. In subsequent rounds, participants used a 5-point Likert-type scale to evaluate EPA statements for importance and relevance to global health across health professions. The authors elevated statements that were rated 4 (important/relevant to most) or 5 (very important/relevant to all) by a minimum of 70% of participants (decided a priori) to the final round, during which participants evaluated whether each statement represented an observable unit of work that could be assigned to a trainee. Descriptive statistics were used for quantitative data analysis. The authors used participant comments to categorize EPA statements into role domains. RESULTS:Twenty-two EPA statements reached at least 70% consensus, and the authors categorized them into 5 role domains: partnership developer, capacity builder, data analyzer, equity advocate, and health promoter. Statements in the equity advocate and partnership developer domains had the highest agreement for importance and relevance. Several statements achieved 100% agreement CONCLUSIONS:: EPAs for global health may be useful to academic institutions and other organizations to guide the assessment of trainees within education and training programs across health professions.
PMID: 33239533
ISSN: 1938-808x
CID: 4702422
Disparities in chronic kidney disease-the state of the evidence
Clark-Cutaia, Maya N; Rivera, Eleanor; Iroegbu, Christin; Squires, Allison
PURPOSE OF REVIEW/OBJECTIVE:The purpose of this review was to assess the prevalence of United States chronic kidney disease (CKD) health disparities, focusing on racial/ethnic groups, immigrants and refugees, sex or gender, and older adults. RECENT FINDINGS/RESULTS:There are major racial/ethnic disparities in CKD, with possible contributions from the social determinants of health, socioeconomics, and racial discrimination. Racial/ethnic minority patients experience faster progression to end-stage kidney disease (ESKD) and higher mortality predialysis, however, once on dialysis, appear to live longer. Similarly, men are quicker to progress to ESKD than women, with potential biological, behavioral, and measurement error factors. There is a lack of substantial evidence for intersex, nonbinary, or transgender patients. There are also strikingly few studies about US immigrants or older adults with CKD despite the fact that they are at high risk for CKD due to a variety of factors. SUMMARY/CONCLUSIONS:As providers and scientists, we must combat both conscious and unconscious biases, advocate for minority patient populations, and be inclusive and diverse in our treatment regimens and provision of care. We need to acknowledge that sufficient evidence exists to change treatment guidelines, and that more is required to support the diversity of our patient population.
PMID: 33464006
ISSN: 1473-6543
CID: 4790902