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1.
J Healthc Manag ; 69(3): 205-218, 2024.
Article in English | MEDLINE | ID: mdl-38728546

ABSTRACT

GOAL: Growing numbers of hospitals and payers are using call centers to answer patients' clinical and administrative questions, schedule appointments, address billing issues, and offer supplementary care during public health emergencies and national disasters. In 2020, the Veterans Health Administration (VA) implemented VA Health Connect, an enterprise-wide initiative to modernize call centers. VA Health Connect is designed to improve the care experience with the convenience, flexibility, and simplicity of a single toll-free number connected to a range of 24/7 virtual services. The services are organized into four areas: administrative guidance for scheduling and general inquiries; pharmacy support for medication matters; clinical triage for evaluation of symptoms and recommended care; and virtual visits with providers for urgent and episodic care. Through a qualitative evaluation of VA Health Connect, we sought to identify the factors that affected the development of this program and to compile considerations to support the implementation of other enterprise-wide initiatives. METHODS: The evaluation team interviewed 29 clinical and administrative leads from across the VA. These leads were responsible for the modernization of their local service networks. PhD-level qualitative methodologists conducted the interviews, asking participants to reflect on barriers and facilitators to modernization and implementation. The team employed a rapid qualitative analytic approach commonly used in healthcare research to distill robust results. PRINCIPAL FINDINGS: A review of the early implementation of VA Health Connect found: (1) deadlines proved challenging but provided momentum for the initiative; (2) a balance between standardized processes and local adaptations facilitated implementation; (3) attention to staffing, hiring, and training of call center staff before implementation expedited workflows; (4) establishing national and local leadership commitment to the innovation from the onset increased team cohesion and efficacy; and (5) anticipating information technology infrastructure needs prevented delays to modernization and implementation. PRACTICAL APPLICATIONS: Our findings suggest that healthcare systems would benefit from anticipating likely obstacles (e.g., delays in software implementations and negotiations with unions), thus providing ample time to secure leadership buy-in and identify local champions, communicating early and often, and supporting flexible implementation to meet local needs. VA leadership can use this evaluation to refine implementation, and it could also have important implications for regulators, federal health exchanges, insurers, and other healthcare systems when determining resource levels for call centers.


Subject(s)
United States Department of Veterans Affairs , United States , United States Department of Veterans Affairs/organization & administration , Humans , Delivery of Health Care/organization & administration , Qualitative Research
2.
Qual Manag Health Care ; 32(2): 75-80, 2023.
Article in English | MEDLINE | ID: mdl-35793546

ABSTRACT

BACKGROUND AND OBJECTIVES: Lean management is a strategy for improving health care experiences of patients. While best practices for engaging patients in quality improvement have solidified in recent years, few reports specifically address patient engagement in Lean activities. This study examines the benefits and challenges of incorporating patient engagement strategies into the Veterans Health Administration's (VA) Lean transformation. METHODS: We conducted a multisite, mixed-methods evaluation of Lean deployment at 10 VA medical facilities, including 227 semistructured interviews with stakeholders, including patients. RESULTS: Interviewees noted that a patient-engaged Lean approach is mutually beneficial to patients and health care employees. Benefits included understanding the veteran's point of view, uncovering inefficient aspects of care processes, improved employee participation in Lean events, increased transparency, and improved reputation for the organization. Challenges included a need for focused time and resources to optimize veteran participation, difficulty recruiting a diverse group of veteran stakeholders, and a lack of specific instructions to encourage meaningful participation of veterans. CONCLUSIONS/IMPLICATIONS: As the first study to focus on patient engagement in Lean transformation efforts at the VA, this study highlights ways to effectively partner with patients in Lean-based improvement efforts. Lessons learned may also help optimize patient input into quality improvement more generally.


Subject(s)
Patient Participation , United States Department of Veterans Affairs , Veterans , Humans , Patient Participation/methods , Qualitative Research , United States , United States Department of Veterans Affairs/organization & administration , Veterans/psychology , Veterans/statistics & numerical data , Male , Aged
3.
Health Serv Res ; 58(2): 343-355, 2023 04.
Article in English | MEDLINE | ID: mdl-36129687

ABSTRACT

OBJECTIVE: To understand what factors and organizational dynamics enable Lean transformation of health care organizations. DATA SOURCES: Primary data were collected through two waves of interviews in 2016-2017 with leaders and staff at seven veterans affairs medical centers participating in Lean enterprise transformation. STUDY DESIGN: Using an observational study design, for each site we coded and rated seven potential enablers of transformation. The outcome measure was the extent of Lean transformation, constructed by coding and rating 11 markers of depth and spread of transformation. Using multivalue coincidence analysis (CNA), we identified enablers that distinguished among sites having different levels of transformation. We identified representative quotes for the enablers. DATA COLLECTION METHODS: We interviewed 121 executive leaders, middle managers, expert consultants, systems redesign staff, frontline supervisors, and staff. PRINCIPAL FINDINGS: Two sites achieved high Lean transformation, three medium, and two low. Together leadership support and capability development were sufficient for the three-level Lean transformation outcomes with 100% consistency and 100% coverage. High scores on both corresponded to high Lean transformation; medium on either one corresponded to medium transformation; and low on both corresponded to low transformation. Additionally, low scores in communication and availability of data and very low scores in alignment characterized low-transformation sites. Sites with high leadership support also had a high veteran engagement. CONCLUSIONS: This multisite study develops a novel measure of the extent of organization-wide Lean transformation and uses CNA to identify enablers linked to transformation. It provides insights into why and how some organizations are more successful at transformation than others. Findings support the applicability of the organization transformation model that guided the study and highlight the roles of executive leadership and capability development in the dynamics of transformation.


Subject(s)
Delivery of Health Care , Veterans , Humans , Hospitals , Leadership
4.
JAMA Netw Open ; 5(4): e226687, 2022 04 01.
Article in English | MEDLINE | ID: mdl-35404460

ABSTRACT

Importance: Telehealth enables access to genetics clinicians, but impact on care coordination is unknown. Objective: To assess care coordination and equity of genetic care delivered by centralized telehealth and traditional genetic care models. Design, Setting, and Participants: This cross-sectional study included patients referred for genetic consultation from 2010 to 2017 with 2 years of follow-up in the US Department of Veterans Affairs (VA) health care system. Patients were excluded if they were referred for research, cytogenetic, or infectious disease testing, or if their care model could not be determined. Exposures: Genetic care models, which included VA-telehealth (ie, a centralized team of genetic counselors serving VA facilities nationwide), VA-traditional (ie, a regional service by clinical geneticists and genetic counselors), and non-VA care (ie, community care purchased by the VA). Main Outcomes and Measures: Multivariate regression models were used to assess associations between patient and consultation characteristics and the type of genetic care model referral; consultation completion; and having 0, 1, or 2 or more cancer surveillance (eg, colonoscopy) and risk-reducing procedures (eg, bilateral mastectomy) within 2 years following referral. Results: In this study, 24 778 patients with genetics referrals were identified, including 12 671 women (51.1%), 13 193 patients aged 50 years or older (53.2%), 15 639 White patients (63.1%), and 15 438 patients with cancer-related referrals (62.3%). The VA-telehealth model received 14 580 of the 24 778 consultations (58.8%). Asian patients, American Indian or Alaskan Native patients, and Hawaiian or Pacific Islander patients were less likely to be referred to VA-telehealth than White patients (OR, 0.54; 95% CI, 0.35-0.84) compared with the VA-traditional model. Completing consultations was less likely with non-VA care than the VA-traditional model (OR, 0.45; 95% CI, 0.35-0.57); there were no differences in completing consultations between the VA models. Black patients were less likely to complete consultations than White patients (OR, 0.84; 95% CI, 0.76-0.93), but only if referred to the VA-telehealth model. Patients were more likely to have multiple cancer preventive procedures if they completed their consultations (OR, 1.55; 95% CI, 1.40-1.72) but only if their consultations were completed with the VA-traditional model. Conclusions and Relevance: In this cross-sectional study, the VA-telehealth model was associated with improved access to genetics clinicians but also with exacerbated health care disparities and hindered care coordination. Addressing structural barriers and the needs and preferences of vulnerable subpopulations may complement the centralized telehealth approach, improve care coordination, and help mitigate health care disparities.


Subject(s)
Breast Neoplasms , Telemedicine , Veterans , Cross-Sectional Studies , Demography , Female , Healthcare Disparities , Humans , Mastectomy , Referral and Consultation , Retrospective Studies , United States , United States Department of Veterans Affairs
5.
Health Care Manage Rev ; 46(4): 308-318, 2021.
Article in English | MEDLINE | ID: mdl-31996609

ABSTRACT

BACKGROUND: The Veterans Health Administration piloted a nationwide Lean Enterprise Transformation program to optimize delivery of services to patients for high value care. PURPOSE: Barriers and facilitators to Lean implementation were evaluated. METHODS: Guided by the Lean Enterprise Transformation evaluation model, 268 interviews were conducted, with stakeholders across 10 Veterans Health Administration medical centers. Interview transcripts were analyzed using thematic analysis techniques. RESULTS: Supporting the utility of the model, facilitators and barriers to Lean implementation were found in each of the Lean Enterprise Transformation evaluation model domains: (a) impetus to transform, (b) leadership commitment to quality, (c) improvement initiatives, (d) alignment across the organization, (e) integration across internal boundaries, (f) communication, (g) capability development, (h) informed decision making, (i) patient engagement, and (j) organization culture. In addition, three emergent themes were identified: staff engagement, sufficient staffing, and use of Lean experts (senseis). CONCLUSIONS: Effective implementation required staff engagement, strategic planning, proper scoping and pacing, deliberate coaching, and accountability structures. Visible, stable leadership drove Lean when leaders articulated a clear impetus to change, aligned goals within the facility, and supported middle management. Reliable data and metrics provided support for and evidence of successful change. Strategic early planning with continual reassessment translated into focused and sustained Lean implementation. PRACTICE IMPLICATIONS: Prominent best practices identified include (a) reward participants by broadcasting Lean successes; (b) provide time and resources for participation in Lean activities; (c) avoid overscoping projects; (d) select metrics that closely align with improvement processes; and (e) invest in coaches, informal champions, process improvement staff, and senior leadership to promote staff engagement and minimize turnover.


Subject(s)
Leadership , Veterans Health , Hospitals , Humans , Organizational Culture , Personnel Turnover
6.
Patterns (N Y) ; 1(2): 100016, 2020 May 08.
Article in English | MEDLINE | ID: mdl-33205093

ABSTRACT

Data provenance is a machine-readable summary of the collection and computational history of a dataset. Data provenance confers or adds value to a dataset, helps reproduce computational analyses, or validates scientific conclusions. The people of the End-to-End Provenance Project are a community of professionals who have developed software tools to collect and use data provenance.

7.
BMC Health Serv Res ; 19(1): 98, 2019 Feb 04.
Article in English | MEDLINE | ID: mdl-30717729

ABSTRACT

BACKGROUND: The goal of Lean Enterprise Transformation (LET) is to go beyond simply using Lean tools and instead embed Lean principles and practices in the system so that it becomes a fundamental, collective mindset of the entire enterprise. The Veterans Engineering Resource Center (VERC) launched the Veterans Affairs (VA) LET pilot program to improve quality, safety, and the Veteran's experience. A national evaluation will examine the pilot program sites' implementation processes, outcomes and impacts, and abilities to improve LET adoption and sustainment. This paper describes the evaluation design for the VA LET national evaluation and describes development of a conceptual framework to evaluate LET specifically in healthcare settings. METHODS: A targeted literature review of Lean evaluation frameworks was performed to inform the development of the conceptual framework. Key domains were identified by a multidisciplinary expert group and then validated with key stakeholders. The national evaluation design will examine LET implementation using qualitative, survey, and quantitative methods at ten VA facilities. Qualitative data include site visits, interviews, and field observation notes. Survey data include an employee engagement survey to be administered to front-line staff at all pilot sites. Quantitative data include site-level quality improvement metrics collected by the Veterans Services Support Center. Qualitative, quantitative, and mixed-methods analyses will be conducted to examine implementation of LET strategic initiatives and variations in implementation success across sites. DISCUSSION: This national evaluation of a large-scale LET implementation effort will provide insights helpful to other systems interested in embarking on a Lean journey. Additionally, we created a multi-faceted conceptual framework to capture the specific features of a Lean healthcare organization. This framework will guide this evaluation and may be useful as an assessment tool for other organizations interested in implementing Lean principles at an enterprise level.


Subject(s)
Quality Improvement/organization & administration , United States Department of Veterans Affairs/organization & administration , Veterans , Delivery of Health Care , Humans , Pilot Projects , Program Evaluation , United States
8.
Genet Med ; 21(5): 1139-1154, 2019 05.
Article in English | MEDLINE | ID: mdl-30353149

ABSTRACT

PURPOSE: Precision medicine promises to improve patient outcomes, but much is unknown about its adoption within health-care systems. A comprehensive implementation plan is needed to realize its benefits. METHODS: We convened 80 stakeholders for agenda setting to inform precision medicine policy, delivery, and research. Conference proceedings were audio-recorded, transcribed, and thematically analyzed. We mapped themes representing opportunities, challenges, and implementation strategies to a logic model, and two implementation science frameworks provided context. RESULTS: The logic model components included inputs: precision medicine infrastructure (clinical, research, and information technology), big data (from data sources to analytics), and resources (e.g., workforce and funding); activities: precision medicine research, practice, and education; outputs: precision medicine diagnosis; outcomes: personal utility, clinical utility, and health-care utilization; and impacts: precision medicine value, equity and access, and economic indicators. Precision medicine implementation challenges include evidence gaps demonstrating precision medicine utility, an unprepared workforce, the need to improve precision medicine access and reduce variation, and uncertain impacts on health-care utilization. Opportunities include integrated health-care systems, partnerships, and data analytics to support clinical decisions. Examples of implementation strategies to promote precision medicine are: changing record systems, data warehousing techniques, centralized technical assistance, and engaging consumers. CONCLUSION: We developed a theory-based, context-specific logic model that can be used by health-care organizations to facilitate precision medicine implementation.


Subject(s)
Implementation Science , Precision Medicine/methods , Stakeholder Participation/psychology , Adult , Decision Making/ethics , Delivery of Health Care , Female , Genomics/methods , Humans , Male , Middle Aged , Models, Theoretical
9.
Genet Med ; 21(6): 1371-1380, 2019 06.
Article in English | MEDLINE | ID: mdl-30377384

ABSTRACT

PURPOSE: Robust evidence about the value of clinical genomic interventions (CGIs), such as genetic/genomic testing or clinical genetic evaluation, is limited. We obtained stakeholders' perspectives on outcomes from CGIs to help inform their value. METHODS: We used an adapted Delphi expert panel process. Two anonymous survey rounds assessed the value of 44 CGI outcomes and whether a third party should pay for them, with discussion in between rounds. RESULTS: Sixty-six panelists responded to the first-round survey and 60 to the second. Policy-makers/payers gave the lowest ratings for value and researchers gave the highest. Patients/consumers had the most uncertainty about value and payment by a third party. Uncertainty about value was observed when evidence of proven health benefit was lacking, potential harms outweighed benefits for reproductive outcomes, and outcomes had only personal utility for individuals or family members. Agreement about outcomes for which a third party should not pay included prevention through surgery with unproven health benefits, establishing ancestry, parental consanguinity, and paternity. CONCLUSION: Research is needed to understand factors contributing to uncertainty and stakeholder differences about the value of CGI outcomes. Reaching consensus will accelerate the creation of metrics to generate the evidence needed to inform value and guide policies that promote availability, uptake, and coverage of CGIs.


Subject(s)
Genetic Testing/economics , Genetic Testing/ethics , Stakeholder Participation/psychology , Attitude of Health Personnel , Delphi Technique , Genetic Testing/trends , Genomics/economics , Genomics/ethics , Genomics/trends , Humans , Surveys and Questionnaires
10.
J Genet Couns ; 26(3): 361-378, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28168332

ABSTRACT

As healthcare reimbursement is increasingly tied to value-of-service, it is critical for the genetic counselor (GC) profession to demonstrate the value added by GCs through outcomes research. We conducted a rapid systematic literature review to identify outcomes of genetic counseling. Web of Science (including PubMed) and CINAHL databases were systematically searched to identify articles meeting the following criteria: 1) measures were assessed before and after genetic counseling (pre-post design) or comparisons were made between a GC group vs. a non-GC group (comparative cohort design); 2) genetic counseling outcomes could be assessed independently of genetic testing outcomes, and 3) genetic counseling was conducted by masters-level genetic counselors, or non-physician providers. Twenty-three papers met the inclusion criteria. The majority of studies were in the cancer genetic setting and the most commonly measured outcomes included knowledge, anxiety or distress, satisfaction, perceived risk, genetic testing (intentions or receipt), health behaviors, and decisional conflict. Results suggest that genetic counseling can lead to increased knowledge, perceived personal control, positive health behaviors, and improved risk perception accuracy as well as decreases in anxiety, cancer-related worry, and decisional conflict. However, further studies are needed to evaluate a wider array of outcomes in more diverse genetic counseling settings.


Subject(s)
Genetic Counseling/standards , Patient Outcome Assessment , Adult , Anxiety , Child , Early Detection of Cancer , Female , Genetic Counseling/psychology , Genetic Testing , Health Behavior , Humans , Middle Aged , Personal Satisfaction , Pregnancy
11.
Genet Med ; 19(7): 763-771, 2017 07.
Article in English | MEDLINE | ID: mdl-27977007

ABSTRACT

OBJECTIVE: To assess the value of genetic testing from the perspective of the Department of Veterans Affairs (VA) clinical leadership. METHODS: We administered an Internet-based survey to VA clinical leaders nationwide. Respondents rated the value (on a 5-point scale) of each of six possible reasons for genetic testing. Bivariate and linear regressions identified associations between value ratings and environmental, organizational, provider, patient, and encounter characteristics. RESULTS: Respondents (n = 353; 63% response rate) represented 92% of VA medical centers. Tests that inform clinical management had the highest value rating (58.6%), followed by tests that inform disease prevention (56.4%), reproductive options (50.1%), life planning (43.9%), and a suspected (39.9%) or established (32.3%) diagnosis. Factors positively associated with high value included a culture that fosters adoption of genomics, specialist versus primary care provider, genetic tests available on laboratory menus, availability of genetic testing guidelines, clinicians knowing when to request genetics referrals, and availability of genetics professionals. CONCLUSION: Our results demonstrate the varied value of genetic testing from the perspective of clinical leadership within a health-care system. Engaging organizational leadership in understanding the various reasons for genetic testing and its value beyond clinical utility may increase adoption of genetic tests to support patient-centered care.Genet Med advance online publication 15 December 2016.


Subject(s)
Attitude of Health Personnel , Genetic Testing/statistics & numerical data , United States Department of Veterans Affairs/organization & administration , Genetic Testing/trends , Hospitals, Veterans , Humans , Internet , Leadership , Patient-Centered Care , Referral and Consultation , Surveys and Questionnaires , United States , Veterans
12.
Qual Manag Health Care ; 25(2): 92-101, 2016.
Article in English | MEDLINE | ID: mdl-27031358

ABSTRACT

OBJECTIVES: Health care organizations have used different strategies to implement quality improvement (QI) programs but with only mixed success in implementing and spreading QI organization-wide. This suggests that certain organizational strategies may be more successful than others in developing an organization's improvement capability. To investigate this, our study examined how the primary focus of grant-funded QI efforts relates to (1) key measures of grant success and (2) organization-level measures of success in QI and organizational learning. METHODS: Using a mixed-methods design, we conducted one-way analyses of variance to relate Veterans Affairs administrative survey data to data collected as part of a 3.5-year evaluation of 29 health care organization grant recipients. We then analyzed qualitative evidence from the evaluation to explain our results. RESULTS: We found that hospitals that focused on developing organizational infrastructure to support QI implementation compared with those that focused on training or conducting projects rated highest (at α = .05) on all 4 evaluation measures of grant success and all 3 systemwide survey measures of QI and organizational learning success. CONCLUSIONS: This study adds to the literature on developing organizational improvement capability and has practical implications for health care leaders. Focusing on either projects or staff training in isolation has limited value. Organizations are more likely to achieve systemwide transformation of improvement capability if their strategy emphasizes developing or strengthening organizational systems, structures, or processes to support direct improvement efforts.


Subject(s)
Capacity Building/organization & administration , Health Services Administration , Organizational Innovation , Quality Improvement/organization & administration , Humans , Inservice Training , Leadership , Quality Indicators, Health Care , Research Support as Topic/statistics & numerical data
13.
J Genet Couns ; 25(4): 625-34, 2016 08.
Article in English | MEDLINE | ID: mdl-26739839

ABSTRACT

There are currently multiple paths through which genetic counselors can acquire advanced knowledge and skills. However, outside of continuing education opportunities, there are few formal training programs designed specifically for the advanced training of genetic counselors. In the genetic counseling profession, there is currently considerable debate about the paths that should be available to attain advanced skills, as well as the skills that might be needed for practice in the future. The Association of Genetic Counseling Program Directors (AGCPD) convened a national committee, the Committee on Advanced Training for Certified Genetic Counselors (CATCGC), to investigate varied paths to post-master's training and career development. The committee began its work by developing three related grids that view career advancement from the viewpoints of the skills needed to advance (skills), ways to obtain these skills (paths), and existing genetic counselor positions that offer career change or advancement (positions). Here we describe previous work related to genetic counselor career advancement, the charge of the CATCGC, our preliminary work in developing a model through which to view genetic counselor advanced training and career advancement opportunities, and our next steps in further developing and disseminating the model.


Subject(s)
Certification , Counselors/education , Education, Continuing , Genetic Counseling , Humans
14.
Genet Med ; 17(11): 919-26, 2015 Nov.
Article in English | MEDLINE | ID: mdl-25741861

ABSTRACT

PURPOSE: Adoption and implementation of evidence-based genetic and genomic medicine have been slow. We describe a methodology for identifying the influence of organizational factors on adoption and implementation of these services in health-care organizations. METHODS: We illustrate a three-component, mixed-methods health services research approach, including expert panels, qualitative interviews with key informants, and quantitative surveys completed by key informants. RESULTS: This research approach yielded a baseline assessment of existing genetic health-care models in the Veterans Health Administration and identified organizational barriers to and facilitators of adoption. In aggregate, the panel and key informant strategies created a communication network of relevant organizational stakeholders and a detailed foundation of organizational knowledge from which to design tools and models for implementation-level genetic/genomic translation. CONCLUSION: Expert panel and key informant strategies can be used to create a backdrop of stakeholder involvement and baseline organizational knowledge within which to plan translation research and to inform strategic planning and policies for adoption and implementation of genetic services in health-care organizations.


Subject(s)
Delivery of Health Care , Genetics, Medical , Genomics , Delivery of Health Care/methods , Delivery of Health Care/organization & administration , Evidence-Based Medicine , Genetics, Medical/methods , Genetics, Medical/organization & administration , Genomics/methods , Genomics/organization & administration , Humans , Models, Theoretical , Pilot Projects , Translational Research, Biomedical , United States , United States Department of Veterans Affairs
15.
Genet Med ; 16(8): 609-19, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24503778

ABSTRACT

OBJECTIVE: To characterize the delivery of genetic consultative services for adults, we examined the prevalence and organizational determinants of genetic consult availability and the organization of these services in the Veterans Health Administration. METHODS: We conducted a Web-based survey of Veterans Health Administration clinical leaders. We summarized facility characteristics using descriptive statistics. Multivariate logistic regression assessed associations between organizational characteristics and consult availability. RESULTS: We received 353 survey responses from key informants representing 141 Veterans Affairs Medical Centers. Clinicians could obtain genetic consults at 110 (78%) Veterans Affairs Medical Centers. Cancer genetic and neurogenetic consults were most common. Academic affiliation (odds ratio = 3.0; 95% confidence interval: 1.1-8.6) and provider education about genetics (odds ratio = 2.9; 95% confidence interval: 1.1-7.8) were significantly associated with consult availability. The traditional model of multidisciplinary specialty clinics or coordinated services between geneticists and other providers was most prevalent, although variability in the organization of these services was described, with consults available on-site, at another Veterans Affairs Medical Center, via telegenetics, or at non-Veterans Health Administration facilities. The emerging model of nongeneticists integrating genetics into their practices was also reported, with considerable variability by specialty. CONCLUSION: Both traditional and emerging models for genetic consultation are available in the Veterans Health Administration; however, there is variability in service organization that could influence quality of care.


Subject(s)
Genetics, Medical/statistics & numerical data , Health Care Surveys/methods , United States Department of Veterans Affairs/statistics & numerical data , Cross-Sectional Studies , Female , Health Services Accessibility/statistics & numerical data , Hospitals, Veterans , Humans , Male , United States , Veterans Health , Web Browser
16.
Patient Educ Couns ; 94(2): 170-9, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24316056

ABSTRACT

OBJECTIVE: To identify and characterize patient-provider communication patterns during disclosure of Alzheimer's disease genetic susceptibility test results and to assess whether these patterns reflect differing models of genetic counseling. METHODS: 262 genetic counseling session audio-recordings were coded using the Roter Interactional Analysis System. Cluster analysis was used to distinguish communication patterns. Bivariate analyses were used to identify characteristics associated with the patterns. RESULTS: Three patterns were identified: Biomedical-Provider-Teaching (40%), Biomedical-Patient-Driven (34.4%), and Psychosocial-Patient-Centered (26%). Psychosocial-Patient-Centered and Biomedical-Provider-Teaching sessions included more female participants while the Biomedical-Patient-Driven sessions included more male participants (p=0.04). CONCLUSION: Communication patterns observed reflected the teaching model primarily, with genetic counseling models less frequently used. The emphasis on biomedical communication may potentially be at the expense of more patient-centered approaches. PRACTICE IMPLICATIONS: To deliver more patient-centered care, providers may need to better balance the ratio of verbal exchange with their patients, as well as their educational and psychosocial discussions. The delineation of these patterns provides insights into the genetic counseling process that can be used to improve the delivery of genetic counseling care. These results can also be used in future research designed to study the association between patient-centered genetic counseling communication and improved patient outcomes.


Subject(s)
Communication , Genetic Counseling , Patient Education as Topic , Patient-Centered Care/methods , Professional-Patient Relations , Adult , Aged , Alzheimer Disease/diagnosis , Alzheimer Disease/genetics , Cluster Analysis , Female , Genetic Predisposition to Disease , Humans , Interviews as Topic , Male , Middle Aged , Risk Assessment , Tape Recording
17.
São Paulo; s.n; 1985. 78 p.
Thesis in Portuguese | LILACS, Sec. Est. Saúde SP, SESSP-ISPROD, Sec. Est. Saúde SP, SESSP-ISACERVO | ID: biblio-1079274

ABSTRACT

O método da "fita de Shakir" foi usado na avaliação do estado nutricional de 633 pré-escolares que frequentavam um programa de atendimento de desnutridos no município de Diadema, Estado de São Paulo


Subject(s)
Male , Female , Humans , Nutrition Assessment , Child , Malnutrition , Nutritional Status/genetics , Body Height , Anthropometry
20.
Rev. nutr ; 13(1): 57-63, jan.-abr. 2000. tab
Article in Portuguese | LILACS, Sec. Est. Saúde SP | ID: lil-341260

ABSTRACT

No ano 2 000 a população brasileira contará com mais de 14 milhões de idosos e a osteoporose se destaca como uma das enfermidades que afetará pelo menos 3 em cada 20 mulheres brasileiras. Uma das medidas preventivas é assegurar o consumo adequado de cálcio dietético para garantir que o indivíduo atinja o pico de massa óssea geneticamente determinado (que se dá entre os 25 e 30 anos), mantenha esta massa na idade adulta e apresente perda mínima na velhice. O objetivo do estudo foi o de conhecer e avaliar o consumo de cálcio por adolescentes de escolas públicas do Município de Osasco, tendo em vista a prevenção da osteoporose. Foi estudado o consumo alimentar de 323 alunos de 5ª e 8ª séries de 8 escolas localizadas nas regiões central e periférica do município. Utilizou-se a média de registro alimentar de 3 dias alternados. O consumo médio diário de cálcio e a porcentagem de cálcio oriunda de alimentos lácteos não foram significativamente diferentes entre homens e mulheres. Somente 6,2 por cento dos homens e 2,8 por cento das mulheres apresentaram consumo de cálcio acima de 1200 mg/dia. Houve diferenças significativas entre as regiões geográficas com relação ao consumo de energia, de cálcio, assim como para a porcentagem de cálcio oriundos de alimentos lácteos e para a densidade do mineral na dieta. A média de cálcio ingerido do quartil mais alto (1015 mg/dia) não atinge a recomendação (1200 mg/dia). Os alimentos lácteos mais consumidos foram leite, queijo, sorvete e iogurte. O leite foi o alimento mais citado por todos os adolescentes, porém a quantidade difere entre os gêneros; as mulheres ingerem cerca de 190 ml por dia enquanto os homens tomam 240 ml.O consumo de cálcio dos adolescentes está muito abaixo das recomendações atuais, refletindo-se na baixa densidade do mineral na dieta diária. Seria desejável uma densidade de pelo menos 550 mgCa/1000 Kcal para alcançar os 1200 mg diários recomendados. É necessário um esforço entre os profissionais da saúde no sentido de estimular o aumento do consumo de alimentos ricos em cálcio visando a prevenção da osteoporose e suas conseqüências


Subject(s)
Humans , Adolescent , Osteoporosis , Calcium , Adolescent Nutrition
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