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1.
BMC Public Health ; 22(1): 888, 2022 05 04.
Artigo em Inglês | MEDLINE | ID: mdl-35509034

RESUMO

BACKGROUND: Cross-sector coalitions can be a powerful vehicle to promote adoption and implementation of evidence-based programs and policies across diverse racial/ethnic communities with a high chronic disease burden. Few studies have examined coalition composition, function, or capacity to promote learning among members. METHODS: We used a mixed methods approach to examine the United for Health coalition's implementation of multiple food environment interventions across five low-income communities of color in Los Angeles, California (USA). At the coalition-level, key measures included the collaborative environment, membership characteristics, process and structure, communication, resources, strengths, challenges/barriers, and community impact. At the organizational- and individual-levels, we collected data on participation, leadership development, intraorganizational change, perceived benefits, and learning outcomes. FINDINGS: Overall, the United for Health coalition produced five community gardens, three pop-up produce markets, and one farmers' market; members also expanded Electronic Benefits Transfer (EBT) access at three existing farmers' markets. Findings indicate early coalition strengths included having a mutual purpose, which was maintained throughout the study period. Coalition participation and engagement was consistently high, while coalition and inter-organizational communication improved over time. Strengths were membership diversity and the availability of learning opportunities. Benefits included leadership development and strategic alignment across organizations. Members demonstrated an increased awareness of the importance of culturally adapted interventions and knowledge of community health planning topics. Key implementation challenges were a lack of resources and social context barriers. CONCLUSIONS: Examining coalition function and maturation in a real-world context reveals important lessons for scholars and practitioners committed to addressing nutrition-related health disparities in marginalized and historically underserved communities. Future work should investigate the sustainability of externally funded cross-sector coalitions after funding ceases.


Assuntos
Planejamento em Saúde Comunitária , Liderança , Humanos , Los Angeles , Grupos Raciais , Estados Unidos
2.
Ann Allergy Asthma Immunol ; 123(1): 35-41, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-31028896

RESUMO

OBJECTIVE: To review the medical literature on hypersensitivity reactions to therapeutic monoclonal antibodies for patients with malignant tumors and chronic inflammatory or connective tissues diseases. DATA SOURCES: We searched the PubMed database using the terms monoclonal antibody, hypersensitivity, and allergy. STUDY SELECTIONS: We selected case reports and cohort studies of patients with hypersensitivity reactions to monoclonal antibodies. We included selected review articles to glean expert opinion on issues for which high-quality data are available. We sought specific information on the incidence, clinical description, pathobiology, and treatment of reactions. RESULTS: Hypersensitivity reactions to therapeutic monoclonal antibodies can be classic type I (mast cell mediated, perhaps IgE dependent) reactions, cytokine release reactions, or type IV cell-mediated reactions. There are limited data on the frequency of such reactions, and because new agents are added to the set at a relatively high rate, it is difficult to determine precisely the incidence of reactions to this class of drugs as a whole. The classification of a specific hypersensitivity reaction depends mainly on the medical history. Skin testing may be available but often is not validated and may be prohibitively expensive. Avoidance of the culpable agent is ideal, but if treatment with the responsible drug is necessary, rapid drug desensitization is an option for type I reactions. Desensitization is less likely to be effective for cytokine release reactions and is contraindicated for type IV reactions. CONCLUSION: Hypersensitivity reactions to therapeutic monoclonal antibodies are heterogeneous. Management depends on accurate identification and thoughtful consideration of the pathobiologic features of the reaction.


Assuntos
Anticorpos Monoclonais/imunologia , Anticorpos Monoclonais/uso terapêutico , Doenças do Tecido Conjuntivo/tratamento farmacológico , Hipersensibilidade a Drogas/imunologia , Inflamação/tratamento farmacológico , Neoplasias/tratamento farmacológico , Animais , Estudos de Coortes , Humanos
3.
Health Promot Pract ; 18(4): 586-597, 2017 07.
Artigo em Inglês | MEDLINE | ID: mdl-28443342

RESUMO

This study is a process evaluation of a clinical-community partnership that implemented evidence-based interventions in clinical safety net settings. Adoption and implementation of evidence-based interventions in these settings can help reduce health disparities by improving the quality of clinical preventive services in health care settings with underserved populations. A clinical-community partnership model is a possible avenue to catalyze adoption and implementation of interventions amid organizational barriers to change. Three Federally Qualified Health Centers in South Los Angeles participated in a partnership led by a local community-based organization (CBO) to implement hypertension interventions. Qualitative research methods were used to evaluate intervention selection and implementation processes between January 2014 and June 2015. Data collection tools included a key participant interview guide, health care provider interview guide, and protocol for taking meeting minutes. This case study demonstrates how a CBO acted as an external facilitator and employed a collaborative partnership model to catalyze implementation of evidence-based interventions in safety net settings. The study phases observed included initiation, planning, and implementation. Three emergent categories of organizational facilitators and barriers were identified (personnel capacity, professional development capacity, and technological capacity). Key participants and health care providers expressed a high level of satisfaction with the collaborative and the interventions, respectively. The CBO's role as a facilitator and catalyst is a replicable model to promote intervention adoption and implementation in safety net settings. Key lessons learned are provided for researchers and practitioners interested in partnering with Federally Qualified Health Centers to implement health promotion interventions.


Assuntos
Serviços de Saúde Comunitária/organização & administração , Promoção da Saúde/organização & administração , Provedores de Redes de Segurança/organização & administração , Populações Vulneráveis , Adolescente , Adulto , Idoso , Relações Comunidade-Instituição , Medicina Baseada em Evidências , Estilo de Vida Saudável , Humanos , Hipertensão/diagnóstico , Hipertensão/tratamento farmacológico , Los Angeles , Masculino , Pessoa de Meia-Idade , Pesquisa Qualitativa , Adulto Jovem
4.
Med Educ ; 54(8): 694-695, 2020 08.
Artigo em Inglês | MEDLINE | ID: mdl-32242964
5.
Am J Public Health ; 104(4): 658-64, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24524512

RESUMO

OBJECTIVES: Our study sought to examine associations between the content of outdoor advertising and neighborhood ethnic/racial and socioeconomic composition to see whether particular communities disproportionately host harmful content. METHODS: We constructed a spatial database of photographs taken from June 2012 until December 2012 in 7 identically zoned communities in Los Angeles, California, to compare outdoor advertising area and content. We selected communities to contrast by ethnicity/race, income, education, and youth population. RESULTS: At-risk communities and communities of color hosted more outdoor advertising depicting harmful content than other communities. Among included neighborhoods, harmful content and the proportion of outdoor advertising overall were most prevalent in communities of Asian Americans and Latino Americans. In all communities, harmful content represented at least 24% of outdoor advertising space. CONCLUSIONS: This study provides evidence of the potential for land-use decisions to result in spatially inequitable health impacts. Although dictating the placement of outdoor advertising through zoning may seem sensible, such a decision might have the unintended consequence of disadvantaging the well-being of local communities. Neighborhood factors require more contextually nuanced public health and land-use policy.


Assuntos
Publicidade/estatística & dados numéricos , Saúde Pública , Escolaridade , Etnicidade/estatística & dados numéricos , Humanos , Los Angeles/epidemiologia , Prevalência , Saúde Pública/estatística & dados numéricos , Grupos Raciais/estatística & dados numéricos , Características de Residência/estatística & dados numéricos , Fatores Socioeconômicos , Populações Vulneráveis/estatística & dados numéricos
6.
Fam Community Health ; 34 Suppl 1: S92-S101, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21160336

RESUMO

Confronted by continuing health disparities in vulnerable communities, Community Health Councils (CHC), a nonprofit community-based organization in South Los Angeles, worked with the African Americans Building a Legacy of Health Coalition and research partners to develop a community change model to address the root causes of health disparities within the community's African American population. This article discusses how the CHC Model's development and application led to public policy interventions in a "food desert." The CHC Model provided a systematic approach to engaging impacted communities in support of societal level reforms, with the goal to influence health outcomes.


Assuntos
Negro ou Afro-Americano , Serviços de Saúde Comunitária/organização & administração , Coalizão em Cuidados de Saúde , Conselhos de Planejamento em Saúde , Disparidades em Assistência à Saúde , Saúde da População Urbana/normas , Fortalecimento Institucional , Pesquisa sobre Serviços de Saúde , Humanos , Los Angeles , Modelos Organizacionais , Inovação Organizacional , Organizações sem Fins Lucrativos , Avaliação de Resultados em Cuidados de Saúde , Mudança Social , Análise de Sistemas
7.
J Allergy Clin Immunol ; 124(6): 1259-66, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19910036

RESUMO

BACKGROUND: Rapid desensitization, a procedure for graded drug administration, allows for the safe readministration of a medication after certain types of hypersensitivity reactions (HSRs) and is indicated in cases in which there are no reasonable therapeutic alternatives. The use of rapid desensitization for HSRs to mAbs has not been validated. OBJECTIVE: We sought to describe our experience with rapid desensitization to mAbs, including rituximab, infliximab, and trastuzumab. METHODS: One hundred five rapid desensitizations were performed in 23 patients with a standardized 12-step, 6-hour protocol. Our approach to patient evaluation before desensitization is described. The severity, characteristics, and timing of both initial HSRs and HSRs during desensitization were determined by means of retrospective review of medical records. After a reaction during desensitization, patient-specific protocol modifications were made before each subsequent desensitization. RESULTS: 104 of 105 desensitizations undertaken were successfully completed. We observed HSRs during 29% of desensitizations, including 27 mild reactions, 1 moderate reaction, and 2 severe reactions. Overall, reactions during desensitization were markedly less severe than initial HSRs, but reactions did recur in a minority of successive desensitizations. CONCLUSIONS: Rapid desensitization is a promising method for the delivery of monoclonal therapeutics after an HSR, but the possibility of a reaction remains with each desensitization.


Assuntos
Anticorpos Monoclonais/efeitos adversos , Dessensibilização Imunológica/métodos , Hipersensibilidade a Drogas/terapia , Adulto , Idoso , Anticorpos Monoclonais/administração & dosagem , Anticorpos Monoclonais Humanizados , Anticorpos Monoclonais Murinos , Hipersensibilidade a Drogas/imunologia , Feminino , Humanos , Infliximab , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Rituximab , Testes Cutâneos , Trastuzumab
8.
J Investig Med ; 68(7): 1217-1222, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32699066

RESUMO

As of 2017, 1.8 million people living with HIV (PLWH) were adolescents between ages 10 and 19, accounting for 5% of all PLWH and 590,000 people between the ages 15 and 24 were newly infected with HIV. Between 2004 and 2011, AIDS-related deaths increased 50% among adolescents, and optimal adolescent adherence to antiretroviral treatment (ART) is estimated at only 62% of adolescents worldwide. While there have been great strides toward achieving the UNAIDS 90-90-90 goals, adolescents remain a group lacking appropriate resources and research to achieve these. This review analyzes current interventions aimed toward increasing adolescent ART adherence. Systematic searches of EMBASE, PubMed and PsycINFO were performed using the keywords 'adolescent HIV medication adherence interventions'. The Gain Score effect size was calculated for studies reporting the Cohen's d and variance to include both prestudy and poststudy values. A random-effects model analyzed intervention significance. Authors were contacted to obtain additional data values and study clarification. Twelve studies met inclusion criteria for meta-analysis. There were no significant differences seen between control and intervention groups in medication adherence (z=-1.4714, p<0.1412), viral load (z=-0.1946, p<0.8547) or CD4+ lymphocyte count (z=0.2650, p<0.7910). There was no significant difference between studies in increasing medication adherence. Results indicate that interventions did not improve medication adherence in adolescents with HIV. However, the paucity of quantitative research available speaks to a need for more quantitative intervention studies and standardization of measures of intervention efficacy.


Assuntos
Infecções por HIV/tratamento farmacológico , Adesão à Medicação , Adolescente , Contagem de Linfócito CD4 , Infecções por HIV/imunologia , Infecções por HIV/virologia , Humanos , Carga Viral
9.
J Allergy Clin Immunol Pract ; 8(5): 1668-1680.e2, 2020 05.
Artigo em Inglês | MEDLINE | ID: mdl-32112926

RESUMO

BACKGROUND: Oxaliplatin causes a wider variety of immediate hypersensitivity reactions than do other platin-based chemotherapeutics. Some resemble type 1 reactions that respond to desensitization. Others are atypical, possibly mast cell-independent cytokine release reactions refractory to desensitization. Given this variability, clinicians need an evidence-based strategy to personalize therapy for oxaliplatin-hypersensitive patients. OBJECTIVE: To develop a data-driven algorithm to optimize treatment of oxaliplatin-hypersensitive patients. METHODS: We retrospectively analyzed the baseline clinical characteristics, biomarkers, and reactions of 48 oxaliplatin-hypersensitive patients who received a total of 266 oxaliplatin desensitizations. RESULTS: We characterized 4 endophenotypes: type 1, cytokine release, mixed, and either. A mean 40-fold increase in serum concentration of IL-6 helped define the cytokine release endophenotype. Younger patients were more likely to have a cytokine release endophenotype, whereas older patients were more likely to have a type 1 reaction. Skin testing was not informative for determining endophenotype or risk of reaction during desensitization, and did not associate with initial or desensitization grade of reaction. Patients with a history of atopy and an initial type 1 reaction responded to desensitization with antihistamine premedications, whereas nonatopic patients with the same initial reaction phenotype were more likely to convert to a cytokine release or mixed reaction during desensitization. We combined these reaction patterns with biomarker data and desensitization outcomes to construct an algorithm that helps tailor desensitization protocol design to meet individual patient needs. CONCLUSIONS: Endophenotyping oxaliplatin hypersensitivity reactions may help forecast desensitization outcomes and personalize treatment plans.


Assuntos
Antineoplásicos , Hipersensibilidade a Drogas , Antineoplásicos/efeitos adversos , Dessensibilização Imunológica , Hipersensibilidade a Drogas/diagnóstico , Hipersensibilidade a Drogas/terapia , Humanos , Compostos Organoplatínicos/efeitos adversos , Oxaliplatina , Estudos Retrospectivos
10.
J Allergy Clin Immunol ; 122(3): 574-80, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18502492

RESUMO

BACKGROUND: Hypersensitivity reactions (HSRs) to chemotherapeutic drugs, including mAbs, often require that the provoking medication be discontinued, thus raising a dilemma for the caregiver: further use could precipitate a severe, even fatal, allergic reaction on re-exposure, but alternative drugs might be poorly tolerated or much less effective compared with the preferred agent. OBJECTIVE: We have developed a standardized rapid desensitization protocol for achieving temporary tolerization to drug allergens. In this study we evaluate the safety and efficacy of this protocol. METHODS: Ninety-eight patients who had HSRs in response to treatment with carboplatin, cisplatin, oxaliplatin, paclitaxel, liposomal doxorubicin, doxorubicin, or rituximab received rapid desensitization to these agents. A standardized 12-step protocol was used, with treatment given intravenously or intraperitoneally. Initial desensitizations occurred in the medical intensive care unit, whereas most subsequent infusions took place in an outpatient setting. Safety and efficacy of the protocol were assessed by review of treatment records. RESULTS: Of the 413 desensitizations performed, 94% induced mild or no reactions. No life-threatening HSRs or deaths occurred during the procedure, and all patients received their full target dose. Most reactions occurred during the first desensitization. Reactions were most commonly reported at the last step of the protocol. Desensitizations through the intravenous and intraperitoneal routes were equally effective. CONCLUSIONS: Our standardized 12-step protocol for rapid drug desensitization is safe and effective and has been adopted as the standard of care at our institutions in treating patients with HSRs to chemotherapeutic drugs, including mAbs.


Assuntos
Antineoplásicos/efeitos adversos , Dessensibilização Imunológica/métodos , Hipersensibilidade a Drogas/terapia , Adulto , Idoso , Antineoplásicos/administração & dosagem , Protocolos Clínicos , Dessensibilização Imunológica/efeitos adversos , Hipersensibilidade a Drogas/imunologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Testes Cutâneos , Resultado do Tratamento
11.
J Nutr Educ Behav ; 51(4): 478-485, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30442570

RESUMO

OBJECTIVE: To understand perceived barriers and facilitators to physical activity (PA) among at-risk African American and Hispanic adolescents and adults in a low-income community. DESIGN: Qualitative research was conducted in 2014-2015 using focus groups and a sociodemographic survey. SETTING: Three high schools in South Los Angeles, California. PARTICIPANTS: Eight high school-aged adolescent focus groups (n = 64) and 8 adult focus groups (n = 47). PHENOMENON OF INTEREST: Perceived barriers and facilitators to PA among predominantly obese and overweight African American and Hispanic adolescents and adults. ANALYSIS: Groups were audio recorded, transcribed, coded, and analyzed using an inductive approach. RESULTS: Participants reported that PA resources were available on school campuses (eg, sports teams) and in the community (eg, sidewalks, local parks, fitness classes). Key barriers to PA were intrapersonal (lack of motivation and time constraints) and environmental (safety concerns), whereas facilitators included interpersonal factors (social support). Participants provided valuable insights, including recommendations to increase noncompetitive programs at schools, develop shared-use agreements, and address safety concerns at local parks and public recreational spaces. CONCLUSIONS AND IMPLICATIONS: The findings suggest that future efforts to promote PA among at-risk minority groups should address intrapersonal and social environmental factors. Community-based programmatic and policy recommendations are provided.


Assuntos
Negro ou Afro-Americano , Exercício Físico/psicologia , Acessibilidade aos Serviços de Saúde/estatística & dados numéricos , Hispânico ou Latino , Adolescente , Adulto , Negro ou Afro-Americano/psicologia , Negro ou Afro-Americano/estatística & dados numéricos , Feminino , Grupos Focais , Conhecimentos, Atitudes e Prática em Saúde , Promoção da Saúde , Hispânico ou Latino/psicologia , Hispânico ou Latino/estatística & dados numéricos , Humanos , Los Angeles , Masculino , Pessoa de Meia-Idade , Pobreza , Pesquisa Qualitativa
12.
Endocrinology ; 149(3): 1038-48, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18063676

RESUMO

Mutations in the tyrosine kinase receptor trkB or in one of its natural ligands, brain-derived neurotrophic factor (BDNF), lead to severe hyperphagia and obesity in rodents and/or humans. Here, we show that peripheral administration of neurotrophin-4 (NT4), the second natural ligand for trkB, suppresses appetite and body weight in a dose-dependent manner in several murine models of obesity. NT4 treatment increased lipolysis, reduced body fat content and leptin, and elicited long-lasting amelioration of hypertriglyceridemia and hyperglycemia. After treatment termination, body weight gradually recovered to control levels in obese mice with functional leptin receptor. A single intrahypothalamic application of minute amounts of NT4 or an agonist trkB antibody also reduced food intake and body weight in mice. Taken together with the genetic evidence, our findings support the concept that trkB signaling, which originates in the hypothalamus, directly modulates appetite, metabolism, and taste preference downstream of the leptin and melanocortin 4 receptor. The trkB agonists mediate anorexic and weight-reducing effects independent of stress induction, visceral discomfort, or pain sensitization and thus emerge as a potential therapeutic for metabolic disorders.


Assuntos
Fatores de Crescimento Neural/farmacologia , Obesidade/metabolismo , Receptor trkB/agonistas , Animais , Peso Corporal/efeitos dos fármacos , Modelos Animais de Doenças , Ingestão de Alimentos/efeitos dos fármacos , Metabolismo Energético/efeitos dos fármacos , Glucose/metabolismo , Homeostase/efeitos dos fármacos , Leptina/metabolismo , Cloreto de Lítio/farmacologia , Masculino , Melanocortinas/metabolismo , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Obesos , Ratos , Ratos Sprague-Dawley , Receptor trkB/metabolismo , Receptores para Leptina/metabolismo , Paladar/efeitos dos fármacos , Triglicerídeos/metabolismo
13.
J Allergy Clin Immunol Pract ; 6(1): 90-94, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29037819

RESUMO

Vocal cord dysfunction, also known as paradoxical vocal fold motion (PVFM), is a disorder characterized by abnormal vocal cord adduction during inspiration. PVFM is commonly misdiagnosed as asthma because of the similarity of symptoms: cough, wheezing, chest pain, and dyspnea. We present the clinical vignette of a 36-year-old woman with juvenile rheumatoid arthritis and multiple adverse drug reactions who presented with recurrent episodes of unrecognized PVFM during skin testing for drug allergy, omalizumab treatment, and tocilizumab desensitization. Before the diagnosis of PVFM, these episodes were treated as anaphylaxis, including the administration of epinephrine. Once diagnosed and treated for PVFM, the patient did not present any further events and continued treatment for drug allergy. PVFM may be underreported in hypersensitivity reactions because of the similarity to Type 1-mediated respiratory symptoms and comorbid asthma.


Assuntos
Alérgenos/imunologia , Anticorpos Monoclonais Humanizados/imunologia , Artrite Juvenil/diagnóstico , Asma/diagnóstico , Dessensibilização Imunológica/métodos , Hipersensibilidade a Drogas/diagnóstico , Omalizumab/imunologia , Disfunção da Prega Vocal/diagnóstico , Adulto , Anticorpos Monoclonais Humanizados/uso terapêutico , Diagnóstico Diferencial , Dispneia , Feminino , Humanos , Omalizumab/uso terapêutico , Sons Respiratórios , Testes Cutâneos
14.
Am J Health Behav ; 41(5): 661-669, 2017 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-28760188

RESUMO

OBJECTIVES: We explored how perceived barriers and facilitators influence healthy eating and investigated the acceptability of changes to school lunch meals among adolescents after implementation of the Healthy, Hunger-Free Kids Act of 2010. METHODS: We conducted 8 focus groups with adolescents (N = 64) at 3 South Los Angeles high schools. Data collection instruments included a semi-structured guide and questionnaire. Two researchers independently coded transcripts. RESULTS: Most participants believed fruits and vegetables were available in their community and reported high relative cost, poor quality, and lack of motivation as barriers to consumption. Many said school meals were an important source of healthy food and were aware of recent changes to the school lunch program. A primary facilitator to eating school lunches was access to fresh food items (eg, a salad bar). Perceived barriers included long cafeteria lines, time constraints, lack of variety, and limited quantities of preferred items. Adolescents viewed off-campus food establishments near the school as competition to school meals. CONCLUSIONS: Our findings suggest the need to measure perceived and actual barriers to healthy eating among adolescents and to examine the effect of these barriers on dietary behavior. We provide programmatic and policy recommendations.


Assuntos
Comportamento do Consumidor , Dieta Saudável/psicologia , Serviços de Alimentação , Almoço/psicologia , Instituições Acadêmicas , Estudantes/psicologia , Adolescente , Feminino , Humanos , Los Angeles , Masculino , Pesquisa Qualitativa
15.
J Surg Educ ; 74(2): 286-294, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-27692808

RESUMO

OBJECTIVE: Optimal methods for medical student assessment in surgery remain elusive. Faculty- and housestaff-written evaluations constitute the chief means of student assessment in medical education. However, numerous studies show that this approach has poor specificity and a high degree of subjectivity. We hypothesized that an objective structured clinical examination (OSCE) in the surgery clerkship would provide additional data on student performance that would confirm or augment other measures of assessment. DESIGN: We retrospectively reviewed data from OSCEs, National Board of Medical Examiners shelf examinations, oral presentations, and written evaluations for 51 third-year Harvard Medical School students rotating in surgery at Massachusetts General Hospital from 2014 to 2015. We expressed correlations between numeric variables in Pearson coefficients, stratified differences between rater groups by one-way analysis of variance, and compared percentages with 2-sample t-tests. We examined commentary from both OSCE and clinical written evaluations through textual analysis and summarized these results in percentages. RESULTS: OSCE scores and clinical evaluation scores correlated poorly with each other, as well as with shelf examination scores and oral presentation grades. Textual analysis of clinical evaluation comments revealed a heavy emphasis on motivational factors and praise, whereas OSCE written comments focused on cognitive processes, patient management, and methods to improve performance. CONCLUSIONS: In this single-center study, an OSCE provided clinical skills data that were not captured elsewhere in the surgery clerkship. Textual analysis of faculty evaluations reflected an emphasis on interpersonal skills, rather than appraisal of clinical acumen. These findings suggest complementary roles of faculty evaluations and OSCEs in medical student assessment.


Assuntos
Estágio Clínico , Competência Clínica , Educação de Graduação em Medicina/métodos , Avaliação Educacional/métodos , Cirurgia Geral/educação , Acreditação , Bases de Dados Factuais , Feminino , Cirurgia Geral/estatística & dados numéricos , Humanos , Masculino , Massachusetts , Anamnese , Exame Físico , Estudos Retrospectivos , Faculdades de Medicina/organização & administração , Estudantes de Medicina/estatística & dados numéricos , Adulto Jovem
16.
J Health Care Poor Underserved ; 17(2 Suppl): 146-58, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16809881

RESUMO

The recent emphasis in public health and medicine on the environmental determinants of chronic illness has created the need for a more comprehensive way to assess barriers and facilitators of healthy living. This paper reports on the approach taken by a Centers for Disease Control and Prevention (CDC)-funded project whose goal is to reduce disparities in diabetes and cardiovascular disease in Los Angeles' African American communities. Findings from this community-based participatory research project suggest that while location is an important variable in evaluating nutritional and physical activity resources, quality and price considerations are at least as useful. We argue that every community or neighborhood is located within a resource environment for medical care, recreation, food, and other health-promoting or health-compromising goods and services that affect the lives and health of its residents.


Assuntos
Negro ou Afro-Americano , Doença Crônica/etnologia , Doença Crônica/prevenção & controle , Planejamento em Saúde Comunitária , Meio Ambiente , Recursos em Saúde/provisão & distribuição , Programas Gente Saudável , Serviços Urbanos de Saúde/provisão & distribuição , Adolescente , Adulto , Doenças Cardiovasculares/etnologia , Doenças Cardiovasculares/prevenção & controle , Diabetes Mellitus/etnologia , Diabetes Mellitus/prevenção & controle , Acessibilidade aos Serviços de Saúde , Humanos , Los Angeles/epidemiologia , Características de Residência , Análise de Pequenas Áreas , Fatores Socioeconômicos , Sociologia Médica , Estados Unidos
17.
Health Promot Pract ; 7(3 Suppl): 233S-46S, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16760245

RESUMO

A Los Angeles REACH demonstration project led by Community Health Councils, Inc. adapted and implemented an organizational wellness intervention originally developed by the local health department, providing training in incorporating physical activity and healthy food choices into the routine "conduct of business" in 35 predominantly public and private, nonprofit-sector agencies. A total of 700 staff, members, or clients completed the 12-week or subsequently retooled 6-week curriculum. Attendance and retention rates between baseline and postintervention assessments were improved substantially in the shortened offering. Feelings of sadness or depression decreased significantly (p = .00), fruit and vegetable intake increased significantly (+0.5 servings/day, p = .00), and body mass index decreased marginally (-0.5 kg/m(2), p = .08) among 12-week participants. The numbers of days in which individuals participated in vigorous physical activity increased significantly among 6-week participants (+0.3, p = .00). This model holds promise for extending the reach of environmentally focused work-site wellness programming to organizations and at-risk populations not traditionally engaged by such efforts.


Assuntos
Negro ou Afro-Americano , Serviços de Saúde Comunitária/organização & administração , Participação da Comunidade , Promoção da Saúde/organização & administração , Acessibilidade aos Serviços de Saúde/organização & administração , Feminino , Comportamentos Relacionados com a Saúde , Humanos , Relações Interinstitucionais , Masculino , Saúde Mental , Pessoa de Meia-Idade , Obesidade/prevenção & controle
18.
J Allergy Clin Immunol Pract ; 4(3): 497-504, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26895621

RESUMO

BACKGROUND: Rapid drug desensitization (RDD) is used to address hypersensitivity reactions to chemotherapeutics and monoclonal antibodies, allowing patients to be treated with optimal pharmacological agents. RDD protocols are tailored to each individual patient's reaction and needs, and protect against anaphylaxis, but overall risks, costs, and benefits have not been determined. OBJECTIVE: We investigated the safety, efficacy, costs, and life expectancy of patients in a large population undergoing RDD. METHODS: We analyzed 2177 RDD procedures performed in 370 patients with cancer, vasculitis, and hematological and connective tissue diseases who presented 402 reactions. A subgroup of carboplatin allergic patients with ovarian cancer treated with RDD was analyzed for costs and life expectancy and compared with a nonallergic control group. RESULTS: RDD allowed all patients to receive safely the full dose of the medication to which they were reactive. A gradual increase in the fraction of outpatient desensitizations from 81% to 98% was achieved through risk stratification. Of the 2177 desensitizations, 93% had no or mild reactions whereas 7% had moderate to severe reactions, which did not preclude the completion of the treatment, and there were no deaths. Overall health costs in the carboplatin allergic group were not higher than those in the nonallergic group treated with standard of care. Administration of carboplatin through RDD was as effective as standard administration with a nonsignificant increase in life expectancy in desensitized patients as compared with nonallergic, nondesensitized controls. CONCLUSIONS: RDD is cost effective and safe for allergic patients with cancer and chronic disease to remain on first line therapy.


Assuntos
Anticorpos Monoclonais/efeitos adversos , Antineoplásicos/efeitos adversos , Dessensibilização Imunológica , Hipersensibilidade a Drogas/terapia , Adulto , Idoso , Anticorpos Monoclonais/uso terapêutico , Antineoplásicos/uso terapêutico , Dessensibilização Imunológica/efeitos adversos , Dessensibilização Imunológica/economia , Dessensibilização Imunológica/métodos , Feminino , Custos de Cuidados de Saúde , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias/tratamento farmacológico , Resultado do Tratamento
19.
JEMS ; 32(7): 20; discussion 20, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17631195
20.
Chem Immunol Allergy ; 97: 217-33, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22613865

RESUMO

Rapid drug desensitization (RDD) is a technique that induces temporary tolerance to a drug, allowing a medication-allergic patient to receive the optimal agent for his or her disease. Through RDD, patients with IgE and non-IgE hypersensitivity reactions (HSRs) including anaphylaxis can safely be administered important medications while minimizing or completely inhibiting adverse reactions. Adverse reactions to drugs are increasingly recognized as important contributors to disease as well as impediments to the best treatment of dermatological, infectious, autoimmune, and neoplastic disorders. With the development of novel pharmacologic agents and the evolution of personalized treatments based on pharmacogenetic profiling, clinicians must decide which agent is the best for a particular patient with a given disease. Biological agents have greatly improved the treatment of chronic inflammatory diseases and malignancies while limiting some medication-associated toxicities. Because of better outcomes, longer patient survival, and extended treatment courses, patients are exposed to drugs more frequently and for longer time periods, increasing the risk of sensitization and the potential for HSRs. The frequency of adverse drug reactions has therefore increased in the last 10 years. Because of the severity of some reactions and the fear of inducing a potentially lethal reaction in highly sensitized patients, first-line treatments are sometimes abandoned, relegating hypersensitive patients to secondary, less effective, therapy. Some of these reactions are mast cell-mediated HSRs, a subset of which occur through an IgE-dependent mechanism, and are thus true allergies. Others involve mast cells, but an IgE mechanism cannot be demonstrated. Both types of reactions are amenable to RDD, and our group has successfully performed several hundred desensitizations to chemotherapy, antibiotics and biological agents including monoclonal antibodies with a standardized 12-step protocol that can be universally applied to all desensitizations. The molecular basis of RDD has now been studied, and an in vitro mouse mast cell model has shown that RDD is an antigen-specific process that does not induce subclinical mast cell mediator release, and that blocks the release of acute and late mast cell mediators by preventing calcium influx and antigen/IgE/and IgE receptor internalization.


Assuntos
Dessensibilização Imunológica , Hipersensibilidade a Drogas/terapia , Animais , Antibacterianos/efeitos adversos , Antibacterianos/uso terapêutico , Anticorpos Monoclonais/efeitos adversos , Anticorpos Monoclonais/uso terapêutico , Antígenos/metabolismo , Antineoplásicos/efeitos adversos , Antineoplásicos/uso terapêutico , Cálcio/metabolismo , Cisplatino/efeitos adversos , Cisplatino/uso terapêutico , Hipersensibilidade a Drogas/prevenção & controle , Imunoglobulina E/metabolismo , Mediadores da Inflamação/antagonistas & inibidores , Mediadores da Inflamação/metabolismo , Mastócitos/efeitos dos fármacos , Mastócitos/imunologia , Camundongos , Neoplasias/tratamento farmacológico , Receptores de IgE/metabolismo , Taxoides/efeitos adversos , Taxoides/uso terapêutico
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