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1.
Prog Community Health Partnersh ; 6(4): 499-506, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23221296

RESUMO

BACKGROUND: All parties in community-academic partnerships have a vested interest prevention program success. Markers of success that reflect community's experiences of programmatic prevention success are not always measurable, but critically speak to community-defined needs. OBJECTIVE: The purpose of this manuscript was to (1) describe our systematic process for linking locally relevant community views (community-defined indicators) to measurable outcomes in the context of a youth violence prevention program and (2) discuss lessons learned, next steps, and recommendations for others trying to replicate a similar process. METHODS: A research team composed of both academic and community researchers conducted a systematic process of matching community-defined indicators of youth violence prevention programmatic success to standardized youth survey items being administered in the course of a program evaluation. The research team of three community partners and five academic partners considered 43 community-defined indicators and 208 items from the youth surveys being utilized within the context of a community-based aggression prevention program. At the end of the matching process, 92 youth survey items were identified and agreed upon as potential matches to 11 of the community-defined indicators. CONCLUSIONS: We applied rigorous action steps to match community-defined indicators to survey data collected in the youth violence prevention intervention. We learned important lessons that inform recommendations for others interested in such endeavors. The process used to derive and assess community-defined indicators of success emphasized the principles of community-based participatory research (CBPR) and use of existing and available data to reduce participant burden.


Assuntos
Relações Comunidade-Instituição , Universidades/organização & administração , Violência/prevenção & controle , Adolescente , Participação da Comunidade/métodos , Pesquisa Participativa Baseada na Comunidade , Comportamento Cooperativo , Humanos , Desenvolvimento de Programas , Avaliação de Programas e Projetos de Saúde
2.
Arch Pediatr Adolesc Med ; 166(3): 232-9, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22393181

RESUMO

OBJECTIVES: To measure the effect of rotavirus vaccine (RVV) on acute gastroenteritis (AGE) managed by primary care physicians in the first 2 rotatvirus seasons following the introduction of RVV. DESIGN: Retrospective cohort study. SETTING: Practice-based network composed of 33 ambulatory pediatric practices in Philadelphia, Pennsylvania. PARTICIPANTS: All children born from February 22, 2006 (date of RVV licensure), through February 29, 2008, and who received care at any network site. MAIN EXPOSURE: Receipt of RVV. OUTCOME MEASURES: The primary outcomes were AGE-related office visits, telephone calls, and episodes (composite outcome consisting of all visits and calls within a 10-day period). RESULTS: Rates of AGE visits in the 2 rotavirus seasons following the introduction of RVV steadily decreased from 3.0 AGE visits per 100 total office visits in the 2005 season to 1.8 in the 2008 season. In 2007, vaccinations were administered to 9351 of 13 951 vaccine-eligible children (67.0%), and in 2008, they were administered to 9958 of 10 728 (92.8%). Among RVV-immunized children in 2007, AGE calls and episodes were significantly reduced with vaccine effectiveness of 53% and 46%, respectively. No significant difference was seen between RVV-immunized and RVV-nonimmunized children for any outcome in 2008. CONCLUSIONS: Rotavirus vaccine was associated with a significant reduction in outpatient AGE calls and episodes among immunized children in our network in 2007. Despite a reduction in winter AGE rates in the network, no difference was detected between RVV-immunized and RVV-nonimmunized children for any outcome in 2008. Further study is needed to understand the lack of vaccine effect in 2008.


Assuntos
Gastroenterite/prevenção & controle , Doença Aguda , Assistência Ambulatorial , Feminino , Gastroenterite/epidemiologia , Gastroenterite/microbiologia , Humanos , Incidência , Lactente , Masculino , Análise Multivariada , Estudos Retrospectivos , Vacinas contra Rotavirus
3.
Arch Dermatol ; 147(11): 1261-7, 2011 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21768444

RESUMO

OBJECTIVE: To demonstrate response to antimalarial agents in patients with cutaneous lupus erythematosus (CLE) using activity scores from the Cutaneous Lupus Erythematosus Disease Area and Severity Index, a validated outcome measure. DESIGN: Prospective, longitudinal cohort study. SETTING: University cutaneous autoimmune disease clinic. PARTICIPANTS: A total of 128 patients with CLE who presented from January 2007 to July 2010 and had at least 2 visits with activity scores. INTERVENTION: Administration of antimalarial agents. MAIN OUTCOME MEASURES: Response was defined by a 4-point or 20% decrease in activity score. Response to initiation was determined by the difference between the scores before treatment and at the first visit at least 2 months after treatment. Response to continuation was determined by the difference between the scores at the first visit and the most recent visit while undergoing treatment. RESULTS: Of 11 patients who initiated treatment with hydroxychloroquine, 55% were responders (n = 6), showing a decrease in median (interquartile range [IQR]) activity score from 8.0 (3.5-13.0) to 3.0 (1.8-7.3) (P = .03). Of 15 patients for whom hydroxychloroquine failed, 67% were responders to initiation of hydroxychloroquine-quinacrine therapy (n = 10), showing a decrease in median (IQR) activity score from 6.0 (4.8-8.3) to 3.0 (0.75-5.0) (P = .004). Nine of 21 patients who continued hydroxychloroquine treatment (43%), and 9 of 21 patients who continued hydroxychloroquine-quinacrine (43%) were responders, showing a decrease in median (IQR) activity score from 6.0 (1.5-9.5) to 1.0 (0.0-4.5) (P = .01) and 8.5 (4.25-17.5) to 5.0 (0.5-11.5) (P = .01), respectively. CONCLUSIONS: The use of quinacrine with hydroxychloroquine is associated with response in patients for whom hydroxychloroquine monotherapy fails. Further reduction in disease activity can be associated with continuation of treatment with antimalarial agents.


Assuntos
Antimaláricos/uso terapêutico , Hidroxicloroquina/uso terapêutico , Lúpus Eritematoso Cutâneo/tratamento farmacológico , Quinacrina/uso terapêutico , Adolescente , Adulto , Idoso , Antimaláricos/administração & dosagem , Estudos de Coortes , Quimioterapia Combinada , Feminino , Seguimentos , Humanos , Hidroxicloroquina/administração & dosagem , Estudos Longitudinais , Lúpus Eritematoso Cutâneo/fisiopatologia , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Quinacrina/administração & dosagem , Índice de Gravidade de Doença , Resultado do Tratamento , Adulto Jovem
4.
AIDS Behav ; 14(4): 748-54, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19089608

RESUMO

Antiretroviral medication refill adherence has not been compared directly to electronic drug monitoring (EDM) in any identifiable published study. We retrospectively studied adults with undetectable HIV titers on highly active antiretroviral therapy. We used Pearson correlation coefficients and receiver operating characteristic curves to relate the two adherence measures, and we used the Wilcoxon rank-sum test to assess the relation between adherence and viral load. In sixty-five subjects, the majority of whom were African American and male with median age of 44 years, pharmacy refill adherence was difficult to collect retrospectively, was not significantly correlated with EDM adherence, and was not significantly related to viral load. Ninety-day supply pharmacy refill adherence correctly classified 95% EDM adherence maximally at 94 days between refills, and the measure was most sensitive for non-adherence at <90 days. Reassessment of the relation between pharmacy refill data and EDM would be warranted when pharmacy refill data is collected as soon as feasible from sources with complete data capture.


Assuntos
Fármacos Anti-HIV/uso terapêutico , Monitoramento de Medicamentos/instrumentação , Prescrições de Medicamentos/estatística & dados numéricos , Infecções por HIV/tratamento farmacológico , Adesão à Medicação/estatística & dados numéricos , Cooperação do Paciente/estatística & dados numéricos , Adulto , Idoso , Estudos de Coortes , Feminino , Infecções por HIV/virologia , Humanos , Masculino , Microcomputadores , Pessoa de Meia-Idade , Farmácias , Estudos Retrospectivos , Estatísticas não Paramétricas
5.
J Consult Clin Psychol ; 75(5): 775-84, 2007 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17907859

RESUMO

A previous randomized trial with 224 alcohol and/or cocaine addicts who had completed an initial phase of treatment indicated that 12 weeks of telephone-based continuing care yielded higher abstinence rates over 24 months than did group counseling continuing care. The current study examined mediators of this treatment effect. Results suggested that self-help involvement during treatment and self-efficacy and commitment to abstinence 3 months after treatment mediated subsequent abstinence outcomes. These analyses controlled for substance use prior to the assessment of mediators. Conversely, there was no evidence that self-help beliefs or social support mediated the treatment effect. These results are consistent with a model in which treatment effects are first accounted for by changes in behavior, followed by changes in self-efficacy and in commitment to abstinence.


Assuntos
Assistência ao Convalescente/métodos , Alcoolismo/reabilitação , Transtornos Relacionados ao Uso de Cocaína/reabilitação , Telefone , Adulto , Alcoolismo/psicologia , Assistência Ambulatorial , Transtornos Relacionados ao Uso de Cocaína/psicologia , Terapia Cognitivo-Comportamental , Terapia Combinada , Aconselhamento , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Psicoterapia de Grupo , Prevenção Secundária , Autocuidado , Autoeficácia , Apoio Social , Temperança/psicologia
6.
Gen Hosp Psychiatry ; 25(2): 115-23, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12676425

RESUMO

Recognition of gaps between evidence gained from mental health research and clinical practice in the community together with changes in treatment patterns and patient/provider preferences for care have led to interest in enhancements in the designs and analyses of clinical and community trials of mental health interventions. Gaps between clinical trials and community care include differences in populations and treatment strategies. To bridge these gaps, we propose enhancing the simple randomized trial with several different designs with the immediate aims of improving patient recruitment and adherence in psychiatric intervention studies thus bringing study designs more in line with clinical practice. The goals are to estimate treatment efficacy and effectiveness so that both internal and external validity are optimized. In this discussion, we address design and analytic issues with respect to a number of enhancements of the randomized trial design, including partial patient-provider preference designs, randomized encouragement and consent designs, fixed adaptive design, and random between- and within-patient adaptive designs. Each has advantages and disadvantages depending on the effect under investigation. Some of these enhancements, such as the fixed adaptive design, have begun to be implemented in effectiveness trials in mental health services research, but all are worthy of more attention.


Assuntos
Depressão/terapia , Medicina Baseada em Evidências , Qualidade da Assistência à Saúde , Ensaios Clínicos Controlados Aleatórios como Assunto , Serviços de Saúde/normas , Humanos
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