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1.
Urol Pract ; 11(4): 736-744, 2024 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-38899655

RESUMEN

INTRODUCTION: Previous literature suggests socioeconomic status and racial disparities impact management decisions for patients with small renal masses. We aim to build upon these findings and examine how these modalities impact patient adherence to their management plan. METHODS: This retrospective study analyzed our Kidney Tumor Program database (n = 1476) containing patients from 2000 to 2020. Socioeconomic status was estimated using 2 modalities: Area Deprivation Index and household income. Patients were then evaluated for differences in adherence, nonadherence, and loss to follow-up. Adherent patients completed all recommended appointments within 6 months of their initial follow-up. Nonadherent patients did not complete all recommended appointments within 6 months of their originally scheduled follow-up but eventually did. Patients lost to follow-up were recommended to follow up but never did. RESULTS: Patient adherence was not significantly different across sex or primary treatment method but differed with respect to race/ethnicity. Black patients were significantly more likely to be nonadherent (P = .021) and lost to follow-up (P = .008). After adjusting for race/ethnicity, Area Deprivation Index and income bracket were significantly associated with adherence and loss to follow-up. Patients with a high socioeconomic status had significantly higher rates of adherence (ADI, quartile [Q] 1 vs Q4, P = .038; income, >$120,000 vs $30,000-$59,999, P < .003) and decreased loss to follow-up (ADI, Q1 vs Q4, P = .03; income, >$120,000 vs $30,000-$59,999, P = .002). CONCLUSIONS: Our results demonstrate that Black race and low socioeconomic status are associated with decreased adherence and increased loss to follow-up. Possible strategies to target these disparities include financial assistance programming, social determinants of health screening, and nurse navigator programs.


Asunto(s)
Neoplasias Renales , Cooperación del Paciente , Clase Social , Humanos , Masculino , Estudios Retrospectivos , Neoplasias Renales/terapia , Neoplasias Renales/economía , Neoplasias Renales/etnología , Femenino , Cooperación del Paciente/estadística & datos numéricos , Cooperación del Paciente/etnología , Persona de Mediana Edad , Anciano
2.
Nurs Res ; 73(4): 328-336, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38905624

RESUMEN

BACKGROUND: Chinese American immigrants have been underrepresented in health research partly due to challenges in recruitment. OBJECTIVES: This study aims to describe recruitment and retention strategies and report adherence in a 7-day observational physical activity study of Chinese American immigrants with prior gestational diabetes during the COVID-19 pandemic. METHODS: Foreign-born Chinese women aged 18-45 years, with a gestational diabetes index pregnancy of 0.5-5 years, who were not pregnant and had no current diabetes diagnosis were recruited. They wore an accelerometer for 7 consecutive days and completed an online survey. Multiple recruitment strategies were used: (a) culturally and linguistically tailored flyers, (b) social media platforms (e.g., WeChat [a popular Chinese platform] and Facebook), (c) near-peer recruitment and snowball sampling, and (d) a study website. Retention strategies included flexible scheduling and accommodation, rapid communications, and incentives. Adherence strategies included a paper diary and/or automated daily text reminders with a daily log for device wearing, daily email reminders for the online survey, close monitoring, and timely problem-solving. RESULTS: Participants were recruited from 17 states; 108 were enrolled from August 2020 to August 2021. There were 2,479 visits to the study webpage, 194 screening entries, and 149 inquiries about the study. Their mean age was 34.3 years, and the mean length of U.S. stay was 9.2 years. Despite community outreach, participants were mainly recruited from social media (e.g., WeChat). The majority were recruited via near-peer recruitment and snowball sampling. The retention rate was 96.3%; about 99% had valid actigraphy data, and 81.7% wore the device for 7 days. The majority of devices were successfully returned, and the majority completed the online survey on time. DISCUSSION: We demonstrated the feasibility of recruiting and retaining a geographically diverse sample of Chinese American immigrants with prior gestational diabetes during the COVID-19 pandemic. Recruiting Chinese immigrants via social media (e.g., WeChat) is a viable approach. Nonetheless, more inclusive recruitment strategies are needed to ensure broad representation from diverse socioeconomic groups of immigrants.


Asunto(s)
Asiático , COVID-19 , Emigrantes e Inmigrantes , Selección de Paciente , Adolescente , Adulto , Femenino , Humanos , Persona de Mediana Edad , Embarazo , Adulto Joven , Asiático/estadística & datos numéricos , Asiático/psicología , COVID-19/etnología , COVID-19/epidemiología , Diabetes Gestacional/etnología , Emigrantes e Inmigrantes/psicología , Emigrantes e Inmigrantes/estadística & datos numéricos , Pandemias , Cooperación del Paciente/estadística & datos numéricos , Cooperación del Paciente/etnología , Medios de Comunicación Sociales/estadística & datos numéricos , Estados Unidos/epidemiología
3.
Chest ; 165(2): 437-445, 2024 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-37741324

RESUMEN

BACKGROUND: Although racial and ethnic differences in CPAP adherence for OSA are widely established, no studies have examined the influence of perceived racial discrimination on CPAP usage, to our knowledge. RESEARCH QUESTION: (1) Do Black adults with OSA report experiencing greater amounts of discrimination than non-Hispanic White adults? (2) Is discrimination associated with poorer CPAP adherence over time, independent of self-identified race? (3) Does discrimination mediate the relationship between self-identified Black race and CPAP usage? STUDY DESIGN AND METHODS: In this prospective study, Black and non-Hispanic White adults with OSA initiating CPAP were enrolled from two sleep centers and completed questionnaires including sociodemographics, perceived discrimination, daytime sleepiness, insomnia symptoms, and depressive symptoms. Perceived discrimination was measured using the Everyday Discrimination Scale (EDS). Black and White group comparisons for baseline sociodemographic variables, sleep symptoms, and perceived discrimination were performed with Student t test or χ2/Fisher exact test, as appropriate. A linear regression model was completed with self-identified Black race and EDS total score as the primary independent variables of interest and mean daily CPAP usage at 30 and 90 days serving as the dependent outcomes. This regression modeling was repeated after adjusting for psychosocial variables known to be associated with CPAP usage. EDS total score was explored as a potential mediator of the association between self-identified Black race and mean daily CPAP adherence at 30 and 90 days. RESULTS: The sample for this analysis consisted of 78 participants (31% female, 38% Black) with a mean age of 57 ± 14 years. Sixty percent of the Black adults reported they experienced racial discrimination at least a few times each year. Relative to White adults, Black adults were also more likely to indicate more than one reason for discrimination (27% vs 4%, P = .003). Adjusting for discrimination, self-identified Black race was associated with 1.4 (95% CI, -2.3 to -0.4 h; P = .006) and 1.6 (95% CI, -2.6 to -0.6 h; P = .003) fewer hours of mean daily CPAP usage at 30 and 90 days, respectively. In the fully adjusted model, a 1-unit change in the total discrimination score (more discrimination) was associated with a 0.08-h (95% CI, 0.01-0.15 h; P = .029) and 0.08-h (95% CI, 0.01-0.16 h; P = .045) change in mean daily CPAP usage at 30 and 90 days, respectively. INTERPRETATION: Adults with OSA who encountered racial discrimination experienced greater decrement in CPAP usage than those who did not experience racial discrimination.


Asunto(s)
Negro o Afroamericano , Presión de las Vías Aéreas Positiva Contínua , Cooperación del Paciente , Racismo , Apnea Obstructiva del Sueño , Población Blanca , Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Presión de las Vías Aéreas Positiva Contínua/psicología , Cooperación del Paciente/etnología , Cooperación del Paciente/psicología , Estudios Prospectivos , Sueño , Apnea Obstructiva del Sueño/etnología , Apnea Obstructiva del Sueño/terapia , Trastornos del Inicio y del Mantenimiento del Sueño/etnología , Trastornos del Inicio y del Mantenimiento del Sueño/terapia , Población Blanca/psicología , Racismo/etnología , Racismo/psicología , Negro o Afroamericano/psicología
4.
Acta Biomed ; 94(S3): e2023182, 2023 08 30.
Artículo en Inglés | MEDLINE | ID: mdl-37695183

RESUMEN

BACKGROUND AND AIM: as a reaction to the COVID-19 pandemic, countries all over the world have undertaken wide-scale measures to prevent and limit the spread of the virus. Suggested preventative measures mainly included "lockdown", social distancing, wearing facemasks, and vaccinations. The success of these measures was widely dependent on the cooperation of citizens. However, people reacted differently to the several types of restrictions and recommendations. Even if the majority followed the rules, others ignored them. This study aims to investigate the reasons for the compliance or violation of the rules developed to fight against the COVID-19 pandemic in Italy. METHODS: to answer the research question, the analysis of two different surveys conducted on a representative sample of Italians (N=2000) were conducted and analysed through descriptive statistics. RESULTS: the data collection agreed with published literature. Compliance with rules during emergencies followed diligence and altruistic patterns. Fear of sanctions did not seem to work in relation to rules compliance during emergency situations. The lack of clarity of regulations in terms of complexity or constant changes led to non-compliance even intervening as a neutralization technique. CONCLUSIONS: government's fear-based interventions did not seem to work since Italians tended to adhere to the rules primarily out of respect for legitimate authority. Future research should focus more on the topic of trust in institutions in emergency situations with the aim of highlighting the key points for successful governance, also in terms of rules compliance.


Asunto(s)
COVID-19 , Control de Enfermedades Transmisibles , Pueblo Europeo , Pandemias , Cooperación del Paciente , Humanos , COVID-19/etnología , COVID-19/prevención & control , COVID-19/psicología , Italia/epidemiología , Pandemias/prevención & control , Cooperación del Paciente/etnología , Cooperación del Paciente/psicología , Pueblo Europeo/psicología , Actitud Frente a la Salud/etnología , Control de Enfermedades Transmisibles/métodos , Control de Enfermedades Transmisibles/normas
5.
J Immigr Minor Health ; 25(4): 849-853, 2023 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-37079241

RESUMEN

The objective of this study was to explore the experience of Hispanic cancer survivors participating in Active Living After Cancer (ALAC), a community-based physical activity program. We analyzed participation and satisfaction data from 250 participants who completed the program from 2017 to 2020 (55% Hispanic, 28% Black, 14% non-Hispanic White). Using a hybrid coding approach, open-text survey comments responses from Hispanic participants (n = 138) were qualitatively analyzed and key themes developed to better contextualize the quantitative results. Quantitative analysis revealed that Hispanic participants attended an average of 9.44 out of 12 sessions. There were no differences in attendance by race/ethnicity; however, Hispanic participants reported significantly higher overall satisfaction ratings than non-Hispanic White participants (4.93 vs 4.65 on a 5-point scale). Open-ended comments indicated that Hispanic ALAC participants experience collective efficacy, self-efficacy, and self-regulation, through observational learning enabled by program facilitation. The ALAC program is highly acceptable and relevant to Hispanic cancer survivors and will inform the continued expansion of other community-based survivorship programs for Hispanic communities throughout Texas.


Asunto(s)
Supervivientes de Cáncer , Servicios de Salud Comunitaria , Ejercicio Físico , Neoplasias , Humanos , Negro o Afroamericano/psicología , Negro o Afroamericano/estadística & datos numéricos , Supervivientes de Cáncer/psicología , Supervivientes de Cáncer/estadística & datos numéricos , Etnicidad , Ejercicio Físico/psicología , Ejercicio Físico/estadística & datos numéricos , Hispánicos o Latinos/psicología , Hispánicos o Latinos/estadística & datos numéricos , Neoplasias/epidemiología , Neoplasias/etnología , Neoplasias/rehabilitación , Neoplasias/terapia , Cooperación del Paciente/etnología , Cooperación del Paciente/psicología , Cooperación del Paciente/estadística & datos numéricos , Satisfacción del Paciente/etnología , Satisfacción del Paciente/estadística & datos numéricos , Encuestas y Cuestionarios , Blanco/psicología , Blanco/estadística & datos numéricos , Servicios de Salud Comunitaria/estadística & datos numéricos
6.
Behav Sleep Med ; 21(3): 242-253, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-35583497

RESUMEN

RATIONALE: Despite having a higher prevalence and severity of obstructive sleep apnea (OSA), African Americans have lower adherence to continuous positive airway pressure (CPAP) compared to other groups. Information regarding challenges faced by African Americans prescribed CPAP are lacking. OBJECTIVES: To determine the barriers and facilitators to optimal management of OSA with CPAP among African Americans and to understand the role bed partners may play. METHODS: We conducted semi-structured in-depth interviews via video conferencing with African American patients of an urban safety-net health care system with OSA prescribed CPAP and their bed partners. Recruitment continued until theoretical saturation was achieved. Verbatim transcripts were analyzed using the principles of thematic analysis. RESULTS: 15 patients (12 women) diagnosed with OSA and prescribed CPAP a mean 2.6 years prior along with 15 bed partners (3 women) were individually interviewed. Four themes emerged regarding impediments to CPAP use: 1) inadequate education and support, 2) CPAP maintenance and hygiene, 3) inconvenient design of CPAP interfaces, and 4) impediment to intimacy. Four themes emerged as facilitators to CPAP use: 1) provider and technical support, 2) properly fitted CPAP masks, 3) active support from partner and family, and 4) experiencing positive results from CPAP. CONCLUSIONS: African American patients with OSA and their bed partners identified several unique barriers and facilitators to CPAP use. Active involvement by bed partners was considered by both patients and partners as helpful in improving CPAP adherence. Interventions to improve OSA outcomes in this population should focus on patients and their bed partners.


Asunto(s)
Negro o Afroamericano , Presión de las Vías Aéreas Positiva Contínua , Cooperación del Paciente , Parejas Sexuales , Apnea Obstructiva del Sueño , Femenino , Humanos , Presión de las Vías Aéreas Positiva Contínua/métodos , Cooperación del Paciente/etnología , Apnea Obstructiva del Sueño/terapia , Apnea Obstructiva del Sueño/diagnóstico , Apoyo Social
7.
J Racial Ethn Health Disparities ; 10(4): 1910-1917, 2023 08.
Artículo en Inglés | MEDLINE | ID: mdl-35876984

RESUMEN

OBJECTIVES: The purpose of this pilot study was to explore the effect of HIV-related stigma and everyday major experiences of discrimination on medication and clinic visit adherence among older African Americans living with HIV in Ohio. METHODS: We collected data from 53 individuals who were living with HIV in Ohio, ≥ 50 years of age, and who identified as Black or African American. We conducted logistic regression models to examine the impact of HIV-related stigma and experiences of discrimination on medication and visit adherence. Each model controlled for age, time since diagnosis, and sexual orientation. RESULTS: The average age was 53.6 ± 2.1 years and 94.3% were men. Almost half (49.1%) of the participants reported poor medication adherence and almost a third (31.4%) reported poor visit adherence. HIV-related stigma (adjusted odds ratio (aOR) = 1.39; 95% confidence interval (CI) = 1.02-1.89) and major experiences of discrimination (aOR = 1.70; 95% CI = 1.11-2.60) were associated with a greater odds of poor medication adherence. Additionally, major experiences of discrimination were associated with a threefold increase in the odds of poor visit adherence (aOR = 3.24; 95% CI = 1.38-7.64). CONCLUSIONS: HIV-related stigma and major experiences of discrimination impede optimal medication and HIV clinic visit adherence for older African Americans living with HIV. To reduce the impact of stigma and discrimination on HIV care engagement, our first step must be in understanding how intersecting forms of stigma and discrimination impact engagement among older African Americans living with HIV.


Asunto(s)
Atención Ambulatoria , Negro o Afroamericano , Infecciones por VIH , Cooperación del Paciente , Discriminación Social , Estigma Social , Femenino , Humanos , Masculino , Persona de Mediana Edad , Negro o Afroamericano/psicología , Negro o Afroamericano/estadística & datos numéricos , Población Negra/psicología , Población Negra/estadística & datos numéricos , Infecciones por VIH/epidemiología , Infecciones por VIH/etnología , Infecciones por VIH/psicología , Infecciones por VIH/terapia , Cumplimiento de la Medicación/etnología , Cumplimiento de la Medicación/psicología , Cumplimiento de la Medicación/estadística & datos numéricos , Proyectos Piloto , Ohio/epidemiología , Cooperación del Paciente/etnología , Cooperación del Paciente/psicología , Cooperación del Paciente/estadística & datos numéricos , Atención Ambulatoria/psicología , Atención Ambulatoria/estadística & datos numéricos , Racismo/etnología , Racismo/psicología , Racismo/estadística & datos numéricos , Discriminación Social/etnología , Discriminación Social/psicología , Discriminación Social/estadística & datos numéricos
8.
Artículo en Inglés | MEDLINE | ID: mdl-38248484

RESUMEN

Hispanic and American Indian (AI) women experience lower breast cancer incidence than non-Hispanic White (NHW) women, but later-stage diagnoses and lower survival rates, suggesting issues with screening and healthcare access. Between 1999-2015, NHW breast cancer incidence decreased by 10% but increased by 8% for AI women. This study used 2016 and 2018 Behavioral Risk Factor Surveillance System data for Arizona and New Mexico to explore mammography screening. Analyses included Hispanic, AI, and NHW women aged ≥40 years (n = 12,830) to calculate age-specific compliance by race/ethnicity, logistic regression, and adjusted and sample-weighted evaluated associations between compliance and socio-economic covariates. In total, 75.1% of Hispanic women aged 50-74 reported mammography in the past two years (United States Preventive Services Task Force compliant) compared to 73.9% of NHW and 71.0% of AI women. Women who reported doctor visits in the past 12 months were likelier to comply than those without (AOR = 4.2 for Hispanic, 2.9 for AI, and 3.2 for NHW women). Reporting access to a personal doctor was related to compliance, except for AI women. While screening compliance was over 74%, visiting a healthcare provider in the past 12 months was essential. AI women reported issues that suggest unique challenges when deciding on mammography.


Asunto(s)
Indio Americano o Nativo de Alaska , Neoplasias de la Mama , Hispánicos o Latinos , Mamografía , Cooperación del Paciente , Femenino , Humanos , Indio Americano o Nativo de Alaska/estadística & datos numéricos , Arizona/epidemiología , Neoplasias de la Mama/diagnóstico por imagen , Neoplasias de la Mama/epidemiología , Neoplasias de la Mama/etnología , Mamografía/estadística & datos numéricos , New Mexico/epidemiología , Hispánicos o Latinos/estadística & datos numéricos , Cooperación del Paciente/etnología , Cooperación del Paciente/estadística & datos numéricos
9.
Chest ; 161(1): 266-275, 2022 01.
Artículo en Inglés | MEDLINE | ID: mdl-34390706

RESUMEN

BACKGROUND: In 2013, the United States Preventive Services Taskforce instituted recommendations for annual lung cancer screening (LCS) with low-dose chest CT imaging for high-risk individuals. LCS reduces lung cancer mortality, with greater reduction observed in Black participants in clinical trials. Although racial disparities in lung cancer mortality have been well documented, less is known about disparities in LCS participation and adherence to follow-up in clinical practice. RESEARCH QUESTION: What is the association between race and adherence to LCS follow-up? STUDY DESIGN AND METHODS: A systematic review was conducted through a search of published studies in MEDLINE, PubMed, EMBASE, Web of Science, and Cumulative Index to Nursing and Allied Health Literature Database from database inception through October 2020. We included studies that examined rates of adherence to LCS follow-up and compared rates by race. Studies were pooled using random-effects meta-analysis. RESULTS: We screened 18,300 titles and abstracts, and 229 studies were selected for full-text review. Nine studies met inclusion criteria; seven were included in the meta-analysis. Median adherent follow-up rate was 37% (range, 16%-82%). Notable differences among the studies included the proportion of the Black population (range, 4%-47%) and the structure of the LCS programs. The meta-analyses showed lower adherence to LCS follow-up in the Black population (OR, 0.67; 95% CI, 0.55-0.80). This disparity persisted across all malignancy risk levels determined by initial screening results. INTERPRETATION: Lower adherence to LCS follow-up in Black compared with White patients occurs despite the higher potential lung cancer mortality benefit. Literature specifically addressing race-related barriers to LCS adherence remains limited. To ensure equity in LCS benefits, greater outreach to eligible Black patients should be implemented through increased physician education and use of screening program coordinators to focus on this patient population. TRIAL REGISTRY: PROSPERO; No.: CRD42020214213; URL: http://www.crd.york.ac.uk/PROSPERO.


Asunto(s)
Negro o Afroamericano , Disparidades en Atención de Salud/etnología , Neoplasias Pulmonares/diagnóstico , Cooperación del Paciente/etnología , Población Blanca , Cuidados Posteriores , Detección Precoz del Cáncer , Humanos
10.
Ophthalmic Epidemiol ; 29(6): 613-620, 2022 12.
Artículo en Inglés | MEDLINE | ID: mdl-34895007

RESUMEN

PURPOSE: To explore individual and community factors associated with adherence to physician recommended urgent eye visits via a tele-triage system during the COVID-19 pandemic. METHOD: We retrospectively reviewed acute visit requests and medical exam data between April 6, 2020 and June 6, 2020. Patient demographics and adherence to visit were examined. Census tract level community characteristics from the U.S. Census Bureau and zip code level COVID-19 related death data from the Cook County Medical Examiner's Office were appended to each geocoded patient address. Descriptive statistics, t-tests, and logistic regression analyses were performed to explore the effects of individual and community variables on adherence to visit. RESULTS: Of 229 patients recommended an urgent visit, 216 had matching criteria on chart review, and 192 (88.9%) adhered to their visit. No difference in adherence was found based on individual characteristics including: age (p = .24), gender (p = .94), race (p = .56), insurance (p = .28), nor new versus established patient status (p = .20). However, individuals who did not adhere were more likely to reside in neighborhoods with a greater proportion of Blacks (59.4% vs. 33.4%; p = .03), greater unemployment rates (17.5% vs. 10.7%; p < .01), and greater cumulative deaths from COVID-19 (56 vs. 31; p = .01). Unemployment rate continued to be statistically significant after controlling for race and cumulative deaths from COVID-19 (p = .04). CONCLUSION: We found that as community unemployment rate increases, adherence to urgent eye visits decreases, after controlling for relevant neighborhood characteristics. Unemployment rates were highest in predominantly Black neighborhoods early in the pandemic, which may have contributed to existing racial disparities in eye care.


Asunto(s)
COVID-19 , Ojo , Visita a Consultorio Médico , Oftalmología , Cooperación del Paciente , Humanos , COVID-19/epidemiología , Pandemias , Características de la Residencia/estadística & datos numéricos , Estudios Retrospectivos , Cooperación del Paciente/etnología , Cooperación del Paciente/estadística & datos numéricos , Triaje/métodos , Telemedicina/métodos , Disparidades en Atención de Salud/economía , Disparidades en Atención de Salud/etnología , Disparidades en Atención de Salud/estadística & datos numéricos , Visita a Consultorio Médico/economía , Visita a Consultorio Médico/estadística & datos numéricos , Oftalmología/estadística & datos numéricos , Desempleo/estadística & datos numéricos , Examen Físico/economía , Examen Físico/estadística & datos numéricos
11.
PLoS One ; 16(8): e0255353, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34383803

RESUMEN

More physical activity and less sedentary behavior is beneficial for children and adolescents. Worldwide, gender differences are >8% favorable for men and the Latin-American region presents an even higher level of insufficient physical activity among women, with a lack of information in young population. Thus, the aim of the current study was to describe the gender differences in physical activity and recreational sedentary behavior in children and adolescents from Latin-American countries. The targeted age range was 5 to 17 years and included 219,803 participants (106,698 boys and 113,105 girls) from 33 out of 47 Latin-American countries identified. Physical activity guidelines from the World Health Organization (≥60 minutes of moderate-to-vigorous physical activity seven days of the week) and <3 hours recreational sedentary behavior daily were the references. In general, boys showed a higher prevalence of meeting physical activity guidelines in comparison with girls. A higher proportion of girls met the <3 hours recreational sedentary behavior cut-point in only ten countries. Thirty percent of the identified countries had no available data. The majority had data from the Global School-based Student Health Survey with data principally on adolescents and only 11/33 countries reported data in the last 5-year period. In conclusion, gender differences in the compliance with physical activity guidelines and the <3 hours recreational sedentary behavior cut-point are evident among children and adolescents from Latin-American countries, with boys being more active than girls.


Asunto(s)
Ejercicio Físico/fisiología , Cooperación del Paciente/estadística & datos numéricos , Conducta Sedentaria/etnología , Adolescente , Niño , Estudios Transversales , Femenino , Guías como Asunto , Encuestas Epidemiológicas , Humanos , América Latina , Masculino , Cooperación del Paciente/etnología , Caracteres Sexuales
12.
Am Surg ; 87(10): 1545-1550, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34130523

RESUMEN

BACKGROUND: Social determinants of health challenge in at-risk patients seen in safety net facilities. STUDY DESIGN: We performed a retrospective review of surgical oncology specialty clinic referrals at a safety net institution evaluating referral compliance and times to first appointment and initiation of definitive treatment. Main outcomes measured included completion of initial visit, initiation of definitive treatment, time from referral to first appointment, and time from first appointment to initiation of definitive treatment. RESULTS: Of 189 new referrals, English was not spoken by 52.4% and 69.4% were Hispanic. Patients presented without insurance in 39.2% of cases. Electronic patient portal was accessed by 31.6% of patients. Of all new referrals, 55.0% arrived for initial consultation and 53.4% initiated definitive treatment. Malignant diagnosis (P < .0001) and lack of insurance (P = .01) were associated with completing initial consultation. Initiation of definitive treatment was associated with not speaking English (P = .03), malignant diagnosis (P < .0001), and lack of insurance (P = .03). Times to first appointment and initiation of definitive treatment were not significantly affected by race/ethnicity, language, insurance, treatment recommended, or electronic patient portal access. CONCLUSION: Access to surgical oncology care for at-risk patients at a safety net facility is not adversely affected by lack of insurance, primary spoken language, or race/ethnicity. However, a significant proportion of all patients fail to complete the initial consultation and definitive treatment. Lessons learned from safety net facilities may help to inform disparities in health care found elsewhere.


Asunto(s)
Accesibilidad a los Servicios de Salud , Cooperación del Paciente/estadística & datos numéricos , Proveedores de Redes de Seguridad , Oncología Quirúrgica , Adulto , California , Femenino , Humanos , Masculino , Persona de Mediana Edad , Cooperación del Paciente/etnología , Derivación y Consulta , Estudios Retrospectivos , Determinantes Sociales de la Salud
13.
J Racial Ethn Health Disparities ; 8(3): 559-565, 2021 06.
Artículo en Inglés | MEDLINE | ID: mdl-32643126

RESUMEN

INTRODUCTION: Disparities observed in colorectal cancer (CRC) incidence and mortality among blacks and Hispanics compared with whites may be in part due to lower screening rates. The New York City (NYC) Department of Health and Mental Hygiene (DOHMH) has implemented a patient navigator (PN) program at NYC hospitals serving lower-income patients to promote high adherence by patients referred for screening colonoscopy. A prior study showed this PN program increased adherence at 3 public hospitals. The aim of this study was to determine the feasibility of expanding the PN program to 10 hospital sites by assessing the impact of the PN program on adherence to screening colonoscopy in a large, urban, lower-income population. METHODS: Data were collected from 2007 through the first quarter of 2012 from PN sites. One site also contributed data from the pilot phase of the project, from 2005 to 2006. Adherence to scheduled screening colonoscopy among those ≥ 50 years was assessed among 10 hospital sites in NYC participating in the colonoscopy PN program. RESULTS: Among the 37,077 asymptomatic adults ≥ 50 years who were scheduled for a screening colonoscopy from 2005 to the first quarter of 2012, 84.2% (83.2% of black, 84.9% of Hispanic, and 87.5% of white adults) were adherent to scheduled colonoscopy. CONCLUSIONS: Expansion of PN programs to navigate all patients referred for a colonoscopy was feasible in a large, urban setting. This can be implemented resulting in high overall adherence rates to screening colonoscopies. The program likely did not result in large ethnic disparities.


Asunto(s)
Colonoscopía/estadística & datos numéricos , Diversidad Cultural , Detección Precoz del Cáncer/estadística & datos numéricos , Cooperación del Paciente/etnología , Navegación de Pacientes/organización & administración , Población Urbana/estadística & datos numéricos , Anciano , Neoplasias Colorrectales/diagnóstico , Neoplasias Colorrectales/etnología , Estudios de Factibilidad , Femenino , Disparidades en el Estado de Salud , Humanos , Masculino , Persona de Mediana Edad , Ciudad de Nueva York/epidemiología , Cooperación del Paciente/estadística & datos numéricos , Pobreza , Evaluación de Programas y Proyectos de Salud
14.
AIDS Care ; 33(1): 54-62, 2021 01.
Artículo en Inglés | MEDLINE | ID: mdl-31969007

RESUMEN

Limited health literacy may contribute to racial disparities in retention in HIV care. The purpose of this study was to evaluate the effects of health literacy and patient and social-level factors on retention in care among African Americans living with HIV. This study included 699 participants recruited from outpatient HIV clinics and retention in care was defined as visit adherence. Multivariable logistic regression models were used to assess predictors of visit adherence among persons with 100% visit adherence compared to less than 100% visit adherence. Controlling for demographic factors, the odds of 100% visit adherence was greater among non-African Americans compared to African Americans. In models that included health literacy, race was no longer significant and health literacy was a significant predictor of 100% visit adherence. Among participants with less than 100% visit adherence, health literacy was not a significant predictor of visit adherence; however, age, marital status, and patient attitudes towards the health care provider were significant predictors. Findings suggest that health literacy may mediate the relationship between race and visit adherence. Future studies should further examine these relationships and develop interventions that target modifiable factors, with a goal of improving health equity and minimizing disparities.


Asunto(s)
Negro o Afroamericano/estadística & datos numéricos , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/psicología , Alfabetización en Salud , Disparidades en Atención de Salud/estadística & datos numéricos , Cooperación del Paciente/estadística & datos numéricos , Retención en el Cuidado/estadística & datos numéricos , Adulto , Femenino , Infecciones por VIH/etnología , Conocimientos, Actitudes y Práctica en Salud , Humanos , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Cooperación del Paciente/etnología
15.
Australas Psychiatry ; 29(3): 266-271, 2021 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-32910691

RESUMEN

OBJECTIVE: Obesity is associated with co-morbid mental illness. The Canberra Obesity Management Service (OMS) supports adults with severe obesity who have the psychosocial capacity to engage. This study will determine whether mental illness is a predictor of OMS attendance and anthropometric changes. METHOD: A retrospective audit was performed from July 2016 to June 2017. Baseline characteristics, attendance and anthropometrics were stratified according to the presence of mental illness. Outcomes included weight stabilisation and clinically significant weight loss. Descriptive analyses were performed. RESULTS: Mental illness was present in 60/162 patients (37%). Attendance was similar for those with and without mental illness. Patients with mental illness had twice as many co-morbidities (p = .001). Depressive disorders were most common (n = 28, 47%). Anxiety, schizophrenia spectrum and other psychotic disorders, and trauma- and stressor-related disorders also featured. Weight stabilisation was achieved by 25 patients (66%) with mental illness and 25 (35%) without. Clinically significant weight loss was observed in 10 patients (26%) with and 26 (40%) without mental illness. CONCLUSION: The presence of mental illness did not impact OMS attendance or weight stabilisation. The higher rate of co-morbidities in those with mental illness highlights the challenges faced by this vulnerable population.


Asunto(s)
Trastornos Mentales/psicología , Manejo de la Obesidad/estadística & datos numéricos , Obesidad Mórbida/psicología , Cooperación del Paciente/psicología , Adulto , Australia/epidemiología , Comorbilidad , Depresión/epidemiología , Femenino , Humanos , Masculino , Trastornos Mentales/epidemiología , Persona de Mediana Edad , Obesidad Mórbida/epidemiología , Cooperación del Paciente/etnología , Prevalencia , Estudios Retrospectivos , Esquizofrenia/epidemiología , Psicología del Esquizofrénico
16.
Am Surg ; 87(5): 818-824, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-33231485

RESUMEN

Financial and educational barriers significantly impact low socioeconomic status racial and ethnic minority groups in their pursuit of health care, though less is known about the interplay of these factors in the pursuit of surgical care. This study was designed to uncover the challenges to patient understanding and compliance with pre- and postsurgical clinical advice in low-income urban environments. The data for this study were collected in spoken survey with eighty patients in 9 surgery clinics at Temple University Hospital in Philadelphia. Survey responses were coded into various groups until categories emerged. Relationships among categories were identified to generate themes and subthemes. Key facilitators of patient understanding and compliance were physician likeability and communication. Eighty (100%) patients reported that the physician always treated them with respect, which was important in their interpretation of their experience with the physician. Eighteen (23%) patients identified a language other than English as their primary language and 57 (71%) patients completed high school or less schooling, which likely influenced their communication with the physician. Eighty (100%) patients expressed that the physician always explained things in a way they could understand, focusing on clarity and thoroughness. Challenges to patient understanding and compliance were finances and social resources. Patients noted difficulty paying for medical care and a lack of support at home. Agency could facilitate use of surgical care while a lack thereof could challenge motivation. Ultimately, these themes showed how patients in this environment interact with surgical care.


Asunto(s)
Hospitales de Enseñanza , Hospitales Urbanos , Cooperación del Paciente , Atención Perioperativa , Pobreza , Salud Urbana , Barreras de Comunicación , Comprensión , Etnicidad , Femenino , Encuestas de Atención de la Salud , Alfabetización en Salud , Humanos , Lenguaje , Masculino , Grupos Minoritarios , Motivación , Cooperación del Paciente/etnología , Cooperación del Paciente/psicología , Philadelphia , Relaciones Médico-Paciente , Autoeficacia , Clase Social , Medio Social , Apoyo Social , Procedimientos Quirúrgicos Operativos
17.
Isr J Health Policy Res ; 9(1): 71, 2020 11 30.
Artículo en Inglés | MEDLINE | ID: mdl-33256830

RESUMEN

BACKGROUND: Anemia is common during pregnancy and the puerperium. The association of ethnicity as well as other characteristics with anemia and compliance with healthcare recommendations has not been studied sufficiently and needs to be explored in order to implement a targeted health policy. We examined the association between ethnicity and the risk for prenatal and puerperium anemia and the compliance with healthcare recommendations. This effort aims to guide reforms in policies and practices that will assist in decreasing anemia prevalence in Israel. METHODS: This study was a secondary analysis of a prospective cohort study database including 1558 women who delivered vaginally at Emek Medical Center. Anemia was assessed before delivery by obtaining a complete blood count (CBC). After delivery, CBCs were taken in cases of postpartum hemorrhage, symptoms consistent with anemia, prenatal anemia or other clinical indications. The study population was divided according to their ethnicity (Jews and Arabs). The primary outcomes were anemia before delivery, anemia in the immediate postpartum and 6 weeks postpartum, and compliance with healthcare recommendations, which was defined as the rate of women who performed a routine CBC test 6-weeks-postpartum. RESULTS: The rates of anemia before delivery and in the puerperium period were similar between Jews and Arabs (before delivery: 88 (11%) versus 98 (14%); 6 weeks postpartum: 55 (21%) vs 68 (28%), respectively;p > 0.05). Iron supplementation was high in both groups during pregnancy (~ 90%) and lower during the postpartum for Jews compared to Arabs (72% vs 83%,respectively; P < .0001). Only one third of the patients performed a CBC 6-weeks-postpartum regardless of ethnicity. CONCLUSION: Overall compliance with health recommendation was high during pregnancy but low postpartum and was reflected in anemia persistence regardless of ethnicity. Because of the adverse long term impact of anemia on patient's health, new policies need to be developed to improve patient's compliance postpartum. A possible strategy is to combine the follow-up of the mother with the one of the newborn in the family health stations (Tipat Halav) and the community clinics similarly to the close follow-up during pregnancy. Additional methods may include active summoning for CBC test and assuring iron supplement consumption.


Asunto(s)
Anemia/epidemiología , Política de Salud , Compuestos de Hierro/administración & dosificación , Complicaciones Hematológicas del Embarazo/epidemiología , Adulto , Anemia/etnología , Árabes/estadística & datos numéricos , Estudios de Cohortes , Bases de Datos Factuales , Femenino , Humanos , Israel , Judíos/estadística & datos numéricos , Cooperación del Paciente/etnología , Cooperación del Paciente/estadística & datos numéricos , Periodo Posparto , Embarazo , Complicaciones Hematológicas del Embarazo/etnología , Estudios Prospectivos , Adulto Joven
18.
PLoS One ; 15(8): e0236775, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32756585

RESUMEN

BACKGROUND: Options to increase the ease of testing for SARS-CoV-2 infection and immune response are needed. Self-collection of diagnostic specimens at home offers an avenue to allow people to test for SARS-CoV-2 infection or immune response without traveling to a clinic or laboratory. Before this study, survey respondents indicated willingness to self-collect specimens for COVID-related tests, but hypothetical willingness can differ from post-collection acceptability after participants collect specimens. METHODS: 153 US adults were enrolled in a study of the willingness and feasibility of patients to self-collect three diagnostic specimens (saliva, oropharyngeal swab (OPS) and dried blood spot (DBS) card) while observed by a clinician through a telehealth session. After the specimens were collected, 148 participants participated in a survey about the acceptability of the collection, packing and shipping process, and their confidence in the samples collected for COVID-related laboratory testing. RESULTS: A large majority of participants (>84%) reported that collecting, packing and shipping of saliva, OPS, and DBS specimens were acceptable. Nearly nine in 10 (87%) reported being confident or very confident that the specimens they collected were sufficient for laboratory analysis.There were no differences in acceptability for any specimen type, packing and shipping, or confidence in samples, by gender, age, race/ethnicity, or educational level. CONCLUSIONS: Self-collection of specimens for SARS-CoV-2 testing, and preparing and shipping specimens for analysis, were acceptable in a diverse group of US adults. Further refinement of materials and instructions to support self-collection of saliva, OPS and DBS specimens for COVID-related testing is needed.


Asunto(s)
Betacoronavirus/aislamiento & purificación , Infecciones por Coronavirus/diagnóstico , Orofaringe/virología , Cooperación del Paciente , Neumonía Viral/diagnóstico , Saliva/virología , Manejo de Especímenes/métodos , Adulto , Betacoronavirus/genética , COVID-19 , Infecciones por Coronavirus/virología , Pruebas con Sangre Seca/métodos , Escolaridad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pandemias , Cooperación del Paciente/etnología , Neumonía Viral/virología , SARS-CoV-2 , Autocuidado , Encuestas y Cuestionarios , Telemedicina
19.
J Health Commun ; 25(7): 531-542, 2020 07 02.
Artículo en Inglés | MEDLINE | ID: mdl-32673182

RESUMEN

This study examines how family history-related factors and causal beliefs affect underserved women's cancer risk perceptions and adherence to mammography. 1,010 patients at a primary care safety net clinic at a large urban hospital completed a survey in 2015. Of the 1,010 patients, 467 women 45 years of age or older were included in this analysis. The majority of participants were African American (68%). We built multivariable linear and logistic regression models to examine the dependent variables of cancer risk perception and mammography screening adherence. According to the results, those with a family history of cancer were significantly more likely to be adherent to mammography. Perceived importance of family health history also significantly predicted their mammography screening adherence. However, cancer risk perceptions did not predict underserved women's mammography adherence. Significant interaction effects on the associations 1) between family cancer history, cancer risk perceptions, and mammography screening adherence and 2) between race, behavioral causal beliefs, and risk perceptions were found. Findings suggest that implementing different strategies across racial groups and by cancer history may be necessary to promote regular mammography screening.


Asunto(s)
Neoplasias de la Mama/genética , Detección Precoz del Cáncer/estadística & datos numéricos , Conocimientos, Actitudes y Práctica en Salud , Mamografía/estadística & datos numéricos , Anamnesis , Cooperación del Paciente/estadística & datos numéricos , Negro o Afroamericano/psicología , Negro o Afroamericano/estadística & datos numéricos , Anciano , Neoplasias de la Mama/diagnóstico , Neoplasias de la Mama/etnología , Femenino , Predisposición Genética a la Enfermedad/etnología , Encuestas de Atención de la Salud , Conocimientos, Actitudes y Práctica en Salud/etnología , Humanos , Área sin Atención Médica , Persona de Mediana Edad , Missouri , Cooperación del Paciente/etnología , Medición de Riesgo , Población Urbana/estadística & datos numéricos
20.
J Pain Symptom Manage ; 60(2): e90-e92, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32360238

RESUMEN

The coronavirus disease 2019 (COVID-19) pandemic presents unique challenges to Asian countries like Singapore with a predominantly Confucian culture. Palliative care providers play an important role in supporting their patients and family members in these difficult times.


Asunto(s)
Infecciones por Coronavirus/etnología , Infecciones por Coronavirus/psicología , Neumonía Viral/etnología , Neumonía Viral/psicología , COVID-19 , Infecciones por Coronavirus/terapia , Asistencia Sanitaria Culturalmente Competente , Cultura , Familia/etnología , Familia/psicología , Humanos , Cuidados Paliativos/métodos , Pandemias , Cooperación del Paciente/etnología , Cooperación del Paciente/psicología , Neumonía Viral/terapia , Singapur
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