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1.
J Cancer Educ ; 38(4): 1383-1390, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-36884133

RESUMO

While the incidence of cervical cancer continues to decrease, there is a significant discrepancy in incidence rates and screening behaviors among Hispanic and non-Hispanic white patients in the USA. This project examines the relationship between Spanish health literacy and cervical cancer screening knowledge, attitudes, and practices among native Spanish-speaking patients at risk for cervical cancer at the USF BRIDGE Healthcare Clinic, a student-run free clinic in Tampa, FL. Spanish-speaking patients ≥21 years (n = 34) participated in a quality improvement project that included an assessment of Spanish health literacy and a written survey on cervical cancer knowledge. Chi-squared tests were performed to assess potential relationships between health literacy and cervical cancer knowledge, attitudes, health behaviors, and demographics. Seven participants (20.6%) scored between 0 and 14 on the SAHL-S, indicating inadequate health literacy. A significant difference in cervical cancer health knowledge was found between patients with adequate health literacy compared to patients with inadequate health literacy (p = 0.002). There is a potential association between low Spanish health literacy and subsequent poorer understanding of cervical cancer in BRIDGE patients. This implies that patients of low health literacy may have poorer comprehension of other aspects of their care beyond cervical cancer screening. Strategies are discussed to improve communication with BRIDGE patients of low Spanish health literacy that may be applicable to other patient populations.


Assuntos
Letramento em Saúde , Clínica Dirigida por Estudantes , Neoplasias do Colo do Útero , Feminino , Humanos , Neoplasias do Colo do Útero/diagnóstico , Neoplasias do Colo do Útero/prevenção & controle , Conhecimentos, Atitudes e Prática em Saúde , Detecção Precoce de Câncer
2.
South Med J ; 114(6): 361-367, 2021 06.
Artigo em Inglês | MEDLINE | ID: mdl-34075429

RESUMO

OBJECTIVE: This study describes the prevalence of negative healthcare experiences, depression, and anxiety in the Tampa Bay transgender and gender non-conforming population. METHODS: Participants completed a survey encompassing healthcare interactions and validated mental health questionnaires. RESULTS: In total, 61% of participants experienced conversion therapy and 54% have been denied care. Depression and anxiety are prevalent, with higher levels statistically associated with denial of care; 60.5% and 43% fear seeking mental health or medical care, respectively. CONCLUSIONS: Self-reported negative experiences are prevalent in this population, with a potential association with avoidance of care. Further research is necessary to clarify these potential relationships.


Assuntos
Atenção à Saúde/normas , Comportamento de Busca de Ajuda , Serviços de Saúde Mental/normas , Minorias Sexuais e de Gênero/psicologia , Adulto , Atenção à Saúde/estatística & dados numéricos , Feminino , Florida , Humanos , Masculino , Serviços de Saúde Mental/estatística & dados numéricos , Satisfação do Paciente , Psicometria/instrumentação , Psicometria/métodos , Autorrelato , Minorias Sexuais e de Gênero/estatística & dados numéricos , Inquéritos e Questionários
3.
Cureus ; 13(6): e15690, 2021 Jun 16.
Artigo em Inglês | MEDLINE | ID: mdl-34159040

RESUMO

Lynch syndrome is the most common form of hereditary colorectal cancer and is associated with an increased incidence of endometrial cancer, small bowel cancer, and other malignancies. The advent of immune checkpoint blockade, next-generation sequencing, and precision medicine molecular tumor boards have revolutionized the current treatment landscape for many cancers and allowed for more creative approaches to treating patients. In addition, tissue agnostic approvals have also served as valid treatment options for patients with otherwise untreatable cancers. In this report, we discuss the case of a 70-year-old woman with Lynch syndrome found to have retroperitoneal lymphadenopathy with p16-negative squamous cell carcinoma, diagnosed as carcinoma of unknown primary (CUP). To our knowledge, this is the first report of Lynch syndrome-associated squamous cell CUP. More research is needed on newly emerging cancer presentations in Lynch syndrome patients as they achieve longer lifespans.

4.
JCO Oncol Pract ; 16(10): e1192-e1201, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32525751

RESUMO

PURPOSE: Biobanks usually do not collect transgender and gender-diverse (TGD) demographic information, hindering research on cancer risk and biological effects related to gender-affirming interventions. METHODS: In August 2019, 172 scientists involved in biobanking research at a single institution (H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL) were invited to complete a survey measuring knowledge and attitudes about TGD health and research practices. Quantitative and qualitative analyses were performed. RESULTS: Among 47 respondents, there was high agreement (77%) regarding the importance of collecting TGD identities and histories of gender-affirming treatments with biospecimens, which was contrasted by low self-reported rates of respondents' biorepositories allowing for the entry of TGD identities (14.9%) and histories of gender-affirming interventions (8.5%). There was high interest in receiving education regarding the unique cancer health needs of TGD patients (74%), and knowledge questions yielded high percentages of "neutral" and "don't know or prefer not to answer" responses. After completing the survey, confidence in knowledge of health needs for TGD patients decreased significantly (48.9% were confident during the presurvey assessment v 36.2% in the postsurvey assessment; P < .001). Qualitative analysis of open-ended questions indicated overall support of TGD data inclusion in biobanks along with perceived barriers to inclusion of such data in biobanks. CONCLUSION: To our knowledge, this was the first study of researchers to assess knowledge, attitudes, and research practices regarding TGD patients. Overall, there was limited knowledge about TGD health and cancer needs and low rates of TGD demographic data collection but a high interest in receiving education regarding this community.


Assuntos
Atitude do Pessoal de Saúde , Bancos de Espécimes Biológicos , Conhecimentos, Atitudes e Prática em Saúde , Neoplasias , Pesquisadores/psicologia , Pessoas Transgênero , Humanos , Inquéritos e Questionários
5.
Contemp Clin Trials Commun ; 19: 100597, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32613134

RESUMO

Biobanks have the potential to be robust resource for understanding potential cancer risks associated with gender-affirming interventions. In this narrative review, we synthesized the current published literature regarding the inclusion of TGD health data in cancer biorepositories and cancer research conducted on biospecimens. Of the 6986 initial results, 153 (2.2%) assessed the biological effects of gender-affirming interventions on TGD tissues. Within that category, only one paper examined transgender tissues in relation to cancer biobanks. Strategies are offered to address the inequities in TGD tissue-based research and diversify the field of biobanking as a whole.

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