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1.
Eur J Cancer Care (Engl) ; 27(2): e12758, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28892208

RESUMO

This study aimed to ascertain the systemic barriers encountered by oncology health professionals (HPs) working with patients from ethnic minorities to guide the development of a communication skills training programme. Twelve medical and five radiation oncologists and 21 oncology nurses were invited to participate in this qualitative study. Participants were interviewed individually or in a focus group about their experiences working with people from minority backgrounds. All interviews were transcribed verbatim and analysed thematically. HPs encountered language and communication barriers in their interactions with patients and their families, which were perceived to impact negatively on the quality and amount of information and support provided. There was a shortage of, and poor processes for engaging, interpreters and some HPs were concerned about the accuracy of interpretation. HPs expressed a need for training in cultural awareness and communication skills with a preference for face-to-face delivery. A lack of funding, a culture of "learning on the job", and time constraints were systemic barriers to training. Oncologists and oncology nurses encounter complex challenges in clinical interactions with minority patients and their families, including difficulties working with interpreters. Formal training programmes targeted to the development of culturally competent communication skills are required.


Assuntos
Atitude do Pessoal de Saúde , Barreiras de Comunicação , Competência Cultural , Oncologistas/psicologia , Enfermagem Oncológica , Adulto , Etnicidade , Feminino , Acessibilidade aos Serviços de Saúde , Humanos , Masculino , Pessoa de Meia-Idade , Grupos Minoritários , Neoplasias/terapia , Serviço Hospitalar de Oncologia/normas , Relações Profissional-Paciente , Pesquisa Qualitativa , Tradução
2.
Eur J Hum Genet ; 24(11): 1517-1523, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27329735

RESUMO

Selection of women for treatment-focused genetic testing (TFGT) following a new diagnosis of breast cancer is changing. Increasingly a patient's age and tumour characteristics rather than only their family history are driving access to TFGT, but little is known about the impact of receiving carrier-positive results in individuals with no family history of cancer. This study assesses the role of knowledge of a family history of cancer on psychosocial adjustment to TFGT in both women with and without mutation carrier-positive results. In-depth semistructured interviews were conducted with 20 women who had undergone TFGT, and who had been purposively sampled to represent women both family history and carrier status, and subjected to a rigorous qualitative analysis. It was found that mutation carriers without a family history reported difficulties in making surgical decisions quickly, while in carriers with a family history, a decision regarding surgery, electing for bilateral mastectomy (BM), had often already been made before receipt of their result. Long-term adjustment to a mutation-positive result was hindered by a sense of isolation not only by those without a family history but also those with a family history who lacked an affected relative with whom they could identify. Women with a family history who had no mutation identified and who had not elected BM reported a lack of closure following TFGT. These findings indicate support deficits hindering adjustment to positive TFGT results for women with and without a family history, particularly in regard to immediate decision-making about risk-reducing surgery.


Assuntos
Proteína BRCA1/genética , Proteína BRCA2/genética , Neoplasias da Mama/psicologia , Testes Genéticos , Mutação , Revelação da Verdade , Adulto , Neoplasias da Mama/diagnóstico , Neoplasias da Mama/genética , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Heterozigoto , Humanos , Pessoa de Meia-Idade , Inquéritos e Questionários
3.
Psychooncology ; 22(9): 1994-2000, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23382138

RESUMO

BACKGROUND: Providing ongoing clinical care that adequately addresses patients' medical, psychosocial and information needs is challenging, particularly for patient groups at increased risk of developing life-threatening disease such as malignant melanoma. This study examined a model of clinical care developed by the High Risk Clinic (HRC) of the Sydney Melanoma Diagnostic Centre in relation to patient satisfaction. METHODS: Semi-structured telephone interviews were conducted and analyzed using the framework of Miles and Huberman, and themes were organized using the qualitative software package, QSR NVivo8. RESULTS: Twenty HRC patients participated in the study (nine men, 11 women; mean age 57.6 years, age range 34-74 years; response rate 91%). Satisfaction with clinical care at the HRC was high. Factors contributing to patient satisfaction included: rapid and regular access to physicians who were perceived by participants as experts, the development of confidence and trust in one's treating doctor, and a sense of being cared about and understood by one's healthcare team. Although one-third of the participants reported some inconveniences in attending the clinic, these were viewed as minor difficulties and not significant barriers to care. Formal psychological support was not sought or expected by participants, although many expressed long-standing melanoma-related fears and concerns. CONCLUSIONS: Accessible, expert medical attention, delivered in a patient-centered manner was integral to melanoma survivors' satisfaction with clinical management. Appropriate referrals to psychological support may further increase satisfaction with clinical care.


Assuntos
Melanoma/psicologia , Satisfação do Paciente , Neoplasias Cutâneas/psicologia , Sobreviventes/psicologia , Adulto , Idoso , Austrália , Feminino , Humanos , Masculino , Melanoma/terapia , Pessoa de Meia-Idade , Avaliação das Necessidades , Risco , Neoplasias Cutâneas/terapia , Inquéritos e Questionários
4.
J Parasitol ; 87(2): 322-9, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11318562

RESUMO

Heads of 109,597 mosquitoes collected during 1996 and 1997 from Gainesville, Florida (1996, n = 39,131; 1997, = 34,209), Bartow, Florida (1996, n = 12,000; 1997, n = 12,000), and Baton Rouge, Louisiana (1996, n = 12,257) were tested by a polymerase chain reaction and Southern hybridization-based test for the presence of third-stage larvae of the canine heartworm Dirofilaria immitis. Mosquito heads were pooled (1-200 heads) by month, locality, and species for testing. The test used was species specific for D. immitis and was capable of detecting DNA from a single larva in a pool of 200 mosquito heads. Specificity for the third larval stage was achieved by probing only mosquito heads. One or more D. immitis-infected mosquito heads were detected in each month of the year from Barrow in both 1996 and 1997. No infected mosquito heads were detected from Gainesville or Baton Rouge in December, January, February, or March. These results are in general agreement with previous sentinel dog and model prediction studies that showed heartworm transmission in the warm temperate Gulf coast region of the United States to be seasonal rather than continuous as previously believed.


Assuntos
Culicidae/parasitologia , Dirofilaria immitis/isolamento & purificação , Insetos Vetores/parasitologia , Animais , Southern Blotting , Dirofilariose/epidemiologia , Dirofilariose/transmissão , Doenças do Cão/epidemiologia , Doenças do Cão/transmissão , Cães , Ecossistema , Florida/epidemiologia , Larva , Louisiana/epidemiologia , Reação em Cadeia da Polimerase , Prevalência , Estações do Ano , Vigilância de Evento Sentinela/veterinária
5.
J Clin Microbiol ; 39(5): 2009-14, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11326037

RESUMO

The functional significance of sequence variation within the upstream regulatory region (URR) of six human papillomavirus type 16 (HPV16) cervical cancer isolates from Australia was investigated. Specific changes in transcription factor binding sites leading to increased promoter activity may explain the transforming ability of some episomal HPV16 isolates.


Assuntos
Variação Genética/genética , Proteínas Oncogênicas Virais/genética , Papillomaviridae/genética , Regiões Promotoras Genéticas/genética , Proteínas Repressoras , Neoplasias do Colo do Útero/virologia , Austrália , Feminino , Células HeLa , Humanos , Mutagênese Sítio-Dirigida , Proteínas Oncogênicas Virais/metabolismo , Papillomaviridae/isolamento & purificação , Proteínas E7 de Papillomavirus , Infecções por Papillomavirus/virologia , Reação em Cadeia da Polimerase , Infecções Tumorais por Vírus/virologia
6.
Mol Cell Probes ; 13(6): 425-30, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10657147

RESUMO

The mosquito-borne filarial worm, Dirofilaria immitis, causes heartworm disease in dogs. Detection of this parasite in its mosquito intermediate host currently involves dissection and microscopic examination for larval stages. Although this method is used commonly as a screening tool for epidemiological surveys, it lacks both sensitivity and specificity. In this study, a more efficient PCR- and probe-based diagnostic assay was developed. The target selected for this assay is a segment of the 16 S rRNA gene. The assay specifically detects as little as 10 pg of D. immitis genomic DNA, equivalent to DNA derived from one third stage larva (L(3)), but does not detect 100 ng (10 000-fold excess) of the purified DNA from several other filarial nematodes, including Dirofilaria striata, Dirofilaria tenuis, Dipetalonema reconditum, Wuchereria bancroftii, Brugia pahangi, B. malayi, Onchocerca volvulus or Loa loa. This assay also detects one L(3)of D. immitis, the minimal biological unit of infection, in a pool of 200 mosquito heads. This assay can serve as a highly specific and sensitive tool for efficiently screening the large numbers of mosquitoes to determine, with statistical validity the seasonal transmission pattern of D. immitis in a locality prior to designing a rational preventive medication program for that parasite.


Assuntos
Culicidae/parasitologia , Sondas de DNA , Dirofilaria immitis/genética , Dirofilaria immitis/isolamento & purificação , Dirofilariose/diagnóstico , Doenças do Cão/diagnóstico , Reação em Cadeia da Polimerase/métodos , Reação em Cadeia da Polimerase/veterinária , Animais , Sequência de Bases , Clonagem Molecular , Culicidae/genética , DNA de Helmintos/isolamento & purificação , Dirofilariose/genética , Doenças do Cão/genética , Cães , Genes de Helmintos , Interações Hospedeiro-Parasita/genética , Dados de Sequência Molecular , RNA de Helmintos/genética , RNA de Helmintos/isolamento & purificação , RNA Ribossômico 16S/genética , RNA Ribossômico 16S/isolamento & purificação , Sensibilidade e Especificidade
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