RESUMO
Importance: The pathway to kidney transplantation (KT) begins with the patient's acceptance of this surgical procedure after discussion with the nephrologist. The patients' perceptions of the disease and of KT may influence their willingness to undergo transplantation. Objective: To describe patients' experiences of kidney disease and their perceptions of KT and the nephrologists' perceptions of the patient experience. Design, Setting, and Participants: This qualitative study collected data through semistructured interviews with patients with chronic kidney disease and nephrologists in the Bretagne, Île-de-France and Normandie regions, France. Researchers involved in the study in each region purposely selected 99 patients with chronic kidney disease who initiated dialysis in 2021, based on their age, sex, dialysis facility ownership, and also 45 nephrologists, based on their sex and years of experience. Data analysis was performed from January to October 2023. Main Outcomes and Measures: Themes were identified using inductive thematic analysis. Specific characteristics of men and women as well as the nephrologist's views for each theme were described. Results: This study included 42 men and 57 women (56 [57%] aged 60 years or older) who started dialysis in 2021 and 45 nephrologists (23 women and 22 men). Six major themes were identified: (1) burden of chronic kidney disease on patients and their families, (2) health care professional-patient relationship and other factors that modulate chronic kidney disease acceptance, (3) dialysis perceived as a restrictive treatment, (4) patients' representation of the kidney graft, (5) role of past experiences in KT perception, and (6) dualistic perception of KT. In some cases, women and nephrologists indicated that women's perceptions and experiences were different than men's; for example, the disease's psychological impact and the living donor KT refusal were mainly reported by 8 women. Conclusions and Relevance: Patients' past experience of chronic kidney disease in general and of KT in particular, as well as their relationship with their family and nephrologist, were substantial determinants of KT perception in this qualitative study. Targeted policies on these different factors might help to improve access to KT, and more research is needed to understand whether there are sex-based disparities.
Assuntos
Transplante de Rim , Pesquisa Qualitativa , Insuficiência Renal Crônica , Humanos , Masculino , Transplante de Rim/psicologia , Feminino , Pessoa de Meia-Idade , Insuficiência Renal Crônica/psicologia , Insuficiência Renal Crônica/cirurgia , Insuficiência Renal Crônica/terapia , França , Idoso , Fatores Sexuais , Adulto , Nefrologistas/psicologia , Diálise Renal/psicologiaAssuntos
Atitude do Pessoal de Saúde , Pesquisa Biomédica , Cuidadores/psicologia , Nefropatias/terapia , Nefrologistas/psicologia , Defesa do Paciente/psicologia , Relações Profissional-Família , Pesquisa Biomédica/organização & administração , Humanos , Equipe de Assistência ao Paciente , Participação do Paciente , Assistência Centrada no Paciente , Relações Médico-PacienteRESUMO
Clinical practice guidelines (CPGs) are systematically developed statements backed by scientific evidence to assist practitioners in management in clinical practice. An international cross-sectional survey was conducted by the IPNA to examine the perceptions of pediatric nephrologists on guidelines and their usage and to identify important diseases for future clinical practice guidelines (CPGs). The survey found that the majority of pediatric nephrologists find CPGs useful in clinical practice and admitted to using them most of the time. Developing CPGs is challenging and there are standards available to develop trustworthy guidelines. While evidence-based global guidelines are ideal, pediatric nephrologists expressed the desire that they address regional differences. Most respondents (89.2%) to the survey agreed that adult guidelines did not cover the pediatric perspective adequately and 71.4% opined that consensus-based pediatric guidelines can be developed when evidence for the pediatric population is lacking. The development of high-quality practice guidelines requires substantial resources and may not be feasible in resource-poor countries. Adaptation of an existing guideline has been suggested as an alternative and the ADAPTE collaboration provides a systematic approach to adapting guidelines. Several diseases where pediatric guidelines are needed as a priority including IgA and C3 glomerulopathy were identified in the survey. Implementation of guideline-based care is challenging and the survey found that lack of availability of guidelines (43%) and resources (22.8%) are important reasons for poor implementation in lower-middle and low-income countries. Perceived complexity of guidelines, physician attitudes, and lack of training also contribute to non-adherence to guidelines.
Assuntos
Atitude do Pessoal de Saúde , Nefrologistas , Pediatria , Guias de Prática Clínica como Assunto , Estudos Transversais , Humanos , Nefrologistas/psicologia , Inquéritos e QuestionáriosRESUMO
OBJECTIVES: To explore nephrologists' concerns and recommendations in counseling their advanced chronic kidney disease (CKD) patients on Ramadan fasting. METHODS: This cross-sectional study was carried out in King Khalid University Hospital, Riyadh, Saudi Arabia between January 2019 and January 2020. An electronic survey was completed by 48 nephrologists practicing in Saudi Arabia. The questionnaire focused on demographics, clinical experience, and factors to consider when advising CKD patients about fasting. Statistical analysis was performed by the Statistical Package for Social Sciences for Windows, version 21 (IBM Corp, Armonk, NY, USA). Statistics include frequency and percentages using multiple response dichotomy analysis and thematic analysis. RESULTS: Most respondents were consultant nephrologists (75%), practicing nephrology for over 10 years (68.8%). The majority of responding nephrologists (85.4%) were concerned about estimated glomerular ltration rate (eGFR), diabetes (68.8%), patient age (64.6%), use of diuretics (62.5%), body uid volume (60.4%), and blood pressure (60.4%). CONCLUSION: This research addresses nephrologists' perspectives about Ramadan fasting for patients with advanced CKD. It highlights factors they consider when advising CKD patients about fasting, which were used to suggest applications in practice. Further studies are needed to comprehend nephrologists' and CKD patients' perspectives on fasting.
Assuntos
Atitude do Pessoal de Saúde , Aconselhamento Diretivo , Jejum/efeitos adversos , Conhecimentos, Atitudes e Prática em Saúde , Islamismo , Nefrologistas/psicologia , Insuficiência Renal Crônica , Fatores Etários , Pressão Sanguínea , Líquidos Corporais , Estudos Transversais , Diabetes Mellitus , Diuréticos , Feminino , Taxa de Filtração Glomerular , Humanos , Masculino , Pessoa de Meia-Idade , Arábia Saudita , Índice de Gravidade de Doença , Inquéritos e QuestionáriosAssuntos
Betacoronavirus , Infecções por Coronavirus , Hospitais Públicos , Hospitais Urbanos , Unidades de Terapia Intensiva , Nefrologistas/psicologia , Ruído , Pandemias , Pneumonia Viral , Atitude do Pessoal de Saúde , COVID-19 , Ambiente de Instituições de Saúde , Humanos , Cidade de Nova Iorque , Quartos de Pacientes , SARS-CoV-2RESUMO
BACKGROUND: Burnout syndrome in physicians is associated with adverse patient safety events, poorer quality of care and reduced patients' satisfaction. There has been scarce information on the risk factors of burnout affecting professionals working in the renal care settings. As yet the phenomenon has not been studied in the population of Polish nephrologists therefore a nationwide cross-sectional study was established by the Polish Society of Nephrology to assess the prevalence of the syndrome. METHODS: The survey, that consisted of the abbreviated Maslach Burnout Inventory, questions about strategies for dealing with burnout symptoms and demographic data, was distributed during two main national meetings that gather nephrologists in Poland. 177 participants filled out the survey - 64% of participants were women, 88% were specialists and 12% - doctors in training. RESULTS: 52% of participants demonstrated a high level of depersonalization and almost half of the study group showed high level of emotional exhaustion. Reduced personal accomplishment was more pronounced in doctors working mostly in dialysis units compared to other nephrologists (p = 0.017). 37% of participants reported that they treat some patients as they were impersonal objects and 48% felt emotionally drained from their work. 59% of participants would like to take part in the remedy program. CONCLUSIONS: Burnout syndrome seems to be an important problem in the population of Polish nephrologists. Doctors working mostly in dialysis settings might be at increased risk of reduced personal accomplishment. The results of the survey may be useful to prepare burnout remedy program.
Assuntos
Esgotamento Profissional/epidemiologia , Nefrologistas/estatística & dados numéricos , Adulto , Idoso , Instituições de Assistência Ambulatorial , Esgotamento Profissional/psicologia , Estudos Transversais , Feminino , Unidades Hospitalares de Hemodiálise , Humanos , Masculino , Pessoa de Meia-Idade , Nefrologistas/psicologia , Admissão e Escalonamento de Pessoal , Polônia/epidemiologia , Prevalência , Diálise Renal , Sociedades Médicas , Inquéritos e Questionários , Carga de TrabalhoRESUMO
BACKGROUND AND OBJECTIVES: Hospital rounds are a traditional vehicle for patient-care delivery and experiential learning for trainees. We aimed to characterize practices and perceptions of rounds in United States nephrology training programs. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: We conducted a national survey of United States nephrology fellows and program directors. Fellows received the survey after completing the 2019 National Board of Medical Examiners Nephrology In-Training Exam. Program directors received the survey at the American Society of Nephrology's 2019 Nephrology Training Program Directors' Retreat. Surveys assessed the structure and perceptions of rounds, focusing on workload, workflow, value for patient care, and fellows' clinical skill-building. Directors were queried about their expectations for fellow prerounds and efficiency of rounds. Responses were quantified by proportions. RESULTS: Fellow and program director response rates were 73% (n=621) and 70% (n=55). Most fellows (74%) report a patient census of >15, arrive at the hospital before 7:00 am (59%), and complete progress notes after 5:00 pm (46%). Among several rounding activities, fellows most valued bedside discussions for building their clinical skills (34%), but only 30% examine all patients with the attending at the bedside. Most directors (71%) expect fellows to both examine patients and collect data before attending-rounds. A majority (78%) of directors commonly complete their documentation after 5:00 pm, and for 36%, after 8:00 pm. Like fellows, directors most value bedside discussion for development of fellows' clinical skills (44%). Lack of preparedness for the rigors of nephrology fellowship was the most-cited barrier to efficient rounds (31%). CONCLUSIONS: Hospital rounds in United States nephrology training programs are characterized by high patient volumes, early-morning starts, and late-evening clinical documentation. Fellows use a variety of prerounding styles and examine patients at the beside with their attendings at different frequencies. PODCAST: This article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2020_03_17_CJN.10190819.mp3.
Assuntos
Atitude do Pessoal de Saúde , Educação de Pós-Graduação em Medicina , Bolsas de Estudo , Conhecimentos, Atitudes e Prática em Saúde , Nefrologistas/educação , Nefrologia/educação , Visitas de Preceptoria , Competência Clínica , Currículo , Feminino , Humanos , Masculino , Nefrologistas/psicologia , Inquéritos e Questionários , Estados Unidos , Carga de TrabalhoAssuntos
Consentimento Livre e Esclarecido , Nefropatias/terapia , Nefrologistas , Nefrologia , Educação de Pacientes como Assunto , Diálise Renal , Atitude do Pessoal de Saúde , Termos de Consentimento , Tomada de Decisão Compartilhada , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Consentimento Livre e Esclarecido/ética , Consentimento Livre e Esclarecido/legislação & jurisprudência , Nefropatias/diagnóstico , Nefropatias/fisiopatologia , Nefropatias/psicologia , Nefrologistas/ética , Nefrologistas/legislação & jurisprudência , Nefrologistas/psicologia , Nefrologia/ética , Nefrologia/legislação & jurisprudência , Participação do Paciente , Formulação de Políticas , Prognóstico , Qualidade de Vida , Diálise Renal/efeitos adversos , Diálise Renal/ética , Medição de Risco , Fatores de RiscoRESUMO
OBJECTIVES: Older patients with end-stage renal disease are willing participants in advance care planning but just over 10% are engaged in this process. Nephrologists fear such conversations may upset patients and so tend to avoid these discussions. This approach denies patients the opportunity to discuss their end-of-life care preferences. Many patients endure medically intensive end-of-life scenarios as a result. This study aims to explore the rationale underpinning nephrologists' clinical decision-making in the management of older patients with end-stage renal disease and to make recommendations that inform policymakers and enhance advance care planning for this patient group. METHODS: A qualitative interview study of 20 nephrologists was undertaken. Nephrologists were asked about their management of end-stage renal disease in older patients, conservative management, dialysis withdrawal and end-of-life care. Eligible participants were nephrologists working in Ireland. Five nephrologists participated in a recorded focus group and 15 nephrologists participated in individual digitally recorded telephone interviews. Semistructured interviews were conducted; thematic analysis was used to distil the results. RESULTS: Three key themes emerged: barriers to advance care planning; barriers to shared decision-making; and avoidance of end-of-life care discussion. CONCLUSIONS: Advance care planning is not an integral part of the routine care of older patients with end-stage renal disease. Absence of formal training of nephrologists in how to communicate with patients contributes to poor advance care planning. Nephrologists lack clinical experience of conservatively managing end-stage renal disease and end-of-life care in older patients. Key policy recommendations include formal communication skills training for nephrologists and development of the conservative management service.
Assuntos
Planejamento Antecipado de Cuidados/organização & administração , Barreiras de Comunicação , Falência Renal Crônica/psicologia , Nefrologistas/psicologia , Relações Médico-Paciente , Assistência Terminal/psicologia , Idoso , Tomada de Decisão Clínica , Tratamento Conservador , Feminino , Humanos , Irlanda , Falência Renal Crônica/terapia , Masculino , Pessoa de Meia-Idade , Pesquisa Qualitativa , Diálise Renal/psicologiaRESUMO
O adoecimento crônico se apresenta atualmente como uma problemática de enorme relevância para as políticas públicas de saúde. Este artigo relata uma investigação realizada com médicos de um serviço especializado no atendimento a pessoas com condições crônicas de adoecimento em um hospital público no Rio de Janeiro. Partindo dos conceitos de Canguilhem sobre saúde e doença foram entrevistados cinco médicos deste serviço especializado de modo a analisar os projetos terapêuticos voltados às condições de cronicidade. No discurso dos entrevistados ressalta-se a referência a diferentes ordens de dificuldades observadas por eles no universo dos pacientes atendidos. Dificuldades de adesão ao tratamento causadas pela angústia diante da ausência da perspectiva de cura, poucos recursos para acesso a uma alimentação saudável e mesmo para a locomoção ao hospital, impossibilitam, segundo os entrevistados, o cuidado necessário ao trabalho de normatividade de um corpo acometido de uma doença crônica.
Chronic illness is currently a problem of enormous relevance for public health policies. This article reports an investigation carried out with physicians of a specialized service in the care of people with chronic conditions of illness in a public hospital in Rio de Janeiro. Based on the concepts of Canguilhem on health and illness, five physicians of this specialized service were interviewed in order to analyze the therapeutic projects focused on the conditions of chronicity. In the interviewees' speech the reference to different orders of difficulties observed by them in the universe of the patients attended is highlighted. Difficulties of adherence to treatment caused by anguish in the absence of the prospect of cure, few resources for access to a healthy diet and even for the locomotion to the hospital, make it impossible, according to the interviewees, to take care of the normative work of a body affected by a chronic disease.
La enfermedad crónica se presenta actualmente como una problemática de enorme relevancia para las políticas públicas de salud. Este artículo relata una investigación realizada con médicos de un servicio especializado en la atención a personas con condiciones crónicas de enfermedad en un hospital público en Río de Janeiro. A partir de los conceptos de Canguilhem sobre salud y enfermedad fueron entrevistados cinco médicos de este servicio especializado para analizar los proyectos terapéuticos orientados a las condiciones de cronicidad. En el discurso de los entrevistados se resalta la referencia a diferentes órdenes de dificultades observadas por ellos en el universo de los pacientes atendidos. Dificultades de adhesión al tratamiento causadas por la angustia ante la ausencia de la perspectiva de curación, pocos recursos para acceder a una alimentación sana e incluso para la locomoción al hospital, imposibilitan, según los entrevistados, el cuidado necesario al trabajo de normatividad de un cuerpo acometido de un cuerpo una enfermedad crónica.
Assuntos
Humanos , Insuficiência Renal Crônica/terapia , Nefrologistas/psicologia , Insuficiência Renal Crônica/psicologiaRESUMO
BACKGROUND: Conservative management, an approach to treating end-stage kidney disease without dialysis, while generally associated with shorter life expectancy than treatment with dialysis, is associated with fewer hospitalizations, better functional status and, potentially, better quality of life. Conservative management is a well-established treatment approach in a number of Western countries, including the United Kingdom (U.K.). In contrast, despite clinical practice guidelines in the United States (U.S.) recommending that nephrologists discuss all treatment options, including conservative management, with stage 4 and 5 chronic kidney disease patients, studies suggest that this rarely occurs. Therefore, we explored U.S. nephrologists' approaches to decision-making about dialysis and perspectives on conservative management among older adults. METHODS: We conducted a qualitative research study. We interviewed 20 nephrologists - 15 from academic centers and 5 from community practices - utilizing a semi-structured interview guide containing open-ended questions. Interview transcripts were analyzed using grounded thematic analysis in which codes were generated inductively and iteratively modified, and themes were identified. Transcripts were coded independently by two investigators, and interviews were conducted until thematic saturation. RESULTS: Twenty nephrologists (85% white, 75% male, mean age 50) participated in interviews. We found that decision-making about dialysis initiation in older adults can create emotional burden for nephrologists. We identified four themes that reflected factors that contribute to this emotional burden including nephrologists' perspectives that: 1) uncertainty exists about how a patient will do on dialysis, 2) the alternative to dialysis is death, 3) confronting death is difficult, and 4) patients do not regret initiating dialysis. Three themes revealed different decision-making strategies that nephrologists use to reduce this emotional burden: 1) convincing patients to "just do it" (i.e. dialysis), 2) shifting the decision-making responsibility to patients, and 3) utilizing time-limited trials of dialysis. CONCLUSIONS: A decision not to start dialysis and instead pursue conservative management can be emotionally burdensome for nephrologists for a number of reasons including clinical uncertainty about prognosis on dialysis and discomfort with death. Nephrologists' attempts to reduce this burden may be reflected in different decision-making styles - paternalistic, informed, and shared decision-making. Shared decision-making may relieve some of the emotional burden while preserving patient-centered care.
Assuntos
Tomada de Decisões , Emoções , Falência Renal Crônica/terapia , Nefrologistas/psicologia , Adulto , Idoso de 80 Anos ou mais , Tratamento Conservador , Morte , Feminino , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Participação do Paciente , Preferência do Paciente , Prognóstico , Pesquisa Qualitativa , Diálise Renal , IncertezaRESUMO
The number of new patients with chronic kidney diseases strongly increases while the one of nephrologists does not: this is developing new challenges, in which e-health will take a special part. This field is poorly investigated: so, we developed a dedicated survey. Telenephrology is a new approach that includes all what nephrologists can do in their routine practice: especially, telehealth with teleconsulting, telesurvey, and helpline. We also studied their relationship with m-health. The questionnaire was developed and validated by members from the Club des Jeunes Néphrologues and the Société Francophone de Néphrologie, Dialyse et Transplantation: it was then broadcast to all french nephrologists, thru web media. From June to July, 2017, we collected 175 answers: they represented all kinds of practices of the profession. Results show that French nephrologists are connected: most of them are present on social network(s) and/or uses connected objects, mostly for personal reasons. They communicate a lot, between them and/or with patients, mainly via email. Computerized medical records are mostly used in the follow-up of patients on renal dialysis or with chronic kidney diseases. Most of French nephrologists are satisfied by telenephrology but there are still obstacles to its deployment: mainly, technical, administrative, and/or billing difficulties. All should be taken into account to help telenephrology developing. In conclusion, French nephrologists are yet connected but they really need more help again to face new challenges raised by e-health.
Assuntos
Nefrologistas/psicologia , Nefrologia/métodos , Telemedicina/métodos , Adulto , Atitude do Pessoal de Saúde , Feminino , França/epidemiologia , Humanos , Masculino , Pessoa de Meia-Idade , Padrões de Prática Médica , Prevalência , Prática Profissional , Insuficiência Renal Crônica/economia , Insuficiência Renal Crônica/epidemiologia , Insuficiência Renal Crônica/terapia , Rede Social , Inquéritos e Questionários , Telemedicina/economia , Telemedicina/organização & administraçãoRESUMO
BACKGROUND: Patients with end-stage kidney disease (ESKD) on hemodialysis have limited life expectancy, yet their palliative care needs often go unmet. The aim of this study was to identify barriers and facilitators for implementation of "Shared Decision Making and Renal Supportive Care" (SDM-RSC), an intervention to improve advance care planning (ACP) for patients with ESKD on hemodialysis. METHODS: The Consolidated Framework for Implementation Research (CFIR) was the organizing framework for this study. CFIR is a theory-based implementation framework consisting of five domains (Intervention Characteristics, Inner Setting, Outer Setting, Characteristics of Individuals, and Process), each of which has associated constructs. Potential barriers and facilitators to implementation of the SDM-RSC intervention were identified through observation of study procedures, surveys of social workers nephrologists, study participants, and family members, and assessment of intervention fidelity. RESULTS: Twenty-nine nephrologists and 24 social workers, representing 18 outpatient dialysis units in Massachusetts (n = 10) and New Mexico (n = 8), were trained to conduct SDM-RSC intervention sessions. A total of 102 of 125 patient enrolled in the study received the intervention; 40 had family members present. Potential barriers and facilitators to implementation of the SDM-RSC intervention were identified in each of the five CFIR domains. Barriers included complexity of the intervention; challenges to meeting with patients on non-dialysis days; difficulties scheduling intervention sessions due to nephrologists' and social workers' caseloads; perceived need for local policy change regarding ACP; perceived need for additional ACP training for social workers and nephrologists; and lack of endorsement of the intervention by some staff members. Facilitators included: training for social workers, national dialysis chain leadership engagement and the institution of social worker/nephrologist clinic champions. CONCLUSIONS: ACP for patients on hemodialysis can have a positive impact on end-of-life outcomes for patients and their families but does not take place routinely. The barriers to effective implementation of interventions to improve ACP identified in this study might be addressed by: adapting the intervention for local contexts with input from clinicians, dialysis staff, patients and families; providing nephrologists and social workers additional training prior to delivering the intervention; and developing policy that routinizes ACP for hemodialysis patients. TRIAL REGISTRATION: Clinicaltrials.gov NCT02405312. Registered 04/01/2015.
Assuntos
Planejamento Antecipado de Cuidados , Falência Renal Crônica/psicologia , Nefrologistas/psicologia , Diálise Renal/métodos , Assistentes Sociais/psicologia , Adulto , Idoso , Tomada de Decisão Compartilhada , Feminino , Humanos , Falência Renal Crônica/terapia , Masculino , Pessoa de Meia-Idade , Nefrologistas/estatística & dados numéricos , Cuidados Paliativos/métodos , Cuidados Paliativos/psicologia , Diálise Renal/psicologia , Assistentes Sociais/estatística & dados numéricos , Inquéritos e QuestionáriosRESUMO
PURPOSE: Patients with end-stage renal disease (ESRD) seem to have a negative attitude towards physical activity, which is mainly favored by the lack of counseling provided by the medical and nursing staff. The aim of this study was to investigate the attitudes of both ESRD patients and medical staff on the participation and promotion of physical activity and identify the obstacles that discourage patients' involvement in intervention programs. STUDY DESIGN: Subjective assessment questionnaires and the International Physical Activity Questionnaire were administrated to hemodialysis patients and medical staff, to investigate the association between patient's barriers to physical activity, the total intensity level of physical activity, and attitudes of both ESRD patients and medical staff on the participation and promotion of physical activity. RESULTS: A total of 103 ESRD patients (61 men, 59.2%), 20 nephrologists (12 men, 60.0%), and 72 nurses (61 women, 84.7%) participated in the study. Most commonly reported patient's barriers were fatigue on dialysis (97.4%) and non-dialysis days (55.1%). Healthcare staff showed positive attitude towards renal rehabilitation exercise programs. However, most of physicians (85.0%) and nurses (83.3%) did not have previous experience with interventional exercise rehabilitation programs. Binary logistic regression revealed significant association between patients' inactivity, demographic data, and barriers towards physical activity, such as fatigue and pain in dialysis and non-dialysis days (p < 0.05), family's and physician's concern (p < 0.05), too many medical problems (p < 0.05), the fear of getting hurt (p = 0.01), and unwillingness for exercise (p < 0.05). Interestingly, healthcare staff's negative attitudes toward patient's physical activity seem to be strongly associated with patient's inactivity status. CONCLUSION: Healthcare staff negative attitudes and multiple related barriers especially fatigue on dialysis and non-dialysis days, towards ESRD patient's physical activity, suppress desire for exercise and active patients' status, leading them to abstain from it.
Assuntos
Atitude do Pessoal de Saúde , Atitude Frente a Saúde , Terapia por Exercício , Exercício Físico , Falência Renal Crônica , Participação do Paciente/psicologia , Diálise Renal , Adulto , Aconselhamento , Exercício Físico/fisiologia , Exercício Físico/psicologia , Terapia por Exercício/métodos , Terapia por Exercício/psicologia , Fadiga/etiologia , Fadiga/psicologia , Feminino , Humanos , Falência Renal Crônica/psicologia , Falência Renal Crônica/reabilitação , Falência Renal Crônica/terapia , Masculino , Pessoa de Meia-Idade , Nefrologistas/psicologia , Recursos Humanos de Enfermagem/psicologia , Diálise Renal/efeitos adversos , Diálise Renal/métodos , Diálise Renal/psicologia , Comportamento SedentárioAssuntos
Atenção à Saúde/economia , Equipamentos e Provisões Hospitalares , Unidades Hospitalares de Hemodiálise , Nefrologistas , Greve , Adulto , Brasil , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Veículos Automotores , Nefrologistas/psicologia , Fatores Sexuais , Inquéritos e QuestionáriosRESUMO
AIM: Patients with chronic kidney disease (CKD) have an increased risk of cancer compared with the general population. Despite this, there is considerable variability in cancer screening practices among nephrologists that may reflect uncertainties about the benefits and harms of screening, the additional costs, and competing priorities among the complex issues that patients are confronted with. We aimed to describe nephrologists' perspectives and approaches to cancer screening in CKD. METHODS: Semi-structured interviews were conducted with 29 nephrologists from 15 units across Australia and New Zealand. Interviews were transcribed and thematically analyzed. RESULTS: Five themes were identified: empowering patients to make informed decisions (respecting patient preferences, communicating evidence-based recommendations, creating awareness of consequences, preparing for transplantation); justifiable risk taking (avoiding undue consequences in vulnerable populations, balancing the costs and benefits, warranted by long term immunosuppression, assurance of reasonable survival gains); ambiguity of evidence in supporting decisions (absence of standardized recommendations, limited transferability of population-based data); depending on a shared multidisciplinary approach (collaboration with primary health care, access to coordinated skin cancer clinics); and prioritizing current or imminent complications. CONCLUSION: Nephrologists approach decisions about cancer screening in patients with CKD based on patient preferences, assessment of risk, justifiable survival gains, and current health priorities. Evidence-based guidelines, communication frameworks and specialist clinics may support informed and shared decision making about cancer screening in CKD.