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1.
Support Care Cancer ; 30(10): 8339-8347, 2022 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-35869370

RESUMEN

PURPOSE: Palliative radiotherapy (PRT) in advanced cancer improves symptom control and quality of life. PRT consultations take place in various clinical settings, including through dedicated rapid access clinics. We examined holistic assessment and PRT delivery by consultation setting. METHODS: We analyzed patients with breast cancer who died (01/04/2013-31/03/2014), after at least one lifetime PRT consultation. Data abstracted included Karnofsky Performance Status (KPS), Edmonton Symptom Assessment System Revised (ESAS-r) ratings, and PRT timelines. Descriptive statistics, t tests of proportions, independent t tests, and chi-square tests were calculated. RESULTS: One hundred thirty patients were assessed for PRT over 224 consults, 28/224 (12.5%) in the rapid access clinic. In non-rapid access versus rapid access visits, KPS was documented in 30.1% versus 89.3%, and medication history in 53.6% versus 96.4%, respectively (both p < 0.0001). Baseline ESAS-r scores were available for 67.9% of rapid access visits, versus no non-rapid access visit. Rapid access consults had a higher proportion of subsequent supportive care referrals (46.4% versus 8.2%; p < 0.0001). Same day PRT start occurred in 37% of rapid access versus 23.4% of non-rapid access visits (p = 0.13). CONCLUSIONS: Assessment for PRT by a dedicated multidisciplinary team provides a comprehensive picture of patient needs and streamlines PRT delivery, essential to personalizing supportive care.


Asunto(s)
Neoplasias de la Mama , Neoplasias , Neoplasias de la Mama/radioterapia , Femenino , Humanos , Estado de Ejecución de Karnofsky , Neoplasias/radioterapia , Cuidados Paliativos , Calidad de Vida , Derivación y Consulta
2.
Semin Oncol Nurs ; 38(2): 151279, 2022 04.
Artículo en Inglés | MEDLINE | ID: mdl-35491333

RESUMEN

OBJECTIVES: We provide a review of external beam radiotherapy for pain associated with bone metastases, to summarize evidence associated with different radiotherapy fraction prescriptions, and outline the oncology nursing roles in a rapid-access palliative radiotherapy clinic. Additionally, we describe the clinical capacity contributed by a nurse practitioner working at full clinical scope. DATA SOURCES: Data derived from literary databases (PubMed, CINAHL); an ethics-approved, prospective data set; and clinical expertise. CONCLUSION: Nursing provides essential contributions in the treatment and holistic symptom management in patients undergoing radiation therapy for painful bone metastases. IMPLICATIONS FOR NURSING PRACTICE: The roles of nursing in radiation oncology have been poorly elucidated within the existing literature. This evaluation provided valuable insights into the contribution of oncology nursing roles in providing timely access for individuals with painful metastasis.


Asunto(s)
Neoplasias Óseas , Oncología por Radiación , Neoplasias Óseas/radioterapia , Neoplasias Óseas/secundario , Humanos , Enfermería Oncológica , Dolor/etiología , Dolor/radioterapia , Cuidados Paliativos , Estudios Prospectivos
3.
J Med Imaging Radiat Sci ; 50(1): 17-23.e1, 2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30777240

RESUMEN

BACKGROUND: Palliative radiation therapists (PRTs) have been integrated in varying capacities into outpatient palliative radiation therapy (RT) services across Canada for over 2 decades. At our institution, PRTs have developed an essential role over 11 years within a palliative radiation oncology (PRO) clinic that focuses on integrating symptom management with radiation oncology assessment for palliative RT. PRTs have had direct clinical, technical, research, and administrative involvement as the clinic evolved from a pilot in 2007 supporting one half-day per week to the current model of five full clinical days. METHODS: Using collaborative reflection, we explored the PRTs' experience and insight. Twelve PRTs who contributed to the PRO clinic for varying lengths of time from 2007 through to 2016 were invited to participate in the development of a collective expression of the PRT experience. Seven PRTs consented to completing an electronic survey consisting of fifteen open-ended questions regarding individual roles and perspectives relating to our PRO clinic. Survey answers were enhanced by semistructured interviews when needed for clarification. Responses were contextualized within the operational changes to our multidisciplinary clinical model, from pilot to integrated service. RESULTS/DISCUSSION: Five respondents answered all of the questions. From the narratives, PRT roles and responsibilities were outlined and their insights and reflections included to contextualize clinical changes. Four phases of the clinic were identified and elucidated. Beginning in January 2007, three PRTs staffed a multidisciplinary clinical pilot one half-day per week for single-fraction, symptomatic bone metastases. The clinic has now evolved through various iterations to the current model with four PRTs sharing a "navigator" role with two registered nurses five full clinic days per week. The range of PRT experiences, responsibilities, and challenges encountered reflected specific clinical and operational conditions. CONCLUSION: As our clinical service model evolved from short-term pilot to fully integrated departmental service, so did the PRT role. PRTs contributing to RT as part of a multidisciplinary model support and advance nontraditional involvement in the holistic care of patients with advanced cancer.


Asunto(s)
Prestación Integrada de Atención de Salud/organización & administración , Personal de Salud , Medicina Paliativa/organización & administración , Rol Profesional , Oncología por Radiación/organización & administración , Actitud del Personal de Salud , Humanos
4.
J Palliat Med ; 16(8): 915-21, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23819731

RESUMEN

OBJECTIVE: Health related quality of life (HRQOL) is a multidimensional concept that is especially important for cancer patients with bone metastases, as maintaining and improving HRQOL is often the main focus of treatment. This study aims to determine factors that may influence HRQOL, which may in turn influence treatment and care of patients. METHODS: Patients (n=396) completed the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ) Bone Metastases module (BM22) at baseline. The EORTC QLQ-BM22 consists of four scales: painful site (PS), pain characteristics (PC), functional interference (FI), and psychosocial aspect (PA) scales. EORTC QLQ-BM22 data, together with sociodemographic and medical factors were analyzed by univariate analysis of variance (ANOVA). Items of significance were determined through backward selection, which were then put through multivariate analysis to determine further significance. RESULTS: Through ANOVA analysis, KPS>80 and breast primary histology were predictive of better HRQOL in the PS scale, while KPS>80, female gender, and breast primary histology were predictive of better HRQOL in the PC and FI scales. KPS>80 and prostate primary histology were predictive of better HRQOL in the PA scale. KPS>80 and primary cancer site were confirmed as significant predictive factors in multivariate analysis. RECOMMENDATIONS: This study identified baseline factors of gender, performance status, and primary histology as determinants of HRQOL in patients with bone metastases. Further study focusing on current treatment (chemotherapy, bisphosphonates, and radiotherapy) and spiritual well-being may identify additional factors affecting HRQOL. Understanding the influence of these factors will allow health care professionals to provide more effective palliative care.


Asunto(s)
Neoplasias Óseas/psicología , Neoplasias/psicología , Cuidados Paliativos/métodos , Calidad de Vida , Adulto , Anciano , Anciano de 80 o más Años , Análisis de Varianza , Neoplasias Óseas/secundario , Neoplasias de la Mama/patología , Neoplasias de la Mama/psicología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Metástasis de la Neoplasia , Neoplasias/patología , Neoplasias de la Próstata/patología , Neoplasias de la Próstata/psicología , Estudios Retrospectivos , Factores Sexuales , Perfil de Impacto de Enfermedad , Apoyo Social , Espiritualidad , Encuestas y Cuestionarios
5.
Int J Radiat Oncol Biol Phys ; 78(2): 527-32, 2010 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-20100640

RESUMEN

PURPOSE: Patients with bone metastases may experience pain, fatigue, and decreased mobility. Multiple medications for analgesia are often required, each with attendant side effects. Although palliative-intent radiotherapy (RT) is effective in decreasing pain, additional supportive care interventions may be overlooked. Our objective was to describe the feasibility of multidisciplinary assessment of patients with symptomatic bone metastases attending a dedicated outpatient palliative RT clinic. METHODS AND MATERIALS: Consecutive patients referred for RT for painful bone metastases were screened for symptoms and needs relevant to their medications, nutritional intake, activities of daily living, and psychosocial and spiritual concerns from January 1 to December 31, 2007. Consultations by appropriate team members and resulting recommendations were collected prospectively. Patients who received RT were contacted by telephone 4 weeks later to assess symptom outcomes. RESULTS: A total of 106 clinic visits by 82 individual patients occurred. As determined by screening form responses, the clinical Pharmacist, Occupational Therapist, Registered Dietician and Social Worker were consulted to provide assessments and recommendations within the time constraints presented by 1-day palliative RT delivery. In addition to pain relief, significant improvements in tiredness, depression, anxiety, drowsiness and overall well-being were reported at 4 weeks. CONCLUSIONS: Systematic screening of this population revealed previously unmet needs, addressed in the form of custom verbal and written recommendations. Multidisciplinary assessment is associated with a high number of recommendations and decreased symptom distress. Our findings lend strong support to the routine assessment by multiple supportive care professionals for patients with advanced cancer being considered for palliative RT.


Asunto(s)
Neoplasias Óseas/radioterapia , Dolor/radioterapia , Cuidados Paliativos/estadística & datos numéricos , Grupo de Atención al Paciente/organización & administración , Actividades Cotidianas , Adulto , Anciano , Anciano de 80 o más Años , Alberta , Instituciones de Atención Ambulatoria/estadística & datos numéricos , Ansiedad/terapia , Neoplasias Óseas/psicología , Neoplasias Óseas/secundario , Distribución de Chi-Cuadrado , Depresión/terapia , Servicios Dietéticos/estadística & datos numéricos , Fatiga/terapia , Estudios de Factibilidad , Femenino , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Humanos , Masculino , Persona de Mediana Edad , Evaluación Nutricional , Terapia Ocupacional/estadística & datos numéricos , Dolor/etiología , Dolor/psicología , Cuidados Paliativos/métodos , Grupo de Atención al Paciente/estadística & datos numéricos , Servicio de Farmacia en Hospital/estadística & datos numéricos , Estudios Prospectivos , Servicio Social/estadística & datos numéricos , Espiritualidad
6.
Curr Opin Support Palliat Care ; 4(1): 11-5, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20040878

RESUMEN

PURPOSE OF REVIEW: Cancer pain remains inadequately treated, despite internationally accepted management guidelines and a myriad of treatment options. Risk factors for undertreatment are reviewed, along with possible explanations. Recent studies documenting the scope of the problem as well as investigating solutions are discussed with clinical-practice recommendations outlined. RECENT FINDINGS: Women over 65 years of age representative of a cultural minority, with earlier stage disease, cared for at home, and with high-school education or less are at highest risk of having uncontrolled cancer pain. Optimal treatment is impeded by patients' maladaptive beliefs, nonadherence, underreporting or miscommunication with caregivers; from a healthcare provider perspective, it may be due to inadequate assessment, documentation, knowledge, and communication. Emerging data support the vital influence of lay caregivers on appropriate pain management. Although home-education programs may decrease pain and improve quality of life, there are also less intensive approaches deliverable by individuals to holistically address pain. SUMMARY: Prospective study of barriers to both delivery and receipt of adequate pain management is needed, as the majority of published literature is based on survey studies. Treatment must be individualized based on clinical circumstances and patient wishes, with the goal of maximizing function and quality of life.


Asunto(s)
Analgésicos/uso terapéutico , Neoplasias/complicaciones , Dolor/tratamiento farmacológico , Anciano , Femenino , Conocimientos, Actitudes y Práctica en Salud , Humanos , Cumplimiento de la Medicación , Dolor/etiología , Dimensión del Dolor , Educación del Paciente como Asunto , Pautas de la Práctica en Medicina
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