Introducción: La Facultad de Medicina de la Pontificia Universidad Javeriana ha venido implementando un plan curricular basado en competencias para garantizar la formación holística de los médicos generales a partir de una estrategia pedagógica denominada actividad integradora (AI), que busca incentivar conocimientos, habilidades y destrezas para el desarrollo de competencias de los médicos en formación. Objetivo: Explorar las percepciones y experiencias de estudiantes, docentes y directivos en el desarrollo de competencias a partir de la implementación de la AI. Método: Estudio cualitativo, descriptivo e interpretativo que se hizo a partir de entrevistas y grupos focales con estudiantes, docentes y personal directivo. Resultados: Se encontró que la AI se constituye como una estrategia de aprendizaje que permite el desarrollo de competencias a través de una didáctica específica que trasforma el escenario pedagógico en un espacio de construcción conjunta de saberes a partir del trabajo en grupo. Conclusiones: Los resultados muestran que, a pesar de que la definición de competencias no es unánime entre los actores, la implementación de la AI ha favorecido que los estudiantes desarrollen conocimientos, habilidades y destrezas desde los saberes propuestos por Miller en el marco de un currículo basado en competencias.
Background In Colombia, cancer incidence is increasing, as is the demand for end-of-life care. Understanding how patients who die from cancer experience this phase will allow the identification of factors associated with greater suffering and actions to improve end-of-life care. We aimed to explore associations between the level of suffering of patients who died from cancer and were cared for in three Colombian hospitals with patient, tumor, treatment, and care characteristics and provided information. Methods Data on the last week of life and level of suffering were collected through proxies: Bereaved caregivers of patients who died from cancer in three participating Colombian hospitals. Bereaved caregivers participated in a phone interview and answered a series of questions regarding the last week of the patient’s life. An ordinal logistic regression model explored the relationship between the level of suffering reported by bereaved caregivers with the patient’s demographic and clinical characteristics, the bereaved caregivers, and the care received. Multivariate analyses were adjusted for place of death, treatments to prolong of life, prolongation of life during the dying process, suffering due to prolongation of life, type of cancer, age, if patient had partner, rural/urban residence of patient, importance of religion for the caregiver, caregivers´ relationship with the patient, and co-living with the patient. Results A total of 174 interviews were included. Median age of the deceased patients was 64 years (IQR 52–72 years), and 93 patients were women (53.4%). Most caregivers had rated the level of suffering of their relative as “moderately to extremely” (n = 139, 80%). In multivariate analyses, factors associated with a higher level of suffering were: unclear information about the treatment and the process before death Odds Ratio (OR) 2.26 (90% CI 1.21–4.19), outpatient palliative care versus home care OR 3.05 (90% CI 1.05–8.88), procedures inconsistent with the patient’s wishes OR 2.92 (90% CI 1.28–6.70), and a younger age (18–44 years) at death versus the oldest age group (75–93 years) OR 3.80 (90% CI 1.33–10.84, p = 0.04). Conclusion End-of-life care for cancer patients should be aligned as much as possible with patients´ wishes, needs, and capacities. A better dialogue between doctors, family members, and patients is necessary to achieve this.
There is limited knowledge regarding Colombian patients with advanced cancer preferences regarding their final moments, place of death, and post-death wishes. To better understand these preferences, we conducted 23 in-depth interviews with patients between the ages of 28 and 78 receiving treatment at two academic hospitals and the National Cancer Institute. While many participants desired a peaceful death, few were comfortable discussing the topic of death directly. Some younger participants expressed an interest in euthanasia but had not received any guidance or support. While several participants preferred a home death, some expressed a desire to die in a hospital due to better symptom control. Additionally, when discussing post-death wishes, some participants expressed frustration about being unable to have these conversations with their loved ones and their preferences for funeral arrangements. Socioeconomic and geographical factors significantly impacted the wishes and preferences expressed, with many individuals hesitant to initiate difficult conversations.
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