@article{TamargoAllué:70856,
      author        = "Tamargo Allué, Laura and Estrada Fernández, María
                       Eugenia",
      title         = "{Sobrecarga del cuidador de un enfermo oncológico y
                       cuidados de enfermería. Revisión bibliográfica}",
      year          = "2018",
      note          = "INTRODUCTION: Cancer is the second cause of death in the
                       world and is seen in the coming years in the number of
                       cases. Due to the great impact that the disease caused on
                       health, patient care burned both the patient and his
                       family, providing the necessary support. The disease and
                       hospitalization took on the role of new roles, which can
                       affect the family and generate future growth and
                       development of the patient, education and emotional
                       relationships. OBJECTIVES: The main objective is to analyze
                       through a bibliographic review through the physical and
                       emotional repercussions of the informal caregiver of the
                       adult oncological patient. METHODOLOGY: A bibliographic
                       search was conducted between December 2017 and February
                       2018, using the following databases: PubMed, Cuiden,
                       Cochrane Library, Bibliographic Index in Health Sciences
                       (IBECS) and Scielo. Also, articles have been searched in
                       Elsevier. DEVELOPMENT: 26 articles have been selected with
                       the search profiles. The literary review indicates that the
                       most frequent physical repercussions are fatigue, fatigue
                       and pain; while the psychological ones focus on anxiety,
                       depression, sleep disorders and anguish. CONCLUSIONS: The
                       caregiver has an important role in the patient's illness,
                       therefore, the need for interventions and health programs
                       aimed at education and support to the caregiver to improve
                       their quality of life and that is reflected in the care of
                       the patient. KEY WORDS: "Caregiver", "Psycho-oncology",
                       “Family”, "Emotions", "Quality of life"",
}