Symptom Assessment and Early Access to Supportive and Palliative Care for Patients With Advanced Solid Tumors in Mexico. Issue 1 (January 2020)

• Record Type: Journal Article
• Authors: Alcalde-Castro, Mirza Jacqueline; Soto-Perez-de-Celis, Enrique; Covarrubias-Gómez, Alfredo; Sánchez-Román, Sofía; Quiróz-Friedman, Paulina; Navarro-Lara, África; Ramos-Lopez, Wendy Alicia; Moreno-García, María Luisa; Contreras-Garduño, Sergio; Perez-Montessoro, Viridiana; Goss, Paul E.; Chávarri-Guerra, Yanin
• Is Part Of: Journal of palliative care. Volume 35:Issue 1(2020)
• Page Start: 40
• Page End: 45
• Publication Date: 2020-01
• Subjects: palliative care -- palliative medicine -- symptom assessment -- advance care planning -- developing countries -- Mexico; Terminal care -- Periodicals; 362.17505
• DOI: 10.1177/0825859719834920
• Languages: English
• ISSNs: 0825-8597

Abstract

Background: Early specialized palliative care improves quality of life of patients with advanced cancer, and guidelines encourage its integration into standard oncology care. However, many patients fail to obtain timely palliative/supportive care evaluations, particularly in limited-resource settings. We aimed to determine the proportion of patients with advanced cancer who received an assessment of symptoms and were referred to supportive and palliative care services during the first year after diagnosis in a Mexican hospital. Methods: Individuals with newly diagnosed advanced solid tumors and 1 year of follow-up at the oncology clinics in the Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran in Mexico City from October 2015 to April 2016 were included in this retrospective study. Results: Seventy-seven patients were included. Forty-two (54.5%) were referred to the various supportive care services during the first year after diagnosis, and 23 (29.8%) were referred to the palliative care clinic. The most commonly assessed symptoms by oncologists were pain (77.9%), anorexia (74.0%), fatigue (68.8%), and nausea (55.8%), while depression/anxiety were evaluated in 10 (12.9%) patients. The oncologist offered to clarify treatment goals in 39 (50.6%) cases and evaluated the understanding of diagnosis/illness and prognosis in 22 (28.5%). Conclusion: Palliative and supportive care services were widely underutilized, which may be related to a lack of standardized symptom assessments and poor end-of-life communication. Novel strategies are needed to improve the implementation of tools for systematic symptom assessment and to optimize the integration of supportive care interventions into oncology care in developing countries.