Introduction
Cancer is among the main Chronic No Communicable
Diseases (NCDs) and represents the second leading cause
of death in the world, with one in every six deaths being
related to the disease. Among the most common types of
lung cancer (2.09 million cases), breast (2.90 million cases),
colorectal (1.8 million cases), prostate (1.28 million cases),
non-melanoma skin cancer (1.04 million cases) and
stomach cancer (1.03 million cases).
1
Regarding the severity of NCDs, an analysis by the World
Economic Bank estimated that countries such as Brazil,
China, India, and Russia lose, annually, more than 20
million productive years of life due to NCDs.
2
From this
perspective, Oncological diseases represent a major public
health problem, due to the significant cost of treatment,
hospitalization, and the need for continuity of care for
individuals in palliative care.
According to the World Health Organization (WHO), in a
concept defined in 1990 and updated in 2002 and 2017,
3
palliative care refers to actions that improve the quality of
life of patients and families facing problems associated with
life-threatening illnesses. It aims to prevent and alleviate
suffering, through early identification, correct assessment,
and treatment of pain and other physical, psychosocial, or
spiritual problems.
It is noteworthy that contingency plans focused on de-
hospitalization, and optimization of financial resources are
extremely relevant, as they constitute strategies that aim to
analyze resources and health actions that favor adequate
planning, as well as targeting to the various levels of health
care.
4
Assistance or home care (HC) corresponds to the set of
health actions, integrated into the Health Care Network
(HCN), to guarantee the continuation of care for the
individual who needs care. This service is available in Brazil
through the Unified Health System (SUS), through
multidisciplinary teams and is also offered by other private
service providers, known as home care services.
5
Within this scenario and perspective, in Brazil, Resolution
No. 41/2018 defined together with the Tripartite
Intermanagers Commission of the National Council of
Health Secretaries (CONASS) and municipal secretariats,
provided for guidelines for the organization of palliative
care, in light of continued care integrated, within the scope
of the Unified Health System (SUS). According to Article
5, palliative care must be offered anywhere in the health
care network, at no cost to the patient and their family,
notably in primary care, home care, outpatient care,
urgent/emergency care, and hospital care.
6
Across the world, healthcare costs are expensive. When it
comes to hospital care, it is even higher. Depending on the
evolution of the disease, patients undergoing oncology
palliative care undergo several readmissions. When it is
possible to decrease readmission rates and shift care to
home care, it can lead to a significant difference in hospital
expenses.
7
The cost is the sum of expenses with personnel, material,
physical structure, and equipment used and must be
understood as an important management tool for analyzing
performance, productivity and quality of services.
8
The first stage of the process consists of verifying the costs
of health services, procedures, and treatments. According
to the analysis carried out, pharmacoeconomic evaluations
have different denominations, including: cost-
minimization, cost-effectiveness, cost-utility and cost-
benefit.9 In this sense, economic evaluation in health plays
a prominent role, requiring managers to face new
challenges in the continuous search for efficiency and
effectiveness of activities. Quality associated with the
rational use of resources must be the new challenge for
health service managers.
10-11
Therefore, it is essential to measure health costs, for a
careful analysis of the service scenario to support decision-
making by managers in the selection of tools and
management models that qualify the care provided to the
population involved, especially people with cancer in
palliative care. In view of the above, the objective of this
study was to investigate scientific articles related to the cost
of the Home Care Service for patients undergoing
oncology palliative care.
Methods
This is an Integrative Literature Review that followed six
standardized steps:
12
in step I, the definition of the research
problem and the guiding question were established, using
the acronym PICo,
13
where the “P” refers to the population
study or the patient, or the problem addressed
(Population/Patient/Problem), which in this review refers
to cancer patients; the “I” is the phenomenon of Interest
(Interest), which were the costs of the home care service
for palliative care and the “Co” to the context (Context),
what was home care. Therefore, the guiding question of
the research was: “What is the cost of home care for
patients undergoing oncology palliative care?”
In stage II, the inclusion criteria were defined, which were
indexed articles, complete texts without definition of
temporality or country of publication, in Portuguese,
Spanish and English, related to the guiding question and
developed in human beings, without restriction on age
range in palliative oncology care.
Studies that addressed palliative care in the hospital area,
letters to the editor, duplicates, opinion and review articles
of any nature, theoretical reflection, comments, essays,
preliminary notes, editorials, letters, theses and
dissertations, course completion works, manuals,
summaries in annals or periodicals, dossiers, official
documents, health policies, hospital management reports,
books and book chapters were excluded.
Data collection took place in October 2021 in databases
and electronic libraries: Scopus; BASIS; Science Direct,
PubMed (MedLine), Scielo, Web of Science and the Virtual
Health Library (VHL), with the descriptors presented by
the search strategy in Table 1.