Lifestyle Choices and Chronic Kidney Disease:: Dietary Habits and Nutritional Management
Lifestyle Choices and Chronic Kidney Disease:: Dietary Habits and Nutritional Management
the study if there are other researches relevant to this study or related to the
content of this study and the past research conducted.
The reserachers can identify and gather differently related and relevant literatures
underfeed primary and secondary sources and electronic sources such as reserach
journals, surveys, statistics, reliable websites and others.
Chronic Kidney Disease (CKD) is a prevalent health condition that affects lots of
individuals worldwide. In the Philippines, particularly in Tabuk City, Kalinga, CKD has
been identified as a significant public health concern. This review of related
literature aims to provide a comprehensive overview of the lifestyle choices,
challenges, and coping mechanisms among CKD patients in Tabuk City, Kalinga,
drawing on existing research in the field of nursing and related disciplines.
Chronic Kidney Disease (CKD) poses several significant challenges for patients in the
Philippines, impacting their overall quality of life and well-being. Nursing research in
the Philippines has shed light on the specific challenges faced by CKD patients in this
context. Below are some of the key challenges documented in nursing research:
The high prevalence rates of depression and anxiety in patients with CKD as
compared to other chronic diseases is of an important concern. It is unfortunate that
compared to other chronic illnesses such as coronary heart diseases and cancers, the
study of CKD and related psychological disorders are far less extensive. Existing
epidemiological studies have revealed important insights and factors that contribute
to the development of depression and anxiety in patients with CKD. Patients with
certain social, psychological, and clinical characteristics were found to be more
prone to falling into depression. These associations provide practitioners vital
indicators to identify and assess patients for psychiatric disorders more efficiently.
In the Philippines, its prevalence is 35.94%, which is much higher than estimated
global rates. Aside from its contribution to mortality, the growing burden of CKD is
also illustrated by its associated financial costs. Locally, 94% of end stage renal
disease (ESRD) patients are undergoing center-based hemodialysis, 4% are on
peritoneal dialysis and only 2% had kidney transplantation. Despite Kidney
Transplantation being the gold standard treatment for CKD, Hemodialysis is still
preferred by most Filipino patients due to transplant costs, low organ donations, lack
of capable infrastructures, and long term immunosuppression therapy.
The Philippines depends on the national health insurance program, PhilHealth, which
ideally guarantees all citizens automatic enrollment pursuant to the Universal Health
Care Law of 2019. However, data of registered beneficiaries from 2018 to 2021
observed geographical discrepancies, with a few remote provinces noted to have
coverages of only 52% and below. There are also some gaps in provision of financial
assistance to the beneficiaries. PhilHealth covers the costs of Hemodialysis,
Peritoneal dialysis and Kidney Transplant in varying degrees. However, most patients
still choose Hemodialysis over Peritoneal dialysis, despite better coverage of
Peritoneal dialysis in the past. It was only in June 2023 when PhilHealth's coverage
was expanded to 156 Hemodialysis sessions to fully cover the recommended thrice-
weekly annual treatments. This is an improvement from the 45, 90, and 144
Hemodialysis sessions previously amended in years 2013, 2015, and 2020,
respectively, wherein patients had to resort to twice-weekly sessions or pay out-of-
pocket.
Transportation Issues
Transportation to and from healthcare facilities can be a significant challenge for
CKD patients, particularly in rural areas.
Social Support
Family and peer support are essential coping mechanisms for CKD patients. A
qualitative study by Christina Seery (2022) The psychosocial needs of patients who
have chronic kidney disease without kidney replacement therapy: a thematic
synthesis of seven qualitative studies emphasizes that the present review aimed to
synthesise qualitative research on the experiences of patients who have CKD without
KRT, to provide additional insight into their potential psychosocial needs. Some
patients reported finding information about CKD confusing or inadequate. Peers are
identified as a helpful resource and could be capitalised on for an educational group
intervention. Patients can feel conscious of burdening their friends and family. The
review also observed several concerns for patients regarding the psychological
effects of CKD without KRT. Patients appeared to feel helpless, as if they had lost
control, had challenges adjusting and were fearful of the future. Therefore, the
review highlights several psychosocial needs for patients who have CKD without KRT
and potential areas for interventions.
Patients with CKD have many different characteristics, perspectives, and lived
experiences that impact their treatment decisions. These include social influences,
values and beliefs, level of comprehension, need for autonomy, and
sociodemographics. These factors influence the way patients receive education and
make medical decisions, which is why clinicians must value and participate in SDM to
navigate potential conflicts. Through the recommendations laid out in this narrative
review, the number of informed patients can be maximized, allowing SDM involving
RRT to be fulfilled.
Cultural Perspectives
It is important to consider cultural and regional factors when examining lifestyle
choices, challenges, and coping mechanisms among CKD patients in Tabuk City,
Kalinga. The cultural norms, beliefs, and healthcare access in this region may
influence the unique experiences of CKD patients.