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Epidemiology Paper Final Draft
Epidemiology Paper Final Draft
Zabrina Thein
Chosen Disease
Chronic Kidney Disease (CKD) is defined by the Centers for Disease Control and
Prevention (CDC) as “a condition in which the kidneys are damaged and cannot filter blood as
well as they should,” (CDC, 2020). Due to the improper filtration, other health problems; such as
heart disease, stroke, and depression; may result from the excess fluid and waste from blood that
Those diagnosed with CKD often do not experience any symptoms or illness. Rather, to
determine if a patient has CKD they must receive a series of specific blood and urine tests.
Similar to most diseases, CKD can worsen over time and possibly progress to kidney failure,
such as end-stage renal disease. For instance, recent findings indicate that “fifteen percent of US
adults are estimated to have CKD,” (CDC, 2020). Moreover, kidney diseases are said to be “the
ninth leading cause of death in the United States,” (CDC 2020). The CDC provides a few
which a dialysis machiene and a special filter are used to clean and filter your blood. In order to
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perform a hemodialysis, the patient must have a minor surgery to implant a catheter which is
Current Research
In the first article, Epidemiology of chronic kidney disease in children, they note that
CKD can progress to further irreversible kidney damage, known as end-stage renal disease
(ESRD). The study defines that the causes of CKD are very different in children than those in
adults. For example, in children, CKD can “impair growth and psychosocial adjustment, which
severely impact upon the quality of life,” (Harambat et al., 2011). The most recent report by the
North American Pediatric Renal Trials and Collaborative Studies show congenital causes, such
as congenital anomalies of the kidney and urinary tract (CAKUT) at 46% and hereditary
nephorapathies at 10%, being the most common. Additionally, in the United States, the recorded
annual incidence of ESRD in children slowly rose during the 1980s and then marginally
increased from 14 to 15 pmarp between 1990 and 2008. The adjusted prevalence rose from 60 to
85 in the same period. Furthermore, at the start of renal replacement therapy (RRT) programs in
the 1960s, the fatality rate was 11% for every 100 patient years. It has improved since then,
showing a stable case-fatality rate of 1.3-18 per 100 patient years in the past 15 years. Among
adults who started this kind of therapy during childhood, the average life expectancy was 63
years for those with a functioning graft compared to 38 years for those remaining on dialysis.
The external validity in this study can be found in the North American Pediatric Renal
Trials and Collaborative Studies (NAPRTCS) data collection. For example, they receive their
data from “pediatric nephrology centers on a voluntary basis and include more than 7,000
children aged under 21 years,” (Harambat et al., 2011). Due to this large sample size and the
wide range of ages, their findings have generalizability and can therefore be applied to a
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population. In addition, NAPRTCS include race in their data collection which is another
important factor when considering external validity. As for the internal validity of this study, this
can be found within the sections treatment modalities and modifiable progressions factors. These
sections detail different types of treatment and what type of treatment that countries offer as well
In the second article, Long-term outcome of chronic dialysis in children, states the
increase in mortality rate is specified as an outcome for pediatric patients on chronic dialysis.
The prevalence of children on renal replacement therapy (RRT) has increased world wide and
therefore consists of at least 2% of any national dialysis or transplant programme. This article
has collected their data from a number of organizations in different countries. For example, the
United States Renal Data System’s (USRDS) data from the 2006 reports an altered “mortality
rate for dialysis patients (age 0–19 years) who started treatment between 1995 and 1999 of
56.5/1,000 patient years at risk,” (Shroff & Ledermann, 2009). In their most recent report the
North American Pediatric Renal Trials and Collaborative Studies (NAPRTCS) declared that the
patient survival rates were “95%, 90.1% and 85.7% at 1 year, 2 years, and 3 years, respectively,”
(Shroff & Ledermann, 2009). Therefore, meticulous care to reduce modifiable risk factors is
important for this group who still have a lifetime chance of renal replacement.
The external validity in this article can be found in the data they have compiled from
NAPRTCS, United States Renal Data System (USRDS), United Network for Organ Sharing
(ERA-EDTA) as well as the Australia and New Zealand Dialysis and Transplant Assosciation
(ANZDATA). To be more specific, this study has collected data from a variety of organizations
which allows for a diverse amount of demographical factors. Therefore, this would make the
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studies findings generalizable and applicable to a population. On the other hand, threats to the
internal validity of this study relate to the different types of instrumentation, participation, and
testing amongst the variety of organizations they collected data from. More specifically, this
In the third article, Social support of adults and elderly with chroinc kidney disease on
dialysis, the studies main objective is to “evaluate the instrumental and emotional support of
patients with chronic kidney disease on hemodialysis” (Silvia et al., 2016). To collect a suffiecnt
amount of reliable data, a descriptive cross-sectional study was conducted using a Questionnaire
of the Sociodemographic and Clinical Characterization and the Social Support Scale for people
living with the Human Immunodeficiency Virus (HIV) - adapted for renal patients. There was a
convenience sample of 103 participants with an average age of 54.81 years who met the
following criteria: “18 years or older, be diagnosed with terminal CKD and be on hemodialysis,”
(Silvia et al., 2016). As defined in the results, the main causes of CKD include: the prevalence of
systemic arterial hypertension (53.4%) and type 2 diabetes mellitus (16.5%). After analyzing the
collected data, the article states there was a significant relationship between the level of
Sociodemographic and Clinical Characterization and the Social Support Scale for People Living
with the Human Immunodeficiency Virus (HIV) - adapter for renal patients,” (Silvia et al.,
2016). The internal validity in this article can be found in the data collected from the Social
Support Scale. The average score of social support of patients with CKD on hemodialysis
resulted in 3.92 emotional support and 3.81 for the instrumental support, indicating a good
availability of perceived support. 45% of the participants were satisfied with the availability of
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support in the management and resolution of operational issues of treatment, practical activities
As stated earlier, the risk of developing CKD is higher if you have diabetes, high blood
pressure, heart disease, family history of CKD, obesity. Perceived susceptibility of CKD will
vary among those who are either high or low risk. For instance, a patient who is at higher risk of
developing CKD has a higher perceived susceptibility and, therefore, is more likely to engage in
preventative behaviors, such as lowering sodium intake and staying active. However, individuals
who are at low-risk, they will have a lower perceived susceptibility and continue any unhealthy
behaviors as they may deny the possibility of developing CKD. For example, females who had
low health literacy had lower perceived susceptibility to CKD compared to males and those with
higher health literacy, (Boulware et al., 2009). This study also concluded that race and poorer
blood pressure management adherence scores were related to a greater perceived susceptibility.
and its progression to ESRD so they can make changes to any unhealthy behaviors. In a study
conducted among CKD patients living in a district in Sri Lanka, they administered a locally
validated questionnaire to assess the presence and severity of symptoms of 1174 randomly
selected CKD patients. Common symptoms of CKD include fatigue, pruritus, irritability, anxiety,
and nausea. According to the study, the most prevalent symptoms during the first week were
bone/joint pain (87.6%; 95% CI 85.6–89.5), feeling irritable (78.6%; 95% CI 76.2–81.0), muscle
cramps (77.5%; 95% CI 75.0–79.9), lack of energy (75.7%; 95% CI 73.2–78.2) and difficulty in
sleeping (68.5%; 95% CI 65.8–71.2). The least prevalent symptoms were diarrhea (5.8%; 95%
CI 4.4–7.2), vomiting (13.7%; 95% CI 11.7–15.7), hiccups (16.5%; 95% CI 14.3–18.6) and
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change in skin color (17.5%; 95% CI 15.3–19.8). As for the perceived benefits of preventative
behaviors and treatments for CKD, goals, such as monitoring and maining a low blood pressure,
will effectively decrease the severity of CKD. Also, although dialysis is only necessary in the
later stages of CKD, the procedure is meant to efficiently clean and filter the blood. For instance,
patients with ESRD who undergo dialysis have been known to experience a drastic improvement
That being said, there are a number of barriers patients must overcome when battling
with CKD, such as difficulty sustaining improved behavior and medical costs. Generally, it is
difficult for most people to break unhealthy habits. To illustrate, a poor diet can negatively
impact someone with diabetes which could further progress to CKD. Therefore, taking control of
dietary meals, such as sodium intake and blood sugar, could assist in preventing the development
of CKD. In terms of costs, the CDC states that “overall Medicare costs for people with CKD
were over $84 billion in 2017, or more than $22,000 per person,” (Centers for Disease Control
and Prevention, 2020). On top of that, the CDC also notes that “total Medicare spending
(excluding prescription drugs) for patients with ESRD or kidney failure reached $36 billion in
2017, or nearly $80,000 per person, accounting for about 7% of the Medicare paid claims costs,”
(2020). Therefore, due to these sizable costs, care for patients with CKD is quite expensive and
is a significant barrier for those who are unable to access affordable healthcare.
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References
Boulware, L. E., Carson, K. A., Troll, M. U., Powe, N. R., & Cooper, L. A. (2009). Perceived
susceptibility to chronic kidney disease among high-risk patients seen in primary care
Chronic kidney disease basics. (2020, March 4). Retrieved November 14, 2020, from Cdc.gov
website: https://www.cdc.gov/kidneydisease/basics.html
Harambat, J., van Stralen, K. J., Kim, J. J., & Tizard, E. J. (2012). Epidemiology of chronic
Hemodialysis. (2016, January 11). Retrieved November 14, 2020, from Kidney.org website:
https://www.kidney.org/atoz/content/hemodialysis
Senanayake, S., Gunawardena, N., Palihawadana, P., Bandara, P., Haniffa, R., Karunarathna, R.,
& Kumara, P. (2017). Symptom burden in chronic kidney disease; a population based
Shroff, R., & Ledermann, S. (2009). Long-term outcome of chronic dialysis in children.
Silva, S. M. da, Braido, N. F., Ottaviani, A. C., Gesualdo, G. D., Zazzetta, M. S., & Orlandi, F.
de S. (2016). Social support of adults and elderly with chronic kidney disease on dialysis.