Thursday, March 8, 2007 is World Kidney Day! World Kidney Day was proposed by the International Society of Nephrology (ISN) and International Federation of Kidney Foundations (IFKF) in 2006 to broadcast a message about kidney diseases to the public, government health officials, general physicians, allied health professionals, individuals, and families. It was launched on March 9, 2006, and will be fully inaugurated this year (https://doi.org/www.worldkidneyday.org/).
The message is that kidney disease is common, harmful and treatable. In this article we focus on chronic kidney disease (CKD), as a global public health problem, and the urgent need for all countries to have a public health policy for CKD. Until recently, decision makers in public health and biomedical science had viewed CKD as uncommon, without consequences, and untreatable until the stage of kidney failure. The care of patients with CKD had been marginalized, relegated to the subspecialty of nephrology, with payment primarily directed at dialysis and transplantation, which are too costly for the vast majority of people living outside the developed world. At the same time, costs for other chronic diseases have been mounting. In developed countries, hypertension, diabetes and cardiovascular disease consume a large fraction of resources for health care. The epidemic of obesity, in the young as well as in the elderly, will magnify these costs. In developing countries the burden of these non-communicable diseases is rising, even though communicable diseases are not yet under control. We now recognize that CKD is especially common in people with other chronic diseases and multiplies the risk for adverse outcomes and costs. The public health mandate is now clear. No country can afford to overlook the burden of CKD; prevention, early detection and intervention are the only cost-effective strategies. In the following paragraphs we outline the rationale for key elements of a public health policy for CKD and for integrating these elements with programs for other chronic diseases.
Rationale
Figure 1 shows a conceptual model for CKD as the basis for a public health approach, emphasizing stages of CKD, as well as antecedents, outcomes and risk factors for development and progression of CKD. CKD is defined as either kidney damage, estimated from markers such as albuminuria, or as a glomerular filtration rate (GFR) <60 ml/min per 1.73 m2 body surface area for 3 months or more [1–3]. Albuminuria is usually defined as a spot urine protein-to-creatinine ratio >30 mg/g, and GFR is usually estimated from serum creatinine, age, gender and race. In the USA, recent data from the National Health and Nutrition Examination Survey (NHANES) estimate the prevalence of CKD as 9.6% in non-institutionalized adults, corresponding to approximately 19 million people (Table 1) [4, 5]. The elderly, racial and ethnic minorities, and those with lower socioeconomic status are disproportionately affected. Prevalence estimates in other countries are difficult to interpret because of differences in serum and urine creatinine levels due to variability among studies in assays, muscle mass and diet. Nonetheless, in both developed and developing nations, a consistent picture is emerging of increased risk for CKD among people with cardiovascular disease (CVD) risk factors or established CVD.
The most important adverse outcomes of CKD include not only complications of decreased GFR and progression to kidney failure, but also increased risk of CVD. Many studies show that albuminuria and decreased estimated GFR each consistently, and in a graded fashion, increases the risk of CVD [7]. Indeed, recent studies show that patients with CKD are 100-times more likely to die, principally from CVD, than to develop kidney failure [8]. There is now convincing data for efficacy of treatment to prevent complications of decreased GFR, to slow progression of kidney disease, and to reduce CVD risk [1–3]. Testing for CKD is feasible in clinical practice, and the same methods can be applied in large-scale screening of people at increased risk. Thus, the tools to improve outcomes for CKD are already available. It is now time to establish policies to translate these advances to public health.
Detection
CKD detection programs could focus on people with CVD risk factors, such as older age, hypertension, diabetes, hyperlipidemia, and people with CVD. The prevalence of CKD is higher in these groups, and many studies have demonstrated that CKD is a “multiplier” for CVD risk [7, 9]. As with all CVD risk factors, the increase in absolute risk is greater in people with other risk factors. The “CKD subgroup”, particularly in the elderly, constitutes an especially high risk group who need special attention (Table 2). Among the “CKD subgroup”, CVD risk factor levels are higher and more difficult to control, outcomes are worse, and costs are higher. Many clinical trials of CVD risk reduction or treatment have excluded patients with later stages of CKD [10]. However, analyses of trials that included patients with earlier stages of CKD have generally revealed that the beneficial effect of treatment in the CKD subgroup is as large as, or larger than, in the group without CKD [11–13]. Most guidelines for CVD risk factor conditions and for CVD now recommend testing for CKD and different treatments for people found to have CKD compared to treatments for people without CKD [14–16].
Children, adolescents and young adults with obesity, hypertension or diabetes are also at increased risk of adverse outcomes related to CKD. It is anticipated that these younger patients have a higher risk for CKD and a higher life-time risk for CVD due to their long exposure to CVD risk factors [17]. CVD risk factor detection programs are beginning for this population and could include testing for CKD.
CKD testing can be implemented within the same infrastructure used for CVD risk factor testing and should include an assessment for albuminuria and a serum creatinine measurement to estimate GFR [1, 3, 5]. These measures should detect most cases of CKD in adults due to hypertension and diabetes. Additional testing for hematuria may be worthwhile in countries with a high prevalence of glomerular diseases. The condition of patients with positive test results for CKD should be evaluated and treated according to established guidelines for CKD [1]. In principle, earlier evaluation of the condition would increase the number of patients with CKD who receive treatment and should increase the effectiveness of such treatment by beginning it at an earlier stage of the disease. In the USA, the incidence of kidney failure due to diabetes is now declining among young whites [6], likely due to their being tested for albuminuria and treated with angiotensin-converting enzyme inhibitors and angiotensin-receptor blockers. These improved outcomes need to be extended to young blacks and to older people.
Surveillance
CKD surveillance programs could focus initially on patients with severe CKD (stages 4, 5). These patients are at greatest risk for CVD and death, for the occurrence of common and treatable complications of decreased GFR, such as hypertension, anemia, malnutrition, and bone and mineral disease, and for progression to kidney failure. Specific treatments are now available for each of these complications and to slow progression, yet, many studies demonstrate suboptimal utilization of effective therapies [18]. In the USA, the average age of people with CKD stage 4 is 75 years, and more than 95% have two or more complications of decreased GFR [1, 5]. In one study, 46% died and 18% were treated by dialysis and transplantation during an average follow-up of 3.1 years [8]. Current guidelines now recommend referral of all patients with CKD stages 4–5 to nephrologists for specialized care and for preparation for dialysis and transplantation where these treatments are offered [1]. Many countries have surveillance programs for patients treated by dialysis and transplantation. However, these programs do not include people with severe CKD who die before the onset of kidney failure or who are not treated with dialysis and transplantation despite the onset of kidney failure. In principle, a surveillance program for CKD stages 4–5 would enable all countries to monitor the magnitude and the care of this high-risk, high-cost population, and possibly to reduce the risk of progression to kidney failure and reduce the cost of dialysis and transplantation.
A surveillance program for patients with CKD stage 3 would reach many more people (Table 1) and might be an effective way to lower rates of CVD and death, especially among the elderly with CVD risk factors or CVD. However, a larger surveillance program would require more resources. One possible strategy would be first to implement a surveillance program directed at CKD stages 4–5, then to use the experience gained to implement a program directed at high-risk subgroups of CKD stage 3.
Prevention
It is not too ambitious to consider CKD prevention. Hypertension and diabetes are the major causes of CKD in developed nations. In developing nations, chronic viral infections may contribute substantially to the burden of CKD from glomerular diseases. Strong, effective public health policies focusing on prevention, detection and treatment of these common chronic diseases may reduce the risk of developing CKD. Reduction in the incidence and prevalence of CKD could be a measure of success of public health programs for these other chronic diseases.
Improving and paying for patient care
Detection, surveillance and prevention programs will bring more patients with CKD and CKD risk factors into the health care delivery system. As for all chronic diseases, commitment and innovation will be necessary to treat more patients, improve quality and remain within public and employer group health plan budgets. Partnerships with government and payers are necessary to establish appropriate measures, standardized information technology platforms, appropriate incentives for improving quality, responsible analysis of the cost of care, and novel reimbursement methods.
Research
Finally, a health care policy for CKD must include investment in basic and clinical research. Research priorities could include studies of the causes of CKD, its progression, complications and relationship to CVD and aging; new markers of kidney damage and better estimating equations for GFR; new treatments to slow progression, ameliorate complications of decreased GFR, and reduce CVD risk; and more effective strategies to implement existing and new treatments across populations.
What should nephrologists do?
Nephrologists cannot care for all those with CKD, but we must join the effort to focus worldwide attention on CKD. We can educate our colleagues, government officials and the public that CKD is common, harmful, and, most importantly, that we have treatment. We can participate with professional, public and governmental groups to develop public health policy for CKD. We can work collaboratively with primary care physicians and other specialists to establish care models, within nephrology and within primary care, including clear recommendations for consultation, co-management and communication among treating physicians. We can develop estimates for the nephrology workforce to care for CKD, and we can develop strategies to train and maintain the workforce. We can improve the quality of care for patients with CKD stages 4–5. Nephrologists will continue to shoulder the burden of care for these severely ill and challenging patients, and we must strive to do so with diligence, technical skill, and compassion. We must recognize that improving the care and outcomes for CKD is a long process. World Kidney Day 2007 is an opportunity to begin this process. Hereafter, each year on World Kidney Day, we should measure our progress.
Andrew S. Levey, MD
Editor-in-Chief, American Journal of Kidney Diseases
Sharon P. Andreoli, MD
President, American Society of Pediatric Nephrology
Thomas DuBose, MD
President, American Society of Nephrology
Robert Provenzano, MD
President, Renal Physicians Association
Allan J. Collins, MD, FACP
President, National Kidney Foundation
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Levey, A.S., Andreoli, S.P., DuBose, T. et al. Chronic kidney disease: common, harmful and treatable—World Kidney Day 2007. Pediatr Nephrol 22, 321–325 (2007). https://doi.org/10.1007/s00467-006-0423-9
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DOI: https://doi.org/10.1007/s00467-006-0423-9