Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Association of pre-ESRD care education with patient outcomes in a 10-year longitudinal study of patients with CKD stages 3–5 in Taiwan


There is little comprehensive education for people with end-stage renal disease (ESRD) progress. We investigated the differences in terms of outcomes between patients with CKD stages 3–5 who enrolled and did not enroll in the pre-ESRD care education in Taiwan. This retrospective cohort study was conducted using data from the National Health Insurance Research Database (NHIRD). All patients diagnosed with CKD stages 3–5 who received the pre-ESRD care education through the pay for performance (P4P) program were enrolled. Based on whether or not they participated in the program, they were categorized into P4P or non-P4P groups. All analyses were performed from January 2006 through December 2015. Study outcomes were risk of hemodialysis dependency, hospitalization, and all-cause mortality. In this study of 29,337 patients, those with CKD stages 3–5 in the P4P group had lower events of hemodialysis, hospitalization, and all-cause mortality compared to patients in the non-P4P group. This study suggested that pre-ESRD care education is associated with increased patient outcomes, resulting in lower hemodialysis and hospitalization events and a higher overall survival rate in patients with CKD stages 3–5. Patient education could raise opportunities to improve pre-ESRD care by reaching patients outside the traditional health care setting.


The prevalence of chronic kidney disease (CKD) in Taiwan is approximately 11.9% higher and affects more than 2.5 million people1. Recent data on prevalence rates of CKD stages in Taiwan showed that CKD 3A, 3B, 4, and 5 were 8.3%, 1.9%, 0.3%, and 0.2%, respectively2. A systematic review and meta-analysis of 100 observational studies indicated that global prevalence of CKD stage 3, CKD stage 4, and CKD stage 5 were 7.6% (6.4–8.9%), 0.4% (0.3–0.5%), and 0.1% (0.1–0.1%), respectively3. CKD has a high global prevalence with a constant estimated global prevalence of CKD with majority stage 33. Therefore, CKD is a global health issue with a high economic cost associated with increased cardiovascular morbidity, early mortality, and decreased life quality4.

It has been widely reported that CKD with end-stage renal disease (ESRD) progress is primarily associated with accelerated hypertension, diabetes mellitus (DM), gout, primary renal disorders, older age, and drug side effects5. Moreover, CKD progression with reduced glomerular filtration rate has been associated with increased cardiovascular disease (CVD) risk4,6, greater severity of vascular disease7,8,9, increased all-cause, and CVD mortality10,11, acute stroke12,13, and increased mortality in heart failure14,15,16. It is crucial to ameliorate a decrease in the glomerular filtration rate and educate CKD patients to prevent kidney disease progress through multidisciplinary care education programs.

In terms of CKD prevention and treatment, the main goal is to slow the CKD progression to ESRD and its subsequent adverse effects through early CKD diagnosis and control of the underlying causes. In addition to these strategies, multidisciplinary care education programs have been widely adopted during CKD treatment, and they resulted in a more effective therapy, slowing the CKD progression to ESRD, and improving dialysis quality17,18,19,20. Thus, it is crucial to include care education programs in the prevention and treatment of CKD.

Pay for performance (P4P) programs used for pre-end-stage renal disease (pre-ESRD) care education in Taiwan is a proper strategy and a promising approach through value-based purchasing on incentives and renal indicators to improve health care quality and disease prognosis for CKD stages 3–5 patients since 200621,22. In other words, the P4P is an encouraging approach to improving health care quality and self-awareness education by connecting financial incentives to supplier performance. The rationale for the initiative is that by explicitly paying for recommended care, quality improvement can be promoted, resulting in better patient outcomes21,22. Under this financial incentive program, nephrologists are asked to provide care by more closely following clinical guidelines and by a multidisciplinary care team21,22. Before P4P programs began, health care providers were traditionally involved in improving CKD care through multidisciplinary care education programs without financial incentives23. This multidisciplinary care has become a focal point for discussing the cases of different professionals with the ultimate goal of establishing a consensus on the diagnosis, education, evaluation, and treatment of patients24,25,26,27,28. In addition, as reported previously, multidisciplinary care education programs have been introduced to assist quality of care, including CKD, dialysis, chronic obstructive pulmonary disease, and coronary artery disease, and DM in many countries17,29,30,31,32,33,34. However, there are few studies on the efficiency of pre-ESRD care education with P4P programs in improving the pre-dialysis outcomes. In this study, using the National Health Insurance Research Database (NHIRD), we explored the outcomes of pre-ESRD care education in patients with CKD stage 3–5 who benefited of the P4P program in Taiwan.


Data sources

The ethical committee, the Institutional Review Board of the Tri-Service General Hospital, approved this retrospective study (TSGH IRB No. B-109-10) and all experimental protocols. Also, informed consent was waived by the ethical committee of the Tri-Service General Hospital. All methods were carried out in accordance with relevant guidelines and regulations. The Taiwan National Health Insurance system is a universal single-payer insurance system and enrolled all these insurance schemes into a single national insurance system. The NHIRD provides longitudinal databases with a detailed description of the database guidelines and regulations which randomly sampled two million beneficiaries from the original NHIRD35. The representativeness of NHIRD has been validated by Taiwan’s National Health Research Institutes35. In this study, we obtained the original data of Taiwan NHIRD, which ranged between 2000 and 2015, to investigate the outcome of the P4P programs for pre-ESRD care education in patients with CKD stage 3–5 since 2006. This study enrolled all patients diagnosed with CKD stages 3–5 who received the P4P program linked with the NHIRD. All the target patients were identified based on the Clinical Modification (ICD-9-CM) codes determined by the International Classification of Diseases (Ninth Revision). If patients with CKD stages 3–5 had enrolled in the P4P program before dialysis, they were allocated to the P4P group. The information related to the cohort identification was collected for a period of 10 years, specifically from 2006 to 2015.

Study design and outcomes

Using the Taiwan NHIRD, the subjects were enrolled in the following two groups: P4P and non-P4P. This study was conducted using the data from the inpatient and outpatient claims recorded between 2006 and 2015. The P4P group comprised patients with CKD stages 3–5 who received the complete P4P program and had no dialysis records. The control group, referred to as the non-P4P group, included patients with CKD stages 3–5 who did not receive the complete P4P program and had no dialysis records in the database.

We excluded patients whose age and sex was not recorded, who were aged < 40 years, for whom a minimum of two years of data was unavailable after the initiation of the program, who had a history of cancer and human immunodeficiency virus, and who received renal replacement therapy and kidney transplantation before the initiation of the P4P program. The last exclusion criterion was applied to ensure that ESRD with renal replacement therapy occurred only after the initiation of the P4P program.

The index date was defined as the onset date of the P4P program initiation. The study follow-up period started from this date and lasted until the onset date of ESRD, with the endpoints being the occurrence of dialysis therapy or kidney transplantation, hospitalization, and mortality events due to any cause. We assigned a date to the control patients who did not receive the P4P program, which matched their corresponding case patients (referred to as the index date).

Finally, in this cohort study, cases and controls were matched according to age, gender, socioeconomic status, CKD stages 3–5, comorbidities (DM, hypertension, hyperlipidemia, myocardial infarction, congestive heart failure, cerebrovascular disease, chronic pulmonary disease, chronic liver disease, peptic ulcer, and dementia), and medications used in the six months before program initiation (specifically: metformin, sulfonylureas, thiazolidinediones, α-glucosidase inhibitors, dipeptidyl peptidase 4, insulins, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, beta-blockers, calcium channel blockers, diuretics, antiplatelet drugs, statins, nonsteroidal anti-inflammatory drugs, and steroids). The incidence density sampling approach was used to match controls with each case according to age (± 1 year), sex, and the follow-up period of the P4P program initiation. This approach allowed the observation of both patient groups during similar periods, thereby eliminating the bias caused by differences in sampling time.

The study outcomes were the rate of dialysis dependency, hospitalization, and mortality. Dialysis dependency was measured from the date of dialysis initiation for at least three consecutive months or from the approval date appearing on the catastrophic illness certificate for ESRD, whichever occurred first, to ensure the actual need of dialysis and its administration. The dialysis modes included hemodialysis (HD) (ICD-9-CM procedure codes: 58027C, 58029C), and the participants were followed up to their first hospitalization. The outcome of interest was the first hospitalization for any cause reported in the NHI claim database after study initiation. Mortality within the 10-year follow-up period was considered noteworthy. Also, the causes of mortality after study initiation—such as ischemic heart disease, heart failure, arrhythmia, out-of-hospital cardiac arrest, cerebrovascular accident, infectious disease, and DM complications—were assessed based on the primary diagnostic codes entered in the inpatient and emergency claims 30 days before death. Patients were followed up from the index date to the earliest of the following events: outcome occurrence, death, disenrollment from the NHI program, or study end date (December 31, 2015).

Review of the P4P program for pre-ESRD care education

To enhance the quality of CKD care, the NHI Administration in Taiwan initiated the P4P program for pre-ESRD care education in 2006. The program’s multidisciplinary care members include nephrologists, nurses and dietitians and it enrolled patients with indications including individuals with CKD stage 3b (glomerular filtration rate (GFR) ~ 30–44.9 mL/min/1.73 m2) or CKD stage 4 (GFR ~ 15–29.9 mL/min/1.73 m2) or CKD stage 5 (GFR < 15 mL/min/1.73 m2), and heavy proteinuria regardless of CKD stage (24-h urine total protein excretion > 1,000 mg or urine protein and creatinine ratio > 1,000 mg/g). Besides offering an appropriate CKD education knowledge, the multidisciplinary care team could track the patient health status and provide nephrologists and family members with the necessary information and communication. The care indicators included renal function maintenance, improvement of proteinuria, continuous multidisciplinary care, pre-inserted HD access, and CKD management and education.


Baseline demographics and clinical characteristics were recorded before obtaining the index date. Socioeconomic status was based on monthly income calculated from the insurance premium provided in the patient enrollment profile, and it was divided into six categories. CKD stages were divided into 3, 4, and 5 based on the ICD code. The comorbidities included DM, hypertension, hyperlipidemia, myocardial infarction, congestive heart failure, cerebrovascular disease, chronic pulmonary disease, chronic liver disease, peptic ulcer, and dementia. We collected the data of patients who had received medications within six months before the index date. The prescribed medications included DM and non-DM medications; among DM medications were insulins, biguanides, sulfonylureas, meglitinides, α-glucosidase inhibitors, and thiazolidinediones; while the non-DM medications included angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, nonselective and selective beta-blockers, calcium channel blockers, loop diuretics, aspirin, and statins. The ICD-9-CM disease diagnostic codes used for previous or coexisting diseases, and the Anatomical Therapeutic Chemical codes used for medications are listed in Supplemental Table 1.

Statistical analysis

Statistical analyses were performed in S.A.S. (S.A.S. System for Windows, version 9.1.3; S.A.S. Institute, Cary, NC, USA). The χ2 test and t-test were used to analyze and evaluate the differences in age or comorbidities and medications between the P4P and non-P4P groups to assure proper matching. Fisher's exact test was applied for categorical variables. The Cox proportional regression hazards model was used to compare the incidence rates of dialysis dependency/kidney transplant, hospitalization, and mortality between the two groups, after modifying comorbidities. The Kaplan–Meier method and the log-rank test were used to estimate the outcomes of the two groups. A two-tailed P value < 0.05 was considered statistically significant.


Study selection

This study enrolled a total of 32,231 individuals diagnosed with CKD stages 3–5 who received the P4P program for the first time, and 2,894 of these were excluded (specifically, those with CKD stages 3–5/P4P before the index date, HD before tracking, without tracking, and of unknown gender). After applying the exclusion criteria and the propensity score matching according to CKD stage, gender, age, comorbidities, medication, and index date, a total of 29,337 patients with matched controls participating in the P4P program were enrolled in this study, as shown in Fig. 1. During the 10-year follow-up study, we identified 14,182 HD events (48.3%), 13,099 hospitalization events (44.6%), and 7,352 mortality events (25.0%) in the P4P group and 18,165 HD events (61.9%), 15,510 hospitalization events (52.8%), and 9,534 mortality events (32.5%) in the control group.

Figure 1
figure 1

Cohort Assembly in This Study. Abbreviations: CKD = chronic kidney disease; HD = hemodialysis; P4P = pay for performance program.

Study characteristics

The baseline characteristics of P4P patients with CKD stages 3–5 and those of controls are shown in Table 1. No differences were observed in gender, age, insurance premiums, comorbidity, and medication between the groups. The P4P group was associated with a significantly decreased risk of HD, hospitalization, and all-cause mortality events (log-rank P < 0.001), as shown by the respective Kaplan–Meier curves for cumulative risks in Fig. 2. The HD events were lower in the P4P patients than in the control group from the second year of follow-up to the 10th year.

Table 1 Baseline characteristics of study subjects.
Figure 2
figure 2

Kaplan–Meier Curves for the Cumulative Incidence of (A) Hemodialysis, (B) Hospitalization, and (C) All-cause Mortality with Log-Rank Test in Patients with CKD Stages 3–5 Enrolled or Not in the Pay for Performance Program Intervention.

Study outcome

The adjusted hazards ratios (aHR) of HD, hospitalization, and all-cause mortality events in patients with CKD stages 3–5 in the P4P group and the matched controls are presented in Table 2. Results showed that these patients had fewer events of HD [aHR, 0.766; 95% confidence interval CI 0.746–0.797; P < 0.001], hospitalization (aHR, 0.790; 95% CI 0.766–0.814; P < 0.001), and mortality (aHR, 0.794; 95% CI 0.766–0.823; P < 0.001) than the control subjects during the follow-up period, after adjusting for age, sex, insurance premium, comorbidities, urbanization level, patient care quality, area of residence in Taiwan. Regardless of CKD stages, comorbidities and medication, the P4P program proved effective, contributing to a decrease in HD, hospitalization, and all-cause mortality events.

Table 2 Hazard ratio of hemodialysis, hospitalization, and mortality in patients with CKD stages 3–5 in the pay for performance program in the cox model with competing risks.

The median follow-up periods in the P4P and control groups were 5.87 ± 6.46 and 6.91 ± 6.42 years, respectively (Table 3). The onset duration values for CKD stages 3–5 in P4P patients in relation to HD, hospitalization, and mortality events were 2.52 ± 2.44, 2.86 ± 2.70, and 3.47 ± 2.80 years, respectively. In contrast, the duration of the same events in the matched control group was 2.28 ± 2.22, 2.53 ± 2.46, and 3.43 ± 2.81 years, respectively. The P4P patients showed delayed HD, hospitalization, and all-cause mortality compared to patients in the matched control group during the follow-up course.

Table 3 Years to hemodialysis, hospitalization, and mortality in patients with CKD stages 3–5 with or without pay for performance program.


The purpose of pre-ESRD care education is to ameliorate patients’ conditions and counteract the progression of CKD-to-ESRD. Our study explored the outcomes of the P4P program for pre-ESRD care education in patients with CKD stages 3–5. After performing multivariate adjustments and subgroup analysis, our results indicated that the P4P program had beneficial effects on patient outcomes, such as lower HD, hospitalization, and all-cause mortality events.

Preventing CKD development and its complications is possible through early diagnosis and by treating any underlying disease to slow its progression. Pre-ESRD care education is an effective and beneficial strategy for CKD prognosis. Devins GM et al. found that it delayed dialysis time in a prospective, randomized and controlled trial36, which was similarly found in our study. The authors suggested that pre-ESRS care education is an essential approach to delay CKD progression and extend time to dialysis therapy in patients with advanced CKD36. A randomized trial of a pre-ESRD care education two-phase intervention (phase 1 using educational booklets and video; phase 2 using an interactive educational group session) significantly increased the self-care dialysis ability37. Furthermore, innovative education methods, including family and community engagement, self-management care, shared decision-making, and digital media, were also proved as additional successful tools38. The results of our study demonstrated again that pre-ESRD care education is essential for CKD prevention and treatment.

In relation to hospitalization risk in advanced CKD cases, a study of 170,897 patients who initiated dialysis with linked Medicare claims from the United States Renal Data System, showed a higher one-year mortality associated with pre-dialysis cardiovascular-related or infection-related hospitalization events39. In our study, data indicated that pre-ESRD care education effectively lowered hospitalization risk (aHR, 0.790; 95% CI 0.766–0.814; P < 0.001) in patients with advanced CKD. We observed that the decreased risk could be achieved through health education on dietary control, care continuity, and compliance with clinical guidelines, leading to an improved life quality and subsequent delay of complications in patients with advanced CKD.

Education is key to reducing mortality in patients with CKD. One study on patients sourced from the United States Renal Data System database showed that educational programs improved dialysis preparation and patient survival (aHR, 0.80; 95% CI, 0.68–0.94) in CKD patients40. Another study of 1,256,640 patients initiated on chronic dialysis sourced from the same database, also demonstrated that patients receiving pre-ESRD care education had a better survival rate than those without41, showing that the education program was associated with significantly higher pre-ESRD nephrologist care rates, preemptive transplant wait-listing, transplantation occurrences, and a lower mortality risk40,41. A meta-analysis of early versus late referrals to nephrologists indicated a significantly higher overall mortality, longer hospital stay, and early at the time of renal replacement therapy initiation in the late referrals compared with the early referrals42. It was previously reported in a study of 32,084 early CKD patients from the NHIRD in Taiwan that an early CKD P4P intervention resulted in a significantly better prognosis in all-cause mortality among matched participants in both P4P programs43. Furthermore, the analysis of advanced CKD cases in the present study confirmed that the P4P program for pre-ESRD care education is a crucial tool to improve survival and patient outcomes. Besides, we further analyzed the causes of all-cause mortality in patients with advanced CKD and observed that there were lower events of ischemic heart disease, heart failure, arrhythmia, out-of-hospital cardiac arrest, cerebrovascular accident, infectious disease, and DM complications in those patients receiving pre-ESRD care education. We infer that its main advantages reside in helping patients understand their disease, ameliorating conditions during treatment, and offering strategies to improve patients’ knowledge and outcomes.

Limitations of this study

This study minimized the selection bias and confounding factors by matching the control group for age, sex, comorbidities, and medications. To correct the confounding bias, we applied a propensity score from the baseline population to match the diversity in characteristics between P4P and non-P4P groups. Despite its strengths and novelty, this study has some limitations that require clarifications. First, the NHIRD does not provide individual laboratory data for further analysis. Second, personal habits and lifestyle cannot be obtained from the NHIRD.


This study indicated that the P4P program for pre-ESRD care education is an optimal strategy for achieving a higher quality nephrology care, as it was related to reduce the incidence of complications related to hemodialysis, hospitalization rate, and all-cause mortality. These findings suggested that patient education maybe plays an important role in the improvement of pre-ESRD care by reaching patients outside the traditional health care setting. The positive results of the education program are a slower disease progression, lifestyle changes, and the achievement of interdisciplinary care education in group settings.



Chronic kidney disease


Diabetes mellitus


End-stage renal disease


National Health Insurance Research Database


Pay for performance


  1. Tsai, M. H. et al. Incidence, prevalence, and duration of chronic kidney disease in Taiwan: Results from a community-based screening program of 106,094 individuals. Nephron 140, 175–184 (2018).

    PubMed  Google Scholar 

  2. Wu, M. J. et al. High risk of renal failure in stage 3B chronic kidney disease is under-recognized in standard medical screening. J. Chin. Med. Assoc. 73, 515–522 (2010).

    PubMed  Google Scholar 

  3. Hill, N. R. et al. Global prevalence of chronic kidney disease—A systematic review and meta-analysis. PLoS ONE 11, e0158765 (2016).

    PubMed  PubMed Central  Google Scholar 

  4. Go, A. S., Chertow, G. M., Fan, D., McCulloch, C. E. & Hsu, C. Y. Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization. N Engl. J. Med. 351, 1296–1305 (2004).

    CAS  PubMed  Google Scholar 

  5. Gansevoort, R. T. et al. Chronic kidney disease and cardiovascular risk: Epidemiology, mechanisms, and prevention. Lancet 382, 339–352 (2013).

    PubMed  Google Scholar 

  6. Di Angelantonio, E., Danesh, J., Eiriksdottir, G. & Gudnason, V. Renal function and risk of coronary heart disease in general populations: New prospective study and systematic review. PLoS Med 4, e270 (2007).

    PubMed  PubMed Central  Google Scholar 

  7. Abaci, A. et al. Renal dysfunction is the most important predictor of the extent and severity of coronary artery disease in patients with diabetes mellitus. Coron. Artery Dis. 18, 463–469 (2007).

    PubMed  Google Scholar 

  8. Weiner, D. E. et al. Chronic kidney disease as a risk factor for cardiovascular disease and all-cause mortality: A pooled analysis of community-based studies. J. Am. Soc. Nephrol. 15, 1307–1315 (2004).

    PubMed  Google Scholar 

  9. Ford, I. et al. Reduced glomerular filtration rate and its association with clinical outcome in older patients at risk of vascular events: Secondary analysis. PLoS Med. 6, e16 (2009).

    PubMed  Google Scholar 

  10. Chronic Kidney Disease Prognosis. Association of estimated glomerular filtration rate and albuminuria with all-cause and cardiovascular mortality in general population cohorts: A collaborative meta-analysis. Lancet 375, 2073–2081 (2010).

    Google Scholar 

  11. Van Biesen, W. et al. The glomerular filtration rate in an apparently healthy population and its relation with cardiovascular mortality during 10 years. Eur. Heart J. 28, 478–483 (2007).

    PubMed  Google Scholar 

  12. Zhang, R. et al. Decreased glomerular filtration rate is associated with mortality and cardiovascular events in patients with hypertension: A prospective study. PLoS ONE 6, e27359 (2011).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  13. Lee, M. et al. Low glomerular filtration rate and risk of stroke: Meta-analysis. BMJ 341, c4249 (2010).

    PubMed  PubMed Central  Google Scholar 

  14. Chen, Z. et al. Estimated glomerular filtration rate is associated with an increased risk of death in heart failure patients with preserved ejection fraction. Front Cardiovasc. Med. 8, 643358 (2021).

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Damman, K. et al. Worsening renal function and prognosis in heart failure: systematic review and meta-analysis. J. Card Fail 13, 599–608 (2007).

    PubMed  Google Scholar 

  16. Heywood, J. T. et al. High prevalence of renal dysfunction and its impact on outcome in 118,465 patients hospitalized with acute decompensated heart failure: A report from the ADHERE database. J. Card Fail 13, 422–430 (2007).

    PubMed  Google Scholar 

  17. Desai, A. A., Garber, A. M. & Chertow, G. M. Rise of pay for performance: Implications for care of people with chronic kidney disease. Clin. J. Am. Soc. Nephrol. 2, 1087–1095 (2007).

    PubMed  Google Scholar 

  18. Bayliss, E. A., Bhardwaja, B., Ross, C., Beck, A. & Lanese, D. M. Multidisciplinary team care may slow the rate of decline in renal function. Clin. J. Am. Soc. Nephrol. 6, 704–710 (2011).

    PubMed  PubMed Central  Google Scholar 

  19. Chen, Y. R. et al. Effectiveness of multidisciplinary care for chronic kidney disease in Taiwan: A 3-year prospective cohort study. Nephrol. Dial. Transplant 28, 671–682 (2013).

    CAS  PubMed  Google Scholar 

  20. Chen, P. M. et al. Multidisciplinary care program for advanced chronic kidney disease: Reduces renal replacement and medical costs. Am. J. Med. 128, 68–76 (2015).

    ADS  PubMed  Google Scholar 

  21. Lin, M. Y. et al. Effect of national pre-ESRD care program on expenditures and mortality in incident dialysis patients: A population-based study. PLoS ONE 13, e0198387 (2018).

    PubMed  PubMed Central  Google Scholar 

  22. Hsieh, H. M. et al. Economic evaluation of a pre-ESRD pay-for-performance programme in advanced chronic kidney disease patients. Nephrol. Dial. Transplant 32, 1184–1194 (2017).

    PubMed  Google Scholar 

  23. Goldstein, M., Yassa, T., Dacouris, N. & McFarlane, P. Multidisciplinary predialysis care and morbidity and mortality of patients on dialysis. Am. J. Kidney Dis. 44, 706–714 (2004).

    PubMed  Google Scholar 

  24. Harris, D. L., Henry, R. C., Bland, C. J., Starnaman, S. M. & Voytek, K. L. Lessons learned from implementing multidisciplinary health professions educational models in community settings. J. Interprof Care 17, 7–20 (2003).

    PubMed  Google Scholar 

  25. Howard, J. P., Bruce, J. & Powell-Tuck, J. Nutritional support: A course for developing multidisciplinary clinical teams. Education Committee, British Association for Parenteral and Enteral Nutrition. J. R Soc. Med. 90, 675–678 (1997).

    CAS  PubMed  PubMed Central  Google Scholar 

  26. MacDonald, N. Limits to multidisciplinary education. J. Palliat Care 12, 6 (1996).

    CAS  PubMed  Google Scholar 

  27. Moss, L. Thyroid Cancer Forum-UK (TCF-UK): a free, independent, multidisciplinary education resource and peer support organisation for consultants. Clin. Oncol. (R Coll Radiol) 22, 508–511 (2010).

    CAS  Google Scholar 

  28. Wright, I. M., Wake, C. H., Anderson, H. & Graham, S. Assessment of the multidisciplinary education for a major change in clinical practice; a prospective cohort study. BMC Health Serv. Res. 9, 28 (2009).

    PubMed  PubMed Central  Google Scholar 

  29. Hemmelgarn, B. R. et al. Association between multidisciplinary care and survival for elderly patients with chronic kidney disease. J. Am. Soc. Nephrol. 18, 993–999 (2007).

    PubMed  Google Scholar 

  30. Karunaratne, K. et al. The impact of pay for performance on the control of blood pressure in people with chronic kidney disease stage 3–5. Nephrol. Dial Transplant 28, 2107–2116 (2013).

    CAS  PubMed  Google Scholar 

  31. Kondo, M. et al. Cost-effectiveness of chronic kidney disease mass screening test in Japan. Clin. Exp. Nephrol. 16, 279–291 (2012).

    PubMed  Google Scholar 

  32. Kuzma, A. M. et al. Multidisciplinary care of the patient with chronic obstructive pulmonary disease. Proc. Am. Thorac Soc. 5, 567–571 (2008).

    PubMed  PubMed Central  Google Scholar 

  33. Sandhoff, B. G., Kuca, S., Rasmussen, J. & Merenich, J. A. Collaborative cardiac care service: A multidisciplinary approach to caring for patients with coronary artery disease. Perm. J. 12, 4–11 (2008).

    PubMed  PubMed Central  Google Scholar 

  34. Odgers-Jewell, K. et al. Effectiveness of group-based self-management education for individuals with Type 2 diabetes: A systematic review with meta-analyses and meta-regression. Diabet Med. 34, 1027–1039 (2017).

    CAS  PubMed  Google Scholar 

  35. Hsieh, C. Y. et al. Taiwan’s national health insurance research database: past and future. Clin. Epidemiol. 11, 349–358 (2019).

    PubMed  PubMed Central  Google Scholar 

  36. Devins, G. M., Mendelssohn, D. C., Barre, P. E. & Binik, Y. M. Predialysis psychoeducational intervention and coping styles influence time to dialysis in chronic kidney disease. Am. J. Kidney Dis. 42, 693–703 (2003).

    PubMed  Google Scholar 

  37. Manns, B. J. et al. The impact of education on chronic kidney disease patients’ plans to initiate dialysis with self-care dialysis: A randomized trial. Kidney Int. 68, 1777–1783 (2005).

    PubMed  Google Scholar 

  38. Narva, A. S., Norton, J. M. & Boulware, L. E. Educating patients about CKD: The path to self-management and patient-centered care. Clin. J. Am. Soc. Nephrol. 11, 694–703 (2016).

    CAS  PubMed  Google Scholar 

  39. Shah, S., Meganathan, K., Christianson, A. L., Leonard, A. C. & Thakar, C. V. Pre-dialysis acute care hospitalizations and clinical outcomes in dialysis patients. PLoS ONE 14, e0209578 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  40. Kurella Tamura, M. et al. Educational programs improve the preparation for dialysis and survival of patients with chronic kidney disease. Kidney Int. 85, 686–692 (2014).

    PubMed  Google Scholar 

  41. Nee, R., Fisher, E., Yuan, C. M., Agodoa, L. Y. & Abbott, K. C. Pre-end-stage renal disease care and early survival among incident dialysis patients in the US military health system. Am. J. Nephrol. 45, 464–472 (2017).

    PubMed  Google Scholar 

  42. Chan, M. R., Dall, A. T., Fletcher, K. E., Lu, N. & Trivedi, H. Outcomes in patients with chronic kidney disease referred late to nephrologists: a meta-analysis. Am. J. Med. 120, 1063–1070 (2007).

    PubMed  Google Scholar 

  43. Liao, P. J. et al. Long-term and interactive effects of pay-for-performance interventions among diabetic nephropathy patients at the early chronic kidney disease stage. Medicine (Baltimore) 95, e3282 (2016).

    Google Scholar 

Download references


We want to acknowledge the authors and other investigators of the articles included in this study for their valuable contributions.


This study was supported by the Tri-Service General Hospital Research Foundation (TSGH-B-110012) and was financially sponsored by the Taipei Medical University (TMU108-AE1-B23). We also appreciate the Health and Welfare Data Science Center, Ministry of Health and Welfare (HWDC, MOHW), Taiwan, for providing the National Health Insurance Research Database (NHIRD).

Author information

Authors and Affiliations



C.L.C., C.H.C., Y.H.H., and W.C.C. involved in the conception of the study protocol, the design, selection of articles, data extraction, statistical analysis, and manuscript writing of this review. C.H.C. and W.C.C. were involved in the selection of articles, data extraction, and reviewing and editing the final manuscript. All authors approved the final manuscript.

Corresponding authors

Correspondence to Yung-Ho Hsu or Wu-Chien Chien.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Chou, CL., Chung, CH., Chiu, HW. et al. Association of pre-ESRD care education with patient outcomes in a 10-year longitudinal study of patients with CKD stages 3–5 in Taiwan. Sci Rep 11, 22602 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing