Budget Impact Associated With Converting Dialysis Patients With a High Pill Burden on Sevelamer to Lanthanum Carbonate: Opportunities for Cost-Efficiencies

2013 ◽  
Vol 61 (4) ◽  
pp. B66
2014 ◽  
Vol 18 ◽  
pp. 2-8
Author(s):  
Ryoichi Ando ◽  
Satomi Yama ◽  
Tsuyoshi Ohnishi ◽  
Shunsuke Iwamoto ◽  
Hitoshi Kimura ◽  
...  

2014 ◽  
Vol 34 (7) ◽  
pp. 749-757 ◽  
Author(s):  
Frank X. Liu ◽  
Surrey M. Walton ◽  
Robert Leipold ◽  
Deborah Isbell ◽  
Thomas A. Golper

Background The economic burden of treating end-stage renal disease (ESRD) continues to grow. As one response, effective January 1, 2011, Medicare implemented a bundled prospective payment system (PPS, including injectable drugs) for dialysis patients. This study investigated the 5-year budget impact on Medicare under the new PPS of changes in the distribution of patients undergoing peritoneal dialysis (PD), in-center hemodialysis (ICHD), and home hemodialysis (HHD). Methods An Excel-based budget impact model was created to assess dialysis-associated Medicare costs. The model accounted for dialysis access establishment, the current monthly capitation physician payment for ESRD, Medicare dialysis payments (including start-up costs), training, oral drug costs, and the costs and probabilities of adverse events including access failure, hospitalization for access infection, pneumonia, septicemia, and cardiovascular events. United States Renal Data System (USRDS) data were used to project the US Medicare dialysis patient population across time. The baseline scenario assumed a stable distribution of PD (7.7%), HHD (1.3%) and ICHD (91.0%) over 5 years. Three comparison scenarios raised the proportions of PD and HHD by ( 1 ) 1% and 0.5%, ( 2 ) 2% and 0.75%, and ( 3 ) 3% and 1% each year; a fourth scenario held HHD constant and lowered PD by 1% per year. Results Under the bundled PPS, scenarios that increased PD and HHD from 7.7% and 1.3% over 5 years resulted in cumulative savings to Medicare of $114.8M (Scenario 1, 11.7% PD and 3.3% HHD at year 5), $232.9M (Scenario 2, 15.7% PD and 4.3% HHD at year 5), and $350.9M (Scenario 3, 19.7% PD and 5.3% HHD at year 5). When the PD population was decreased from 7.7% in 2013 to 3.7% by 2017 with a constant HHD population, the total Medicare payment for dialysis patients increased by over $121.2M. Conclusions Under Medicare bundled PPS, increasing the proportion of patients on PD and HHD vs ICHD could generate substantial savings in dialysis-associated costs to Medicare.


2019 ◽  
Vol 34 (Supplement_1) ◽  
Author(s):  
Berfu Korucu ◽  
Ozant Helvaci ◽  
Rezzan Eren Sadioglu ◽  
Burak Ozbas ◽  
Hasan Yeter ◽  
...  

2018 ◽  
Vol 47 (3) ◽  
pp. 153-161 ◽  
Author(s):  
Kamyar Kalantar-Zadeh ◽  
Vidhya Parameswaran ◽  
Linda H. Ficociello ◽  
Ludmila Anderson ◽  
Norma J. Ofsthun ◽  
...  

Background: A database analysis was conducted to assess the effectiveness of sucroferric oxyhydroxide (SO) on lowering serum phosphorus and phosphate binder (PB) pill burden among adult peritoneal dialysis (PD) patients prescribed SO as part of routine care. Methods: Adult PD patients (n = 258) prescribed SO through a renal pharmacy service were analyzed. Baseline was 3 months before SO prescription. SO-treated follow-up was for 6 months or until either a new PB was prescribed, SO was not refilled, PD modality changed, or patient was discharged. In-range serum phosphorus was defined as ≤5.5 mg/dL. Results: At baseline, mean serum phosphorus was 6.59 mg/dL with 10 prescribed PB pills/day. The proportion of patients achieving in-range serum phosphorus increased by 72% from baseline to month 6. Prescribed PB pills/day decreased by 57% (10 at baseline to 4.3 at SO follow-up, p < 0.0001). The mean length of SO follow-up was 5.1 months; SO follow-up ended for 38, 27, and 50 patients at months 4, 5, and 6, respectively, due to no further PB fills, and for 10, 11, and 4 patients at months 4, 5, and 6, respectively, due to another PB prescribed. In patients with baseline serum phosphorus >5.5 mg/dL who achieved in-range serum phosphorus during SO follow-up for ≥1 quarter, a notable improvement in serum phosphorus (6.54 to 5.10 mg/dL, p < 0.0001) was observed, and there was a 53% reduction in PB pill burden (9.9 to 4.7, p < 0.0001). Conclusion: Among PD patients prescribed SO as part of routine care, improvements in serum phosphorus control and >50% reduction in PB pills/day were observed.


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