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Standardized Emergency Department Encounter Ratio (SEDR) for Dialysis Facilities

CBE ID
3565
Endorsement Status
1.0 New or Maintenance
1.1 Measure Structure
Previous Endorsement Cycle
Is Under Review
Yes
Next Maintenance Cycle
Spring 2026
1.6 Measure Description

The Standardized Emergency Department Encounter Ratio is the ratio of the observed number of emergency department (ED) encounters that occur for adult Medicare ESRD dialysis patients treated at a particular facility to the number of ED encounters that would be expected given the characteristics of the dialysis facility’s patients and the national event rate for dialysis facilities. Medicare patients include those with traditional Fee for Service Medicare and those with Medicare Advantage. The time period for the measure calculation is one calendar year. 

 

Note that for this measure an “ED encounter” always refers to an outpatient encounter that does not end in a hospital admission, but does include observation stays. This measure is calculated as a ratio but can also be expressed as a rate.

1.6a Material Specification Change(s)
Yes
1.6b Summary of Specification Changes

Since the previous endorsement cycle, we have made the following changes:

  1. Denominator:  the measure now includes Medicare Advantage (MA) patients that had previously been excluded due to lack of outpatient claims data.
  2. Risk Adjustment: the measure includes Medicare Advantage as a covariate in the risk adjustment model. 
    Measure Specs
      General Information
      1.7 Measure Type
      1.3 Electronic Clinical Quality Measure (eCQM)
      No
      1.8 Level of Analysis
      1.9 Care Setting
      1.9b Other Care Setting
      Dialysis Facility
      1.10 Measure Rationale

      Emergency department (ED) encounters are an important indicator of care coordination.  In addition, observation stays, generally defined as < 48 hours, have become more frequent since CMS adopted the “Two-Midnight rule” in 2013 to define more highly reimbursed inpatient care. Furthermore, the Hospital Readmissions Reduction Program placed further pressure on health systems to use observation stays to avoid triggering financial penalties. Traditional measures of inpatient hospitalization do not include outpatient ED encounters or observation stays and thus an important arena for unscheduled acute care had been largely unmeasured.

       

      More than half (55.0%) of all patients with ESRD visit the ED during their first year of dialysis, and patients with ESRD have a mean of 2.7 ED visits per patient-year [1]. This rate is 6-fold higher than the national mean for US adults in the general population [1]. Furthermore, the Lovasik study notes that among Medicare beneficiaries with ESRD, 30% of hospital admissions that originate in the ED are for diagnoses that are often dialysis-related such as complications of vascular access, congestive heart failure/fluid overload, septicemia, and hyperkalemia. A study by Zhang and colleagues reported that rates of ED visits among patients on thrice weekly in-center hemodialysis vary by dialysis schedule (Mon/Weds/Fri; Tues/Thurs/Sat) and by day of week [2]. For example, the ED visit rate (without hospital admission) was highest on the day following the longer interdialytic interval over the weekend (Mondays), suggesting an association with facility structure and treatment schedule. 

       

      Missed dialysis treatments are associated with an over two-fold higher risk of an ED visit, suggesting an opportunity for dialysis facilities to establish or strengthen facility practices that can help to reduce skipped or shortened treatments through increased communication, care coordination, and patient education. This, in turn, has the potential to reduce avoidable ED visits. Such a strategy was used by several dialysis providers participating in the Centers for Medicare and Medicaid Innovation’s Comprehensive End Stage Renal Disease Care model. For example, participants would keep an extra chair/station available at their facilities, or have arrangements with a sister facility to take a patient that needed an extra dialysis treatment. The result was more diversions of patients from the ED [3].  

       

      Finally, the CMS Centers for Medicare and Medicaid Innovation’s Comprehensive End Stage Renal Disease Care model, and more recent ETC and Kidney Care Choices Models emphasize care coordination as a central feature of care delivery in order to reduce unnecessary utilization and improve outcomes.  During the second performance year, the original Wave 1 cohort of ESCOs (ESRD Seamless Care Organizations) experienced about a 3% reduction in ED use relative to the period before the CEC model was launched [3-5]. 

      Measures of the frequency of ED use may help dialysis facility level efforts to prevent emergent unscheduled care and control escalating medical costs. 

       

      Inclusion of Medicare Advantage Patients

      Legislative changes that became effective in January 2021 removed barriers that had previously prevented ESRD patients from enrolling in Medicare Advantage (MA) plans.  In the subsequent years, there have been a substantial increase in the number of ESRD beneficiaries covered by MA plans, now approaching 45% of the dialysis population.  Unlike FFS beneficiaries, MA outpatient encounters and administrative records had not been readily available for analyzing facility quality, and so MA patients had been excluded from the previously endorsed version of this measure. With the recent availability of Part C Medicare Advantage encounter data, MA patients can now be included in this measure.  Adjustment for MA coverage is important in order to control for potential difference in outcomes related to coverage type since there is wide variation in the frequency of MA patients at the dialysis facility level.  In addition, our internal analyses indicate that MA patients have significantly higher rates of ED encounters compared to FFS patients. 

       

       While the currently endorsed version of this measure does not include MA patients, this submission includes MA patients by: (1) incorporating Part C outpatient encounter data to identify ED visits for MA patients, (2) addition of all prevalent comorbidity from Part C encounter data in comorbidity adjustment, and (3) adjusts for MA coverage by including a time dependent covariate.

       

      References:

      [1] Lovasik BP, Zhang R, Hockenberry JM, Schrager JD, Pastan SO, Mohan S, Patzer RE. Emergency Department Use and Hospital Admissions Among Patients With End-Stage Renal Disease in the United States. JAMA Intern Med. 2016 Oct 1; 176(10):1563-1565. 

       

      [2] Zhang S, Morgenstern H, Albertus P, Nallamothu B, He K, and Saran R. Emergency department visits and hospitalizations among hemodialysis patients by day of the week and dialysis schedule in the United States. PLOS ONE. https://doi.org/10.1371/journal.pone.0220966 August 15, 2019.

       

      [3] Marrufo G, Negrusa B, Ullman D, Hirth R, Messana J, Maughan B, Nelson J, Lindsey N, Gregory D, Svoboda R, Melin C, Chung A, Dahlerus C, Nahra T, Jiao A, McKeithen K, and Gilfix Z. Comprehensive End-Stage Renal Disease Care (CEC) Model. Performance Year 2 Annual Evaluation Report. Prepared for: Centers for Medicare & Medicaid Services. September 2019. https://innovation.cms.gov/Files/reports/cec-annrpt-py2.pdf

       

      [4] https://www.cms.gov/priorities/innovation/innovation-models/kidney-care-choices-kcc-model

       

      [5] https://www.cms.gov/priorities/innovation/innovation-models/esrd-treatment-choices-model

      1.11 Measure Webpage
      None.
      1.20 Types of Data Sources
      1.25 Data Source Details

      Data are derived from the EQRS patient-specific clinical and administrative data, including ESRD patient list, CMS-2728 Medical Evidence Form, CMS-2746 Death Notification Form, and patient admission and discharge data, from all Medicare certified dialysis facilities, the Medicare Enrollment Database (EDB), and Medicare claims data.  

       

      In addition, the database includes transplant data from the Scientific Registry of Transplant Recipients (SRTR), data from the Nursing Home Minimum Dataset, and the provider and survey and certification data from the Internet Quality Improvement and Evaluation System (iQIES) data.

       

      Information on ED visits is obtained from Medicare FFS and Part C outpatient claims, and past-year comorbidity data are obtained from multiple claim types (inpatient, home health, hospice (Part A only), skilled nursing facility claims).

       

      Fee-for-service (FFS) Medicare Part A (inpatient) and Part B (outpatient and physician supplier, hospice, home health, and skill nursing) claims for dialysis patients are included in the current database; additionally, the database incorporates Part C Medicare Advantage (MA) data for the MA enrollees. This database ensures that hospital, outpatient dialysis, and other billable services under Medicare – whether FFS or MA – are captured.

      1.14 Numerator

      The observed number of outpatient Emergency Department encounters among eligible adult Medicare patients at a facility during the reporting period.

      1.14a Numerator Details

      Emergency department (ED) encounters are identified from Medicare FFS and Part C outpatient claims using revenue center codes that indicate an ED visit (0450, 0451, 0452, 0453, 0454, 0455, 0456, 0457, 0458, 0459, 0981). We include both outpatient ED visits and those that result in an observation stay, but not those that result in a hospital admission. Outpatient ED claims that have overlapping or consecutive dates of service are combined and considered as a single ED encounter. To further ensure that these outpatient ED encounters are distinct from those associated with hospitalizations, we exclude ED encounters where there is an inpatient claim for the patient that has dates of service including any of the same time period covered by the ED encounter.

       

      The total number of emergency department encounters includes multiple encounters (i.e., second, third, etc.) for the same patient during the reporting period. 

       

      See denominator details for additional criteria for a patient to be assigned to a particular facility and criteria for identifying emergency department encounters.

       

      The time period for the measure calculation is one calendar year.

      1.15 Denominator

      The expected number of Emergency Department encounters among eligible Medicare patients at the facility during the reporting period adjusted for the characteristics of the patients at the facility.

      1.15a Denominator Details

      General Inclusion Criteria for Dialysis Patients 

      Adult patients are included in the measure only after they have had ESRD for greater than 90 days. This minimum 90-day period assures that patients are eligible for Medicare, either as their primary or secondary insurer, and that follow-up is complete. Thus, the measure excludes ED encounters during the first 90 days of ESRD as well as patients who die or recover kidney function during that time period. 

       

      In order to exclude patients who only received temporary dialysis therapy, we assign patients to a particular facility only after they have been on chronic dialysis there for the past 60 days. This 60-day period is used both for patients who started ESRD for the first time and for those who returned to dialysis after a failed transplant. Emergency Department encounters during the first 60 days of dialysis at a facility do not affect the facility’s Standardized Emergency Department Encounter Ratio.

       

      In order to assure completeness of information on ED encounters for all patients included in the analysis, we restrict to Medicare patients who are either enrolled in Medicare Advantage or who reach a certain threshold of Medicare outpatient dialysis and inpatient claims indicating that Medicare is the primary payor. Specifically, months within a given dialysis patient-period are used for the Standardized Emergency Department Encounter Ratio calculation when the patient is enrolled in Medicare Advantage or meets the criterion of being within two months after a month with either: (a) $1200+ of Medicare dialysis claims OR (b) at least one Medicare inpatient claim. 

       

      Identifying Facility Treatment Histories for Each Patient

      For each patient, we identify the dialysis provider at each point in time. Starting with day 91 after onset of ESRD, we attribute patients to facilities according to the following rules. A patient is attributed to a facility once the patient has been treated there for the past 60 days. When a patient transfers from one facility to another, the patient continues to be attributed to the original facility for 60 days and then is attributed to the destination facility. In particular, a patient is attributed to his or her current facility on day 91 of ESRD if that facility had treated him or her for the past 60 days. If on day 91, the facility had not treated a patient for the past 60 days, we wait until the patient reaches day 60 of continuous treatment at that facility before attributing the patient to that facility. When a patient is not treated in a single facility for a span of 60 days (for instance, if there were two switches within 60 days of each other), we do not attribute that patient to any facility. Patients who withdrew from dialysis or recovered kidney function remain assigned to their treatment facility for 60 days after withdrawal or recovery.

       

      If a period of one year passes with neither Medicare dialysis claims nor EQRS information to indicate that a patient was receiving dialysis treatment, we consider the patient lost to follow-up and do not include that patient in the analysis. If dialysis claims or other evidence of dialysis reappears, the patient is entered into analysis after 60 days of continuous therapy at a single facility.

       

      Days at Risk for Medicare Dialysis Patients

      After patient treatment histories are defined as described above, periods of follow-up in time since ESRD onset are created for each patient. To adjust for duration of ESRD appropriately, we define six time intervals with cut points at 3-6 months, 6-12months, 1-2 years, 2-3 years, 3-5 years, and 5+ years. A new time period begins each time the patient is determined to be at a different facility, or at the start of each calendar year or when crossing any of the above cut points. 

       

      The number of days at risk in each of the time intervals listed above is used to calculate the expected number of emergency department encounters for the patient during that period. The Standardized Emergency Department Encounter Ratio for a facility is the ratio of the total number of observed emergency department encounters to the total number of expected emergency department encounters during all time periods at the facility. Based on a risk adjustment model for the overall national emergency department encounter rate, we compute the expected number of emergency department encounters that would occur for each month that each patient is attributed to a given facility. The sum of all such expectations for patients and months yields the overall number of emergency department encounters that would be expected at the facility given the specific patient mix. This forms the denominator of the measure.

       

      The denominator of the Standardized Emergency Department Encounter Ratio is derived from a proportional rates model [3-5]. This is the recurrent event analog of the well-known proportional hazards or Cox model [2-3].  To accommodate large-scale data, we adopt a model with piecewise constant baseline rates [1] and the computational methodology developed in Liu, Schaubel and Kalbfleisch [3].

       

      References:

      [1] Cook, R. and Lawless, J. The Statistical Analysis of Recurrent Events. New York: Springer. 2007.

       

      [2] Cox, D.R. (1972) Regression Models and Life Tables (with Discussion). J. Royal statistical Society, Series B, 34, 187-220.

       

      [3] Kalbfleisch, J.D. and Prentice, R. L. The Statistical Analysis of Failure Time Data. Wiley, New York, 2002.

       

      [4] Lawless, J. F. and Nadeau, C. Some simple and robust methods for the analysis of recurrent events, Technometrics, 37 1995, 355-364.

       

      [5] Lin, D.Y., Wei, L.J., Yang, I. and Ying, Z. Semi parametric regression for the mean and rate functions of recurrent events, Journal of the Royal Statistical Society Series B, 62, 2000, 771-730

      1.15d Age Group
      Adults (18-64 years)
      Older Adults (65 years and older)
      1.15b Denominator Exclusions

      Exclusions that are implicit in the denominator definition include time at risk while a patient:

      • Has had ESRD for 90 days or less
      • Is less than 18 years of age
      • Non-Medicare primary insurance 

      The denominator also excludes patient time at risk for calendar months in which a patient is:

      • Actively enrolled in hospice at any time during the calendar month
      1.15c Denominator Exclusions Details

      We exclude from the time at risk for the measure all calendar months in which a patient spends any time enrolled in hospice (enrollment is determined from Medicare hospice claims). Hospice patients are considered to be under the purview of hospice care givers and may have other reasons for Emergency Department use.

      1.13 Data Dictionary
      Attached
      1.13a Attach Data Dictionary
      1.16 Type of Score
      1.17 Measure Score Interpretation
      Better performance = Lower score
      1.18 Calculation of Measure Score

      The numerator is the observed number of ED encounter events for a facility, and the denominator for the same facility is the expected number of ED encounter events adjusted for patient mix. The measure for a given facility is calculated by dividing the numerator by the denominator. See 1.18a for SEDR_Flowchart_Final_04-2026_508.pdf attachment. 

      1.18a Attach measure score calculation diagram
      1.19 Measure Stratification Details

      N/A

      1.26 Minimum Sample Size

      There is not a minimum sample size needed to calculate the performance score. Public reporting of this measure on DFCC would be restricted to facilities with at least five patient years at risk to ensure stable estimates and for the measure to comply with restrictions on reporting of potentially identifiable patient information related to small cell size.

      Supplemental Attachment
      7.1 Supplemental Attachment
      Initial Endorsement
      Steward Organization
      Centers for Medicare & Medicaid Services
      Steward POC email
      Steward Organization Copyright

      Not applicable

      Steward Address

      Wilfred  Agbenyikey
      Baltimore, MD
      United States

      Measure Developer POC

      Jonathan Segal
      UM-KECC
      Ann Arbor, MI
      United States

        Evidence
        2.2 Evidence of Measure Importance

        Among Medicare beneficiaries, 30% of hospital admissions that originate in the ED are for diagnoses that are often dialysis related such as complications of vascular access, congestive heart failure/fluid overload, septicemia, and hyperkalemia [1].  Recent research points to many additional opportunities to further reduce unnecessary ED use in this population.   Programs developed to impact dialysis provider practices have been shown to improve intermediate outcomes (reduced catheter vascular access [3], small solute adequacy, anemia management volume overload [1], hospitalization, and mortality. 

         

        Cohen and colleagues [9] reported that missed dialysis treatments are associated with an over two-fold higher risk of an ED visit, suggesting an opportunity for dialysis facilities to establish or strengthen facility practices that can help to reduce skipped treatments through increased communication, care coordination, and patient education. This, in turn, has the potential to reduce avoidable ED visits. Given the association between missed dialysis treatments and increased risk of an ED visit [4], dialysis facility interventions that improve adherence to the treatment schedule would be expected to decrease ED utilization. Other interventions, such as telehealth, have been demonstrated to reduce ED utilization in high-risk dialysis patients [5]. 

         

        Zhang and colleagues [10] reported that rates of ED visits among patients receiving thrice weekly in-center hemodialysis vary by dialysis schedule (Mon/Weds/Fri; Tues/Thurs/Sat) and by day of week. For example, the ED visit rate (without hospital admission) was highest on the day following the longer interdialytic interval over the weekend (Mondays), suggesting an association with facility structure and treatment schedule. 

         

        In the general population, outpatient ED visits were reported to have increased more slowly for Medicare patients being treated by patient-centered medical home practices when compared to non-patient-centered medical homes [6]. PCMH provide comprehensive care and treat all the patient’s clinical and mental and health issues; rely on care coordination across providers and provide expanded access to care around the clock (AHRQ; https://www.ahrq.gov/ncepcr/research/care-coordination/pcmh/define.html). A comparable example that may hold promise of reducing ED use among ESRD dialysis patients is the recent CMS Centers for Medicare and Medicaid Innovation’s Comprehensive End Stage Renal Disease (ESRD) Care model that emphasizes care coordination as a central feature of care delivery in order to reduce utilization and improve outcomes. During the second performance year, the original Wave 1 cohort of ESCOs (ESRD Seamless Care Organizations) experienced about a 3% reduction in ED use relative to the period before the CEC model was launched [11].

         

        Finally, low health literacy has been associated with increased use of ED services [7] and some studies have indicated that patient education interventions can reduce ED utilization [8].

         

        In-Line References:

         

        [1] Emergency Department Use Among Adults Receiving Dialysis. Ronksley PE, Scory TD, McRae AD, MacRae JM, Manns BJ, Lang E, Donald M, Hemmelgarn BR, Elliott MJ. JAMA Netw Open. 2024 May 1;7(5):e2413754. doi: 10.1001/jamanetworkopen.2024.13754.

         

        [2] Defragmentation of care in complex patients with ESKD improves clinical outcomes. Moore N, Roer D.Am J Manag Care. 2024 May 1;30(5):e165-e168. doi: 10.37765/ajmc.2024.89544.      

         

        [3] Fast track dialysis: Improving emergency department and hospital throughput for patients requiring hemodialysis. O'Donnell C, Molitch-Hou E, James K, Leong T, Perry M, Wood D, Masud T, Thomas B, Ross MA, Franks N.Am J Emerg Med. 2021 Jul;45:92-99. doi: 10.1016/j.ajem.2021.02.035. Epub 2021 Feb 22.     

         

        [4] Insurance Status and Emergency Department Visits Associated With Hemodialysis in Texas West J, Chan HK, Molony DA, Robinson DJ, Foringer JR, Wang HE. JAMA Netw Open. 2020 Feb 5;3(2):e1921447. doi: 10.1001/jamanetworkopen.2019.21447.   

                  

        [5] Effects of Early Frequent Nephrology Care on Emergency Department Visits among Patients with End-stage Renal Disease Chen YY, Chen L, Huang JW, Yang JY. Int J Environ Res Public Health. 2019 Mar 31;16(7):1158. doi: 10.3390/ijerph16071158.      

              

        [6] Failed Target Weight Achievement Associates with Short-Term Hospital Encounters among Individuals Receiving Maintenance Hemodialysis Assimon MM, Wang L, Flythe JE. J Am Soc Nephrol. 2018 Aug;29(8):2178-2188. doi: 10.1681/ASN.2018010004. Epub 2018 May 23.  

         

        [7] Burden of Emergency Medical Services Usage by Dialysis Patients Bartolacci J, Goldstein J, Kiberd B, Swain J, Vinson A, Clark D, Tennankore KK. Prehosp Emerg Care. 2018 Nov-Dec;22(6):698-704. doi: 10.1080/10903127.2018.1454558. Epub 2018 Apr 19. 

          

        [8] Patterns of emergency department utilization by patients on chronic dialysis: A population-based study. Komenda P, Tangri N, Klajncar E, Eng A, Di Nella M, Hiebert B, Strome T, Lobato de Faria R, Zacharias JM, Verrelli M, Sood MM, Rigatto C.      PLoS One. 2018 Apr 17;13(4):e0195323. doi: 10.1371/journal.pone.0195323. eCollection 2018.    

         

        [9] Lovasik, B.P., et al., Emergency Department Use and Hospital Admissions Among Patients With End-Stage Renal Disease in the United States. JAMA Intern Med, 2016. 176(10): p. 1563-1565.

        [10] Centers for Disease Control and Prevention. National hospital ambulatory medical care survey: 2011 emergency department summary tables. http://www.cdc.gov/nchs/fastats/injury.htm 2011  [cited 2017 January 9].

         

        [11] Ng LJ, Chen F, Pisoni RL, Krishnan M, Mapes D, Keen M, Bradbury BD. Hospitalization risks related to vascular access type among incident US hemodialysis patients. Nephrol Dial Transplant. 26(11):3659-66, 2011

         

        General References:

         

        [12] Chan, K. E.;Thadhani, R. I.;Maddux, F. W. Adherence barriers to chronic dialysis in the United States. J Am Soc Nephrol. 2014 25(11):2642-8 doi:10.1681/asn.2013111160

         

        [13] Minatodani, D. E.;Berman, S. J. Home telehealth in high-risk dialysis patients: a 3-year study. Telemed J E Health. 2013 19(7):520-2 doi:10.1089/tmj.2012.0196

         

        [14] Pines, J. M.;Keyes, V.;van Hasselt, M.;McCall, N. Emergency department and inpatient hospital use by Medicare beneficiaries in patient-centered medical homes. Ann Emerg Med. 2015 65(6):652-60 doi:10.1016/j.annemergmed.2015.01.002

         

        [15] Green, J. A.;Mor, M. K.;Shields, A. M.;Sevick, M. A.;Arnold, R. M.;Palevsky, P. M.;Fine, M. J.;Weisbord, S. D. Associations of health literacy with dialysis adherence and health resource utilization in patients receiving maintenance hemodialysis. Am J Kidney Dis. 2013 62(1):73-80 doi:10.1053/j.ajkd.2012.12.014

         

        [16] Morgan, S. R.;Chang, A. M.;Alqatari, M.;Pines, J. M. Non-emergency department interventions to reduce ED utilization: a systematic review. Acad Emerg Med. 2013 20(10):969-85 doi:10.1111/acem.12219

         

        [17] Cohen D, Gray K, Colson C, Van Wyck D, Tentori F, and Brunell S. Impact of Rescheduling a Missed Hemodialysis Treatment on Clinical Outcomes. Kidney Med. 2(1):12-19. Published online December 11, 2019

         

        [18] Zhang S, Morgenstern H, Albertus P, Nallamothu B, He K, and Saran R. Emergency department visits and hospitalizations among hemodialysis patients by day of the week and dialysis schedule in the United States. PLOS ONE. https://doi.org/10.1371/journal.pone.0220966 August 15, 2019.

         

        [19] Grecia Marrufo, Brighita Negrusa, Darin Ullman, Richard Hirth, Claudia Dahlerus Jennifer Wiens, Ariana Ackerman, Daniel Gregory, Kelsey Bacon, Jonathan Segal, Yi Li, Tammie Nahra, Amy Jiao, Joseph Gunden, Kathryn Sleeman, Daniel Strubler, Katherine B. McKeithen, and Rebecca Braun. https://www.cms.gov/priorities/innovation/data-and-reports/2022/cec-ann…

        2.6 Meaningfulness to Target Population

        During the 2015 ED Technical Expert Panel (TEP) which included 3 patient members, some TEP members cited care fragmentation and lack of ownership over patient outcomes that often occur within the U.S. health care system contribute to avoidable ED use. They noted that many dialysis patients rely heavily on their nephrologists (versus primary care physicians) for more comprehensive as well as primary care due to their frequent interactions as part of the regular dialysis treatment schedule. There was agreement that better communication among providers including the dialysis facility is needed to avoid preventable ED visits. 

         

        The TEP agreed that ED encounters that do not result in admission are not well monitored as a quality indicator. Panelists recommended both the development of a measure of overall ED use that did not result in an admission along with a measure focused on ED visits occurring shortly after an inpatient discharge. ED encounter measures would provide facilities with a more complete picture of their performance on key clinical outcomes of mortality, hospitalization, readmission, and ED usage. 

        2.4 Performance Gap

        Data for Table 1 are from the ESRD patient treatment history file described above in 1.15a for the year 2023. The total number of dialysis facilities included in the performance scores was 7,488. The total number of patients included in the performance scores was 517,165.

        Table 1. Performance Scores by Decile

        See 2.4a for attached table

        2.4a Attach Performance Gap Results
          Closing Care Gaps
          3.1 Contributions Toward Closing Care Gaps

          This domain is optional for the Spring 2026 cycle.

            Feasibility
            4.1a Data Structure and Availability

            All the data incorporated into our database come from structured data. Data collection for this measure is accomplished via data sources including EQRS, a web-based and electronic batch submission platform maintained and operated by CMS contractors, Medicare Claims, and other supplemental data sources (see Section 1.25 Data Source Details). Publicly reported measures like this one are reviewed on a regular basis by dialysis facility providers and rare instances of inaccurate or missing data are present (based on comments received during facility previews). For this measure maintenance submission, Medicare Advantage patients are now being included in the measure through the addition of Medicare Advantage Part C encounter data.

            4.1b Implementation Costs and Burden

            As the data required for this measure are already part of routine data collection, no additional costs or burden are anticipated. 

            4.1c Confidentiality

            A public reporting threshold of at least 5 patient-years at risk in a given facility is in place for Dialysis Facility Care Compare on Medicare.gov (DFCC) to avoid potential compromise of confidentiality.

            4.3 Feasibility Informed Final Measure

            No feasibility challenges have been identified that resulted in a change to the measure. Changes to the measure were made to include Medicare Advantage patients that had previously been excluded and do not affect the feasibility profile.

            4.4 Proprietary Information
            Not a proprietary measure and no proprietary components
              Testing Data
              5.1.1 Data Used for Testing

              Data are derived from registry and claims data explained in more detail in question 1.25, encompassing the years 2020-2023. 

              5.1.1a Dates of Testing Data

              January-December 2020-2023

              5.1.2 Differences in Data

              None

              5.1.3 Characteristics of Measured Entities

              See 7.1 Supplemental Attachment for a PDF of the text and table for 5.1.3 

              5.1.4 Characteristics of Units of the Eligible Population

              See 7.1 Supplemental Attachment for a PDF of the text and table for 5.1.4

              5.2.2 Method(s) of Reliability Testing

              We evaluated the reliability of the SEDR using 2023 data from Medicare End-Stage Renal Disease (ESRD) dialysis patients. A key metric for this evaluation is the inter-unit reliability (IUR), which quantifies the proportion of total variation in a measure that is attributable to true differences between facilities, rather than to random variation. By definition, IUR ranges from 0 to 1, with higher values indicating that most of the observed variation in the quality measure reflects actual differences in facility performance—thereby implying higher precision in comparing facilities.

               

              However, due to the ratio form of SEDR, directly estimating the within-facility variance is not straightforward. We use a bootstrap-based approach to estimate this component of variability.

               

              Let T1,…,TN represent the SEDR values for N facilities. For each facility i with ni subjects, r, we draw  bootstrap samples with replacement from its patients (we found B=100 to be sufficient based on numerical experiments). For each sample, we compute the corresponding bootstrapped SEDRs, denoted of T*i,1, … T*i,B.  We then compute the sample variance of these bootstrapped SEDRs for each facility, denoted Si*2

               

              An estimate of the within-facility variance of SEDR, namely, σ t,w2, is given by the bootstrap variance:

               

              St,w2= ΣNi=1[(ni-1) S i*2]/ ΣNi=1(ni-1).

               

              Calling on formulas from the one-way analysis of variance, an estimate of the overall variance of Tis

               

              St2= ΣNi=1[ni (Ti -Ť)2]/ [n’(N-1)],

               

              where 

               

              Ť = SnTi / Sni

               

              is the weighted mean of the observed SEDR and

               

              n’ = (Sn- Sni2/Sni)/(N-1)

               

              is approximately the average facility size (number of patients per facility). Note that  St2is the total variation of SEDR and is an estimate of σ b+ σ t,w2, where σ bis the between-facility variance, the true signal reflecting the differences across facilities. Thus, the estimated IUR, which is defined by

               

              IUR = σ b/( σ b+ σ t,w2),

               

              can be estimated with (St2- St,w2)/St2.

               

              Note: SEDR calculations were restricted to facilities with at least five patient-years at risk to ensure stable estimates and comply with restrictions on reporting of potentially identifiable patient information related to small cell size.

              5.2.3 Reliability Testing Results

              The overall IUR for SEDR is 0.62. 

              See 5.2.3a for SEDR_5.2.3a_Table 2A_Table 2B_IUR Additional Info_Final_04-2026_508.pdf, which contains additional information about SEDR's IUR

              5.2.3a Attach Additional Reliability Testing Results
              5.2.4 Interpretation of Reliability Results

              The IUR for SEDR in 2023 is 0.62 which indicates that almost two-thirds of the variation can be attributed to the between-facility differences and less than roughly one-third to within-facility variation. 

              Table 2a. Accountable Entity Level Reliability Testing Results by Denominator, Target Population Size

              See 5.2.3a for SEDR_5.2.3a_Table 2A_Table 2B_IUR Additional Info_Final_04-2026_508.pdf

              Table 2b. Accountable Entity Level Reliability Testing Results by Reliability Score

              See 5.2.3a for SEDR_5.2.3a_Table 2A_Table 2B_IUR Additional Info_Final_04-2026_508.pdf

              5.3.3 Method(s) of Validity Testing

              Empirical validity testing - validation of performance measure scores: 

              To validate SEDR we first stratified facilities into the ‘better than/as expected’ and ‘worse than expected’ categories of SEDR. Next, we calculated mean performance scores for several quality measures: Standardized Mortality Ratio (SMR), Standardized Transfusion Ratio (STrR), Standardized Fistula Rate (SFR), Percentage of Prevalent Patients Waitlisted (PPPW), Standardized Hospitalization Ratio (SHR), and Emergency Department Visit within 30 days of discharge (ED30). We then compared mean performance scores across the combined strata of ‘better than/as expected’ ‘and ‘worse than expected’ performance categories for SEDR. 

               

              We expect better mean performance on the above quality measures for facilities classified as ‘better than/as expected’ for SEDR compared to facilities classified as ‘worse than expected.’ Compared to facilities that perform ‘worse than expected’, facilities that perform ‘better than/as expected’ on SEDR are likely to have more successful care coordination and other processes of care in place that may help patients avoid an ED visit:

              • SMR: We expect to observe a lower mean standardized mortality ratio for facilities in the ‘better than/as expected’ category for SEDR compared to facilities classified as ‘worse than expected.’ Facilities with a higher rate of ED utilization may not have care processes in place to support management of acute crises such as cardiovascular related events, infections, and others that places patients at risk of dying.   
              • STrR: We expect to observe a lower mean standardized transfusion event ratio for facilities in the ‘better than/as expected’ category for SEDR compared to facilities classified as ‘worse than expected.’ Facilities that have a lower STrR likely have processes of care in place to support robust anemia management and other care processes compared to facilities with a higher STrR. 
              • Standardized Fistula Rate (SFR): We expect to observe a higher mean standardized fistula rate for facilities in the ‘better than/as expected’ category for SEDR compared to facilities classified as ‘worse than expected.’ AVFs are typically considered to be the preferred vascular access due to lower risk of infection and potential need for hospitalization or other acute care.  Higher standardized fistula rates suggest facilities are successful at creating AVFs due to more robust processes to coordinate care outside of the dialysis facility. Facilities that do a better job at care coordination reduce the likelihood that patients will experience a preventable and unscheduled acute event resulting in an ED visit. 
              • PPPW: We expect to observe a higher mean standardized percentage of prevalent patients on the waitlist for facilities in the ‘better than/as expected’ category for SEDR compared to facilities classified as ‘worse than expected.’ Facilities that have a higher standardized percentage of patients on the transplant waitlist suggest they may have more robust processes to coordinate care outside of the dialysis facility with other providers and the transplant center, compared to facilities with lower percentages. This includes the facility taking steps to ensure patients maintain sufficient health status in order to be placed on the waitlist. Therefore, facilities that have higher standardized waitlist percentages are likely deploying effective care coordination and other care processes that may reduce the likelihood of patients getting preventable and unscheduled acute care from the ED. 
              • SHR: We expect that facilities classified as ‘worse than expected’ for SEDR will have a standardized hospitalization ratio that is close to the national norm. SEDR only captures outpatient ED visits that do not result in an admission which, by definition, is a different patient subpopulation than SHR. Patients that require acute care from the ED without an admission likely have lower acuity medical needs that can be handled in an outpatient setting without admission. Therefore, we expect this measure will have the weakest relationship to the current measure as we do not expect SEDR flagging to be related to how facilities perform on SHR. 
              • ED30: We expect to observe a lower mean ED30 ratio for facilities classified as ‘better than/as expected’ for SEDR compared to facilities classified as ‘worse than expected’ since both measures are a reflection of outpatient ED use.  As such, we expect that this will have the strongest relationship with the current measure.  However, the measures represent two different aspects of dialysis patients’ emergency department use that assess complementary elements of facility care. A low SEDR, corresponding to low overall emergency department encounter rates, indicates that the facility has processes (e.g. patient/staff education, assistance with primary care, frequent evaluation of target weight) in place to avoid the need for unscheduled acute care. A low ED30 indicates that a facility is successful in managing the transition of care (e.g. medication reconciliation, evaluation of target weight, assistance with follow up appointments) that occurs after a hospital discharge.
              5.3.4 Validity Testing Results

              See 5.3.4a for SEDR_5.3.4_Final_508.pdf, which contains the text and table for this question

              5.3.4a Attach Additional Validity Testing Results
              5.3.5 Interpretation of Validity Results

              On average, the standardized mortality ratio was 8% higher than the national average for facilities that were ‘worse than expected,’ and 2% lower from the national average (SMR = 0.98) for facilities that were ‘better than/as expected’ for SEDR. 

               

              On average, the standardized transfusion event ratio was 5% higher than the national average for facilities classified as ‘worse than expected’ while the ‘better than/as expected’ classification group of facilities were 6% lower than the national average. This suggests that facilities which have lower numbers of transfusion events likely have better processes of care in place to support robust anemia management and other care processes, thus reducing patient utilization of the ED for some acute care needs.

               

              Overall, the average SFR was 58.57% for facilities classified as ‘better than/as expected’ and 55.63% in facilities classified as ‘worse than expected.’ The results reinforce the observation that patients with AVFs have lower risk of infection and potential need for acute care or hospitalization compared to patients with other access types, such as long-term catheter. Higher facility standardized fistula rates suggests facilities may be doing a better job at care coordination, reducing patient utilization of the ED for many acute care needs. While the difference in fistula rates was small between facilities this may reflect that national trends in AVF rates have generally plateaued across many US dialysis facilities.

               

              The mean facility standardized percentage of patients waitlisted (PPPW) in facilities classified as ‘better than/as expected’ was 16.05% compared to facilities classified as ‘worse than expected’ (14.94%), suggesting that facilities that have higher rates of patients on the transplant waitlist may have more robust processes to coordinate care outside of the dialysis facility with other providers. These facilities could be deploying more effective care coordination and other care processes that may reduce the likelihood of patients utilizing the ED for many acute care needs. 

               

              Facilities classified as ‘better than/as expected’ and those classified as ‘worse than expected’ for SEDR performed similarly on SHR. The mean SHR was 0.98 for ‘better than/as expected’ and 1.01 for facilities classified as ‘worse than expected’ for SEDR. These respective values are close to the national mean of 1.0 indicating flagging for SEDR is not related to how facilities perform on SHR. This suggests that both measures are capturing different patient subpopulations and different facets of facility care quality.

               

              The ED30 ratio on average for facilities classified as ‘better than/as expected’ for SEDR was close to the national average (1.03), while facilities classified as ‘worse than expected’ had an ED30 ratio 47% higher than the national average. These results reinforce that both ED30 and SEDR assess complementary elements of care that are likely reflected by internal processes that support greater access to care and other clinical triaging of patients that may be experiencing onset of an acute event, which may help reduce patient utilization of the ED for preventable acute care needs.

               

              Taken together these results provide validation support for SEDR. Performance on key quality measures that were expected to be related to ED use was also related to facility flagging in the respective ‘better than/as expected’ or ‘worse than expected’ categories. 

              5.4.1 Methods Used to Address Risk Factors
              5.4.2 Conceptual Model Rationale

              See 5.4.2a for SEDR_Conceptual Model_5.4.2 Rationale_04-2026_508.pdf, which contains the text and table for this question, along with the conceptual model on Page 1

              5.4.3 Variable Distribution Across Measured Entities

              See 5.4.3a for SEDR_5.4.3 Variable Distribution Across Measured Entities_04-2026_508.pdf, which contains the text and table for this question

              5.4.3a Attach Descriptive Statistics for Risk/Case-mix Variables
              5.4.4 Risk/Case-Mix Adjustment Modeling and/or Stratification Results

              See 5.4.4a for SEDR_5.4.4 Risk_Case-Mix Adjustment Modeling_04-2026_508.pdf, which contains the text and tables for this question

              5.4.4a Attach Risk/Case-mix Adjustment Modeling and/or Stratification Specifications
              5.4.5 Calibration and Discrimination

              The c-statistic for a recurrent event model measures the concordance between the observed rate of recurrent events and the model-based rate. The C-statistic for SEDR is 0.61.

              See 5.4.5a for calibration and discrimination testing results, found in SEDR_5.4.5a_Final_508.pdf.

              5.4.5a Attach Calibration and Discrimination Testing Results
              5.4.6 Interpretation of Risk/Case-mix Factor Findings

              See 7.1 Supplemental Attachment section for SEDR_5.4.6. Interpretation of Risk_04-2026_508.pdf, which contains the text and table for this question.

              5.4.7 Final Approach to Address Risk Factors
                Use
                6.1.1 Current Status
                In use
                6.1.2 Current or Planned Use(s)
                6.1.3 Program Details
                Name of the program and sponsor
                Dialysis Facility Care Compare, Centers for Medicare and Medicaid Services
                Purpose of the program

                Dialysis Facility Care Compare helps patients find detailed information about Medicare-certified dialysis facilities. They can compare the services and the quality of care that facilities provide.

                Geographic area and percentage of accountable entities and patients included

                United States. All Medicare-certified dialysis facilities that have at least 5 patient years at risk are included in the measure calculation for the program. Five patient-years at risk means that the total time at risk in the measure denominator for the reporting period of calendar year 2023 must meet or exceed 5 patient-years exposure. For the October 2024 Dialysis Facility Compare refresh, 7,106 U.S. dialysis facilities serving 278,531 patients had SEDR results reported.

                Applicable level of analysis and care setting

                Facility level, Dialysis Facilities

                Name of the program and sponsor
                Dialysis Facility Reports, Centers for Medicare and Medicaid Services
                Purpose of the program

                The Dialysis Facility Reports (DFRs) are provided as a resource for characterizing selected aspects of clinical experience at this facility relative to other caregivers in this state, End Stage Renal Disease (ESRD) Network, and across the United States. Since these data could be useful in quality improvement and assurance activities, each state’s surveying agency may utilize the DFRs as a resource during their survey and certification process. Measures included in the DFRs are updated annually and available to dialysis facilities to review and submit comments prior to their release to State Survey Agencies and Regional Offices in September of each year.

                Geographic area and percentage of accountable entities and patients included

                United States. All Medicare-certified dialysis facilities and have at least 5 patient years at risk are included in the measure calculation for the program.  Five patient-years at risk means that the total time at risk in the measure denominator for the reporting period of calendar year 2023 must meet or exceed 5 patient-years exposure. For the FY 2025 Dialysis Facility Reports, 7,106 U.S. dialysis facilities serving 278,531 patients had SEDR results reported.

                Applicable level of analysis and care setting

                Facility level, Dialysis Facilities

                6.1.4 Attributes for Accountability Use

                This measure is best suited for an accountability program that focuses on End Stage Renal Disease (ESRD) patients.  Specifically, ESRD patients with Medicare coverage (either traditional Medicare or a Medicare Advantage Plan) would be the target population.  Programs that focus on the dialysis facility as the accountable entity are ideal, as opposed to programs that focus on the Nephrologist or provider.  As such, this is an outpatient measure with limited adjustments for social risk factors.  However, additional adjustments could be made at the program level based on the needs or design of the program.  

                6.2.1 Actions of Measured Entities to Improve Performance

                As described in the logic model there are multiple resources facilities have available which can help them prevent avoidable ED events. These include:

                • Identification of patients with missed/shortened treatments and counseling or removal of barriers (e.g. assistance with transportation) to improve adherence to dialysis prescription 
                • Tracking patients who do not achieve target weight for improved fluid management by offering additional or prolonged dialysis treatments
                • Reconcile medications after hospitalization or change in care setting to avoid medication errors
                • Establish relationships with outpatient vascular access centers so that efficient management of vascular access problems (e.g. access thrombosis or malfunction) can be achieved without reliance on the Emergency Department
                • Regular review and training refresher for infection control
                • Educate patients about when to receive care in the ED vs. dialysis clinic or primary care and who to contact if questions or concerns arise between treatments
                6.2.2 Feedback on Measure Performance

                For DFCC, feedback can be provided any time through contacting the dialysisdata.org helpdesk. Preview periods allow for specific times for facilities to review and comment on measure calculations, and provide an opportunity to request a list of patients included in the measure calculation.

                 

                Comments received during DFCC preview periods tend to be rare. What few questions we get are generally technical in nature, asking for clarification on how the SEDR is calculated for particular facilities, including questions about patient assignment and application of risk adjustment criteria. 

                6.2.3 Consideration of Measure Feedback

                The revisions made to the measure specifications during this maintenance review were not directly in response to specific feedback received during public reporting (which, as described above, was more general in nature).

                 

                Based on enrollment information from the Medicare Enrollment Database (EDB), the percentage of ESRD dialysis beneficiaries enrolled in Medicare Advantage (MA) has steadily increased over time. From 12% in 2010, the proportion rose to 22% by 2020. Prior to 2020, there was an annual increase of approximately 1%. However, since 2021, the annual increase has been more than 5%.

                 

                The growth in ESRD beneficiaries joining MA plans carries significant implications for the metrics used to assess dialysis facility performance. Contrary to the data from Fee-For-Service (FFS) Medicare beneficiaries, MA outpatient encounters and administrative records had not been readily available for the purposes of analyzing facility quality, except for internal CMS use in risk adjustment and performance assessment.

                6.2.4 Progress on Improvement

                See 7.1 Supplemental Attachment section for SEDR_6.2.4 Progress on Improvement_04-2026_508.pdf, which contains the text and table for this question

                6.2.5 Unexpected Findings

                None

                  Public Comments

                  Submitted by Patrick S Romano (not verified) on Wed, 07/08/2026 - 00:00

                  Permalink

                  "Methodology for prevalent comorbidity selection: We began the selection process with the 283 AHRQ CCS groupers for calendar year 2015."

                  This approach is antiquated. The Clinical Classification Software (CCS) is a dead grouper that was designed for ICD-9-CM and is no longer supported or recommended by AHRQ for ANY purpose. The current diagnosis grouper is the Clinical Classification Software Refined (CCSR), which was purpose-built for ICD-10-CM. Unlike CCS, CCSR is updated annually and therefore properly handles the 5,000 or more new ICD-10-CM codes that have been introduced over the past decade. For example, 1504 new codes were introduced in 2023 alone, and these codes cannot be handled by a dead grouper such as CCS. The CCSRs are designed for backward compatibility to October 2015, and must therefore be used for any purpose where CCS would have been used prior to that date. Please refer to these websites or consult with the AHRQ HCUP Research Tools team for further information.

                  https://www.icd10data.com/ICD10CM/Codes/Changes/New_Codes?year=2025

                  https://hcup-us.ahrq.gov/tools_software.jsp 

                  https://hcup-us.ahrq.gov/toolssoftware/ccsr/ccs_refined.jsp 

                  Organization
                  UC Davis Center for Healthcare Policy and Research

                  Submitted by Lauren Ahearn (not verified) on Fri, 06/19/2026 - 09:44

                  Permalink

                  ASN supports expanding the denominators for CBE 3565 and CBE 3566 to include Medicare Advantage (MA) beneficiaries. With MA enrollment among ESRD patients now exceeding 50% and continuing to grow, inclusion of these patients is essential to ensure that quality measures fully and accurately represent the entire ESRD population[i]. ASN also supports inclusion of MA status as a covariate in the measures’ risk adjustment models, as this could help account for some differences in patient demographics and utilization patterns between MA and traditional Fee-for-Service Medicare.

                  At the same time, ASN urges CMS to maintain oversight of known limitations in MA encounter data. ASN has consistently raised concerns regarding the completeness and transparency of MA data, challenges that have also been documented by the Medicare Payment Advisory Commission (MedPAC)[ii]. As these measures are implemented for public reporting and accountability programs, CMS must carefully monitor MA data completeness and timeliness to prevent distortions in facility-level performance scores.


                   

                  [i] United States Renal Data System. 2025 USRDS Annual Data Report: Epidemiology of kidney disease in the United States. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, 2025

                  [ii] https://www.medpac.gov/wp-content/uploads/import_data/scrape_files/docs… source/reports/jun19_ch7_medpac_reporttocongress_sec.pdf

                  Organization
                  American Society of Nephrology

                  Importance

                  Importance Rating
                  Importance

                  Strengths:

                  • A clear logic model is provided, depicting the relationships between inputs (e.g., Quality Improvement Staff and facility-specific policies and procedures that reflect requirements in CMS’ Conditions for Participation in the Medicare ESRD Chronic Dialysis Program) activities (e.g., identification of high-risk patients and root cause analysis for common emergency department (ED) visits, delivery of education to patients on when to visit the emergency department and who they can call if questions arise between visits), and desired outcomes (e.g., improved identification of high-risk patients and sustained reduction in ED encounter rates). This model demonstrates how the measure's implementation will lead to the anticipated outcomes.
                  • The problem this measure addresses presents a significant burden for patients including negative health consequences associated with ED visits such as hyperkalemia, infection, and fluid overload, and significant cost and utilization associated with ED visits.
                  • Data from ESRD patient treatment history from 2023 show a performance gap, with decile ranges from 0.51 in the lowest decile to 1.65 in the highest decile, indicating variation in measure performance. 

                  Limitations:

                  • The literature review includes studies and reports that are more than 5 years old and only includes one systematic review.The submission could be strengthened by including more recent and higher quality empirical studies.
                  • The patient input obtained through a technical expert panel (TEP) is more than 10 years old (2015). The submission could be strengthened by expanding the discussion of how meaningfulness was established and providing more feedback. 

                  Rationale:

                  • This new/maintenance measure meets all criteria for 'Met' for importance due to the significance of the problem it addresses and well-articulated logic model.

                  Closing Care Gaps

                  Closing Care Gap Rating
                  Closing Care Gaps

                  The developer did not address this optional domain. 

                  Feasibility Assessment

                  Feasibility Assessment Rating
                  Feasibility Assessment

                  Strengths:

                  • All required data elements are routinely generated during care delivery, and required elements are available from digital or electronic sources. The developer described that the recent inclusion of Medicare Advantage patients does not affect data availability. The developer stated that no feasibility issues were found requiring adjustment of the final measure’s specifications.
                  • The developer noted that there are no additional costs or burden associated with data collection and data entry, validation, and analysis as all data are routinely generated during care delivery.
                  • The developer described how all required data elements can be collected without risk to patient confidentiality, including limiting public reporting of the measure on Dialysis Facility Care Compare to facilities with at least 11 eligible index discharges to avoid reporting potentially identifiable patient information.
                  • There are no fees, licensing, or other requirements to use any aspect of the measure (e.g., value/code set, risk model, programming code, algorithm). 

                  Limitations:

                  • None identified.

                  Rationale:

                  • This maintenance measure meets all criteria for 'Met' for feasibility due to its well-documented feasibility assessment, clear and implementable data collection strategy, and transparent handling of patient confidentiality, burden, licensing, and fees. 

                  Scientific Acceptability

                  Scientific Acceptability Reliability Rating
                  Scientific Acceptability Reliability

                  Strengths:

                  • Data used for reliability testing were sourced from EQRS patient-specific clinical and administrative data during the year 2023.

                  Limitations:

                  • The developer conducted bootstrap inter-unit reliability (IUR) at the accountable entity-level. Around 50% of accountable entities meet the expected threshold of 0.6 for accountable entity-level reliability. Between 10% and 20% of accountable entities had reliability below 0.4, and the developer provided an interpretation of and a rationale for these results, stating that because dialysis facilities in the United States are extremely small they lack sufficient sample size to achieve the reliability threshold of 0.6. The developer provides a rationale for why facilities should be included in the measure to help with the overall quality of care provided by dialysis facilities.

                  Rationale:

                  • This maintenance measure is rated as 'Not Met But Addressable' for reliability because the current reliability metrics do not meet the established thresholds for this measure, indicating potential issues with the consistency and accuracy of the results across different settings and populations. However, the identified limitations are deemed addressable, as the developer may consider aggregating data across multiple years to increase sample size. Data were sourced for years 2020 to 2022 in addition to year 2023 which was used for reliability testing. By addressing this issue, there is potential to enhance the reliability.
                  Scientific Acceptability Validity Rating
                  Scientific Acceptability Validity

                  Strengths:

                  • The developer performed the required validity testing for this maintenance measure; specifically, they performed accountable entity validity testing at the level the measure is specified (dialysis facility). The data used for validity testing come from an initial 8,098 facilities (598,274 total patients) that reported the measure in 2023.
                  • The developer performed a classification analysis comparing the meaure to six other measures reported by many dialysis facilities, where the mean performance on each of the comparator measures was calculated for dialysis facilities that performed "better than or as expected" vs. "worse than expected" on the SEDR measure. The developer hypothesized that better performance on the SEDR measure (where a lower score = better performance) would be associated with lower scores on the standardized mortality ratio (SMR), the standardized transfusion ratio (STrR), and the ED30 (a meaure reflecting ED use, but not otherwise defined in the submission), higher scores on the standardized fistula rate (SFR) and percentage of patients waitlisted for transplant (PPPW), and no significant relationship with the standardized hospitalization ratio (SHR). The developer's reasoning for each of these hypothesized relationships was detailed in the submission.
                  • The developer reported findings in line with their hypotheses; for example, facilities that performed better than or as expected on SEDR had lower (better) performance scores for SMR (0.98), and facilities that performed worse than expected on SEDR had higher (worse) scores for SMR (1.08, p<0.0001). Other results aligned with the developer's hypotheses. For SHR, the developer interpreted the finding of no significant difference to indicate that the SHR and SEDR measures capture different patient populations, i.e., patients with lower acuity (SEDR) vs. higher acuity (SHR) needs.
                  • The developer conducted statistical risk adjustment, based on a conceptual model, selecting risk factors that are present at the start of care, have a significant association with the outcome, and vary in prevalence across measured entities. The model has acceptable calibration.

                  Limitations:

                  • The developer reported a concordance index of 0.61, indicating moderate model discrimination.

                  Rationale:

                  • This maintenance measure is rated as ‘Met’ for validity because the developer performed the required validity testing for this measure, and validity testing results support a strong inference of validity for the measure, confirming that the measure accurately reflects performance on quality and can distinguish good from poor performance.
                  • The risk adjustment methods used are appropriate and demonstrate variation in the prevalence of risk factors across measured entities. The model performance is acceptable.

                  Use and Usability

                  Use and Usability Rating
                  Use and Usability

                  Strengths:

                  • The measure is currently used in the Dialysis Facility Care Compare (DFCC) and Dialysis Facility Reports (DFRs) Public Reporting Programs.  
                  • Attributes of a suitable program for this measure are described, and these include an accountability program that focuses on End Stage Renal Disease (ESRD) patients with Medicare coverage as the target population and the dialysis facility as the accountable entity.
                  • The developer provided a summary of how accountable entities can use the measure results to improve performance. Specifically, identifying patients with missed/shortened treatments and who don’t achieve target weight for improved fluid management, refresher training for infection control, and education for patients around when to use the emergency department (ED) and who to contact for questions or concerns between treatments. These possible actions are reflected in the measure’s logic model.  
                  • Stakeholders can submit questions about the measure at any time through an online helpdesk. The developer noted that only clarification questions have been received.  
                  • The developer noted that the feedback received did not lead to any changes in the measure specifications.  
                  • The developer reported no unexpected findings. 

                  Limitations:

                  • The developer reported no changes in performance from calendar years 2020 to 2023 and did not provide a rationale for the lack of improvement. The developer should consider collecting additional feedback from providers to ascertain the reasons why the measure is leveling off and describe appropriate mitigation approaches.  

                  Rationale:

                  • This maintenance measure is rated ‘Not Met, but Addressable’ for use and usability because while the measure is actively used in at least one accountability application, there was no improvement in the measure score and the developer did not provide a sufficient rationale.
                  First Name
                  Abate
                  Last Name
                  Mammo

                  Submitted by Abate on Tue, 06/30/2026 - 11:04

                  Permalink

                  Importance

                  Importance Rating
                  Importance

                  Importance of the measure is well described. The logic model is clear and detailed.  However, I have a few comments that I think could enhance the application.

                  1. It would have benefited form clarification upfront on what facilities the measures would be estimated for.  Since it is mostly describing avoidable ED visits, it is easy to assume that the measures could be referring to acute care facilities. I suggest clarifying that from the start.
                  2. Wouldn't excluding Inpatient admissions through ED bias the results since such patients could be sicker? Please explain.
                  3. The number of technical experts and patients used to guide the measure look too small for comfort.

                   

                  Closing Care Gaps

                  Closing Care Gaps Rating
                  Closing Care Gaps

                  Not required

                  Feasibility Assessment

                  Feasibility Assessment Rating
                  Feasibility Assessment

                  Data availability adequately described and the study feasibility is properly explained. 

                  Scientific Acceptability

                  Scientific Acceptability Reliability Rating
                  Scientific Acceptability Reliability

                  Unless I have missed it, the analysis includes several factors that can easily have collinearity problems.  Could the applicant address how that problem is handled? One simple example is age and age-squared. Another examples can be listed among the diseases (health conditions) listed.

                  Scientific Acceptability Validity Rating
                  Scientific Acceptability Validity

                  Detailed examples and estimates provided to show validity of measures though the classifications of facilities by their performance would lead one  to expect final outcomes. 

                  Use and Usability

                  Use and Usability Rating
                  Use and Usability

                  It is currently in use much like other measures that only show starred ratings that may not be very useful to patients.

                  Summary

                  The measure is adequately presented but needs some more improvement on a couple of areas mentioned above. One of the concerns I have is excluding admissions who came through ED and another one is the possible collinearity of factors used in the modeling which needs some explanation how that was handled. 

                  First Name
                  Lauren
                  Last Name
                  Agoratus

                  Submitted by Lauren Agoratus on Thu, 07/02/2026 - 14:52

                  Permalink

                  Importance

                  Importance Rating
                  Importance

                  General: “More than half (55.0%) of all patients with ESRD visit the ED during their first year of dialysis,  Noted that ESRD patients can now enroll in Medicare Advantage but may be better for duals to have 2 plans (formularies).  Noted “care fragmentation and lack of ownership over patient outcomes that often occur within the U.S. health care system contribute to avoidable ED use.”

                  Closing Care Gaps

                  Closing Care Gaps Rating
                  Closing Care Gaps

                  optional

                  Feasibility Assessment

                  Feasibility Assessment Rating
                  Feasibility Assessment

                  “As the data required for this measure are already part of routine data collection, no additional costs or burden are anticipated. "

                  Scientific Acceptability

                  Scientific Acceptability Reliability Rating
                  Scientific Acceptability Reliability

                  –“ However, due to the ratio form of SEDR, directly estimating the within-facility variance is not straightforward.”

                  Scientific Acceptability Validity Rating
                  Scientific Acceptability Validity

                  Validity-done at the entity level using empirical validity testing.

                  Risk adj. –statistical risk adjustment models with risk factors.

                  Use and Usability

                  Use and Usability Rating
                  Use and Usability

                  Use -Currently in use; public reporting.

                  Usability –“ As described in the logic model there are multiple resources facilities have available which can help them prevent avoidable ED events.”

                  Summary

                  Similar to the other 3 measures, if unmet issues are address accept.  Note:  American Society of Nephrology supports.

                  First Name
                  Tarik
                  Last Name
                  Yuce

                  Submitted by tyuce on Wed, 07/08/2026 - 09:32

                  Permalink

                  Importance

                  Importance Rating
                  Importance

                  Clearly an important topic to address. 

                  Closing Care Gaps

                  Closing Care Gaps Rating
                  Closing Care Gaps

                  Did not complete, but optional

                  Feasibility Assessment

                  Feasibility Assessment Rating
                  Feasibility Assessment

                  No concerns, authors did a nice job of describing this.

                  Scientific Acceptability

                  Scientific Acceptability Reliability Rating
                  Scientific Acceptability Reliability

                  Agree with staff comments

                  Scientific Acceptability Validity Rating
                  Scientific Acceptability Validity

                  No concerns

                  Use and Usability

                  Use and Usability Rating
                  Use and Usability

                  Agree that developer should consider including additional feedback from users to understand why the measure is leveling off.

                   

                  First Name
                  John
                  Last Name
                  Wagner

                  Submitted by John Wagner on Thu, 07/09/2026 - 00:56

                  Permalink

                  Importance

                  Importance Rating
                  Importance

                  Agree with staff assessment 

                  Closing Care Gaps

                  Closing Care Gaps Rating
                  Closing Care Gaps

                  Optional

                  Feasibility Assessment

                  Feasibility Assessment Rating
                  Feasibility Assessment

                  Agree with staff assessment 

                  Scientific Acceptability

                  Scientific Acceptability Reliability Rating
                  Scientific Acceptability Reliability

                  Agree with staff assessment. Note public comment on comorbidity adjustment

                  Scientific Acceptability Validity Rating
                  Scientific Acceptability Validity

                  Agree with staff assessment 

                  Use and Usability

                  Use and Usability Rating
                  Use and Usability

                  Agree with staff assessment 

                  First Name
                  Eleni
                  Last Name
                  Theodoropoulos

                  Submitted by Eleni Theodoropoulos on Thu, 07/09/2026 - 17:54

                  Permalink

                  Importance

                  Importance Rating
                  Importance

                  Addresses important health care area and provides a clear logic model.

                  Closing Care Gaps

                  Closing Care Gaps Rating
                  Closing Care Gaps

                  Developer did not address

                  Feasibility Assessment

                  Feasibility Assessment Rating
                  Feasibility Assessment

                  All required data elements are routinely generated during care delivery, and required elements are available from digital or electronic sources.  No barrier to use (i.e., licensing, additional costs).

                  Scientific Acceptability

                  Scientific Acceptability Reliability Rating
                  Scientific Acceptability Reliability

                  Thresholds not met for measure in presented data set.  May need to increase sample size to address consistency and accuracy.

                  Scientific Acceptability Validity Rating
                  Scientific Acceptability Validity

                  Agree with Battelle's comments

                  Use and Usability

                  Use and Usability Rating
                  Use and Usability

                  Measure is currently in use but developer needs to provide rationale related to performance improvement levels.

                  Summary

                  Developer should address the reliability and use areas to strengthen measure for re-endorsement.  

                  First Name
                  Lisa
                  Last Name
                  Suter

                  Submitted by Lisa Gale Suter MD on Thu, 07/09/2026 - 21:23

                  Permalink

                  Importance

                  Importance Rating

                  Feasibility Assessment

                  Feasibility Assessment Rating

                  Scientific Acceptability

                  Scientific Acceptability Reliability

                  unsure if measure will be as meaningful when aggregated across years

                  Scientific Acceptability Validity Rating

                  Use and Usability

                  Use and Usability Rating
                  Use and Usability

                  while I understand performance gap has not closed, not sure that justifies not measuring any more and 2020-2023 period complicated by global pandemic that might make it confound assessing improvements

                  Advisory Committee Comments
                  Advisory Group Feedback

                  A committee member and the patient co-chair asked the developer to provide more detail about including MA patients in the overall measure and in the risk adjustment model. One committee member questioned the conceptual rationale for including MA as a risk-adjustment variable after already adjusting for patient characteristics.

                  In Meeting Developer Responses

                  The developer added the MA population to the measure due to an increasing number of individuals enrolling in MA.

                  In terms of adding MA to the risk adjustment, even after accounting for other factors, the measure needed to adjust for facilities that had very high or very low proportions of MA patients. Emergency department (ED) utilization patterns differ between MA and traditional Medicare fee-for-service populations.

                  Advisory Group Feedback

                  The patient co-chair noted the lack of improvement in performance over time, while other committee members questioned the value of continued measurement without improvement, sought examples of dialysis facility changes resulting from the measure, and asked why the developer had not convened a more recent technical expert panel (TEP).

                  In Meeting Developer Responses

                  While the measure received initial endorsement in fall 2020, it was first reported in Care Compare in 2023, meaning it has been in use for a relatively short amount of time, which was part of why the developer has not convened a new TEP. 
                  The developer cited quality improvement efforts through end-stage renal disease (ESRD) networks and alternative payment models as examples of interventions that have reduced ED utilization in some settings.

                  Advisory Group Feedback

                  A committee member expressed concern that the measure misses an important population by excluding inpatient admissions, particularly patients who present to the ED and require subsequent hospitalization.

                  In Meeting Developer Responses

                  The developer has a separate, complementary measure for in-patient admissions. This measure complements the hospitalization measure by capturing ED encounters and observation stays that do not result in admission.

                  Advisory Group Feedback

                  A few committee members expressed concern that because the measure captures all ED visits, patients may be dissuaded from going to the ED for appropriate reasons. One committee member noted that a ratio does not guarantee quality but rewards adherence. Committee members also questioned whether the measure appropriately distinguishes avoidable ED utilization from clinically necessary ED use among a medically complex dialysis population and whether dialysis facilities should be held accountable for ED visits unrelated to dialysis care.

                  In Meeting Developer Responses

                  The measure is a ratio, and the expectation is not that any facility should have an emergency utilization rate of 0. Rather, the ratio helps facilities compares their performances against their peers. Patients will have appropriate ED use unrelated to dialysis care, but facilities have control over providing their patients with education about when they should go to the ED. The developer acknowledged that some ED visits are clearly dialysis-related, some are unrelated, and others fall into a gray area, making attribution difficult.

                  Advisory Group Feedback

                  A few committee members expressed concern about the measure’s low reliability. One committee member questioned how the reliability concerns could realistically be addressed if small facility size is an inherent characteristic of dialysis facilities.

                  In Meeting Developer Responses

                  Dialysis facilities are smaller than most measured entities and need special considerations. A potential mitigation strategy is to allow smaller facilities to have a larger deviation from the mean when compared against larger facilities. Additional protections for small facilities are incorporated into public reporting and accountability programs.

                  Advisory Group Feedback

                  A committee member raised several methodological concerns regarding the measure’s risk-adjustment approach, questioning whether a C-statistic alone is sufficient to evaluate model performance. The member noted concerns about the model’s discrimination, potential overfitting, the use of stepwise variable selection methods, and the absence of training, testing, or validation data splits to assess generalizability. They also questioned the use of Clinical Classifications Software (CCS)-based comorbidity groupings and whether the classification approach adequately reflects updates to International Classification of Diseases, Tenth Revision, (ICD-10) coding, suggesting that additional evaluation of model performance and validation methods may be warranted.

                  In Meeting Developer Responses

                  The developer will respond to technical modeling questions in writing following the meeting.
                  The measure does not rely on the 2015 CCS software. Rather, the developer used the CCS groupings as a schema for organizing comorbidities, while ICD-10 codes are reviewed and updated on a regular basis.