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Cover of End-stage Renal Disease in the Medicare Population: Frequency and Duration of Hemodialysis and Quality of Life Assessment

End-stage Renal Disease in the Medicare Population: Frequency and Duration of Hemodialysis and Quality of Life Assessment

Technology Assessment Program

Investigators: , MBBS, MHS, , MS, , MD, MHS, , BS, , MD, MHS, , DO, MPH, and , MD, MPH.

Structured Abstract

Objective:

To study effects of more frequent or longer hemodialysis on clinical outcomes, quality of life (QOL), and symptoms in end-stage renal disease (ESRD) patients.

Data sources:

We searched through October 21, 2019 for studies in PubMed, Embase®, and other sources.

Methods:

We focused on studies assessing the frequency or duration of hemodialysis using a comparison group and at least 6 months of followup. We defined usual care as hemodialysis three times per week with less than 4 hours per treatment, more frequent hemodialysis as four or more treatments per week, and longer hemodialysis as 4 or more hours per treatment. We considered study limitations, directness, consistency, and precision to grade strength of evidence (SOE). We included studies assessing QOL in ESRD patients receiving dialysis and evaluated QOL tools using the COnsensus-based Standards for selection of health status Measurement Instruments (COSMIN).

Results:

We found 17 studies (3 randomized controlled trials (RCTs), one non-randomized trial, and 13 observational studies) reported in 39 articles that addressed the impacts of increased frequency or duration of hemodialysis. Compared to the U.S. hemodialysis population, study populations were younger, healthier, and had a longer life expectancy. The SOE was low that more frequent hemodialysis compared to usual care: lowered mortality, the composite outcome of risk of death or increase in left ventricular (LV) mass, and risk of death or decrease in physical health; lowered LV mass and heart rate variability; and improved quality of life and patient reported symptom measures, blood pressure, and metabolic measures. The SOE was low that more frequent and longer hemodialysis compared to usual hemodialysis: improved blood pressure; and shortened time to recovery after hemodialysis; The SOE was low that vascular access complications were more frequent with either more frequent or more frequent and longer hemodialysis, compared to usual care.

We identified 125 QOL or symptom measure tools used in 165 studies. Ten tools were designed for use in, and validated in dialysis populations. Six tools were not designed for dialysis populations but were validated in that population. COSMIN assessments were good in four or more domains for the Kidney Disease Quality of Life instrument, and Pediatric Quality of Life Inventory.

Conclusions:

More frequent in-center hemodialysis may improve clinical outcomes, mortality, and quality of life or patient-reported symptom measures. The trial populations were younger, healthier, and had a longer life-expectancy than the broader U.S. dialysis population, limiting applicability to patients with similar characteristics. Further research may increase our confidence in the findings.

Contents

Prepared for: Agency for Healthcare Research and Quality, US Department of Health and Human Services, 5600 Fishers Lane, Rockville, MD 20857; www.ahrq.gov Contract No. HHSA 290-2015-00006I Prepared by: The Johns Hopkins University Evidence-based Practice Center, Baltimore, MD

Suggested citation:

Shafi T, Wilson RF, Greer R, Zhang A, Sozio S, Tan M, Bass EB. End-stage Renal Disease in the Medicare Population: Frequency and Duration of Hemodialysis and Quality of Life Assessment. Technology Assessment Program Project ID No. JHE51000. (Prepared by the Johns Hopkins University Evidence-based Practice Center under contract number HHSA 290-2015-00006I) Rockville, MD: Agency for Healthcare Research and Quality. July 2020. Available at: http://www.ahrq.gov/research/findings/ta/index.html.

This report is based on research conducted by the Johns Hopkins University Evidence-based Practice Center (EPC), under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. HHSA 290-2015-00006-I). The findings and conclusions in this document are those of the author(s) who are responsible for its contents; the findings and conclusions do not necessarily represent the views of AHRQ. No statement in this article should be construed as an official position of the Agency for Healthcare Research and Quality or of the U.S. Department of Health and Human Services.

The Johns Hopkins University Evidence Based Practice Center and study authors have not financial interests or other relationships with the manufacturers of commercial products, suppliers of commercial services, or commercial supporters.

None of the investigators have any affiliations or financial involvement that conflicts with the material presented in this report.

The information in this report is intended to help healthcare decision makers—patients and clinicians, health system leaders, and policymakers, among others—make well-informed decisions and thereby improve the quality of healthcare services. This report is not intended to be a substitute for the application of clinical judgment. Anyone who makes decisions concerning the provision of clinical care should consider this report in the same way as any medical reference and in conjunction with all other pertinent information, i.e., in the context of available resources and circumstances presented by individual patients.

This report is made available to the public under the terms of a licensing agreement between the author and the Agency for Healthcare Research and Quality. This report may be used and reprinted without permission except those copyrighted materials that are clearly noted in the report. Further reproduction of those copyrighted materials is prohibited without the express permission of copyright holders.

AHRQ or U.S. Department of Health and Human Services endorsement of any derivative products that may be developed from this report, such as clinical practice guidelines, other quality enhancement tools, or reimbursement or coverage policies may not be stated or implied.

This report may periodically be assessed for the currency of conclusions. If an assessment is done, the resulting surveillance report describing the methodology and findings will be found on the Effective Health Care Program website at www.effectivehealthcare.ahrq.gov. Search on the title of the report.

Persons using assistive technology may not be able to fully access information in this report. For assistance contact ude.hpshj@nosliwer.

Bookshelf ID: NBK576034PMID: 34990092

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