Abstract
Hemodialysis is an intensive treatment with a substantial time burden for patients. Generally, a standard hemodialysis schedule consists of three treatments per week, each lasting 4 hours. However, it can be debated whether this schedule is appropriate for all patients. Incremental hemodialysis refers to a treatment approach where hemodialysis is initiated with a less intensive schedule (i.e., fewer sessions per week) and gradually increased as residual kidney function declines. The effects of incremental hemodialysis on key outcomes—health-related quality of life, vascular access-related complications, and fluid overload—were discussed in this review. Although incremental hemodialysis is hypothesized to improve health-related quality of life, most studies found no significant difference. Similarly, most studies did not report significant differences in vascular access-related complications. Concerns have been raised regarding fluid overload due to extended intervals between sessions and underdialysis, especially when the transition to a thrice-weekly schedule is delayed. However, most studies found no difference in fluid overload related outcomes. Incremental hemodialysis is a promising, personalized treatment that could reduce the socioeconomic burden of dialysis. Given the methodologic limitations of available studies, ongoing trials will contribute to a clearer understanding of the role of incremental hemodialysis with varying residual kidney function at initiation.
Keywords: arteriovenous access, chronic hemodialysis, hemodialysis adequacy, patient-centered care, vascular access
Introduction
Hemodialysis is a time-intensive treatment for kidney failure, typically requiring three sessions per week, each lasting about 4 hours.1 Despite improvements in care, hemodialysis continues to impose a significant disease burden, including high cardiovascular mortality rates, frequent hospitalizations, and an impaired health-related quality of life (HRQoL).2–4 These persistent challenges underscore the need for standardized research outcomes meaningful to all stakeholders, especially patients. In response, the Standardized Outcomes in Nephrology initiative was established.5 As part of this initiative, a Delphi study identified dialysis-free time, HRQoL, the reduction of vascular access-related complications, and cardiovascular disease as among the most important research outcomes. In light of these outcomes, incremental hemodialysis, where patients with sufficient residual kidney function (RKF) begin hemodialysis at a lower frequency, transitioning to more frequent sessions as RKF declines, is an interesting treatment option.6 This typically involves a twice-weekly schedule although practical implementation varies.
In Figure 1, several potential benefits and concerns of incremental hemodialysis are summarized. It is hypothesized that incremental hemodialysis could improve HRQoL, reduce vascular access-related complications, and prolong preservation of RKF. Dialysis facilities can reduce costs by lowering the use of resources such as dialysate, dialyzers, saline, bloodlines, bicarbonate cartridges, and needles as well as by reducing staff workload.7 Several high-quality cohort studies have shown that incremental hemodialysis does not pose a higher mortality risk compared with standard treatment.8 However, if deteriorating RKF is recognized too late, incremental hemodialysis may lead to complications. Incremental hemodialysis in patients with residual urea clearance ≤3.0 ml/min per 1.73 m2 was associated with higher mortality in one study, potentially due to fluid overload.9 However, it is important to recognize that, beyond RKF, factors such as comorbid conditions, dietary and fluid intake, and medication adherence also significantly influence outcomes in incremental hemodialysis.10 Fluid overload could lead to an increased pill burden or hospitalizations.11 In addition, since RKF helps maintain plasma urea levels in twice-weekly hemodialysis patients, delayed detection of its decline may lead to reduced clearance of uremic solutes.12 Incremental hemodialysis is mentioned in several guidelines, but the implementation is not yet standardized.1,13,14 The 2019 British guideline mentions that an incremental schedule may be optimal in patients with significant RKF.14 However, as with the decision to initiate conventional dialysis, the choice to start incremental hemodialysis is not based solely on RKF. There is no international consensus on the other specific eligibility criteria, but Kalantar-Zadeh et al. proposed eight criteria based on expert opinion.15 Key eligibility criteria among these, in addition to residual diuresis >500 ml/24 hours, include minimal fluid retention between sessions, manageable comorbidities, and controllable electrolyte imbalances, particularly potassium and phosphate levels. Although most literature regarding incremental hemodialysis is observational, several studies suggest a beneficial association between incremental hemodialysis and the preservation of RKF and no increased mortality risk.8,16,17 Several studies have shown that RKF preservation may contribute to improved fluid homeostasis and HRQoL.18,19 However, less is known about the effect of incremental hemodialysis on HRQoL, vascular access-related complications, or fluid overload.
Figure 1.

Potential benefits and concerns of incremental hemodialysis. This figure was created in BioRender (Roos S, 2025, https://BioRender.com/j97b522). HRQoL, health-related quality of life; RKF, residual kidney function.
This narrative review will explore the key aspects of incremental hemodialysis aligned with the Standardized Outcomes in Nephrology initiative, focusing on potential benefits on HRQoL and vascular access-related complications, as well as addressing concerns related to fluid overload. An overview of the discussed studies including their specific definitions of incremental hemodialysis is presented in Supplemental Table 1.11,20–30
History of Hemodialysis Schedules
The Social Security Amendments in 1972 marked hemodialysis as a lifesaving treatment, resulting in financial reimbursement and widespread adoption in the United States.31–33 Since that time, the frequency, duration, and dose of hemodialysis sessions have varied significantly.33 Initially, sessions often exceeded 6 hours due to technical limitations such as inefficient small dialyzer surfaces. Inconvenient locations and manual setup added to the time burden, creating a demand for shorter schedules. As the dialyzer became more efficient, treatment times could be substantially reduced.34,35 Observational studies showed that thrice-weekly was superior compared with twice-weekly, especially for cognitive function.36,37 Following the National Cooperative Dialysis Study in 1981, thrice-weekly schedules with shorter durations became the standard.38 This trial demonstrated that low BUN concentration, rather than session duration, was crucial for preventing death or medical illness, shifting the focus to urea clearance and the Kt/V metric. However, in 2002, the Hemodialysis (HEMO) study demonstrated no significant differences in mortality or hospitalization between high and conventional urea clearance in thrice-weekly hemodialysis patients, although the difference in weekly standard Kt/V between intensive and standard regimens was marginal (3.60±0.57 versus 2.57±0.26, respectively).39,40 Of course, this finding was done against a background of enhanced efficiency over the previous decades. Several studies have shown beneficial effects of hemodialysis schedules with longer durations. Although based only on the observational studies, longer hemodialysis sessions lasting over 4 hours may decrease mortality.41,42 The effect of more than thrice-weekly hemodialysis on overall mortality is still uncertain, but the Frequent Dialysis Network trial demonstrated that six weekly hemodialysis sessions reduced mortality and improved hypertension control and cardiac function by reducing left ventricular mass compared with thrice-weekly hemodialysis.40,43,44 On the other hand, the nocturnal Frequent Dialysis Network trial showed that more frequent dialysis sessions can lead to an accelerated loss of RKF.45 A key limitation of many of these studies is the exclusion of patients with substantial RKF or the lack of adjustment for it.38,39,41 As a result, it remains unclear whether these findings are applicable to incident hemodialysis patients with substantial RKF, for whom incremental hemodialysis may be considered.
HRQoL
Incremental hemodialysis has been linked to both improved and decreased HRQoL. It has been suggested that HRQoL may be enhanced due to the reduced time burden resulting from fewer sessions.14 In addition, incremental hemodialysis most likely preserves RKF, which is associated with an improved HRQoL.17,19 On the other hand, it is conceivable that increased fluid overload, potentially associated with incremental hemodialysis, could exacerbate symptoms such as dyspnea and edema, thereby decreasing HRQoL.
Studies on HRQoL in incremental hemodialysis are scarce. A systematic review in 2022 yielded no studies reporting on HRQoL.46 However, there is one randomized controlled trial (RCT) and one observational study that reported on this outcome (Table 1). Vilar et al. demonstrated no significant difference in the Europe Quality of Life 5-Dimension 5-Level index value after 6 and 12 months in a small feasibility RCT, but the number of participants was very limited.11 Park et al. found no difference in the physical component score or mental component score of the Kidney Disease Quality of Life-Short-Form 12 between the incremental group, including once-weekly schedules, and the conventional group, measured at 3 and 12 months, but only 27% of patients completed the 12-month questionnaire.28
Table 1.
Comparison of incremental and conventional hemodialysis schedules on health-related quality of life–related outcomes
| Author (Year) | Study Design | Outcome | Results | P Value | ||
|---|---|---|---|---|---|---|
| Score | Incremental | Conventional | ||||
| Vilar et al. (2022)11 | RCT | EQ-5D-5L index valuea | Total score at 6 mo | 0.83 (IQR, 0.70–0.91) | 0.74 (IQR, 0.61–0.93) | P = 0.81b |
| Total score at 12 mo | 0.81 (IQR, 0.69–0.93) | 0.81 (IQR, 0.70–0.92) | ||||
| Park et al. (2016)28 | Observational | KDQOL-SF12 | PCS at 3 mo | 41.6±8.4 | 39.8±9.8 | P = 0.27 |
| PCS at 12 mo | 43.4±10.2 | 41.9±9.4 | P = 0.48 | |||
| MCS at 3 mo | 40.8±8.5 | 39.9±10.0 | P = 0.61 | |||
| MCS at 12 mo | 42.5±9.9 | 40.6±8.6 | P = 0.36 | |||
EQ-5D-5L, Europe Quality of Life-5-Dimension5-Level; IQR, interquartile range; KDQOL, Kidney Disease Quality of Life; MCS, mental component score; PCS, physical component score; RCT, randomized controlled trial; SF12, Short-Form 12.
Ranges from 1.0 (best possible score) to 0.0 (worst possible score).
Statistical significance of the difference in scores between the schedules from baseline to the last available score in the study.
Two Chinese studies compared the effect of maintenance twice-weekly hemodialysis on HRQoL. One RCT reported a higher total score of the Kidney Disease Quality of Life Short Form-36 in the twice-weekly group after 1 year.47 Another cross-sectional study found no significant differences in the Kidney Disease Quality of Life-Short-Form 12.48 However, these studies do not examine incremental hemodialysis, and patients on maintenance twice-weekly hemodialysis in China had a lower socioeconomic status, less health insurance, and the age in general was about 15 years lower than Western populations.11,28,47,48
Despite the fact that data on HRQoL are limited, some studies have examined outcomes which could affect HRQoL. In the TwoPlus Pilot RCT, conventional hemodialysis was compared with a schedule of twice-weekly hemodialysis during 6 weeks, followed by a transition to thrice-weekly hemodialysis.49 The dialysis symptom index (DSI), the generalized anxiety (Generalized Anxiety Disorder 7-Item [GAD-7]), and depression scores (Patient Health Questionnaire-9 [PHQ-9]) were examined after 6 and 12 weeks. The DSI scores regarding physical symptoms were slightly, but not significantly, better in the conventional group. On the other hand, the GAD-7 and PHQ-9 scores were better in the incremental group. Although psychologic symptoms were better in the incremental group, an increased number of physical symptoms could negatively affect HRQoL. Furthermore, assessments in this study stopped after 12 weeks, thus possibly missing long-term negative effects on HRQoL. Theoretically, psychologic symptoms could worsen as RKF declines and transitioning to thrice-weekly sessions becomes necessary, as this transition may be more difficult than starting with thrice-weekly sessions from the start. In a different observational study, Davenport et al. found no difference in the Beck Depression scale among prevalent hemodialysis patients on an incremental schedule and those on a conventional schedule but performed no follow-up of this questionnaire.24
In conclusion, evidence on HRQoL difference between incremental and conventional hemodialysis is limited with only two studies, both with small sample sizes and short follow-up periods. Future larger randomized trials or observational studies with extended follow-up are needed. Furthermore, qualitative studies could explore how patients experience specific aspects of HRQoL with incremental versus conventional hemodialysis.
Vascular Access-Related Complications
It is hypothesized that twice-weekly hemodialysis could reduce vascular access-related complications compared to thrice-weekly hemodialysis, particularly in patients with an arteriovenous fistula (AVF) or arteriovenous graft (AVG). Vascular access-related complications are a significant cause of hospitalization for patients on hemodialysis.50,51 Supposed mechanisms of the relationship between incremental hemodialysis and vascular access-related complications are summarized in Figure 2. First, fewer punctures can reduce local inflammation, cytokine release, and intimal proliferation, all of which may contribute to stenosis.52 Fewer punctures may also lower the risk of infection, but studies comparing six-weekly hemodialysis to thrice-weekly hemodialysis found no relation between dialysis frequency and infection risk.53 The risk of hematoma formation, which can progress to pseudo-aneurysms, may also be lowered.54 Second, reduced shear forces during blood return may lower the risk of intimal proliferation and therefore of stenosis of the AVF or AVG.55 Finally, the HEMO study found an association between intradialytic hypotension and an increased risk of fistula thrombosis.56 Since RKF is a key eligibility criterion for starting with incremental hemodialysis, these patients more often have RKF, require less ultrafiltration, and therefore experience intradialytic hypotension less frequently, which may help reduce fistula thrombosis.15,17
Figure 2.

Supposed mechanisms of the relationship between incremental hemodialysis and the possible reduction of vascular access-related complications. Incremental hemodialysis is associated with less intradialytic hypotension, which is associated with fistula thrombosis, and it decreases the number of punctures, possibly reducing stenosis, (pseudo)aneurysms, and infections.52–54,56 Reduced shear forces may decrease the risk of stenosis.55 This figure was created in BioRender (Roos S, 2025, https://BioRender.com/i12e044).
It is important to note that the hypothesis of a relationship between hemodialysis frequency and the risk of vascular access-related complications originates from studies comparing six-weekly dialysis with thrice-weekly dialysis, which observed a higher incidence of vascular access-related complications in the frequent dialysis schedule.53 Notably, the difference in puncture frequency is more pronounced in these comparisons: 12 punctures versus six for double-needle cannulations. It remains unclear whether these results extend to the comparison between thrice-weekly and twice-weekly schedules, where the difference is smaller. In Figure 3, two RCTs and seven observational studies comparing incremental and conventional schedules on vascular access-related events are summarized. Details of these results are presented in Supplemental Table 2. In a RCT by Vilar et al., the conventional group demonstrated nonsignificantly higher vascular access-related complication rates compared with the incremental group.11 In a pilot trial by Murea et al., which reported on the causes of hospitalization over a mean follow-up of 9 months, the low number of events in both groups made it difficult to draw any meaningful conclusions.20 In the most recent study of Lucas et al., the complication rates of AVFs in 112 patients on an incremental schedule were compared with those in 76 patients on a conventional schedule, all from a single dialysis unit.26 After a mean follow-up of 2 years, no difference was found and AVG or catheter complications were not reported. Chen et al. was the only study to report a significant reduction in vascular access-related complications in the incremental group.23 However, this study included once-weekly schedules in the incremental group, with fewer punctures, potentially contributing to a greater difference. Caria et al. compared a schedule of once-weekly hemodialysis, combined with a low-protein diet, with conventional thrice-weekly hemodialysis and found no significant difference in vascular access-related hospitalizations.21 Two studies did not focus on incremental hemodialysis but compared long-term hemodialysis patients that maintained on twice-weekly versus thrice-weekly schedules and they found no difference in dysfunction of the AVF or vascular access-related hospitalizations.57,58
Figure 3.

Comparison of incremental and conventional hemodialysis schedules on vascular access-related complications. aNo incidence rate ratio could be calculated because zero events occurred in the incremental group. bHR reported. Murea et al.20 and Vilar et al.11 were the only RCTs reporting this outcome. Both the study of Lin et al.57 and Panaput et al.58 compared maintenance twice-versus thrice weekly hemodialysis instead of incremental hemodialysis. HR, hazard ratio; RCT, randomized controlled trial.
Several methodologic limitations of the abovementioned studies must be taken into account. Most studies were observational, and prospective studies were small with <100 inclusions per the treatment group. Many studies only examined complications of AVF or grouped all types of vascular access-related complications together, including catheter-related complications, without distinguishing the results by access type. The relatively small sample sizes of many of the studies limit their ability to detect any significant differences in vascular access-related complications. Furthermore, the inclusion of once-weekly schedules into two studies complicates comparisons between the studies.21,23
Fluid Overload
Several studies have reported an increased risk of cardiovascular events on Mondays or on the day after a 2-day interdialytic interval for patients on hemodialysis.59–61 This may be explained by electrolyte imbalances as well as by fluid accumulation after the dialysis break. However, RKF (daily urine output or average creatinine-urea clearance) was not accurately reported in some of these studies, and no increased risk was found in the subgroup of patients with <12 months of dialysis treatment history, where the proportion of RKF is likely higher.60 Therefore, it remains unclear whether the longer dialysis-free interval in incremental hemodialysis poses a risk for fluid overload. Mathew et al. reported that in facilities practicing incremental hemodialysis, about 56% (interquartile range, 37%–64%) of patients had urine collection within the first 91 days of dialysis.62 Lack of serial assessment of RKF could lead to late recognition of deteriorating RKF in patients on incremental hemodialysis and, consequently, a delay in schedule intensification. In addition, although no study has yet investigated this, patients may find it psychologically challenging to increase hemodialysis frequency as soon as this becomes necessary, which can contribute to a delay. A delay in schedule intensification could lead to an inadequate dialysis efficiency which could lead to fluid overload. The results of some small descriptive studies suggest that interdialytic weight gain was increased at the moment before transitioning from twice-weekly to thrice-weekly hemodialysis, providing some indication that delayed transitioning could be a potential concern in incremental hemodialysis.62,63 Furthermore, some studies of patients on maintenance twice-weekly hemodialysis reported an increased risk of volume overload.64,65
As no standard measurement method exists for the evaluation of fluid overload, we discussed studies that reported on outcomes related to fluid overload such as fluid overload related hospitalizations or events, ultrafiltration, BP (N-terminal pro [NT-pro]), brain natriuretic peptide (BNP), bioimpedance measurements, interdialytic weight gain, number of antihypertensive drugs, or fluid overload-related symptoms. The results of one RCT and five observational studies that evaluated any of these outcomes are presented in Table 2. The study of Vilar et al. was the only RCT that examined outcomes related to fluid overload.11 Although, after 12 months, the incremental group had 1 L more extracellular water on bioimpedance and both the number of antihypertensive drugs used and the number of fluid overload-related events were higher in the incremental group, none of these differences were statistically significant.
Table 2.
Comparison of incremental and conventional hemodialysis schedules on outcomes related to fluid overload
| Author (Year) | Study Design | Outcome | Results | P Value | Conclusion | |
|---|---|---|---|---|---|---|
| Incremental | Conventional | |||||
| Vilar et al. (2022)11 | RCT | Amount of antihypertensives at 12 mo | 3.1 pills (95% CI, 2.5 to 3.8) | 2.1 pills (95% CI, 0.9 to 3.2) | NSa | No difference |
| Fluid overload related events | Three per person-year | Two per person-year | P = 0.49 | No difference | ||
| Pre-dialysis systolic BP at 12 mo | 158 mm Hg (95% CI, 146 to 170) | 160 mm Hg (95% CI, 143 to 176 | NSa | No difference | ||
| Extracellular water on bioimpedance measurement | 20.8 L (95% CI, 19 to 23) | 19.9 L (95% CI, 18 to 22) | NSa | No difference | ||
| Caria et al. (2014)21 | Observational | Fluid overload related events | 0 | Two (acute pulmonary edema and congestive heart failure) | NR | N/A |
| Casino et al. (2022)22 | Observational | Ultrafiltration at 3 mo | 1×/wk: 1.95±1.06 L/session | 2.2±0.84 L/session | P = 0.04b | N/A |
| 2×/wk: 2.3±1.07 L/session | ||||||
| Davenport et al. (2019)24 | Observational | Pre-dialysis systolic BP | 149±25 mm Hg | 139±24 mm Hg | P < 0.001 | Increased risk incremental group |
| Pre-dialysis diastolic BP | 77±16 mm Hg | 71±16 mm Hg | P < 0.001 | |||
| Kaja Kamal et al. (2017)25 | Observational | Ultrafiltration | 568 ml more compared to incremental group | P < 0.001 | Increased risk conventional group | |
| Torreggiani et al. (2022)30 | Observational | Median NT-pro-BNP | 1×/wk: 1970 ng/L (IQR, 1471–8018) | 3×/wk: 4122 ng/L (IQR, 2103–9180) | P = 0.59a | N/A |
| 2×/wk: 3734 ng/L (IQR, 1590–10028) | ||||||
Reported outcomes related to fluid overload: fluid overload related events/hospitalizations (n); ultrafiltration (ml or l or kg/session); systolic BP (mm Hg); N-terminal pro-brain natriuretic peptide (ng/ml); amount of antihypertensives (N); extracellular water (L). CI, confidence interval; IQR, interquartile range; N/A, not applicable; NR, not reported; NT-pro-BNP, N-terminal pro-brain natriuretic peptide; RCT, randomized controlled trial.
Based on 95% confidence intervals instead of P value.
Statistical significance between three groups is reported, no pairwise comparisons were performed.
Caria et al. reported no fluid overload-related events in 38 patients from the incremental group with a follow-up of 2 years.21 Davenport et al. was the only study that reported results that may indicate an increased risk of fluid overload in the incremental group.24 In this observational study, a higher predialysis systolic and diastolic BP was reported in the incremental group. However, neither baseline BP nor RKF was reported.
Two studies reported results that may indicate a higher risk of fluid overload in the conventional group. First, Kaja Kamal et al. reported higher ultrafiltration in the conventional group.25 This may partly be explained by selection bias, as patients in the conventional group were significantly older and had more diabetes and peripheral vascular disease compared with the incremental group. Second, Casino et al. conducted a one-way ANOVA to compare the ultrafiltration among patients with diuresis above 500 ml, divided into three groups: once-weekly, twice-weekly, and thrice-weekly dialysis schedules.22 The analysis revealed a significant difference between the groups, with lower ultrafiltration in the once-weekly group. However, pairwise comparisons between the twice-weekly and thrice-weekly groups were not specifically tested, and the difference between these two groups was minimal (0.1 L).
Effects of hemodialysis frequency on (NT-pro) BNP have been reported in one study, which found no difference between the two schedules.30 However, both NT-pro BNP and BNP are partially cleared by the kidneys, meaning their levels are influenced by kidney function, and no definitive optimal cutoff for these biomarkers has been established.66,67 Both biomarkers are partially cleared by dialysis, which further complicates their interpretation. The dry-weight reduction In hypertensive hemodialysis patients trial demonstrated that in hypertensive hemodialysis patients, BNP levels are primarily influenced by baseline BNP concentrations, and a decline in BNP levels did not predict reduction in dry weight.68
To the best of our knowledge, there are no studies that report on symptoms related to fluid overload, such as dyspnea, coughing, or edema. Although these symptoms rely on subjective reporting, they are clinically relevant and the use of the DSI could provide more objective measurements. Furthermore, the clinically relevant effect of incremental hemodialysis on long-term fluid overload and more severe hypertension has not been evaluated but may contribute to the high prevalence of diastolic dysfunction in dialysis patients.69
Conclusion
Since the initiation of chronic hemodialysis in 1960, several developments have led to the adoption of a standard thrice-weekly schedule. This schedule is now being reevaluated with the concept of incremental hemodialysis. Multiple studies have demonstrated the safety of incremental hemodialysis regarding mortality and the positive effect on RKF. Some guidelines also mention the option of incremental hemodialysis for patients with RKF, but its implementation is not yet standardized. Evidence regarding its effect on HRQoL remains limited. This is largely due to the small number of studies, limited sample sizes, and short follow-up periods. Furthermore, most studies regarding vascular access-related complications showed no difference between the conventional and the incremental group. Finally, the heterogeneity in reported outcomes is high, but most studies did not show an increased risk of fluid overload with the incremental schedule. Regular serial urine collections remain crucial for detecting declining RKF in a timely manner and enabling appropriate intensification of the dialysis schedule.
It is important to recognize that the absence of standardized protocols for implementing incremental hemodialysis leads to variability in outcomes across studies. Therefore, ongoing trials will contribute to a clearer understanding of the role of incremental hemodialysis. We identified 11 ongoing RCTs, of which ten will report on quality of life,70–79 four on vascular access-related complications,73,75,76,79 and seven on outcomes related to fluid overload.73–77,79,80 Since RCTs often face challenges such as limited sample sizes or short follow-up periods, large observational cohort studies with extended follow-up can offer additional valuable insights. As long as patients are counseled that schedules generally need to be intensified over time and that twice-weekly dialysis will not be permanent, this treatment approach undoubtedly has a place in the current era of personalized medicine.
Supplementary Material
Disclosures
Disclosure forms, as provided by each author, are available with the online version of the article at http://links.lww.com/KN9/B314.
Author Contributions
Conceptualization: Erik L. Penne, Sanne Roos, Thomas S. van Lieshout.
Supervision: Erik L. Penne.
Visualization: Sanne Roos, Thomas S. van Lieshout.
Writing – original draft: Sanne Roos, Thomas S. van Lieshout.
Writing – review & editing: Alferso C. Abrahams, Erik L. Penne, Sanne Roos, Frans J. van Ittersum, Brigit C. van Jaarsveld, Thomas S. van Lieshout.
Funding
None.
Supplemental Material
This article contains the following supplemental material online at http://links.lww.com/KN9/B315.
Supplemental Table 1. Discussed observational and randomized studies comparing incremental with conventional hemodialysis schedules.
Supplemental Table 2. Comparison of incremental and conventional hemodialysis schedules on vascular access-related events.
References
- 1.Tattersall J Martin-Malo A Pedrini L, et al. EBPG guideline on dialysis strategies. Nephrol Dial Transplant. 2007;22(suppl 2):ii5–21. doi: 10.1093/ndt/gfm022 [DOI] [PubMed] [Google Scholar]
- 2.Collins AJ Foley RN Herzog C, et al. US renal data system 2012 annual data report. Am J Kidney Dis. 2013;61(1 suppl 1):A7, e1-476. doi: 10.1053/j.ajkd.2012.11.031 [DOI] [PubMed] [Google Scholar]
- 3.Fletcher BR Damery S Aiyegbusi OL, et al. Symptom burden and health-related quality of life in chronic kidney disease: a global systematic review and meta-analysis. PLoS Med. 2022;19(4):e1003954. doi: 10.1371/journal.pmed.1003954 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Grams ME Coresh J Matsushita K, et al.; Writing Group for the CKD Prognosis Consortium. Estimated glomerular filtration rate, albuminuria, and adverse outcomes: an individual-participant data meta-analysis. JAMA. 2023;330(13):1266–1277. doi: 10.1001/jama.2023.17002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Evangelidis N Tong A Manns B, et al. Developing a set of core outcomes for trials in hemodialysis: an international Delphi survey. Am J Kidney Dis. 2017;70(4):464–475. doi: 10.1053/j.ajkd.2016.11.029 [DOI] [PubMed] [Google Scholar]
- 6.Wong J, Vilar E, Davenport A, Farrington K. Incremental haemodialysis. Nephrol Dial Transplant. 2015;30(10):1639–1648. doi: 10.1093/ndt/gfv231 [DOI] [PubMed] [Google Scholar]
- 7.Erickson KF, Sirich TL. Economic considerations of incremental hemodialysis. Kidney360. 2025;6(5):854–856. doi: 10.34067/KID.0000000812 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Caton E, Sharma S, Vilar E, Farrington K. Impact of incremental initiation of haemodialysis on mortality: a systematic review and meta-analysis. Nephrol Dial Transplant. 2023;38(2):435–446. doi: 10.1093/ndt/gfac274 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Obi Y Streja E Rhee CM, et al. Incremental hemodialysis, residual kidney function, and mortality risk in incident dialysis patients: a cohort study. Am J Kidney Dis. 2016;68(2):256–265. doi: 10.1053/j.ajkd.2016.01.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Murea M Torreggiani M Deira J, et al. From niche to norm: a multiaction plan to close gaps and mainstream incremental hemodialysis. Kidney Int. 2025;108(2):201–213. doi: 10.1016/j.kint.2025.03.032 [DOI] [PubMed] [Google Scholar]
- 11.Vilar E Kaja Kamal RM Fotheringham J, et al. A multicenter feasibility randomized controlled trial to assess the impact of incremental versus conventional initiation of hemodialysis on residual kidney function. Kidney Int. 2022;101(3):615–625. doi: 10.1016/j.kint.2021.07.025 [DOI] [PubMed] [Google Scholar]
- 12.Leong SC, Sao JN, Taussig A, Plummer NS, Meyer TW, Sirich TL. Residual function effectively controls plasma concentrations of secreted solutes in patients on twice weekly hemodialysis. J Am Soc Nephrol. 2018;29(7):1992–1999. doi: 10.1681/ASN.2018010081 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.National Kidney Foundation. KDOQI clinical practice guideline for hemodialysis adequacy: 2015 update. Am J Kidney Dis. 2015;66(5):884–930. doi: 10.1053/j.ajkd.2015.07.015 [DOI] [PubMed] [Google Scholar]
- 14.Ashby D Borman N Burton J, et al. Renal association clinical practice guideline on haemodialysis. BMC Nephrol. 2019;20(1):379. doi: 10.1186/s12882-019-1527-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Kalantar-Zadeh K Unruh M Zager PG, et al. Twice-weekly and incremental hemodialysis treatment for initiation of kidney replacement therapy. Am J Kidney Dis. 2014;64(2):181–186. doi: 10.1053/j.ajkd.2014.04.019 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Campo A, Goia F, Cottino R, Gandolfo C, Viglino G. Reduced intensity incremental hemodialysis start does not decrease life expectancy and saves money: results of the RIDDLE study. J Nephrol. 2025;38(3):1043–1048. doi: 10.1007/s40620-025-02271-z [DOI] [PubMed] [Google Scholar]
- 17.Takkavatakarn K, Jintanapramote K, Phannajit J, Praditpornsilpa K, Eiam-Ong S, Susantitaphong P. Incremental versus conventional haemodialysis in end-stage kidney disease: a systematic review and meta-analysis. Clin Kidney J. 2024;17(1):sfad280. doi: 10.1093/ckj/sfad280 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Marquez IO Tambra S Luo FY, et al. Contribution of residual function to removal of protein-bound solutes in hemodialysis. Clin J Am Soc Nephrol. 2011;6(2):290–296. doi: 10.2215/CJN.06100710 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Shafi T Jaar BG Plantinga LC, et al. Association of residual urine output with mortality, quality of life, and inflammation in incident hemodialysis patients: the choices for healthy outcomes in caring for end-stage renal disease (CHOICE) study. Am J Kidney Dis. 2010;56(2):348–358. doi: 10.1053/j.ajkd.2010.03.020 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Murea M Patel A Highland BR, et al. Twice-weekly hemodialysis with adjuvant pharmacotherapy and transition to thrice-weekly hemodialysis: a pilot study. Am J Kidney Dis. 2022;80(2):227–240.e1. doi: 10.1053/j.ajkd.2021.12.001 [DOI] [PubMed] [Google Scholar]
- 21.Caria S, Cupisti A, Sau G, Bolasco P. The incremental treatment of ESRD: a low-protein diet combined with weekly hemodialysis may be beneficial for selected patients. BMC Nephrol. 2014;15:172. doi: 10.1186/1471-2369-15-172 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Casino FG Lopez T Santarsia G, et al. Could incremental haemodialysis be a new standard of care? A suggestion from a long-term observational study. G Ital Nefrol. 2022;39(3):2022-vol3. PMID: 35819039 [PubMed] [Google Scholar]
- 23.Chen W Wang M Zhang M, et al. Benefits of incremental hemodialysis seen in a historical cohort study. Ther Clin Risk Manag. 2021;17:1177–1186. doi: 10.2147/tcrm.S332218 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Davenport A Guirguis A Almond M, et al. Comparison of characteristics of centers practicing incremental vs. conventional approaches to hemodialysis delivery - postdialysis recovery time and patient survival. Hemodial Int. 2019;23(3):288–296. doi: 10.1111/hdi.12743 [DOI] [PubMed] [Google Scholar]
- 25.Kaja Kamal RM Farrington K Busby AD, et al. Initiating haemodialysis twice-weekly as part of an incremental programme may protect residual kidney function. Nephrol Dial Transplant. 2019;34(6):1017–1025. doi: 10.1093/ndt/gfy321 [DOI] [PubMed] [Google Scholar]
- 26.Fernández Lucas M, Piris González M, Díaz Domínguez ME, Collado Alsina A, Rodríguez Mendiola NM. Incremental hemodialysis and vascular access complications: a 12-year experience in a hospital hemodialysis unit. J Nephrol. 2024;37(7):1929–1937. doi: 10.1007/s40620-024-01932-9 [DOI] [PubMed] [Google Scholar]
- 27.Lucas MF Teruel JL Ruíz-Roso G, et al. Incremental hemodialysis schedule in patients with higher residual renal function at the start of dialysis. Adv Nephrol. 2014;2014(1):236245. doi: 10.1155/2014/236245 [DOI] [Google Scholar]
- 28.Park JI Park JT Kim YL, et al. Comparison of outcomes between the incremental and thrice-weekly initiation of hemodialysis: a propensity-matched study of a prospective cohort in Korea. Nephrol Dial Transplant. 2017;32(2):355–363. doi: 10.1093/ndt/gfw332 [DOI] [PubMed] [Google Scholar]
- 29.Tawfik AAS, Ahmed SAE, Abd-Elaziz HE, Mady GES. Incremental versus conventional hemodialysis: which is better for prevalent hemodialysis patients? Egypt J Hosp Med. 2022;87(1):1848–1855. doi: 10.21608/ejhm.2022.231634 [DOI] [Google Scholar]
- 30.Torreggiani M Fois A Chatrenet A, et al. Incremental and personalized hemodialysis start: a new standard of care. Kidney Int Rep. 2022;7(5):1049–1061. doi: 10.1016/j.ekir.2022.02.010 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Lacson EJ, Brunelli SM. Hemodialysis treatment time: a fresh perspective. Clin J Am Soc Nephrol. 2011;6(10):2522–2530. doi: 10.2215/CJN.00970211 [DOI] [PubMed] [Google Scholar]
- 32.Rettig RA. Origins of the Medicare Kidney Disease Entitlement: The Social Security Amendments of 1972. National Academy Press; 1991. [Google Scholar]
- 33.Van Stone JC. Dialysis equipment and dialysate, past, present and the future. Semin Nephrol. 1997;17(3):214–217. PMID: 9165650 [PubMed] [Google Scholar]
- 34.Scribner BH, Cole JJ, Ahmad S, Blagg CR. Why thrice weekly dialysis? Hemodial Int. 2004;8(2):188–192. doi: 10.1111/j.1492-7535.2004.01094.x [DOI] [PubMed] [Google Scholar]
- 35.Gotch F Lipps B Weaver J Jr., et al. Chronic hemodialysis with the hollow fiber artificial kidney (HFAK). Trans Am Soc Artif Intern Organs. 1969;15:87–96. PMID: 5791436 [PubMed] [Google Scholar]
- 36.Teschan PE, Ginn HE, Bourne JR, Ward JW. Assessing the adequacy of dialysis. Proc Eur Dial Transplant Assoc. 1981;18:697–705. PMID: 7329997 [PubMed] [Google Scholar]
- 37.Teschan PE, Ginn HE, Walker PJ, Bourne JR, Fristoe M, Ward JW. Quantified functions of the nervous system in uremic patients on maintenance dialysis. Trans Am Soc Artif Intern Organs. 1974;20a:388–392. PMID: 4450361. [PubMed] [Google Scholar]
- 38.Lowrie EG, Laird NM, Parker TF, Sargent JA. Effect of the hemodialysis prescription on patient morbidity: report from the National Cooperative Dialysis study. N Engl J Med. 1981;305(20):1176–1181. doi: 10.1056/nejm198111123052003 [DOI] [PubMed] [Google Scholar]
- 39.Eknoyan G Beck GJ Cheung AK, et al. Effect of dialysis dose and membrane flux in maintenance hemodialysis. N Engl J Med. 2002;347(25):2010–2019. doi: 10.1056/NEJMoa021583 [DOI] [PubMed] [Google Scholar]
- 40.Chertow GM Levin NW Beck GJ, et al.; FHN Trial Group. In-center hemodialysis six times per week versus three times per week. N Engl J Med. 2010;363(24):2287–2300. doi: 10.1056/NEJMoa1001593 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Jansz TT Noordzij M Kramer A, et al. Survival of patients treated with extended-hours haemodialysis in Europe: an analysis of the ERA-EDTA registry. Nephrol Dial Transplant. 2020;35(3):488–495. doi: 10.1093/ndt/gfz208 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Saran R Bragg-Gresham JL Levin NW, et al. Longer treatment time and slower ultrafiltration in hemodialysis: associations with reduced mortality in the DOPPS. Kidney Int. 2006;69(7):1222–1228. doi: 10.1038/sj.ki.5000186 [DOI] [PubMed] [Google Scholar]
- 43.Chertow GM Levin NW Beck GJ, et al. Long-term effects of frequent In-Center hemodialysis. J Am Soc Nephrol. 2016;27(6):1830–1836. doi: 10.1681/ASN.2015040426 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Natale P Green SC Rose M, et al. Frequent hemodialysis versus standard hemodialysis for people with kidney failure: systematic review and meta-analysis of randomized controlled trials. PLoS One. 2024;19(9):e0309773. doi: 10.1371/journal.pone.0309773 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Daugirdas JT Greene T Rocco MV, et al. Effect of frequent hemodialysis on residual kidney function. Kidney Int. 2013;83(5):949–958. doi: 10.1038/ki.2012.457 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Moorman D Pilkey NG Goss CJ, et al. Twice versus thrice weekly hemodialysis: a systematic review. Hemodial Int. 2022;26(4):461–479. doi: 10.1111/hdi.13045 [DOI] [PubMed] [Google Scholar]
- 47.Dai L Lu C Liu J, et al. Impact of twice- or three-times-weekly maintenance hemodialysis on patient outcomes: a multicenter randomized trial. Medicine (Baltimore). 2020;99(20):e20202. doi: 10.1097/md.0000000000020202 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Bieber B Qian J Anand S, et al. Two-times weekly hemodialysis in China: frequency, associated patient and treatment characteristics and quality of life in the China dialysis outcomes and practice patterns study. Nephrol Dial Transplant. 2014;29(9):1770–1777. doi: 10.1093/ndt/gft472 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Murea M, Highland BR, Yang W, Dressler E, Russell GB. Patient-reported outcomes in a pilot clinical trial of twice-weekly hemodialysis start with adjuvant pharmacotherapy and transition to thrice-weekly hemodialysis vs conventional hemodialysis. BMC Nephrol. 2022;23(1):322. doi: 10.1186/s12882-022-02946-w [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.van Eck van der Sluijs A Bonenkamp AA van Wallene VA, et al. Differences in hospitalisation between peritoneal dialysis and haemodialysis patients. Eur J Clin Invest. 2022;52(6):e13758. doi: 10.1111/eci.13758 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Manns B Tonelli M Yilmaz S, et al. Establishment and maintenance of vascular access in incident hemodialysis patients: a prospective cost analysis. J Am Soc Nephrol. 2005;16(1):201–209. doi: 10.1681/ASN.2004050355 [DOI] [PubMed] [Google Scholar]
- 52.Stracke S Konner K Köstlin I, et al. Increased expression of TGF-beta1 and IGF-I in inflammatory stenotic lesions of hemodialysis fistulas. Kidney Int. 2002;61(3):1011–1019. doi: 10.1046/j.1523-1755.2002.00191.x [DOI] [PubMed] [Google Scholar]
- 53.Suri RS Larive B Sherer S, et al. Risk of vascular access complications with frequent hemodialysis. J Am Soc Nephrol. 2013;24(3):498–505. doi: 10.1681/ASN.2012060595 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Mudoni A Cornacchiari M Gallieni M, et al. Aneurysms and pseudoaneurysms in dialysis access. Clin Kidney J. 2015;8(4):363–367. doi: 10.1093/ckj/sfv042 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Browne LD, Bashar K, Griffin P, Kavanagh EG, Walsh SR, Walsh MT. The role of shear stress in arteriovenous fistula maturation and failure: a systematic review. PLoS One. 2015;10(12):e0145795. doi: 10.1371/journal.pone.0145795 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Chang TI Paik J Greene T, et al. Intradialytic hypotension and vascular access thrombosis. J Am Soc Nephrol. 2011;22(8):1526–1533. doi: 10.1681/ASN.2010101119 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Lin YF Huang JW Wu MS, et al. Comparison of residual renal function in patients undergoing twice-weekly versus three-times-weekly haemodialysis. Nephrology (Carlton). 2009;14(1):59–64. doi: 10.1111/j.1440-1797.2008.01016.x [DOI] [PubMed] [Google Scholar]
- 58.Panaput T Thinkhamrop B Domrongkitchaiporn S, et al. Dialysis dose and risk factors for death among ESRD patients treated with twice-weekly hemodialysis: a prospective cohort study. Blood Purif. 2014;38(3-4):253–262. doi: 10.1159/000368885 [DOI] [PubMed] [Google Scholar]
- 59.Bleyer AJ, Russell GB, Satko SG. Sudden and cardiac death rates in hemodialysis patients. Kidney Int. 1999;55(4):1553–1559. doi: 10.1046/j.1523-1755.1999.00391.x [DOI] [PubMed] [Google Scholar]
- 60.Foley RN, Gilbertson DT, Murray T, Collins AJ. Long interdialytic interval and mortality among patients receiving hemodialysis. N Engl J Med. 2011;365(12):1099–1107. doi: 10.1056/NEJMoa1103313 [DOI] [PubMed] [Google Scholar]
- 61.Fotheringham J Smith MT Froissart M, et al. Hospitalization and mortality following non-attendance for hemodialysis according to dialysis day of the week: a European cohort study. BMC Nephrol. 2020;21(1):218. doi: 10.1186/s12882-020-01874-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Mathew A Obi Y Rhee CM, et al. Treatment frequency and mortality among incident hemodialysis patients in the United States comparing incremental with standard and more frequent dialysis. Kidney Int. 2016;90(5):1071–1079. doi: 10.1016/j.kint.2016.05.028 [DOI] [PubMed] [Google Scholar]
- 63.Ghahremani-Ghajar M Rojas-Bautista V Lau WL, et al. Incremental hemodialysis: the University of California Irvine experience. Semin Dial. 2017;30(3):262–269. doi: 10.1111/sdi.12591 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Fang N Che M Shi L, et al. B-type natriuretic peptide levels and volume status in twice-weekly hemodialysis patients. Ren Fail. 2021;43(1):1259–1265. doi: 10.1080/0886022x.2021.1971091 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Mukherjee T, Devi G, Geetha S, Anchan NJ, Sankarasubbaiyan S. A comparison of practice pattern and outcome of twice-weekly and thrice-weekly hemodialysis patients. Indian J Nephrol. 2017;27(3):185–189. doi: 10.4103/0971-4065.202844 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Davies SJ, Davenport A. The role of bioimpedance and biomarkers in helping to aid clinical decision-making of volume assessments in dialysis patients. Kidney Int. 2014;86(3):489–496. doi: 10.1038/ki.2014.207 [DOI] [PubMed] [Google Scholar]
- 67.Wang AY. Clinical utility of natriuretic peptides in dialysis patients. Semin Dial. 2012;25(3):326–333. doi: 10.1111/j.1525-139X.2012.01079.x [DOI] [PubMed] [Google Scholar]
- 68.Agarwal R. B-type natriuretic peptide is not a volume marker among patients on hemodialysis. Nephrol Dial Transplant. 2013;28(12):3082–3089. doi: 10.1093/ndt/gft054 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Laddha M, Sachdeva V, Diggikar PM, Satpathy PK, Kakrani AL. Echocardiographic assessment of cardiac dysfunction in patients of end stage renal disease on haemodialysis. J Assoc Physicians India. 2014;62(1):28–32. PMID: 25327089 [PubMed] [Google Scholar]
- 70.Courivaud C. Quality of Life of Frail Aged Patients in Incremental Hemodialysis: A Phase III Study, 2022. ClinicalTrials.gov. Accessed September 12, 2025. https://clinicaltrials.gov/study/NCT03782519 [Google Scholar]
- 71.Rhee CM Kovesdy CP Unruh M, et al. Incremental hemodialysis transition in veterans and nonveterans with kidney failure. Curr Opin Nephrol Hypertens. 2025;34(1):33–40. doi: 10.1097/mnh.0000000000001040 [DOI] [PubMed] [Google Scholar]
- 72.Deira J Suárez MA López F, et al. IHDIP: a controlled randomized trial to assess the security and effectiveness of the incremental hemodialysis in incident patients. BMC Nephrol. 2019;20(1):8. doi: 10.1186/s12882-018-1189-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73.Kaja Kamal RM Farrington K Wellsted D, et al. Impact of incremental versus conventional initiation of haemodialysis on residual kidney function: study protocol for a multicentre feasibility randomised controlled trial. BMJ Open. 2020;10(8):e035919. doi: 10.1136/bmjopen-2019-035919 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Fernández Lucas M Ruíz-Roso G Merino JL, et al. Initiating renal replacement therapy through incremental haemodialysis: protocol for a randomized multicentre clinical trial. Trials. 2020;21(1):206. doi: 10.1186/s13063-020-4058-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75.Murea M Raimann JG Divers J, et al. Comparative effectiveness of an individualized model of hemodialysis vs conventional hemodialysis: a study protocol for a multicenter randomized controlled trial (the TwoPlus trial). Trials. 2024;25(1):424. doi: 10.1186/s13063-024-08281-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Kerr P. The INCremental Dialysis to Improve Health Outcomes in People Starting Haemodialysis (INCH-HD) Study: A Randomised Controlled Trial, 2024. ClinicalTrials.gov. Accessed September 12, 2025. https://clinicaltrials.gov/study/NCT04932148 [Google Scholar]
- 77.White CA, Wellihinda H, Day AG, Heyland DK, Holden RM. Pilot randomized trial of dialysis less frequently in the elderly: the D-LITE study. Kidney Int Rep. in press. doi: 10.1016/j.ekir.2025.08.043 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Zhang W. Feasibility and Safety of Incremental Hemodialysis in Initial Dialysis Patients - A single-center Randomized Controlled Study. WHO International Clinical Trials Registry Platform, 2023. Accessed September 12, 2025. https://trialsearch.who.int/Trial2.aspx?TrialID=ChiCTR2300078656 [Google Scholar]
- 79.Lok C. CANadian INCremental Dialysis to Improve Health Outcomes in People Starting Hemodialysis (CAN INCH-HD) Study. ISRCTN, 2023. Accessed September 12, 2025. https://www.isrctn.com/ISRCTN78497421 [Google Scholar]
- 80.Casino FG Basile C Kirmizis D, et al. The reasons for a clinical trial on incremental haemodialysis. Nephrol Dial Transplant. 2020;35(11):2015–2019. doi: 10.1093/ndt/gfaa220 [DOI] [PubMed] [Google Scholar]
