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JSM Renal Medicine

Clinical and Biological Benefits of Daily Online Hemodiafiltration

Research Article | Open Access | Volume 1 | Issue 1

  • 1. Institute of Nephrology, Université Medecine Paris Descartes, France
  • 2. Institute of Nephrology, Centre AURA Paris Plaisance, France
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Corresponding Authors
Caroline Créput, Centre AURA Paris Plaisance Nephrology and Hemodialysis Center, 185 rue Raymond Losserand, 75014 PARIS, France, Tel: 33181696000 ; Fax: 33181696049;
Abstract

Introduction: Daily Online Hemodiafiltration (D-OL-HDF), by combining OL-HDF and daily hemodialysis, is an interesting alternative modality for ESKD patients. First results were reported by Fischbach et al., on children and by Maduell et al., on adult’s patients in 2003: excellent clinical tolerance and better dialysis adequacy allowing a better quality of life, an improvement in nutritional status, a better control of anemia and blood pressure and a reduction of left ventricular mass were reported. However, there is no data regarding this technique since 2003. We studied here retrospectively ten patients treated with D-OL-HDF and followed them during twelve-months to evaluate the benefits of this modality.

Materiel and Methods: All 10 patients, treated with D-OL-HDF between 2011 and 2015 in our centre, were included in this study. Data were collected monthly after changing three times a week OL-HDF to D-OL-HDF (six or five times a week, 2 to 2.5 hours by session respectively): dialysis adequacy, hemodynamic and cardiovascular parameters, bone’s parameters and nutritional status have been evaluated.

Results and Discussion: As expected, the Interdialytic Weight Gain (IDWG) was significantly lower as well as the value of Brain Natriuretic Peptid (BNP) and, in meanwhile, a gain in Left Ventricular Ejection Fraction (LVEF) after twelve months was obtained. We observed also a significant increase in haemoglobin value and in serum albuminemia whereas other parameters remained stable. Moreover, phosphate binders and oral calcium supplementation were reduced during the follow-up.

Discussion: These benefits are consistent with those presented by Maduell et al: D-OL-HDF seems to be an excellent technique and should be considered as an alternative treatment to three times a week conventional treatment.

Keywords

•    Hemodiafiltration
•    Daily hemodialysis
•    Dialysis efficiency

Citation

Roux A, Fumeron C, Petitclerc T, Créput C (2016) Clinical and Biological Benefits of Daily Online Hemodiafiltration. JSM Renal Med 1(1): 1005.

ABBREVIATIONS

β2m: Beta-2-microglobulin; BNP: Brain Natriuretic Peptid; BMI: Body Mass Index; BP: Blood Pressure; ESRD: End Stage Renal Disease; FAT: Fat Adipose Tissue; FHN: Frequent Hemodialysis Network; FTI: Fat Tissue Index; HDF: Hemodiafiltration; IDWG: Interdialytic Weight Gain; LVEF: Left Ventricular Ejection Fraction; OL-HDF: Online-Hemodiafiltration; SD: Standard Deviation D-OL-HDF: Daily-Online-Hemodiafiltration.

INTRODUCTION

For forty years, dialysis techniques have been dramatically improved. Latest publications have described the superiority in terms of morbidity and mortality of the Online-Hemodiafiltration (OL-HDF) technique [1], as well as the daily and long hemodialysis techniques [2]. However, there are very few studies regarding the short daily OL-HDF (D-OL-HDF) technique.

By combining diffusive and convective solute transfer through high flux dialyzer membrane, OL-HDF is considered the most efficient technique for both small and large uremic toxins elimination [3]. Uremic toxins are shown to have a pathogenic role in the occurrence of long-term complications affecting hemodialysed patients [4,5]. OL-HDF improves clinical and biochemical parameters as well as patients’ quality of life, when compared with conventional hemodialysis [6]. Although, the primary analyses of three large randomized controlled trials showed inconclusive results due to a non-significant difference in all-cause mortality or cardiovascular events between OL-HDF and HD [7-9]. Post-hoc analysis of these studies, as well as the meta analysis conducted by Mostovaya et al, suggests a positive effect of post-dilution OL-HDF modality over standard hemodialysis in reducing cardiovascular and all-cause mortality [1,3]. Moreover, the relationship between a convective volume over 23 L/session and a decrease in mortality rate was demonstrated in theses post-hoc analysis [3,9].

Daily hemodialysis compared to three-weekly hemodialysis, increases the nutritional status, and decreases the over hydration allowing a better tolerance of ultrafiltration rate and, subsequently, a better blood pressure control [10]. Moreover, Frequent Hemodialysis Network (FHN) randomized trials showed that daily dialysis improves mental and physical health and is associated with reduction in left ventricular mass [11-13]. A recent study conducted by Chertow et al. showed that frequent hemodialysis reduces long-term mortality of selected patients with End Stage Renal Disease (ESRD) [2].

Daily OL-HDF, by combining OL-HDF and daily hemodialysis is an interesting alternative modality, firstly described by Fischbach et al in children [14]. These authors reported good benefits of this technique such as: less tiredness, better appetite, increase in Body Mass Index (BMI) and catch up growth, optimal blood pressure control and less interdialytic weight gain associated to a reduction of left ventricular hypertrophy [15].

Recently, Maduell et al., in a prospective study of eight patients followed for six months, described a better control of anemia, nutrition, blood pressure, as well as a reduction of phosphate binders and a noticeable regression of left ventricular hypertrophy in daily OL-HDF than with standard Hemodialysis [10]. At this time, this study was the only one reporting this technique for adult patients.

We studied here retrospectively ten patients treated with D-OL-HDF and followed them for twelve-month to evaluate and confirm the benefits of this modality.

MATERIALS AND METHODS

The study was conducted retrospectively over a period of 12 months between 2011 and 2015 in our centre, starting at the beginning of daily OL-HDF.

All of the patients treated with D-OL-HDF in our centre were included (6 men and 4 women). They all gave their informed consent to participate in the study.

The median age was 55.5 ± 18 (range 29 to 86 years), and the median dialysis vintage was 1.6 years (range: 0.08 to 26.7 years). The underlying renal diseases were glomerular nephropathy (n=5), diabetic nephropathy (n=1), polycystic kidney disease (n=1), others (n=3). The baseline residual renal function was lower than 4 mL/min.

Eight patients were included in daily OL-HDF technique while they were already treated at least 3 months with three-weekly OL-HDF. The two others were immediately treated with D-OLHDF at the initiation of hemodialysis treatment.

Daily-OL-HDF modality was indicated either for medical intolerance to standard hemodialysis (n=2) or for personal convenience (n=8).

All patients were hemodialysed with a native arterio-venous fistula allowing a bipuncture and a blood flow ≥ 300 mL/min.

The session length of daily-OL-HDF was 2 hours six times a week (n=6) or 2.5 hours 5 times a week (n=4). In all cases, the weekly treatment duration was 12 hours and similar in both techniques.

Fresenius 5008 dialysis monitors were used in post-dilution D-OL-HDF with Autosub® retro-control mode. Dialysate flow was automatically adapted to the blood flow in Autoflow® mode. All patients were treated with high flux polysulfone membrane with an effective surface area of 2.10 m2 (ELISIO 21H Nipro® or TS 2.1 SL Toray®) and with an acetate-free concentrate.

Anticoagulation in D-OL-HDF modality was either suppressed (8 patients) either decreased with very low doses of non fractional heparin for the two others patients. Five of the ten patients were treated with antiplatelet therapy and two were treated with anti-vitamine-K therapy.

Data were collected every month for one year, and compared to the data after 3 months before daily OL-HDF when data were available or to baseline.

Usual hemodialysis parameters were obtained at each dialysis session. Blood samples for biological tests were periodically taken from the arterial line according to the K-DOQI recommendations at midweek session, every month for routinely tests or every 3 months (prealbumin) or 12 months (troponin, β2m and cholesterol) [16].

The value of single-pool Kt/VDaug (spKt/VDaug) was estimated using the second generation equation of Daugirdas with measurement of urea concentration at H0 and H2.

Bio-impedancemetry analysis was performed on five patients to assess the corporeal composition with the Body Composition Monitor Fresenius®.

Quantitative variables are expressed as mean and standard deviation (SD). Categorical variables are expressed as percentages. Median and means were compared and when it was significant by bilateral paired Wilcoxon Signed-Ranks Test. The probability p < 0.05 was considered statistically significant.

RESULTS

Blood flow was similar for both compared techniques: 362.5 ± 25 mL/min at baseline vs 352.1 ±10.5 mL/min in D-OL-HDF. The mean value of infusion volumes (Vs) was 74 ± 1.65 L/week in daily OL-HDF and the convection volumes (Vc) was 81 ± 2 L/ week. The dialysis adequacy was similar for both modalities. The mean value of weekly spKt/VDaug was 5.8 ± 1.29 at baseline and 6.6 ± 1.18 at 12 months of D-OL-HDF (ns). The blood purification of middle Molecular Weight (MW) assessed by β2m pre-dialysis value, was significantly better after 12 months of daily OL-HDF (Table 2). The Inter-Dialytic Weight Gain (IDWG) was significantly lower at 12 months in daily OL-HDF (1.12 ± 0.63 kg vs 1.96 ± 0.55 kg, p < 0.05).

However, the total IDWG per week was similar in both modalities (Table 1).

Table 1:  Clinical characteristics.

 

M-3  

M0

M+6

M+12             

P

Blood Pressure:

SBP (mmHg)

DBP (mmHg)

Weight:

DW (kg)

IDWG (kg)

IDWG (kg/week)

BMI (kg/m2)

FTI (kg/m2)

LTI (kg/m2)

 

140 ± 20

73 ± 9

 

65.3 ± 9.2

1.96 ± 0.55

6.1 ± 2.9

22.7 ± 3.2

     -

     -

 

143 ± 24

78 ± 18

 

65.0 ± 9.5

0.84 ± 0.71

6.3 ± 2.6

22.6 ± 3.2

10.9 ± 5.4

11.0 ± 3.3

 

142 ± 21

74 ± 20

 

65.6 ± 10.6

0.93 ± 0.57

5.6 ± 3.6

22.9 ± 3.1

     -

     -

 

139 ± 24            

72 ± 17              

 

65.9 ± 11.6        

1.12 ± 0.63     

6.5 ± 3.1            

23.0 ± 3.1          

11.8 ± 4.0          

10.3 ± 2.8          

 

ns

ns

 

ns

0,01

ns

ns

ns

ns

Values are expressed as mean  ±  SD or median.

Abbreviations: SBP: Systolic Blood Pressure; DBP: Diastolic Blood Pressure; DW: Dry Weight; IDWG: Interdialytic Weight Gain; BMI: Body Mass Index; FTI: Fat Tissue Index; LTI: Lean Tissue Index.

The predialysis blood pressure (BP) was similar for all patients; six of the ten patients were receiving antihypertensive drugs (one or two different molecules). At the end of the observation time, anti-hypertensive treatment has remained stable for all patients with fully controlled blood pressure (Table 1). Moreover, the value of Brain Natriuretic Peptid (BNP) monitored every month decreased significantly after one year of daily-OL-HDF treatment from 564.7 ± 164 to 313.5 ± 17 pg/ml (p < 0.05). Left Ventricular Ejection Fraction (LVEF) was evaluated for seven of the ten patients by echocardiographic assessment and compared from baseline to one year of D-OL-HDF. The LVEF was significantly increased from 59.1 ± 9.6 to 68.5 ± 9.0 % (p < 0.05) (Figure 1).

Cardiovascular parameters. BNP (Brain Natriuretic Peptid) and LVEF (Left Ventricular Ejection Fraction) are represented and compared from the beginning and the end of the study.

Figure 1 Cardiovascular parameters. BNP (Brain Natriuretic Peptid) and LVEF (Left Ventricular Ejection Fraction) are represented and compared from the beginning and the end of the study.

During the 12 months study period, the haemoglobin value increased from 10.9 ± 1.9 to 11.8 ± 0.07 g/dl (p<0.05), whereas erythropoietin doses, ferritinemia and saturation coefficient remained stable (Table 2).

Table 2: Biological characteristics of the patients.

 

M-3   

M0

M + 6

M + 12

p

Hématologic parameters:

Hémoglobin (g/dl)

Ferritinemia (µg/l)

CS (%)

EPO doses (UI/kg/week)

Phosphocalcique metabolism:

Calcium (mmol/L)

Phosphorus (mmol/L)

PTH (ng/mL)

PAL (UI)

Nutritional parameters:

Albumin (g/l)

Prealbumin (mg/l)

Total Cholesterol (g/l)

Cardiovascular parameters:

Total Protein (g/l)

BNP (pg/ml)

Troponin US (µg/l)

Hemodialysis parameters:

Weekly spKt/Vd

β2m (mg/dl)

 

10.9 ± 1.9

395 ± 140

26.0 ± 6.3

195 ± 217

 

2.11 ± 0.12

1.42 ± 0.4

360 ± 25

77.4 ± 3.5

 

 34.2 ± 2-

NA-

NA-

     

68 ± 8.4

564 ± 164

NA-

 

5.81 ± 1.29

NA-

 

11.2 ± 0.2

357 ± 292

24.5 ± 4.2

126 ± 110

 

2.25 ± 0.23

1.38 ± 1.0

310 ± 12

65.9 ± 5.6 

 

34.3 ± 2.2 

0.32 ± 0.0

4.69 ± 1.9  

 

70.3 ± 1.4

462 ± 63

0.05

 

6.42 ± 1.41

24.8 ± 1.0

 

 

11.5 ± 2.4

325 ± 170

26.5 ± 12

144 ± 146

 

2.18 ± 0.09

1.51 ± 0.14

439 ± 10

85.2 ± 2.1

 

34.2 ± 0.49

0.32 ± 0.0

NA-

 

67.9 ± 0.7

315 ± 36

NA-

 

6.49 ± 0.94

NA-

 

11.8 ± 0.07

220 ± 390

29.1 ± 45

190 ± 182

 

2.26 ± 0.09

1.55 ± 0.46

487 ± 45

89.8 ± 11.3

 

36.6 ± 2.5

0.34 ± 0.0

4.81 ± 1.55

 

71.5 ± 0

313 ± 17

0.05

 

6.60 ± 1.18

22.9 ± 2.1

 

 

0.036

ns

ns

ns

 

ns

ns

ns

ns

 

0.028

ns

ns

 

ns

0.028

ns

 

ns

0.035

 

Values are expressed as mean  ±  SD.

Abbreviations: CS: Saturation Coefficient; PTH: Parathyroid Hormone; PAL: Alkaline Phosphatase; BNP: Brain Natriuretic Pep tid; β2m: Beta2-microglobulin

Serum calcium and phosphate were unchanged after 12 months of D-OL-HDF as well as PTH value (Table 2). However, the oral calcium supplementation was disrupted for two of the five patients treated, and three of seven patients stopped their phosphate binder treatment. All patients were supplemented with native Vitamin D as recommended. Hyperparathryroiditis was treated with Alfacalcidol® for one patient and with Cinacalcet® for another one. These treatments remained stable all over the study. The serum albumin increased significantly after 12 months of daily OL-HDF (36.6 ± 2.5 vs 33.73 ± 2.0 g/l) (p < 0.05), when the total protidemia remained stable. In the same time, dry weight and BMI were unchanged. The bioimpedancemetric analysis displayed a stable Fat Adipose Tissue (FAT) mass as well as a stable Fat Tissue Index (FTI) mass (Figure 2).

Nutritional parameters are represented between first month (M0) and the end of the study (M12). BMI: Body Mass Index; FTI: Fat Tissue Index; LTI: Lean  Tissue Index.

Figure 2 Nutritional parameters are represented between first month (M0) and the end of the study (M12). BMI: Body Mass Index; FTI: Fat Tissue Index; LTI: Lean Tissue Index.

Regarding the daily use of vascular access, we did not observe any increase of thrombosis or stenosis events compared to a three-weekly-HDF treatment.

DISCUSSION

Mortality rates remain high for ESRD patients: more than fifty percents at five years after diagnosis [17]. Also worrying is the health-related quality of life of these patients, a predictive factor for mortality [18]. Publications from Fischbach et al., using D-OLHDF in children reported a better quality of life, an improvement in nutritional status and a reduction of morbi-mortality [14,15]. These results were found and confirmed in adults by Maduell et al. in a study covering a six months period[10]. The authors showed a better quality of solute clearance of small, middle and high weight molecules in D-OL-HDF comparing to standard OL-HDF and good benefits regarding clinical and biological parameters.

Since Maduell et al., in 2003, there hasn’t been any publication regarding this technique in hemodialysis literature, even though the results published by Maduell were very encouraging.

We started to use this modality in our center in 2012 and report in this study the results of 12 months of follow up to confirm Maduell’s results.

Despite the lack of analyzed data, daily OL-HDF was very well accepted by the ten patients who reported an increase of their quality of life (less tiredness and a better quality of sleep), a better restless after hemodialysis session and less hypotension episodes. The low duration of hemodialysis session and the lack of anticoagulation allowing a decrease in the vascular access compression time decreased daily impact of hemodialysis treatment.

The quality of solute removal regarding small and middlesized molecules was similar to the two treatments modalities assessed by the spKt/VDaug.. However, we observed, as described by Maduell et al. [10], a significantly decrease of the predialytic β2m value. This better elimination of MW-molecules could be explained by higher weekly blood purification with daily convective treatment as well as a lower production of β2m.

In this study, the change from three times a week OL-HDF to D-OL-HDF results in an improvement of the nutritional status.

The albumin concentration increases significantly. There is also a tendency for an increase of body weight, body mass index and fat tissue index. Theses results could be explained by a better appetite noticed in our patients and also observed by Maduell; or by a better solute clearance of the leptin as others middle-sized molecules. This could also be explained by an overestimated dry weight before the beginning of daily OL-HDF; patients could be over-hydrated as suggested by the results of BNP values. Our results are in accordance with the recent data published by the FHN describing an increase of the patients’ body weight in frequent (6 times/week) hemodialysis. They also report an increase in estimated adiposity in the 6 times per week group and a relative decrease in the lean body mass which might be explained by the decrease of overweight. This has been associated with improved appetite and increase of protein and caloric intake in frequent hemodialysis modality [20].

It has to be noticed that, D-OL-HDF might decrease albuminemia, as albumin loss is more important during the first two hours of HDF [19]. However, we choose polysulfone membranes with a very low protein loss (<1.5 g/session) to limit this well known risk.

Our cohort of patients displayed a controlled blood pressure before beginning the daily OL-HDF and remained stable all over the study without any change in antihypertensive drugs. It is important to note that most of them were treated with small doses of Beta-blocker or/and Renin-angiotensin system antagonist for their cardioprotective properties and not used for their anti hypertensive effects.

IDWG and the BNP value decreased significantly in short daily OL-HDF. The increase of hemodialysis frequency results in lower volume fluctuations assessed by the lower IDWG and probably a lower overhydration explained by better tolerance to ultrafiltration.

The repercussion on heart is understandable because of the better control of volume variations and extracellular overload increasing the heart post charge, as well as the better nutritional status.

We also showed, by echographic measurements, a significant improvement of LVEF for five patients whereas there was no change for the others (Figure 2). Maduell et al., with magnetic resonance imaging (MRI), described a significant reduction in left ventricular mass at six months [10]. They although explained the reduction of LVM by a better elimination of homocystein, a better control of blood pressure and anemia.

Furthermore, we observed a significant increase in hemoglobin level during the study period while erythropoietin doses remained stable. This result might be explained by several factors such as a better nutritional status, a better blood purification of uremic toxins and at least by the better control of over hydration and IDWG (lower BNP).

In our study, there was no difference in calcemia, phosphoremia and PTH values at 12 months. However, forty percent of patients treated with phosphate binder or with calcium supplementation stopped their treatment. This result is even more relevant that patients have a better appetite as shown by the increase of albuminemia. The reduction of these medications could have a positive effect on treatment adhesion and obviously on patients’ quality of life.

CONCLUSION

D-OL-HDF seems to be an excellent therapeutic alternative to three times a week conventional treatment. In our observational retrospective study, we showed an improvement in nutritional status and a better left ventricular ejection fraction. Patients describe a better quality of life with a better tolerance of dialysis sessions and an improvement of their well-being. These benefits are consistent with those presented by Maduell et al. and should be considered to initiate this hemodialysis modality in a certain type of patients. However, to our knowledge, very few centers are using currently this technique. Further prospective trials are needed to confirm these preliminary results.

ACKNOWLEDGEMENTS

The authors thank Catherine Maheas for her technical assistance. They also thank the medical and nurses staffs of Hemodialysis Center Henri Küntziger and AURA APP for their valuable assistance during the study.

REFERENCES

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2. Chertow GM, Levin NW, Beck GJ, Daugirdas JT, Eggers PW, Kliger AS, et al. Long-Term Effects of Frequent In-Center Hemodialysis. J Am Soc Nephrol. 2016; 27: 1830-1836.

3. Mostovaya IM, Blankestijn PJ, Bots ML, Covic A, Davenport A, Grooteman MP, et al. Clinical evidence on hemodiafiltration: a systematic review and a meta-analysis. Semin Dial. 2014; 27: 119-127.

4. Liabeuf S, Lenglet A, Desjardins L, Neirynck N, Glorieux G, Lemke HD, et al. Plasma beta-2 microglobulin is associated with cardiovascular disease in uremic patients. Kidney Int. 2012; 82: 1297-1303.

5. Vanholder R, Glorieux G, De Smet R, Lameire N. European Uremic Toxin Work Group. New insights in uremic toxins. Kidney Int Suppl. 2003; 6-10.

6. Kantartzi K, Stelios P, Efthemia M, Athanasios R, Konstantinos L, Vassilios D, et al. Can Dialysis Modality Influence Quality of Life in Chronic Hemodialysis Patients? Low-Flux Hemodialysis versus High Flux Hemodiafiltration: A Cross-Over Study. Ren Fail. 2013; 35: 216- 221

7. Grooteman MP, van den Dorpel MA, Bots ML, Penne EL, van der Weerd NC, Mazairac AH, et al. Effect of online hemodiafiltration on all-cause mortality and cardiovascular outcomes. J Am Soc Nephrol. 2012; 23: 1087-1096.

8. Ok E, Asci G, Toz H, Ok ES, Kircelli F, Yilmaz M, et al. Mortality and cardiovascular events in online haemodiafiltration (OL-HDF) compared with high-flux dialysis: results from the Turkish OL-HDF Study. Nephrol Dial Transplant. 2013; 28: 192-202.

9. Maduell F, Moreso F, Pons M, Ramos R, Mora-Macià J, Carreras J, et al. High-efficiency postdilution online hemodiafiltration reduces allcause mortality in hemodialysis patients. J Am Soc Nephrol. 2013; 24: 487-497.

10. Maduell F, Navarro V, Torregrosa E, Rius A, Dicenta F, Cruz MC, et al. Change from three times a week on-line hemodiafiltration to short daily on-line hemodiafiltration. Kidney Int. 2003; 64: 305-13.

11. Hall Y, Larive B, Painter P, Kaysen G, Lindsay RM, Nissenson AR, et al. Effects of Six versus Three Times per Week Hemodialysis on Physical Performance, Health, and Functioning: Frequent Hemodialysis Network (FHN) Randomized Trials. Clin J Am Soc Nephrol. 2012; 7: 782-794.

12. Unruh M, Larive B, Chertow G, Eggers PW, Garg AX, Gassman AJ, et al. Effects of 6-Times-Weekly Versus 3-Times-Weekly Hemodialysis on Depressive Symptoms and Self-reported Mental Health: Frequent Hemodialysis Network (FHN) Trials. Am J Kidney Dis. 2013; 61: 748- 758.

13. FHN Trial Group, Chertow GM, Levin NW, Beck GJ, Depner TA, Eggers PW, et al. In-center hemodialysis six times per week versus three times per week. N Engl J Med. 2010; 363: 2287-2300.

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15. Fischbach M, Zaloszyc A, Shroff R. The interdialytic weight gain: a simple marker of left ventricular hypertrophy in children on chronic haemodialysis. Pediatr Nephrol. 2015; 30: 859-863.

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17. ERA-EDTA Registry Annual Report 2012. Amsterdam, The Netherlands: Academic Medical Center, Department of Medical Informatics. 2014.

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19. Combarnous F, Tetta C, Cellier CC, Wratten ML, Custaud, De Catheu T, et al. Albumin loss in on-line hemodiafiltration. Int J Artif Organs. 2002; 25: 203-209.

20. Kaysen GA, Greene T, Larive B, Mehta RL, Lindsay RM, Depner TA, et al. The effect of frequent hemodialysis on nutrition and body composition: frequent Hemodialysis Network Trial. Kidney Int. 2012; 82: 90-99.

Roux A, Fumeron C, Petitclerc T, Créput C (2016) Clinical and Biological Benefits of Daily Online Hemodiafiltration. JSM Renal Med 1(1): 1005

Received : 22 Aug 2016
Accepted : 04 Nov 2016
Published : 06 Nov 2016
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ISSN : 2573-105X
Launched : 2014
JSM Health Education & Primary Health Care
ISSN : 2578-3777
Launched : 2016
JSM Communication Disorders
ISSN : 2578-3807
Launched : 2016
Annals of Musculoskeletal Disorders
ISSN : 2578-3599
Launched : 2016
Annals of Virology and Research
ISSN : 2573-1122
Launched : 2014
Journal of Muscle Health
ISSN : 2578-3823
Launched : 2016
JSM Genetics and Genomics
ISSN : 2334-1823
Launched : 2013
JSM Anxiety and Depression
ISSN : 2475-9139
Launched : 2016
Clinical Journal of Heart Diseases
ISSN : 2641-7766
Launched : 2016
Annals of Medicinal Chemistry and Research
ISSN : 2378-9336
Launched : 2014
JSM Pain and Management
ISSN : 2578-3378
Launched : 2016
JSM Women's Health
ISSN : 2578-3696
Launched : 2016
Clinical Research in HIV or AIDS
ISSN : 2374-0094
Launched : 2013
Journal of Endocrinology, Diabetes and Obesity
ISSN : 2333-6692
Launched : 2013
Journal of Substance Abuse and Alcoholism
ISSN : 2373-9363
Launched : 2013
JSM Neurosurgery and Spine
ISSN : 2373-9479
Launched : 2013
Journal of Liver and Clinical Research
ISSN : 2379-0830
Launched : 2014
Journal of Drug Design and Research
ISSN : 2379-089X
Launched : 2014
JSM Clinical Oncology and Research
ISSN : 2373-938X
Launched : 2013
JSM Bioinformatics, Genomics and Proteomics
ISSN : 2576-1102
Launched : 2014
JSM Chemistry
ISSN : 2334-1831
Launched : 2013
Journal of Trauma and Care
ISSN : 2573-1246
Launched : 2014
JSM Surgical Oncology and Research
ISSN : 2578-3688
Launched : 2016
Annals of Food Processing and Preservation
ISSN : 2573-1033
Launched : 2016
Journal of Radiology and Radiation Therapy
ISSN : 2333-7095
Launched : 2013
JSM Physical Medicine and Rehabilitation
ISSN : 2578-3572
Launched : 2016
Annals of Clinical Pathology
ISSN : 2373-9282
Launched : 2013
Annals of Cardiovascular Diseases
ISSN : 2641-7731
Launched : 2016
Journal of Behavior
ISSN : 2576-0076
Launched : 2016
Annals of Clinical and Experimental Metabolism
ISSN : 2572-2492
Launched : 2016
Clinical Research in Infectious Diseases
ISSN : 2379-0636
Launched : 2013
JSM Microbiology
ISSN : 2333-6455
Launched : 2013
Journal of Urology and Research
ISSN : 2379-951X
Launched : 2014
Journal of Family Medicine and Community Health
ISSN : 2379-0547
Launched : 2013
Annals of Pregnancy and Care
ISSN : 2578-336X
Launched : 2017
JSM Cell and Developmental Biology
ISSN : 2379-061X
Launched : 2013
Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
JSM Ophthalmology
ISSN : 2333-6447
Launched : 2013
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
JSM Clinical Case Reports
ISSN : 2373-9819
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
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