6. Introduction To Adequacy
â Main target in dialysis is to improve the patientâs quality of life e.g.
⢠Feeling more healthy
⢠Less uremic complications
⢠Less degree of anemia
⢠Better control of BP
â Target can be achieved by giving your patient an adequate dose of
dialysis
â Urea Kinetic modeling is a useful tool in calculating the dose of
dialysis
7. Filters
Efficiency and Flux
â˘Efficiency: ability to achieve large small solute clearance with
high blood flows (all filters are high efficiency these days)
â˘Flux: ability to achieve high middle molecule clearance and
ultrafiltration rate (determined by the average pore size)
Diffusion and Convection
⢠Diffusion: solutes move by diffusion between blocks of fluid separated by the membrane
â˘Convection: solutes move en mass with a block of fluid across the membrane (more effective for
moving large molecules)
11. First Randomised Controlled Trial In Dialysis
⢠The National Cooperative Dialysis Study (NCDS) was
the first multicentric, randomized and controlled trial to
investigate the impact of dialysis dose on patients'
outcome.
⢠160 patients were randomized to two different urea
timeâaveraged concentrations (TAC; 100 vs 5
0
mg/dl) and
to two different treatment times (2.5â3.5 vs 4.5â5.5
h) and
followedâup for 6months.
NCDS 1980
12. First Randomised Controlled Trial In Dialysis
NCDS 1980
Predialysis urea 38 vs 26 mmol. Dialysis 2.5-35h vs 4.5-5 h
high kt/v and long
dialysis
high kt/v and short
dialysis
low kt/v and long
dialysis
low kt/v and short
dialysis
13. Secondary analysis of NCDS
⢠A quantification of dialysis dose using spKt/V was first
proposed by Gotch in a secondary analysis of NCDS
data.
⢠In his analysis, probability of dialysis failure was higher
for Kt/V â¤0.8 and abruptly decreased for Kt/V >0.9.
14. Higher Kt/V has better outcome
Gotch FA,Sargent Kidney Int 1985;28:526
Kt/v=1.2
15. NCDS Conclusion
⢠Thus, according to NCDS patient
morbidity and treatment failure are
related to the dialysis dose
16. Why Should We Measure Dialysis Dose?
ď§ There is a correlation between delivered
dose of hemodialysis and patient morbidity
and mortality
ď§ Clinical symptoms are not reliable
19. âŤAt the end of dialysis BUN from blood (first pool).
âŤBut not in other tissues, muscles, (the other pool).
âŤOrgans with low blood flow (skin, bone, muscles) may serve as reservoir for
urea
âŤUrea then diffuses from tissues to blood to equilibrate.
âŤRebound, sharp increase in urea post dialysis.
lower Kt/V.
âŤTakes about 45- 60 minutes to complete
âŤUsually 0.21 less than single pool.
âŤAlmost all centers use single pool analysis.
Single pool or double pool
20. Hemodialysis Dose Measurement
ď§ Kt/V
K= dialyzer urea clearance L/h
t = dialysis session length hr
v = distribution volume of urea L
ď§ URR
22. Urea Reduction Volume (URR)
ď§ Simple
ď§ Prediction of mortality
Limitation:
Does not account for the contribution of
UF to dialysis dose
Kt/V=1.1 (UF=0)
Kt/v = 1.35 (UF=10%BW)
URR=65
25. Kt/V
Computerized software
Mathematical logarithm
Kt/v = -Ln (R-0.008t)+(4-3.5xR) x UF
W
Ln = natural logarithm
R = postdialysis BUN
predialysis BUN
UF = Ultrafiltration volume in liters
W = Postdialysis weight in kg
26. âŤPre-sample: After insertion of the needle.
âŤPost sample :
A. To prevent rebound ; sequestration of urea from other tissues into
blood to reach equilibrium less than 2 min after ending,
B. To prevent recirculation ; blood pump is slowed to 30 ml/min for
one minute and a sample is taken from art. line.
BUN SAMPLING OF KT/V &URR
27. Post Dialysis BUN Sampling
Avoid 2 rebound:
Early (<3min post dialysis)
ď§ Access recirculation,begin immediately post
hemodialysis and rebound in 20 seconds
ď§ Cardiopulmonary recirculation, begin 20 seconds
post hemodialysis and is completed in 2-3 minutes
after slowing or stopping the blood pump.
Late (>3 min)
ď§ Completed within 30-60 minutes due to flow-volume
disequilibrium.
29. Equilibrated Kt/V
ď§ eKt/v is 0.2 units less than single-pool kt/v, but it can be as great 0.6
unit less.
ď§ For most patient, urea rebound is nearly complete in 15 minutes
after hemodialysis but for minority, it may require up to 50-60 minutes
ď§ The degree of rebound is high in small patient
⢠eKt/V= spKt/V - 0.6 x (spKt/V) / t + 0.03 (for arterial access)
⢠eKt/V= spKt/V - 0.47 x (spKt/V) / t + 0.02 (for venous access)
34. DEFENITION of Kt/V
⢠K= urea clearance of a dialyzer
â This depends on two factors
⢠the ability of the hollow fiber to clear urea
â The pore size and specification
â The surface are of the dialyzer
⢠The rate of blood flow through the hollow fiber
â Supplied by manufacturer and should be checked
⢠t =during a certain time of dialysis (minutes)
⢠V =Volume of dissolved urea in the body
â urea is equally distributed in all body compartments
â water is also equally distributed in all body compartment Volume of urea almost equals
total body water
35.
36. How to calculate V or
Total Body Water (TBW)
⢠Simplest: 2/3 of body weight
⢠Bio-Electrical Impedance
â Elctrical Measurement of TBW
⢠Kinetic measure for TBW
⢠Anthropometric measures
for TBW
TBW = -0.07493713 x age - 1.01767992
x male + 0.12703384 x ht
-0.04012056 x wt + 0.57894981
x diabetes - 0.00067247
x wt2 - 0.03486146 x (age x male)
+ 0.11262857 x (male x wt)
+ 0.00104135 x (age x wt)
+ 0.00186104 x (ht x wt)
37. Calculate the dose of Dialysis
⢠K= clearance of hollow fiber
â Available from producer
â Urea clearance for a given blood flow
⢠V= Calculated by any method
â Weight, height, age, gender ..etc
⢠You decided on the duration of dialysis
â t= time expected on dialysis in minutes
CALCULATE DOSE OF DIALYSIS =Kt/V
38. Dose of dialysis
⢠Depends on three factors
â 1. The time of dialysis (t) đĄđĄ
â 2. The amount of urea a hollow fiber can clear when blood
passes through it (K) đĄđĄ
â 3. The total volume of urea in the patientâs body that needs
to be dialyzed (V) đĄđĄ
Kt/V= dose of dialysis
39. Automated monitoring of hemodialysis
adequacy by dialysis machines
⢠Has potential benefits to patients and cost savings
⢠Kidney International 2010 78, 833-835
41. What Happens if a smaller dose is given?
Worse outcome :
⢠Death
⢠Fall in albumin level
⢠Hospitalization (not related to access)
⢠Infections
42. Prescribed vs. delivered Kt/V
Prescribed Kt/V is a computerized
estimation of what the patients Kt/V would
be, based on the prescription
Delivered Kt/V is actual results based on
how the patient really dialyzed the day the
kinetic labs were drawn
43. How to make sure patient has actually received his dose of
dialysis
Delivered KT/V
⢠Variables Used
⢠R= BUN before -BUN after
⢠UF/W= wt removed during Dx/ post Dx weight
â Deducted using one of the following formulas
a. 2.2 - 3.3x (R - 0.3 - UF/W) (bedside)
b. -ln(R-0.3) + (4-35xR) x UF/W (logarithmic)
⢠Daugirdas JT in Daugirdas and Ing in Handbook of dialysis Little Brown and Co 2nd ed
44. Discrepancies Between Delivered and Prescribed
Dialysis Dose
Delivered less than the prescribed:
ď§ Low blood flow
ď§ Inadequate dialyzer performance
ď§ Low dialysate flow
ď§ Dialysis machine programmed incorrectly
ď§ Hemodialysis ended prematurely
ď§ The predialysis BUN was drained after
initiation of hemodialysis
ď§ Access recirculation
ď§ Weak vascular access
50. Discrepancies Between Delivered and Prescribed
Dialysis Dose
Delivered Dose More than the Prescribed:
ď§ Postdialysis BUN was drained from venous
bloodline
ď§ The post dialysis BUN was diluted with saline
ď§ Small (V)
51. THE HEMO STUDY (2002)
⢠1846 patients under hemodialysis
52. The HEMO Study (2002)
Standard dose group
⢠SpKt/V 1.3
⢠eKt/V 1.16
⢠URR 66.3
⢠Dialysis T 190 min
High dose group
⢠SpKt/V 1.7
⢠eKt/V 1.53
⢠URR 75.2
⢠Dialysis T 219 min
53. The HEMO Study (2002)
⢠Tests for outcome:
â Death
â Fall in albumin level
â Hospitalization (not related to access)
â Infections
⢠Results of outcome were the same in the two groups
55. The HEMO Study (2002)
EKNOYAN et al N Engl j Med.2002 ;347:2010
56. Conclusions Of HEMO
⢠Dialysis prescription of KT/V Values less than 1.2 may
carry a high mortality and morbidity
⢠Increasing the dose of dialysis of a KT/V more than 1.4
does not carry any significant benefit
⢠Recommended dose is a KT/V which lies between 1.3
and 1.4 (single pool)
⢠No benefit from the use of high Flux dialyzers
59. ďą Complex, may be difficult to understand.
ďą Urea is not associated with toxicity.
ďą It assumes urea diffusion across the membrane is comparable to other
toxins.
ďą Dosing is depends on V (TBW),V in females is < V in males with the
same surface area lower calculated dose.
ďą Kt/V is a poor measure of control of extracellular fluid overload, and it
certainly does not reflect the rate of fluid removal.
ďą Kt/V urea does not reflect control of serum phosphorus;
Criticism of KT/V
66. Frequency of dialysis:
⢠Thrice, quotidian
⢠every other day
⢠Daily in-center
⢠Daily Home Dialysis
⢠Nocturnal Dialysis
⢠Inâcenter Nocturnal Dialysis
⢠Other
71. âŤReflects protein intake in steady state patients.
âŤIncreased kt/v leads to increase in PCR and more protein intake.
âŤnPCR is of great value predicting morbidity.
âŤAdequate Dx recommended > 1.1 gm/kg/day
Normalized protein catabolic rate IMPORTANCE
72. Residual Renal Function (Kr)
Effect on KT/V and URR
⢠Has insignificant effect on urea clearance during hemodialysis
⢠But has a significant effect on lowering predialysis BUN
⢠Every 1ml/min of Kr offers a KT/V of 0.13
⢠Consequently patients with Kr needs less KT/V but donât
decrease dialysis dose
80. Maximize Middle Molecule Removal
1. Use High Flux membranes (more permeable membranes for larger toxins).
2. Apply more convection, i.e. Haemodiafiltration (HDF).
82. Reduced Ă2-microglobulin levels
F Locatelli et al, Kid Int, 50: 1293-1302, 1996.
Lower incidence of CTS / amyloidosis
F Locatelli et al, Kid Int, 55: 286-293, 1999.
J. Berland et al, NDT, 10 (Suppl.10): 45-47 (1995).
Improved safety (endotoxin retention)
GrĂśtsch et al & Weber et al, Dialyse J, 1998
Improved lipid status
P J Blankestijn et al, JASN, 5: 1703-1708, 1995
P B Forster et al, NDT, 14 (Suppl. 4) 49-51, 1999.
Lower mortality risk
F Port, USRDS; ASN 1998.
Treatment with high flux
83.
84. The MPO Study (2009)
Significance:
⢠Large, randomized clinical outcomes trial for 3x/week intermittent HD for incident patients
⢠Compared low versus high flux filters (Kuf, β2M-sieving coefficient) with equal urea Kt/V
⢠Stratified patients based on albumin (âĽ4 g/dL or <4 g/dL)
Conclusions:
⢠âIn summary, we did not detect a significant survival benefit with either high-flux or low-flux
membranes in the population overall,
⢠The use of high-flux membranes conferred a significant survival benefit among patients with
serum albumin <4 g/dl.
⢠âthe results of the MPO Study can be interpreted as a supporting rationale for the use of high-
flux dialysis membranes if they are financially affordable.â
85. Comparison between predialysis PTH for patients with low flux and
high flux dialysis membranes
Ahmed Rabie El Arbagy et al. Study of Effect of High-Flux Versus Low-Flux Dialysis Membranes on Parathyroid
Hormone. American Journal of Clinical Medicine Research, 2014, Vol. 2, No. 1, 36-42. doi:10.12691/ajcmr-2-1-9
Š The Author(s) 2014. Published by Science and Education Publishing.
87. KDOQI Clinical Practice Guideline for Hemodialysis Adequacy: 2015 Update
John T. Daugirdas, MD, Thomas A. Depner, MD, Jula Inrig, MD, MHS, Rajnish Mehrotra, MD, Michael V. Rocco, MD, MSCE, Rita S.
Suri, MD, MSc, FRCPC, Daniel E. Weiner, MD, MS, Nancy Greer, PhD, Areef Ishani, MD, MS, Chief, Roderick MacDonald, MS, Carin
Olson, MD, MS, Indulis Rutks, BS, Yelena Slinin, MD, MS, Timothy J. Wilt, MD, MPH, Michael Rocco, MD, MSCE, Holly Kramer, MD,
Michael J. Choi, MD, Milagros Samaniego-Picota, MD, Paul J. Scheel, MD, MBA, Kerry Willis, PhD, Jessica Joseph, MBA, Laura
Brereton, MSc John T. Daugirdas, MD, Thomas A. Depner, MD, Jula Inrig, MD, MHS, Rajnish Mehrotra, MD, Michael V. Rocco, MD,
MSCE, Rita S. Suri, MD, MSc, FRCPC, Daniel E. Weiner, MD, MS, Nancy Greer, PhD, Areef Ishani, MD, MS, Chief, Roderick
MacDonald, MS, Carin Olson, MD, MS, Indulis Rutks, BS, Yelena Slinin, MD, MS, Timothy J. Wilt, MD, MPH, Michael Rocco, MD,
MSCE, Holly Kramer, MD, Michael J. Choi, MD, Milagros Samaniego-Picota, MD, Paul J. Scheel, MD, MBA, Kerry Willis, PhD, Jessica
Joseph, MBA, Laura Brereton, MSc
American Journal of Kidney Diseases
Volume 66, Issue 5, Pages 884-930 (November 2015)
DOI: 10.1053/j.ajkd.2015.07.015
Copyright Š 2015 National Kidney Foundation, Inc. Terms and Conditions
KDOQI Clinical Practice Guideline for
Hemodialysis Adequacy: 2015 Update
88. American Journal of Kidney Diseases 2015 66, 884-930DOI: (10.1053/j.ajkd.2015.07.015)
Copyright Š 2015 National Kidney Foundation, Inc. Terms and Conditions
89. Timing of Hemodialysis Initiation
⢠Education about different forms of renal replacement therapy (RRT)
should be started once eGFR reaches <30 mL/min/1.73m2 or the
eminent need for RRT approaches. No change from 2006. (No grade)
⢠The timing of therapy should be driven by signs and symptoms of
uremia, evidence of protein-energy wasting, or metabolic
abnormalities/volume overload refractory to medical management.
The 2015 guideline removes any suggested eGFR (which was
previously given as 15 mL/min/1.73m2 in 2006). (No grade).
90. Frequent and Long Duration Hemodialysis
In-center Frequent HD
⢠Suggest: Patients with ESRD should be offered in-center short frequent
HD as an alternative to thrice weekly HD, with discussion of patient
preference and risk/benefit. Not in 2006 guideline. Grade of 2C.
⢠Recommend: All patients need to be informed of risk of in-center frequent
HD, including increase in vascular access complications and potential
hypotension during HD. Not in 2006 guideline. Grade of 1C.
91. Home Long HD
⢠Consider home long HD for patients with ESRD who
prefer this therapy for lifestyle considerations. Not in
2006 guideline. (No grade).
⢠Recommend: All patients need to be informed of risk
of home long HD, including increase in vascular
access complications, potential for increased
caregiver burden and accelerated decline of residual
kidney function. [Not in 2006 guideline]. (Grade 1C).
92. Pregnancy
⢠During pregnancy, women with ESRD should receive
long frequent HD either in center or at home.
Not in 2006 guideline. No grade given.
93. Measurement of Dialysis: Urea Kinetics
⢠Recommend: Target single pool Kt/V of 1.4 and minimum Kt/V of 1.2 per HD
session in thrice weekly HD. No change from 2006. (Grade 1B).
⢠Dose may be reduced in patients with significant residual kidney function
provided residual kidney function is measured periodically. No change from
2006. (No grade).
⢠For schedules other than thrice weekly, suggest a target Kt/V of 2.3 volumes
per week with minimum Kt/V of 2.1 using a method of calculation that includes
ultrafiltration and residual kidney function. Not in 2006 guideline. (No grade).
94. Volume and Blood Pressure Control: Treatment
Time and Ultrafiltration Rate
⢠Recommend: Patients with low residual kidney function
(<2mL/min) undergoing thrice weekly dialysis need a
minimum of 3 hours per treatment. No change from
2006. Grade of 1D.
⢠Consider longer session or extra session if large
weight gains, high BP, high UF rates, metabolic
complications, or inability to achieve dry weight. No
change from 2006. No grade given for this
95. Volume and Blood Pressure Control: Treatment
Time and Ultrafiltration Rate
⢠Reduce dietary sodium intake and ensure adequate
sodium/water removal with HD to manage HTN and
volume. Grade of 1B.
⢠Prescribe UF rate balancing risk of hemodynamic
instability with benefit of volume removal. No change
from 2006. No grade
97. Guides to dialysis prescription
⢠Patient weight
â dry weight
â IDWG
⢠Co-morbidities.
⢠Recent lab work.
⢠Medications.
⢠Current clinical condition.
⢠Dietary status
⢠Mode
98. Basic goals of adequate dialysis:
Fluid removal to expected 'dry weight' at end of dialysis.
Predialysis BP < 140/90 mmHg with or without antihypertensive drugs.
Predialysis plasma concentrations:
-Potassium: â¤5.5 mmol/l without using ion exchange resins.
-Bicarbonate: âĽ24 mmol/l .
-Inorganic phosphate: â¤5.5 mg/dl without oral binding agents.
-Urea: <35 mmol/l with daily protein-intake1.2 g/kg/BW .
-Albumin: âĽ40 g/l & Cholesterol= 200-300 mg%
-Haemoglobin: 11â12 g/100ml with or without ESA.
Rodriegaz handbook of dialysis 2012
99. TECHNICAL REQUIREMENTS FOR DELIVERY OF ADEQUATE DIALYSIS:
Vascular access: blood flow ⼠300 ml/min .
Dialysis fluid: bicarbonate buffered, sterile, pyrogen-free.
Volumetric machine.
Dialyzer: -Highly permeable, biocompatible membrane.
- Surface area: âĽ1.3 m2.
Dose of dialysis:
-Minimum Kt/V urea: 1.2â1.3 (single pool).
-Minimum URR : 65â70%.
-Measurement of dialysis dose: once / month.
- Weekly dialysis time:
- HD Vs HDF
Rodriegaz handbook of dialysis 2012