Dialysis prescription 2

61
By Dr. Iheme, C.P. M.B.B.Ch

Transcript of Dialysis prescription 2

Page 1: Dialysis prescription 2

By

Dr. Iheme, C.P.

M.B.B.Ch

Page 2: Dialysis prescription 2

Outline Introduction

Epidemiology

Haemodialysis apparatus

Mechanisms of solute transport

Indications for dialysis

Components of dialysis prescription

Dialysis Adequacy

Complications of Haemodialysis

Conclusion

Page 3: Dialysis prescription 2
Page 4: Dialysis prescription 2

Introduction Definition: Dialysis is a process whereby the solute

composition of blood is altered by exposing it to a dialysate through a semipermeable membrane.

Page 5: Dialysis prescription 2

Introduction ctd Functions of the kidney

• Remove excess salt, water, and acid.

• Remove or regulate other electrolytes (e.g. K + , Ca 2+ , Mg 2+ , PO 4 ).

• Remove waste products of metabolism (Ur and Cr routinely measured, but there are many others).

• Make erythropoietin.

• 1 ά -hydroxylates and activates vitamin D.

Page 6: Dialysis prescription 2

Epidemiology US: 490,000 ESRD patients, 300,000 currently on HD

UK: 23,500 HD patients, 74000 PD patients

White population predominant

Diabetes is the most common underlying diagnosis, followed by hypertension in the US.

Nigeria:17ooo new cases yearly. Prevalence of 79,050

Page 7: Dialysis prescription 2

Renal Replacement Therapies

offered to the patients

556, 73%

9, 1%

7, 1%

188, 25%

Haemodialysis

CAPD

RenalTransplant

ConservativeArogundade et al, WCN 2009

Page 8: Dialysis prescription 2

Epidemiology Mortality rate in RRT patients age 30–34 is 25x higher

age >85,mortality is 73x higher

Median survival

age 45–54 is currently 10.5 years

age 55–64 it is 5.6 years

age 65–74, 3 years

Page 9: Dialysis prescription 2

Haemodialysis apparatus

Page 10: Dialysis prescription 2

Mechanisms of solute transport1. Diffusion: movement of substances from an area of

higher concentration to an area of lower concentration of solutes.

2. Ultrafiltration (convective Transport): water driven by a hydrostatic is pushed through the membrane .

Solutes that can pass easily through the membrane pores are swept along with the water ( “solvent drag”).

Page 11: Dialysis prescription 2
Page 12: Dialysis prescription 2

Mechanisms of solute transport Hemodiafiltration: hemodialysis and hemofiltration

are combined. Seen in newer models of machines

“Countercurrent” flow : Maximize the concentration difference of waste products between blood and dialysate in all parts of the dialyzer.

Page 13: Dialysis prescription 2
Page 14: Dialysis prescription 2
Page 15: Dialysis prescription 2

Indications for dialysis in AKI

AEIOU

Acidosis: pH<7.2

Electrolyte abnormalities:

life-threatening hyperkalemia associated with ECG changes

symptomatic hypermagnesemia and hypercalcemia

Page 16: Dialysis prescription 2

Indications for dialysis Intoxications: Xtics of dialysable substances

Low molecular weight (<500 Da)

High water solubility

Low degree of protein binding

Small volumes of distribution (<1 L/kg)

High dialysis clearance relative to endogenous clearance

E.g. barbiturates, bromides, chloral hydrate, alcohols, lithium, theophylline, procainamide, salicylates, atenolol, and sotalol.

Page 17: Dialysis prescription 2

Indications for dialysis in AKI

Overload: fluid overload or pulmonary edema not responsive to aggressive diuresis

Uremia: mental status changes attributable to uremia, uremic pericarditis, or neuropathy, bleeding diatheses, or vomiting associated with uremia.

Page 18: Dialysis prescription 2

Initiation of dialysis in CKD CKD stage 4 (GFR < 30 mL/min/1.73 m2) pts and

family members, should receive education about kidney failure and options for its treatment.

Initiate maintenance dialysis after an assessment of

uremic features

evidence of protein-energy wasting

metabolic abnormalities and/or volume overload mgt

Page 19: Dialysis prescription 2

Components of dialysis Prescription Haemodialysis is a form of treatment and requires a

prescription

Prescription depends on individual characteristics and should be tailored to suit the individual needs

Choosing a prescription depends on the dialysis modality to be employed

Page 20: Dialysis prescription 2

Goal of HD is to achieve

Dialysis adequacy

Electrolyte balance

Volume regulation

Page 21: Dialysis prescription 2

Dialysis Prescription For the goal of attaining adequate Kt/V and URR

values, the principle variables are:

duration of treatment,

Frequency

blood flow,

dialysate flow,

dialyzer size.

Page 22: Dialysis prescription 2

Dialysis Prescription Duration of treatment:

typically btw 3-4 hours in length

thrice weekly

Time can be ↑ if Kt/V and/or URR reflect poor dialysis

Page 23: Dialysis prescription 2

Dialysis Prescription Frequency: Different dialysis modalities exist

Intermittent in-center HD: usually 3x weekly

Intermittent home HD

Short daily HD (about 6x weekly)

Nocturnal HD (6-8hrs, 6x weekly)

Page 24: Dialysis prescription 2

Dialysis Prescription KDOQI guidelines recommend in-center short

frequent hemodialysis as an alternative to conventional Rx after considering

individual patient preferences,

the potential quality of life and

physiological benefits, and

the risks of these therapies.

Page 25: Dialysis prescription 2

Dialysis Prescription

Blood flow rate: Largely depends on type

of access used.

1. Arteriovenous fistulas (AVFs): Best. Flow rates of 600-800cc/min. Can maintain patency at flows of 200cc/min.

2. Arteriovenous grafts (AVG): Flow rates of 1000 to 1500 cc/min.

Page 26: Dialysis prescription 2

Dialysis Prescription3. Cuffed tunneled dialysis catheters: Placed in IJV

4. Femoral catheters

Aim is to achieve blood flow rates of 400-500cc/min for fistula and graft, 350-400cc/min for catheters.

Page 27: Dialysis prescription 2

AV Fistula

Page 28: Dialysis prescription 2

PTFE Graft

Page 29: Dialysis prescription 2

Cuffed TunneledCatheter

Page 30: Dialysis prescription 2

Dialysate flow: btw 500-800cc/min. Increasing the flow beyond 800 has no added benefit

Page 31: Dialysis prescription 2

Dialyzer size: A dialyzer is a rigid polyurethrane shell ( ≈30cm long), containing hollow fibres (capillaries) of dialysate membrane.

A larger exposed surface area can be used to help improve adequacy

Dialyser efficiency: measured as KoA (mass transfer urea coefficient). Could be high flux >600 or low flux <300

Page 32: Dialysis prescription 2

Electrolyte balance Dialysate: A solution of ultrapure water,

Na + (132-150mmol/L),

K + (usually 1.0 – 3.0mmol/L),

Ca 2+ (1.0 – 1.25mmol/L),

Mg 2+,

Cl – ,

dextrose,

Buffer(usually HCO3)

Ultrapure water is generated in a treatment plant

Page 33: Dialysis prescription 2

Dialysate Potassium concentration Depends on the patient’s pre-HD K+ concentration.

Serum K+ ≥5.5 mEq/L→ a dialysate K+ of 2- 3 mEq/L

If propensity toward arrhythmias, 3 mEq/L bath is preferred to avoid precipitating hypokalemia.

A dialysate K+ of 4 mEq/L →patients with hypokalemia or persistent serum K+ <3.5 mEq/L.

Serum K+ >6.5 to 7.0 mEq/L or ECG changes hyperkalemia, → 0 or 1 mEq/L dialysate K+.

Page 34: Dialysis prescription 2

Sodium modelling 140 - 145 mEq/L is appropriate in most cases

↓ serum Na+ levels indicate excessive free water intake and managed through fluid restriction.

Serum sodium <130mEq/L→ the dialysate sodium conc<= 15 - 20 mEq/L above the serum levels.

Hypernatremia should also be corrected slowly.

Dietary Na+ <100mmol/day intake (equivalent to 6g NaCl)

Page 35: Dialysis prescription 2

Calcium concentrations Guidelines recommend ↓ dialysate Ca 2+ to maintain

neutral or negative Ca 2+ balance to prevent vascular calcification.

↑ patient: dialysate gradients associated with SCD

Dialysate Ca 2+ of 1.25mmol/L normally used.

May be increased to 3-3.5mmol/l in persistent hypercalcemia,

concurrent acidosis

Page 36: Dialysis prescription 2

Dialysate bicarbonate Usually of 35 - 38 mEq/L to correct the metabolic

acidosis associated with chronic renal failure.

For those susceptible to alkalosis, lower bath of 20 - 28 mEq/L can be used. E.g.

total parenteral nutrition (TPN),

vomiting or nasogastric suction,

poor protein intake,

Respiratory alkalosis.

Page 37: Dialysis prescription 2
Page 38: Dialysis prescription 2

Volume Regulation: Ultrafiltration Fluid restriction to limit intradialytic weight gains to

<4 kg

Ultrafiltrate should not be ˃ 10% of patient’s body water

>4 to 5 L of ultrafiltrate → uncomfortable fluid shifts and intradialytic hypotension.

Patients with low residual kidney function (< 2 ml/min) undergoing 3x weekly HD require 3 hours minimum.

Page 39: Dialysis prescription 2

Volume Regulation: Ultrafiltration Additional sessions or longer treatment times for pts

with

large weight gains,

high ultrafiltration rates,

poorly controlled blood pressure,

difficulty achieving dry weight,

poor metabolic control (such as hyperphosphatemia, metabolic acidosis, and/or hyperkalemia).

Page 40: Dialysis prescription 2

Anticoagulation Heparinization during HD minimizes clotting of the

dialysis circuit during the treatment.

For patients with evidence of bleeding, no heparin is prescribed. This includes

Uraemic gastritis,

GI bleeding

Pericardial effusion

Haemorrhagic stroke

Recent surgery

Post transplant patients

Page 41: Dialysis prescription 2

Anticoagulation

Risk factors for Clotting include

high hemoglobin and hematocrit,

a high rate of ultrafiltration,

low blood flow on dialysis.

Both unfractionated and LMWH can be used.

Page 42: Dialysis prescription 2

Dialysis Adequacy Dialysis can be considered adequate if it

provides relief of uraemic symptoms

controls acidosis, fluid balance, and serum K +.

It should also allow a feeling of physical and psychological well-being.

Adequacy is mainly modelled by 2 equations

Kt/V

urea reduction ratio.

Page 43: Dialysis prescription 2

Urea as a surrogate marker Small, water-soluble breakdown of amino acids and

dependent on protein intake and breakdown.

Now considered a good surrogate marker for other pathogenic solutes

Advantages include

Abundance in renal failure

Ease of measurement,

Wide volume of distribution

Good dialyzability

Page 44: Dialysis prescription 2

Dialysis Adequacy Kt/V: is a ratio that relates the volume of cleared

plasma (Kt) to the volume of urea distribution (V).

K = dialyser urea clearance.(ml/min)

t = time on dialysis.(min)

V = volume of distribution of Ur (estimated from patient size).(ml)

Page 45: Dialysis prescription 2

Dialysis Adequacy Describes the volume of urea cleared during a dialysis

session relative to the volume of urea distributed throughout the body.

spKt/V: single pool urea clearance

eKt/V: equilibrated urea clearance

stdKt/V: Weekly standard urea clearance

Page 46: Dialysis prescription 2

KDOQI guidelines on Adequacy A target single pool Kt/V (spKt/V) of 1.4 per session

for patient treated thrice weekly, with a minimum delivered spKt/V of 1.2.

If significant residual native kidney function (Kr), the dose of hemodialysis may be reduced.

For hemodialysis schedules other than thrice weekly, a target standard Kt/V of 2.3 volumes per week with a minimum delivered dose of 2.1

Page 47: Dialysis prescription 2

Dialysis Adequacy Urea reduction rate (URR) similarly reflects the

removal of urea

URR = (BUNpre–BUNpost)/BUNpre

K/DOQI guidelines recommend the attainment of a minimal URR of 65% and a target URR of 70%.

Page 48: Dialysis prescription 2
Page 49: Dialysis prescription 2
Page 50: Dialysis prescription 2

Complications of Haemodialysis The most common complications during hemodialysis

are,

hypotension,

cramps,

nausea and vomiting,

Page 51: Dialysis prescription 2

Complications of Haemodialysis headache,

chest pain,

back pain,

itching.

Haemolysis

Clotting of extra-corporeal unit

First use syndrome/dialyser reaction

Accidental disconnection

Hard water syndrome,

Air embolism

Page 52: Dialysis prescription 2

Intradialytic hypotension IDH is defined as a fall in SBP >20mmHg (or MAP

>10), associated with symptoms, or a fall to SBP <100mmHg.

Symptoms associated with IDH include:

Cramps, abdominal pain, or nausea (reduced gut perfusion).

Yawning, sighing, anxiety, or dizziness (reduced cerebral perfusion).

Chest pain or arrhythmias

Page 53: Dialysis prescription 2

IDH Causes

Volume-related

Large weight gain (high ultrafiltration rate)

Short weekly dialysis time (high ultrafiltration rate)

Excessively low target (“dry”) weight

Antihypertensive medications

Eating during treatment

Anemia

Page 54: Dialysis prescription 2

IDH

2. Inadequate vasoconstriction

High dialysis solution temperature

Autonomic neuropathy

3. Cardiac factors

Diastolic dysfunction

Page 55: Dialysis prescription 2

IDH 4. Other causes

a. Pericardial tamponade

b. Myocardial infarction

c. Occult hemorrhage

d. Septicemia

e. Dialyzer reaction

Page 56: Dialysis prescription 2

Immediate management of IDH:

Stop ultrafiltration (UF).

Trendelenburg position.

IVF 0.9% NaCl as a 250mL bolus.

Recheck BP.

Thorough clinical review (including medications) to prevent future episodes

Page 57: Dialysis prescription 2

Disequilibrium Syndrome

Clinical features: nausea and vomiting, agitation, headache, seizures, loss of consciousness.

Cause: high blood urea levels being reduced too rapidly. Usually occurs during first dialysis session (with high blood flows). Leads to cerebral edema

Prevention: use a dialyser with small surface area, commence blood flow rate at 150-200mL/min. Limit first session to 2h. Mannitol infusion,50% dextrose infusion

Page 58: Dialysis prescription 2

Conclusion Haemodialysis is a life-sustaining procedure for the

treatment of ESRD

In AKI, it provides rapid correction of fluid and electrolyte abnormalities that pose an immediate threat to the patient’s well-being.

In CKD, it results in a dramatic reversal of uremic symptoms and helps improve the patient’s functional status and survival.

To achieve these goals, the dialysis prescription must ensure that an adequate amount of dialysis is delivered to the patient.

Page 59: Dialysis prescription 2

Thanks for listening

Page 60: Dialysis prescription 2
Page 61: Dialysis prescription 2

References Cheng,S., Vijayan,A. The Washington Manual Nephrology

Subspecialty Consult.3rd Edition.St. Louis,Missouri: Lippincott Williams and Wilkins; 2012: 538-562

Daudirdas,J.T.,Blake,P.G., Ing,T.S. Handbook of Dialysis. 5th

Edition. Philadelphia: Lippincott Williams and Wilkins; 2015 Steddon,S., Ashman,N.,Chesser, A.,Cunningham,J. Oxford

Handbook of Nephrology.2nd Edition. Oxford, UK: Oxford University Press;2014:274-308

Bamgboye,E.L. The looming epidemic of kidney failure in Nigeria. MetroHealth: 2015

Hemodialysis Prescription & Adequacy, KDOQI guidelines,Oct2015

Palmer,B.F., The Dialysis Prescription and Urea modelling. www.kidneyatlas.org