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84 Cards in this Set

  • Front
  • Back
What happens in Uremia?
Bun increases
why is cardiovascular events significant in Uremia?
Because pts w/ ESRD have really high rates of death due to cardiovascular events.

more than 50% will die.
What Clinical Manifestations happen in Cardiovascular **
Volume overload, LVH, HTN
What are Indications For Dialysis?
Acid-base imbalance: Metabolic acidosis resulting from the accumulation of organic and inorganic acids

Electrolyte imbalance:Hyperkalemia, Hyperphosphotemia

Intoxications:Salicylates, lithium, methanol, ethylene glycol, theophylline, phenobarb

Overload-fluid:Postoperative fluid gain

Uremia:High catabolism of acute renal failure
What electrolyte is the most concerning in dialysis?
K is most concerning (if increased, patients get EKG changes, ventricular fibrillation
When is dialysis initiated?
CrCl < 9-14ml/min

Anuria or oliguria
What are Subjective symptoms of dialysis?
Persistent anorexia, nausea, vomiting
When will diabetic pts intiate dialysis?
@ 15ml/min
What are Three basic components: of dialysis?
Blood-filled compartment
Dialysate-filled compartment
Semi-permeable membrane
What are two main processes of dialysis?
Diffusion
Ultrafiltration
What is diffusion?
Movement of solute down a concentration gradient
What is the diffusion rate dependent on? (4)
Difference between blood and dialysate
Solute characteristics: the smaller the solute the easier it will cross the semi permeable membrane
Dialyzer membrane composition: how big are the pores?
Blood and dialysate flow rates: the faster the rates the better diffusion will be
What is Convection / ultrafiltration ?
Movement of water across dialyzer membrane as a result of hydrostatic or osmotic pressure
What is convection?
Dissolved solutes are “dragged” across membrane with fluid transport
What are the three types of dialysis?
Intermittent Hemodialysis (IHD)

Peritoneal Dialysis (PD)

Continuous Renal Replacement Therapy (CRRT)
Intermittent Hemodialysis (IHD)
How long is each session? How often is it done?

What do the solutes in the blood come in direct contact with?

What does it require?
Efficient form of dialysis
3-5 hour session
3 times per week
Solutes in blood come in direct contact with dialyzing membrane (filter)
Requires anticoagulation
What are the 3 different membranes of dialyzers?
Conventional/standard:
Small pore size (<500 daltons) limited solute removal eg. Urea, Scr

High efficiency
Increased surface area increased ability to remove water, urea, Scr and other small molecules

High flux
Increased pore size  increased removal of large molecules (< 40,000 daltons)
What are standard dialysates for IHD?
Dextrose: 100mg.dl
Potassium: 2 meq/L
Sodium: 140meq/l
Chloride: 116 meq/l
Magnesium Sulfate: 1.5meq/l
Calcium Gluconate: 2.5 meq/l
Sodium Bicarbonate: ~20-30meq/l
What does the rate of ultra filtration depend on?
The rate of ultrafiltration depends upon the porosity of the membrane and the hydrostatic pressure of the blood, which depends upon blood flow.  This is very effective in removal of fluid and middle-sized molecules, which are thought to cause uremia
Who can venous catheters be used in? what is it good for?
Small children
Diabetics with severe vascular disease
Morbidly obese
No AV access sites

Good for acute dialysis so can be done immediately
Goals of Hemodialysis?
1.Achieve desired/optimal dry weight
Dry weight: target post-dialysis weight at which patient is normotensive and non-edematous

2.Achieve adequate removal of endogenous waste products
When pts are first initated on IHD, what happens?
Very short session ares done first. 1-2 hours at most and are done daily to allow the body to adjust correctly
What are the 2 methods of Dialysis Adequacy?
1.Urea reduction ratio (URR) > 65%
2.Kt/V >1.2
k = dialyzer clearance of urea
t = duration of dialysis (hrs)
V = urea distribution volume of patient (L)
What are 3 Causes of Inadequate Dialysis?
Patient non-adherence

Access stenosis or thrombosis

Use of catheters
What happens to patients that have high sodium food?
Even though on dialysis, it still can"t remove a lot of the phosphorus, so a lot of patients will be given phosphorus binders--> tums, phoslo or none Ca binders like sevelmar or renagel. These must be taken with meals.
What are 3 common complications of IHD?
1.Hypotension (20-30%)
Nausea & cramping (with acute decrease in BP) especially in elderly and DM patients
2.Muscle cramps (10-20%)-->occur due to low muscle perfusion
3.Pruritis (5%)
What are Non-Rx measures for hypotension?
Trendelenburg position
Decreased UF rate
NS bolus 100-200ml
Evaluate BP meds
What are pharmacologic therapies for hypotension?
½ hr before dialysis:
Midodrine 2.5 – 10mg
Fludrocortisone 0.1mg
Albumin 50 to 100 ml infusion
What are Non-Rx measures for muscle cramps?
NS bolus 100- 200ml
Reset dry weight
Stretches
What are pharmacologic therapies for
Vitamin E 400 IU qhs
what are vascular access complications of IHD?
Catheters > grafts > fistulas

Thrombosis
Infection: Mostly due to S. Aureus (often MRSA)
Risk factors: Type of access, DM, immunosuppression, h/o bacteremia, S. aureus nasal carriage.
What are non RX measures in IHD of access thrombosis?
Forced NaCl flush
Medical thrombectomy
Change catheter
What are pharmacologic measures in IHD of access thrombosis?
Alteplase 2mg/2ml
Retaplase 0.5mg/2ml
What are non RX measures in IHD of infxn?
Obtain blood culture
Change catheter +
Culture catheter tip
What are pharmacologic measures in IHD of infxn?
Antibiotics
Gram+ coverage +/-
Gram - coverage
What are two kinds of PD?
Continuous Ambulatory PD (CAPD)
4-5 exchanges per day

Automated PD (APD)
Performed by machine called cycler while patient sleeping
What are advantages of PD?
It can be done at home, there are no traveling restrictions with it either.
How often is PD performed?
What does it rely on?
What dont solutes come in contact with?
What do solutes meet more of?
Can blood be regulated?
What flow doesnt it have?
Must be performed daily
Relies entirely on passive diffusion
Solutes not in direct contact with dialyzing membrane
Solutes meet more barriers
Blood flow cannot be regulated
No countercurrent dialysate flow
explain the Peritoneal Dialysis Process?
1-3L dialysate solution is instilled into peritoneal cavity & left for prescribed time (“dwell time”)

Dialysate fluid is drained out and new bag is instilled (~30 min)

Frequency: 2-3L exchanges 4 to 5 times/day
Less efficient than IHD as there is no way to regulate dialysate flow or blood flow

PD catheter is placed in permanently
What are standard dialysates in PD?
Dextrose: 100md/dl
Potassium: 2meq/L
Sodium: 140 meq/l
Chloride: 116 meq/L
Magnesium Sulfate: 1.5 meq/l
Calcium Gluconate: 2.5 meq/l
Sodium Bicarbonate
PD and HD dialysate only differ how?
on dextrose content.
What is an alternative to dextrose? why is it used?
Icodextrin…as dextrose can be toxic to peritoneal cavityicodextran is not.
How can Dialysate drugs be delivered?
By doing this, what don't these drugs have to pass through?
delivered IP. ..Drugs that are delivered IP do not have systemic absorbtion, but can adhere to polyvinil bags therefore must consider adherence of drug.
how are PD Dialysate Solutions available ?
Commercially available in 1-3L polyvinyl chloride bags
PD Dialysate Solutions Contain varying concentrations of what?
Electrolytes: Na, CL, Ca, Mg, lactate
Dextrose: 1.5%, 2.5%, 3.85%, 4.25% or
Icodextrin: 7.5%
Additives: insulin, heparin, antibiotics
How is PD adequacy assesed?
1.Kt/V x 7 days > 1.7
2.Contribution of residual renal function
CrCl 9-12 ml/min ~Kt/V 0.2-0.4

Important to preserve residual fxn
Use ACEI/ARBs
Avoid drugs/procedures associated with kidney insult--> AG, NSAIDS
Do PD patients have residual renal function?
Do they have to restrict fluid?
What is the monitoring of Kt/V?
PD patient usually have some residual renal function, not as fluid restricted, Kt/v should be monitored over first month, than every 4 months after for possible decrease in residual kidney function.
What are mechanical complications of PD?
Mechanical:
Catheter obstruction

Excessive catheter motion  infection, tissue aggravation

Catheter tip impinging on viscera  pain
What are medical complications of PD?
1.Diabetes
Increased insulin requirements

2.Fluid overload
Edema, CHF, or pulmonary exacerbations and HF

3.Electrolyte abnormalities

4.Malnutrition
Albumin and amino acid loss in PD fluid

5.Infection
Exit site, tunnel infections or peritonitis
Management of PD Complications
Glucose load leads to what complication? What is pharmacologic therapy?
Exacerbation of diabetes

IP insulin
Management of PD Complications

Fluid overload leads to what complication? What is pharmacologic therapy?
Exacerbation of CHF
Edema
Pulmonary congestion

Increase Ultrafiltration
Diuretics if patient has residual renal fxn (urine output > 100ml/day)
Management of PD Complications

Electrolyte abnormalities leads to what complication? What is pharmacologic therapy?
Hypo and hyper
-calcemia
-kalemia

Alter dialysate Ca and K content
Management of PD Complications

Malnutrition leads to what complication? What is pharmacologic therapy?
Albumin loss, loss of amino acids, muscle wasting and increase in adipose tissue

Dietary change, TPN, d/c PD
What is number 1 reason for PD failure
?
Peritonitis
What are signs and symptoms of peritonitis?

How is it diagnosed?
1. Cloudy dialysate effluent* (95%)
Lab tests: dialysate WBC > 100/mm3

2.Abdominal pain* or Rebound tenderness* (75-80%)

3. Fever >38 C* or NV--> 25-30%

4. Chills

* Diagnosis includes two of these
Diagnosis of Peritonitis consists of what bugs?
Gram positives
Enterococcus
S. aureus or S. Epi

Gram negatives
E. coli, Pseudomonas or Klebsiella
Gram negatives usually found around bowel area, may find way to catheter due to lack of hand washing.
What is Empiric Antibiotic Dosing of PD based on?
1. GFR < 15ml/minute

2.Based on residual urine output

< 100 ml per day
Cefazolin 1 gm per bag daily
Ceftazidime 1 gm per bag daily

> 100 ml per day
Cefazolin 20mg/kg per bag daily
Ceftazidime 20mg/kg per bag daily
Empiric Antibiotic for PD last how long?
Treatment duration: IP antibiotics x 14-21 days
What are Peritonitis Treatment Guidelines? (6)
Prompt initiation of empiric therapy
IP administration of antibiotics
Adjust treatment based on C & S
Re-evaluate on day 4
Consider catheter removal in patients with consistent positive cultures
If infection is systemic drugs are given IV or PO
What are Infectious Complications?

What are sx?

What organism is it usually?
Catheter-related (exits site infection)

Sx: purulent drainage, with or without erythema at catheter exit site

Organism: usually S. aureus
Risk increased in patients who are nasal carrier of S. aureus
What is a major risk factor for infections?
Nasal carriage of S. aureus is major risk factor
Nasal carriage of S. aureus is major risk factor

What are Tx of infections?
ntranasal mupirocin BID x 5 days (every month)

Topical mupirocin daily to exit site

Rifampin 300mg po BID x 5 days (every 3 months)
Rifampin is not a favored method as the resistance occurs quite quickly.
What are additional risk factors of infections?
Additional risk factors: elderly, diabetics and immunocompromised patients
PD is favored in the following patients?
1.Infants, very young children
2.Severe cardiac disease
3.Hemodynamic stability
4.Difficult vascular access
5.Significant residual renal function
6.Desire for greater freedom, autonomy and ability to travel
When can is PD contraindicated in pts?
Unsuitable peritoneum ( adhesions, fibrosis, malignancy)
Most common reasons for PD failure?
Peritonitis
Patient burnout
What is CRRT?
is a means of dialyzing critically ill patients without compromising hemodynamic stability
In CRRT, how are large volumes of fluids infused?
infused through the hemodialyzer and must be replaced in the form of buffered, electrolyte solutions supplied by the pharmacy
CRRT

What process is it similar to?
How does it run?
What is the dosing estimated on?
Same basic process as IHD with respect to hemofiltration, access and anticoagulation
Runs continuously with rate changes
Pharmacy supplies high volumes of dialysate and replacement fluid
Drug dosing for estimated ClCr ~ 30ml/min
What are advantages of IHD?
Higher efficiency
-Closer patient monitoring
-Low failure rate
What are disadvantages of IHD?
Travel to dialysis clinic
-Cramps, hypotension
-Rapid decline in renal function
What are advantages of PD?
Freedom to move around
-Hemodynamic stability
- Preserved renal function
What are disadvantages of PD?
Peritonitis
-High failure rate
-Catheter malfunction
What are advantages of CRRT?
Highest efficiency
-Hemodynamic stability
-Mimics natural physilogy
What are disadvantages of CRRT?
Frequent clotting of filter
-Highly labor intensive
-Expensive
What are 3 Membrane and Dialysis characteristics in IHD, PD and CRRT?
1.Rate of blood and dialysate flow

2.Porosity of the hemodialyzer
Large or small size pores
Number of pores

3.Composition of the hemodialyzer
Increased binding of drug molecules or endogenous substances
What are drug characteristics in IHD, PD and CRRT?
Molecular weight  Larger molecules less likely to be cleared (> 40 kDa)

Water solubility  Lipophilic molecules more likely to bind to the hemodialyzer

Protein binding  protein bound substances less likely to be cleared

Volume of Distribution  drugs with higher Vd less likely to be cleared efficiently
How is PD and IHD dosed?
PD and IHD – Dose for clearance < 15 ml/minute
Adjust dose of all renally cleared drugs and administer dose after dialysis (IHD)
CRRT is dosed how??
Dose for clearance 30 ml/minute
What are 5 drugs and there dosing in HD?
Acyclovir 5mg/kg q24h after HD
Levofloxacin 250mg q48h after HD
Cefazolin 1 gm q 48 after HD
Ciprofloxacin 400mg q 24 after HD
Metronidazole 500 mg q8h
What are 5 drugs and there dosing in CRRT?
Acyclovir 10mg/kg q24h
Levofloxacin 250mg q24h
Cefazolin 2gm q24h
Ciprofloxacin 400mg q12h
Metronidazole 500 mg q8h
What is the dose and
What do you monitor in Gentamicin?
Gentamicin 1-2 mg/kg based on levels
Peaks and troughs
What is the dose and what do you monitor in vanco?
Vancomycin 20mg/kg based on levels
Troughs only
In Monitoring Serum Drug Levels, when do you obtain peaks? How often are troughs taken?
When do you hold and give doses?
Peaks: Obtain 1 hour after infusion stopped
Troughs: IHD (after IHD), CRRT – daily, PD ~48 hours after loading dose
Hold dose until trough desirable
Give dose if trough desirable