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Please note: The following guidelines have not been assessed using the AGREE
(Appraisal of Guidelines for Research and Evaluation) criteria. This will take place
at the next guideline review.
Version: 1.0
Authorised by: Dr J Beattie
Q-Pulse Ref: YOR-REN-008
Page 1 of 6
Issue Date: Jan 2011
Contents
Page Number(s)
1. Introduction
2. Definition
3. Aetiology
4. Clinical Assessments 3
5. Investigations
6. Urinary Electrolytes in Renal Failure
7. Management of Acute Renal Failure
7.1 Fluid Management
7.2 Electrolyte Abnormalities
7.2.1 Hyponatraemia
7.2.2 Hypernatraemia
7.2.3 Hyperkalaemia
7.2.4 Hypocalcaemia
7.2.5 Hyperphosphataemia
7.2.6 Hypophosphataemia
8. Acid-Based Disorders
9. Nutrition
10. Hypertension
11. Future Guideline Development
2
2
2
3
4
4
4-5
5
5
5
6
6
6
6
7
7
7-8
8
1. Introduction
The following guideline has been developed by clinicians within the Renal Unit at
Yorkhill. This document is intended for use by clinicians in the Management and
Investigation of Acute Renal Failure. For further information, contact a clinician within the
Renal Unit.
3. Aetiology
Pre-Renal
Intrinsic Renal
Post-Renal
Hypovolaemia
Peripheral vasodilatation
Impaired Cardiac Output
Renal Vessel occlusion
Drugs
Hepatorenal Syndrome
Increased intraabdominal
pressure
Circulatory Insufficiency
Nephrotoxins
Renal Disease
Myo/haemoglobinuria
Tumour infiltrate
Intratubular obstruction
Latrogenic Factors
Version: 1.0
Authorised by: Dr J Beattie
Q-Pulse Ref: YOR-REN-008
Page 2 of 6
Issue Date: Jan 2011
Blood Pressure
Neurological Examination
Bruising/Bleeding
Cardiorespiratory Examination
Drug History
5. Investigations
Version: 1.0
Authorised by: Dr J Beattie
Q-Pulse Ref: YOR-REN-008
Page 3 of 6
Issue Date: Jan 2011
Urine
Output
Uosm
(mosm)
(newborn)
UNa
(mmol/L)
(newborn)
FENa (%)
(newborn)
Lab
studies
Pre - renal
Oliguria
Intrinsic
Oliguria - Polyuria
Post renal
Variable
>500
(>350)
<10
(3119)
<1
(<2.5)
<300
(<300)
>40
(6335)
>2
(>3)
<350
(<300)
>40
Increased
Urea
Lower
Creatinine
Hypocalcaemia
Hyperphosphataemia
Creatinine increases
by 45 130
mmol/L/day
Hyponatraemia
Hyperkalaemia
Hyperchloraemic
Acidosis
<2
(<3)
Correction of Hypovolaemia
Fluid Overload:
o Frusemide 2 - 10mg/kg bolus
o Fluid restriction
o Minimalise drug infusion volumes
Accurate input/output
Daily weight
Dialysis
Beware Polyuria
25ml/kg
12.5ml/Kg
5ml/Kg
Version: 1.0
Authorised by: Dr J Beattie
Q-Pulse Ref: YOR-REN-008
Page 4 of 6
Issue Date: Jan 2011
8. AcidBase Disorders
These are invariably acidosis and are often mixed respiratory and metabolic especially in
the intensive care setting. Treatment is generally only indicated if there is associated
hyperkalaemia or if the acidosis is profound.
Treatment of Acid-Based Disorders
Base Deficit (mmol) = Base Excess x Weight/3
Replace half of the deficit initially
Sodium Bicarbonate is hypertonic with a risk of CNS complications or
hypernatraemia and is only effective with adequate ventilation.
Rapid correction of acidosis may cause hypocalcaemia and tetany or seizures
Therefore rapid correction to be avoided
Version: 1.0
Authorised by: Dr J Beattie
Q-Pulse Ref: YOR-REN-008
Page 5 of 6
Issue Date: Jan 2011
Dose
1-5 mg/kg/hr
Onset
3-5 min
Nifedipine
0.25-0.5 mg/kg
sublingual
Nitrogylcerin
1-10 ug/kg/min
as IV infusion
Instant
Sodium
Nitroprusside
0.5-8 ug/kg/min
as IV infusion
Phentolamine
Clonidine
Hydralazine
Frusemide
Diazoxide
Action
Alpha & beta
Blocker
5-10 min Ca
channel
blocker
Direct
vasodilator
Complications
Hypoglycaemia
Well tolerated
Headache,
nausea,
Syncope
Tachycardia,
bradycardia
Instant
Direct
vasodilator
Thiocyanate
poisoning
0.1mg/kg stat
5-50ug/kg/min
IVI
2-6 ug/kg
5-10 min
Alpha blocker
~10 min
0.2 to 15
mg/dose IV
bolus
4-6ug/kg/min
IVI
1-3mg/kg over
15min
0.1-1mg/kg/hr
IVI
5 mg/kg (max
300) IV bolus
5-10 min
Central alpha 2
Agonist
Direct
vasodilator
Tachycardia,
vomiting
arrythmias
Depression
Rebound
Headache,
vomiting,
tachycardia
3-5 min
Diuretic
Volume depletion
Electrolyte abn
Direct
vasodilator
Hyperglycaemia
Nausea &
vomiting
Should any aspect of this guideline change before the planned review in
February 2007 (i.e. new technology or procedural change) then this guideline
should be updated accordingly.
Future review of this guideline should make use of the AGREE document to
ensure that up-to-date evidence and best clinical practice has been used to
inform this guideline. For further information on guideline development, contact
the Multi-Professional Clinical Practice Group.
Version: 1.0
Authorised by: Dr J Beattie
Q-Pulse Ref: YOR-REN-008
Page 6 of 6
Issue Date: Jan 2011