Monday, 27 June 2011

Chronic Renal Failure (CRF)


Definition
Irreversible deterioration in renal function


Classification – 5stages
Stage
Description
GRF (ml/min/ 1.73m3)
Action
1
Kidney damage with N/↑GFR
>90
Investigate
2
Kidney damage w slightly low GFR
60-89
Renoprotection – BP, diet
3
Moderately low GFR
30-59
4
Severe low GFR
15-29
Consider RRT
5
Kidney failure
<15 or dialysis

Aetiology
Disease
%
DM
20-40
HTN
5-25
Glomerular disease
-IgA nephropathy common
10-20
Interstitial disease
5-15
Systemic inflammatory e.g. SLE, vasculitis
5
RAS
5
Congenital/inherited
-PKD, Alports disease
5
Unknown
5-20

History
Symptoms
Fluid overload – ankle swelling, SOB,urine output
Uraemic symtoms
·         Anorexia, vomiting, , metalic taste
·         Fatigue, weakness,hiccup
·         Pruritus,bruise

Signs
Pallor,  yellow skin pigmentation
V/S: ↑BP, ↑RR, Kussmaul’s respiration, pulsus paradoxus
Brown nail
Purpura, bruising, excoriation, AV fistulae
Conjuctival pallor
JVP ↑
Displaced apex beat, pericardial friction rub
Bibasal Crepitation
Tenckhoff catheter
Leg swelling

I(x)
Blood
HB ↓ (normochromic, normocytic)
ESR
U&E (↑ urea, ↑creatinine)
↓Ca2+, ↑PO43-, ↑ ALP (renal osteodystrophy)
↑PTH
Urine
MC&S, dipstick, urine PCI or 24h urine protein
Imaging
Renal US – TRO obstruction, measure size
Small <9cm
Large -DM, PKD, amyloidosis, myeloma, systemic sclerosis, asymmetrical renal vascular
DTPA scan
CXR – cardiomegaly, pleural/pericardial effusion, pulmonary oedema
Bone  X-ray – TRO renal osteodystrophy
Renal biopsy

Complications
Anaemia

Def of EPO
Diminished erythropoisis dt toxic effect of uraemia on BM
↓red cell survivors
↓dietary intake and absorption of iron
Bleeding
Capillary fragility, poor platelet function
Fluid and electrolyte balance
↓concentrating ability
Acidosis

Infection
Cellular and humoral immunity are impaired
Renal osteodystrophy
Impaired renal function
(1) ↓PO43-  secretion à ↑plasma [PO43- ]
(2)↓1,25 (OH)2Vit D à↓Ca2+ absorption à↓plasma [Ca2+]
Both (1),(2) àstimulate PTH gland (hyperplasia) à↑PTHà↑osteoclastic activityà↑bone resorption
Generalised myopathy
Dt combination of poor nutrition, hyperparathyroidism, Vid D def, disorder of  electrolyte metabolism
Neuropathy
Dt demyelination of medullated fibres, longer fibres – earlier stage
Sensory
-paraesthesia
-tx:amytriptaline, gabapentin
Motor
-foot drop
Autonomic
-delayed gastric emptying
-diarrhoea
-postural hypotension

Treatments

Refer to nephrologist
Treat reversible causes
        I.            HTN
      II.            ↓ renal perfusion
    III.            RAS
    IV.            Hypotension dt drug treatment

      V.            Sodium, water depletion
    VI.            Poor cardiac output
  VII.            UT obstruction
VIII.            UTI
    IX.            Nephrotoxic med

HTN – small Bp dropàimprove significant renal function
-Tx: ACE-i, A2A
-target: 130/80, (125/75 if >1g proteinuric/d)
Oedema
– frusemide 250mg-2g/24h ± metolazone 5-10mg/24h PO mane
-fluid restriction
Anaemia
EPO
Renal osteodystrophy
Restrict dietary phosphate e.g. egg, cheese, milk
Vit D analogue – Alphacalcidol=1α-hydroxycholecalciferol
Ca2+ supplement
Phosphate binder in gut (e.g. Calchichew)
Restless legs
Clonazepam -0.5-2mg/d

Renal replacement therapy
Indications (7)
1.       Fluid overload
2.       ↓urine output
3.       Uraemic symptoms
4.       Uraemic encephalopathy
5.       ↑urea
6.       Hyperkalaemia
7.       Metabolic acidosis

Methods  of RRT
1.       Haemodialysis (HD)
Blood flows on one side of semi-permeable membrane, while dialysate flows in the opposite direction
Solute transfers occur by diffusion.
Ultrafiltration is the removal of excess fluid by creating negative transmembrane perssure.
Problems
                                i.            Disequilibrium syndrome
                               ii.            hypotension, arrhythmias
                             iii.            Bleeding, haemolysis, air embolism
                             iv.            Time consuming
                              v.            Access
Fistula - thrombosis, stenosis, aneurysm, steal syndrome, ischaemic
Temporary line -  infection, blockage
2.       Haemofiltration
Blood is filtered continuously acoss highly permeable synthetic membrane.
Removal of waste product by a process called convection.
Ultrafiltrate is substituted with an equal volume of replacement fluid.
Advantage – less haemodynamical instability
Disadvantages – > expensive, longer than HD
3.       Peritoneal dialysis
                                I.            CAPD (continuous ambulatory
peritoneal dialysis)
2L bags aer changed 3-5 times/day, total dialysate of 10L
                              II.            Automated peritoneal dialysis
Use cyler machine to enhance solute and fluid removal
Techniques (4)
                                                 i.            CCPD (continuous cylic PD)
                                               ii.            IPD (Intermitted PD)
                                              iii.            NIPD (Night intermittent PD)
                                             iv.            TIPD (tidal intermittent PD)
Problems with PD
exit site leak
 poor inflow/ outflow
 pelvic/ abdo pain
 faeculent/ bloody effluent
unilat pleural effusion
poor metabolic control
hyperglycaemia in DM patients
peritonitis

Haemodialysis vs  peritoneal dialysis
Haemodialysis
PD
Efficient
Less efficient
4hrs, 3 times / week
4 exchanges/day
2-3 days bet treatment
Few hours bet treatment
Visit to hosp
Performed at home
Requires adequate venous circulation
Require intact peritoneal membrane
Compliance with diet and fluid restriction
Diet and fluid less restricted
Symptoms and haemodynamic instability
Asymptomatic, less haemodynamic instability
Infection related to vascular access
Peritonitis and catheter-related infection

Complication of dialysis
1.       Cardiovascular diseases
e.g IHD, CF, stroke > common
2.       HTN
3.       Anaemia – Rx: EPO ±haematinics
4.       Bleeding tendency
-dt platelet dysfunction
-Rx – desmopressin, transfusion
5.       Renal bone disease
-Rx: diet, alfacalcidol, Ca2+supplement, phospate binders
6.       Infection –dt non-sterility procedure
7.       Β2-microglobulin amyloidosis
-dt accumulation of amyloid
-compl: Carpal tunnel syndrome, arthralgia, #
8.       Acquired renal cyst
-present with haematuria or malignant transformation
9.       Malignancy
e.g. urothelial tumour in analgesic nephropath

Discussion

Haemodialysis fluid (dialysate)
1.       K3 (low calcium)
2.       K5 (standard calcium)
3.       K6 (high calcium)

3 types of fistula (AVF)
1.       Brachiocephalic fistula (BCF)
2.       Brachiobasillic fistula (BBF)
3.       Radio cephalic fistula (RCF)

Factors involved in determining site of fistula
1.       Non dominant hand
Risk of steal syndrome
2.       Distil first – radio àbrachial

Types of Temporary line
1.       Femoral catheter – last  <1w
2.       IJC – last up to 2 months
Only for good cardiac function
Buy time for AVF to mature
Hand grip exercise 3h/d àspeed up maturity of fistula

Screening before starting HD
1.       Hep B
2.       Hep C
3.       HIV
Aim: to avoid contamination of the machine, thus transmission of infection

Eat High calcium food

Avoid high phosphate food

Hyperkalaemia findings on ECG
1.       Absent P wave
2.       Prolong PR interval
3.       Widening of QRS complex
4.       Tall T wave

Hyperkalaemia in CRF
Rule out causes for hyper K
1.       ACE-i, suxamethonium
2.       K-sparing diuretics
3.       Massive blood transfusion
4.       Delay in analysis – K leak out of RBC
5.       Rhabdomyolysis, burn
6.       Metabolic acidosis
7.       Addison’s disease
8.       Excess K therapy

Treatment of hyperkalaemia
1.       Calcium
10ml of 10% calcium gluconate IV over 2min
2.       IV glucose + insulin
50ml Dextrose 50% + 10U Actrapid insulin IV over 30min
MOA: insulin stimulates intracellular uptake of K+, lowering serum K+ by 1-2mmol/l over 60min
3.       Salbutamol 5mg nebulizer
4.       Haemodialysis


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