Renal Flashcards
Tx of AKI
A-E assessment
Correction of any hypoxia
Halt any potentially damaging drugs
Restrict potassium intake
Pre-renal causes
Treat shock
Post-renal causes
Refer to urology
Renal causes
Assess fluid status with volume replacement to match known insensible losses
CVP measurement may be necessary
If there is urine output after fluid replacement continue large quantities of fluids +/- diuretics
If there is no urine output or complications are present nephrologist intervention is required
Indications for acute dialysis with AKI
refractory hyperkalaemia pulmonary oedema acidosis uraemic pericarditis/encephalopathy complete anuria drug OD
what is a good indicator of AKI severity
furosemide stress test
Furosemide 1mg/kg is give after fluid resus, and urine output over 2 hours is measured and replaced
Volume of fluid output at 2 hours can then be used to demonstrate likelihood of progression to AKI stage III
Generally after a week of oliguria, if the AKI is improving there will be one week of polyuria before return to normal kidney function at week 3
what are common electrolyte abnormalities in AKI
Rapidly progressive uraemia
Symptoms progress from anorexia, pruitis, vomiting to encephalopathy (confusion, drowsiness, fitting) and haemorrhagic episodes
Hyperkalaemia
Hypernatraemia (unless pre-renal)
Metabolic acidosis
Hypocalcaemia/hypophosphataemia (more common in CKD)
Tx of Hyperkalaemia
Start continuous ECG monitoring
10ml 10% calcium gluconate IV
Repeat at 5 minute intervals to a max of 3 doses until ECG stabilises
50ml of 50% glucose with 10U ACTRAPID insulin into a large vein over 30 mins to decrease K+ concentration
Consider 10mg salbutamol neb (also lowers potassium)
If pH <7.2 consider sodium bicarbonate IV if advised by renal registrar
Recheck K+ after 2 hours
Calcium resonin can then be given orally/rectally, however this is a long term management option
Tackle underlying issue
Tx of CKD
Treat reversible causes
First line is blood pressure/diabetic control
<130/80
If proteinuric BP should be <125/75
ACE inhibitors first line
Primary CV prevention is also important
Statin + low dose aspirin
Second line is control of complications
Recombinant EPO for those with anaemia
Calcium/Vit D supplementation
K+ restriction is there is any suggestion of hyperkalaemia
Renal replacement therapy is indicated in those with ESRD
Guidelines suggest this should be for any symptomatic CKD 5 patient however many consultants will delay starting dialysis
Tx of renal bone disese
Restrict dietary phosophate
Giving phosphate binders
Adcal supplementation
whats the difference between haemodialysis and haemofiltration
Hameofiltration differs from haemodialysis by not transfering solutes via diffusion but via filtration
what are the 2 peritoneal dialysis regimes
Continuous ambulatory peritoneal dialysis (CAPD) or continuous cycling peritoneal dialysis (CCPD)
CAPD = every 2 hours up to 3-4 times a day 2L of peritoneal fluid is drained out and a fresh 2L is reinserted into the peritoneal cavity
CCPD = over a 12 hour period fluid is continuously pumped through the abdomen
what is the major risk of peritoneal dialysis
peritonitis
dialysis complications
Annual mortality is 20%
Infection
Cardiovascular disease
Renal bone disease
Anaemia
Bleeding tendencies
Increased risk of renal malignancy
what assessments are required prior to transplantation
Virology/TB assessment
Active infection contraindicated due to risks of immunosuppression
Blood group/HLA matching
Full systemic examination – comorbid disease is a contraindication
operative complications of renal transplantation
Bleed
Thrombosis
Infection
Urinary leaks
post-surgical complications of transplant
Rejection
Risk highest in the first 3 months
Lifelong immunosuppression because of this
Most episodes of rejection are reversible and in most cases immunological tolerance develops
Ciclosporin/tacrolimus toxicity
Infection/malignancy due to immuosuppression
Skin cancer
Anal cancer
Lymphoma
prognosis of a transplant
5 year 80-95% graft survival rate depending on how good the HLA match is
what drugs need adjusting in renal impairment
Gentamicin
Cephalosporins
Heparin
Lithium
Opiates
Digoxin
How do you manage minimal change disease in children
try steroids and if the child responds within a month biopsy is not required, otherwise biopsy is indicated
steroids tend to resolve it in 4-6 weeks
most common cause of glomerulonephritis in adults
beurgers disease (IgA nephropathy)
Tx of Beurgers disease/IgA nepropathy
supportive therapy
prognosis of beurgers disease
20% progress to ESRD in 20 years
prognosis of minimal change disease
1% progress to ESRD
Tx of HSP
Attacks are usually self limiting but if there are relapses and evidence of progressive renal involvement then corticosteroids are inidicated
Tx of goodpastures disease
plasma exchange and corticosteroids +/- cytotoxics
Tx of RPGN
Aggressive immunosuppression (high dose steroid and cyclophosphamide)
Prognosis depends on how early treatment is initiated
Tx of cystitis (empirical)
3 days of Nitrofurantoin (100mg BD) /Trimethoprim
Tx of pyelonephritis
IV tazocin 4.5g TDS
At least 7 days
Tx of asymptomatic UTI in pregnant women
Always treat, for at least 7 days
avoid nitrofurantoin at term due to neonatal haemolysis risk + avoid trimethoprim in first trimester as it is teratogenic
consult local guidelines but generally nitrofurantoin/amoxicillin/cefalexin advised by NICE
Tx of recurrent UTI
Advice on high fluid intake , frequent voiding (specifically after sex), avoidance of spermicidal jellies and avoidance of constipation
If this fails trimethoprim/nitrofurantoin prophylaxis may be started
Tx of hydronephrosis secondary to ureteric obstruction
Nephrostomy
If there is significant enough hydronephrosis
Prevents fluid accumulation and damage
Surgical stenting, depending on cause