CKD Flashcards
(121 cards)
What is the definition of CKD?
Chronic Kidney Disease - abnormal kidney structure or function, present for more than 3 months with implications for health - can also include those with just a reduced GFR of less than 60.
Irreversible.
Which things do we use to categorise CKD?
GFR
Albuminuria
Pathological cause
Describe the classification using GFR
G1 = above 90 G2 = 60-89 G3a = 45-59 (mild) G3b = 30-44 (moderate) G4 = 15-29 (severe) G5 = lower than 15 (failure)
Describe the classification of CKD with albuminuria
This is based on the ACR, and sometimes just use the Cr
A1 = 0-30
A2 = 30-300
A3 = above 300
What are the different types of renal pathology that can cause a CKD?
Glomerular Tubulointerstitial Vascular Cystic/congenital Transplant
What is the prognosis like for CKD?
This varies depending on the GFR and albuminuria.
If low GFR or high albuminuria, this is associated with a higher risk of:
mortality
CVD
ESRD
AKI
A1, G1/2 = low risk
A1, G3a = moderate risk
A1 G3b = high risk
A1 G4 = v high risk
A2 G1/2 = moderate risk
A2 G3a = high risk
A2 G3b = v high risk
A3 G1/2 = high risk
A3 G3-5 = v high risk
What are the most common causes of CKD in the UK?
Diabetes
Glomerulonephritis
Renovascular disease
What do you ask about in PMH to try to determine the cause of CKD?
Previous UTI Previous transplant LRT symptoms HTN DM IHD Renal colic
DRUGS WHAT HAS BEEN RECENTLY STARTED
What do you ask about in the family to see what the risk of CKD is?
Renal disease
SAH
What sort of things cause vascular kidney disease?
Renal vasculitis
HF
TTP
What sorts of things cause glomerular CKD?
Membranous change
DM
Amyloidosis
What can cause tubulointerstitial CKD?
UTI
Pyelonephritis
Stones
Drugs
Toxins
Sarcoidosis
What can cause cystic/congenital CKD?
Renal dysplasia
Alport syndrome
Fabry disease
What can cause transplant CKD?
Recurrence of renal disease
Rejection
Calcineurin toxicity
What do we ask in a systems review for CKD?
Eyes, skin, join problems?
Malignancy signs
What are the symptoms of CKD?
Fluid overload (SOB, PO, HTN) Fatigue Anorexia Nausea/Vomiting Pruritis
Bone pain
Arthralgia
Foamy or cola urine
Retinopathy
What are the risk factors of CKD?
Over 50
PMH of KD
DM
HTN
Male Black/hispanic FH Smoking Obesity Long term analgesic/NSAIDs AI
What peripheral signs indicate CKD?
Vascular disease signs Joint disease Gouty tophi Fistula Bruising (steroids) Encephalopic flap (high urea)
Anaemia Xanthelasma Uraemia (yellow tinge) Jaundice (hepatorenal) Gum hypertrophy (ciclosporin) Cushingoid (steroids) Periorbital oedema (nephrotic syndrome) Taut skin (scleroderma) Facial lipodystrophy (glomerulonephritis)
JVP (overload)
Parathyroidectomy scar
Lymphadenopathy
What signs from a CV exam can suggest potential kidney problems?
High BP
Sternotomy (recent mitral valve)
Cardiomegaly
Peripheral oedema
What signs from a resp exam indicate potential kidney problems?
Pulmonary oedema
Peripheral oedema
Pulmonary effusion
What signs from an abdo exam suggest potential kidney problems?
Ballotable kidneys
Palpable liver
Transplant scars
Catheter
What investigations do we do for CKD?
FBC - ACD Glc - DM Serum Cr - raised MSU - protein/blood/albumin/Bence Jones - Multiple myeloma/uPCR/uACR MCS GFR
ANA, ANCA - AI
Low calcium - kidneys aren’t converting vit D so no Ca absorption
High phosphate - kidneys aren’t excreting
High PTH - stimulated by low Ca - renal osteodystrophy
Renal USS - usually small unless infiltrative disease (amyloid, myeloma), APKD and DM. Asymmetry in congenital and vascular diseases
Consider renal biopsy
What are ANA and ANCA?
Antinuclear antibodies
Anti-Neutrophilic Cytoplasmic Autoantibodies
Present in autoimmune disease
How often do we monitor those with CKD?
GFR and albuminuria:
Annually if low risk
6 monthly if moderate
3 monthly if high
Worry if eDFR drop >25%