Nephrology Presentations Flashcards

1
Q

Outline the pathophysiology of haematuria

A

Gross = blood that you can see
- 10% chance of finding cancer

Microscopic = blood that can only be seen under the microscope
- 3% chance of finding cancer

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2
Q

Outline the aetiology of haematuria

A

UTI

Pyelonephritis

Bladder/kidney stone

BPH

Prostatitis

Glomerulonephritis – IgA nephropathy

Cancer

Sickle cell anaemia

Kidney injury

Medication = anti-cancer drug cyclophosphamide, penicillin, aspirin, heparin

Strenuous exercise

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3
Q

What are the symptoms of haematuria?

A

Pink/red coloured urine

Passing clots = pain

UTI = persistent urge to urinate, pain and burning with urination, and extremely strong-smelling urine, fever

Pyelonephritis = fever, flank pain

Anaemia = pallor

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4
Q

How is haematuria investigated?

A

Urine dipstick

Urine analysis

Urine culture = suspected infection

Bloods = FBC, U+Es, coag

Imaging = CT, MRI, US

Cystoscopy

Abdo exam = assess for palpable kidneys

Genitalia exam

Kidney biopsy = in cases of: significant haematuria, abnormal renal function, recurrent persistent haematuria, serologic abnormalities, recurrent gross haematuria, FH of end-stage renal disease

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5
Q

How would you manage haematuria?

A

Asymptomatic = generally doesn’t require treatment

Abx = UTI

Medication to shrink prostate

Shock wave therapy to break up stones

Tumour/cancer = surgery

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6
Q

Outline HTN in children

A

HTN = BP above the 95th percentile for height, age, sex

Aetiology = renal parenchymal disease, renal vascular disease, aortic coarctation, endocrine causes, essential HTN, iatrogenic, renal tumours

S+S = vomiting, headache, facial palsy, HTN retinopathy, convulsions, proteinuria

Mx = weight loss, low salt, exercise, avoid smoking/alcohol, ACEi, BB, CCB, thiazide diuretic

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7
Q

What is Acute renal failure, how does it present and what is its DDx?

A

Acute decline in renal function characterized by an increase in blood urea nitrogen (BUN) and serum creatinine values, often accompanied by hyperkalaemia, metabolic acidosis, and HTN

S+S = haemorrhage, fever, rash, abdo pain, pale skin, swelling, abdo mass, oliguria (<0.5ml/kg/h)

DDx =

  • prerenal (most common) = sepsis, D+V, dehydration, DI, diuretics, adrenal insufficiency, shock burns, pancreatitis
  • intrinsic = haemolytic uraemic syndrome (HUS)
  • postrenal = stones, posterior urethral valves

stage 1 = SCr 150-200% baseline, <0.5ml/kg/h >8h
stage 2 = SCr 200-300% baseline, <0.5ml/kg/h >16h
stage 3 = SCr >300% baseline, 0.3ml/kg/h, >24h

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8
Q

What is Chronic renal failure, how does it present and what is its DDx?

A

GFR <15ml/min per 1.73 m2

S+S = poor appetite, bone pain, vomiting, headache, stunted growth, recurrent UTI, tissue swelling, poor muscle tone, anorexia, polydipsia, HTN, normochromic normocytic anaemia

DDx =

  • Prolonged obstruction
  • Alport syndrome = deafness, progressive kidney damage, and eye defects.
  • Nephrotic syndrome = proteinuria, low protein in the blood, high cholesterol levels, oedema
  • Polycystic kidney disease = growth of numerous cysts
  • Cystinosis = amino acid cystine accumulates within lysosomes in the kidney
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9
Q

What is glomerulonephritis, how does it present and what is its DDx?

A

Glomeruli become inflamed and impair the kidney’s ability to filter urine

S+S = HTN, dark brown urine, sore throat, diminished urine output, fatigue, lethargy, increased breathing effort, headache, seizures, rash, weight loss, joint pain, pale, oedema

DDx = strep, Alport syndrome, SLE, polyarteritis nodosa group, Wegener vasculitis

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10
Q

What are the urinary tract abnormalities, how do they present and what is its DDx?

A

Posterior urethral valves, hydronephrosis and hydroureters, severe vesico-ureteric reflux, duplex kidney, ureteropelvic junction obstruction, megaureter, renal agenesis, multicystic dysplastic kidney (MCDK), autosomal recessive/dominant polycystic kidney disease

S+S = recurrent UTI, anatomical abnormality, nonsyndromic

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11
Q

Outline the pathophysiology and aetiology of cystitis (LUTI)

A

Colonization with ascending spread - commonly e.coli

Hematogenous spread

Periurogenital spread

Shorter length of the female urethra allows uropathogens easier access to the bladder

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12
Q

What are the signs and symptoms of cystitis?

A

Parent report = vomiting, fever, lethargy, poor feeding, failure to thrive

Dysuria

Urinary urgency and frequency

Sensation of bladder fullness or lower abdo discomfort

Suprapubic tenderness

Flank pain and costovertebral angle tenderness (present in cystitis but suggest upper UTI)

Bloody, cloudy, offensive smelling urine

Fevers, chills, and malaise (noted in pts with cystitis, more frequently associated with upper UTI)

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13
Q

How is cystitis investigated?

A

Dipstick = leucocytes ++, protein ++, nitrites +

Infant with unexplained temp 38 = urgent urine microscopy + culture (clean catch sample) (10^5 pure growth CFU)/mm3)

USS = <6w old, sepsis, poor urine flow, abdo/bladder mass, raised serum creatinine, no response to Abx in 28h, non-E.coli MO, recurrent (2 UUTI, 1 UUTI 1 lUTI, 3 LUTI)

Dimercaptosuccinic acid (DMSA) 4-6m following acute infection = atypical, recurrent

Micturating cystourethogram (MCUG) (ONLY <6m) = atypical, recurrent

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14
Q

How would you manage cystitis? and how can it be prevented?

A

Lower uncomplicated = 3 day nitrofurantoin

Lower complicated = 5-7 day nitrofurantoin

General = paracetamol, increased fluid intake

PREVENT = hydrated, toilet more often, timed toilet sessions, empty bladder completely, double voiding, front to back wipe, avoid constipation, avoid nylon/synthetic/tight underwear, no bubble baths

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15
Q

Describe the pathophysiology of pyelonephritis

A

Bacterial invasion of the renal parenchyma

Bacteria usually reach the kidney by ascending from the lower urinary tract or the blood stream

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16
Q

What is the aetiology of pyelonephritis?

A

E.coli = 70-95%

Klebsiella spp = 1-2%

Coag-ve staphylococci = 5-10%

17
Q

What are the signs and symptoms of pyelonephritis?

A

Fever

Nausea

Vomiting

Poor feeding

Failure to thrive

Costovertebral angle pain = may be mild, moderate, or severe; flank or costovertebral angle tenderness is most commonly unilateral over the involved kidney, although bilateral discomfort may be present

Gross haematuria

18
Q

Outline how pyelonephritis should be investigated?

A

Dipstick = +ve leukocyte esterase, nitrites

Infant with unexplained temp 38 = urgent urine microscopy + culture (clean catch sample) (>1000 colony-forming units (CFU)/mL)

USS = if atypical, recurrent, or within 6 weeks

Dimercaptosuccinic acid (DMSA) 4-6m following acute infection = atypical, recurrent

Micturating cystourethogram (MCUG) (ONLY <6m) = atypical, recurrent

CT = identify alterations in perfusion, contrast excretion, infection, haemorrhage, masses, obstruction

MRI = detect renal infection, masses, obstruction

19
Q

How should pyelonephritis be managed?

A

IV fluid to maintain hydration

IV Abx =

  • <3m nitrofurantoin
  • > 3m oral cefatexin
  • > 3m IV ceftriaxone

Surgery = renal abscess, renal necrosis

Calculi-related urinary tract infection (UTI) = extracorporeal shockwave lithotripsy (ESWL)

20
Q

Define nephritic syndrome

A

Inflam that can involve any part of the nephron or interstitium

Blood in urine (may have small amount of protein)

Injury to endothelium in capillary loops

In acute renal failure

Hypertensive = normal BP regulation by the kidney is lost

21
Q

What are the common causes of nephritic syndrome?

A

IgA

Anti-GBM disease

Post-infectious

SLE nephritis

Henoch-Schönlein purpura nephritis

22
Q

Define nephrotic syndrome

A

Damaged glomerulus =

  • Generalised oedema
  • Heavy proteinuria (>3g/24h)
  • Hypoalbuminaemia (<25g/L) (usually with hypercholesterolaemia)
23
Q

What are causes of nephrotic disease?

A

Site of injury = podocyte/subepithelial = proteinuria/haematuria

1) minimal change glomerulonephritis
2) focal segmental glomerulosclerosis (FSGS)
3) membranous glomerulonephritis

High protein loss = oedema

24
Q

Give a DDx for a child presenting with oedema

A

Nephrotic syndrome

HF (murmur, breathlessness, cyanosis)

Allergic reaction (rash, wheezing, stridor)

Malnutrition (Kwashiorkor)

Liver failure

25
Q

How should suspected nephrotic syndrome be investigated?

A
  • urine dip
  • urinary protein:creatinine ratio
  • U+Es
  • FBC
  • serum albumin
  • Hep B/C screen
  • C3/4
  • urine MS+C, PCR, analysis
  • serum Ig electrophoresis
  • lipid profile
26
Q

How is nephrotic syndrome be Mx?

A

Oral high dose corticosteroids

Low salt diet (avoid worsening oedema)

Prophylactic Abx (leak Ig)

ACEi/ARBs = reduce proteinuria

Fluid restrict

Loop diuretic = furosemide

Daily weights

27
Q

What are the possible complications of nephrotic syndrome

A

Fluid Mx = intravascularly depleted (shock)

Infection = (loss of Ig) capsulated bacteria, high risk peritonitis

Varicella Zoster (Chicken pox) = VZV immunoglobulin or IV acyclovir

Thrombosis

Spontaneous bacterial peritonitis

28
Q

What is vesicoureteral reflux and its causes

A

Retrograde flow of urine from the bladder into the ureter - ureters displaced laterally and enter bladder directly rather than at an angle

  • Primary = born with defect in valve
  • Secondary = failure of the bladder to empty properly, either due to a blockage or failure of the bladder muscle or damage to the nerves
29
Q

How does vesicoureteral reflux present?

A

Non-specific = failure to thrive, with or without fever; other features include vomiting, diarrhoea, anorexia, and lethargy

Older children may report voiding symptoms or abdominal pain

Pyelonephritis = abdo discomfort, fever

30
Q

How should suspected vesicoureteral reflux be Ix?

A

Urine dip

<2y microscopy (URGENT)

Renal USS

Micturating cystourethrogram (MCUG)

31
Q

Outline the Mx of vesicoureteral reflux

A

Prophylactic Abx - if structural abnormality

Primary = can get better or go away as a child gets older, as a child grows, the entrance of the ureter into the bladder matures and the valve works better

Secondary = surgery, Abx, intermittent urinary catheterization

32
Q

What is enuresis and its causes?

A

Involuntary urination (night time: nocturnal enuresis, daytime: diurnal enuresis)

Most children get control of daytime urination by 2 years and night time urination by 3 – 4 years

Causes =

  • lack of attention to bladder sensation - psychogenic problem
  • neuropathic bladder (enlarges, fails to empty)
  • detrusor instability (overactive bladder)
  • bladder neck weakness
  • fluid intake
  • failure to wake
  • psychological distress
  • sec = chronic constipation, UTI, LD, CP
33
Q

How should enuresis be Ix?

A

2 week diary of toileting, fluid intake and bedwetting episodes

34
Q

Outline how enuresis should be managed?

A

Reassure parents of children under 5 years that it is likely to resolve without any treatment

Lifestyle changes: reduced fluid intake in the evenings, pass urine before bed and ensure easy access to a toilet, avoid fluid irritants

Encouragement, +ve reinforcement. Avoid blame or shame. Punishment should very much be avoided.

Treat any underlying causes or exacerbating factors, such as constipation

Timed urination (every 3h), alarms

Posture = legs wide apart, to relax pelvic floor, must rest legs on something

Double micturition = urinate, top for 30s, continue to urinate

Med: desmopressin, oxybutynin, imipramine

Safeguarding

35
Q

What is Henoch-Schonlein purpura and its causes?

A

Systemic IgA vasculitis which can affect the skin, joints, bowel and kidneys

Often follow infections in the throat, tonsils or bouts of gastroenteritis

Cause = unknown

36
Q

How does Henoch-Schonlein purpura present?

A

3-10y

Fever

Haematuria

Rash = mainly on the backs of the legs, buttocks, trunk and back

Arthralgia

Abdo pain

Proteinuria

Bilateral pedal oedema

Glomerulonephritis

37
Q

How should suspected Henoch-Schonlein purpura be investigated?

A

Urine dip

Bloods = CRP, ESR, WBC, U+Es,

Renal USS

Kidney biopsy = immunoglobulin A(IgA) antibodies present

Skin biopsies = leucocytoclastic vasculitis

38
Q

Outline the management of Henoch-Schonlein purpura

A

Self-resolving

Immunosuppressants may be needed to reduce inflammation