Renal Flashcards

1
Q

UTI - definitions

A
  • Bacteriuria – there is bacteria present in the urine which can be symptomatic or asymptomatic.
  • Urinary tract infection – presence of a pure growth of >105 organisms per mL of fresh MSU. UTIs can be classified as lower - urethritis, cystitis and prostatitis or upper – pyelonephritis.
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2
Q

UTI - classification

A
  • Uncomplicated if there is normal urinary tract and function or complicated if there’s abnormal tract or function, voiding difficulty, outflow obstruction or a virulent organism e.g. S aureus.
  • Recurrent is a further infection with a new organism and relapse is with the same organism.
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3
Q

UTI - risk factors

A

Female, sexual intercourse, exposure to spermicide in females (by diaphragm or condoms), pregnancy, menopause, depleted host defences (e.g. immunosuppression or diabetes mellitus) or a urinary tract abnormality (e.g. obstruction, stones, catheter or malformation).

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4
Q

UTI - in pregnancy

A

UTIs are common and often asymptomatic until serious pyelonephritis or premature labour ± fetal death can occur so urine should be routinely tested at all antenatal appointments.

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5
Q

UTI - in catheterised patients

A

Urine is almost always infected so investigations are pointless unless patient is ill.

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6
Q

UTI - organisms

A

Most commonly E coli (>70% in the community but <41% in hospital) but also Staph saprophyticus or Proteus mirabilis.

Rarer causes include Enterococcus faecalis, Klebsiella, Enterobacter and Acinetobacter species, Psuedomonas aureginosa, Serratia marascens or Staphylococcus aureus.

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7
Q

UTI - symptoms

A
  • Acute pyelonephritis – fever, rigors, vomiting, loin pain and tenderness and oliguria (if ARF).
  • Cystitis – frequency, dysuria, urgency, strangury (strong desire), haematuria or suprapubic pain.
  • Prostatitis – flu like symptoms, back ache, few urinary symptoms, swollen or tender prostate.
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8
Q

UTI - signs

A

Fever, abdo or loin tenderness, foul smelling urine, distended bladder or an enlarged prostate.

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9
Q

UTI - urine dipstick

A

If symptoms are present dipstick the urine and treat empirically if nitrites or leucocytes are positive while awaiting sensitivities on an MSU.

If dipstick is negative consider sending for MC+S to confirm this. Send for a lab MSU anyway if male, a child, pregnant, immunosuppressed or unwell.

A pure growth of >105 organisms per mL is diagnostic.

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10
Q

UTI - pyuria

A

If <105 organisms per mL and >20 WBCs/mm3 the result may still be significant. It can be caused by a treated UTI <2 weeks ago, inadequately treated UTI, fastidious culture requirement, appendicitis, tubulointerstitial nephritis, caliculi, prostatitis, PKD or a tumour.

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11
Q

UTI - bloods and imaging

A
  • Bloods – FBC, Us and Es, CRP and blood culture if systemically unwell – known as urosepsis.
  • Ultrasound, IVU or cystoscopy – consider for UTI in children, men, if failure to respond to treatment, recurrent UTI (>2/year), pyelonephritis, unusual organism or persistent haematuria.
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12
Q

UTI - management

A
  • Lower UTI – consider empirical treatment in otherwise healthy women with 200mg Trimethaprim BD or Nitrofurantoin for 3-6 days. If no response perform urine culture.
  • Upper UTI – culture urine and give 1.5g Cefuroxime TDS IV followed by oral for 7 days.
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13
Q

UTI - management in pregnancy

A

Get expert help, any bacteriuria is treated with Nitrofurantoin whether it as symptomatic or not. Urine cultures should be repeated at each antenatal visit.

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14
Q

UTI - management in men

A

Often results from an anatomical or functional abnormality so should be taken seriously and referred to an urologist. Give a 2 week course of Levofloxacin (a quinolone antibiotic) and if no response consider prostatitis and give 4 weeks of treatment.

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15
Q

UTI - prevention

A

Increase water intake, antibiotic prophylaxis (either continuous or post-coital), drinking 200-750mL of cranberry or lingo berry juice per day or taking oral cranberry concentrate tablets.

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16
Q

GN - definition

A

A common cause of end stage renal failure in adults along with diabetes and hypertension.

They are a group of disorders where damage to the glomerular filtrating apparatus causes a leak of protein ± blood into the urine (which depends on the cause).

Patients may be asymptomatic or present with haematuria (microscopic ± red cell casts), proteinuria, renal failure or hypertension.

17
Q

GN - investigations

A
  • Bloods – FBC, Us and Es, LFTs, ESR and CRP, immunoglobulins, electrophoresis, complement levels (C3 and C4), autoantibodies, ANA, ANCA, anti-ds DNA, anti-GBM and blood cultures.
  • Urine – red cell casts, MC+S and Bence-Jones proteins. Can also measure 24 hr urine protein.
  • Further investigations – a chest x-ray, renal ultrasound or renal biopsy may be useful.
18
Q

Nephritic syndrome - definition

A

A group of signs – haematuria (with RBC casts ± dysmorphic RBCs), proteinuria, hypertension and progressive oliguria and renal impairment – caused by disease of the glomerulus.

19
Q

GN - IgA nephropathy

A

Berger’s disease – the most common glomerulonephritis in the developed world and usually presents with macro or microscopic haematuria or occasionally with nephritic syndrome.

  • Typical patient – a young man with episodic macroscopic haematuria occurring a few days after an upper respiratory tract infection e.g. pharyngitis and recovery is often rapid between attacks. There’s increased IgA which forms immune complexes and deposits on mesangial cells.
  • Renal biopsy – mesangial proliferation and immunofluorescence shows deposits of IgA and C3.
  • Management – the role of immunosuppression is uncertain but steroids may decrease proteinuria and slow down decline in renal function. Cyclophosphamide may also be effective.
  • Prognosis – worse if male, hypertension, proteinuria or renal failure at presentation.
20
Q

GN - SLE

A

Approximately 20% of patients with lupus will have evidence of renal involvement. The mechanism can vary between vascular, glomerular or tubulointerstitial damage.

21
Q

GN - anti-GBM disease

A

Goodpasture’s disease – caused by the development of auto-antibodies to type IV collagen as essential component of the glomerular basement membrane. Type IV collagen is also found in the lung and haemoptysis may also be a feature especially in smokers.

Young males are most commonly affected but can occur at any age and gender. Presentation is with macroscopic haematuria, rapidly progressing oliguria and renal failure within days. This can be prevented with rapid early treatment – plasma exchange, corticosteroids and cytotoxics.

22
Q

GN - proliferative GN

A

Classified histologically – focal, diffuse or mesangialcapillary glomerulonephritis. The main cause is post-streptococcal glomerulonephritis occurring 1-12 weeks after a sore throat or skin infection.

A streptococcal antigen is deposited on the glomerulus causing a host reaction and immune complex formation. It usually presents with nephritic syndrome.

Renal biopsy shows an inflammatory reaction affecting mesangial and endothelial cells, immunofluorescence shows IgG and C3 deposits and ASOT (anti-streptolysin O titre) is raised.

Management is supportive and >95% completely recover.

23
Q

GN - Henoch-Schonlein purpura

A

A systemic variant of IgA nephropathy causing a small vessel vasculitis. It causes a purpuric rash on the extensor surfaces, flitting polyarthritis, scrotal and scalp swelling, abdominal pain (due to bleeding) and nephritis.

Diagnosis is usually clinical but can be confirmed with immunofluorescence for IgA and C3 in skin or renal biopsy.

Management is with steroids or cyclophosphamide for resistant cases but up to 50% can develop end stage renal failure.

24
Q

GN - rapidly progressive GN - definition

A

The most aggressive form that can lead to end stage renal failure in days. There are different causes but all have the same biopsy findings – crescents affecting most glomeruli – a proliferation of parietal epithelial cells and macrophages in Bowman’s capsule.

RPGN is classified pathologically into 3 categories:

  • Immune complex disease (45%) – post-infectious, SLE, IgA nephropathy or HSP.
  • Pauci-immune disease (50% of cases) – 80-90% of cases are ANCA positive – Wegener’s granulomatosis (C-ANCA), microscopic polyarteritis (P-ANCA) or Churg-Strauss.
  • Anti-GBM antibody disease (5%) – 10-40% are ANCA positive – Goodpasture’s disease.
25
Q

GN - RPGN - presentation and management

A
  • Clinical presentation – there are signs of renal failure and of the individual systemic diseases e.g. fever, malaise, myalgia, weight loss or haemoptysis. Massive pulmonary haemorrhage is the most common cause of death in patients who are ANCA positive.
  • Management – aggressive immunosuppression with corticosteroids and cyclophosphamide.
  • Prognosis – around 80% will have some improvement in renal function following treatment.