Nephrology and Genitourinary Flashcards

(38 cards)

1
Q

What causes Henoch-Schonlein purpura?

A

Antigen exposure post URTI causes increased IgA which disrupts IgG synthesis
IgA and IgG react to form complexes which deposit in affected organs

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2
Q

How does HSP present?

A

Urticarial –> purpuric rash over buttocks, arms, legs and ankles

Arthralgia - knees and ankles

Periarticular oedema

Colicky stomach pain

Haematemesis and malaena

Haematuria and proteinuria

Ileus, protein losing enteropathy, orchitis

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3
Q

How is HSP managed?

A

Abdo and testicular USS - obstruction

Barium enema

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4
Q

What are the long term complications of HSP?

A

Proteinuria may result in nephrotic syndrome
RF: oedema, hypertension and deteriorating renal function

Children are followed up for a year to detect persistent anomalies

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5
Q

What is nephrotic syndrome and what causes it?

A

Heavy proteinuria –> low plasma albumin and oedema

HSP
SLE
Malaria
Allergens

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6
Q

What are the presenting features of nephrotic syndrome?

A

Periorbital oedema
Scrotal/vulval, leg and ankle oedema
Ascites
Breathlessness due to pleural effusions and abdo distension

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7
Q

What is steroid sensitive nephrotic syndrome?

A
85-90%
Boys>girls
ASIAN
Oral corticosteroids make urine free of protein
Doesn't progress to renal failure

1/3 resolve
1/3 infrequently relapse
1/3 frequently relapse

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8
Q

What are complications of nephrotic syndrome?

A

Hypovolaemia - intravascular compartment becomes depleted –> abdo pain and fainting

Thrombosis - hypercoaguable state due to urinary loss of antithrombin

Hypercholesterolaemia

Infection

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9
Q

What is steroid resistant nephrotic syndrome?

A

Referral to paediatric nephrologist after 4-8 weeks

Diuretics, salt restriction, ACE inhibitors and NSAIDs

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10
Q

What is congenital nephrotic syndrome?

A

Presents in first 3 months of life
FINNS and INCEST

Hypoalbuminaemia –> mortality
Kidney may need removing

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11
Q

What organisms cause UTIs?

A
E. coli
Klebsiella
Proteus
Pseudomonas (indicates structural abnormalities)
Strep faecalis
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12
Q

What are causes of haematuria?

A
Infection
Trauma
Stones
Tumours
Sickle cell disease
Bleeding disorders
Renal vein thrombosis
Hypercalciuria

Glomerulonephritis
IgA nephropathy
Familial nephritis
Thin basement membrane disease

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13
Q

How does a UTI present in an infant?

A
Fever
Vomiting
Lethargy and irritability
Poor feeding
Jaundice
Septicaemia
Offensive urine
Febrile convulsions
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14
Q

How does a UTI present in a child?

A
Dysuria and frequency
Abdo pain or loin tenderness
Fever +/- rigors
Lethargy and anorexia
Vomiting and diarrhoea
Haematuria
Febrile convulsions
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15
Q

How are urine dipsticks interpreted?

A
Nitrates (N) - produced by bacteria
Leukocyte esterase (LE) - tests for WBC

N+ve LE+ve = UTI

N+ve LE-ve = start Abx and wait for cultures

N-ve LE+ve = start Abx if clinical picture matches

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16
Q

How are atypical and recurrent UTIs investigated?

A

USS during acute infection

DMSA after infection

17
Q

What is vesicoureteric reflux?

A

RED HAIRED GIRLS
Development anomaly of the junction
Ureters are displaced laterally and enter directly into bladder
Severity ranges from mild to intrarenal reflux and renal scarring

18
Q

How does an acute kidney injury present in childhood?

A

Oliguria (less than 0.5ml/kg)

19
Q

What are the most common causes of AKI in childhood?

A

Prerenal

  • hypovolaemia (burns, sepsis, gastroenteritis, haemorrhage, nephrotic syndrome)
  • circulatory failure

Renal (salt and water retention, proteinuria)

  • vascular
  • tubular
  • glomerular
  • interstitial

Post renal
- obstruction

20
Q

How is an AKI managed?

A

Check fluid balance and circulation
USS for masses or renal obstruction

Prerenal - fluid replacement

Renal - restrict fluid intake, diuretic

Post renal - catheter, surgery

21
Q

When is dialysis indicated in AKI?

A
Failure of conservative management
Hyperkalaemia
Severe hypo/hypernatraemia
Pulmonary oedema
Severe acidosis
22
Q

What are the stages of chronic kidney disease?

A
Stage 1: GFR >90
Stage 2: GFR 60-89
Stage 3: GFR 30-59
Stage 4: GFR 12-29
Stage 5 GFR
23
Q

What are the presenting features of CKD?

A
Anorexia/lethargy
Polydipsia and polyuria
Failure to thrive
Bone deformities
Hypertension
\+ acute renal failure
Proteinuria
24
Q

What are the most common causes of acute glomerulonephritis?

A

Follows strep throat/skin infection

Vasculitis (SLE, Wegener’s, HSP)

IgA nephropathy

Anti-glomerular basement membrane disease

25
What happens in glomerulonephritis?
Damaged glomerular cells restricts filtration --> Decreased urine output and volume overload Hypertension --> seizures Oedema Haematuria and proteinuria
26
How is the cause of glomerulonephritis diagnosed?
Post-strep Low C3 Positive ASO and Anti-DNAase B Otherwise renal biopsy and USS
27
What causes haemolytic uraemic syndrome?
Secondary to GI infection with E. coli 0157 Prodrome of bloody diarrhoea Toxins of organism enters GI mucosa and localises to endothelial cells of kidney --> intravascular thrombogenesis
28
What are the abnormalities which define HUS?
Acute renal failure Microangiopathic haemolytic anaemia Thrombocytopenia
29
What are the risks with non-diarrhoea associated HUS?
May be familial and frequently relapses High risk of hypertension Chronic renal failure Mortality
30
What are the common causes of HTN in children?
Renal - renal parenchymal disease - renal artery stenosis - polycystic kidneys - renal tumour Coarctation of the aorta Catecholamine excess - phaechromocytoma (tumour of adrenals) - neuroblastoma Endocrine - CAH - Cushing's or corticosteroid treatment - hyperthyroidism
31
How does HTN present?
``` Vomiting Headaches Facial palsy Hypertensive retinopathy Convulsions Cardiac failure Failure to thrive ```
32
How is pyelonephritis treated?
``` Consider referral to paediatric specialist Oral Abx (co-amoxiclav) for 7-10 days IV Abx (ceftriaxone) for 2-4 days then oral ```
33
How is cystitis treated?
Oral Abx (trimethoprim, nitrofurantoin) for 3 days
34
How does urinary tract anomalies present?
Absence of both kidneys --> severe oligohydramnios Multicystic dysplastic kidney - non functioning kidney Polycystic kidney disease - both kidneys affected but some function is maintained Pelvic or horseshoe shaped kidneys - predisposed to infection/obstructs drainage Duplex system - bifid pelvis -> two ureters Hydronephrosis - dilation and swelling of kidney due to back pressure
35
How does the male urethra develop differently in hypospadias?
Occurs in proximal to distal direction under influence of testosterone Urethral opening lies proximal to normal position
36
How does IgA nephropathy present?
Similar to HSP but restricted to kidney | Macroscopic haematuria after URTI
37
How does neuropathic bladder present?
Urinary incontinence - the need to urinate frequently and with urgency UTI - urine is held in bladder for too long Kidney injury - high pressure caused by urine backlog Kidney stones - pain, haematuria, fever Erectile dysfunction
38
How is vulvo-vaginitis managed?
Hygiene, avoidance of bubble baths and loose fitting underwear Oestrogen cream helps atrophic tissue