Renal and urology Flashcards

1
Q

What is the management of a UTI/ pyelonephritis in children

A

Children under 3 months with a fever- IV antibiotics (ceftriazone)

Oral abx if over 3 months and otherwise well
Trimethoprim, nitrofuratonin, cefalexin, amoxicillin

Any features of sepsis IV abx

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2
Q

When should an USS be carried out if a child has a UTI

When should a DMSA scan be carried out

A

Children under 6 months with 1st UTI/ recurrent UTI/ Atypical bacterial
- USS within 6 weeks

DMSA- 4- 6 months after illness to assess for damage

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3
Q

What are the features of Vesico-ureteric reflux

A

Urine flows from bladder back into ureters
Predisposes to upper urinary tract infections and renal scarring

Diagnosed using a micturating cystourethrogram - Investigates atypical/ recurrent UTIs in under 6 months

Management
Avoid constipation
Avoid excessively full bladder
Prophylactic abx
Surgical input from paediatric urology

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4
Q

What are the features and management of vulvovaginitis in children

A

Inflam/ irritation of vulva and vagina
Ages 3-10

Risk factors
Wet nappies, chemicals and soaps. tight clotting, poor toilet hygiene, constipation, threadworms, pressure on area (horse riding), chlorinated pools

Presentation
Pain itching, erythema around labia, vaginal discharge, constipation
Leukocytes on dipstick but no nitrates

Management
Avoid soaps and perfumes
Good toilet hygiene- front to back wiping
Keep area dry
Sudocream
Loose clothing

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5
Q

What are the features and of nephrotic syndrome in children

A

Protein leakage into urine
Ages 2-5- frothy urine, oedema and pallor

Nephrotic syndrome triad
-Low serum albumin (more in urine)
-High urine protein +++
-Oedema

Will also have
-Deranged lipid profile (Cholesterol, triglycerides and LDLs)
-HTN
-Hypercoagulability- increased clot forming

Most common cause in children
Minimal change disease

Could also be secondary to underlying kidney disease
-Focal segmental glomerulonephritis
-Membranoproliferative glomerulonephritis

Or systemic illness
Henoch Schonlein Purpur
Diabetes or infection

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6
Q

What is minimal change disease

A

Most common cause nephrotic syndrome in children

Oedema, urinary protein, low serum albumin

Treat with oral prednisone

2/3 will reoccur

Urinalysis will show small molecular weight proteins and hyaline casts

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7
Q

What is the management of nephrotic syndrome in children

A

High dose steroids
Given for 4 weeks then weaned over next 8 weeks

If children are steroid resistance can give ACE inhibit or immunosuppressants

Low salt diet
Diuretics for oedema
Albumin infusions
Antibiotic prophylaxis

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8
Q

What are the features of nephritis in children

A

Inflammation of nephrons

Reduced kidney function
Haemoaturia
Proteinuria (less than nephrotic)

Two most common causes
Post strep glomerulonephritis
Berger’s disease (IgA nephropathy)

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9
Q

What are the features of post strep glomerulonephritis

A

1-3 weeks after B-haemolytic strep infection- like tonsillitis from strep progenies

Immune complexes get stuck in kidney glomeruli and cause inflam

This causes an AKI

Diagnosis if evidence of tonsillitis caused by strep- positive that swab and anti-streptolysin antibodies titres

Supportive management
If severe complications of HTN- antihypertensive meds and diuretics

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10
Q

What are the features of IgA nephropathy

A

Berger’s disease
Related to Henoch-Schonlein purpura
IgA vasculitis
IgA deposits in the nephrons cause inflam

Renal biopsy will show IgA deposits and glomerular mesangial proliferation

Teens and young adults

Supportive treatments
Immhnosuppresant meds- steroids and cyclophosphamide to slow disease progression

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11
Q

What are the features of haemolytic uraemic syndrome

A

Thrombosis in small blood vessels
Triggered by Shiga toxin from E.Coli or Shigella

Following gastroenteritis
Use of abx during this can increase it’s risk

Triad of
Microangiopathic haemolytic anaemia (RBCs breaking down in small vessels)
AKI
Thrombocytopenia (Low plts)

Formation of blood clots uses up platelets

Presentation
Fever, abdo pain, lethargy, pallor, reduced urine output, haematuria, HTN, Bruising, jaundice, confusion

Management
Medical emergency
Treat hypovolaemia
HTN
Severe anaemia- transfuse
Severe renal failure- haemdialysis

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12
Q

What are the causes of primary nocturnal enuresis

A

-Most common - variation on normal development (when younger than 5) - perhaps fam history

Other causes
-Overactive bladder
-Fluid intake before bed (fizzy drinks, caffeine)
-Failure to wake
-Psychological distress- pressure in home/ at school
Chronic constipation, UTI, learning disability, cerebral palsy

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13
Q

What is the management of primary nocturnal enuresis

A

2 week diary of fluid intake, toilet and bedwetting

Reassure if under 5 that will likely resolve
Lifestyle changes- reduced fluid intake and pass urine before bed
Encouragement and positive reinforcement
Treat underlying conditions- constipation/ UTI etc
Enuresis alarms

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14
Q

What are the causes of secondary nocturnal enuresis

A

Bed wetting after being dry for at least 6 months
UTI
Constipation
T1DM
Psychosocial issue
Maltreatment (abuse etc)

Treat underlying cause

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15
Q

What are the causes of diurnal enuresis

A

Daytime incontinence

Urge incontinence- overactive bladder gives little warning before emptying
Stress incontinence- leakage of urine during physical exertion, laughing and coughing

Recurrent UTIS
Psychosocial issues
Constipation

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16
Q

What pharmacological treatment can be given for enuresis

A

Desmopressin (ADH)- reduces volume of urine produced by the kidneys - taken at bedtime

Oxybutinin (anticholinergic) - helpful with urge incontinence

Imipramine (tricyclic antidepressant)- relax bladder

17
Q

What are the features of PCKD in children

A

Autosomal recessive PCKD presents in childhood the dominant presents in adulthood

Features on Antenatal USS
-Cystic enlargement of renal collecting ducts
-Oligohydraminos, pulmonary hypoplasia and potter syndrome (lack of amniotic fluid and kidney failure)
-Congential liver fibrosis

Babies born will have resp failure shortly after birth- lungs not developed
May need renal dialysis within 1st few days of life, kidney failure before adulthood

18
Q

What long term problems are associated with PCKD

A

Liver failure (fibrosis)
Portal HTN (oesophageal varices)
Progressive HF
HTN
Chronic lung disease

1/3 will die as neonates

19
Q

What are the features associated with Multicystic dysplastic kidney

A

Seen on antenatal scans
One kidney has multiple cysts and one is fine
Normal life but prone to UTIs, HTN and CKD

20
Q

What are the features of a Wilms tumour

A

Under 5 with abdo mass
Abdo pain, haematuria, lethargy, fever, HTN, weight loss

Diagnosis
USS of abdomen
CT/ MRI to stage
Biopsy for histology

Management
Surgical excision - nephrectomy
Adjuvant chemo or radio

Prognosis - early stage good chance

21
Q

What are the features of a posterior urethral valve

A

Tissue at end or urethra near bladder causes an obstruction to urine
Back pressure on bladder, ureters and kidneys cause hydronephrosis

Difficulty urinating, weak stream, chronic urinary retention, palpable bladder, Recurrent UTIs, impaired kidney function

Investigations
Can be picked up on antenatal scans- oligohydraminos/ hydronephrosis

Abdo USS - enlarged thickened bladder and bilateral hydronephrosis

Micturating cystourethrogram- shows extra urethral tissue and reflux back into bladder

Cystoscopy can ablate or remove tissue

22
Q

What are the features of undescended testes

A

Testes not out of the abdomen after birth- cyrptorchidism
Longer they take to descend less likely this will happen

Risk factors
Fam history
Low BW
Small for gestational age
Prematurity
Maternal smoking

Management
Watch and wait for 3-6 months
If not ny 6 months refer to urologist
Orchidopexy between6- 12 months

23
Q

What are the features of hypospadias

A

Affects boys
Urethral meatus is on the ventral side (underside) of penis

Epispadias- where the meatus is on the top side of penis

Noticed on newborn exam

Management
Mild cases may not need surgery
Surgery at 3-4 months TO CORRECT

24
Q

What are the features of a hydrocele

A

Fluid within the tunica vaginalis surrounding the testes

Simple hydrocele- common in newborn males- fluid trapped in tunica vaginalis

Communicating hydrocele- tunica vaginalis is connected with the peritoneal cavity - fluid can travel to it from peritoneal cavity causing it to grown - size will fluctuate

Examination
Soft, smooth non tender swelling around one testes - swelling infront and below testes

Will transilluminate

Management
USS
Simple hydroceles resolve in 2 yrs - reassure

Communication hydroceles- surgical removal of connection