Renal/urology Flashcards

(183 cards)

1
Q

What makes up the urinary tract?

A

urethra, bladder, ureters and kidneys

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Whatis acute pyelonephritis?

A

Infection of the kidney

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is cystitis?

A

Inflammation of the bladder

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the characteristic feature of a UTI?

A

Fever

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What should always be excluded in any child presenting with a temperature?

A

UTI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How do babies present with UTI?

A
Fever
Lethargy
Irritability 
Vomiting
Poor feeding
Urinary frequency
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How do older infants and children present with UTI?

A
Fever
Abdominal (suprapubic) pain)
Vomiting
Dysuria
Urinary frequency
Incontinence
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the ideal urine sample?

A

Clean catch

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How does a clean catch sample usually have to be taken in younger children/ babies?

A

Parent sits with them without nappy and urine pot held ready to catch sample

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What things are looked for on a urine sample that would indicate infection?

A

Nitrites

Leukocyte esterase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What does the presence of nitrites in the urine indicate and why?

A

Gram negative bacteria break down nitrates (normal waste product in urine) into nitrites, so suggests presence of bacteria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What does the presence of leukocytes in urine suggest?

A

Rise in WBC in the urine indicate infection or inflammation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is leukocyte esterase?

A

A product of leukocytes that gives an indication about the number of leukocytes in the urine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the best indication of infection in a urine sample?

A

Nitrites

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What urine sample results would trigger treatment of UTI?

A

Leukocytes + Nitrites
Just nitrites
(Not just leukocytes unless there is clinical evidence of UTI)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What should happen to the urine sample if nitrites or leukocytes are present?

A

Should be sent to microbiology lab for culture and sensitivities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

How should all children under 3 months with a fever be managed?

A

Start immediate IV antibiotics (Ceftriaxone) and have full septic screen (+ LP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

How are children over 3 months with UTI managed?

A
Oral antibiotics
(Any features of sepsis/ pyelonephritis= inpatient treatment with IV antibiotics)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What are the usual antibiotics of choice in children with UTI’s?

A

Trimethoprim
Nitrofurantoin
Cefalexin
Amoxicillin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What should be investigated for with recurrent UTI’s?

A

Underlying cause and any renal damage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

When should children presenting with a UTI recieve an USS?

A

All under 6 months with first UTI
Those with recurrent UTI’s
Those with atypical UTI’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What scan should be used 4-6 months after illness to assess for damage from atypical/ recurrent UTI’s?

A

DMSA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What is a DMSA scan?

A

Dimercaptosuccinic acid scan- injecting a radioactive material and using a gamma camera to assess how well the material is taken up in the kidneys.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What does a DMSA scan look for?

A

Scarring in the kidneys as a result of previous infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
What is VUR?
Vesico-ureteric reflux
26
What is vesico-ureteric reflux?
Where urine has a tendency to flow from the bladder back into the ureters
27
What predisposes patients to developing upper UTI's?
VUR
28
How is VUR diagnosed?
Using a micturating cystourethrogram
29
How is vesico-ureteric reflux managed?
Avoid constipation Avoid excessively full bladder Prophylactic antibiotics Surgical input
30
What should be used to investigate atypical/ recurrent UTIs in children under 6 months?
Micturating cystourethrogram (MCUG)
31
What does MCUG involve?
Catheterising the child, injecting contrast into the bladder and taking series of Xrays to determine whether contrast is refluxing into ureters
32
When is MCUG used?
To investigate atypical/ recurrent UTI in children under 6 months In family history of VUR When there is dilation of ureter on USS When there is poor urinary flow
33
What is vulvovaginitis?
Inflammation and irritation of the vulva and vagina
34
What age range is usually affected by vulvovaginitis?
3-10 year old girls
35
What causes the irritation in vulvovaginitis?
Sensitive and thin skin and mucosa around the vulva and vagina
36
What factors exacerbate vulvovaginitis?
``` Wet nappies Use of chemicals/ soaps Tight clothing Poor toilet hygeine Constipation Threadworms Pressure on area (e.g. horseriding) Heavy chlorinated pools ```
37
When does vulvovaginitis usually improve and why?
Much less common after puberty as oestrogen helps keeps skin and vaginal mucosa healthy
38
How does vulvovaginitis present?
``` Soreness Itching Erythema Vaginal discharge Dysuria Constipation ```
39
What may a urine dipstick show with vulvovaginitis?
Leukocytes (but no nitrites)
40
How is vulvovaginitis managed?
``` No medical treatment needed: Avoid soap/ chemicals Good toilet hygiene (front to back) Keep area dry Emolients Loose clothing ```
41
What will patients with vulvovaginitis usually have been treated for prior to diagnosis?
UTI and thrush
42
What is nephrotic syndrome?
When the basement membrane in the glomerulus becomes highly permeable to protein, allowing protein to leak into the urine
43
In what age range is nephrotic syndrome most common?
2-5
44
What is the classic triad seen in nephrotic syndrome?
Low serum albumin High proteinuria Oedema
45
What is the usual urine dipstick result in nephrotic syndrome?
>3+ protein
46
How does nephrotic syndrome present?
Frothy urine Generalised oedema Pallor
47
What are three other characteristic features of nephrotic syndrome?
Deranged lipid profile High blood pressure Hyper-coaguability
48
What is the deranged lipid profile usually seen in nephrotic syndrome?
High levels of cholesterol, triglycerides & LDL's
49
What is the most common cause of nephrotic syndrome in children?
Minimal change disease
50
What are the secondary causes of nephrotic syndrome?
Intrinsic kidney disease (focal segmental glomerulosclerosis, membranoproliferative glomerulonephritis) Systemic illness
51
What systemic illnesses may cause secondary nephrotic syndrome?
Henoch schonlein purpura (HSP) Diabetes Infection
52
What systemic illnesses may cause secondary nephrotic syndrome?
Henoch schonlein purpura (HSP) Diabetes Infection
53
How is minimal change disease diagnosed?
Renal biopsy rules out any abnormalities | Urinalysis shows small molecular weight proteins and hyaline casts
54
How is the treatment of change disease treatment?
High dose corticosteroids
55
What is the prognosis of minimal change disease?
Good- most make a full recovery but it may reoccur
56
What is the general management of nephrotic syndrome?
High dose steroids Low salt diet Diuretics
57
How long are steroids given for in nephrotic syndrome?
high dose given for 4 weeks then gradually weaned over next 8 weeks
58
What percentage of children with nephrotic syndrome will respond to steroids?
80% are steroid sensitive
59
What percent of steroid sensitive patients will relapse and need further steroids?
80%
60
What is given to steroid resistant children with minimal change disease?
ACE inhibitors | Immunosuppressants
61
What are the main complications of nephrotic syndrome?
``` Hypovolaemia Thrombosis Infection Acute/ chronic renal failure Relapse ```
62
Why do you get hypovolaemia in nephrotic syndrome?
Fluid leaks from the intravascular space into the interstitial space causing oedema and low BP
63
Why do you get thrombosis in nephrotic syndrome?
Because proteins that normally prevent clotting are lost in the kidneys, and the liver responds to the low albumin by producing pro-thrombotic protiens
64
Why are you more prone to infection in nephrotic syndrome?
The kidneys leak immunoglobulins, weakening the capacity of the immune system. This is exacerbated by steroid treatment
65
What is nephritis?
Inflammation of the nephrons of the kidneys
66
What does nephritis cause?
Reduction in kidney function Haematuria Proteinuria
67
Do you get more proteinuria in nephtrotic syndrome or nephritic syndrome?
Nephrotic syndrome
68
What are the two most common causes of nephritis in children?
Post-strep glomerulonephritis | IgA nephropathy
69
How long after streptococcus infection does glomerulonephritis usually occur?
1-3 weeks
70
Why does streptococcus infection cause nephritis?
Immune complexes get stuck in the glomeruli of the kidney and cause inflammation, which eventually leads to acute kidney injury
71
What are the immune complexes made of?
Streptococcal antigens Antibodies Complement proteins
72
What is the most common streptococcus infection that leads to glomerulonephritis?
Tonsillitis caused by streptococcus pyogenes
73
How is post-strep glomerulonephritis managed?
Supportive | may need antihypertensives/ diuretics if they develop complications
74
What is IgA nephropathy also known as?
Berger's disease
75
What is Berger's disease related to?
HSP (IgA vasculitis)
76
How does IgA nephropathy cause nephritis?
IgA deposits in the nephrons of the kidney cause inflammation
77
What will renal biopsy show with IgA nephropathy?
IgA deposits and glomerular mesangial proliferation
78
How is IgA nephropathy managed?
Supportive treatment of renal failure | Immunosuppressants to slow progression
79
What is haemolytic uraemic syndrome?
Thrombosis within small blood vessels throughout the body
80
What usually triggers haemolytic uraemic syndrome?
Shiga toxin (bacterial toxin)
81
What is the classic triad seen in haemolytic uraemic syndrome?
Haemolytic anaemia Acute kidney injury Thrombocytopenia
82
What is uremia?
'Urine in the blood'- when the waste products usually excreted by the kidney build up in the blood
83
What bacteria produces the shiga toxin?
E.coli 0157 | Shigella
84
What increases the risk of developing HUS?
The use of antibiotics and anti-motility medications to treat gastroenteritis caused by e.coli/ shigella
85
How long after a bout of gastroenteritis do symptoms of HUS usually begin?
Around 5 days later
86
What are the signs/ symptoms of HUS?
``` Reduced urine output Haematuria/ dark brown urine Abdominal pain Lethargy Irritability Confusion Oedema Hypertension Bruising ```
87
How is HUS managed?
MEDICAL EMERGENCY Self- limiting so supportive management Urgent referral to paediatric renal specialist
88
What is the mortality of HUS?
10%
89
What is enuresis?
Involuntary urination
90
What is the medical term for bed wetting?
Nocturnal enuresis
91
What is diurnal enuresis?
Inability to control bladder function during the day
92
By what age should most children have control of daytime urination?
2
93
By what age should most children have control of nighttime urination?
3-4 years
94
What is primary nocturnal enuresis?
Where the child has never managed to stay consistently dry at night
95
What is the most common cause of primary nocturnal enuresis?
Variation on normal development
96
What is common in a history of primary nocturnal enuresis?
A family history of delayed dry nights
97
What are other causes of primary nocturnal enuresis?
Overactive bladder Fluid intake prior to bedtime Failure to wake (deep sleep/ underdeveloped bladder signals) Psychological distress
98
What are the secondary causes of nocturnal enuresis?
Chronic constipation UTI Learning disability Cerebral palsy
99
What is the initial step in management of primary nocturnal enuresis?
Establish underlying cause- keep 2 week diary of toileting, fluid intake and bedwetting episodes
100
What is the management of primary nocturnal enuresis?
Reassure parents- likely to resolve with no treatment Lifestyle changes Encrouagement and positive reinforcement Treat underlying causes/ exacerbating factors Pharmacological treatment
101
What lifestyle changes are recommended in the management of primary nocturnal enuresis?
Reduce fluid intake in evening Pass urine before bed Easy access to toilet Avoid fizzy drinks, juice and caffeine
102
What is secondary nocturnal enuresis?
Where the child begins wetting the bed when they have been dry for at least 6 months
103
What are the causes of secondary nocturnal enuresis?
``` UTI Constipation T1 diabetes Psychosocial problems Maltreatment ```
104
What are the two types of diurnal enuresis?
Urge incontinence | Stress incontinence
105
What are other causes of diurnal enuresis?
Recurrent UTIs Psychosocial problems Constipation
106
What can be used to help with bed wetting?
An enuresis alarm-device that makes a noise at the first sign of bed wetting to wake the child and stop them from urinating
107
What pharmacological treatment can be used for nocturnal enuresis?
Desmopressin Oxybutinin Imapramine
108
How does desmopressin help in the treatment of nocturnal enuresis?
Analogue of ADH, so reduces the volume of urine produces by the kidneys at night if taken at bedtime
109
How does oxybutinin help in the treatment of nocturnal enuresis?
Anticholinergic that reduces the contractility of the bladder
110
What are the two types of polycystic kidney disease?
Autosomal recessive polycystic kidney disease (ARPKD) and Autosomal dominant polycystic kidney disease (ADPKD)
111
Which type of polycystic kidney disease presents in children?
Autosomal recessive polycystic kidney disease (ARPKD)
112
When does ADPKD present?
In adulthood
113
When does ARPKD present?
In neonates/ on antenatal USS
114
What mutation causes ARPKD?
Mutation in the polycystic kidney and hepatic disease 1 (PKHD1) gene on chromosome 6
115
What does the PKHD1 gene code for and why does this cause PKD?
Codes for fibrocystin/ polyductin protein complex, which is responsible for the creation of tubules and the maintenance of healthy epithelial tissue in the kidneys, liver and pancreas
116
What does ARPKD cause?
``` Cystic enlargement of renal collecting ducts Oligohydramnios Pulmonary hypoplasia Potter syndrome Congenital liver fibrosis ```
117
How does ARPKD usually present in the antenatal period?
With oligohydramnios and polycystic kidneys seen on antenatal scans
118
What is oligohydramnios?
Lack of amniotic fluid caused by reduced urine production by the fetus
119
What does a lack of amniotic fluid lead to?
Potter syndrome | Pulmonary hypoplasia
120
What is Potter syndrome?
Syndrome characterised by dysmorphic features
121
What is pulmonary hypoplasia?
Underdeveloped fetal lungs
122
What does pulmonary hypoplasia lead to shortly after birth?
Respiratory failure
123
Why do neonates with PKD often get respiratory failure shortly after birth?
Pulmonary hypoplasia | Large cystic kidneys may take up so much space in abdomen it becomes hard to breathe adequately
124
What ongoing problems due patients with PKD have throughout life?
Liver failure due to liver fibrosis Portal hypertension--> oesophageal varices Progressive renal failure--> Hypertension Chronic lung disease
125
What is the prognosis of ARPKD?
Poor- most develop end stage renal failure before reaching adulthood 1/3 die in neonatal period 1/3 survive to adulthood
126
What is MCDK?
Multicystic dysplastic kidney
127
What is multicystic dysplastic kidney?
Where one of the baby's kidneys is made up of many cysts while the other kidney is normal
128
How is MCDK diagnosed?
On antenatal USS
129
Does MCDK need intervention?
No- the cystic kidney will usually atrophy and disappear and the single healthy kidney is sufficient
130
What can having a single kidney put you at risk of?
UTI Hypertension CKD
131
What is Wilm's tumour?
Specific type of tumour affecting the kidney
132
What age range is affected by Wilm's tumour?
Children under 5
133
In what patients should a Wilms tumour be considered?
Child under 5 presenting with mass in the abdomen
134
How may Wilms tumour present?
``` Mass in abdomen Abdominal pain Haematuria Lethargy Fever Hypertension Weight loss ```
135
How is a Wilms tumour diagnosed?
USS abdomen CT/ MRI for staging Biopsy= definitive diagnosis
136
How are Wilms tumours treated?
Surgical excision of tumour and affected kidney (nephrectomy)
137
What may also be given with nephrectomy to treat Wilms tumour?
Adjuvant treatment (chemo or radiotherapy)
138
What is the prognosis of Wilms tumour?
Early stage tumoour have up to 90% cure rate | Metastatic disease has poorer prognosis
139
What is a posterior urethral valve?
Congenital disorder where obstructive membranes develop in the proximal end of the urethra, causing obstruction of urine output
140
What patients are affected by posterior urethral valve?
Newborn boys
141
What does a posterior urethral valve cause?
Back pressure into the bladder, ureters and kidneys, causing hydronephrosis
142
What is hydronephrosis?
Swelling of kidneys due to a build up of urine in them
143
What does posterior urethral valve increase the risk of?
UTI's
144
How does a posterior urethral valve present?
``` (May be asymptomatic) Difficulty urinating Weak urinary stream Chronic urinary retention Palpable bladder Recurrent UTI's Impaired kidney function ```
145
What may severe cases of posterior urethral valve in a fetus cause?
Bilateral hydronephrosis and oligohydramnios, leading to pulmonary hypoplasia
146
How may posterior urethral valve be diagnosed antenatally?
On USS scans as oligohydramnios and hydronephrosis
147
How might posterior urethral valve be diagnosed after birth?
Abdominal USS Micturating cystourethrogram Cystoscopy
148
What would USS show in posterior urethral valve?
Enlarged, thickened bladder and bilateral hydronephrosis
149
How can posterior urethral valve be managed?
Temporary urinary catheter while waiting for definitive management Ablation of extra tissue during cystoscopy
150
Where do the testes develop in the fetus?
In the abdomen
151
How do the testes descend into the scrotum?
Migrate through the inguinal canal
152
By when have the testes usually reached the scrotum?
Prior to birth
153
What percentages of boys have testes still in the abdomen at birth?
5%
154
What are undescended testes?
When the testes have not migrated into the scrotum
155
What are undescended testes also known as?
Cryptochidism
156
What may undescended testes cause in older children/ after puberty?
Testicular torsion Infertility Testicular cancer
157
What are the risk factors for undescended testes?
``` Family history Low birth weight Small for GA Prematurity Maternal smoking in pregnancy ```
158
How are undescended testes managed?
Watch an wait
159
After how long will most testes spontaneously descend on their own?
Within first 3-6 months
160
What should happen if testes are not descended by 6 months?
Should be seen by paediatric urologist
161
What is orchidopexy?
Surgical correction of undescended testes
162
When should orchidopexy be carried out?
Between 6-12 months
163
What are retractile testicles?
When the testes move out of the scrotum into the inguinal canal
164
Under what circumstances may the testes retract?
In boys who haven't reached puberty when its: Cold Cremasteric reflex
165
What is hypospadias?
Congenital condition affecting males where the urethral opening is not located at the tip of the penis
166
Where does the urethral meatus tend to be in hypospadias?
Ventral (underside) of penis, towards scrotum. Can be towards the bottom of the glans (head), halfway down or at the base of the shaft
167
What is epispadias?
Where the meatus is displaced to the dorsal side (top) of the penis
168
What is chordee?
Where the head of the penis is bent downwards
169
When is hypospadias usually diagnosed?
On examination of the newborn
170
How is hypospadias managed?
Referall to paediatric urologist: Mild= no treatment moderate= surgery after 3-4 months to correct position of opening and straighten penis
171
What are the complications of hypospadias?
Difficulty directing urination Cosmetic/ psychological concerns Sexual dysfunction
172
What is a hydrocele?
A collection of fluid within the tunica vaginalis surrounding the testes
173
What is the tunica vaginalis?
The pouch of serous membrane that covers the testes
174
What is the tunica vaginalis originally part of during development?
Peritoneal membrane
175
What is a simple hydrocele?
When the fluid is trapped in the tunica vaginalis
176
What usually happens to the fluid in a simple hydrocele?
It gets reabsorbed over time
177
What is a communicating hydrocele?
When the tunica vaginalis around the testicle is connected with the peritoneal cavity via a pathway (processus vaginalis), allowing fluid to travel from the peritoneal cavity into the hydrocele
178
What will be found on examination with a hydrocele?
Soft, smooth, non-tender swelling around one of the testes. | Transilluminate with light
179
What is the difference between simple and communicating hydroceles in terms of their presentation?
Communicating hydroceles will fluctuate in size depending on the volume of fluid from the peritoneal cavity
180
What are the differential diagnoses for a scrotal/ inguinal swelling in a neonate?
``` Hydrocele Partially descended testes Inguinal hernia Testicular torsion Haematoma Tumour ```
181
How is the diagnosis of a hydrocele confirmed?
USS
182
What is the management of a simple hydrocele?
Routine follow up with no treatment- will usually resolve within 2 years
183
What is the management of communicating hydroceles?
Treat with surgery to remove/ ligate the connection (processus vaginalis)