Renal Flashcards

(192 cards)

1
Q

What are the five functions of the kidney?

A
  1. volume management 2. vitamin D physiology 3. EPO production 4. waste excretion and metabolism 5. acid-base balance
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2
Q

what does dialysis manage to do?

A

volume management waste excretion and metabolism acid-base balance

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3
Q

describe the RAAS?

A

insert picture

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4
Q

what is nephrotic syndrome?

A

presence of proteinuria causing hypo albumin and peripheral oedema

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5
Q

what is the most common cause of nephrotic syndrome in children?

A

Minimal change disease

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6
Q

What is the most common cause of nephrotic syndrome in young adults?

A

focal segmental glomerulosclerosis (and minimal change disease)

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7
Q

what is the most common cause of nephrotic syndrome in older adults?

A

Membranous neuropathy and systemic diseases such as diabetes

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8
Q

what are the causes of nephrotic syndrome?

A
minimal change disease 
focal segmental glomerulosclerosis  
membranous nephropathy
 diabetic nephropathy  
amyloidosis/SLE
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9
Q

what is minimal change disease?

A

There is Podocyte effacement causing proteins to leak

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10
Q

what is the management of minimal change disease?

A

corticosteroids if it is then steroid resistance you must do a renal biopsy

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11
Q

what is focal segmental glomerulosclerosis?

A

scar tissue forming on some but not all of the glomeruli can be primary or secondary

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12
Q

what are the causes of secondary focal segmental glomerulosclerosis?

A

HIV obesity reflux nephropathy

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13
Q

what is the management of focal segmental glomerul0 sclerosis?

A

biopsies
- required to differentiate between idiopathic and secondary causes which informs management

corticosteroids

and reducing intra-glomeruli pressure with RAAS blockade (ACEi or ARB)

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14
Q

what is membranous nephropathy?

A

basement membrane thickening with IgG deposition through capillary walls causing a spike and dome appearance on electron imaging

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15
Q

what are the causes of membranous nephropathy?

A

usually idiopathic but can be due to: hepatitis B autoimmune diseases like lupus drug reactions (NSAIDs and penicillinamine)

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16
Q

what is the management of membranous nephropathy?

A

symptomatic relief with diuretics and our AAAS blockade plus reducing risk of clots with blood thinners or anticoagulants if there is a high risk of kidney disease developing in the next five years use of high-dose corticosteroids and immunosuppressants

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17
Q

how do you assess the risk of chronic kidney disease in membranous nephropathy/any disease really?

A

assess proteinuria and blood creatinine the amount which they rise in six months

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18
Q

what is diabetic nephropathy?

A

occurs in both type I and type II diabetes with basement membrane dysfunction and thickening, glomerulosclerosis

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19
Q

how often does diabetic nephropathy cause nephrotic syndrome?

A

rarely does it progress to proteinuria significant to be defined nephrotic syndrome usually classed as microalbuminea

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20
Q

how do you manage diabetic nephropathy?

A

diabetic control ACE inhibitors or/and ARB in serious cases dialysis and transplant may be needed

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21
Q

how does amyloidosis cause nephropathy?

A

Ig light chains from amyloid fibres are deposited within the kidney associated with chronic inflammatory disease (AL or AA chains)

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22
Q

what is the management of amyloidosis/ amyloidosis nephropathy?

A

treat amyloidosis with anti-plasma cell chemotherapy

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23
Q

what questions should you ascertain in a history of nephrotic syndrome?

A

looking at differentials of: diabetes malignancy SLE HIV be drug history connective tissue disorders amyloidosis - insert picture

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24
Q

what investigations should you perform in nephrotic syndrome?

A

urine dipstick spot urine protein to creatinine ratio EGFR FPC lipid profile (+)serum albumin(-) then look for differentials: serum-free light chains and urine electrophoresis (amyloidosis) HIV hepatitis syphilis screen ANA (SLE) renal biopsy if corticosteroid resistant

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25
when are renal biopsy is contraindicated?
Avoided in general if possible but contraindicated in children
26
what is the management of nephrotic syndrome?
Corticosteroids in general - may also need ARB/ACE I diuretics
27
why does nephrotic syndrome lead to thromboembolic disease?
As well as albumin being lost clotting inhibitors are also lost
28
why does nephrotic syndrome caused pleural effusions?
Decrease in argument causes oedema and in the lungs this is a pleural effusion
29
why does an nephrotic syndrome cause hypercholesterolaemia?
there is decreased albumin force to bind to
30
what happens to sodium in nephrotic syndrome?
hyponatraemia due to excess bodily fluids (oedema)
31
what is nephrotic syndrome?
Proteinuria and haematuria
32
what are the common causes of nephritic syndrome?
IgA neophropathy, glomeruli nephritis including post infectious haemolytic uraemic syndrome henloch schonlein purpura, goodpasteures, SLE
33
what is the presentation of nephritic syndrome?
Haematuria oedema less than nephrotic reduced urine output/oliguria hypertension
34
what would urinealysis show for nephritic syndrome?
haematuria +++ proteinuria++ red-cell casts
35
what do red cell casts indicates in nephrotic syndrome?
Form in their frown and indicate the glomerular disease
36
what is IgA nephropathy?
a buildup of IgA in the kidneys
37
how do you manage IgA nephropathy?
ACE I or ARB + low sodium diet and water restrictions
38
How do you diagnose IgA nephropathy?
kidney biopsy and serum IgA (+)
39
what is glomerulonephritis?
An umbrella term encompassing minimal change disease FS GS IgA nephropathy post infectious SLE and vascular to causes
40
what is post-streptococcal glomerular nephritis?
Inflammation of the glomerulus after skin or throat infection
41
how do you diagnose post strap glomeruli nephritis?
skin or throat swab (positive) antibiotics to manage infection fluid and electrolyte balance if severe and very symptomatic diuretics and corticosteroids
42
what is haemolytic uraemic syndrome?
A group of syndromes characterised by low red blood cells and acute kidney failure
43
who does haemolytic uraemic syndrome are most affect?
children
44
What is a presentation of haemolytic uraemic syndrome?
Bloody diarrhoea fever vomiting and weakness progressing to kidney injury
45
what is a common trigger for haemolytic uraemic syndrome?
post infectious of E. coli
46
what is the management of haemolytic uraemic syndrome?
dialysis steroids blood transfusions and plasmapheresis
47
how do you diagnose haemolytic uraemic syndrome?
full blood count and blood smear (haemolytic anaemia and thrombocytopenia) EGFR urea and creatinine stool cultures (positive)
48
what is Henloch schonlen purpura?
a vasculitis IgA with a characteristic triad of 1.maculopapular rash 2. arthralgia 3. abdominal pain
49
what does the image below show?
the maculopapular, urticarial, rashassociated with HSP - insert image
50
what is the rash distribution of HSP?
Extensor surfaces and symmetrical, purpuric but blanching
51
what are consequences of HSP?
Intussusception chronic kidney disease
52
how does HSP cause chronic kidney disease?
There is IgA deposition and ischaemia
53
what is the management of HSP?
corticosteroids and one year follow-up
54
how do you diagnose HSP?
Symptomatic triad evidence of nephritic syndrome biopsy showing IGA deposition
55
when is kidney biopsy indicated in children?
unresponsive to corticosteroids or evidence of kidney decline and high blood pressure
56
how do you investigate nephritic syndrome?
Find underlying cause with urea (+) and creatinine (+) ESR potassium(+) igA (+ in IgA neph) ANA (lupus also complement c3 and 4) , dipstick measure BP
57
how do you manage nephritic syndrome?
supportive therapy: low sodium diet and water restrictions treating underlying cause if more severe add a CEI or ARB diuretics and a very severe renal replacement therapy
58
What is goodpasteures syndrome?
also antibodies to Alpha three chain of IV collagen causing pulmonary renal syndrome
59
why does Godpasteures syndrome cause pulmonary renal syndrome?
IV Collagen is primarily found in the basement membrane of the glomeruli and the alveoli thus its destruction will cause pulmonary renal syndrome
60
what are symptoms of Goospatures syndrome?
reduced urine output spontaneous haemoptysis oedema haematuria and accompanying symptoms of shortness of breath fever and nausea
61
what HLA protein is Goodpastueres associated with?
HLA DRB-1 or DR-4
62
what investigations would be diagnostic for Goodpasteures syndrome?
anti-GBM (+ve) biopsy renal showing IgG deposition chest x-ray showing pulmonary infiltrates
63
what is the management of Goodpasteures syndrome?
immunosuppression with oral corticosteroids and plasmapheresis
64
what is Wagner's granulomatosis?
systemic vasculitis typically involving the small and medium vessels of the lower and upper respiratory tract which also affects the glomerulus (causing glomerulonephritis)
65
what does Wagner's granulomatosis cause nephrotic or syndrome
nephritic
66
what is most important to remember about Px of Wagners granulomatosis?
has both respiratory and renal involvement particularly aware of with patients with nosebleeds , Haemoptysis, sob cough … symptoms of upper respiratory tract or lower respiratory tract disorders with also nephrotic syndrome
67
what is diagnostic for Wagner's granulomatosis?
Positive ANCA and renal biopsy showing segmental cruising glomeruli nephritis with immune complex depositions
68
what is the management of Wagner's granulomatosis?
immunosuppressants (corticosteroids) plasmapheresis
69
what is renal colic?
and acute severe flank pain radiating to the groin
70
what are symptoms of renal calculi?
renal colic nausea and vomiting due to pain urinary frequency/urgency haematuria
71
what are risk factors for renal calculi?
high protein intake high salt intake previous stone dehydration white male obesity
72
what investigation is diagnostic for renal calculi?
None contrast CT ultrasound scan can be performed if pregnant
73
what is an important differential in renal calculi?
ectopic pregnancy in females so do a urine pregnancy test
74
what is the management of a renal calculi where the stone is not visible?
conservative management with analgesia And antiemetics (+NSAIDS)
75
what is the management of a stone less than 10 mm?
medical expulsion therapy with tamsulosin
76
what is the management of a stone greater than 10 mm??
ESWL also do this if there is veiled medical expulsion therapy however if the stone is greater than 50 mm than do percutaneous urteroscopy
77
why is an FB C useful in stones?
Can show evidence of infection which can indicate antibiotics
78
what is cystitis?
Infection of the bladder
79
wall usually causes UTIs?
E. coli
80
what can complicated UTIs be caused by?
Steph aureus P aerginosa or enterococci
81
what are symptoms of pyleo nephritis?
Back/flank pain costo vertebral angle tenderness fever
82
what are the general symptoms of a UTI?
Dysuria frequency haematuria urgency suprapubic pain
83
if a man presents with symptoms of a UTI what should you also investigate?
prostate enlargement so do DRE +/- PSA
84
what antibiotics are used for UTI?
nitrofurantoin or trimethoprim
85
what antibiotics are used for complicated UTI?
Cephalexin or fluoroquinolone in males
86
how does the management of UTI for males stiffer than the management for females which are not pregnant?
Two minutes seven days for males (also for pregnant individuals) in complicated/older men you can prescribe for 14 days
87
What is the most common type of bladder cancer?
Transitional cell carcinoma
88
apart from transitional cell carcinoma what are the other types of bladder cancer?
square miss cell carcinoma Adeno carcinoma
89
what is the public health significance of bladder cancer?
It's the 10th most common cancer in the UK
90
what occupational risk factor is significant in bladder cancer
exposure to dies rather leather textiles and paints – aromatic amines are carcinogenic
91
apart from occupational risks what other risk factors are associated with bladder cancer?
male smoking genetic conditions such as HNPCC schistosomiasis chronic cystitis long-term catheterisation or intermittent self catheterisation
92
what is the presentation of bladder cancer?
chemo Tory – painless (usually visible) urgency recurrent UTI suprapubic pain suprapubic pelvic mass may be felt
93
what investigations are required for anyone presenting with haematuria?
a scan such as ultrasound or CT and cystoscopy of the bladder
94
what is diagnostic for bladder cancer?
Imaging showing mass urine cytology and cystoscopy (you should still perform a full set of bloods)
95
where does bladder cancer usually originate from ?
renal power and climbable cortex
96
describe the stages of bladder cancer?
see image below
97
in what type of cancer is renal cancer?
renal cell carcinoma - adenocarcinoma
98
apart from renal cell carcinoma what other types of real cancer are there?
transitional cell carcinoma
99
what is the commonest type of renal cancer in children?
Wilms tumour A.k.a. Nephroblastoma
100
what is the typical presentation of a Wilms' tumour?
Asymptomatic mass unilateral in the abdomen
101
what are the typical symptoms of renal cancer in adults?
Massive haematuria loin pain hypertension possibly a left-sided variocele NB less than 10% of patients present with the classic triad most cancers are identified incidentally
102
what is paraneoplastic syndrome of renal cancer?
Results from polycythaemia due to the paraneoplastic EPO production (causing erythrocytosis)
103
how is calcium affected in renal cancer?
Hypercalcaemia can occur due to the elevation/production of parathyroid hormone related hormone
104
why does anaemia occur in renal cancer?
Haematuria may cause anaemia, chronic disease can cause anaemia
105
what is rhabdomyolysis?
can be the end result of any disease process which causes damage to the myocyte cell membrane of skeletal muscle causing myocyte-lysis
106
what are some causes of rhabdomyolysis?
physical exertion (inc. seizures or severe agitation) electrolyte disturbances (hypokalaemia hypocalcaemia hypophosphataemia hypo or hyponatraemia) muscle hypoxaemia (even from long immobilisation) metabolic disorders (hyperaldosteronism DKA hypothyroidism) direct muscular damage biological agents (including bacteria or viruses) genetic defects drugs and toxins (statins alcohol diuretics cocaine methadone heroin alkaloids antipsychotics)
107
what is the presentation of rhabdomyolysis?
Usually just presents with muscular pain but can also have dark urine general malaise muscular tenderness
108
how do you diagnose rhabdomyolysis?
serum creatine kinase ++++ / urine disptick shows haematuria in 50%
109
what investigations should you do in a patient with rhabdomyolysis to find out the underlying cause?
TSH – hypothyroidism ESR – inflammatory disease ANA – autoimmune cause swabs+cultures - bacterial and a good history
110
how do you treat rhabdomyolysis?
Managing the underlying cause hydration therapy and then diuretic therapy unless it's being caused by diuretics if anuric or unresponsive to hydration therapy give haemodialysis
111
what is polycystic kidney disease?
An inherited renal cystic disease which can be autosomal dominant (most common) or recessive
112
what is the typical presentation of polycystic kidney disease?
Hypertension abdominal flank pain recurrent UTI with fever
113
what are extra renal features of polycystic kidney disease?
Extra renal cysts intracranial aneurysms and elongated and distended arteries aortic root dilatations and aneurysms mitral valve prolapse and abdominal wall hernias polycystic liver disease
114
what features would you find in a family history of polycystic kidney disease?
History of cerebrovascular events family history of cardiovascular events family history of end-stage renal disease
115
what is the management of polycystic kidney disease?
Hypertension mainly treated with ACEi, managed underlying renal pain with analgesia and bed rest give prompt UTI antibiotics and consider prophylaxis if haematuria is present which is not caused by UTI drink lots of water and surgical intervention may be required / in end-stage renal disease give transplant and dialysis
116
what is a common complication of polycystic kidney disease?
Infected renal cysts treated with ciprofloxacin (if that doesn't work sister drainage if that doesn't work in a fracture)
117
what medication should you not give for the management of pain in polycystic kidney disease and why?
NSAIDs because they are nephrotoxic
118
what is obstructive at uropathy?
Blockage of urinary flow which can occur at any level of the urinary tract affecting one or both kidneys depending on the level of obstruction
119
what other causes of unilateral obstructive uropathy?
Renal stones iatrogenic from surgery commonly obstetric/gynaecology malignancy causing compression
120
what causes of obstructive uropathy?
``` The 4 S's Stones Strictures Swelling (trauma etc) Surrounding structures (cancers BHP and neurogenic) ``` ``` ------------------------------------------------------------------------------- BPH neurogenic bladder renal or ureteric stones bladder tumour urethral stricture prostate cancer ```
121
what is the presentation of obstructive uropathy?
Flank pain fever and UTI symptoms L UTS palpable enlarged bladder from inability to urinate and any symptoms of underlying cause
122
what investigations should you perform in obstructive uropathy?
Renal ultrasound scan CT pyelogram CT abdomen and pelvis
123
what is hydronephrosis?
swelling of the kidney due to urine backup this can cause a KI in progress to CKD
124
define AKI stage I?
serum creatinine: 1.5 – 1.9 x baseline or >/0.3 urine output: <0.5 for 6-12h
125
define AKI stage II?
Serum creatinine: 2 – 2.9 x baseline urine output:< 0.5 for 12h +
126
defining AKI stage III?
serum creatinine: 3 x baseline decreasing EGFR to <35ml in patiemts <18 urine output:<0.3 for >24h or anuria for 12h
127
what are pre-renal causes of AKI?
Anything which causes hypoperfusion – hypovolaemia (from haemorrhage ET C) sepsis over diuresis heart failure hepato-renal syndrome
128
what are renal causes of AKI?
Glomeruli nephritis vascular causes such as HUS blood clots
129
what are post renal causes of AKI?
Anything causing outflow obstruction – BPH tumours strictures stones UTI urinary retention
130
what electrolyte disturbances can in acute kidney injury?
Hyperkalaemia so make sure you do an ECG
131
how do you manage hyperkalaemia?
Ivy glucose and insulin
132
when would you need to refer acute kidney injury to specialist?
Signs of abstraction kidney infection and sepsis hypovolaemia or an urgent complication
133
what complications can occur in acute kidney injury?
Pulmonary oedema hyperkalaemia uraemic encephalopathy pericarditis
134
what is the acute management of acute kidney injury?
Fluid bolus with IV fluids and less as congestive heart failure or pulmonary oedema in which case use loop diuretics
135
how would you go about finding the cause of acute kidney injury?
See image
136
what is chronic kidney disease?
Chronic renal failure causing either haematuria and/or proteinuria or a reduction of EGFR to <60 for 3 months +
137
what is the most common cause of chronic kidney disease?
Diabetes then hypertension
138
apart from diabetes and hypertension what other things can cause chronic kidney disease?
Polycystic kidney disease obstructive uropathy causes of nephrotic and nephrotic syndrome such as focal segmental glomerulosclerosis membranous neuropathy SLE amylodosis rapidly progressive glomerulonephritis
139
what is the pathophysiology of chronic kidney disease?
once renal damage has occurred glomerular hypertrophy occurs in order to maintain GFR this increases the intra-glomeruli pressure and inflammatory processes mean that the glimmer glomerular permeability increases and causes the passage of inflammatory substances to their messenger deal matrix causing scarring fibrosis and more information renal injury also causes angiotensin II production which causes an increase in TGF beta causing collagen synthesis and renal scarring
140
what are symptoms/features of CKD?
fatigue oede,a nausea and vomiting pruiritis anorexia - many symptoms caused by build up of toxins
141
what are the stages of CKD?
insert picture
142
when would urine microalbumin be increased in CKD?
diabetes or HTN
143
what can CKD cause as a complication?
amaemia (decreased EPO) 2ry hyperthyroidism (vD conversion is decreased) acidosis (decreased ammonia and bicarbonate excretion)
144
how do you manage stage 1-2 CKD?
Treat HTN and any compliations ... reduce CVS risks with ACEi or ARB (2ry CCB) and statins - treat anaemia with EPO stimulating agent and /or iron suppliments treat 2ry hyperparathyroidism with calcium acetate +/- ercocaliferol +/- active vitamin D analogue treat metabolic acidosis wuth PO socium bicarb.
145
how do you treat anaemia in CKD?
EPO stimulating agent and /or iron suppliments
146
how do you treat 2ry hyperparathyroidism in CKD?
calcium acetate +/- ercocaliferol +/- active vitamin D analogue
147
how do you treat metabolic acidosis in CKD?
PO biacrbonate
148
what is the presentation of a UTI in an infant?
High fever over 39° irritability poor feeding suprapubic tenderness and abdominal/flank pain may be present
149
what are common features of UTI presentation in older children/teens?
Foul-smelling urine dysuria and frequency (tends to be in order children) as well as suprapubic tenderness and abdominal/funk pain
150
as well as the usual UTI investigations what other investigations should you perform in a ? UTI - in children?
do blood cultures and also Brown neonates/infants younger than 24 months
151
What should you do as follow-up for UTIs in children once treatment has commenced?
Cultures are performed after 24 hours of initiation of treatment
152
what should you do in young males presenting with UTIs?
Check genitourinary structures for abnormalities
153
what is the management of UTI in a patient under six weeks old?
IV antibiotics ampicillin/gentamicin
154
what is the management of a UTI and patient over six weeks old?
PO cefexime if stable - if unstable Ivy ampicillin/gentamicin - in teens management is the same as with adults
155
what is nocturnal enuresis?
In voluntary urination whilst asleep after seven years of age
156
what is the definition of primary nocturnal enuresis?
When the child hasn't had a period of dryness and has never stopped bedwetting
157
what is the definition of secondary nocturnal enuresis?
When a child starts bedwetting after period of dryness
158
how do you diagnose nocturnal enuresis?
Take a voiding diary fluid intake diary check blood pressure check random blood glucose perform bladder ultrasound scan
159
why should you check blood pressure in patients with nocturnal enuresis?
Hypertension indicates renal pathology
160
what are the 3 potential mechanisms for nocturnal enuresis?
High nocturnal urine production high nocturnal bladder function sleep and arousal mechanism dysfunction
161
what is the management of nocturnal enuresis?
Motivational therapy watch and wait bedwetting alarms waterproof mattress and absorbent underwear medical therapy with: amitriptyline or desmopressin
162
what is the most common cause of chronic kidney disease in children?
Congenital and hereditary causes such as structural malformations glomerulonephropathies hereditary nephropathy is such as AD-PKD
163
how do you diagnose current kidney disease in children?
Due to the nature of the causes of childhood CKD it is usually detected on faecal ultrasound otherwise : RFT, urinalysis showing + Al + Cr +/- Haematuria ultrasound/CT
164
what is a presentation of CKD in childhood?
Hypertension anorexia and failure to thrive oedema caused by proteinuria possibly bone deformities and anaemia of chronic disease
165
how do you manage childhood CKD?
encourage growth ACEi + Diuretics for HTN and calcium carbonate to decrease potassium
166
how to stimulate growth in children with CKD?
Enteric feeds and caloric supplements controlling protein intake salt and bicarbonate supplements recombinant hGH
167
what is the presentation of acute kidney injury in children?
anurea (<10ml x 24h) or oliguria (<400ml x 24h)
168
what all causes of acute kidney injury in paediatrics?
Pretty much the same as adult however obstruction tends to be congenital rather than because of thrombosis or stone
169
what is the management of acute kidney injury in paediatrics?
treating the underlying cause - if renal AKI Fluid restriction diuretics sodium control high-calorie diet normal protein feeds
170
when is dialysis indicated for acute kidney injury in paediatrics?
If there is hyperkalaemia hypernatraemia or hypo notary mere or if there is a pulmonary oedema/pulmonary hypertension severe acidosis or multisystem organ failure
171
what can precipitate acute on chronic kidney injury?
Dehydration or infection
172
what are the most common congenital abnormalities (renal) in paediatrics?
pelvic ureteric junction obstruction horseshoe kidney renal Genesis and dysplasia renal cysts polycystic kidneys ectopic kidney
173
describe the pelvic ureteric junction obstruction?
Can be caused by many things but is a narrowing in the yurt as it joins the renal pelvis obstructing flow of urine from the kidney
174
What are the consequences of pelvic ureteric junction obstruction?
Risk of infections stones renal failure hydronephrosis
175
what is a horseshoe kidney?
a fusion anomaly of the kidney joined at the isthmus
176
What are the causes or horseshoe kidney?
Increased risk of kidney stones pyelonephritis from reflux and pelvic ureteric junction obstruction
177
when would you treat a horseshoe kidney?
If obstruction is present causing symptoms
178
what is renal agenesis and dysplasia?
The kidney is either absent or underdeveloped
179
what does renal agenesis cause if it is bilateral?
Oligohydramnios pulmonary hypoplasia extremity and facial anomalies – all part of Potter's syndrome – which is fatal within minutes to hours of birth or leads to miscarriage
180
which type of polycystic kidney disease usually affects children?
Autosomal recessive presents in childhood and is much more severe than autosomal dominant leading to renal failure and can involve liver pancreas leads to hypertension intracranial aneurysms and valve abnormalities
181
what are duplex kidneys?
Duplex kidneys share a single renal unit with more than one collecting symptom they are usually asymptomatic and the patient has normal kidney function
182
what duplex kidney is more at risk of developing?
vesico-ureteric reflux uterocele and an ectopic ureter
183
what is vesico ureteric reflux?
urine does not flow out of the bladder properly and instead goes back up the ureter to the kidneys
184
what are consequences of vesico ureteric reflux?
UTI damage and scarring to the kidney - nephropathy possibly hydronephrosis
185
what is a uterocele?
balloon forms like an aneurysm in the ureter where it connects to the bladder urine collected in the balloon involving a narrowing causing obstruction
186
what is the presentation of vesico ureteric refulx?
recurrent and often UTI infections / can have severe UTI symptoms
187
what investigations should you perform for vesico ureteric reflux?
USS - MAG3 sees dye be taken up by the kidneys through x-ray imaging MCUG bladder is catheterisation filled with special dye patient is asked to pass urine while being scanned this is good for detecting severity of reflux DMS a assesses whether the kidneys have been affected by urinary infections
188
what is the management of vesico ureteric reflux?
if reflexes mild key is with preventing kidney infections with good fluid intake and regular urination as well as avoiding constipation add profylaxis if needed and symptomatic and severe = surgery
189
what is congenital nephrotic syndrome?
An inherited disorder characterised by protein in the urine and causing oedema developing shortly after birth
190
what is a presentation of congenital nephrotic syndrome?
Low birthweight oedema decreased urine output for an appearance of your own poor appetite cough because of pulmonary oedema recurrent UTI malnutrition kidney failure if untreated
191
one investigation should you perform for congenital nephrotic syndrome?
Hypertension amniotic fluid can be tested for increased alpha-fetoprotein
192
what is the management of congenital nephrotic syndrome?
Diuretics ACEi NSAIDS prophylaxis/antibiotics sodium restriction dietary supplements fluid restriction to help control oedema in the end is definitively treated through dialysis and transplant it is typically resistant corticosteroids or other immunosuppressant