10 Flashcards

1
Q

Are the kidneys intraperitoneal or retroperitoneal organs?

A

Retroperitoneal

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2
Q

Which surface of the kidneys are covered with peritoneum?

A

Anterior surface

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3
Q

Which muscles lie posterior to the kidneys and offer protection?

A

Psoas major

Quadratus lumborum

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4
Q

Where in the abdomen are the kidneys located?

A

Posterior abdomen

Upper L and R quadrants

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5
Q

What does ‘retroperitoneal’ mean?

A

Behind the peritoneum.

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6
Q

Which vertebral levels do the kidneys level with?

A

T12 to L3

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7
Q

Which kidney is often situated slightly lower and why?

A

Right kidney

Due to liver

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8
Q

Where to the adrenal glands sit?

A
  • Immediately superiorly to the kidneys.

- Within the renal fascia.

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9
Q

The kidneys are encased in complex layers of fascia and fat.

How are they arranged from deep to superficial?

A

Renal capsule – Tough fibrous capsule.

Perirenal (or perinephric) fat – Collection of extraperitoneal fat.

Renal (Gerota’s) fascia – Encloses the kidneys and the suprarenal glands.

Pararenal (or paranephric) fat – Mainly located on the posterolateral aspect of the kidney.

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10
Q

Define ‘parenchyma’

A

Functional tissue of an organ.

Distinguished from the connective and supporting tissue.

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11
Q

Which 2 main areas is the renal parenchyma divided into?

A

– Outer cortex
– Inner medulla

The cortex extends into the medulla, dividing it into triangular shapes – these are known as renal pyramids.

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12
Q

What is the apex of the renal pyramid called?

A

Renal papilla

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13
Q

What is each renal papilla associated with?

A

– Minor calyx

– Which collects urine from the pyramids

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14
Q

What merges to form a major calyx?

A

Several minor calyces.

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15
Q

Urine passess through the major calices into what?

A

Renal pelvis

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16
Q

Describe the structure of the renal pelvis.

A

– Flattened

– Funnel-shaped

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17
Q

What is the medial margin of each kidney marked by?

A

A deep fissure (the renal hilum)

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18
Q

Via which structure does renal vessels and ureter enter/exit the kidney?

A

Renal hilum

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19
Q

What does the left kidney lie posterior to?

A
– Adrenal gland
– Spleen
– Stomach
– Pancreas
– L colic flexure
– Jejunum
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20
Q

What does the left kidney lie anterior to?

A

– Diaphragm
– Ribs: 11th, 12th
– Muscles: Psoas major, Quadratus lumborum, Transversus abdominis.
– Nerves: Subcostal, Iliohypogastric, Ilioinguinal.

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21
Q

What does the right kidney lie posterior to?

A

– Suprarenal gland
– Liver
– Duodenum
– R colic flexure

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22
Q

What does the right kidney lie anterior to?

A

– Diaphragm
– 12th rib
– Muscles: Psoas major, Quadratus lumborum, Transversus abdominis.
– Nerves: Subcostal, Iliohypogastric, Ilioinguinal.

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23
Q

Where does the renal arteries originate from?

A
Abdominal aorta
Immediately distal (below) to the origin of the superior mesenteric A.
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24
Q

Where does the abdominal aorta lie relative to the midline?

What significance does this have in the context of the renal arteries?

A

Slightly L of the midline.

Thus, the R renal A. is longer and crosses the vena cava posteriorly.

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25
What happens once the renal arteries enter the kidneys via the renal hilum?
They divide into segmental branches. Then they further divide to supply the renal parenchyma.
26
What does the segmental arteries of the kidneys divide to form?
Interlobar arteries They are situated on either side of every renal pyramid.
27
Describe the divisions that occur to the renal artery when it enters the kidney via the renal hilum.
1. Segmental A. 2. Interlobar A. 3. Arcuate A. At 90 degrees to arcuate arteries, interlobular arteries arise 4. Interlobular A. Interlobular arteries pass through the cortex and divide 1 last time into: 5. Afferent arterioles
28
What does the afferent arterioles form?
A capillary network, the glomerulus, where filtration takes place.
29
What does the capillaries come together to form?
Efferent arterioles.
30
What is the peritubular network?
The is the formation of the efferent arterioles in the outer 2/3 of the cortex.
31
What does the peritubular network supply?
The nephron tubules w/ oxygen and nutrients.
32
What are straight arteries called?
Vasa recta
33
Which arteries supply the inner 1/3 of the cortex and medulla?
Vasa recta
34
Relative to the renal arteries where to the renal veins lie in the renal hilum?
Anteriorly to renal arteries.
35
Where does the renal veins empty into?
IVC
36
Which renal vein is longer and why?
Left because the vena cava lies slightly to the right of the midline.
37
Which lies more anteriorly: renal veins or renal arteries?
Veins
38
Which kidney is higher?
Left kidney (T12-L3)
39
At which vertebral level does the transpyloric plane lie?
L1
40
Where does the transpyloric plane cut the L and R kidneys?
Left - hilum | Right - superior pole
41
Where does lymph from the kidney drain into?
The lateral aortic nodes
42
What is a pelvic kidney?
Embryologically, the kidneys develop in the pelvis, and ascend into the abdomen. Occasionally, one of the kidneys can fail to ascend, and remains in the pelvis, at the level of the common iliac artery.
43
What is a horseshoe kidney?
A horseshoe kidney (a.k.a a cake kidney or fused kidney) is where the 2 developing kidneys fuse into a single horseshoe-shaped structure. This occurs if the kidneys become too close together during their ascent from the pelvis to the abdomen – they become fused and consequently ‘stuck’ underneath the inferior mesenteric artery. This type of kidney is still drained by two ureters, and is usually asymptomatic, although it can be prone to obstruction.
44
What is renal dysgenesis?
Renal dysgenesis is used to describe any underdevelopment of the kidneys. There are 2 main forms: - Renal agenesis – complete failure of one or both kidneys to develop. It is most commonly unilateral. - Renal hypoplasia – the kidneys develop with a normal architecture, but are of a smaller size.
45
Knowing the length of a kidney helps when interpreting any changes in size on radiographs. Approximately how many vertebral levels does a kidney extend over?
3
46
Which structure encloses the kidneys and suprarenal glands?
Renal fascia
47
The renal vessels and ureter enter and exit the kidney via which structure?
Renal hilum
48
Which artery suspends the ascent of a horseshoe kidney?
Inferior mesenteric A.
49
From anterior to posterior, which structures lie in the renal hilum?
- Vein - Artery - Ureter
50
What is renal cell carcinoma strongly correlated with?
Smoking
51
Describe renal cell carcinoma.
- Linked to smoking. - Metastasizes early - Spreads to other areas in body particularly lungs. - Met Lungs appear like a cannon ball. - Poor chemotherapy response. - Is the most common histology of kidney tumours. - RIsk highest in elderly men and w/ smoking history. - Presents w/ abdominal pain, a mass, haematuria - Paraneoplastic effects: EPO (over excreted from kidney), fever
52
What is the renal medulla responsible for?
Generating very high tonicity that allows us to reabsorb water. The medulla splits into many pyramids which all drain into papillae.
53
What is a renal pyramid?
Area where all collecting ducts drain into 1 papilla.
54
What is a papillae?
Where the collecting ducts of a pyramid drain into a minor calyx.
55
How many papillae drain into a minor calyx?
Several
56
How many minor calyces are there?
7-13
57
Where do minor calyces drain into?
Major calyces which there are 2-3 of.
58
Where do major calyces drain into?
Renal pelvis which connects to the ureter
59
Describe the branching of the renal arteries once they enter the kidneys.
- Renal A. (branches at L1) - Segmental A. - Lobar A. - Interlobar A. - Arcuate A. - Interlobular A. - Afferent arteriole - Glomerular capillaries - Efferent arteriole - Peritubular capillaries
60
Which plane does arcuate vessels run in?
The cortico-medullary plane.
61
Where do the ureters leave the kidneys?
Pelvi-uteritary junction
62
Which wall does the ureters run along?
Posterior abdominal wall
63
Do the ureters pass anterior or posterior at the pelvic brim?
Over the pelvic brim. Which is the same point as the bifurcation of the common iliac vessels. Ureters pass anterior to the bifurcation of the common iliac vessels.
64
Which surface do the ureters approach the bladder from?
Posterior surface
65
Which muscle do the ureters follow?
Psoas major
66
In females where do the ureters descend relative to the cervix?
Lateral
67
Where do the ureters narrow?
Pelvi-ureteric junction Pelvic brim Uretero-vesical junction
68
Describe the path of descent of the ureters.
Inferiorly along path of psoas to pelvic brim where: - Pass anterior to bifurcation of . common iliac A. - Anterior to sacro-iliac joint
69
What passes anterior to ureters?
- Gonadal A. - ovarian and testicular arteries | - Colic A.
70
What passes posterior to ureters?
- Vas deferens | - Uterine A.
71
Which arteries supply the ureters?
- Renal A. - Gonadal A. - testicular/ovarian - Superior and inferior vesical A. Abdominal: Renal artery and testicular/ovarian artery. Pelvic: Superior and inferior vesical arteries.
72
Describe the microanatomy of the ureter.
From the lumen (deep) to superficial: - Transitional epithelium - Subepithelial connective tissue - Inner circular smooth muscle - Outer longitudinal muscle - Fibrous tissue
73
Why is transitional epithelium of the ureters functionally relevant?
Can convert from cuboidal epi to squamous epi. - Can allow dilation in the lumen wo/ sig increase in luminal pressure. Whole urinary tract lined by this transitional epithelium.
74
What is the function of the inner circular and outer longitudinal muscles of the ureter?
Allows forward flow of urine (peristalsis) towards the bladder
75
Describe the bladder anatomy.
- Fundus is superior - Apex lies anteriorly - Ureters open on the inferior posterior surface - Between ureteric orifices + urethral orifices form a triangular area (trigone) - Muscles of bladder = detrusor muscle. - Detrusor allows pressure in bladder to rise greater than pressure in the internal urethral sphincter --> promotes urination - Lined by transitional epithelium w/ rugae (for greater urine capacity wo/ generating bladder pressure)
76
What are most bladder malignancies?
Transitional cell carcinomas
77
What is the muscle of the bladder?
Detrusor
78
What is the function of the detrusor?
Allows pressure in bladder to rise greater than pressure in the internal urethral sphincter --> promotes urination.
79
What is the trigone?
Ureteric orifices + urethral orifices forms a triangular area (trigone) - Flat area of mucosa
80
Where is the internal urethral sphincter?
At bladder neck
81
What is the internal urethral sphincter an extension of?
Detrusor
82
What are the 2 types of capillaries in the kidney and what do they supply?
- Peritubular - supplies PCT DCT | - Vasa recta - supplies loop of Henle therefore go into the medulla
83
What are the branches of the renal artery?
Renal artery --> interlobar arteries --> arcuate arteries --> interlobular arteries --> afferent arterioles --> glomerular capillaries --> efferent arterioles
84
What are the 2 types of nephrons?
Cortical nephrons | Juxtamedullary nephrons - go right into medulla
85
What are the 3 components of the glomerulus?
- Epithelium with podocytes - slit pores between them - Negatively charged basement membrane - Capillary endothelium with fenestration
86
Which cells make up the juxtaglomerular apparatus and their functions?
1. Granular cells - produce renin 2. Macula densa cells - detect NaCl 3. Extraglomerular mesangial cells - smooth muscle and thought to be associated with immune system
87
Where are macula densa cells found?
In the walls of the tubule where the thick ascending limb meets the DCT
88
What are the filtration pressures in the kidney and which way are they acting?
1. Hydrostatic pressure of the capillaries - approx 55mmHg (out of capillaries) 2. Hydrostatic pressure of bowman's capsule - approx 15mmHg (into capillaries) 3. Oncotic pressure of the bowman's capsule - 30mmHg (into capillaries)
89
If you constrict the afferent arteriole, what happens to GFR?
It decreases
90
If you dilate the efferent arteriole, what happens to GFR?
It decreases
91
If you dilate the afferent arteriole, what happens to GFR?
It increases
92
If you constrict the efferent arteriole, what happens to GFR?
It increases
93
What occurs in the myogenic mechanism of autoregulation if blood pressure is too high?
Increased stretch in afferent arterioles (which increases NFP and GFR) --> afferent arteriolar vasoconstriction --> decreased glomerular BP --> decreased NFP and decreased GFR The myogenic mechanism is how arteries and arterioles react to an increase or decrease of blood pressure to keep the blood flow within the blood vessel constant. The smooth muscle of the blood vessels reacts to the stretching of the muscle by opening ion channels, which cause the muscle to depolarise leading to muscle contraction. This significantly reduces the volume of blood able to pass through the lumen, which reduces blood flow through the blood vessel. Alternatively when the smooth muscle in the blood vessel relaxes, the ion channels close, resulting in vasodilation of the blood vessel; this increases the rate of flow through the lumen. This system is especially significant in the kidneys, where the GFR is particularly sensitive to changes in blood pressure. However, with the aid of the myogenic mechanism, the glomerular filtration rate remains very insensitive to changes in human blood pressure.
94
What occurs in the tubuloglomerular feedback mechanism of autoregulation, if blood pressure is too high?
Increased GFR = increased blood flow = increased NaCl detection by macula densa cells = they secrete vasoconstrictor = increased arteriolar vasoconstriction = decreased glomerular BP = decreased NFP andGFR In the physiology of the kidney, tubuloglomerular feedback (TGF) is a feedback system inside the kidneys. Within each nephron, information from the renal tubules (a downstream area of the tubular fluid) is signaled to the glomerulus (an upstream area). Tubuloglomerular feedback is one of several mechanisms the kidney uses to regulate glomerular filtration rate (GFR). It involves the concept of purinergic signaling, in which an increased distal tubular sodium chloride concentration causes a basolateral release of adenosine from the macula densa cells. This initiates a cascade of events that ultimately brings GFR to an appropriate level.
95
What are the effects of angiotensin II?
- Aldosterone secretion | - Vasoconstriction
96
Upper urinary tract symptoms
Loin pain - this may radiate to groin and testicles | Haematuria
97
What are cystatin C based equation?
It is a protein secreted by most body cells which is freely filtered. After filtration it is mostly reabsorbed and there is only a small amount excreted in the urine. If the levels are higher in the urine, glomerular filtration has calcined. Independent of weight, height, muscle mass, age + gender.
98
What are the problems with using creatinine clearance to estimate clearance?
- Affected by muscle mass | - Affected by certain drugs e.g. trimethoprim
99
What are obstructive voiding symptoms?
``` Hesitancy Delay in initiating micturition Weak urinary stream Straining to void Incomplete emptying Terminal dribbling ```
100
What are storage symptoms?
``` Nocturia Urgency Incontinence Bladder pain Dysuria ```
101
What would air in the urine suggest?
Vesico-colic fistula
102
Which electrolyte will rise with kidney injury?
Potassium
103
What does specific gravity on a dipstick show?
Whether ADP is acting or not
104
What is an example of a genetic kidney disease?
Autosomal dominant polycystic kidney disease
105
Nephrotic syndrome signs.
- Proteinuria ++++ - Frothy urine - Hypoalbuminaemia - Oedema - around ankles and face - Hyperlipidaemia
106
Where is the main site for EPO production?
Kidneys - so patients with kidney injury may be anaemic
107
What happens to bicarbonate levels in kidney injury?
They fall as kidneys generate new bicarbonate and excrete hydrogen
108
What happens to calcium and phosphate in a kidney injury?
- Decrease in calcium | - Increase in phosphate
109
Nephritic syndrome signs
- Haematuria +++ - Proteinuria ++ - Hypertension - Low urine volume - less than 300ml/day - Oedema may be present but not as severe as nephrotic
110
Hereditary nephritis
- Nephritic - Caused by mutations in genes encoding glomerular basement membrane proteins - Alport syndrome
111
IgA nephropathy
- Nephritic - Abnormality of IgA production and clearance - Deposition of IgA in mesangium
112
Post streptococcal glomerulonephritis
- Nephritic | - Streptococcal antigens trapped in glomerular basement membrane during infection
113
What is nephritic syndrome?
Inflammatory reaction which seriously damages capillary walls, permitting blood to pass into the urine and reduces GFR
114
Describe minimal change disease?
- Glomerulus look normal under a microscope but have diffuse effacement of podocytes under electron microscope - T cell derived - Basement membrane less negative
115
What is focal segmental glomerulonephrosis?
- Sclerosis affecting some, but not all glomeruli (focal) - Involves only segments of affected glomerulus (segmental) - Injury to podocytes initiating events - Deposition of hyaline masses - IgM and complement commonly seen in lesion
116
What is the paracellular route?
Between tight junctions
117
Which side is the apical membrane?
Lumen side
118
Which side the basolateral side?
Capillary side
119
Describe primary active transport.
- On basolateral surface | - Na+/K+ ATPase pumps 3Na+ out of PCT cell and 2K+ into cell to create concentration gradient
120
Describe secondary active transport
- On apical surface - Sodium gradient created by primary active transport - Amino acids and glucose facilitated with sodium
121
How much sodium is reabsorbed in the PCT?n
65%
122
Why do you get glucose in the urine and polyuria with diabetes mellitus?
Transport maximum of glucose is breached so you get glucose in the urine. Urine is an osmotic diuretic so with more glucose in the urine, there is more water.
123
What secretions are there into the proximal tubule?
Organic acids - penicillins, cephalosporins, bile salts, urate etc. Organic cations - creatinine
124
By which route are chloride ions absorbed?
Paracellular
125
What is the thin descending limb and thin ascending limb of the loop of Henle epermeable to?
(Thin) descending - Low permeability to ions and urea, while being highly permeable to water Thin ascending: - Impermeable to water, but it is permeable to ions
126
Which nerve is firing if you are holding in urine?
Pudendal as it is under voluntary control
127
Which receptors would you find on the external sphincter?
Nicotinic - respond to acetylcholine from pudendal nerve - somatic
128
Which receptors would you find on the internal sphincter?
Alpha-1 - respond to NA from hypogastric nerve - sympathetic
129
Which receptors would you find on the bladder?
M3 - respond to acetylcholine from pelvic nerve - parasympathetic --> parasympathetic detrusor contraction. B3 - respond to NA from hypogastric nerve - sympathetic --> relaxation of the detrusor smooth muscle of the urinary bladder and increases bladder capacity The bladder has mainly M1, M2 (80%) and M3 (20%) cholinergic receptor types, but only M3 cholinergic receptors are responsible for the parasympathetic detrusor contraction. α-receptors are located in the trigonum and in the urethra. α1-Receptors are common in men, α2-receptors are common in women. α-Receptors are rare in the detrusor muscle. α1-receptors are classified into three subtypes (A, B and D), in the urinary bladder and urethra α1A-receptors prevail. The adrenergic stimulation of α1A-receptors leads to an increase of bladder closure.
130
Describe the thin ascending loop of Henle.
Impermeable to water Permeable to ions that cross by diffusion
131
Describe the thick ascending loop of Henle.
NaCl actively pumped out | Impermeable to water
132
What is the relationship between time of half life and steady state?
Quicker the half life, the more difficult it is to achieve a steady state
133
What happens to ionised drugs in the kidney?
They stay in the tubule
134
What is the physiology of normal micturition?
A full bladder causes stretching of the detrusor muscle which is detected by the pelvic nerve (sensory, afferent) which increases the rate of firing of nerve impulses to the sacral region of the spinal cord. This then bypasses the thoracolumbar region to go to the pontine micturition centre.
135
What happens to lipid soluble drugs?
They are almost completely reabsorbed
136
What is the steady state of a drug?
Drug is at peak level in system Around 4 doses needed for drug to attain a steady state
137
What do principal cells respond to and secrete?
ADH Aldosterone - secrete K+ The principal cell mediates the collecting duct's influence on sodium and potassium balance via sodium channels and potassium channels located on the cell's apical membrane. Aldosterone determines expression of sodium channels (especially the ENaC). Increases in aldosterone increase expression of luminal sodium channels. Aldosterone also increases the number of Na⁺/K⁺-ATPase pumps. That allow increased sodium reabsorption and potassium secretion. Vasopressin (ADH) determines the expression of aquaporin channels that provide a physical pathway for water to pass through the principal cells. Together, aldosterone and vasopressin let the principal cell control the quantity of water that is reabsorbed.
138
What happens to acidic drugs in alkaline urine?
More readily ionised so are more soluble in water
139
What happens to alkaline drugs in acidic urine?
More readily ionised so are more soluble in water
140
What do intercalated cells secrete?
H+
141
What happens when the pontine micturition centre is activated?
- Inhibition of hypogastric sympathetic nerve = no relaxation of detrusor muscle (B3) therefore contraction occurs - Inhibition of hypogastric sympathetic nerve = no function of internal sphincter (alpha-1) therefore it relaxes - Inhibition of pudendal nerve = relaxation of external sphincter
142
What is classed as a complicated UTI?
Involves: - Children - Catheters - Haematogenous
143
What are the route of infection of a UTI?
- Ascending | - Haematogenous - through bloodstream, through kidneys descending down
144
What is continuous incontinence?
Continuous loss of urine at all times
145
What is functional incontinence?
Incontinence due to cognitive impairment Causes of functional incontinence: confusion, dementia, poor eyesight, impaired mobility or dexterity or unwillingness to use the toilet due to depression or anxiety. Functional incontinence is more common in elderly people as many of the causes are associated with conditions that affect people as they age. For example, a person with Alzheimer's disease may not plan well enough to reach a bathroom in time or may not remember how to get to the bathroom.
146
What are the main causes of voiding difficulties?
- Increased outflow resistance at bladder neck - Urethral stricture - Detrusor muscle failure
147
What is the pathology of BPH?
Hyperplasia of both the lateral and median lobes leading to compression and urethra and therefore bladder obstruction. Within the prostate there are solid nodules of fibromuscular material.
148
What is urge incontinence?
When you have a sudden urge to urinate. In urge incontinence, the bladder contracts when it shouldn't, causing some urine to leak through the sphincter muscles holding the bladder closed.
149
What is stress incontinence?
Involuntary leakage of small amounts of urine due to high abdominal pressure (e.g. coughing, laughing, sneezing etc.)
150
What is overflow incontinence?
Involuntary leakage when the bladder is full
151
What does nosocomial mean?
Disease originating in hospital
152
Who gets UTIs?
- Infants - Early childhood - male and female same rate at this point - Late teens/early 20's female - Elderly men
153
Describe metanephros.
Develops in sacral region of embryo About 5 weeks of gestation Form final adult kidneys Becomes functional in latter part of pregnancy
154
What is the ureteric bud?
Outgrowth of mesonephric duct Eventually dilates and splits to form the renal pelvis, calyces and collecting tubules
155
What feature of E. Coli allows it to survive in the bladder?
Type I fimbriae which bind to mannose residues on host cells Type P fimbriae can bind to kidney cells as well as bladder cells
156
Main cause of community acquired UTI?
E. Coli
157
Describe mesonephros.
Develops in lumbar region of embryo 4th-5th week of gestation Consists of excretory tubules with their own collecting ducts - mesonephric ducts Mesonephric ducts drain into nephritic duct
158
Main cause of hospital acquired UTI?
E. Coli
159
Other than E coli, what are other causes of UTI?
- Mycobacterium tuberculosis - Adenovirus - JC and BK virus - Schistosoma (parasitic flatworm)
160
What are some host defences against UTIs?
- Urine flow - Urine pH, osmolality - Secretory factors such as secretory IgA and lactoferrin - Mucosal defences - Macrophages
161
Bacterial virulence factors of uropathogenic E. Coli.
- Capsule - Resists phagocytosis - K antigen - can induce immune response - Type I fimbriae - cause cystitis bind to mannose residues - Type P fimbriae - can cause pyelonephritis and cystitis
162
Bacterial virulence factors of Proteus species.
- Gr- - Produces urease - Increases urine pH Three species (P. vulgaris, P. mirabilis, and P. penneri) are opportunistic human pathogens. P. mirabilis, once attached to the urinary tract, infects the kidney more commonly than E. coli. P. mirabilis is often found as a free-living organism in soil and water. P mirabilis - associated with formation of magnesium ammonium phosphate (struvite) stones
163
Describe pronephros.
Develops in cervical region embryo 4th week of gestation Non-functional and regresses soon after formation leaving behind the NEPHRITIC DUCT
164
Risk factors for UTI?
- Female - Anatomical abnormality - MS - Spina Bifida - Catheterisation - Pregnancy - Foreign body
165
What are the 3 embryological stages of the kidney?
1. Pronephros 2. Mesonephros 3. Metanephros
166
Where does the metanephros originally rely on their blood supply from?
Branches of aorta | Later on, kidney ascends into lumbar region and its primary blood supply is from renal arteries
167
How might a UTI present in infants?
Poor feeding and failure to thrive
168
Which results on urinalysis suggest UTI?
- +ve leucocyte esterase | - +ve nitrites
169
How can we prevent UTIs in people who need catheters?
- Not catheterising - Limit duration of catheterisation - Aseptic insertion - Closed drainage system - catheter into sealed bag - Ag++ bonded catheters
170
What is urethral syndrome and its possible causes?
Symptoms of lower UTI without bacteria | STI could cause, non-infective inflammation
171
Which bacteria is Nitrofurantoin not effective against?
Proteus
172
Risk factors for UTI in children?
- Poor urine flow - Constipation - Spinal lesion
173
What is a buffer?
When acid or base is added to it, minimises change in pH
174
What does the Guthrie test test for?
PKU
175
What type of carcinoma is penile cancer?
Squamous cell carcinoma
176
What are risk factors for penile cancer?
- Smoking - HPV - Poor hygiene/smegma
177
What type of carcinoma is prostate cancer?
Adenocarcinoma
178
What is the staging for bladder cancer?
- Tis (transitional cell in situ) --> T4 T1 - just in top cells and part of lamina propria. T2 - In muscle layer T3 - through muscle layer to surrounding fat T4 - gone right through and fixed to pelvic side wall
179
What are the types of bladder/ureter/renal pelvis cancer?
- Transitional cell - Squamous cell carcinoma - Adenocarcinoma
180
What is the henderson-hasselbach equation?
pH = pKa + log (HCO3-/H2CO3)
181
How does haemoglobin act as a buffer?
NH3+ - donates H+ ion if there is a lot of base added. COO- - accepts H+ ion if there is a lot of acid added
182
What are the 2 phosphate salts that act as buffers and how?
Sodium dihydrogen phosphate - acid phosphate Disodium dihydrogen phosphate - alkaline phosphate Alkaline phosphate converted to acid phosphate which generates Na+ and binds to H+ in the lumen, generating HCO3- for plasma
183
How is ammonium generated in proximal tubule lumen?
Deamination of glutamine produces NH4+ and HCO3- in the proximal tubular cell
184
When CO2 increases, what happens to pH?
CO2 increases = [H+] increase = DECREASED PH
185
How do the kidneys prevent acidosis?
- Reabsorption of HCO3- | - Excretion of H+
186
What happens to the ammonium in the proximal tubule?
Secreted into the lumen
187
Why does acidosis increase NH4+ excretion?
- Acidosis stimulates the enzymes that deaminate glutamate = increase in ammonium - Increased H+ secretion results in NH3 production, which results in increased NH4+ in the collecting tubules. The conversion of NH3 to NH4+ maintains a gradient for NH3 secretion so excess NH4+ is removed from the medulla
188
What pH is acidaemia?
Less than 7.35
189
What are some causes of respiratory acidosis?
- COPD - Obstruction of airway - Severe asthma - Morphine, barbiturates
190
What pH is alkalemia?
More than 7.45
191
What would the pH, PCO2 and HCO3- be in respiratory alkalosis?
- pH = high - PCO2 = low Kidneys start to excrete HCO3 and retain H+ to lower pH
192
What are the causes of metabolic alkalosis?
- Loss of acid e.g. vomiting and diarrhoea - Ingestion of alkali e.g. antacid - Depleted ECF
193
What is bladder extrophy?
Where the bladder and cloaca haven't fused properly so bladder is open on the abdomen
194
What is the compensatory mechanism involved in respiratory alkalosis?
- As there is too much CO2 being removed, this causes [H+] levels to fall and therefore increase in pH and decreased [HCO3-] - Reduce H+ secretion - Decreased HCO3- reabsorption
195
What would the pH, PCO2 and HCO3- be in metabolic alkalosis?
- pH = high - PCO2 = normal - HCO3- = high
196
What is hypospadias?
Where the urethra opens on underside of penis
197
What would the pH, PCO2 and HCO3- be in metabolic acidosis?
- pH - low - PCO2 - normal - HCO3 - low
198
What are some causes of respiratory alkalosis?
- Hysterical over breathing - High altitude - Fever - Brainstem damage
199
What is the compensatory mechanism involved in metabolic acidosis?
Increased loss of CO2 from lungs which reduces less H+, allowing pH to rise Renal response - stimulates formation of ammonia and excretion of excess hydrogen ions - this mechanism takes a bit longer
200
What are some causes of metabolic acidosis?
- Ingestion of acids - Excess metabolic production of H+ e.g. lactate acidosis or DKA - Loss of HCO3- e.g. severe diarrhoea - Renal disease e.g. failure to excrete H+
201
What would the pH, PCO2 be in respiratory acidosis?
- pH = low - PCO2 = high To compensate kidneys start to retain HCO3- and excrete H+ to raise pH
202
What are the histological changes in BPH?
Stromal-glandular hyperplasia within the prostate - Circulating testosterone will directly affect both epithelial and stromal cells - DHT mainly formed in stream cells which can move out in paracellular way - Interacts with androgen receptors in epithelial and stromal cells
203
What are the compensation mechanisms for metabolic alkalosis?
- Respiratory compensation | - Increase in pH acts on chemoreceptors which reduce ventilatory rate and increase pCO2
204
What is a horseshoe kidney?
Where kidneys are malrotated and closer than they should be
205
What is epispadias?
Where the urethra opens on the dorsum of the penis
206
How does an absent kidney occur?
Absent kidney occurs if the collecting system (from ureteric bud) fails to fuse with the nephrons (from metanephric mesoderm)
207
What is urethral stricture?
Narrowing of the lumen which may be secondary to infection, trauma, extrinsic compression etc.
208
What are the risk factors for bladder/ureter/renal pelvis cancer?
- Smoking - Arylamines - Chronic irritation
209
What are risk factors for urolithiasis?
- Male - Dehydration - Dietary components - Genetic factors
210
What are risk factors for urolithiasis?
- Male - Dehydration - Dietary components - Genetic factors
211
What is the difference between glomerulonephritis and glomerulopathy?
Glomerulonephritis - inflammation is present Glomerulopathy - inflammation is absent
212
WHy does nephrotic syndrome lead to hyperlipidaemia?
Protein like albumin in the blood area leaked out and excreted in urine. Overzealous body (liver) synthesises more lipoproteins, and reduced clearance of lipoprotein bearing lipoproteins.
213
Why does peripheral oedema occur in nephrotic syndrome?
- Overfill hypothesis: Increase salt and water retention - Underfill hypothesis: reduced oncotic pressure in capillaries around the body due to protein loss, therefore fluid leaks out
214
What does -aemia refer to?
in blood
215
What are the primary causes of nephrotic syndrome?
Direct insult to kidneys
216
What are secondary causes of nephrotic syndrome?
Result of another disease process
217
What is minimal change nephropathy?
Minimal Change Disease (MCD for short) is a kidney disease in which large amounts of protein is lost in the urine. It is one of the most common causes of the Nephrotic Syndrome worldwide.
218
What is focal segmental glomerulosclerosis?
Focal segmental glomerulosclerosis (FSGS) is a cause of nephrotic syndrome in children and adolescents, as well as a leading cause of kidney failure in adults.
219
Name 3 diseases nephrotic syndrome causes.
Focal segmental glomerulosclerosis Membranous nephropathy Minimal change disease
220
What is observed in minimal change histology?
normal on light microscopy but on electron microscopy - fusion of foot processes of podocytes
221
What is the epidemiology of minimal change nephropathy?
- Most common in children (but occurs in adults too) - More common in males - Main cause of nephrotic syndrome in children
222
How does minimal change nephropathy present?
facial swelling(normally the first sign) , ascites, scrotal swelling, peripheral oedema
223
What does damage of podocytes trigger?
Apoptosis causes popcytes to detach from glomerular basement membrane + be destroyed. Glomerular basement membrane is exposed. Maladaptive interactions develop between the glomerular basement membrane and the parietal epithelial cells. This is followed by the proliferation of epithelial, endothelial, and mesangial cells. The combination of cell proliferation and leak of protein into Bowman's space results in the deposition of collagen. Ultimately, the capillary loop collapses and endothelial cells are lost.  The glomerular tuft undergoes sclerosis, creating the characteristic lesion of FSGS. The disease eventually progresses to produce global sclerosis and end-stage renal failure.
224
Why does proteinuria + hypoalbuminaemia occur once podocyte die?
Protein leaks across the glomerular membrane, resulting in proteinuria and hypoalbuminaemia. At the same time, cholesterol levels rise due to increased cholesterol synthesis in the liver and the loss of lipid-regulating proteins in urine;.
225
Pathophysiology of minimal change nephropathy.
Unidentified circulating/permeability factors podocyte damage --> podocyte apoptosis Less podocytes --> protein leaks Proliferation of epithelial, endothelial, and mesangial cells --> proliferation and leak of protein into Bowman's space deposition of collagen Damage to capillary endothelial cells --> scarring
226
How are podocytes affected in primary FSGS?
More podocyte effacement, scarring and sclerosis more likely to be primary. - Podocyte effacement is seen in normal and sclerosed glomeruli in primary - Deeper glomeruli affected first
227
What are the problems with primary FSGS?
- Non responsive to steroid therapy - Commonly recurs in transplanted kidneys - Poor renal prognosis Later progresses to global sclerosis CKD ( 50% ESRD within 10 years)
228
What is secondary FSGS due to?
Underlying acquired disease - Reduction in nephron no. e.g. hypertension, ischaemia, nephrectomy, IgA nephropathy - Viruses e.g. HIV, cytomegalovirus, EBV - Drugs e.g.heroin, anabolic steroids, lithium
229
What does reduced nephron no cause?
Greater blood flow in remaining nephrons which leads to glomerular hypertrophy, hyperfiltration
230
What diseases does nephrotic syndrome in children cause?
Minimal change nephropathy Focal segmental glomerulosclerosis
231
What diseases does nephrotic syndrome in adults cause?
Membranous glomerulopathy Focal segmental glomeruloscleoris Diabetic nephropathy SLE Amyloidosis
232
What is Amyloidosis?
It's a rare disease that occurs when a substance called amyloid builds up in your organs. Amyloid is an abnormal protein that is produced in bone marrow and can be deposited in any tissue or organ.
233
How does membranous glomerulopathy present?
Asymptomatic proteinuria or nephrotic syndrome (+/- haematuria, HTN, renal impairment)
234
What is membranous glomerulopathy secondary to?
Underlying pathology or toxic insult
235
What is sarcoidosis?
Sarcoidosis is a disease involving abnormal collections of inflammatory cells that form lumps known as granulomas. The disease usually begins in the lungs, skin, or lymph nodes. Less commonly affected are the eyes, liver, heart, and brain. Any organ, however, can be affected.
236
What is SLE?
Systemic lupus erythematosus (SLE), also known simply as lupus, is an autoimmune disease in which the body's immune system mistakenly attacks healthy tissue in many parts of the body. Symptoms vary between people and may be mild to severe.
237
HTN + renal impairment --> ?
Poor prognosis signs
238
What is diabetic nephropathy?
Microvascular complication of diabetes and elevated sugars
239
What are risk factors for diabetic nephropathy?
- Poor sugar control - HTN (more insult to kidneys) - Male - Ethnicity (Southeast Asian) - Social deprivation
240
Describe the pathology of diabetic nephropathy.
IgA-containing immune complexes that are prone to mesangial deposition. In susceptible people, the deposited IgA triggers variable degrees of glomerular inflammation and subsequent glomerular and tubulointerstitial scarring. 
241
What is the pathophysiology of diabetes mellitus?
- Both metabolic alterations (hyperglycaemia and possibly hyperlipidaemia) and haemodynamic alterations (systemic and glomerular hypertension) at this level all you need to know - Inflammation, endothelial dysfunction, and oxidative stress are intertwined in a vicious cycle that leads to significant kidney damage and cardiovascular events.  - Ultimately GFR is altered and decreases…which can ultimately lead to Chronic Kidney Disease
242
What is diabetes mellitus characterised by?
High glucose levels and increased glomerular pressure, both of which can cause glomerular mesangium expansion via increased mesangial stretch.
243
What is nephritic syndrome.
Immunological disorder causing thickening of basement membrane HTN, mild oedema, oliguria, dark urine, azotemia, high JVP
244
What are the signs of nephtitic syndrome?
- Hypertension (due to low GFR and increased Renin) - Often some proteinuria - Often oliguria - Oedema may be present (periorbital, sacral, leg) - Acute kidney injury
245
What does nephritic syndrome cause in children?
Haemolytic uraemic syndrome Henoch-schonlein purpura (IgA vasculitis) Post-streptococcal GN
246
What is haemolytic uraemic syndrome?
Damage to endothelium of glomerular capillary bed. Nephritic syndrome Hemolytic-uremic syndrome (HUS) is a disease characterized by a triad of hemolytic anemia (anemia caused by destruction of red blood cells), acute kidney failure (uremia), and a low platelet count (thrombocytopenia).
247
How does haemolytic uraemic syndrome present?
Haemolytic anaemia Acute kidney failure (uraemia) Thrombocytopenia (Thrombocyte – platelets, penia --> deficiency (in blood in this case)
248
List 2 causes for haemolytic uraemic syndrome.
Infectious agents e.g. streptococcus --> No diarrhoea Toxigenic agent E.coli 0157.H7 --> Diarrhoea is present.
249
What is henoch schonlein purpura?
NEPHRITIC Most common vasculitis of children (affects adults too) Skin lesions are characterised as palpable purpura and are typically non-blanching. The lesions are usually 2 to 10 mm in diameter, and represent the extravasation of blood into the skin. Usually occur in crops and fade over several days. Can occur anywhere, but are usually concentrated on the lower extremities. The rash occurs in all patients.
250
What are the classic signs of henoch schonlein purpura (HSP)
- Rash (purpura) --> occurs in all patients - Abdominal pain - Arthritis/arthralgia - Glomerulonephritis --> haematuria - HSP can follow a URTI
251
What is post streptococcal glomerulonephritis?
Acute glomerulonephritis following streptococcal infection is characterized by the sudden appearance of hematuria, proteinuria, red blood cell casts in the urine, oedema, and hypertension with or without oliguria. Occurs 1-3 weeks after streptococcal infection, e.g. - Strep throat - Otitis media - Cellulitis
252
Why is there haematuria of post streptococcal glomerulonephritis?
B haemolytic streptococcus Leads to inflammation of glomerulus But no necrosis
253
What are the causes of nephritic syndrome in adults?
Goodpasture's ANCA-associated vwasculitis SLE Primary or secondary mesangiocapillary GN
254
What is goodpasture syndrome (GPS)?
NEPHRITIC A rare autoimmune disease in which antibodies attack the basement membrane in lungs and kidneys, leading to bleeding from the lungs and kidney failure. It is thought to attack the alpha-3 subunit of type IV collagen, which has therefore been referred to as Goodpasture's antigen.
255
What does ANCA stand for?
Anti-neutrophil cytoplasmic antibodies (ANCAs) - They are a group of autoantibodies mainly of the IgG type, against antigens in the cytoplasm of neutrophil granulocytes (the most common type of white blood cell) and monocytes.
256
Why is Goodpasture syndrome also known as anti-GBM glomerulonephritis.
Anti-GBM (anti-glomerular basement membrane antibodies attacks basement membrane) 2/3 good pastures (lung haemorrhage, due Ab attack on lung vasculature) 1/3 purely renal Patients: >50, affect men + women equally
257
What does acute kidney injury lead to?
Acute decline in the GFR from baseline, with or without oliguria/anuria.
258
Which markers are used to diagnose acute kidney injury?
Creatinine in blood Urine output - Keypoint - AKI is potentially reversible
259
What are the pre-renal causes of acute kidney injury?
- Reduced renal perfusion: Hypovolemia, shock, low cardiac output (heart failure), haemorrhage - Renal artery stenosis
260
What are the renal causes of acute kidney injury?
Tubular: - Acute tubular necrosis - Nephrotoxic drugs - NSAIDS, ACEi, gentamicin Glomerular: - Rapidly progressive glomerulonephritis - Autoimmune - Drugs - Interstitial nephritis Vascular: - Vasculitis - Thrombus - Malignant BP (very high BP)
261
What are the post renal causes of acute kidney injury?
- Mechanical obstruction of the urinary outflow tract. e.g. lymphoma, tumour, prostate hyperplasia, strictures, renal calculi - Ascending urinary infection (including pyelonephritis), and urinary retention
262
What are some important complications for AKI?
Hyperkalaemia - ensure U + E's + ECG are done Uraemia - less urea being filtered into the urine - risk of encephalopathy pericarditis
263
Define chronic kidney disease.
It's a condition characterised by a gradual loss of kidney function over time.
264
Why does intra-glomerular pressure increase in response to injury?
The kidney attepmpts to adapt to nephron loss to maintain constant glomerular filtration.
265
In CKD what can an increase in glomerular permeability to macro-molcules lead to?
An increase in glomerular permeability to macromolecules may result in toxicity to the mesangial matrix, causing mesangial cell expansion, inflammation, fibrosis glomerular scarring.
266
Give examples of macromolecules that the glomerulus may become more permeable to in CKD?
Transforming growth factor-beta (TGF-beta) Fatty acids Pro-inflammatory markers of oxidant stress Protein
267
How is angiotensin II affected in renal injury?
Increases production, causing an upregulation of TGF-beta, contributing to collagen synthesis + renal scarring within the glomerulus
268
List 3 clinical indicators of CKD?
Microalbuminuria: 30 to 300 mg/g creatinine/day Proteinuria: >300 mg proteinuria/day Haematuria: >3 RBCs per high power field on more than 2 occasions
269
Risk factors for CKD.
- Age >50 years - Male sex - Black or Hispanic ethnicity - Family history - Smoking - Obesity - Long-term analgesic use - Diabetes mellitus - HTN - Autoimmune disorders, genetic disorders e.g. polycystic kidneys
270
What is pruritus?
Itch
271
What is uraemia?
A raised level in the blood of urea and other nitrogenous waste compounds that are normally eliminated by the kidneys
272
What is uremic pericarditis?
It causes fibrinous pericarditis + that is an exudative inflammation. The pericardium is infiltrated by the fibrinous exudate. This consists of fibrin strands and leukocytes.
273
What's the problem with hyperkalaemia?
Can lead to arrhythmia Due to less filtration --> poor excretion of potassium
274
What is metabolic acidosis?
Increase in hydrogen loss in blood. Total ammonium excretion begins to fall when the GFR is below 40 - 50 mL/min
275
Why is metabolic acidosis commonly associated w/ CKD?
As the no. of functioning nephrons declines in CKD, acid excretion is initially maintained by an increase in the ammonium excreted per nephron. Total ammonium excretion begins to fall when the GFR is below 40 to 50 mL.min.
276
How is CKD managed?
Main aim = slow progression by managing symptoms + dealing w/ cause. Options: - Dialysis - Kidney transplant
277
What is of acute CKD?
Sudden decline in renal function in patients w/ known chronic kidney disease.
278
What causes CKD?
Causes: pre-renal, renal, post-renal - systemic infection - drugs - dehydration --> hypovolemia - obstruction
279
What opens into the cloaca?
Allantois - ventrally | Hindgut - dorsally
280
Which ducts are connected to the posterior wall of the cloaca?
Mesonephric + paramesonephric
281
What is the cloaca?
A common cavity at the end of the digestive tract for the release of both excretory and genital products in vertebrates (except most mammals) and certain invertebrates.
282
What is the pronephros?
Pronephros is the earliest nephric stage in humans, and constitutes the mature kidney in most primitive vertebrates.
283
Which somites does the pronephros extend from and to?
It extends from the 4th to the 14th somites
284
How many pairs of tubules does the pronephros consist of?
6-10 pairs of tubules
285
Why is the pronephros known as a vestigial structure?
It disappears completely by the 4th week of human embryonic life.
286
How does the mesonephros develop?
By the formation of mesonephric tubules from the intermediate mesoderm It is the principal excretory organ during early embryonic life (4—8 weeks).
287
What is the principal excretory organ during 4-8 weeks of embryonic life?
Mesonephros
288
Although the mesoopherhos gradullary degenerates, pars of its duct system becomes associated with what?
Male reproductive organs
289
From what embryonic tissue is the kidney derived?
Intermediate mesoderm, which then forms the pronephros, mesonephros, metanephros.
290
By what process do the ureteric buds give rise to the collecting tubules?
The ureteric buds form from the lower end of the mesonephric duct, and then reaches and penetrates the metanephric blastemal, which forms a cap over the bud. The bud then enlarges and forms the beginning of the renal pelvis. The stalk becomes the ureter whilst the renal pelvis divides into the major and minor calyces, with the minor calyces forming the collecting tubules
291
How do the kidneys come to reach their adult position?
The definitive adult kidneys (metanephros) develop inferiorly in the pelvic region. During embryonic development they “ascend” such that the adult kidneys come to lie in the lumbar region.
292
What is the metanephros aka?
Adult kidney
293
Where does the metanephros develop?
Pelvic region Then ascend during embryonic development to lumbar region
294
How does this the ascending of the metanephros occasionally lead to the formation of accessory renal arteries?
As the kidneys ascend they do not keep their original blood supply (as is the case with the gonads), instead they form new superiorly positioned blood vessels connecting to the common iliac vessels and then the aorta and inferior vena cava. As these new renal vessels form the older inferiorly positioned vessels typically regress, however sometimes these vessels do not regress, resulting in accessory renal vessels.
295
From what embryonic tissue is the bladder formed?
The bladder forms primarily from the endodermally derived urogenital sinus (formed from the partitioning of the cloaca of the hindgut), and also a contribution from the mesonephric ducts which are derived from (intermediate) mesoderm. The mesonephric contribution forms the trigone of the bladder.
296
How is the trigone of the bladder formed?
Although the trigone is generally accepted to derive from the mesonephric ducts, the manner in which this is accomplished is not completely understood, The trigone may form primarily through vitamin A-mediated apoptosis of the common nephric duct rather than from true incorporation of the inferior portions of the mesonephric ducts with the bladder. An endodermal origin of the trigone has also been postulated.
297
List 5 anomalies of ureters.
``` Retrocaval /retroiliac ureter Anomalies of ureteral diameter Abnormal number of ureters Partial doubling Complete doubling ```
298
Explain partial doubling
Incomplete division of 2 ureters that fuse at different levels. In each case a common section exists with a normal ureteral orifice. A Uretero-ureteral reflux tends to occur at the Y branch.
299
Explain complete doubling
Here a complete doubling of the ureters, and renal pelvis occurs. The ureters empty into the bladder in accordance with Weigart and Meyer’s law. The calyx system of the upper renal pelvis is as not as well differentiated as that of the lower one. This is often asymptomatic, unless there are complications due to the calyx system abnormalities.
300
Explain how there can be an abnormal number of ureters.
These are the most frequent anomalies of the urinary tract, and many are asymptomatic. They arise from a premature branching of the ureter anlage, leading to a partial second ureter, or from an additional ureter anlage, when two complete ureters are generated.
301
Explain how there can be anomalies of ureteral diameter.
Primary megaloureter due to an obstruction: - The cause of constriction of the terminal part of the ureter, leading to dilatation. - The constriction can be anatomic, or purely functional. - Above the constriction the ureter is dilated, bulging and the wall thickened. - The primary megaloureter should be distinguished from the secondary due to a valve or a vesico-ureteral reflux.
302
Explain what retrocaval and retroiliac ureters are.
R ureter traces out an “S” at the L4 level behind the vena cava. A developmental disorder of the vena cava is responsible. In a similar manner the ureter can run behind the common iliac artery at the L5 level.
303
What is the most frequent type of anomalies of the urinary tract?
Abnormal no. of ureters.
304
What is congenital polycystic kidney (CPK)?
Polycystic kidney disease (PKD) is an incurable genetic disorder characterised by the formation of fluid-filled cysts on the kidney that multiply over time. The kidney damage seen in PKD is thought to be the result of the body's immune system, destroying the healthy tissue in its attempts to rid the kidney of the cysts.
305
What is infantile PKD caused by?
A non-sex linked (autosomal) recessive genetic mutation mapped to the short arm of chromosome 6 (6p21). Both parents must be carriers of the mutation for their children to be affected with infantile PKD, with a probability of 25% that their child will be affected by infantile PKD.
306
Describe the phenotype of babies born with infantile PKD?
Floppy, low-set ears A pointed nose Small chin Folds of skin surrounding the eyes (epicanthal folds). Large, rigid masses can be felt on the back of both thighs (flanks), and the baby usually has trouble breathing.
307
How common is renal agenesis?
Unilateral renal agenesis (URA), 1:450-1:1000 newborns, describes the absence of one kidney whilst with bilateral renal agenesis (BRA), 1 in 3,000 babies, the baby is missing both kidneys.
308
What is renal agenesis?
Renal agenesis is a condition in which a baby is missing one or both kidneys at birth.
309
How may bilateral agenesis be manifest in utero?
BRA babies have distinct features, widely separated eyes, ears set too low, a flat broad nose, receding chin, and limb defects.
310
How does a horseshoe kidney form?
Horseshoe kidney is a renal fusion anomaly
311
Where is a horseshoe kidney found?
By the inferior mesenteric artery The normal ascent of the kidney is impaired because the artery hooks over the isthmus
312
How is a horseshoe kidney connected?
90% by an isthmus of functioning renal parenchyma or fibrous tissue between the lower poles. 10% superior or both superior + inferior poles are fused.
313
What is a sigmoid kidney?
When either superior or both the superior and inferior poles of the kidney are fused
314
What is patent urachus?
Failure f the entire course of the urachus to close resulting in an open channel between the bladder and umbilicus. It's normally diagnosed when neonates leak urine from umbilicus.
315
What is exstrophy?
Means 'turned inside out' Bladder exstrophy is a congenital abnormality of the bladder
316
When does bladder exstrophy occur?
It occurs if lower abdominal wall does not form properly, resulting in a bladder which is open anteriorly and exposed on the anterior abdominal wall.
317
Pain from upper ureteral stones radiate where?
To flank + lumbar areas.
318
Stones obstructing the ureteropelvic junction present with what type of pain?
mild-to-severe deep flank pain without radiation to the groin.
319
On the right side (flank + lumbar areas), what can pain from upper ureteral stones be confused with?
Cholecystitis or cholelithiasis
320
What is cholecystitis?
Inflammation of the gallbladder.
321
What is cholelithiasis?
Gallstones Which are concretions that form in the biliary tract, usually in the gallbladder
322
On the left side (flank + lumbar areas), what can pain from upper ureteral stones be confused with?
Acute pancreatitis Peptic ulcer disease Gastritis
323
What is gastritis?
Inflammation of the lining of the stomach. It may occur as a short episode or may be of a long duration. There may be no symptoms but, when symptoms are present, the most common is upper abdominal pain. Other possible symptoms include nausea and vomiting, bloating, loss of appetite and heartburn.
324
Where does miduretheral calculi pain radiate? What can this pain mimic?
Midureteral calculi cause pain that radiates anteriorly and caudally. This pain can mimic appendicitis on the right or acute diverticulitis on the left.
325
Distal uretral stones cause pain that radiates where?
Into the groin / testicle (male) or labia majora (female) because the pain is referred from the ilioinguinal or genitofemoral nerves.
326
Which stones are rare?
Urate stones - they are radiolucent whereas most renal stones are radio-opaque.
327
What are renal stones commonly composed of?
Calcium oxalate | 80%
328
What are renal stones commonly composed of?
Calcium oxalate | 80% of the time
329
Which enzyme does allopurinol inhibit?
Xanthine oxidase
330
How does inhibition of xanthine oxidase reduce the amount of uric acid in the urine?
Inhibits the formation of uric acid from xanthine + hypoxanthine
331
How does leakage of calcium into urine lead to a change in the pH?
Alkalinisation of the urine
332
What is the physiological role of parathyroid hormone?
Primary response to PTH by kidney = to increase renal calcium resorption + phosphate excretion. In the kidney PTH blocks reabsorption of phosphate in the proximal tubule + promote calcium reabsorption in the ascending loop of Henle, distal tubule, collecting duct.
333
What secreted PTH?
Parathyroid glands
334
Where in the nephron does parathyroid hormone block reabsorption of phosphate?
Proximal tubule
335
Where in the nephron does parathyroid hormone promote reabsorption of calcium?
Ascending loop of Henle Distal tubule Collecting duct
336
Why might primary hyperparathyroidism lead to the formation of calcium stones?
Primary hyperparathyroidism is the result of excessive secretion of PTH. PTH regulates serum calcium + phosphate levels. High levels of PTH causes serum calcium levels to increase and serum phosphate levels to fall. This leads to excessive renal calcium excretion (hypercalciuria)
337
What is hypercaliuria?
Excessive renal calcium excretion
338
Urinary tract stones often lead to what?
Urinary stasis this can lead to infection
339
How does increased fluid intake reduce the chances of developing renal stones?
More fluid intake = more dilute urine = reduced concentration of ions within urine = reduces solubility product
340
What measurement on a dipstick urinalysis would be abnormal in a patient with urinary tract stones?
Blood is often present pH will be normal in calcium oxalate stones but may be high in patients with type 1 renal tubular acidosis or in the presence of urease splitting microorganisms
341
Which measurements would be useful on to serum biochemistry to determine the cause of the renal stone a patient had?
Elevated calcium ion levels also check pH, 24 hour urine volume, oxalate, sodium, calcium, citrate, urate excretion, spot sample of cysteine
342
Where is. angiotensinogen produced?
Liver
343
What does hydrolysis of angiotensinogen by renin give rise to?
Angiotensin I
344
What can ACE cleave aside from Ang I?
Bradykinin --> switching it off
345
What is the function of bradykinin?
Dilation of blood vessels
346
What does removal of bradykinin cause?
Less vasodilation Increases the capability of Angiotensin II to increase blood pressure
347
Other than stimulating the secretion of aldosterone, what other effects are caused by angiotensin II?
Constriction of blood vessels --> increased blood pressure Effects on nerves, causing thirst sensation, desire for salt Encouraging release of antidiuretic hormone from pituitary gland Effects on kidneys - increase sodium retention + water reabsorption Therefore increases blood volume and pressure
348
Where is aldosterone secreted?
The zona glomerulosa of the cortex of the adrenal gland
349
As sodium is reabsorbed from the urine, what happens to blood volume and osmolarity?
Osmolarity of blood will increase as the sodium is reabsorbed. The osmolarity increases as the ratio of solute to water molecules increases.
350
What affect does sodium reabsorbtion have on the blood pressure?
Blood volume will increase therefore blood pressure will increase.
351
Describe the MoA of angiotensin converting enzyme inhibitors (e.g. lisinopril, ramipril)
Block convertion of Ang I to Ang II thereby reducing arteriolar constriction and alleviatin high blood pressure. Also causes loss of sodium and water, leading to reduced blood volume. And causes slight increase in potassium blood levels.
352
Describe the MoA of spironolactone.
Potassium sparing diuretic Acts by antagonism of aldosterone in the distal renal tubules. It competitively binds to the mineralocorticoid receptors; these are nuclear receptors that act via gene transcription that results in a decreased production and expression of both the ENaC and ROMK channels in the apical membrane, as well as decreasing the production and expression of Na+K+ATPase on the basolateral membrane. These actions increase sodium + water excretion, while potassium is retained. Thus Spironolactone is a potassium sparing diuretic.
353
What clinical consequences may arise from horseshoe kidney?
Horseshoe kidneys generally function adequately but there is an increased incidence of upper urinary tract obstruction and infection. Furthermore, it has also been reported that horseshoe kidneys can be associated with ureteric abnormalities including duplications (duplex ureters).
354
What are the S+S of polycystic kidney disease?
1) pain or tenderness in the abdomen 2) haematuria 3) urinary tract infection (UTI) 4) kidney stones 5) symptoms of chronic renal failure 6) asymptomatic hypertension 7) asymptomatic presentation through family screening
355
What percentage does autosomal dominant polycystic kidney disease account for of all PKD cases?
90%
356
Autosomal dominant polycystic kidney disease 1 present at what age?
30-40s
357
Autosomal dominant polycystic kidney disease 2 present at what age?
60-70s
358
If symptoms of Autosomal dominant polycystic kidney disease presents in childhood then what might it be instead?
autosomal recessive polycystic kidney disease
359
What is the goal of PKD treatment?
control blood pressure and reduce risk of cardiovascular complications + progressive kidney failure
360
What might PKD treatments include?
1) pain medication 2) blood pressure medication 3) antibiotics (to treat UTI) 4) a low-sodium (salt) diet 5) surgery (to drain cysts and help relieve discomfort – this is rare) 6) novel therapies to alter cyst growth are in development
361
What is the meaning of infarct?
An area of tissue that undergoes necrosis as a result of obstruction of local blood supply, as by a thrombus or embolus
362
What are the causes of infarction?
The most common cause is thromboembolism from either the heart or aorta, or in situ thrombus formation within the renal artery or segmental branch artery. Atrial fibrillation is a risk factor.
363
Why are renal infarcts typically wedge-shaped, as here?
This is due to the segmented nature of the blood supply to the kidney.
364
What would be the implications of this renal infarct for renal function?
It depends on the size of the infarct. - Small infarcts do not affect kidney function, but multiple or large infarcts can lead to kidney failure, depending on the blood vessel that is occluded.
365
What symptoms and signs might you expect in small renal infarcts?
Often asymptomatic
366
What symptoms and signs might you expect in large renal infarcts?
Acute flank pain (mimicking renal colic) and maybe associated with haematuria.
367
What is hydronephrosis?
The swelling of a kidney due to a build-up of urine. It happens when urine cannot drain out from the kidney to the bladder from a blockage or obstruction. Hydronephrosis can occur in one or both kidneys. The main function of the urinary tract is to remove wastes and fluid from the body.
368
What is the pelvicalyceal system?
Pertaining to the renal pelves and calices.
369
What is the renal parenchyma?
Parenchyma = the essential or functional elements of an organ, as distinguished from its framework, which is called the stroma. Renal parenchyma = the functional tissue of the kidney, consisting of the nephrons.
370
What is the renal papillae?
The renal papilla is the location where the renal pyramids in the medulla empty urine into the minor calyx in the kidney. Histologically it is marked by medullary collecting ducts converging to form a papillary duct to channel the fluid. Transitional epithelium begins to be seen.
371
What is hyperplasia?
The enlargement of an organ or tissue caused by an increase in the reproduction rate of its cells, often as an initial stage in the development of cancer.
372
What causes bladder trabeculation?
Secondary to bladder outlet obstruction Cause morphological + histological changes due to hypertrophy and hyperplasia of bladder muscle the infiltration of the connective tissue.
373
What treatments are available for prostatic hyperplasia?
Treatment depends on severity of the disease. Mild and moderate symptoms are usually monitored with regular check-up whilst lifestyle changes are implemented: - Reduced alcohol consumption - Exercise regime
374
What treatments are available for moderate to severe prostatic hyperplasia?
Finasteride and dutasteride are used. These block 5-alfa reductase and reduce dihydrotestosterone production and hence the activity of this hormone on the prostate gland, reducing its size and so improve symptoms. In addition alpha blockers (Tamsulosin, alfuzosin) can be prescribed as a relaxant to aid urination. As a last resort surgery can be used if prostate enlargement does not respond to treatment.
375
What are the causes of hydronephrosis?
There are 2 common causes of hydronephrosis 1) A blockage within the urinary tract between the renal pelvis and vesico-ureteric junction as in this case 2) A disruption in the working of the bladder leading to backflow of urine from the bladder to the kidney.
376
What do the following cause? 1) Kidney stones 2) Pregnancy 3) Bladder or cervical cancer 4) BP hyperplasia or prostate cancer 5) Endometriosis 6) Tuberculosis 7) Pelvicoureteric junction obstruction 8) Neurogenic bladder 9) Urethral obstruction
Hydronephrosis
377
What are the consequences of outflow obstruction for the bladder?
Obstruction in the urethra causes bladder dilation, secondary hypertrophy and diverticulae formation.
378
What are the symptoms of renal cell carcinoma?
Typical symptoms of are: 1) Haematuria 2) A mass in the abdomen. 3) A pain in the side that doesn't go away. 4) Loss of appetite. 5) Weight loss for no known reason. 6) Anaemia. 7) Pyrexia of unknown origin
379
What is the most common type of kidney cancer in adults? | more likely to affect men in 50-70s
Renal cell carcinoma
380
What are risk factors for renal cell carcinoma?
1) Family history of the disease 2) High blood pressure 3) Horseshoe kidney 4) Polycystic kidney disease 5) Smoking 6) Von Hippel-Lindau disease (a hereditary disease that affects blood vessels in the brain, eyes, and other body parts)
381
What is the prognosis for patients with renal cell carcinoma?
Dependent on the level of metastasis, with the highest survival for those patients with early detection. If however, the cancer has metastasised to the lymph nodes or to other organs, the survival rate is much lower.
382
Which factors predispose to transitional cell carcinoma?
The main factors driving the formation of this disease are environmental. Therefore these are the main factors: 1) Smoking 2) Exposure to certain dyes/chemicals in leather/textiles/plastics and rubbers 3) The misuse of pain medicines 4) Exposure to some medicine – especially cyclophosphamide
383
How do the presenting features of transitional cell carcinoma depend on where it occurs in the urinary tract?
Haematuria is the most common presenting complaint, and this can be either visible or non-visible. However if the tumour is present in the vesicouretic junction, this can cause obstruction of the ureter and hydronephrosis. Alternatively if the tumour is present in the urethral orifice, then the patient may suffer from bladder outlet obstruction and urinary retention. Unfortunately, occasionally patients sometimes only present after metastatic spread, due to systemic symptoms associated with the metastasis.
384
What are the complications of transitional cell carcinoma?
* UTI * Urinary retention * Hydronephrosis * Recurrence of tumour * • The risk of upper urinary tract tumour recurrence increases in patients with multiple and high-risk bladder tumours. * Increased risk of urethral transitional cell carcinoma. * Complications of surgery include bowel obstruction, obstruction of the ureter, pyelonephritis and infection of the wound. * Radical cystectomy damages the S2,3,4 outlet and causes complete erectile dysfunction, although a nerve-sparing approach can reduce this to about half. * Orthotopic bladders have a risk of urinary incontinence
385
What can radical cystectomy damage?
The S2,3,4 outlet and causes complete erectile dysfunction, although a nerve-sparing approach can reduce this to about half.
386
Which structure is commonly blocked by prostatic hyperplasia?
The prostatic urethra is commonly obstructed by benign hyperplasia
387
Which structure produces 60% of the seminal fluid?
Prostate
388
Where are openings of the ureters found?
Upper 2 corners of the trigone
389
Which structure is referred to as the trigone?
The trigone is at the base of the bladder, it's made up by different cell types
390
What is the urachus?
A fibrous remnant of the allantois
391
What is the allantois?
A canal that drains the urinary bladder of the foetal that joins + runs within the umbilical cord
392
What biochemical change can cause cardiac arrest due to ventricular arrhythmia?
Raised serum potassium levels
393
What biochemical change can cause hypertension?
Raised blood renin levels
394
What biochemical change can cause normochromic, normocytic anaemia?
Reduced serum EPO levels
395
Erythropoietin deficiency is common in chronic kidney disease and leads to what?
Decreased red cell production and anaemia
396
What is the main vasomotor site of action of Angiotensin II?
Efferent arteriole
397
Where is the site of sodium reabsorption through a channel that is blocked by the diuretic furosemide?
Thick ascending loop of Henle
398
Where is the major site of bicarbonate reabsorption?
Proximal convoluted tubule
399
How does angiotensin II minimised constriction at the afferent arteriole?
Angiotensin II stimulates the release of the vasodilator nitric oxide from the afferent arteriole, thereby minimizing constriction at this site
400
How does furosemide work?
Furosemide is a loop diuretic. It inhibits water reabsorption in the nephron by blocking the sodium-potassium-chloride cotransporter (NKCC2) in the thick ascending limb of the loop of Henle. This is achieved through competitive inhibition at the chloride binding site on the cotransporter, thus preventing the transport of sodium from the lumen of the loop of Henle into the basolateral interstitium.
401
Where is bicarbonate reabsorbed in the nephron?
About 85 to 90% of the filtered bicarbonate is reabsorbed in the proximal tubule The rest is reabsorbed by the intercalated cells of the distal tubule and collecting ducts.
402
After intravenous administration of which highly ionised drug, which has a low therapeutic index, is very rapid plasma clearance by the kidney?
Gentamicin
403
What is gentamicin?
An antibiotic that can be given via injection or intravenous. It is part of the aminoglycoside family of antibiotics, which work via either preventing the growth of bacteria, or inducing bacterial death. However, it may also cause some serious side effects, including damage to your kidneys and the cochlea in the inner ear, which controls hearing and balance. The clearance of Gentamicin depends on both kidney function and body weight.
404
What is gentamicin usd for?
It is typically used for serious gram negative bacterial infections which are difficult to treat with other antibiotics.
405
To what structures can gentamicin cause damage to?
Kidneys | Choclea of inner ear
406
What is methly penicillin more commonl known as?
Penicillin V
407
Is penicillin V or G more effective against gram-negative bacteria?
G
408
Which antibiotic is more acid stable Penicillin V or G? What are the implications of this?
V Therefore can be given orally
409
What is lithium used to treat?
Bipolar affective disorder
410
Which univalent cation of the white metal series has a low therapeutic index and will accumulate rapidly in acute kidney injury?
Lithium
411
Where is lithium absorbed?
Lithium is absorbed by the GI tract, is not protein bound and is filtered at the glomerulus.
412
Where in the nephron is 90% of filtered lithium reabsorbed?
60% in the proximal tubule, 40% in the thick ascending limb of the loop of Henle, the connecting tubule, and the cortical collecting duct.
413
What can lithium be a substitute for in the nephron?
For sodium in several sodium channels Particularly the sodium-hydrogen exchanger in the proximal tubule (NHE3), the sodium/potassium/2chloride exchanger in the thick ascending limb of the loop of Henle (NKCC2), and the epithelial channel of the cortical collecting tubule (ENaC).
414
Why will lithium levels rise rapidly and toxicity occur if patient on lithium develops acute kidney injury?
Because lithium is entirely renally excreted
415
Where does the left and right gonadal vein drain into?
L - left renal vein | R - directly into inferior vena cava
416
How does the gonadal veins ascending with gonadal arteries in the abdomen?
Along the psoas muscle Anterior to. ureters
417
Where does the renal artery arise from?
Abdominal aorta at L1-2, inferior to superior mesenteric artery
418
Pseudomonas spp. are Gram-negative rod bacteria commonly found in where?
Soil, ground water, plants and animals. Pseudomonal infection causes a necrotising inflammation.
419
What family are proteus species part of?
Enterobacteriaceae family of gram-negative bacilli.
420
Name bacterial species implicated as serious causes of infection in humans
Proteus, Escherichia, Klebsiella, Enterobacter, and Serratia species.
421
Which bacteria species are commonly found in the human intestinal tract as part of normal human intestinalgl flora?
Proteus, Escherichia coli, Klebsiella, Enterococci
422
Which physiological change will lead to an increase in the Glomerular filtration rate? a. A decrease in renal blood flow b. A decrease in the concentration of plasma protein c. Compression of the renal capsule d. Constriction of the afferent arteriole e. Decrease in afferent arteriole pressure
A decrease in the concentration of plasma protein Because GFR = (volume of urine x urine flow)/plasma protein concentration When you reduce the denominator, the answer is greater (GFR)
423
What is the principal site for glucose reabsorption within the nephron?
Proximal convoluted tubule
424
What is the term that describes the volume of fluid from which a drug can be completely removed per unit of time (rate of drug removal)?
Clearance volume
425
When is clearance of a drug linear?
Clearance of a drug is linear if the drug is eliminated via first order kinetics. Clearance of a drug can be completed via both renal excretion and liver metabolism, and in this case this clearances are additive (total clearance=clearance via the kidney + clearance via the liver).
426
A 45 year old woman presents with oedema of the face and ankles. She is normally fit and well. Urine dipstick testing shows 4+ of protein, but no glucose or blood. What is the likely pathological basis for this presentation?
An abnormality of the basement membrane of the glomerulus
427
What does proteinuria suggest?
Nephrotic syndrome
428
A 50 year old man has recently noticed ankle swelling. Urine testing reveals non-visible haematuria and 4+ proteinuria. What is likely to be causing the haematuria?
Glomerulonephritis
429
What is haematuria (often visible) without proteinuria suggestive of?
Bladder tumour
430
What does retroperitoneal fibrosis produce?
Renal obstruction at the level of the ureters and progressive renal failure.
431
What might you expect to find as a ‘normal variant’ on inspection of the urine of a dehydrated patient? ``` A. Glucose B. Granular casts C. Hyaline casts D. More than 10 white cells per cubic millimetre E. Red cells ```
Hyaline casts - found in healthy individuals who are dehydrated or who do vigorous exercise.
432
What are hyaline casts formed from?
Excess (Tam-Horsfall) protein in the nephrons
433
A 35 year old woman presents with her first episode of symptoms of urinary frequency and painful micturition. She is normally fit and well Her urine is cloudy and blood, protein and nitrites are detected on a dipstix test. Which antibiotic is the most appropriate choice in this situation?
This is a simple (as opposed to complicated) urinary tract infection. The most common organism is E. Coli which responds well in most circumstances to trimethoprim which is also a cheap drug.
434
What is nitrofurantoin used for? | List it's pros and cons.
Treating bacterial urinary tract infectious that are not caused by Proteus ssp. Nitrofurantoin is concentrated in the urine and is a reasonable choice but not active against Proteus ssp.
435
A 35 year old woman presents with her first episode of symptoms of urinary frequency and painful micturition. What is the most reliable guide to the presence of a bacterial infection in the urine?
Nitrites in urine
436
How are nitrites formed
nitrate (NO3) --> nitrite (NO2) catalysed by bacterial nitrate reductase
437
When might presence of. nitrites be falsely negative in a urine dipstick (when there is a bacterial infection)?
if infections caused by non-nitrate reducing bacteria low no. of bacteria patient taking vitamin C
438
A 76 year old man presents with severe kidney failure. Examination confirms a suprapubic mass consistent with an enlarged bladder. What pathology is most likely to result in this presentation?
Benign hyperplasia of the prostate gland
439
An 82 year old woman presents with a history of nocturia and polyuria. Blood tests show severe kidney failure. You suspect a diagnosis of post-renal kidney failure. What imaging technique would you request to demonstrate this pathology? And why?
Ultrasound - cheap - non-invasive - doesn't involve ionising radiation - doesn't involve administration of. potentially nephrotoxic iodinated contrast
440
Bladder cancer is more likely to. cause obstruction at which level?
Vesico-ureteric junction In which case the bladder would be empty
441
What would an ultrasound reveal in post-renal kidney failure?
Hydronephrosis Distention of the renal calyces and pelvis with urine as a result of obstruction of the outflow of urine distal to the renal pelvis.
442
What is the term for a synthetic non-biological foreign chemical?
Xenobiotic
443
What is an antibiotic?
Anti-bacterial agent (can be natural)
444
What is a probiotic?
A bacteria or yeast culture which have beneficial properties (such as those of the intestinal flora).
445
What is a neurobiotic?
Refers to the study of the nervous system in conjunction with technology.
446
What is a prebiotic?
Type of fibre
447
How is the renal clearance of a drug affected by the urine pH level?
Acidic pH aids basic drugs to be excreted Basic pH aids acidic drugs to be excreted
448
Which part of the nephron is the primary site of action of the thiazide diuretics?
Distal tubule (early) Inhibit the sodium-chloride cotransporter in the distal tubule
449
Why are thiazide diuretics less powerful than loop diuretics?
Because they act on the distal tubule where only 5% of filtered sodium is reabsorbed (less than from the loop of Henle - 20-30%)
450
In which part of the nephron is the majority of filtered sodium bicarbonate reabsorbed?
Proximal tubule (90%)
451
A pharmaceutical company wishes to undertake a study of a new drug that may alter kidney function. In their initial studies they need to measure GFR as precisely as possible in normal volunteers. Which test would give the most accurate measurement of glomerular filtration rate?
Inulin clearance
452
A pharmaceutical company wishes to undertake a study of a new drug that may alter kidney function. In their initial studies they need to measure GFR as precisely as possible in normal volunteers. Which test would give the most accurate measurement of glomerular filtration rate?
Inulin clearance | followed by creatinine clearance
453
What is inulin?
Inulin is the most accurate substance to measure because it is a small, inert polysaccharide molecule that readily passes through the glomeruli into the urine without being reabsorbed by the renal tubules.
454
The right kidney is related posteriorly to what structure?
genitofemoral nerve
455
What is the genitofemoral nerve?
A branch of the lumbar plexus arising within the substance of the psoas major muscle from the inion of the anterior rami of L1 and L2 spinal nerves
456
Which nerve descends in the retroperitoneum to give off genital + femoral terminal ranches supplying the skin over the anterior scrotum or labia majora and lateral femoral triangle respectively?
The genitofemoral nerve
457
What are the 4 muscles which contribute to the posterior abdominal wall?
Psoas major, the Psoas minor, the Quadratus lumborum and the Iliacus.
458
From which embryonic tissue is the nephron of the adult kidney is derived?
Intermediate mesoderm
459
What does the intermediate mesoderm develop into?
Urogenital system (kidneys + gonads) + their respective duct systems Adrenal cortex
460
In which week of foetal development does the intermediate mesoderm differentiate into the kidneys?
3rd week
461
The cortex of the kidney projects into the kidney dividing the medulla into what shapes?
Triangular shaped renal pyramids
462
What are apices of renal pyramids surrounded by?
Minor calices which join to form a. major calyx which unite to form the renal pelvis which exit the kidney to form the ureters
463
During development when do kidneys ascending to assume their adult position?
~9th week
464
Which structure typically prevents the normal ascent of a horseshoe kidney?
Inferior mesenteric artery
465
What does renal pyramids consist of?
Tubules that transport urine from the cortical part of the kidney to the calyces
466
What is the point of each renal pyramid called?
Papilla
467
What pathophysiological mechanism can lead to a sudden fall in GFR following the commencement of treatment with an ACE Inhibitor?
Efferent arteriolar vasodilatation
468
How does inhibition of ACE affect bradykinin levels?
Increase them - because ACE inactivates bradykinin when it's not being inhibited
469
What is bradykinin?
A potent vasodilator
470
Where does acetazolamide (carbonic anhydrase) act in a nephron?
Proximal tubule
471
Where does amiloride and spironolactone act in the nephron?
Inhibition of aldosterone receptor at the distal tubule and cortical collecting duct,
472
Where does furosemide act?
Acesnding limb of the loop of Henle on Na-K-Cl cotransporter
473
Where does bendroflumethiazide work?
Bendroflumethiazide is a thiazide diuretic which works by inhibiting sodium reabsorption at the beginning of the distal convoluted tubule (DCT) via Na-Cl transporter
474
What are the most powerful diuretics?
Loop diuretics which act on ascending loop of Henle
475
GIve examples of loop diruretics
E.g. furosemide, bumetanide, dichlorphenamide, methazolamide
476
When should loop diuretics be avoided?
* Severe hypokalaemia * Severe hyponatraemia * Anuria – non-passage of urine * Comatose + pre-comatose states associated w liver cirrhosis * Renal failure due to nephrotoxic or hepatotoxic drugs
477
Where do thiazides, chlorothiazides, hydrochlorothiazides (diuretics) act?
Distal convoluted tubule
478
Where do potassium sparing antikaliuretic diuretic agents work?
Collecting tubule and duct
479
Where does acetazolamide diuretics act?
Proximal convoluted tubule
480
Upper urinary tract infection pain is localised where?
Loid pain which may radiate to groin/testicles
481
What causes dark urine?
Concentrated bile pigments
482
What causes frothiness of urine?
Excess protein
483
What does urobilionogen in urine dipstick mean?
It is a breakdown product bilirubin which suggests haemolysis
484
Creatine is broken down in muscles, what is the by-product of this catabolism?
Creatinine - used to estimate GFR and hence kidney function
485
What are the following symptoms indicative of? ``` o Urinary frequency (e.g. cystitis) o Nocturia o Urgency o Incontinence o Bladder pain o Dysuria ```
Storage issues lower urinary tract
486
List obstructive voiding symptoms (lower urinary tract).
``` o Hesitancy o Delay in initiating micturition o Weak urinary stream o Straining to void o Incomplete emptying o Terminal dribbling ```
487
What are the 2 broad functionings of the urinary system?
Maintain: water, salt, pH balance Excretion of metabolic waste products
488
As per the endocrine functions of the kidneys, the kidneys produce which 3 important hormones?
- Erythropoietin - Calcitriol (1,25- dihydroxycholecalciferol - Renin They also synthesize prostaglandins (not unique to kidneys), which affect many processes in the kidneys .
489
Which kidney is slightly lower than the other?
Right kidney - due to liver
490
Name 5 renal regions.
```  Bowman’s capsule (cup-shape + surrounds glomerulus)  Proximal convoluted tubule (PCT)  Loop of Henle (LoH)  Distal convoluted tubule (DCT)  Collecting duct (CD) ```
491
The glomerular capsule has 2 layers. | Visceral and parietal, describe their histology.
Between the 2 layers lies the capsular space (lumen of urinary tube) ``` Visceral layer (inner): • Podocytes (modified simple epithelial cells) – stop macromolecules passing • Pedicles (foot-like projections) wrap around endothelial cells of glomerular capillaries to form inner capsule wall • Fenestrated endothelium ``` ``` Parietal layer (outer): • Simple squamous epithelium ```
492
What lies between the parietal and visceral layers of the glomerular capsule?
Capsular space aka lumen of urinary tube
493
What is the function of the capsular space?
Fluid filtered from glomerular capillaries enters this space
494
Describe the histology of the PCT.
* Have apical microvilli - increased SA for absorption + secretion * High no. of mitochondria
495
Histology of the descending limb of the loop of Henle and the thin ascending limb
Simple squamous epithelium
496
What do cortical nephrons lack?
Thin ascending limb of loop of Henle
497
Histology of thick ascending limb of loop of Henle
* Simple cuboidal to low columnar epithelium * Final part of ascending limb makes contact w/ afferent arteriole (because columnar tubule cells in this region are crowded together they as known as macula densa)
498
What type of cells lie alongside macula densa?
Wall of afferent arteriole (and sometimes effect) containing modified smooth muscle fibres (juxtaglomerular cells)
499
What is the juxtaglomerular apparatus make up of?
Specialized structure formed by the distal convoluted tubule (macula densa) and the glomerular afferent arteriole (juxtaglomerular cells) The juxtaglomerular apparatus consists of three cell types. They are: the macula densa, a part of the distal convoluted tubule of the same nephron. juxtaglomerular cells, which secrete renin, specialized smooth muscle cells of the afferent arteriole, which supplies blood to the glomerulus.
500
Functoin of juxataglomerular apparatus
It is located near the vascular pole of the glomerulus and its main function is to regulate blood pressure and the filtration rate of the glomerulus.
501
Name the cells in the kidney that synthesize, store and secrete renin. They are specialised smooth muscle cells mainly in the walls of the afferent arterioles and some in the efferent arterioles.
The juxtaglomerular cells (JG cells, or granular cells)
502
What begins a short distance past macula densa?
Distal convoluted tubule cells
503
In the last part of the DCT and collecting duct what cells are present?
Principal cells and intercalated cells
504
Function of intercalated cells?
Maintain acid-base balance
505
Function of principal cells?
Reabsorb Na+ + secrete K+
506
What 2 ways can K+ secretion be increased?
K+ secretion can be increased by aldosterone + by increasing Na+ delivery to CD
507
Which part of the kidneys have receptors that bind ADH (vasopressin) and aldosterone?
Collecting duct
508
Where do collecting ducts drain into?
Large papillary ducts
509
What are papillary duct cells lined with?
Simple columnar epithelium
510
Is glomerular filtration passive or active?
Passive process in which hydrostatic pressure forces fluids and solutes through a membrane
511
What do podoytes prevent?
Prevents macromolecules from travelling further
512
What does the basement membrane in kidneys prevent?
Plasma proteins from entering capsular space
513
What is tubular reabsorption and tubular secretion?
o Tubular reabsorption: movement of solutes + water from lumen of renal rubble across epithelial cells + back into blood o Tubular secretion: movement of solutes directly from blood across the epithelial cells into luminal filtrate
514
What does aldosterone do?
Increases sodium reabsorption which increases water reabsorption which leds to more concentrated urine Increases sympathetic activity Stimulates posterior pituitary gland to secrete ADH, which causes water reabsorption in collecting duct which increases concentration of urine
515
What are the branches of the renal arteries called?
The segmental arteries are branches of the renal arteries. There are five named segmental arteries: - superior - inferior - anterior superior - anterior inferior - posterior
516
Name the arteries which which supply the renal lobes.
Interlobar arteries
517
From the renal artery until glomerular capillaries list all the names of the arteries.
Renal artery - segmental arteries - interlobar arteries - arcuate arteries - cortical radiate arteries - afferent arterioles - glomerular capillaries
518
From glomerular capillaries to renal vein name all the veins in the kidneys.
Glomerular capillaries - efferent arterioles - peritubular capillaries + vasa recta - cortical radiate veins - arcuate veins - interlobar veins - renal vein
519
Where does the renal veins lie relative to the renal arteries?
Anterior
520
Which renal vein is longer and why?
The left renal vein is longer because the vena cava lies slightly to the right so the vein travels anteriorly to abdominal aorta
521
Lymph from kidneys drain where?
Into lateral aortic nodes located at origin of renal arteries
522
NaCl is actively transported out of which limb of the loop of henle? What does this do?
Ascending limb  This increases interstitial fluid osmolality + creating an osmotic gradient
523
Where is water passively transported out of?
The descending limb of LoH (down it’s conc. gradient)
524
Common causes of chronic kidney disease?
Diabetes LT uncontrolled hypertension Polycystic kidney disease
525
Why is creatinine used to measure GFR?
Freely filtered, not secreted, not absorbed
526
WHat filters out of the blood at the glomerulus and what does not unless there is pathology?
 Blood cells + proteins don’t filter through unless there’s pathology  NaCl, K+, H2O, glucose, aa, creatinine, urea filter out
527
The proximal convoluted tubule lies in the renal cortex. What is absorb here?
Na+ (65%) H2O (65%) HCO3- (90%) Cl- (50%) Glucose + aa (~100%)
528
What is secreted in the PCT?
Uric acid + organic acids are secreted into nephron from capillaries
529
The primary role of the loop of henle is what?
Concentrate the salt in the interstitium
530
What is the descending limb of the loop of Henle permeable to? And what is it impermeable to?
Permeable to water + impermeable to solutes (salt particles)
531
What is the ascending limb of the LoH permeable and impermeable to?
Impermeable to water + actively transports NaCl to interstitial fluid of medullary pyramids
532
What is the renal corpuscle made up of?
* Glomerulus (capillary network) | * Glomerular capsule (Bowman’s capsule) – double walled epithelial cup surrounding glomerulus
533
What is the 3 main sectionsl of the renal tubule?
* Proximal convoluted tubule (PCT) – renal cortex * Nephron loop (LoH) – renal medulla * Distal convoluted tubule (DCT) – renal cortex
534
Differences between thin and thick ascending limb histology.
 Thin ascending limb – lumen same as other areas but thinner simple squamous epithelium  Thick ascending limb – thicker simple cuboidal epithelium
535
Name the 2 classes of nephrons.
``` Cortical nephrons (majority) Juxtamedullary pehrons ```
536
Describe the cortical neprhones
 Renal corpuscles – lie in outer portion of real cortex  Short loops of Henle – lie mainly in cortex + penetrate only into outer region of renal medulla  Blood supply – peritubular capillaries (that arise from efferent arterioles)
537
Describe the juxtamedullary nephrons
Renal corpuscles – lie deep to cortex, close to medulla Long loops of Henle – extend deep into medulla • Enable kidneys to excrete v. dilute or conc. urine Blood supply – vasa recta (that arise from efferent arterioles)
538
Do cortical or uxtamedullary nephrons have longer loops of Henle?
Juxtamedullary
539
Summaries histology of the different parts of the renal tubule.
PCT = Simple cuboidal w/ prominent microvilli LoH (descending + thin ascending) = Simple squamous LoH (thick ascending )= Simple cuboidal + low columnar DCT (majority) = Simple cuboidal DCT (last part) + CD = Simple cuboidal w/ principal + intercalated cells
540
What is the major stimuli that triggers release of Ang II?
Low blood volume/pressure causes stimulation of renin-induced Ang II production
541
What major stimuli triggers aldosterone release?
Increased Ang II level + increased plasma K+ level --> promote aldosterone release by adrenal cortex
542
What stimulates ANP (atrial natriuretic peptide) secretion?
Stretching of atria
543
Causes of urological pathology.
Congenital, infection, inflammation, stones, cancer, trauma, neurological
544
Describe what horse-shoe kidney is?
* Kidneys rotated lying lower than normal, over poles close together, bridge of tissue between kidneys * Kidneys have failure to depart from midline
545
What is BPH associated with histologically?
Histological changes of stromal-glandular hyperplasia seen within the prostate
546
When is benign prostatic hyperplasia clinically significant?
When this overgrowth of benign tissue is associated with bothersome lower urinary tract symptoms: frequency, urgency, nocturia, weak stream
547
The enzymes aromatase and 5-alpha reductase are responsible for converting androgen hormones into what?
Aromatase = oestrogen 5-alpha reductase = DHT respectively
548
DHT is a potent anabolic hormone that promotes what?
Prostate cell proliferation
549
What is urolithiasis?
Formation of stony concretions in the bladder or urintary tract
550
What percentage of stones are made up of: calcium (oxalate + phosphate), uric acid, struvite (magnesium ammonium phosphate)?
 Calcium stones: 75-80% (oxalate + phosphate)  Uric acid: 4-15%  Struvite (magnesium ammonium phosphate): 4-12% (F>M), urease producing bacteria – staghorn calculus
551
What is the commonest cancer in men?
Adenocarcinoma of prostate | 90% of over 90 year olds
552
What is rate of drug elimination known as?
Clearance
553
What is volume of distribution?
Fluid volume that would be required to contain the amount of drug present in the body at the same conc. as in the plasma
554
List drugs than can cause acute interstitial nephritis?
Beta-lactam antibiotics, vancomycin, NSAIDs, furosemide, thiazides
555
What are aminoglycosides?
Bactericidal antibiotics which act by inhibiting bacterial protein synthesis
556
Why can't you give aminoglycosides to patients with renal failure?
Decreased clearance, this can lead to excess levels of the drug building up + causing ototoxicity Half-life of aminoglycosides: • Healthy patients: 1.5 hours • Renal failure patients: 25 hours
557
Which drugs can cause ototoxicity?
Aminoglycosides and loop diuretics
558
Which antibiotics cause tubular toxicity?
Aminoglycosides | Tetracyclines
559
Where do carbonic anhydrase inhibitors act?
Proximal rubule
560
Where does osmotic diuretics act?
In the nephron, osmotic diuretics act at the portions of the nephron that are water-permeable. Proximal convoluted tubule and the descending limb of Henle's loop.
561
Where do thiazides, chlorothiazides, hydrochlorothiazides act?
DCTreab
562
What are furosemide, bumetanide, dichlorphenamide, methazolamide examples of and where do they work?
Loop diuretics Inhibit Na+/K+/2Cl- co-transporter in thick ascending limb
563
What are substances that donate protons called?
Acids Bases accept protons
564
What causes nephrotic syndrome?
Loss of function of glomerular basement membrane
565
Common primary causes of nephrotic syndrome in children?
* Minimal change glomerulonephritis (MCG) | * Focal segmental glomerulosclerosis (FSGS)
566
Common primary causes of nephrotic syndrome in adults?
* Focal segmental glomerulosclerosis (FSGS) | * Membranous glomerulonephritis - Second most common nephrotic disease in adults after FSGS
567
List secondary causes of nephrotic syndrome?
 Diabetic nephropathy  Systemic Lupus Erythematosus (SLE)  Amyloidosis  Chronic viral infection
568
Causes of acute renal injury
o Glomerular injury (irreversible) o Interstitial injury o Acute tubular necrosis
569
Names of nephritic syndrome in adults.
Goodpasture’s syndrome ANCA-associated vasculitis SLE MCGN
570
Examples of nephrotic syndrome in adults
Focal segmental glomerulosclerosis Membranous glomerulonephritis IgA nephropathy (berger disease)
571
Examples of nephrotic syndrome in children
Minimal change glomerulonephritis Focal segmental glomerulosclerosis
572
Treatment of nephrotic syndrome.
Water given with negative balance High protein and high calcium Salt restriction and potassium given freely
573
Treatmenft of nephritic syndrome.
Water with negative balance (less than normal as pt. is hypervolemic) Sodium, potassium, protein restriction
574
In nephritic syndrome which 2 immunological disorders cause thickening of the basement membrane?
Anti-basement membrane antibody Immune complex (ppt of BM)
575
What is the mechanism of nephrotic syndrome?
Any inflammation causes proteinuria then oedema then hypovolemia then more hypoalbuminemia and hyperlipideia
576
How much urine does the bladder normally store?
300-400ml
577
Histology of the lower urinary tract
o Outer – adventitial connective tissue layer o Middle – smooth muscle coat (detrusor) o Innermost – transitional cell epithelium – an elastic barrier that is impervious to urine
578
How does the urethra differ in. males and females?
 Urethra is 5 times longer in males  Urethra is divided into 3 segments in males, but is 1 short tube in females  Urethra is a common duct for the urinary + reproductive system in males (separate in females)
579
What are the nerve roots for micturition?
S2-4 (parasympathetic)
580
Which nerve controls bladder contraction and which nerve controls relaxation of sphincter?
o Pelvic nerve (efferent + afferents) control bladder contraction o Pudendal nerve S2, S3 – relaxation of sphincter
581
What is the most common bacterial infection seen in primary care?
UTI
582
Commonest cause of UTI
UTI-causing (uropathogenic) E. coli (UPEC
583
Risk factors for UTI
- Female sex (shorter urethra) - Anatomic abnormality - Functional abnormality - Neurological disorders (spinda bifida, MS) - Catherisation - Pregnancy - Foreign body (e.g. stones) - UT surgery/instrumentation
584
Name some viruses which can cause UTIs
Adenoviruses  Associated w/ haemorrhagic cystitis BK + JC viruses  Associated w/ infection + graft failure in patients following kidney transplants
585
What is the main host defense against UTIs?
Urine flow and micturition
586
List host defences against UTI
Urine flow and micturition Urine chemistry (osmolality; pH; organic acids) Secreted factors o sIgA (secretory IgA) o Lactoferrin: an iron chelator Mucosal defences o Mucopolysaccharides – glucoseaminoglycan o Few receptors
587
What is urethritis, cystitis, pyelonephritis?
rethritis – involvement of urethra (lower UTI) o Cystitis – involvement of bladder (lower UTI) o Pyelonephritis – involvement of kidney (upper UTI)
588
Name the 3 routes of acquisition of a urinary infection.
Ascending (commonest) - Bacteria transmitted from bowel to urethra then to bladder then to kidney Haematogenous Lymphatic spread
589
List gram-negative bacteria than can cause UTIs
``` Klebsiella Enterobacter Serratia Pseudomonas aeruginosa Proteus mirabilis ```
590
List gram-positive bacteria than can cause UTIs
Staphylococcus epidermidis S. aureus S. saprophyticus Enterococcus faecalis
591
50% of women w/ clinical features of cystitis have negative urine cultures. What are the possible explanations?
o Low bacteria count --> low nitrites o Fastidious bacteria which don’t grow on routine culture media – e.g. ureoplasma o Non-infective inflammation o Sexually transmitted pathogens – e.g. chlamydia trachomatis
592
Which antimicrobial agent is not active against proteus species so should not be given if that is the cause of a UTI?
Nitrofuratoin
593
Which antimicrobials are given for lower urinary tract infections?
Amoxicillin (high resistance) Trimethoprim Cephalexin
594
Which antimicrobials should be given in a mild and severe upper UTI?
o Upper tract (mild): co-amoxiclav | o Upper tract (severe): cefotaxime, gentamicin
595
List the types of urinary incontinences.
Urge incontinence due to an overactive bladder Stress incontinence due to poor closure of the bladder Overflow incontinence due to either poor bladder contraction or blockage of the urethra Functional incontinence due to medications or health problems making it difficult to reach the bathroom