Urology and Renal conditions Flashcards

(134 cards)

1
Q

Renal and uro conditions:

A
  • Acute kidney injury (AKI)
  • Amyloidosis
  • Benign prostatic hyperplasia
  • Bladder cancer
  • Chronic kidney disease (CKD)
  • Epididymitis and orchiditis
  • Glomerulonephritis
  • Hydrocoele
  • Nephrotic syndrome
  • Polycystic kidney disease
  • Prostate cancer
  • Renal artery stenosis
  • Renal cell carcinoma
  • Testicular cancer
  • Testicular torsion
  • Urinary tract calculi
  • Urinary tract infection
  • Varicocoele
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2
Q

Acute kidney injury:

Define

A
  • An abrupt loss of kidney function resulting in the retention of urea and other nitrogenous waste products and the dysregulation of extracellular volume and electrolytes.
    • NOTE: this can occur in patients with previously normal kidneys or in patients with pre-existing renal disease
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3
Q

Acute kidney injury:

Define

A
  • An abrupt loss of kidney function resulting in the retention of urea and other nitrogenous waste products and the dysregulation of extracellular volume and electrolytes.
    • NOTE: this can occur in patients with previously normal kidneys or in patients with pre-existing renal disease
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5
Q

AKI Classification:

A
  • KDIGO Classification of AKI
    • Increase in serum creatinine > 26 mmol/L within 48 hrs
    • Increase in serum creatinine to > 1.5 times baseline within the preceding 7 days
    • Urine volume < 0.5 ml/kg/hr for 6 hours
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6
Q

Explain the aetiology/risk factors of AKI:

A
  • Pre-Renal (90%)
    • Hypovolaemia (e.g. haemorrhage, severe vomiting)
    • Heart failure
    • Cirrhosis
    • Nephrotic syndrome
    • Hypotension (e.g. shock, sepsis, anaphylaxis)
    • Renal hypoperfusion (e.g. NSAIDs, ACE inhibitors, ARBs, renal artery stenosis)
  • Intrinsic Renal
    • Glomerular - glomerulonephritis, haemolytic uraemic syndrome
    • Tubular - acute tubular necrosis
    • Interstitial - acute interstitial nephritis (e.g. NSAIDs, autoimmune)
    • Vasculitides (e.g. Wegener’s granulomatosis)
    • Eclampsia
  • Post-Renal (due to obstruction)
    • Calculi
    • Urethral stricture
    • Prostatic hypertrophy or malignancy
    • Bladder tumour
  • RISK FACTORS
    • Age
    • Chronic kidney disease
    • Comorbidities (e.g. heart failure)
    • Sepsis
    • Hypovolaemia
    • Use of nephrotoxic medications
    • Emergency surgery
    • Diabetes mellitus
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7
Q

Summarise the epidemiology of AKI

A
  • 15% of adults admitted to hospital will develop an AKI
  • Most common in the ELDERLY
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8
Q

Recognise the presenting symptoms of AKI

A
  • Depends on underlying CAUSE
  • Oliguria/anuria
    • NOTE: abrupt anuria suggests post-renal obstruction
  • Nausea/vomiting
  • Dehydration
  • Confusion
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9
Q

Recognise the signs of AKI on physical examination

A
  • Hypertension
  • Distended bladder
  • Dehydration - postural hypotension
  • Fluid overload (in heart failure, cirrhosis, nephrotic syndrome) - raised JVP, pulmonary and peripheral oedema
  • Pallor, rash, bruising (vascular disease)
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10
Q

Identify appropriate investigations for AKI

A
  • Urinalysis
    • Blood - suggests nephritic cause
    • Leucocyte esterase and nitrites - UTI
    • Glucose
    • Protein
    • Urine osmolality
  • Bloods
    • FBC
    • Blood film
    • U&Es
    • Clotting
    • CRP
    • Immunology
      • Serum immunoglobulins and protein electrophoresis - for multiple myeloma
        • Also check for Bence-Jones proteins in the urine
      • ANA - associated with SLE
        • Also check anti-dsDNA antibodies (high in active lupus)
      • Complement levels - low in active lupus
      • Anti-GBM antibodies - Goodpasture’s syndrome
      • Antistreptolysin-O antibodies - high after Streptococcal infection
    • Virology - check for hepatitis and HIV
  • Ultrasound
    • Check for post-renal cause
    • Look for hydronephrosis
  • Other Imaging
    • CXR - pulmonary oedema
    • AXR - renal stones
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11
Q

Generate a management plan for AKI

A
  • Treat the cause
  • FOUR main components to management:
    • Protect patient from hyperkalaemia (calcium gluconate)
    • Optimise fluid balance
    • Stop nephrotoxic drugs
    • Consider for dialysis
  • Monitor serum creatinine, sodium, potassium, calcium, phosphate and glucose
  • Identify and treat infection
  • Urgent relief of urinary tract obstruction
  • Refer to nephrology if intrinsic renal disease is suspected
  • Renal Replacement Therapy (RRT) considered if:
    • Hyperkalaemia refractory to medical management
    • Pulmonary oedema refractory to medical management
    • Severe metabolic acidaemia
    • Uraemic complications
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12
Q

Identify possible complications of AKI

A
  • Pulmonary oedema
  • Acidaemia
  • Uraemia
  • Hyperkalaemia
  • Bleeding
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13
Q

Summarise the prognosis for patients with AKI

A

Summarise the prognosis for patients with AKI

  • Inpatient mortality varies depending on cause and comorbidities
  • Indicators of poor prognosis:
    • Age
    • Multiple organ failure
    • Oliguria
    • Hypotension
    • CKD
  • Patients who develop AKI are at increased risk of developing CKD
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14
Q

Summarise the prognosis for patients with AKI

A

Summarise the prognosis for patients with AKI

  • Inpatient mortality varies depending on cause and comorbidities
  • Indicators of poor prognosis:
    • Age
    • Multiple organ failure
    • Oliguria
    • Hypotension
    • CKD
  • Patients who develop AKI are at increased risk of developing CKD
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15
Q

Identify possible complications of AKI

A
  • Pulmonary oedema
  • Acidaemia
  • Uraemia
  • Hyperkalaemia
  • Bleeding
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16
Q

Generate a management plan for AKI

A
  • Treat the cause
  • FOUR main components to management:
    • Protect patient from hyperkalaemia (calcium gluconate)
    • Optimise fluid balance
    • Stop nephrotoxic drugs
    • Consider for dialysis
  • Monitor serum creatinine, sodium, potassium, calcium, phosphate and glucose
  • Identify and treat infection
  • Urgent relief of urinary tract obstruction
  • Refer to nephrology if intrinsic renal disease is suspected
  • Renal Replacement Therapy (RRT) considered if:
    • Hyperkalaemia refractory to medical management
    • Pulmonary oedema refractory to medical management
    • Severe metabolic acidaemia
    • Uraemic complications
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17
Q

Identify appropriate investigations for AKI

A
  • Urinalysis
    • Blood - suggests nephritic cause
    • Leucocyte esterase and nitrites - UTI
    • Glucose
    • Protein
    • Urine osmolality
  • Bloods
    • FBC
    • Blood film
    • U&Es
    • Clotting
    • CRP
    • Immunology
      • Serum immunoglobulins and protein electrophoresis - for multiple myeloma
        • Also check for Bence-Jones proteins in the urine
      • ANA - associated with SLE
        • Also check anti-dsDNA antibodies (high in active lupus)
      • Complement levels - low in active lupus
      • Anti-GBM antibodies - Goodpasture’s syndrome
      • Antistreptolysin-O antibodies - high after Streptococcal infection
    • Virology - check for hepatitis and HIV
  • Ultrasound
    • Check for post-renal cause
    • Look for hydronephrosis
  • Other Imaging
    • CXR - pulmonary oedema
    • AXR - renal stones
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18
Q

Recognise the signs of AKI on physical examination

A
  • Hypertension
  • Distended bladder
  • Dehydration - postural hypotension
  • Fluid overload (in heart failure, cirrhosis, nephrotic syndrome) - raised JVP, pulmonary and peripheral oedema
  • Pallor, rash, bruising (vascular disease)
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19
Q

Recognise the presenting symptoms of AKI

A
  • Depends on underlying CAUSE
  • Oliguria/anuria
    • NOTE: abrupt anuria suggests post-renal obstruction
  • Nausea/vomiting
  • Dehydration
  • Confusion
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20
Q

Summarise the epidemiology of AKI

A
  • 15% of adults admitted to hospital will develop an AKI
  • Most common in the ELDERLY
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21
Q

Explain the aetiology/risk factors of AKI:

A
  • Pre-Renal (90%)
    • Hypovolaemia (e.g. haemorrhage, severe vomiting)
    • Heart failure
    • Cirrhosis
    • Nephrotic syndrome
    • Hypotension (e.g. shock, sepsis, anaphylaxis)
    • Renal hypoperfusion (e.g. NSAIDs, ACE inhibitors, ARBs, renal artery stenosis)
  • Intrinsic Renal
    • Glomerular - glomerulonephritis, haemolytic uraemic syndrome
    • Tubular - acute tubular necrosis
    • Interstitial - acute interstitial nephritis (e.g. NSAIDs, autoimmune)
    • Vasculitides (e.g. Wegener’s granulomatosis)
    • Eclampsia
  • Post-Renal (due to obstruction)
    • Calculi
    • Urethral stricture
    • Prostatic hypertrophy or malignancy
    • Bladder tumour
  • RISK FACTORS
    • Age
    • Chronic kidney disease
    • Comorbidities (e.g. heart failure)
    • Sepsis
    • Hypovolaemia
    • Use of nephrotoxic medications
    • Emergency surgery
    • Diabetes mellitus
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22
Q

AKI Classification:

A
  • KDIGO Classification of AKI
    • Increase in serum creatinine > 26 mmol/L within 48 hrs
    • Increase in serum creatinine to > 1.5 times baseline within the preceding 7 days
    • Urine volume < 0.5 ml/kg/hr for 6 hours
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23
Q

Bladder Cancer

Define bladder cancer

A
  • Malignancy of bladder cells
    • Most bladder cancers are transitional cell carcinomas
    • RARELY, bladder cancers may be squamous cell carcinomas associated with chronic inflammation (e.g. schistosomiasis)
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24
Q

Explain the aetiology/risk factors of bladder cancer

A
  • UNKNOWN
  • Risk Factors
    • Smoking
    • Dye stuffs (naphthylamines and benzidine)
    • Cyclophosphamide treatment
    • Pelvic irradiation
    • Chronic UTIs
    • Schistosomiasis
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25
Q

Summarise the epidemiology of bladder cancer

A
  • 2% of cancers
  • 2nd most common cancer of the genitourinary tract
  • 2-3 x more common in MALES
  • Peak incidence: 50-70 yrs
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26
**Recognise the presenting symptoms of bladder cancer**
* Painless macroscopic haematuria * Irritative/storage symptoms * Frequency * Urgency * Nocturia * Recurrent UTIs * Rarely: ureteral obstruction
27
**Recognise the signs of bladder cancer on physical examination**
* Often NO SIGNS * Bimanual examination may be performed as part of disease staging
28
**Identify appropriate investigations for bladder cancer**
* **Cystoscopy** - allows visualisation, biopsy or removal * Ultrasound * Intravenous urography * CT/MRI for staging
29
**Prostate Cancer** **Define prostate cancer**
* *Primary malignant neoplasm of the prostate gland*
31
**Explain the aetiology/risk factors of pancreatic cancer**
* UNKNOWN * **Risk Factors** * Age * Afro-Caribbean * Family history * Dietary factors * Occupational exposure to cadmium
32
**Summarise the epidemiology of prostate cancer**
* COMMON * 2nd most common cause of male cancer deaths
33
**Recognise the presenting symptoms of prostate cancer**
* Often ASYMPTOMATIC * **Lower Urinary Tract Obstruction** * Frequency * Hesitancy * Poor stream * Terminal dribbling * Nocturia * **Metastatic Spread** * Bone pain * Cord compression * Systemic symptoms: malaise, anorexia, weight loss * Paraneoplastic syndromes (e.g. hypercalcaemia)
34
**Recognise the signs of prostate cancer on physical examination**
* Asymmetrical hard nodular prostate * Loss of midline sulcus
35
**Identify appropriate investigations for prostate cancer**
* **Bloods** * FBC * U&Es * PSA * NOTE: not a very specific test for prostate cancer * Acid phosphatase * LFTs * Bone profile * **CT/MRI Scan** * Assesses extent of local invasion and lymph node involvement * **Transrectal Ultrasound and Needle Biopsy** * **Isotope Bone Scan** - check for bone metastases
36
**Renal Cell Cancer** **Define renal cell cancer** * *Primary malignancy of the kidneys* **Explain the aetiology/risk factors of renal cell cancer**
* Renal clear cell carcinoma (80%) - UNKNOWN CAUSE * Papillary carcinoma (10%) - UNKNOWN CAUSE * Transitional cell carcinoma (10%) * NOTE: these occur at the **renal pelvis** * **Risk Factors** * Associated with certain _inherited_ conditions: * von Hippel-Lindau disease * Mutation in the von Hippel-Lindau protein, which causes headaches, balance issues, dizziness, limb weakness, vision problems and high blood pressure * Tuberous sclerosis * A rare genetic disease that causes _benign tumours_ to grow in the brain and other organs (e.g. skin, kidneys, lungs, eyes) * Polycystic kidney disease * Familial renal cell cancer * Smoking * Chronic dialysis * NOTE: renal cell cancer can cause _abnormal LFTs_ in the absence of liver metastases = **Strauffer's Syndrome**
37
**Summarise the epidemiology of renal cell cancer**
* UNCOMMON * 3% of all adult malignancies * Peak incidence: 40-60 yrs
38
Recognise the signs of renal cell cancer on physical examination
* Palpable renal mass * Hypertension * Plethora * Anaemia * A left-sided tumour can obstruct the _left testicular vein_ as it joins the left renal vein, and cause a **left-sided varicocoele**
39
**Identify appropriate investigations for renal cell cancer**
* **Urinalysis** * Haematuria * Cytology * **Bloods** * FBC * U&Es * Calcium * LFTs * High ESR (in 75%) * **Abdominal Ultrasound** * Best first-line investigation * Can distinguish between solid masses and cystic structures * **CT/MRI** * Useful for staging * Staging system: **Robson Staging**
40
**Testicular Cancer** **Define testicular cancer**
* *Malignant tumour of the testes* * Types: * Seminomas - 50% * Non-seminomatous germ-cell tumours and teratomas - 30% * RARE: gonadal stromal tumours (Sertoli and Leydig cell tumours) and non-Hodgkin's lymphoma
41
**Recognise the presenting symptoms of renal cell cancer**
* **Renal Cell Carcinoma** * Usually present LATE * Asymptomatic in 90% * Triad of Symptoms: * Haematuria * Flank pain * Abdominal mass * **Transitional Cell Carcinoma** * Presents _EARLIER_ with haematuria * **Systemic Signs of Malignancy** * Weight loss * Malaise * Paraneoplastic syndromes (e.g. fever, hypercalcaemia, polycythaemia)
45
**Explain the aetiology/risk factors of testicular cancer**
* UNKNOWN * **Risk Factors** * Maldescended testes * Ectopic testes * Atrophic tests
46
**Summarise the epidemiology of testicular cancer**
* UNCOMMON * 1% of male malignancies * Common age of onset: 18-35 yrs
47
**Recognise the presenting symptoms of testicular cancer**
* Swelling or discomfort of the testes * Backache due to para-aortic lymph node enlargement * Lung metastases --\> SOB, haemoptysis
48
**Recognise the signs of testicular cancer on physical examination**
* Painless, hard testicular mass * There may be a secondary hydrocoele * Lymphadenopathy (e.g. supraclavicular, para-aortic) * Gynaecomastia (tumour produces hCG)
49
**Identify appropriate investigations for testicular cancer**
* **Bloods** * FBC * U&Es * LFTs * Tumour Markers * a-fetoprotein * b-hCG * LDH * **Urine Pregnancy Test** - will be positive if the tumour produces b-hCG * **CXR** - show lung metastases * **Testicular Ultrasound** * Allows visualisation of the tumour * Can see associated hydrocoele * **CT Abdomen and Thorax** - allows staging * Staging System: **Royal Marsden Hospital Staging**
50
Benign Prostatic Hyperplasia Define benign prostatic hyperplasia
* *Slowly progressive nodular hyperplasia of the **periurethral (transitional) zone** of the prostate gland* * It is the **most frequent cause of LUTS in adult males**
51
Explain the aetiology/risk factors of benign prostatic hyperplasia
* UNKNOWN * Link with hormonal changes (e.g. androgens) * Risk Factors: reduced risk with soya/vegetable based diets and negative association with cirrhosis
52
Summaries the epidemiology of benign prostatic hyperplasia
* COMMON * 70% of men \> 70 yrs have _histological_ BPH (50% of them will experience symptoms) * More common in the west than the east * More common in Afro-Caribbeans
53
Recognise the presenting symptoms of benign prostatic hyperplasia
* **Obstructive Symptoms** * Hesitancy * Poor or intermittent stream * Terminal dribbling * Incomplete voiding * **Irritative/Storage Symptoms** * Frequency * Urgency * Urge incontinence (leakage of urine that accompanies an intense desire to pass water with failure of restraint) * Nocturia * **TIP**: the obstructive and irritative symptoms can be remembered using the mnemonic **FUND HIPS** * **F**requency * **U**rgency * **N**octuria * **D**ysuria * **H**esitancy * **I**ncomplete voiding * **P**oor stream * **S**mell/odour * **Acute Retention Symptoms** * Sudden inability to pass urine * Associated with _SEVERE PAIN_ * **Chronic Retention Symptoms** * _Painless_ * Frequency - with passage of _small volumes_ of urine * Nocturia is a major feature
54
Recognise the signs of benign prostatic hyperplasia on physical examination
* **DRE** - the prostate is usually smoothly enlarged with a palpable midline groove * NOTE: there is poor correlation between the size and the severity of the symptoms * **Signs of Acute Retention** * Suprapubic pain * Distended, palpable bladder * **Signs of Chronic Retention** * A large distended painless bladder (volume \> 1 L) * Signs of _renal failure_
55
Identify appropriate investigations for benign prostatic hyperplasia
* **Urinalysis** * Check for UTI signs and blood * **Bloods** * U&Es - check for impaired renal function * PSA * **Midstream Urine** * MC&S * **Imaging** * US of urinary tract (check for **hydronephrosis**) * Bladder scanning to measure pre- and postvoiding volumes * **Transrectal Ultrasound Scan (TRUS)** - allows assessment of bladder size and volume * **Flexible Cystoscopy**
56
Generate a management plan for benign prostatic hyperplasia
* **In Emergency** (acute urinary retention) * Catheterisation * **Conservative** (if mild) * Watchful waiting * **Medical** * Selective **a****-blockers** (e.g. tamsulosin) relax the smooth muscle of the internal urinary sphincter and prostate capsule * **5****a****-reductase inhibitors** (e.g. finasteride) will inhibit the conversion of testosterone to dihydrotestosterone, which can reduce prostate size by around 20% * **Surgery** * TURP * Open prostatectomy
57
Identify possible complications of benign prostatic hyperplasia
* Recurrent UTI * Acute or chronic urinary retention * Urinary stasis * Bladder diverticula * Stone development * Obstructive renal failure * Post-obstructive diuresis * **Complications of TURP** * Retrograde ejaculation (you ejaculate up into your bladder because the internal urinary sphincter is relaxed) * Haemorrhage * Incontinence * TURP syndrome * DEFINITION: seizures or cardiovascular collapse caused by _hypervolaemia_ and _hyponatraemia_ due to absorption of glycine irrigation fluid * Urinary infection * Erectile dysfunction * Urethral stricture
58
Summarise the prognosis for patients with benign prostatic hyperplasia
* Mild symptoms are usually well controlled medically * Most patients get significant relief from surgery
59
Chronic Kidney Disease Define chronic kidney disease (CKD)
* *Progressive loss of kidney function over a period of months or years* * The definition is based on the presence of kidney damage or decreased kidney function (i.e. eGFR \< 60 ml/min per 1.73 m2) for three months or more * **Classification of CKD** * **Stage 1: Normal** * eGFR \> 90 ml/min per 1.73 m2 with other evidence of CKD (microalbuminuria, proteinuria, haematuria, structural abnormalities, biopsy showing glomerulonephritis) * **Stage 2: Mild Impairment** * eGFR 60-89 ml/min per 1.73 m2 with other evidence of CKD * **Stage 3a: Moderate Impairment** * eGFR 45-59 ml/min per 1.73 m2 * **Stage 3b: Moderate Impairment** * eGFR 30-44 ml/min per 1.73 m2 * **Stage 4: Severe Impairment** * eGFR 15-29 ml/min per 1.73 m2 * **Stage 5: Established Renal Failure** * eGFR \< 15 ml/min per 1.73 m2 or on dialysis
60
Explain the aetiology/risk factors of CKD
* In developed countries it is mainly associated with: * Age * Diabetes mellitus * Hypertension * Obesity * Cardiovascular disease * Other risk factors: * Arteriopathic renal disease * Nephropathies * Family history * Neoplasia * Myeloma * Systemic disease (e.g. SLE) * Smoking * Chronic use of NSAIDs
61
Summarise the epidemiology of CKD
* COMMON * Risk increases with age * Often associated with other diseases (e.g. cardiovascular disease)
62
Recognise the presenting symptoms of CKD
* Often ASYMPTOMATIC * May be an incidental finding of a routine blood or urine test * Symptoms of Severe CKD: * Anorexia * Nausea and vomiting * Fatigue * Pruritus * Peripheral oedema * Muscle cramps * Pulmonary oedema * Sexual dysfunction is common
63
Recognise the signs of CKD on physical examination
* Physical examination rarely reveals many clues * May show signs of underlying disease (e.g. SLE) * May show complications of CKD (e.g. anaemia) * Signs of CKD: * Skin pigmentation * Excoriation marks * Pallor * Hypertension * Peripheral oedema * Peripheral vascular disease
64
Identify appropriate investigations for CKD
* **Assessment of Renal Function** * **Urea** - not ideal because it varies massively depending on hydration status and diet * **Creatinine** - useful but has limitations. Renal function can drop considerably with minimal change in serum creatinine * **Isotopic GFR** - GOLD STANDARD but expensive * **Biochemistry** * Glucose - check for undiagnosed diabetes and diabetic control * Potassium - raised * Also check sodium, bicarbonate, calcium, phosphate * **Serology** * Antibodies * ANA - SLE * c-ANCA - granulomatosis with polyangiitis (Wegener's) * Anti-GBM - Goodpasture's syndrome * Hepatitis serology * HIV serology * **Urinalysis** * Check for proteinuria/haematuria * 24 hr urine collection * Serum or urine protein electrophoresis - check for multiple myeloma * **Imaging** * Ultrasound - check for structural abnormalities * CT/MRI * X-Ray KUB - check for stones * **Renal Biopsy**
65
Epididymitis and Orchitis Define epididymitis and orchitis
* *Inflammation of the epididymis or testes* * 60% of epididymitis is associated with orchitis * Most cases of orchitis are associated with epididymitis
67
Explain the aetiology/risk factors of epididymitis and orchitis
* Most cases are **INFECTIVE** in origin * **Bacterial** * If \< 35 yrs: *Chlamydia* and *Gonococcus* * If \> 35 yrs: mainly coliforms (e.g. *Enterobacter*, *Klebsiella*) * RARE: TB, syphilis * **Viral** * Mumps * **Fungal** * *Candida* if immunocompromised * 1/3 are **IDIOPATHIC** * **Risk Factors** * Diabetes * Rare: vasculitis (e.g. Henoch-Schonlein purpura)
68
Summarise the epidemiology of epididmytis and orchitis
* COMMON * Affects _all_ age groups * Most commonly: 20-30 yrs
69
Recognise the presenting symptoms of epididymitis and orchitis
* Painful, swollen and tender testis or epididymis * NOTE: less acute onset than testicular torsion * Penile discharge * **IMPORTANT**: ask about _sexual history_
70
Recognise the signs of epididymitis and orchitis on physical examination
* Swollen and tender epididymis or testis * Scrotum may be erythematous and oedematous * Pyrexia * Walking will be painful * Eliciting a cremasteric reflex may be painful
71
Identify appropriate investigations for epididymitis and orchitis
* **Urine** * Dipstick * Early morning urine collections for MC&S * **Bloods** * FBC - high WCC * High CRP * U&Es * **Imaging** * Increased blood flow on duplex examination
72
Generate a management plan for epididymitis and orchitis
* **Medical** * Antibiotics * **Surgical** * Exploration of testicles if testicular torsion _cannot_ be excluded clinically * Required if an abscess develops
73
Identify possible complications of epididymitis and orchitis
* Pain * Abscess * Fournier's gangrene (if the infection is left untreated and spreads) * **Mumps orchitis** could cause testicular atrophy and fertility issues
74
Summarise the prognosis for patients with epididymitis and orchitis
* GOOD if treated * May take up to 2 months for the swelling to resolve
75
Urinary Tract Infection Define urinary tract infection
* *The presence of a pure growth of **\> 105 organisms per mL** of fresh MSU* * Sub-Classification * **Lower UTI** - affecting the urethra (urethritis), bladder (cystitis) or prostate (prostatitis) * **Upper UTI** - affecting the renal pelvis (pyelonephritis) * NOTE: the laboratory classification mentioned above isn't a complete necessity for the diagnosis of UTI - 1/3 women with symptoms of UTI will have negative MSU * **Other Classification** * **Uncomplicated UTI** - normal renal tract and function * **Complicated UTI** - abnormal renal/genitourinary tract, voiding difficulty/obstruction, reduced renal function, impaired host defences, virulent organism (e.g. *S. aureus*)
76
Explain the aetiology/risk factors of urinary tract infection
* MOST UTIs are caused by ***Escherichia coli*** * Other causative organisms: * *Staphylococcus saprophyticus* * *Proteus mirabilis* * *Enterococci* * Atypical organisms that can cause UTI (usually in immunocompromised individuals): * *Klebsiella* * *Candida albicans* * *Pseudomonas aeruginosa* * **Risk Factors** * FEMALE * Sexual intercourse * Exposure to spermicide * Pregnancy * Menopause * Immunosuppression * Catheterisation * Urinary tract obstruction * Urinary tract malformation
77
Recognise the presenting symptoms of urinary tract infections
* **Cystitis** * Frequency * Urgency * Dysuria * Haematuria * Suprapubic pain * **Prostatitis** * Flu-like symptoms * Low backache * Few urinary symptoms * Swollen or tender prostate on PR * **Acute Pyelonephritis** * High fever * Rigors * Vomiting * Loin pain and tenderness * Oliguria (if AKI)
78
Summarise the epidemiology of urinary tract infections
* VERY COMMON * 1-3% of GP consultations * The majority of women will have a UTI in their lifetime * MUCH more common in FEMALES
80
Recognise the signs of urinary tract infection on physical examination
* Fever * Abdominal or loin tenderness * Foul-smelling urine * Distended bladder (occasionally) * Enlarged prostate (if prostatitis)
81
Identify appropriate investigations for urinary tract infection
* **Urine Dipstick** * Positive leucocyte esterase and nitrites * **Urine Microscopy** * Presence of leucocytes indicates infection * **Urine Culture** * To exclude diagnosis or if the patient failed to respond to empirical antibiotics * **Ultrasound** * Rule out obstruction * **Bloods** * FBC * U&Es - check renal function * CRP * Blood cultures - if systemically unwell and risk of urosepsis
82
Generate a management plan for urinary tract infection
* Empirical treatment of uncomplicated UTI: **TRIMETHOPRIN _or_ NITROFURANTOIN** * Treat for 3-6 days * NOTE: men with UTI may need a _longer_ course of antibiotics * Alternative Treatments: **Co-amoxiclav** or **Cefalexin** * Prophylactic antibiotics may be used in certain circumstances (e.g. recurrent cystitis associated with sexual intercourse)
83
Identify possible complications of urinary tract infection
* Ascending infection can lead to: * Pyelonephritis * Perinephric and intrarenal abscess * Hydronephrosis or pyonephrosis * AKI * Sepsis * Prostatic involvement (e.g. prostatitis) in men with UTIs is common **Summarise the prognosis for urinary tract infection** * GOOD prognosis with appropriate treatment
84
Amyloidosis Define amyloidosis
* *Heterogenous group of diseases characterised by **extracellular deposition of amyloid fibrils***
85
Explain the aetiology/risk factors of amyloidosis
* Amyloid fibrils are _polymers_ of low-molecular-weight subunit proteins * These are derived from proteins that undergo conformational changes to adopt an anti-parallel beta-pleated sheet configuration * Their deposition progressively _disrupts the structure and function of normal tissue_ * Amyloidosis is classified according to the **fibril subunit proteins** * **Type AA** - serum amyloid A protein * **Type AL** - monoclonal immunoglobulin light chains * **Type ATTR** (familial amyloid polyneuropathy) - genetic-variant transthyretin
86
Summarise the epidemiology of amyloidosis
* **AA** - incidence of 1-5% amongst patients with chronic inflammatory diseases * **AL** - 300-600 cases in the UK per year * **Hereditary Amyloidosis** - accounts for 5% of patients with amyloidosis
87
Recognise the presenting symptoms and signs of amyloidosis
* **Renal** - proteinuria, nephrotic syndrome, renal failure * **Cardiac** - restrictive cardiomyopathy, heart failure, arrhythmia, angina * **GI** - macroglossia (characteristic of **AL**), hepatosplenomegaly, gut dysmotility, malabsorption, bleeding * **Neurological** - sensory and motor neuropathy, autonomic neuropathy, carpal tunnel syndrome * **Skin** - waxy skin and easy bruising, purpura around the eyes (characteristic of **AL**), plaques and nodules * **Joints** - painful asymmetrical large joints, enlargement of anterior shoulder * **Haematological** - bleeding tendency
89
Identify appropriate investigations for amyloidosis
* **Tissue Biopsy** * **Urine** - check for proteinuria, free immunoglobulin light chains (in AL) * **Bloods** * CRP/ESR * Rheumatoid factor * Immunoglobulin levels * Serum protein electrophoresis * LFTs * U&Es * **SAP Scan** - radiolabelled SAP will localise the deposits of amyloid
90
Glomerulonephritis Define glomerulonephritis
* *An _immunologically mediated_ inflammation of the renal glomeruli*
91
Explain the aetiology / risk factors of glomerulonephritis
* There are loads of different types of glomerulonephritis with different aetiologies * Some types are caused by the **deposition of antigen-antibody complexes in the glomeruli** * This leads to inflammation and activation of complement and coagulation cascades * The immune complexes may form within the glomerulus (more common) or be deposited from the circulation * The antigens to which the antibodies are produced are _UNKNOWN_ but may be associated with: * Bacteria (e.g. *Streptococcus viridans*, Staphylococci) * Viruses (e.g. HBV, HCB, measles, mumps, EBV) * Protozoal (e.g. *Plasmodium malariae*, schistosomiasis) * Inflammatory/Systemic diseases (e.g. SLE, vasculitis, cryoglobulinaemia) * Drugs (e.g. gold, penicillinamine) * Tumour * **Classification** is based on the site of nephron pathology and its distribution * **Minimal-change Glomerulonephritis** * Light microscopy - minimal change * Electron microscopy - loss of epithelial foot process * **Membranous Glomerulonephritis** * Thickening of glomerular basement membrane (GBM) from _immune complex deposition_ * Associated with **Goodpasture's Syndrome** * **Membranoproliferative Glomerulonephritis (MPGN)** * Thickening of GBM * Mesangial cell proliferation and interdeposition * **Focal segmental glomerulosclerosis** * Glomerular scarring * Associated with HIV * **Focal segmental proliferative glomerulonephritis** * Mesangial and endothelial cell proliferation * Focal = involvement of some glomeruli * Segmental = involvement of parts of individual glomeruli * **Diffuse proliferative glomerulonephritis** * Same as above but affects _ALL_ glomeruli * **IgA Nephropathy** * Mesangial cell proliferation * Mesangial IgA and C3 deposits * **Crescentic Glomerulonephritis** * Crescent formation by macrophages and epithelial cells, which fills up Bowman's space * **Focal Segmental Necrotising Glomerulonephritis** * Peripheral capillary loop necrosis (occurs in granulomatosis with polyangiitis, microscopy polyarteritis and other vasculitides) * Often evolves into crescentic glomerulonephritis NOTE: **cryoglobulins** are immunoglobulins that _precipitate in the cold_
92
Summarise the epidemiology of glomerulonephritis
* Accounts for 25% of the cases of chronic renal failure
93
Recognise the presenting symptoms of glomerulonephritis
* Haematuria * Subcutaneous oedema * Polyuria or oliguria * History of recent infection * Symptoms of **uraemia** or **renal failure** (acute and chronic)
94
Recognise the signs of glomerulonephritis on physical examination
* Hypertension * Proteinuria * Haematuria (especially in IgA nephropathy) * Renal failure * Nephrotic syndrome - consists of a TRIAD of: * Proteinuria **\> 3.5 g/24 hrs** * Low serum albumin **\< 24 g/L** * Oedema * NOTE: due to the hypoalbuminaema, the liver tries to compensate and increases production of lipids, causing **hyperlipidaemia** * Nephritic syndrome (TRIAD: **hypertension** + **proteinuria** + **haematuria**) * Syndrome comprising of signs of nephritis * Pores in the podocytes are large enough to allow protein _AND_ red blood cells to pass into the urine * MAIN FEATURE: **Haematuria** * This is in contrast to nephrotic syndrome, which is mainly concerned with **proteinuria** * There may also be **red cell casts** in the urine - indicative of glomerular damage * Other features: * Proteinuria * Hypertension * Low urine output (due to decreased renal function) * NOTE: in _nephrotic_ syndrome, **only PROTEINS** are moving into the urine
95
Identify appropriate investigations for glomerulonephritis
* **Bloods** * FBC * U&Es + creatinine * LFTs (check albumin) * Lipid profile * Complement studies * Antibodies: * ANA * Anti-dsDNA * ANCA * Anti-GBM antibody * Cryoglobulins * **Urine** * Microscopy - check for red cell casts * 24 hr collection: creatinine clearance and protein * **Imaging** * Renal tract ultrasound to exclude other pathology (e.g. obstruction) * **Renal Biopsy** * For microscopy * **Investigations for associated conditions** (e.g. HBV, HCV and HIV serology)
96
Hydrocoele Define hydrocoele
* *The excessive collection of serous fluid within the **tunica vaginalis***
97
Explain the aetiology/risk factors of hydrocoeles
* Congenital * Idiopathic * Tumour * Infection * Trauma * Underlying testicular torsion * Testicular appendage * **Risk Factors/Associations** * Indirect inguinal hernias in children * Epididymo-orchitis * Filariasis (in countries of high prevalence)
98
Summarise the epidemiology of hydrocoeles
* VERY COMMON in **CHILDREN** in the _first year of life_ * Common in **older men**
99
Recognise the presenting symptoms of hydrocoeles
* Scrotal swelling * Usually ASYMPTOMATIC * Patients may complain of _pain_ or _urinary symptoms_ due to the **underlying cause**
100
Recognise the signs of hydrocoeles on physical examination
* Scrotal swelling * It is possible to get above the swelling * Transilluminates * Difficult to separate the swelling from the testicle
101
Identify appropriate investigations for hydrocoeles
* Ultrasound - exclude tumour * Urine - dipstick and MSU for infection * Blood - markers of testicular tumours: * a-fetoprotein * b-HCG * Lactate dehydrogenase
102
Nephrotic Syndrome Define nephrotic syndrome
* *Nephrotic syndrome is characterised by a triad of:* * ***Proteinuria*** *(\> 3 g/24 hr)* * ***Hypoalbuminaemia*** *(\< 30 g/L)* * ***Oedema*** * *Hypercholesterolaemia is also a common feature*
103
Explain the aetiology / risk factors of nephrotic syndrome
* Most commonly caused by: **minimal change glomerulonephritis in children** * However, _ALL_ forms of glomerulonephritis can cause nephrotic syndrome * Other causes: * Diabetes mellitus * Sickle cell disease * Amyloidosis * Malignancies (lung and GI adenocarcinomas) * Drugs (e.g. NSAIDs) * Alport's syndrome * HIV
104
Summarise the epidemiology of nephrotic syndrome
* 90% of nephrotic syndrome in _CHILDREN_ is due to **minimal change glomerulonephritis** * Most common cause of nephrotic syndrome in _ADULTS_: * Diabetes mellitus * Membranous glomerulonephritis
105
Recognise the presenting symptoms of nephrotic syndrome
* Family history of atopy (in those with minimal change glomerulonephritis) * Family history of renal disease * Swelling of face, abdomen, limbs, genitalia (due to hypoalbuminaemia) * Symptoms of the underlying cause (e.g. SLE) * Symptoms of complications
106
Recognise the signs of nephrotic syndrome on physical examination
* Oedema: periorbital, peripheral, genital * Ascites: fluid thrill, shifting dullness
107
Identify appropriate investigations for nephrotic syndrome
* **Bloods** * FBC * U&E * LFTs (low albumin) * ESR/CRP * Glucose * Lipid profile (check for secondary hyperlipidaemia) * Immunoglobulins * Complement * **Tests to identify the cause** * **SLE** - ANA, anti-dsDNA antibodies * **Infections**: * Group A b-haemolytic streptococcal infection (ASO titre) * HBV infection (serology) * *Plasmodium malariae* (blood film) * **Goodpasture's Syndrome** - anti-glomerular basement antibodies * **Vasculitides** - polyangiitis with granulomatosis, microscopic polyarteritis (check ANCA) * **Urine** * Urinalysis (check protein and blood) * MC&S * 24 hr collection (calculate creatinine clearance and 24 hr protein excretion) * **Renal Ultrasound** * Exclude other causes (e.g. reflux nephropathy) * **Renal Biopsy** * **Other imaging**: Doppler ultrasound, renal angiogram, CT or MRI (if renal vein thrombosis suspected)
108
Polycystic Kidney Disease Define polycystic kidney disease
* *_Autosomal dominant_* *inherited disorder characterised by the development of **multiple renal cysts** that gradually expand and replace normal kidney substance, variably associated with extrarenal (liver and cardiovascular) abnormalities*
109
Explain the aetiology / risk factors of polycystic kidney disease
* 85% caused by mutations in **PKD1** on chromosome 16 * This is a membrane-bound multidomain protein involved in cell-cell and cell-matrix interactions * 15% caused by mutations of **PKD2** on chromosome 4 * **Pathophysiology** * Proliferative/hyperplastic abnormality of the tubular epithelium * Early on, the cysts are connected to the tubules from which they arise and the fluid content is _glomerular filtrate_ * When cyst diameter \>2 mm, they detach from the tubule and the fluid content is derived from _secretion of the lining epithelium_ * With time, the cysts enlarge and **cause progressive damage to adjacent functioning nephrons**
110
Summarise the epidemiology of polycystic kidney disease
* MOST COMMON inherited kidney disorder * Responsible for **10%** of end-stage renal failure
111
Recognise the presenting symptoms of polycystic kidney disease
* Present at **30-40 yrs** * 20% have _no family history_ * May be **asymptomatic** * **Flank Pain** - may result from cyst enlargement/bleeding, stone, blood clot migration, infection * Haematuria * Hypertension * Associated with **berry aneurysms** and may present with **subarachnoid haemorrhage**
112
Recognise the signs of polycystic kidney disease on physical examination
* Abdominal distension * Enlarged cystic kidneys * Palpable liver * Hypertension * Signs of chronic renal failure (at late stage) * Signs of associated AAA or aortic valve disease
113
Identify appropriate investigations for polycystic kidney disease
* **US or CT** * Will show multiple cysts bilaterally in _enlarged kidneys_ * Liver cysts may also be seen
114
**Renal Artery Stenosis** **Define renal artery stenosis** * *Stenosis of the renal artery* **Explain the aetiology / risk factors of renal artery stenosis**
* **Atherosclerosis** (older patients) - widespread aortic disease involving the _renal artery ostia_ * **Fibromuscular Dysplasia** (younger patients) * Unknown aetiology * May be associated with collagen disorders, neurofibromatosis and Takayasu's arteritis * May be associated with micro-aneurysms in the mid and distal renal arteries (resembling a _string of beads_ on angiography) * **Pathogenesis/Pathophysiology** * Renal hypoperfusion (due to the stenosis) stimulates the renin-angiotensin system leading to **increased angiotensin II** and **increased aldosterone** * This leads to **increased blood pressure** * The high blood pressure leads to **fibrosis**, **glomerulosclerosis** and **renal failure**
115
Summarise the epidemiology of renal artery stenosis
* Prevalence unknown * Accounts for 1-5% of all hypertension * Fibromuscular dysplasia occurs mainly in _women with hypertension \< 45 yrs_
116
Recognise the presenting symptoms of renal artery stenosis
* History of hypertension in \< 50 yrs * Hypertension _refractory to treatment_ * Accelerated hypertension and renal deterioration on starting ACE inhibitors * History of flash pulmonary oedema * **IMPORTANT: ACE INHIBITORS ARE BAD IN RENAL ARTERY STENOSIS**
117
Recognise the signs of renal artery stenosis on physical examination
* Hypertension * Signs of renal failure in advanced bilateral disease * Renal artery bruits
118
Identify appropriate investigations for renal artery stenosis
* **Non-Invasive** * Duplex ultrasound * Ultrasound measurement of kidney size * **CT Angiogram or MR Angiography**: risk of contrast nephrotoxicity * **Digital Subtraction Angiography** = GOLD STANDARD * **Renal Scintigraphy** * Uses radio-agent that is either excreted by glomerular filtration or by the tubules * Addition of an ACE inhibitor causes _delayed clearance_ by the affected kidney (may not be useful in bilateral renal artery stenosis)
119
Testicular Torsion Define testicular torsion
* *A* ***SURGICAL EMERGENCY****. Twisting or torsion of the spermatic cord results, initially, in venous outflow obstruction from the testicle, progressing to arterial occlusion and testicular infarction if not corrected.*
120
Explain the aetiology/risk factors of testicular torsion
* **Intravaginal (MOST COMMON)** * The spermatic cord twists _within_ the tunica vaginalis * **Extravaginal** (usually in _neonates_) * The entire testis and tunica vaginalis twist in a vertical axis on the spermatic cord * Due to incomplete fixation of the gubernaculum to the scrotal wall allowing free rotation * **Risk Factors** * Imperfectly descended testes * High investment of the tunica vaginalis
121
Summarise the epidemiology of testicular torsion
* Most common cause of _acute scrotal pain_ in 10-18 yr olds
122
Recognise the presenting symptoms of testicular torsion
* Sudden-onset severe hemiscrotal pain * Abdominal pain * Nausea and vomiting
123
Recognise the signs of testicular torsion on physical examination
* Swollen, erythematous scrotum on the affected side * Swollen testicle will lie _slightly higher_ than the unaffected one * Testicle might lie horizontal * Thickened cord * **Testicular Appendix** * There may be a visible necrotic lesion on transillumination * **Differential Diagnosis** * Epididymo-orchitis * Incarcerated inguinal hernia
124
Identify appropriate investigations for testicular torsion
* **Doppler/Duplex Imaging of the Testes** * Do _NOT_ delay surgery * Arterial inflow * REDUCED in testicular torsion * INCREASED in epididymo-orchitis
125
Generate a management plan for testicular torsion
* Exploration of the scrotum **within 6 hrs** of onset of symptoms * After the testicle is twisted back into place, a **bilateral orchidopexy** is performed * This involves suturing the testicle to the scrotal tissue to prevent recurrence * If the testicle is **necrotic**, orchidectomy may be performed
126
Identify possible complications of testicular torsion
* Testicular infarction * Testicular atrophy * Infection * Impaired fertility (due to production of anti-sperm antibodies)
127
Summarise the prognosis for patients with testicular torsion
* From the onset of torsion, a testicle may only survive **4-6 hrs** * With prompt surgical intervention, most testicles are salvaged
128
Urinary Tract Calculi Define urinary tract calculi
* *Crystal deposition within the urinary tract. Also known as **nephrolithiasis**.* * Types of Stone: * Calcium oxalate - MOST COMMON * Struvite - quite common * Urate - 5% * Cysteine - 2%
129
Explain the aetiology/risk factors of urinary tract calculi
* Many cases are IDIOPATHIC * **Metabolic Causes** * Hypercalciuria * Hyperuricaemia * Hypercystinuria * Hyperoxaluria * **Infection** * Hyperuricaemia * **Drugs** * Indinavir * **RISK FACTORS**: * Low fluid intake * Structural urinary tract abnormalities (e.g. horseshoe kidney)
130
Summarise the epidemiology of urinary tract calculi
* COMMON * 2-3% of general population * 3 x more common in MALES * Age group affected: 20-50 yrs * Bladder stones more common in developing countries * Upper urinary tract stones more common in industrialised countries
131
Recognise the presenting symptoms of urinary tract calculi
* Often ASYMPTOMATIC * **SEVERE loin to groin pain** * Nausea and vomiting * Urinary urgency, frequency or retention * Haematuria
132
Recognise the signs of urinary tract calculi on physical examination
* Loin to lower abdominal tenderness * _NO_ signs of peritonism * **Leaking AAA** is the main differential to consider in older men * Signs of _systemic sepsis_ if there is an obstruction and infection above the stone
133
Identify appropriate investigations for urinary tract calculi
* **Bloods** * FBC - high WCC if infection * U&Es - check renal function * Calcium * Urate * Phosphate * **Urine** * Dipstick - haematuria is common * MC&S * **X-Ray KUB** * 80% of kidney stones are radio-opaque * **Intravenous Urography (IVU)** * Allows visualisation of the kidneys and ureters * **Ultrasound** * May show hydronephrosis and hydroureter * **Non-enhanced Spiral CT** * Can also be used to image stones * **Isotope Radiography** * Used to assess kidney function
134
Generate a management plan for urinary tract calculi
* **ACUTE PRESENTATION** * Analgesia * Bed rest * Fluid replacement * Urine collection to try and retrieve any stone that has passed * NOTE: most stones **\< 5 mm** will pass spontaneously * An **obstructed, infected kidney** is an EMERGENCY and should be treated as soon as possible to relieve the obstruction (e.g. by placing a percutaneous nephrostomy) * **REMOVAL OF CALCULI** * **Urethroscopy** * A scope is passed into the bladder and up the ureter to visualise the stone * It can then be removed by a basket or broken up with a laser * If the stone cannot be removed, a **JJ stent** should be placed to allow urine drainage * **Extracorporeal Shock-Wave Lithotripsy (ESWL)** * Non-invasive * An electromagnetic shockwave is focused onto the calculus to break it up into smaller fragments that can pass spontaneously * **Percutaneous Nephrolithotomy (PCNL)** * Performed for large, complex stones (e.g. staghorn calculi) * After making a nephrostomy tract, a nephroscope is inserted, which allows disintegration and removal of stones * **TREATMENT OF CAUSE** * Depends on the cause (e.g. parathyroidectomy if hypercalcaemia due to hyperparathyroidism, allopurinol if hyperuricaemia) * **ADVICE** * Increase oral fluid intake
135
Identify possible complications of urinary tract calculi
* **Of Stones** * Infection (**PYELONEPHRITIS**) * Septicaemia * Urinary retention * **Of Ureteroscopy** * Perforation * False passage * **Of Lithotripsy** * Pain * Haematuria
136
Summarise the prognosis for patients with urinary tract calculi
* GOOD * However, infection of the calculus could lead to irreversible renal scarring * Recurrence of about **50%** over 5 yrs
137
Varicocoele Define varicocoele
* DEFINITION: *dilated veins of the **pampiniform plexus** forming a scrotal mass.*
138
Explain the aetiology/risk factors of varicocoele
* More common on the **LEFT** (80-90%) because of: * The angle at which the left testicular vein meets the left renal vein * Lack of effective valves between the left testicular vein and left renal vein * Increased reflux from compression of the renal vein (between the superior mesenteric artery and the aorta) * Due to venous incompetence (sort of like varicose veins)
139
Summarise the epidemiology of varicocoele
* Unusual in boys under 10 yrs old * Incidence increases after puberty * Incidence: 15% in general population * Associated with infertility
140
Recognise the presenting symptoms of varicocoele
* Usually ASYMPATOMATIC * Only 2-10% have symptoms * Scrotum feels like a ***bag of worms*** * Scrotal heaviness * Incidental finding at examination
141
Recognise the signs of varicocoele on physical examination
* Patient must be _STANDING_ for examination * The side of the scrotum with the varicocoele will _hang lower_ * The swelling may _reduce_ when lying down * **Valsalva manouevre** whilst standing will increase dilatation * Cough impulse
142
Identify appropriate investigations for varicocoele
* Sperm count - done as part of fertility investigation * Colour Doppler scan