Questions I got wrong from 2004 Flashcards

1
Q

Diagnosis?
A 22-year-old woman, on treatment for nephrotic syndrome due to minimal change glomerulonephritis. She is concerned by increasing weight gain and easy bruising. Blood tests show plasma creatinine 65 μmol/L and albumin 31 g/L.

A

Cushing’s syndrome.
Corticosteroids remain the mainstay of treatment for minimal change disease and is given to all patients. Minimal change disease is the most common form of nephrotic syndrome in children and it is so named as there are minimal histological changes in renal tissue. 90% are idiopathic. Long term coricosteroid treatment here has induced iatrogenic Cushing’s syndrome with associated signs of hypercorticalism (weight gain and easy bruising). Corticosteroid-sparing therapies can be added here.

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

Diagnosis?
A 45-year-old HCV positive Egyptian journalist presents with acute renal failure. He is complaining of increasing abdominal distension, pruritis, ankle oedema and weight gain. Serum albumin is low and there is hyponatraemia and thrombocytopenia.

A

Portal hypertension.
HCV in this patient is causing hepatic cirrhosis which has decompensated resulting in ascites, secondary to portal hypertension. The hypoalbuminaemia is a sign of decreased hepatic synthetic function. Hyponatraemia is a common finding associated with ascites. It arises due to reduced protein synthesis and therefore a loss of colloid osmotic pressure and increased fluid loss from the intravascular compartment, stimulating ADH secretion. There is peripheral oedema here which is due to low albumin. The pruritis is due to reduced hepatic excretion of conjugated bilirubin and there may be accompanying jaundice too. The cause of his renal failure may well be hepatorenal syndrome in the context of his severe liver disease. His prognosis is poor.

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

What analgesia should NOT be used in the postoperative period?
An 85-year-old who is known to be hypertensive and has mild impaired renal function presents with signs of dehydration and undergoes a laparotomy for small bowel obstruction.

A

Diclofenac.
NSAIDS may impair renal function and provoke renal failure, especially in patients with pre-existing impairment. NSAIDs should be avoided if possible in these patients or used with caution at the lowest effective dose for the shortest possible time. The mechanism of damage involves reducing creatinine clearance. NSAIDs are also contraindicated in asthmatics as it causes bronchospasm due to the accumulation of leukotrienes.

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

What analgesia should NOT be used in the postoperative period?
A 60-year-old man with diabetes is transferred from another hospital for urgernt femoral-distal bypass surgery and arrives with a heparin infusion in situ. His APTT is 2.4.

A

Epidural bupivacaine and fentanyl.
Epidurals are relatively contraindicated in anticoagulated patients. Insertion of the epidural needle may lead traumatic bleeding into the epidural space and with clotting abnormalities, the development of a haematoma which can lead to spinal cord compression. Coagulopathy, raised ICP and infection at the injection site are absolute contraindications. Relative contraindications include anticoagulated patients and those with anatomical abnormalities of the vertebral column. NSAIDs do not increase the risk of epidural haematoma.

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

What analgesia should NOT be used in the postoperative period?
A 62-year-old man who requires a knee replacement gives a history of allergy to dihydrocodeine.

A

Codydramol.
Co-dydramol is a combination of dihydrocodeine and paracetamol and the patient is known to be allergic to dihydrocodeine.

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

What analgesia should NOT be used in the postoperative period?
A 65-year-old man with a history of peptic ulceration requires an aortic aneurysm repair electively.

A

Diclofenac.
NSAIDs inhibit COX which has the effect of reducing PGE2 levels. PGE2 plays a role in gastric cytoprotection by downregulating HCl production and increasing mucus and the production of bicarbonate. This leads to gastric irritation and ulceration. A PPI can be prescribed alongside NSAIDs or misoprostol can be used, which is a stable PGE1 analogue which mimics local PG to maintain the gastroduodenal mucosal barrier.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Diagnosis?
A middle-aged tramp presents in A&E intoxicated and confused. He has a half-finished bottle of vodka in his pocket. Additionally there is horizontal gaze palsy and severe ataxia with vertigo and headache.

A

Wernicke’s encephalopathy.
Wernicke’s is due to acute thiamine deficiency, which is a problem in alcoholics. Others at risk include those with AIDS, cancer and treatment with chemotherapy, malnutrition and GIT surgery, especially bariatric procedures. It is a clinically under-diagnosed condition. The classic EMQ triad is of mental change, ophthalmoplegia and gait dysfunction, which is actually only seen in 10% of cases. In reality, the manifestations are varied and a high index of suspicion is needed. Despite there, the manifestiations typically include altered consciousness, gait disorders and eye movement abnormalities. This is an emergency and treatment is with parenteral replacement of thiamine. This avoids permanent neurological damage including later development of Korsakoff’s psychosis, which is irreversible. Note that thiamine should be given before dextrose! Magnesium deficiency also needs to be corrected as it is a co-factor in the functioning of thiamine dependent enzymes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Most appropriate treatment?

A 55-year-old Asian man complaining of nocturia. Random blood glucose 10.2 mmol/L. He was overweight.

A

Dietary advice alone.
This patient is symptomatic and has a random blood glucose of 10.2. This patient does not quite meet the diagnostic criteria for DM. Symptomatic patients need a single random blood glucose of >11.1 or single fasting glucose of >7. Asymptomatic patients need two separate elevated readings for a diagnosis. Alternatively if there are borderline results, an OGTT can be conducted to see if plasma glucose is raised >11.1 two hours after an oral glucose load of 75g. A patient is said to have impaired fasting glucose if fasting glucose falls between 6.1-6.9. Impaired glucose tolerance is present if plasma glucose 2 hours after oral glucose load in OGTT falls between 7.8-11.0. First line intervention in this situation, and in newly diagnosed DM is diet and lifestyle advice and changes.

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

Most appropriate treatment?

A 47-year-old man with diabetes for 10 years. At review, his BP was 130/80, a glycosylated haemoglobin was 8.2% (normal

A

Oral hypoglycaemic drug.
Careful dietary intervention has failed to keep HbA1c in check so the patient will need to be started on an oral hypoglycaemic drug. First line is metformin. It is worth noting that HbA1c values, since June 2011, are no longer expressed as a percentage and are now given in mmol/mol. HbA1c is glycated Hb and provides an estimation of glycaemic control over the life span of red blood cells (around 60 days). Fructosamine is measured instead if there is a Hb disorder or RBC life span is decreased as HbA1c is only reliable if normal Hb is present with normal RBC life spans. Fructosamine is a glycated plasma protein which provides information on glucose levels over the previous 1-3 weeks.

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

Diagnosis?
An 80-year-old woman is admitted from a residential home with a two week history of purulent sputum and pyrexia (38ºC). Examination reveals a constant wheezing in inspiration and expiration localised over the right lung base.

A

Inhaled foreign body.
This is aspiration pneumonia. There are symptoms of pneumoia with pyrexia and purulent sputum, along with risk factors for aspiration in this elderly person who may have difficulties swallowing or altered mental status from, for example, dementia. The location of the wheeze is also consistent with this diagnosis as the RLL is the most common site due to the anatomy of the bronchial tree. Complications include abscess and empyema. Treatment is predominantly with antibiotics and supportive care.

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

Diagnosis?
A 64-year-old diabetic man presents with sudden onset of severe SOB and cough productive of frothy sputum. Examination reveals BP 70/50 mmHg; P 90/min, faint wheeze and scattered fine rales.

A

Left ventricular failure.
DM is a cardiovascular risk factor. There are no expressed signs or symptoms of RVF here such as peripheral oedema, ascites, elevated JVP and hepatomegaly. Nocturia may be a symptom as fluid returns from the legs when the patient lies down flat. RVF leads to a backlog of blood and congestion of the systemic capillaries. LVF, on the other hand, causes congestion in the pulmonary circulation so the symptoms are respiratory. As seen in this patient, there is SOB and the classic cough productive of frothy sputum – a sign of pulmonary oedema. On respiratory examination, pulmonary oedema due to LVF may give audible fine late inspiratory crepitations at the bases. There may also be orthopnoea. This is why you can ask patients in a cardiac history how many pillows they sleep with. PND can also occur as well as ‘cardiac asthma’.

Initial investigations should include ECG, CXR, TTE and bloods including BNP levels. First line treatment is with an ACE inhibitor which reduces morbidity and mortality. Salt and fluid restriction is also beneficial. All patients with chronic heart failure will also receive a beta blocker such as carvedilol. Other adjuncts include spironolactone, diuretics, hydralazine and a nitrate, and digoxin. The NYHA classification criteria can be used based on symptoms to describe functional limitations and ranges from Class I to Class IV with symptoms occuring at rest. Many patients are asymptomatic for long periods of time because mild cardiac impairment is balanced by compensation.

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

Diagnosis?
A 65-year-old man had an inferior myocardial infarct 10days ago. His initial course was uncomplicated. He suddenly deteriorates with acute left ventricular failure. On examination the pulse is regular 100/min and normal volume and character. BP 110/60. The apex beat is dynamic. There is a loud grade 3/6, apical pansystolic murmur which radiates to the axilla.

A

Mitral regurgitation.
MR is loudest at the apex and radiates to the axilla and tends to be around grade 4. It is associated with a systolic thrill at the apex. TTE is the investigation of choice for diagnosis. Chronic MR is associated with a laterally displaced apex beat with LV dilatation. Mitral valve prolapse is a strong risk factor for development of MR.

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

Most appropriate professional to expedite discharge?
A 75-year-old woman was admitted to Care of the Elderly ward having had a couple of falls at home. No other medical problems are found. She lives on her own in a ground floor flat and has home help once a week.

A

Occupational therapist.
Occupational therapists will visit the patient’s home and help determine tools and facilities the patient can benefit from for their day to day life e.g. stairlifts, bath rails

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

Most appropriate professional to expedite discharge?
A 78-year-old woman was admitted six weeks ago with a fractured neck of femur. She lives with her husband in a first-floor flat with no lift. The nurses are worried how she is going to manage at home because she is not mobilising in the ward.

A

Physiotherapist.
Physiotherapists work with patients who have physical difficulties to identify and improve movement and function. This will involve, for example, encouraging movement and exercise using a range of techniques.

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

Most appropriate professional to expedite discharge?
A 65-year-old man with a long history of hypertension. He is admitted with sudden loss of speech. He is found to be aphasic and has minimal right-sided weakness. He is keen to go home.

A

Speech and language therapist.
Would you discharge this patient in their present state? This patient needs a swallowing assessment and speech therapy from a SALT. SALTs deal with disorders of speech, communication, language and swallowing. They are particularly useful after neurological impairments and conditions including stroke, head injury, Parkinson’s and dementia. In the film ‘The King’s Speech’ starring acclaimed actor and heartthrob Colin Firth, George VI gets help with his stammer from Logue who is a speech and language therapist.

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

Most appropriate professional to expedite discharge?
A 56-year-old man is admitted with chest pain. Exercise ECG is normal but his random blood sugar on admission was 23 mmol/l. He is overweight and being referred to the diabetic clinic as an outpatient.

A

Dietician.
This patient has possible DM (needs a second test result to be diagnostic or needs to be symptomatic). The first line intervention is dietary and lifestyle changes. The most useful person this patient will benefit from is a dietician who will be able to give him advice on his eating habits – a diet high in fibre and low in fat is recommended and to also cut, to a degree, carbohydrate intake or at least resort to carbohydrates with a high glycaemic index such as lentils and sweet potato. The GI measures the effect carbohydrates have on blood sugar levels – a lower GI has more of an impact on blood sugar levels in a shorter amount of time. Advice will also be given on how to deal with hypoglycaemic episodes if the patient is being treated with medication which predisposes to this risk, such as insulin.

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

Most appropriate professional to expedite discharge?
A 68-year-old diabetic woman with venous ulcers was admitted with cellulites. The acute infection has now cleared but she needs regular compression dressings to help the ulcers heal.

A

District nurse.
District nurses visit people in their homes or in care homes and provide care in that context. They also provide teaching in the community.
Always remember that an MDT ethos is needed for most cases. This is especially true for stroke patients.

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

Diagnosis?

A 35-year-old woman has a 10-year history of low retrosternal dysphagia and painless regurgitation of food in the mouth.

A

Hiatus hernia.
A hiatus hernia is where intraabdominal contents protrude through the oesophageal hiatus of the diaphragm. Risk factors inclyde obesity and high intra-abdominal pressure. The condition may be asymptomatic, or it may present with symptoms (which are non-specific) such as heartburn, dysphagia, pain on swallowing, wheezing, hoarseness and chest pain. A CXR is the first test done and may show an air bubble in the wrong place but barium studies are diagnostic and treatment depends on the symptoms and anatomy of the hernia. Hernias can be sliding or rolling (or mixed, or giant), uncomplicated or complicated by, for instance, obstruction and bleeding. Do you know the difference between a sliding and a rolling hiatal hernia?

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Diagnosis?

A 45-year-old lady presents with retrosternal dysphagia. She has spoon-shaped nails and is noted to be pale.

A

Plummer-Vinson syndrome.
Plummer-Vinson syndrome is the association of chronic IDA (shown here by the koilonychia and paleness on examination) with dysphagia due to a post cricoid web. Roughly 7% of those with IDA may complain of gradual onset dysphagia with the discomfort found in the area of the cricoid cartilage. Invasive procedures may be needed for management such as endoscopic dilation of the web but treatment is largely aimed at correcting the IDA.

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

Diagnosis?
A 50 year old describes a 5 month history of heartburn and cramp-like chest pain relived by drinking cold water, both unrelated to food. There has also been intermittent dysphagia to both liquids and solids, regurgitation and weight loss of 2kg.

A

Achalasia.
This is achalasia which is a motility disorder with loss of peristalsis in the distal oesophagus and failure of the LOS to relax in response to swallowing. This presents commonly with dysphagia to both liquids and solids, regurgitation and retrosternal chest pain, which can be slowly progressive over time. In structural obstruction such as cancer, dysphagia to liquids is uncommon unless the disease is very advanced. Retrosternal pressure experienced can be precipitated by drinking liquids but is eased by continuing to drink, and the pain may be relieved by cold water. This may wake the individual from sleep. A UGI endoscopy is needed to exclude malignancy as a cause of dysphagia. The diagnosis is established on manometry or barium studies. Treatment is symptomatic.

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

Diagnosis?
A 22-year-old student went to Thailand on holiday. A week following his return, he presented to his GP with a flu like illness and high fever. His GP presumed it was flu and told him to go home. Two days later, he re-presented to A&E, this time vomiting.

A

Falciparum malaria.
In the Western world, almost all cases of malaria occurs in travellers so an adequate travel history is crucial or the diagnosis may be missed. Patients typically present with non-specific symptoms such as a fever, sweats, chills and myalgia. This student has just returned from an endemic area. Sometimes EMQs will describe patterns of fevers occuring at regular intervals of 48-72 hours associated with P. vivax, P. ovale and P. malariae infections but in most patients there is no specific pattern. Hepatosplenomegaly is a common presenting sign although not common at presentation in a first world setting. Thrombocytopenia is common with falciparum infection and a mild degree of anaemia are commonly seen. WCC can be high, low or normal.
Dengue presents abruptly with typically headache and retrobulbar pain worsening with eye movement. There may also be a rash and leukopenia and thrombocytopenia are common.

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

Most appropriate initial management?
A 80-year-old woman is admitted with vomiting. Her blood pressure is 120/80 mmHg, pulse rate 90/min, with warm peripheries. Plasma urea is 25 mmol/l, and creatinine 120 μmol/l.

A

Intravenous saline.

This patient is very dehydrated

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

Most appropriate initial management?
A 25-year-old woman is admitted semi-comatose. She has been complaining of increasing thirst and lethargy over the previous few weeks. BM stick result is 36 mmol/l. Blood pH is 7.10 with a HCO3- of 15 mmol/l.

A

Intravenous saline.
Initial treatment of DKA aims at correcting severe volume depletion (the main problem), again with IV saline infusion at a rate of 1-1.5L for the first hour. When glucose reaches 11.1mmol, fluid should be changed to 5% dextrose to prevent hypoglycaemia.

24
Q

Most appropriate treatment?

The immediate management of an acute deep vein thrombosis in someone who is at a high risk of bleeding.

A

Unfractionated heparin.
The mainstay of treatment for acute DVT is anticoagulation. This can be either unfractionated heparin, a LMWH or a factor Xa inhitor like fondaparinux. Fondaparinux has a higher half life than LMWH and there is no effective way of reversing it. LMWH have a shorter half life and some of it can be removed with protamine. Heparin though can be reversed quickly with protamine. Hence, if the patient is at a high risk of bleeding, they should be treated with unfractionated heparin and you should avoid fondaparinux. If they start bleeding you can just chuck them protamine. This however requires monitoring of APTT and platelet counts. If the patient has heparin-induced thrombocytopenia, you can try using fondaparinux. LMWH is recommended in those with active cancer and preferred in pregnancy, and consideration needs to be given in those with renal impairment.

25
Q

Most appropriate treatment?

Disseminated intravascular coagulation.

A

Platelet concentrates plus fresh frozen plasma.
DIC is a syndrome where coagulation pathways activate resulting in intravascular thrombosis, platelet and clotting factor depletion. The underlying disorder needs to be treated and FFP with platelet concentrate needs to be given. A platelet infusion should be considered and FFP is preferred for replacement of clotting factors and clotting inhibitors. Complications of DIC include life-threatening bleed, ARF and gangrene.

26
Q

Diagnosis?
A 60-year-old life-long non-smoker with a 6-month history of lower back pain has an ESR of 105 and a serum calcium of 3.0.

A

Myeloma.
This patient has multiple myeloma. This is characteristed by clonal proliferation of plasma cells in BM and commonly presents with bony pain and symptoms of anaemia. There may also be infections present in 10%. Elevated ESR agrees with this diagnosis. The diagnostic test is serum or urine electrophoresis looking for a paraprotein spike of IgG or IgA and light chain urinary excretion (Bence Jones proteins). Bone marrow examination and skeletal survey will also need to be conducted. Bone marrow analysis will help differentiate this from MGUS and solitary plasmacytoma. Bone changes include osteopenia, osteolytic lesions and fractures. Younger patients may be candidates for high-dose chemotherapy and autologous transplantation.

27
Q

Most likely underlying cause for their hypertension?

A 44-year-old man, BP 175/110 mmHg plasma potassium 2.2 mmol/L.

A
Primary hyperaldosteronism (Conn’s syndrome)
The normal range for potassium 3.5-5mmol/l. You should really know the normal ranges for common values like sodium, potassium and urea by this stage. In Conn’s, potassium is normal or low. It is important when drawing blood to avoid haemolysing the sample, which will cause a falsely elevated potassium level. It is important for screening to calculate the aldosterone/renin ratio, with >30 being suggestive of Conn’s. In Conn’s, aldosterone is raised and renin is low due to negative feedback. This is in contrast to renal artery stenosis where both aldosterone and renin will be raised. It is important to discontinue diuretics and other interfering medications for at least 6 weeks prior to measuring the ratio. The most reliable diagnostic test is a fludrocortisone suppression test. Treatment can be surgical with excision of the adenoma (if aldosterone production is lateralised to one side) or medical with spironolactone and amiloride. There are also familial forms of primary hyperaldosteronism which show an autosomal dominant mode of inheritance. 

Spironolactone is an aldosterone receptor antagonist. Amiloride inhibits aldosterone-sensitive sodium channels. They are both examples of potassium sparing diuretics acting on the DCT.

28
Q

Most useful test in establishing the diagnosis?

Renal artery stenosis

A

Duplex ultrasound
Renal artery stenosis is basically narrowing of the renal artery. There may not be any clinical consequences of this – just because someone’s renal arteries are narrowed does not mean they are suffering worsening kidney function, although this may be the case, especially after blockade of the renin-angiotensin system, and patients may have difficult to control and accelerated hypertension. A definitive diagnosis is made on imaging, where there is some controversy on what is most appropriate to use. USS is safe and non-invasive but the sensitivity and specificity is low. CT/MR angiography has the risk of contrast nephropathy and nephrogenic systemic fibrosis. Conventional angiography (the best test available) has the risk of bleeding and emboli as well as contrast related risks already mentioned.

Generally, the recommendation is to start with renal duplex ultrasound. This would not be an unreasonable approach. This can be followed by further tests. Although, in some centres in the country, the first line is CT or MR angiography and duplex USS is only done if there is a contra-indication to CT/MR angiography. However, the only reasonable option on this list is duplex USS.

29
Q

Most useful test in establishing the diagnosis?

Pituitary tumour

A

MRI head.
Pituitary MRI is preferred over CT and you will be able to see if the tumour has invaded, for example, the sphenoid sinus and cavernous sinuses or any compression of the optic chiasma. MRI is contra-indictaed in some cases such as those with a permanent pacemaker or those with ESRF on dialysis – in which case you would perform a CT. Both are done with contrast enhancement. A sellar mass will be seen.

30
Q

Most appropriate diagnostic investigation?
A 32-year-old man attends your surgery saying he brought up blood every morning for the last week. He is unsure whether he is vomiting or coughing it up. His haemoglobin (done yesterday) is 14 g/dL.

A

Chest x-ray.
The blood being brought up here occurs at a fixed time period every day and he is not anaemic. This makes you suspect a respiratory cause of his haemoptysis such as pneumonia – particularly TB, cancer, vasculitis like Wegener’s, bronchiectasis and bronchitis.

31
Q

Most appropriate diagnostic investigation?
A 55- year-old lady on Warfarin for recurrent pulmonary emboli presents having vomited a small amount of blood that morning. She has been on antibiotics for a presumed chest infection for the last week.

A

Clotting profile.
This woman is on prophylactic warfarin anticoagulation. There is an interaction here with the antibiotics this woman is taking which has resulting in enhanced anticoagulation effects of warfarin, causing her to bring up the blood. Cepahalosporins, chloramphenicol, ciprofloxacin, clarithryomycin, erythromycin and metronidazole are all examples which increase the effect of warfarin. Any P450 inducer will have this effect as warfarin is a drug metabolised by cytochrome P450 enzymes. Antibiotics can also upset the gut flora which reduces vitamin K levels.

32
Q

Most appropriate diagnostic investigation?
A 65-year-old man with a six-month history of ischaemic heart disease on Aspirin presents with a one-month history of epigastric pain and two days of dark stools. He has vomited a ‘cupful’ of fresh blood this morning.

A

Upper GI endoscopy.
NSAID use is a key risk factor for a peptic ulcer. Other key risks include H. pylori infection, smoking and FH of PUD. Zollinger-Ellison syndrome should be considered if there are multiple ulcers or ulcers refractory to treatment. The epigastric pain and symptoms of dark stools are consistent with a bleeding peptic ulcer. The most specific and sensitive test is an upper GI endoscopy which also allows management of the bleed. A biopsy may also be done to rule out malignant transformation. Gastric ulcers require a compulsory biopsy but duodenal ulcers rarely undergo malignant change. Management here can be aimed at discontinuing NSAIDs which are the cause in this case.

33
Q

Most appropriate diagnostic investigation?
A 22-year-old medical student has several episodes of vomiting blood after a period of forceful retching. He had been binge drinking for the last 3 days after failing his OSCE.

A

Upper GI endoscopy.
The definitive diagnosis for a Mallory-Weiss tear is made by OGD. This tear in the oesophageal mucosa occurs after a rise in abdominal pressure, causing subsequent GI bleeding. It commonly presents with haematemesis after an episode of retching/vomiting/coughing/straining. Hence, risk factors include anything which can cause vomiting like heavy alcohol use, which is commonly the case in EMQs. Also, other conditions would include food poisoning, bowel obstruction, hyperemesis gravidarum, bulimia, the chronic cough of COPD, meningitis etc… you name it really. Classically, MWT presents with a small self limiting episode of haematemesis. Treatment is supportive because most cases are self limiting and emergency treatment is not offered unless the patient is showing signs of clinical instability. If the patient is actively bleeding, treatment will be with therapeutic endoscopy in most cases, and very very few cases will require more intervention such as angiography with embolisation.

34
Q

Most appropriate diagnostic investigation?
A 72-year-old man, admitted to hospital with a single large haematemesis and continuing abdominal pain. Upper and lower GI endoscopy were reported as ‘unremarkable’

A

CT scan abdomen.
The cause here could be an aortoenteric fistula or AVM. You have to assume with endoscopy here that upper and lower GI endoscopy were unremarkable. The next step on this list would be a CT scan with contrast to detect the GI bleed. You would expect to see the active bleeding with contrast leaking into the bowel lumen.

35
Q

Most likely investigation that will reveal the cause of the renal failure?
A 46-year-old woman complains of right loin pain. Her mother had been on dialysis in Australia for 10 years. Plasma creatinine 180 μmol/l. No abnormalities were detected on urinalysis

A

Renal ultrasound.
A dominantly inherited cause of renal failure is likely to be polycystic kidney disease which is best noted on ultrasound

36
Q

Most likely investigation that will reveal the cause of the renal failure?
A 28-year-old woman with a carcinoma of the cervix was admitted with plasma creatinine of 250μmol/l. BP was 130/80. Urinalysis was negative

A

Renal ultrasound.
A patient with cervical carcinoma is at risk of ureteric obstruction and then hydronephrosis. Ultrasound is the test of choice

37
Q

Most likely investigation that will reveal the cause of the renal failure?
An 82-year-old man admitted through A&E with confusion. BP 90/60. JVP not seen. His hands and feet were cool. Plasma creatinine 420 μmol/l, urea 55 mmol/l. After catheterisation, 200mls mucky urine was drained from his bladder

A

CVP measurement.
A confused hypotensive shocked patient might be hypotensive because of cardiac disease (which will cause a raised JVP) or due to sepsis (which will cause a low JVP). If you can’t see the JVP, then you should put in a central line to measure the CVP accurately to tell you if the cause of the low blood pressure here is sepsis or cardiac failure.

38
Q

Most likely investigation that will reveal the cause of the renal failure?
A 32-year-old man presents with oedema. Plasma creatinine 150 μmol/l, urea 15 mmol/l, albumin 15 g/l. Urine protein excretion 8.5 gm/24 hour. Routine immunescreen (antinuclear antibody, complement levels, CRP) is normal.

A

Renal biopsy.
When the cause of renal failure might be nephritis (as in nephrotic syndrome) a renal biopsy will be needed to make the diagnosis. Occasionally this is urgent, so that potent immunosuppresives can be administered.

39
Q

Most likely investigation that will reveal the cause of the renal failure?
A 76-year-old man presents with lethargy and back pain. Plasma creatinine 220 μmol/l, urea 18 mmol/l, calcium 2.9 mmol/l (2.2 – 2.6), albumin 29 g/l. Urine protein excretion 1.5 gm/24 hours.

A

Plasma electrophoretic strip.
Renal impairment in myeloma results from a combination of factors: deposition of light chains, hypercalcaemia, hyperuricaemia and (rarely) in patients who have had the disease for some time, deposition of amyloid. Serum protein electrophoresis characteristically shows a monoclonal band.

40
Q

Initial investigation to confirm the diagnosis?
A 45-year-old man wakes in the night with severe pain in his right flank radiating round to the front and into his groin. He can’t get comfortable, but on examination his abdomen is soft with no masses. His urine shows a trace of blood but no other abnormality.

A

Helical CT.
This patient has renal colic which classically presents with severe flank pain radiating to the groin. Microscopic haematuria is present in up to 90% of cases. Up to 85% of stones are visible on a plain KUB although urate stones are radiolucent. If the stone is radio-opaque, calcification will be seen within the urinary tract. In pregnancy, a renal USS is first line. The IVP has now been replaced by the CT scan which is the new diagnostic standard. A non-contrast helical (or spiral) CT is preferred due to high sensitivity and specificity and accurately determines presence, site and size of stones. Stones are analysed after they are extracted or when they are expelled to check their composition. It is worth noting that in all females of child bearing age, a urine pregnancy test is necessary to exclude an ectopic pregnancy.

41
Q

Most appropriate investigation?
An 80 year old man presents with severely painful feet with mottled and purple toes with black areas. He tells you that he has also had constant severe back pain for a few days.

A

CT scan.
This patient has a dissecting aortic aneurysm which can be diagnosed with a CT scan showing the presence of an intimal flap. The CT scan should include chest, abdomen and pelvis to visualise the extent of the aneurysm. Dissecting aneurysms are either type A, which involves the ascending aorta, or type B. Type A dissections require urgent surgery whereas type B can be managed medically if it is not complicated by end organ ischaemia. The aortic dissection has led to a cholesterol embolism. This can be diagnosed histopathologically with the finding of cholesterol crystals. The phenomenon where cholesterol is released from an atherosclerotic plaque is called ‘trash foot’. A highly technical medical term. This results in the mottled appearance of distal embolism associated with livedo reticularis. You can search the internet for some case reports of this phenomenon.

42
Q

Most appropriate investigation?
A 25-year-old university student presents with high fevers. He has a petechial rash, black areas on his digits and a blood pressure of 70/50.

A

Blood cultures.
This patient has sepsis. Sepsis is the presence of SIRS with a likely infectious cause. This patient’s profound arterial hypotension means he has severe sepsis (dysfunction of one or more organ systems). The patient being a young university student most likely has meningitis even though symptoms of headache, photophobia and neck stiffness are not mentioned. Hence, a LP would be performed but it is not the 1st test to order in a patient who presents with sepsis.
It is important in the first instance to obtain a blood culture immediately, and preferably before antibiotics are started. If this is bacterial meningitis, you would expect to see a raised WCC on the LP with elevated protein, normal/reduced glucose and predominantly neutrophils in the white cell differential. Early blood cultures allows you to either broaden your empirical antibiotic spectrum or narrow it in those with sensitive organisms. It is worth noting that in sepsis, the patient may have a low temperature <36. A source of infection should be sought unless it is immediately evident such as the signs and symptoms of pneumonia being present. Petechial haemorrhage is a sign of organ dysfunction although a petechial rash may be due to meningococcal septicaemia.

43
Q

Most appropriate investigation?
An 80-year-old man with diabetes presents with black right great and second toes. He also has an ulcer on the ball of the foot.

A

Arteriogram.
Diabetic neuropathy has lead to the painless ulcer developing over pressure points in the foot such as on the ball of this man’s foot. This may have resulted from an object becoming lodged in the shoe and eroding through the skin with walking. This is why it is important for diabetics to check their feet regularly and to wear specialised footwear. The black toes on his right foot are likely due to peripheral vascular disease. It is worth noting that peripheral vascular disease refers specifically to peripheral arterial disease. The first line study is an ABPI although an arteriogram can be done to identify areas of stenoses which can be treated surgically. The black mummified toes may have to be amputated.

44
Q

Most appropriate investigation?
A 55 year old woman presents with painful joints, a purpuric rash on her arms and legs. Systems review reveals heamoptysis and ear pain. On examination you find black patches on her toes.

A

Anti-neutrophil cytoplasmic antibody.
This patient has Wegener’s granulomatosis, a systemic vasculitis affecting small and medium sized vessels. The classic triad includes upper and lower respiratory tract involvement and GN. Musculoskeletal manifestations such as arthralgia and signs of thromboembolism are commonly seen. A positive cANCA (antigen being proteinase 3) in the setting of the classic triad is sufficient to diagnose Wegener’s. Urinalysis and microscopy is also indicated to reveal renal involvement and a CT chest may reveal lung involvement, particularly in those who are asymptomatic for pulmonary involvement. This may show nodules or infiltrates.

45
Q

Most appropriate investigation?

A 41-year-old woman of Mediterranean descent is found to be anaemic. She has hepatosplenomegaly and normal haematinics.

A

Haemoglobin electrophoresis.
This is beta-thalassaemia, either major or intermedia due to the findings of abdominal distension, skeletal changes and hepatosplenomegaly which is not seen in heterozygoud beta-thalassaemia trait. The pallor is highly suggestive of moderate to severe anaemia, confirmed by the test results. Beta-thalassaemia major (or Cooley anaemia) is due to a complete abscence of HbA and often presents at a few months of age with pallor and abdominal distension, both described by parents as being progressive in nature. HSM and bony abnormalities (most often the frontal and parietal bossing mentioned, as well as ‘chipmunk facies’) are often present at presentation. Intermedia has a similar presentation but in a toddler or older child, with less pronounced symptoms and a more insidious course. Blood transfusions are required though stem cell transplant offers a hope of a cure. Hb electrophoresis will reveal minimal or no HbA and elevated HbF and HbA2.

46
Q

Most appropriate investigation?
A 40-year-old man who has been investigated for iron deficiency anaemia has a normal upper GI endoscopy and colonoscopy. A barium meal and follow through was also unhelpful.

A

Anti-gliadin antibodies.
This man is being investigated for a microcytic IDA here. The cause is not dietary iron intake given the history. So this could still be due to inadequate absorption such as coeliac disease or loss from GI bleeding. The unremarkable endoscopy results and barium studies indicate the absence of GI bleeding. This leaves coeliac disease, or potentially idiopathic, but the next thing to do here is to investigate the possibility of coeliac disease. Coeliac most common presents with IDA, although it can also lead to a macrocytic anaemia with mainly folate deficiency (though B12 is also affected but hepatic stores last several years). It is an autoimmune condition triggered by gluten peptides found in wheat, rye and barley. The ultimate best test is duodenal biopsy and histology to show intra-epithelial lymphocytes, villous atrophy and crypt hyperplasia. Macroscopic changes may be present but endoscopy is generally unhelpful, as in this case. The test of choice before performing such an invasive confirmatory test is to look for elevated anti-gliadin antibodies. Anti-tissue transglutaminase is less accurate and endomysial antibody is more expensive and has lower sensitivity.

47
Q

Most appropriate investigation?
An 18-year-old African woman presents in A&E with severe right shin pain. She has had similar previous episodes. She is found to be anaemic.

A

Haemoglobin electrophoresis.
Africans have higher incidence of sickle cell anaemia. This is a presentation of bone pain. About 8% of black people carry the gene and the prevalence is high in sub-Saharan Africa. Sickling occurs when RBCs containing HbS become distorted into a crescent shape. Patients with sickle cell anaemia have no HbA at all. If both parents carry the sickle cell gene, there is a 1 in 4 chance of giving birth to a child with sickle cell anaemia. Sickle cell disease also includes other conditions such as HbS from one parent with another abnormal Hb or beta thalassaemia from the other parent such as HbS-Beta thal and HbSC.

48
Q

Most likely investigation to give the diagnosis?
A 45-year-old man with a long history of excess alcohol consumption presents with haematemesis. On examination he is clubbed and has spider naevi.

A

Abdominal ultrasound scan.
This is clubbing due to cirrhosis as a result of chronic alcohol excess. Ultrasound here is the only feasible option on the list and can detect advanced cirrhosis and possible signs of portal hypertension, such as ascites, splenomegaly and increased portal vein diameter. The ultrasound may show a nodular liver surface, the liver may itself be shrunk due to cirrhosis and the left hand side of the liver may be hypertrophied. USS findings with a good clinical suspicion is enough for diagnosis.

49
Q

Diagnosis?
A 56 year old man on NSAIDs and amoxicillin for bronchitis develops a rash. He is mildy febrile despite the resolution of his bronchitis. The patient is confirmed to be in acute renal failure with elevated urea and creatinine and there is also pedal oedema. He is not oliguric. FBC shows eosinophilia.

A

Acute interstitial nephritis.
Acute interstitial nephritis classically presents with acute renal failure associated with oliguria and the ‘hypersensitivity triad’ of rash, fever and eosinophilia triggered by a drug. This can commonly be antibiotics, especially beta-lactams, and NSAIDs, though the range of triggering medications is vast. Oliguria can be present in more severe cases. There is inflammation of the renal interstitium, as suggested by the name, and this is likely a hypersensitivity reaction. It can also occur in the setting of a chronic inflammatory disease instead of being drug triggered. It will usually resolve once you stop the offending drug and treatment is supportive, though corticosteroids can be given to dampen the reaction. Most patients recover but have some residual impairment.

50
Q

Diagnosis?
A 32 year old woman at 34 weeks gestation presents with acute RUQ pain and a frontal headache. There is oliguria and increasing oedema as well as proteinuria of 3+ on urinalysis. Creatinine is elevated. The doctor starts her on labetalol.

A

Pre-eclampsia
This is a syndrome characterised by new onset hypertension and proteinuria in pregnant women after 20 weeks gestation. The only definitive treament is to deliver the placenta and a risk-benefit to the mother and baby should be carried out to determine the best clinical step. The doctor starts her on an antihypertensive here so while the question does not directly tell you she is hypertensive, this can be inferred. If the patient doesn’t have either hypertension or proteinuria, then they do not have pre-eclampsia. The woman may be asymptomatic, or like this case, may present with symptoms indicating a more severe disease such as a headache which is usually frontal and upper abdominal pain usually in the RUQ (a clinical symptom of HELLP syndrome which is a subtype of severe disease characterised by Haemolysis, ELevated liver enzymes and Low Platelets). Oedema is very common but quite non-specific as a presentation. Oliguria may be present and again is a sign that the pre-eclampsia is severe. The raised creatinine indicates underlying renal impairment and renal failure can be a rare complication, often occuring as ATN with either sepsis or placental abruption.

51
Q

Most appropriate management action?
A 17-year-old woman with a FH of headaches has now herself developed headaches which are throbbing in character and preceded by flashing lights. She wonders what her GP can do for her.

A

Aspirin.
Migraine is a chronic condition, with genetic determinants, which usually presents in early to mid life. The typical migraine aura this patient describes (which can be visual, sensory or speech symptoms) which can occur during or before the headache, is pathognomic, but is not seen in the majority of patients. The aura can be positive phenomena (for example this patient seeing flashing lights) or negative phenomena (for example visual loss). Nausea, photophobia and disability (the headache gets in the way with the patient’s ability to function) accompanying a headache also suggest a migraine diagnosis. The headache of a migraine tends to be prolonged if untreated, and tends to be unilateral and pounding (but does not have to be). Tests aim to rule out other differentials, although if the history is compatible and neurological examination is unremarkable, further testing is not needed.

Treatment of this chronic condition aims at treating acute attacks to restore function. Triptans can be used in specialist care for severe symptoms. These are 5HT1 agonists. Effective initial treatment in a primary care setting can involve NSAIDs, which are available OTC and include aspirin, as well as indometacin and naproxen. Paracetamol is less effective than NSAIDs but is still better than placebo – it is first line in those who are pregnant. Treatment should be taken as soon as a patient realises they are having an attack and may need to be repeated after the attack. A few patients who have frequent, severe or disabling headaches may require daily prophylaxis such as anticonvulsants, TCAs and beta blockers.

52
Q

Most appropriate management action?
A 32-year-old man presents 24 hours after the sudden onset of the worst headache of his life. He has no history of headaches, is afebrile but has neck stiffness and is drowsy. CT scan is normal.

A

Lumbar puncture.
SAH (bleeding into the subarachnoid space) presents with sudden severe headache patients will often describe as the worst headache of their life, and can often be so bad that they feel like they’ve been kicked in the back of the back. Half of all patients lose consciousness and eye pain with exposure to light can also be seen. Altered mental status is common. SAH occurs most commonly in the 50-55 age group and affects women and black people more than men and white people. The most common cause of non-traumatic SAH is an aneurysm which ruptures. Conditions which predispose to aneurysm formation and SAH include adult PKD, Marfan’s, NF1 and Ehlers-Danlos. Cerebral aneurysms arise around the circle of Willis. A CT scan is indicated, and if unrevealing, this should be followed by an LP. Cerebral angiography can confirm the presence of aneurysms. The patient should be stabilised and this followed by surgical clipping or endovascular coil embolisation, the choice is subject to much current controversy sparked by relatively recent research. Complications can commonly occur and include rebleeding, hydrocephalus and vasospasm.

53
Q

Diagnosis?
A 65-year-old man presents with a large painless bladder and overflow incontinence at night and a raised creatinine level.

A

Hydronephrosis.
This patient has BPH which has caused hydronephrosis. This is an example of bilateral obstructive uropathy. Acute presentations are often painful whereas chronic presentations are more insidious in onset. Blockage of urinary flow by the enlarged prostate has led to urinary retention and overflow incontinence. Initial treatment aims to relieve the pressure on the kidneys. This involves catheterisation as the first line treatment. The patient should be started on alpha blockers at the time of catheterisation.

54
Q

Most appropriate monitoring investigation?

Cyclophosphamide

A

White cell count.
This drug is used mainly with other drugs for treating malignancies including leukaemias, lymphomas and solid tumours. The rare and serious complication is haemorrhagic cystitis as a result of the urinary metabolite acrolein and mesna can be given as prophylaxis. It is an alkylating agent which damages DNA and interferes with cell replication. The only feasible option on this list is WCC where we have to assume this drug is being used for a leukaemia or lymphoma and we want to measure whether it is working.

55
Q

Most appropriate next step in management?
A 50-year-old man presents with acute ST elevation MI to London’s best hospital. He has already been given aspirin, oxygen, morphine and GTN and is haemodynamically stable. 20 minutes have passed since symptom onset.

A

Perform coronary angioplasty.
For confirmed ST elevation MI the 1st line treatment which gives the best results is primary PCI with stenting and is indicated if the person presents to A&E within 90 minutes of first presentation. CABG should be strongly considered if the patient fails PCI and should be done within 12 hours of onset of symptoms, ideally within 6. This is London’s best hospital but if this were Orkney and they did not have PCI capacity or the ability to transfer to a PCI facility within 30 minutes or so, then you would thrombolyse if there are no contraindications. This must be done within 12 hours of symptom onset and ideally within 3 hours as the efficacy of fibrinolytics diminishes over time. You should be aware of the absolute contraindications to thrombolysis such as suspected aortic dissection and prior intracranial haemorrhage. This patient has already been given some treatment for suspected MI (aspirin, oxygen, morphine and GTN). Post-treatment this patient will need aspirin therapy and clopidogrel for at least a year – aspirin should be continued indefinitely. Patients should also be started on a beta blocker, ACE inhibitor and a statin, indefinitely.

56
Q

Most appropriate next step in management?

A 55-year-old woman with a 6-week history of intermittent angina is found to have a serum cholesterol of 7.9 mmol/l.

A

Perform exercise ECG.
This patient has presented with stable angina. Resting ECG is often normal however during exercise stress ECG (most often the Bruce Protocol) there will be ST segment depression during exercise indicative of ischaemia. Those unable to exercise to an adequate level may need stress myocardial perfusion imaging or stress echocardiography. 1st line treatment involves lifestyle changes and antiplatelet therapy with aspirin. Anti-anginal theray will also be given, first line being beta-blockade. Statin therapy, blood sugar control in diabetics and BP control with antihypertensives may also be necessary. Those with LMS disease, 3 vessel disease or a reduced EF may benefit from CABG. Single vessel disease may benefit from PCI.

57
Q

Diagnosis?
An 82-year-old woman woke up at night acutely short of breath, with a frothy cough and wheeze. She had a myocardial infarction 6 months previously.

A

Acute left ventricular failure.
You should know the distinction between LVF and RVF. RVF leads to a backlog of blood and congestion of the systemic capillaries. This causes peripheral oedema and ascites and hepatomegaly may develop. Nocturia may be a symptom as fluid returns from the legs when the patient lies down flat. LVF causes congestion in the pulmonary circulation so the symptoms are respiratory. As seen in this patient, there is SOB and the frothy cough suggestive of pulmonary oedema. In a hospital setting, patients need to be sat upright to improve the SOB and IV access needs to be established. Oxygen, morphine, diuretics (frusemide or another loop diuretic) and nitrates will be given. Once stable, medical treatment of heart failure should be started which involves in the first instance, an ACE inhibitor followed by beta blockade.