MEGA EMRCS Flashcards
(2135 cards)
Which of the following drugs increases the rate of gastric emptying in the vagotomised stomach?
A Ondansetron
B Metoclopramide
C Cyclizine
D Erythromycin
E Chloramphenicol
D Erythromycin
Vagotomy seriously compromises gastric emptying which is why either a pyloroplasty or gastro- enterostomy is routinely performed at the same time.
Chloramphenicol has no effect on gastric emptying. Ondansetron slows gastric emptying slightly. Metoclopramide increases the rate of gastric emptying but its effects are mediated via the vagus nerve. Erythromycin enhances gastric emptying by acting via the motilin receptor in the gut.
A 36-year-old man with end-stage renal disease who is undergoing haemodialysis has normocytic normochromic anaemia. Which of the following is the most appropriate therapy?
A. Erythropoietin
B. Ferrous sulphate
C. Folate
D. Vitamin B6
E. Vitamin B12
ANSWER IS A
Erythropoietin, or EPO, is a glycoprotein hormone that is a cytokine for erythrocyte
(red blood cells) precursors in the bone marrow. Also called haematopoietin or haemopoietin, it is produced by the kidney and is the hormone regulating red blood cell production.
Erythropoietin is available as a therapeutic agent produced by recombinant DNA technology in mammalian cell culture. It is used in treating anaemia resulting from chronic renal failure or from cancer chemotherapy. Its use is also believed to be common as a doping agent in endurance sports such as bicycle racing, triathlons and marathon running.
A blood sample taken from the umbilical artery of a newborn was subjected to electrophoresis to detect antibodies (immunoglobulins). Which of the following antibodies will have the highest percentage in a newborn?
A. IgA
B. IgD
C. IgE
D. IgG
E. IgM
ANSWER IS D
IgG is a monomeric immunoglobulin, built of two heavy chains γ and two light chains. Each molecule has two antigen-binding sites.
This is the most abundant immunoglobulin and is approximately equally distributed in blood and in tissue liquids, constituting 75% of serum immunoglobulins in humans. This is the only isotype that can pass through the placenta, thereby providing protection to the newborn in its first weeks of life before its own immune system has developed.
It can bind to many kinds of pathogens, for example viruses, bacteria and fungi, and protects the body against them by complement activation (classic pathway),opsonisation or phagocytosis and neutralization of their toxins. There are four subclasses:
→IgG1 (66%), IgG2 (23%), IgG3 (7%) and IgG4 (4%):
- IgG1, IgG3 and IgG4 cross the placenta easily
- IgG3 is the most effective complement activator, followed by IgG1 and then IgG2
- IgG4 does not activate complement
- IgG1 and IgG3 bind with high affinity to Fc receptors on phagocytic cells
- IgG4 has intermediate affinity and IgG2 affinity is extremely
A 58-year-old male patient needed a blood transfusion after repair of an abdominal aortic aneurysm. His blood was sent to the laboratory. The technician, while checking for this patient’s blood group, said that the patient’s blood agglutinates with antisera anti-A and anti-D, while the patient’s serum agglutinates cells of blood group B. What is the blood group of this patient?
A. A positive
B. B positive
C. A negative
D. B negative
E. O positive
ANSWER IS A
According to the ABO blood typing system there are four different kinds of blood types: A, B, AB or O.
❖Blood groups A - If you belong to the blood group A, you have A antigens on the surface of your red blood cells and B antibodies in your blood plasma.
❖Blood group B - If you belong to the blood group B, you have B antigens on the surface of your red blood cells and A antibodies in your blood plasma.
❖Blood group AB - If you belong to the blood group AB, you have both A and B antigens on the surface of your red blood cells and no A or B antibodies at all in your blood plasma.
❖Blood group O - If you belong to the blood group O, you have neither A nor B antigens on the surface of your red blood cells but you have both A and B antibodies in your blood plasma.
Many people also have a so-called Rh factor on the red blood cell’s surface. This is also an antigen and those who have it are called Rh+. Those who have not are called Rh–. A person with Rh– blood does not have Rh antibodies naturally in the blood plasma (as one can have A or B antibodies, for instance) but they can develop Rh antibodies in the blood plasma if they receive blood from a person with Rh+ blood, whose Rh antigens can trigger the production of Rh antibodies.
A person with Rh+ blood can receive blood from a person with Rh– blood without any problems. So, in this vignette the patient’s blood group is A positive as he has antigen A, antibody B and Rh antigens.
In humans there are five types of antibody: IgA, IgD, IgE, IgG and IgM. Which of the following statements regarding IgM is CORRECT?
A. It binds to allergens
B. It functions mainly as an antigen receptor on B cells
C. It is the largest immunoglobulin molecule
D. It is the most abundant immunoglobulin
E. It is a tetramer of four
ANSWER IS C
IgM forms polymers where multiple immunoglobulins are covalently linked together
with disulphide bonds, normally as a pentamer or occasionally as a hexamer. It has a large molecular mass of approximately 900 kDa (in its pentamer form).
The J chain is attached to most pentamers, while hexamers do not possess the J chain due to space constraints in the complex. Because each monomer has two antigen binding sites, an IgM has 10 of them; however, it cannot bind 10 antigens at the same time because they hinder each other.
Because it is a large molecule, it cannot diffuse well and is found in the interstitium only in very low quantities. IgM is primarily found in serum; however, because of the J chain, it is also important as a secretory immunoglobulin.
Due to its polymeric nature, IgM possesses high avidity and is particularly effective at complement activation. It is sometimes called a ‘natural antibody’, but it is likely that the antibodies arise due to sensitization in the very young to antigens that are naturally occurring in nature. For example anti-A and anti-B IgM antibodies can be formed in early life as a result of exposure to anti-A- and anti-B-like substances that are present on bacteria or perhaps also on plant materials.
In germ-line cells, the gene segment encoding the μ constant region of the heavy chain is positioned first among other constant-region gene segments. For this reason, IgM is the first immunoglobulin expressed by mature B cells.
IgM is also by far the physically largest antibody in the circulation. IgM antibodies are mainly responsible for the clumping (agglutination) of red blood cells if the recipient of a blood transfusion receives blood that is not compatible with his/her blood type. IgM antibodies appear early in the course of an infection and usually do not reappear after further exposure. IgM antibodies do not pass across the human placenta. These two biological properties of IgM make it useful in the diagnosis of infectious diseases. Demonstrating IgM antibodies in a patient’s serum indicates recent infection or, in serum from a neonate, indicates intrauterine infection such as congenital rubella.
The lack of normal factor VIII causes haemophilia A, an inherited bleeding disorder. Factor VIII is synthesized predominantly in:
A. Hepatocytes
B. Histiocytes
C. Kupffer cells
D. Platelets
E. Vascular endothelium
ANSWER IS E
Factor VIII (FVIII) is an essential clotting factor. The lack of normal FVIII causes haemophilia A, an inherited bleeding disorder. The gene for Factor VIII is located on the X chromosome (Xq28). FVIII is a glycoprotein pro-cofactor. Factor VIII is synthesized predominantly in the vascular endothelium and is not affected by liver disease. In fact, levels usually are elevated in such instances. It is also synthesized and released into the bloodstream by the liver.
In the circulating blood, it is mainly bound to von Willebrand factor (vWF, also known as factor VIII-related antigen) to form a stable complex. Upon activation by thrombin or factor Xa, it dissociates from the complex to interact with factor IXa in the coagulation cascade. It is a co-factor to factor IXa in the activation of factor X, which, in turn, with its co-factor factor Va, activates more thrombin. Thrombin cleaves fibrinogen into fibrin, which polymerises and cross links (using factor XIII) into a blood clot. No longer protected by vWF, activated FVIII is proteolytically inactivated in the process (most prominently by activated protein C and factor IXa) and quickly cleared from the bloodstream.
FVIII concentrated from donated blood plasma or alternatively recombinant FVIII can be given to haemophiliacs to restore haemostasis. So, FVIII is also known as antihaemophilic factor. The transfer of a plasma by-product into the bloodstream of a patient with haemophilia often led to the transmission of diseases such as HIV and hepatitis before purification methods were improved. In the early 1990s, pharmaceutical companies began to produce recombinant synthesized factor products, which now prevent nearly all forms of disease transmission during replacement
A 45-year-old woman, with a past history of easy bruising and heavy menstrual periods, was admitted for elective cholecystectomy and was diagnosed with von Willebrand’s disease on routine preoperative investigations. von Willebrand’s disease is:
A. Autosomal dominant
B. Characterized by decreased bleeding time
C. Characterized by decreased factor VII
D. Characterized by decreased platelets
E. X-linked
ANSWER IS A
Von Willebrand’s disease (vWD) is the most common hereditary coagulation abnormality described in humans, although it can also be acquired as a result of other medical conditions. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. It is known to affect humans and, in veterinary medicine, dogs.
There are three types of hereditary vWD, but other factors such as ABO blood group may also play a part in the cause of the condition. The various types of vWD present with varying degrees of bleeding tendency. Severe internal or joint bleeding is rare (only in type 3 vWD); bruising, nosebleeds, heavy menstrual periods (in women) and blood loss during childbirth (rare) may occur. Death may occur The vWF gene is located on chromosome 12 (12p13.2). It has 52 exons spanning 178 kbp. Types 1 and 2 are inherited as autosomal dominant traits and type 3 is inherited as autosomal recessive.
Occasionally type 2 also inherits recessively. In humans, the incidence of vWD is roughly about 1 in 100 individuals. Because most forms are rather mild, they are detected more often in women, whose bleeding tendency shows during menstruation. The actual abnormality (which does not necessarily lead to disease) occurs in 0.9–3% of the population. It may be more severe or apparent in people with blood group O. Acquired vWD can occur in patients with autoantibodies. In this case the function of vWF is not inhibited but the vWF– antibody complex is rapidly cleared from the circulation. A form of vWD occurs in patients with aortic valve stenosis, leading to gastrointestinal bleeding (Heyde’s syndrome). This form of acquired vWD may be more prevalent than is presently thought.
Acquired vWF has also been described in the following disorders: Wilms’ tumour, hypothyroidism and mesenchymal dysplasias. Patients with vWD normally require no regular treatment, although they are always at increased risk for bleeding. Prophylactic treatment is sometimes given for patients with vWD who are scheduled for surgery. They can be treated with human-derived medium purity factor VIII concentrates. Mild cases of vWD can be trialed on desmopressin (1-desamino-8-D- arginine vasopressin, DDAVP) (antihaemophilic factor, more commonly known as humate-P), which works by raising the patient’s own plasma levels of vWF by inducing release of vWF stored in the Weibel–Palade bodies in the endothelial cells
A 68-year-old woman complaining of easy fatigability and shortness of breath after abdominal aortic aneurysm repair was diagnosed with iron-deficiency anaemia and prescribed an oral iron preparation. Which of the following statements about iron metabolism is CORRECT?
A. Ferritin is a plasma protein that transports iron in the blood
B. Haemosiderin is a product of haemoglobin degradation
C. Iron is more efficiently absorbed in the ferrous state (Fe2+) than in the ferric
state (Fe3+)
D. Most iron in the body is stored as haemosiderin
E. The gastrointestinal rate of iron absorption is extremely high
ANSWER IS C
The absorption of non-haem iron in any food is strongly affected by the composition of the meals. Iron is more efficiently absorbed in the ferrous state (Fe2+) than in the ferric state (Fe3+) and commercial iron preparations often contain vitamin C to prevent oxidation of Fe2+ to Fe3+. Still, only 3–6% of the ingested daily iron is actually absorbed in the upper gastrointestinal tract.
Seventy per cent of the total body iron is used for haemoglobin and myoglobin; the remainder is stored as readily exchangeable ferritin and some is stored in less easily mobilized haemosiderin. When old red blood cells are destroyed by the tissue macrophage system, haem is separated from globin and degraded to biliverdin. Iron in the plasma is bound to the iron transporting protein transferrin. Transferrin level (total iron-binding capacity) and saturation are clinically important indicators of iron deficiency anaemia.
A 45-year-old man on warfarin for a mechanical mitral valve was admitted in the Accident and Emergency Department with persistent bleeding following dental extraction. He was told that his coagulation was deranged. Which of the following statements about blood coagulation is CORRECT?
A. Absence of Ca2+ promotes blood coagulation
B. Disseminated intravascular coagulation (DIC) results in depletion of fibrin
split products
C. Patients with haemophilia A usually have a normal bleeding time
D. von Willebrand factor suppresses platelet adhesion
E. von Willebrand factor suppresses blood coagulation
ANSWER IS C
Prolonged bleeding time is characteristic of platelet disorders, e.g., thrombocytopaenia. Patients with haemophilia A or B (i.e. absence of factor VIII or IX, respectively) have a prolonged partial thromboplastin time (PTT), but do not have a prolonged bleeding time. Ca2+ is a necessary co-factor for blood coagulation, and chelation of Ca2+ ions by citrate inhibits coagulation.
Von Willebrand factor is part of the factor VIII complex and also promotes platelet adherence to the vascular subendothelium. Patients who lack this factor (von Willebrand’s disease) have both a prolonged PTT and a prolonged bleeding time. Disseminated intravascular coagulation results in depletion of coagulation factors and accumulation of fibrin split products.
Nerve gas (organophosphate) is a weapon of chemical warfare that kills by causing respiratory and cardiovascular failure. The expected effect of organophosphate poisoning on the heart would be:
A. Decrease the force of myocardial contractions by potentiating the vagal tone to the ventricular muscle
B. Decrease the rate of rhythmicity of the sinoatrial (SA) node by inducing hyperpolarisation
C. Depolarize cells of the SA node by closing potassium channels under the control of the muscarinic acetylcholine receptor
D. Increase the rate of rhythmicity of the SA node by increasing the upward drift in membrane potential caused by sodium leakage
E. Increase conductivity at the atrioventricular (AV) junction by inducing depolarization
ANNSWER IS B
The toxic effects of nerve gas derive from its ability to inhibit the enzyme cholinesterase. The inhibition of this naturally occurring degradative enzyme engenders a massive accumulation of acetylcholine evoking an overstimulation of the acetylcholine receptors throughout the body. In the heart, specifically, acetylcholine released by the vagal nerve stimulates muscarinic receptors in the cells of the sinoatrial (SA) node.
This results in the opening of potassium channels and hyperpolarisation of the SA node. It therefore takes longer for sodium leakage to cause the membrane potentials of these cells to reach the threshold required for an action potential. The rate of rhythmicity is so decreased. A similar hyperpolarisation of the fibers at the atrioventricular (AV) junction decreases conduction velocity of atria impulses to the ventricle. The force of ventricular contractions is not affected by the vagus nerve.
The resting membrane potential of a neuronal cell body is –60 mV. Opening chloride channels in the neuronal membrane will most likely cause:
A. Depolarization to about –30 mV
B. Depolarization to about +30 mV
C. Hyperpolarisation to about –70 mV
D. Initiation of an action potential
E. No change in membrane potential
ANSWER IS C
Increasing the membrane’s conductance to chloride will result in chloride influx and the membrane potential approaching the value dictated by the chloride equilibrium potential (calculated from the Nernst equation), which is about –70 mV for neurons.
A value of –30 mV is near the Nernst potential for Cl− ions in smooth muscle cells, but not in neurons; +30 mV is near the Nernst potential for Na+ ions. The membrane potential would remain unchanged only if the cell resting membrane potential is already at the Nearest potential of the ion channels that were opened. Action potentials occur if the cell membrane is depolarised above threshold.
Chloride ions are associated with changes in neuronal membrane potential. Which of the following statements most accurately describes the response of a neuron to a decrease in the conductance of the cell membrane to chloride ions?
A. The cell will depolarize if its membrane potential is positive with respect to the equilibrium potential for chloride ions
B. The cell will hyperpolarize if its membrane potential is positive with respect to the equilibrium potential for chloride ions
C. The cell will hyperpolarize if the external chloride concentration is greater than the internal chloride concentration
D. The cell will hyperpolarize if the external chloride concentration is less than the internal chloride concentration
E. No change in membrane potential will occur if the external and internal chloride ion concentrations are equal
ANSWER IS A
Although electrogenic pumps may contribute to the membrane potential of certain cells, the major determinants of membrane potential are the external and internal concentrations of permanent ions and their relative permeabilities in the membrane. Decreasing the conductance causes the membrane potential to move away from the equilibrium potential for that ion. So, a decrease in the conductance of a membrane to chloride ions causes the cells to depolarize – that is, become more positive – if the membrane potential is positive with respect to the chloride equilibrium potential.
Conversely, increasing the conductance for an ion causes the membrane potential to approach the equilibrium potential for that ion. External and internal ion chloride concentrations are needed to calculate the Nernst potential for this ion, but a simple comparison of these two values does not allow predictions about the change in membrane potential.
Which of the following is not secreted by the parietal cells?
A-Hydrochloric acid
B-Mucus
C-Magnesium
D-Intrinsic factor
E-Calcium
Answer is B. Parietal cells: secrete HCl, Ca, Na, Mg and intrinsic factor Chief cells: secrete pepsinogen
Surface mucosal cells: secrete mucus and bicarbonate.
Gastric secretions
A working knowledge of gastric secretions is important for surgery because peptic ulcers are common, surgeons frequently prescribe anti secretory drugs and because there are still patients around who will have undergone acid lowering procedures (Vagotomy) in the past.
Gastric acid
Is produced by the parietal cells in the stomach
pH of gastric acid is around 2 with acidity being maintained by the H /K ATP ase pump. As part of the process bicarbonate ions will be secreted into the surrounding vessels.
Sodium and chloride ions are actively secreted from the parietal cell into the canaliculus. This sets up a negative potential across the membrane and as a result sodium and potassium ions diffuse across into the canaliculus.
Carbonic anhydrase forms carbonic acid which dissociates and the hydrogen ions formed by dissociation leave the cell via the H /K antiporter pump. At the same time sodium ions are actively absorbed. This leaves hydrogen and chloride ions in the canaliculus these mix and are secreted into the lumen of the oxyntic gland.
A 65 year old man is admitted for a below knee amputation. He is taking digoxin. Clinically the patient has an irregularly irregular pulse. What would you expect to see when you examine the jugular venous pressure?
A-Absent y waves
B-Slow y descent
C-Cannon waves
D-Steep y descent
E-Absent a waves
Jugular venous pressure
Absent a waves = Atrial fibrillation
Large a waves = Any cause of right ventricular hypertrophy, tricuspid stenosis Cannon waves (extra large a waves) = Complete heart block
Prominent v waves = Tricuspid regurgitation
Slow y descent = Tricuspid stenosis, right atrial myxoma
Steep y descent = Right ventricular failure, constrictive pericarditis, tricuspid regurgitation
Which part of the ECG represents atrial depolarization?
A-P wave
B-Q wave
C-T wave
D-QRS complex
E-P-R interval
Theme from April 2013 exam
Theme from April 2014 exam
The P wave represents atrial depolarization. Note that atrial repolarization is obscured within the QRS complex.
P wave
Represents the wave of depolarization that spreads from the SA node throughout the atria
Lasts 0.08 to 0.1 seconds (80-100 ms)
The isoelectric period after the P wave represents the time in which the impulse is traveling within the AV node
P-R interval
Time from the onset of the P wave to the beginning of the QRS complex
Ranges from 0.12 to 0.20 seconds in duration
Represents the time between the onset of atrial depolarization and the onset of ventricular depolarization
QRS complex
Represents ventricular depolarization
Duration of the QRS complex is normally 0.06 to 0.1 seconds
ST segment
Isoelectric period following the QRS
Represents period which the entire ventricle is depolarized and roughly corresponds to the plateau phase of the ventricular action potential
T wave
Represents ventricular repolarization and is longer in duration than depolarization
A small positive U wave may follow the T wave which represents the last remnants of ventricular repolarization.
Q-T interval
Represents the time for both ventricular depolarization and repolarization to occur, and therefore roughly estimates the duration of an average ventricular action potential.
Interval ranges from 0.2 to 0.4 seconds depending upon heart rate.
At high heart rates, ventricular action potentials shorten in duration, which decreases the Q-T interval. Therefore the Q-T interval is expressed as a “corrected Q-T (QTc)” by taking the Q- T interval and dividing it by the square root of the R-R interval (interval between ventricular depolarizations). This allows an assessment of the Q-T interval that is independent of heart rate.
Normal corrected Q-Tc interval is less than 0.44 seconds.
A 53 year old man undergoes a reversal of a loop colostomy. He recovers well and is discharged home. He is readmitted 10 days later with symptoms of vomiting and colicky abdominal pain. On examination he has a swelling of the loop colostomy site and it is tender. What is the most likely underlying diagnosis?
A-Haematoma
B-Intra abdominal adhesions
C-Anastomotic leak
D-Anastomotic stricture
E-Obstructed incisional hernia
In this scenario the most likely diagnosis would be obstructed incisional hernia. The tender swelling coupled with symptoms of obstruction point to this diagnosis. Prompt surgical exploration is warranted. Loop colostomy reversals are at high risk of this complication as the operative site is at increased risk of the development of post operative wound infections.
Acute incisional hernia
Any surgical procedure involving entry into a cavity containing viscera may be complicated by post operative hernia
The abdomen is the commonest site
The deep layer of the wound has usually broken down, allowing internal viscera to protrude through
Management is dictated by the patients clinical status and the timing of the hernia in relation to recent surgery
Bowel obstruction or tenderness at the hernia site both mandate early surgical intervention to reduce the risk of bowel necrosis Mature incisional hernias with a wide neck, and no symptoms, may be either left or listed for elective repair
Risk factors for the development of post operative incisional hernias include; post operative wound infections, long term steroid use, obesity and chronic cough
Theme: Abdominal stomas
A. End ileostomy
B. End colostomy
C. Loop ileostomy
D. Loop colostomy E. End jejunostomy F. Loop jejunostomy G. Caecostomy
For each of the following scenarios, please select the most appropriate type of stoma to be constructed. Each option may be selected once, more than once or not at all.
A 56 year old man is undergoing a low anterior resection for carcinoma of the rectum. A primary anastomosis is planned.
Loop ileostomy
Theme from April 2014 Exam
Colonic resections with an anastomosis below the peritoneal reflection may have an anastomotic leak rate (both clinical and radiological) of up to 15%. Therefore most surgeons will defunction such an anastomosis to reduce the clinical severity of an anastomotic leak. A loop ileostomy will achieve this end point and is relatively easy to reverse.
Theme: Abdominal stomas
A. End ileostomy
B. End colostomy
C. Loop ileostomy
D. Loop colostomy E. End jejunostomy F. Loop jejunostomy G. Caecostomy
For each of the following scenarios, please select the most appropriate type of stoma to be constructed. Each option may be selected once, more than once or not at all.
A 23 year old man with uncontrolled ulcerative colitis is undergoing an emergency sub total colectomy.
The correct answer is End ileostomy
Following a sub total colectomy the immediate surgical options include an end ileostomy or ileorectal anastomosis. In the emergency setting an ileorectal anastomosis would be unsafe.
Theme: Abdominal stomas
A. End ileostomy
B. End colostomy
C. Loop ileostomy
D. Loop colostomy E. End jejunostomy F. Loop jejunostomy G. Caecostomy
For each of the following scenarios, please select the most appropriate type of stoma to be constructed. Each option may be selected once, more than once or not at all.
A 63 year old women presents with large bowel obstruction. On examination she has a carcinoma 10cm from the anal verge.
The correct answer is Loop colostomy
Large bowel obstruction resulting from carcinoma should be resected, stented or defunctioned. The first two options typically apply to tumours above the peritoneal reflection. Lower tumours should be defunctioned with a loop colostomy and then formal staging undertaken prior to definitive surgery. An emergency attempted rectal resection carries a high risk of involvement of the circumferential resection margin and is not recommended.
Abdominal stomas
Stomas may be sited during a range of abdominal procedures and involve bringing the lumen or visceral contents onto the skin. In most cases this applies to the bowel. However, other organs or their contents may be diverted in case of need.
With bowel stomas the type method of construction and to a lesser extent the site will be determined by the contents of the bowel. In practice, small bowel stomas should be spouted so that their irritant contents are not in contact with the skin. Colonic stomas do not need to be spouted as their contents are less irritant.
In the ideal situation the site of the stoma should be marked with the patient prior to surgery. Stoma siting is important as it will ultimately influence the ability of the patient to manage their stoma and also reduce the risk of leakage. Leakage of stoma contents and subsequent maceration of the surrounding skin can rapidly progress into a spiraling loss of control of stoma contents.
Types of stomas
Name of stoma Use Common sites
Gastrostomy Gastric decompression or fixation Epigastrium Feeding
Loop jejunostomy
Seldom used as very high output
May be used following emergency laparotomy with planned early closure
Any location according to need
Percutaneous Usually performed for feeding purposes and site in the Usually left upper quadrant jejunostomy proximal bowel
Loop ileostomy
Defunctioning of colon e.g. following rectal cancer surgery
Does not decompress colon (if ileocaecal valve competent)
Usually right iliac fossa
End ilestomy
Usually following complete excision of colon or where ileo- colic anastomosis is not planned
May be used to defunction colon, but reversal is more difficult
Usually right iliac fossa
A 48 year old woman presents to the A&E department with a sudden onset, severe headache peaking within seconds. On examination, she appears anxious but has no focal neurological deficits. A non-contrast CT scan of the head is performed urgently and is found to be normal. There is no family history of aneurysms or other vascular abnormalities. What is the most appropriate next step in the management of this patient?
A. Prescribe subcutaneous sumatriptan
B. Perform lumbar puncture
C. Initiate antiviral therapy
D. Arrange outpatient neurology follow-up without further investigation
E. Request a magnetic resonance imaging (MRI) of the brain
B: In a patient with a sudden onset, severe headache, and normal CT scan, SAH must still be ruled out, as the CT scan may not detect biood if performed very early in the course of SAH. Lumbar puncture is the next step to look for xanthochromia and red blood cells in the cerebrospinal fluid. This will confirm or exclude the diagnosis of SAH Even if you were thinking migraine, you still need to do an LP first because a CT scan was arranged (which means that the clinicians originally thought it was a SAH) So commit to your suspected diagnosis.
A 32 year old woman attends her General Practice due to frequent migraines. She has 1-2 migraines a month which prevent her from going to work. She has a background of asthma controlled with salbutamol and inhaled steroids. She is in a long term relationship and uses condoms for contraception. What is the SINGLE most appropriate medication to offer for migraine prophylaxis?
A. Propranolol
B. Amitriptyline
C. Topiramate
D. Aspirin
E. Sumatriptan
Given the patient’s background and the need for migraine prophylaxis in a woman of childbearing age with a history of asthma, the most appropriate medication to offer would be Amitriptyline.
Explanation:
• Amitriptyline: This tricyclic antidepressant is effective for migraine prophylaxis and is generally safe for women of childbearing age. It is not contraindicated in asthma and does not have the teratogenic risks associated with Topiramate. • Propranolol: Should be avoided due to the patient’s asthma. • Topiramate: Should be avoided in women of childbearing age due to potential teratogenic effects. • Aspirin: Used for acute treatment, not for prophylaxis. • Sumatriptan: Used for acute treatment of migraines, not for prophylaxis.
Correct Answer:
B. Amitriptyline
A 30 year old man presents to the clinic with a 6 day history of nasal congestion, headache, a feeling of pressure behind the eyes, and a fever. The symptoms have been progressively worsening, and the patient reports difficulty sleeping due to the congestion. There is no history of allergies or any other significant past medical history. On examination, there is tenderness over the frontal and maxillary sinuses. What is the most appropriate initial management for this patient?
A. Oral paracetamol
B. Oral amoxicilin
C. Nasal pseudoephedrine
D. Oral cetirizine
E. Nasal fluticasone
A: The patient presents with symptoms suggestive of acute sinusitis and has a fever, which suggests an inflammatory process. According to NICE CKS guidelines, the management of acute sinusitis is primarily focused on symptomatic relief Oral paracetamol can be used to relieve pain, reduce inflammation, and lower the fever. Nasal pseudoephedrine is a decongestant, but there is insufficient evidence to recommend its use, and the same applies to oral cetirizine, an antihistamine Nasal corticosteroids can reduce inlammation, but are not recommended as firstline treatment by NICE CKS Nasal steroids should be considered if the patient has been having symptoms for 10 days or more.
A 77 year old man presents to A&E with chest pain, An ECG demonstrates ST-depression and T-wave inversion in the lateral leads. Serum troponin is 88 mmoll (+5). He is offered Aspirin and Fondaparinux. A decision is made for an urgent angiogram with coronary intervention, where the left circumflex artery requires insertion of a drug-eluting stent. His background includes atrial fibrillation for which takes apixaban. He is told he will require lifelong aspirin treatment together with 12 months of another antiplatelet agent. What is the SINGLE most appropriate antithrombotic medication?
A. Clopidogrel
B. Prasugrel
C. Ticagrelor
D. Bisoprolol
E. Ramipril
A: Clopidogrel should be used as a second antiplatelet medication in the context of anticoagulated patients (warfanin/DOAC). Usually patients will be started on aspinin and ticagrelor post-MI.
A 35 year old man presents to the Emergency Department with a history of ingesting a large number of aspirin tablets about 4 hours ago. He appears restless, and on examination, his respiratory rate is 30 breaths per minute. His arterial blood gas (ABG) shows: pH 7.50 (7.35-7.45) PaO2: 12.7 kPa (10-14) PaCO2: 4 kPa (4.7-6.0) Bicarbonate 22 mmol/L (22-26) The salicylate level is found to be elevated. What is the most likely acid-base disturbance?
A. Metabolic Alkalosis
B. Metabolic Acidosis
C. Respiratory Acidosis
D. Respiratory Alkalosis
E. Mixed metabolic acidosis and respiratory alkalosis
D: The patient has salicylate poisoning, as indicated by the history of aspirin ingestion and the elevated salicylate level Salicylate poisoning initially causes a respiratory alkalosis due to direct stimulation of the respiratory centre in the medulla, leading to hyperventilation. This is reflected in the ABG with a high pH and low PaCO2 Though salicylate poisoning can also lead to a metabolic acidosis, in this case, the bicarbonate level is 22 mmolit, which does not support a concurrent metabolic acidosis Therefore, the primary acid-base disturbance is respiratory alkalosis