Multiple Choice Questions: Physiology of Apnoea and The Benefits of Preoxygenation

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Multiple Choice Questions

Physiology of apnoea and the benefits of (d) One tablets of chloroquine 300 mg.
preoxygenation (e) Two tablets of digoxin 250 mg.

1. Time for desaturation to occur following the onset of apnoea is 6. The following properties of a maternal drug can confer an
influenced by the following: increased risk of toxicity to a breastfeeding infant:
(a) Thyroid state of the patient. (a) Highly protein-bound.
(b) The efficacy of preoxygenation. (b) Long half-life.
(c) The muscle relaxant used. (c) Small molecular weight.
(d) Age of the patient. (d) Acidity of compound.
(e) Weight of the patient. (e) Degree of lipid solubility.
2. Time for desaturation to occur following the onset of apnoea 7. The following features increase an infant’s susceptibility to
can be delayed by: toxicity:
(a) Head down position. (a) Increased glomerular filtration rate (GFR).
(b) Insufflation of air. (b) Higher minute ventilation.
(c) Preoxygenation. (c) A thin stratum corneum.
(d) Sepsis. (d) Increased plasma protein binding.
(e) Maintaining a patent airway. (e) Immature Phase II metabolic pathways.

3. During apnoea: 8. The following drugs may be removed by haemodialysis:


(a) In a 1-month old child, the rate of decline of PaO2 is three (a) Salicylates.
times that of an adult. (b) Lithium.
(b) Increasing the oxygen fraction applied to the patent (c) Barbiturates.
airway from 90–100% more than doubles open airway (d) Tricyclic antidepressants.
apnoea. (e) Metformin.
(c) Closed-airway apnoea results in a negative intrathoracic
9. Enhanced elimination by urinary alkalinization:
pressure, hastening hypoxia.
(a) Is best for drugs with a pKa of 3.0– 7.2.
(d) Equal amounts of O2 and CO2 leave and enter the alveoli.
(b) May be enhanced by a degree of hypokalaemia.
(e) The SaO2 starts to fall at a PaO2 of 10 kPa.
(c) Is more suitable for highly protein-bound drugs.
4. Apnoeic mass movement of oxygen can: (d) Is effective in the management of quinidine poisonings.
(a) Be used without problem to ensure oxygenation without (e) Aims to promote a urine output of 5–10 ml kg21 h21.
ventilation.
(b) Reverse hypoxia.
Antibiotic resistance in the intensive
(c) Only occur with a ‘perfect’ airway. care unit
(d) Significantly extend survivable duration of apnoea and buy
time to rescue the airway. 10. Regarding resistant bacteria:
(e) Cause temporary reversal of haemoglobin desaturation. (a) Organisms with intrinsic resistance are often of low
virulence.
(b) Mutation is the most important mechanism of acquisition of
Poisoning in children resistance.
5. Significant toxicity could occur in a healthy 10 kg toddler after (c) Gene transfer is the most important method of acquisition of
ingestion of the following: resistance.
(a) Two tablets of paracetamol 500 mg. (d) Pseudomonas can become a problem in vulnerable patients
(b) Two tablets of aspirin 300 mg. managed in selection pressure environments.
(c) Two tablets of amitryptilline 50 mg. (e) MRSA is resistant to all antibiotics.

136 doi:10.1093/bjaceaccp/mkp022
Continuing Education in Anaesthesia, Critical Care & Pain | Volume 9 Number 4 2009
# The Author [2009]. Published by Oxford University Press on behalf of The Board of Directors of the British Journal of Anaesthesia. All rights reserved.
For Permissions, please email: journals.permissions@oxfordjournal.org
Multiple Choice Questions

11. Considering the transfer of resistance: (c) Bleeding complications following thrombolysis are lethal in up
(a) Plasmids are the most important routes of transmission of to 1 per 400 treatment years.
genetic information within the intensive care unit. (d) Vena cava filters should be used as first line therapy in patient
(b) Corynebacterium diptheriae and Vibrio cholerae are examples with PE following surgery.
of bacteria that commonly receive genetic information from (e) Thrombolysis is associated with decreased mortality following
bacteriophages. sub-massive PTE
(c) Naked bacterial DNA is uncommonly found in ICU patients.
(d) Transposons can encode resistance and move between Anaesthesia for robot-assisted laparoscopic
plasmids. surgery
(e) Acquisition of resistance may be associated with a metabolic
17. The following physiological changes are usually associated
cost.
with a surgical pneumo-peritoneum in the Trendelenberg position:
12. Biochemical mechanisms occurring in bacterial resistance (a) Increased mean arterial pressure.
include: (b) Increased systemic vascular resistance.
(a) Active efflux of antibiotics. (c) Increased renal blood flow.
(b) Modifications to cell wall permeability. (d) Decreased intraocular pressure.
(c) The development of alternative biochemical pathways. (e) Decreased pulmonary compliance.
(d) Producing enzymes that break down antibiotic.
18. Reported complications associated with robot assisted prosta-
(e) Reverse chemotaxis away from areas of high antibiotic
tectomy include:
concentration.
(a) Brachial plexus neuropraxia.
13. Considering common resistant organisms: (b) An increased incidence of on table cardiac arrest.
(a) Restricting glycopeptide use can reduce the incidence of VRE. (c) Erroneous pulse oximetry readings when the probe is placed
(b) Carbapenems can prevent ESBL development. on the ear.
(c) Pseudomonas colonization is uncommon in burns patients. (d) An incidence of robot failure requiring the procedure to be
(d) Handwashing does not reduce rates of MRSA. abandoned of 10%.
(e) MRSA infections are associated with excess mortality. (e) Facial oedema and stridor on extubation.

14. Strategies to reduce resistance include: 19. Regarding conduct of anaesthesia for robot-assisted
(a) Promotion of handwashing and basic hygiene measures. prostatectomy:
(b) Contact isolation and screening. (a) Arterial and central venous pressure monitoring is mandatory.
(c) Genetic typing of bacteria to determine transmission route. (b) The patient is positioned in a steep reverse Trendelenberg
(d) De-escalation and restrictive antibiotic policies. position.
(e) Greater use of broad spectrum agents. (c) A laryngeal mask is appropriate for airway management.
(d) The patient should be cross matched for 8 units, as blood loss
Diagnosis and initial treatment of patients is usually substantial.
with suspected pulmonary (e) Isoflurane is the ideal inhalational agent.
thromboembolism
20. Postoperative care after a robot-assisted prostatectomy usually
15. Regarding diagnosis of PE: includes:
(a) Pulmonary angiography requires right heart catheterization. (a) Analgesia provided by a lumbar/low thoracic epidural.
(b) D-dimers are a useful screening test in the outpatient setting. (b) Routine admission to the intensive care unit.
(c) Pulmonary scintigraphy is best interpreted in the light of the (c) Observations for signs of compartment syndrome.
clinical presentation. (d) Analgesia with large doses of opiates.
(d) Ultrasonography of the leg veins in the absence of leg symp- (e) Suitability for discharge within 24–48 h.
toms is an effective tool for exclusion of venous
thromboembolism. Transcutaneous electrical nerve stimulation
(e) Echocardiography may be a first line investigation.
Choose one single best answer, from (a) to (e), for each question for
16. Regarding treatment and prognosis of PE: questions 21-25:
(a) Patients who remain breathless at three months following pul- 21. For patients with normal skin sensation transcutaneous electri-
monary embolism are at high risk of developing CTEPH. cal nerve stimulation (TENS) should initially be given to generate:
(b) Following pulmonary embolus related to surgery, long-term (a) A strong painful paraesthesiae over acupuncture points.
anticoagulation over a period in excess of three months is not (b) A strong non-painful paraesthesiae over vertebrae segmentally
normally needed related to the pain.

Continuing Education in Anaesthesia, Critical Care & Pain j Volume 9 Number 4 2009 137
Multiple Choice Questions

(c) A strong painful paraesthesiae over the site of pain. (c) Blocking impulses travelling in peripheral nociceptive
(d) A strong non-painful paraesthesiae over the site of pain. afferents.
(e) A paraesthesiae that is barely perceptible over the site of pain. (d) Long-term depression of central nociceptor cell activity.
(e) Inhibiting second order central nociceptor cell activity in
22. The purpose of conventional TENS is to:
somatic receptive fields.
(a) Stimulate large diameter, low threshold afferents (A-b) and
small diameter, high threshold afferents (A-d). 24. Clinical research on TENS demonstrates that:
(b) Stimulate large diameter, low threshold afferents (A-b) (a) TENS is definitely effective for the relief of all chronic pains.
without simultaneously stimulating small diameter, high (b) TENS has no value as an adjunct for the relief of acute pain.
threshold afferents (A-d). (c) TENS may be effective for the relief of chronic pain although
(c) Generate muscle twitches in order to activate small diameter evidence is often inconclusive due to methodological
muscle afferents. shortcomings.
(d) Stimulate small diameter, higher threshold afferents (A-d) (d) TENS should be used as a stand alone treatment for moderate
without simultaneously stimulating large diameter, low to severe pain.
threshold afferents (A-b). (e) TENS is definitely not effective for the relief of chronic pain.
(e) Directly stimulate neurones in the spinal cord.
25. Suitable choice for electrode placement may include:
23. The mechanism of action of conventional TENS is predomi- (a) Anterior and posterior over chest wall to treat angina pain.
nantly by: (b) Over an area of diminished skin sensation to treat neuropathic
(a) Activating structures on the descending pain inhibitory pain.
pathways. (c) On the contralateral site in the treatment of phantom pain.
(b) Resetting central sensitization and reorganizing aberrant (d) Over the abdomen for pain relief during childbirth.
neuronal pathways. (e) Over the anterior neck for acute tonsillitis.

We no longer publish the answers to the journal’s MCQs in the journal. Instead, you are invited to take part in a web-based, self test.
Visit the web site: www.ceaccp.oxfordjournals.org to obtain a certificate and CME points. Please see the editorial in Volume 7, Number 1
(February, 2007) for further details.

138 Continuing Education in Anaesthesia, Critical Care & Pain j Volume 9 Number 4 2009

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