Posttest
Posttest
- Which of the following community emergency response agencies should be involved in planning for disasters such as those involving mass exposures to cholinesterase inhibitors? (Choose ALL correct answers)
- Emergency management/disaster offices
- All area hospitals
- The poison center
- Fire departments
- EMS providers
- The Local Emergency Planning Committee (LEPC)
- None of the above
- Which of the following should be assumed to happen with incidents involving patients acutely exposed to cholinesterase inhibitors (Choose ALL correct answers)
- Patients will be transported to the hospital without having been decontaminated
- Chemically exposed patients will be sent to a single hospital in the community designated for chemical casualties
- Contaminated patients will arrive unannounced
- None of the above
- Cholinesterase inhibitor toxicity leads to (Choose ALL correct answers)
- Excessive cholinesterase activity
- Depression of cholinesterase activity
- Excessive amounts of acetylcholine
- Occupation of cholinesterase binding sites by the cholinesterase inhibitor
- None of the above
- Which of the following are among the 4 major types of pathology caused by cholinesterase inhibitors? (Choose ALL correct answers)
- The cholinergic toxidrome
- The acute polyneuropathic syndrome
- The intermediate syndrome
- Organophosphate-induced delayed neuropathy
- None of the above
- The key function of nicotinic receptors is to (Choose ALL correct answers)
- Trigger excretion of exocrine glands
- Trigger rapid neural and neuromuscular transmission
- Suppress rapid neural and neuromuscular transmission
- Modulate intrinsic rhythmic electrical and mechanical activity
- None of the above
- Which of the following effects of acute cholinesterase toxicity involve nicotinic receptors? (Choose ALL correct answers)
- Sweating
- Miosis (pupillary constriction)
- Hyperglycemia
- Fasciculations
- None of the above
- In which of the following anatomical locations are nicotinic receptors found? (Choose ALL correct answers)
- Neuromuscular junctions
- Sympathetic nervous system
- Autonomic ganglia
- Central nervous system
- None of the above
- Muscarinic receptors (Choose ALL correct answers)
- Are faster to respond than nicotinic receptors
- Are not found in the central nervous system
- Trigger bronchodilation
- Trigger mostly sympathetic nervous system effects
- None of the above
- Which of the following are true about the cholinergic toxidrome? (Choose ALL correct answers)
- CNS effects are mediated by both nicotinic and muscarinic receptors
- CNS effects can mimic mental illness
- Uncontrolled seizures can lead to long-term CNS effects
- Seizures are more common in adults than children
- None of the above
- Acute cholinesterase inhibitor toxicity has been known to result in the following laboratory abnormalities (Choose ALL correct answers)
- Leukocytosis
- Peaked T-waves on EKG
- Elevated serum glucose
- Hyperkalemia or hypokalemia
- None of the above
- Which of the following medical conditions can be mimicked by cholinesterase inhibitor toxicity? (Choose ALL correct answers)
- Mental illness
- Food poisoning
- Opiate overdose
- Influenza
- None of the above
- Pediatric cholinesterase inhibitor poisoning differs from that in adults in the following ways (Choose ALL correct answers)
- Seizures are less likely
- Nicotinic effects are more likely
- Fasciculations are more common
- Bradycardia is less common
- None of the above
- Potential sources of exposure to cholinesterase inhibitors include which of the following (Choose ALL correct answers)
- Insecticides
- Antiparkinson drugs
- Snake venom
- Malaysian Bean sprouts
- None of the above
- Which of the following questions should be included in history for suspected cholinesterase inhibitor exposure? (Choose ALL correct answers)
- Typical work activities
- Medications
- Hobbies
- Use of traditional or ethnic remedies
- None of the above
- Which of the following are true about laboratory tests for cholinesterase inhibitor toxicity? (Choose ALL correct answers)
- The rapid availability of RBC cholinesterase levels, compared to serum cholinesterase levels makes them a useful tool for the emergency management of acutely toxic patients
- Reduction in RBC cholinesterase levels to normal is a good end point for titration for initial doses of 2-PAM
- Normal ranges of serum cholinesterase vary widely among individuals, but RBC cholinesterase level normals vary little among individuals
- Since the imposition of federal laboratory standards, the normal ranges for serum and RBC cholinesterase levels are the same for each laboratory
- None of the above
- Supportive care is an important aspect of treatment for the cholinergic toxidrome and should be focused primarily on maintaining and improving (Choose the ONE BEST answer)
- Renal function
- Hepatic function
- Respiratory function
- CNS function
- None of the above
- Atropine counteracts cholinesterase inhibitor toxicity by (Choose the ONE BEST answer)
- Competitively occupying muscarinic receptor sites
- Competitively occupying nicotinic receptor sites
- Competitively occupying nicotinic and muscarinic receptor sites
- Neutralizing acetylcholine
- None of the above
- Which of the following is/are the best end-points against which to titrate the dose of atropine in acute cholinesterase poisoning? (Choose the ONE BEST answer)
- Pupillary dilation
- Pupillary constriction
- Clinically significant reduction of bronchorrhea and bronchoconstriction, (as reflected by level of oxygenation and ease of ventilation)
- Development of heart rate of between 100-150/min
- Return of consciousness
- Return of muscle strength
- All of the above
- None of the above
- In order of preference, the best routes of atropine administration are: (Choose the ONE BEST answer)
- Intramuscular is better than Intravenous which is better than Autoinjector
- Intravenous is better than Autoinjector which is better than Intramuscular
- Autoinjector is better than Intravenous which is better than Intramuscular
- Intravenous is better than Intramuscular which is better than Autoinjector
- Intravenous is best; Intramuscular and Autoinjector are equally good
- None of the above
- Which type of cholinesterase toxicity can require the highest doses of atropine? (Choose the ONE BEST answer)
- Inhalation of nerve agent
- Dermal exposure to organophosphorus agents
- Suicidal ingestion of organophosphorus agents
- Ingestion of carbamates
- Which of the following are true about 2-PAM? (Choose ALL correct answers)
- It should never be used in carbamate poisoning
- It works by attaching to the cholinesterase inhibitor bound to cholinesterase, attaching to and removing the inhibitor
- It reduces the effectiveness of atropine
- It is ineffective after aging occurs
- None of the above
- Which of the following are reasons for treatment failure with 2-PAM? (Choose ALL correct answers)
- Inadequate dose
- Co-administration of atropine
- Redistribution of cholinesterase inhibitor from fat tissue
- Aging has already occurred
- None of the above
- Which of the following lead to delayed aging, and therefore prolongation of the time course when 2-PAM is still effective? (Choose ALL correct answers)
- Co-administration of atropine
- Poisoning from fat-soluble organophosphorus compounds
- Dermal exposure
- Poisoning with chemicals that must be metabolically converted before they possess cholinesterase inhibiting properties
- None of the above
- Which of the following is true about seizures resulting from cholinesterase inhibitors? (Choose ALL correct answers)
- They are more common in adults than in children
- Although diazepam is effective in controlling seizures, it has not been shown to improve clinical outcome
- Diazepam should not be used unless seizures occur
- CNS damage from cholinesterase inhibitors is due to a direct toxic effect, not seizure activity
- None of the above
- Which of the following are currently recommended in the routine treatment of poisoning?
- Syrup of ipecac
- Gastric lavage
- Cathartics
- Activated charcoal
- None of the above
- Which of the following is true regarding the intermediate syndrome? (Choose ALL correct answers)
- It most commonly occurs after nerve agent poisoning
- If good supportive care has been given and there is no hypoxic damage, the condition usually resolves spontaneously
- Atropine is indicated if muscarinic signs are present
- Delayed, but sudden-onset of respiratory weakness or paralysis may occur, leading to respiratory failure
- None of the above
- Which of the following are true about Organophosphate-induced delayed neuropathy (OPIDN)? (Choose ALL correct answers)
- It is caused by a molecular alteration of nicotinic receptors at the neuromuscular junction of distal skeletal muscle groups
- Pain is not a characteristic symptom
- If there has not been any hypoxic damage, and good supportive care has been given, full recovery is the rule
- Early and adequate doses of 2-PAM and atropine have been shown to prevent this condition
- None of the above
- Which of the following are true about Organophosphorus ester-induced neurotoxity (OPICN) (Choose ALL correct answers)
- It is a set of long-term, persistent neuropsychiatric signs and symptoms
- No specific treatment has been identified
- Studies carried out to assess whether the condition can occur after asymptomatic exposures to cholinesterase inhibitors have suffered from methodological problems
- It occurs when cholinesterase inhibitors trigger a permanent defect in neurotarget esterase
- None of the above
- Which of the following are true about cholinesterase inhibitors? (Choose ALL correct answers)
- Chronic, asymptomatic exposure to cholinesterase inhibitors is associated with an increased risk of chronic lymphocytic leukemia
- Neural tube defects have been associated with symptomatic exposures during the first trimester of pregnancy
- The available evidence does not explain the myriad of symptoms of Gulf War Illness on the basis of exposure to cholinesterase inhibitors
- The Wenger-Herzold study demonstrated clinically significant long-term decrements in immunity in those with long-term exposure to organophosphorus compounds, but not carbamates
- None of the above
- The most characteristic early finding in intermediate syndrome is: (Choose the ONE BEST answer)
- Loss of sensation in distal extremities
- Inability of the patient to lift his/her head off the pillow
- Muscle fasciculations
- Profound salivation (liters per day)
- None of the above
- Muscarinic receptors are found in: (Choose ALL correct answers)
- Skeletal muscle
- Smooth muscle
- Exocrine glands
- Sweat glands
- None of the above
- Which of the following are true about the central nervous system effects of cholinesterase inhibitors (Choose the ONE BEST answer)
- The pathology can be explained on the basis of increased muscarinic, as opposed to nicotinic, receptor activity
- The pathology can be explained on the basis of increased nicotinic, as opposed to muscarinic, receptor activity
- The pathology is poorly understood but involves both nicotinic and muscarinic receptors
- None of the above
- Which of the following central nervous system signs and symptoms have been reported in cases of cholinesterase inhibitor poisoning? (Choose ALL correct answers)
- Anxiety
- Emotional lability
- Convulsions
- Excess dreaming
- None of the above
- Which of the following questions on an exposure history are appropriate for the physician to ask in a patient suffering from signs and symptoms suggestive of cholinesterase inhibitor poisoning? Choose ALL correct answers
- What are your hobbies?
- Do you cook with wild mushrooms?
- Does anyone at home have similar signs or symptoms?
- Do you handle venomous snakes?
- None of the above
- Cholinesterase inhibitors block the ability of acetylcholinesterase to break down acetylcholine by? (choose the ONE best answer)
- Occupying the binding site on cholinesterase to which the acetylcholine would attach
- Preventing the release of acetylcholine from its attachment on cholinesterase
- Attaching to acetylcholine which prevents its attachment to cholinesterase
- None of the above
- What causes the cholinergic toxidrome? (Choose the ONE best answer)
- An excess of acetylcholine
- A deficiency of acetylcholine
- An excess of acetylcholinesterase
- None of the above
- Where are cholinergic receptors are found? (Choose ALL correct answers)
- At the neuromuscular junction
- In the central nervous system
- In the sympathetic, peripheral nervous system
- In the parasympathetic, peripheral nervous system
- None of the above
- Nicotinic and muscarinic receptors differ in which the following ways (Choose ALL correct answers)
- They have different functions
- They have different mechanism by which they trigger signal transmission
- They may exist at different anatomical locations
- None of the above
- Why do excessive levels of acetylcholine (“The cholinergic toxidrome”) cause different signs and symptoms, depending on whether the nicotinic or muscarinic receptors are involved? (Choose ALL correct answers)
- Because some nicotinic and muscarinic receptors are located in and affect different anatomic structures
- Because nicotinic and muscarinic receptors are triggered by different neurotransmitters
- Because nicotinic and muscarinic receptors have different mechanisms of action
- None of the above
- Factors that account for variation in the clinical presentation of cholinesterase toxicity include: (Choose ALL correct answers)
- Route of exposure
- The balance of nicotinic and muscarinic effects on the sympathetic and parasympathetic nervous system
- Age of the patient
- The specific cholinesterase-inhibiting chemical
- None of the above
- Which of the following are major factors leading to respiratory failure in cases of cholinesterase inhibitor poisoning? (Choose ALL correct answers)
- Bronchodilation
- Central respiratory depression
- Weakness or paralysis of the respiratory muscles
- Excessive respiratory tract secretions
- None of the above
- Which of the following statements are true regarding serum or red blood cell cholinesterase levels? (Choose ALL correct answers)
- The use of these tests helps to avoid serious errors in emergency treatment
- With current technology, interindividual variation in results, is no longer a significant problem
- While percentage of inhibition in the same person may be different in different laboratories, the absolute cholinesterase values are usually the same
- None of the above
- Which of the following statements are true about the laboratory measurement of cholinesterase inhibitors themselves or their metabolites? (Choose ALL correct answers)
- Each test can measure only one chemical, so it is only useful if you know the specific chemical to which the patient was exposed
- The results are not usually available in time to guide emergency treatment
- The test results are usually very accurate
- None of the above
- Which of the following statements is true about the patient with exposure to cholinesterase inhibitors? (Choose ALL correct answers)
- If the patient has only been exposed to cholinesterase inhibitor vapor, there is no risk of secondary exposure
- If the patient has ingested a cholinesterase inhibitor, others can be exposed if the patient vomits
- More important than which decontamination fluid is used is how rapidly decontamination is initiated
- Water and soapy water are very effective decontamination fluids
- None of the above
- If a hospital receives a patient with cholinesterase inhibitor toxicity and there is the potential that others were also exposed at the scene, which of the following should be notified (Choose ALL correct answers)
- All other area hospitals
- The local fire department
- The poison center
- Area EMS providers
- None of the above
Relevant Content
To review content relevant to the posttest questions, see:
Question | Location of Relevant Content |
---|---|
1 | Community preparedness |
2 | Community preparedness |
3 | What type of patdology do cholinesterase inhibitors cause? |
4 | What type of patdology do cholinesterase inhibitors cause? |
5 | Nicotine acetylcholine receptors |
6 | Nicotine acetylcholine receptors |
7 | Nicotine acetylcholine receptors |
8 | Muscarinic acetylcholine receptors |
9 | What is the cholinergic toxidrome? |
10 | Effects on routine laboratory tests |
11 | Differential diagnosis |
12 | Signs and symptoms: differences in pediatric cases |
13 | Who is at risk for exposure? the exposure history |
14 | Who is at risk for exposure? the exposure history |
15 | Effects on routine laboratory tests |
16 | Management strategy 2: Supportive care |
17 | Management strategy 3: Medications – Atropine |
18 | Management strategy 3: Medications |
19 | Management strategy 3: Medications |
20 | Management strategy 3: Medications |
21 | Management strategy 3: Medications – 2-PAM |
22 | Management strategy 3: Medications |
23 | Management strategy 3: Medications |
24 | Management strategy 3: Medications – Diazepam |
25 | Syrup of ipecac, gastric lavage, catdartics, and activated charcoal |
26 | the intermediate syndrome |
27 | Organophosphate-induced delayed neuropatdy (OPIDN) |
28 | Organophosphorus ester-induced chronic neurotoxicity (OPICN) |
29 | Other issues related to cholinesterase inhibitor toxicity |
30 | the intermediate syndrome |
31 | Muscarinic acetylcholine receptors |
32 | Clinical findings are due to a mixture of nicotinic and muscarinic effects |
33 | Clinical findings are due to a mixture of nicotinic and muscarinic effects |
34 | Who is at risk for exposure? the exposure history |
35 | What are cholinesterase inhibitors? |
36 | the cholinergic toxidrome: What is the cholinergic toxidrome? |
37 | the cholinergic toxidrome: What is the cholinergic toxidrome? |
38 | the cholinergic toxidrome: What is the cholinergic toxidrome? |
39 | the cholinergic toxidrome: What is the cholinergic toxidrome? |
40 |
the cholinergic toxidrome: Clinical findings in cholinesterase inhibitor toxicity are due to a mixture of nicotinic and muscarinic effects. the cholinergic toxidrome: Signs and Symptoms: differences in pediatric cases |
41 | Management strategy 2: supportive care |
42 | Laboratory Assessment of the Cholinergic Toxidrome: Red Blood Cell (RBC) and Serum Cholinesterase Levels |
43 | Laboratory Assessment of the Cholinergic Toxidrome: Direct Measurement of Cholinesterase Inhibitors and their Metabolic Byproduct |
44 | Management of the Cholinergic Toxidrome: Management Strategy 1: Prevention of Secondary Exposure |
45 | Public Healtd and Medico-Legal Issues |