Which of the following is NOT a contraindication for spinal anaesthesia?
Who is known for demonstrating the levels of ether anesthesia?
In which context can helium replace nitrogen as a diluent gas in oxygen mixtures?
Which of the following cannot be given by epidural anaesthesia?
Ayre's T-piece is which type of circuit
Stages of anesthesia were established by
What is the most reliable indicator to prevent esophageal intubation?
What is a significant disadvantage of ketamine?
What is the maximum concentration allowed for epidural block?
The inducing agent of choice in shock -
NEET-PG 2012 - Anesthesiology NEET-PG Practice Questions and MCQs
Question 11: Which of the following is NOT a contraindication for spinal anaesthesia?
- A. Raised intracranial tension
- B. Bleeding disorder
- C. Hypertension (Correct Answer)
- D. Infection at injection site
Explanation: ***Hypertension*** - While **severe uncontrolled hypertension** may necessitate blood pressure stabilization before surgery, **mild to moderate hypertension** is not an absolute contraindication for spinal anesthesia. - In fact, spinal anesthesia can sometimes be beneficial in hypertensive patients due to its **vasodilatory effects**, which may help lower blood pressure. *Bleeding disorder* - A **bleeding disorder** (e.g., thrombocytopenia, coagulopathy) is a **major contraindication** due to the high risk of **epidural or spinal hematoma** formation. - A hematoma can lead to **spinal cord compression** and irreversible neurological damage. *Raised intracranial tension* - **Raised intracranial tension (ICT)** is a **strict contraindication** because the drop in cerebrospinal fluid (CSF) pressure during spinal anesthesia can worsen the pressure gradient across the foramen magnum. - This can precipitate **herniation of the brainstem** and lead to catastrophic neurological injury or death. *Infection at injection site* - The presence of an **infection at the injection site** is an absolute contraindication as it poses a significant risk of introducing bacteria into the **subarachnoid space**. - This can lead to serious complications such as **meningitis** or a **spinal abscess**.
Question 12: Who is known for demonstrating the levels of ether anesthesia?
- A. Morton
- B. Guedel (Correct Answer)
- C. Thompson
- D. None of the options
Explanation: ***Guedel*** - Arthur Guedel developed and refined the **stages and planes of ether anesthesia** based on clinical observations of respiratory patterns, eye signs, and muscle tone. - His classification system, known as the **Guedel stages**, provided a systematic approach to monitoring anesthetic depth, especially useful before the advent of modern anesthetic agents and monitoring equipment. *Morton* - **William T.G. Morton** is credited with the first successful public demonstration of sulfuric ether as a surgical anesthetic in 1846 during a tooth extraction. - While he pioneered the use of ether for anesthesia, he did not develop the classic stages of anesthetic depth. *Thompson* - There is no widely recognized historical figure named Thompson who is primarily known for defining the **levels or stages of ether anesthesia**. - This name is not associated with the primary discovery or classification of anesthetic depth. *None of the options* - This option is incorrect because **Guedel** is specifically known for his work in defining the stages of ether anesthesia. - Guedel's contributions were significant in standardizing anesthetic practice for many years.
Question 13: In which context can helium replace nitrogen as a diluent gas in oxygen mixtures?
- A. Argon
- B. Xenon
- C. Helium
- D. None of the options (Correct Answer)
Explanation: **None of the options** - This question implies that helium might replace *another noble gas* as a diluent, but the correct application is for helium to replace **nitrogen** in oxygen mixtures, particularly in **diving applications**. This question likely has a flaw in its premise if expecting one of the noble gases listed to be the 'replacement' for nitrogen, as helium *is* the replacement. - Helium is used instead of nitrogen in diving gases (**trimix, heliox**) for deep dives because it is less narcotic than nitrogen under pressure, reducing the risk of **nitrogen narcosis**. *Argon* - **Argon** is denser than nitrogen and has a higher narcotic potential at depth, making it unsuitable as a replacement for nitrogen in diving gases. - It is sometimes used during **dry suit inflation** for insulation due to its low thermal conductivity, but not as a breathing gas diluent. *Xenon* - **Xenon** is a potent anesthetic agent, even at atmospheric pressure, due to its high lipid solubility. - Its use as a diluent would cause severe **narcosis** and render a diver unconscious, making it entirely inappropriate for diving mixtures. *Helium* - While helium is indeed the gas that replaces nitrogen as a diluent in oxygen mixtures for deep diving, it being listed as an option here suggests a misunderstanding of the question's phrasing. The question is asking for **in which context** helium can replace nitrogen, not asking to identify helium itself as the replacement. - Given the other options are noble gases that *cannot* replace nitrogen in this context, "None of the options" is the most accurate answer if the question implies picking from the provided list for a replacement *for helium* or a suitable *alternative* to helium, which isn't the case here.
Question 14: Which of the following cannot be given by epidural anaesthesia?
- A. Morphine
- B. Remifentanil (Correct Answer)
- C. Alfentanil
- D. Fentanyl
Explanation: ***Remifentanil*** - **Remifentanil** is specifically designed for **intravenous administration** and is rapidly metabolized by plasma esterases, making it unsuitable for epidural use. - Due to its short half-life and rapid metabolism, epidural administration would provide inconsistent and fleeting analgesia, and its breakdown products are not inert in the epidural space, potentially causing **neurotoxicity**. *Morphine* - **Morphine** is a commonly used opioid for **epidural analgesia** due to its hydrophilicity, allowing for prolonged action in the cerebrospinal fluid. - It provides effective **postoperative pain relief** and has a relatively slow onset but long duration of action when administered epidurally. *Alfentanil* - **Alfentanil** is a synthetic opioid that has been used for **epidural analgesia**, though less commonly than fentanyl or sufentanil, sometimes in conjunction with local anesthetics. - It has a faster onset and shorter duration of action compared to morphine, but still provides effective **analgesia** when administered epidurally. *Fentanyl* - **Fentanyl** is a widely used lipophilic opioid for **epidural analgesia**, often combined with local anesthetics, for both surgical and obstetric pain. - Its lipophilicity allows for rapid absorption and a relatively quick onset of action, providing effective **segmental analgesia**.
Question 15: Ayre's T-piece is which type of circuit
- A. Type A
- B. Type B
- C. Type E (Correct Answer)
- D. Type D
Explanation: ***Type E*** - The **Ayre's T-piece** is classified as a **Type E breathing circuit** according to the classification of Mapleson circuits. - It is a modification of the Mapleson A circuit, widely used in pediatric anesthesia due to its high efficiency and low resistance. *Type A* - **Mapleson A circuits** have the fresh gas flow (FGF) inlet near the patient and a reservoir bag at the circuit's most distal end. - While very efficient for spontaneous ventilation, they are not the same as an Ayre's T-piece. *Type B* - **Mapleson B circuits** have the fresh gas flow inlet and the reservoir bag near the patient, with the expiratory valve further away. - This configuration is generally inefficient for both spontaneous and controlled ventilation. *Type D* - **Mapleson D circuits** have the fresh gas flow inlet near the patient and the expiratory valve close to the reservoir bag, which is distal to the patient. - These circuits are commonly used for controlled ventilation, but are not the Ayre's T-piece.
Question 16: Stages of anesthesia were established by
- A. Diethyl ether (Correct Answer)
- B. Nitrous oxide
- C. Halothane
- D. Chloroform
Explanation: ***Diethyl ether** - The classic stages of anesthesia (analgesia, excitement, surgical anesthesia, medullary depression) were originally described in relation to the administration of **diethyl ether**. - Its slow onset and prolonged half-life allowed for the clear observation and definition of these distinct stages. *Nitrous oxide* - This gaseous anesthetic has a rapid onset and offset, making it difficult to clearly delineate all four classical stages with its use. - It is often used as an adjunct to other anesthetics rather than as a sole agent for prolonged surgical anesthesia. *Halothane* - Halothane is a potent volatile anesthetic that became popular after ether, but its use also does not typically involve the clear, step-wise progression through all four anesthetic stages as seen with ether. - It was one of the first widely used inhaled anesthetics that largely replaced ether due to better patient control and fewer side effects. *Chloroform* - Chloroform was another early anesthetic but was associated with significant cardiac and hepatic toxicity, leading to its limited use and eventual discontinuation. - While it induced anesthesia, the clear staging of anesthetic depth was primarily established and standardized using diethyl ether.
Question 17: What is the most reliable indicator to prevent esophageal intubation?
- A. Oxygen saturation on pulse oximeter
- B. Direct visualization of passing tube beneath vocal cords
- C. Auscultation over chest
- D. Measurement of CO2 in exhaled air (EtCO2). (Correct Answer)
Explanation: ***Measurement of CO2 in exhaled air (EtCO2)*** - The presence of **carbon dioxide** in exhaled air confirms tracheal intubation as the esophagus does not contain CO2. - This method provides a **real-time**, objective assessment of tube placement that is highly reliable because even small amounts of CO2 are detected. *Oxygen saturation on pulse oximeter* - This indicator measures **oxygenation**, which can remain adequate for several minutes after esophageal intubation due to pre-oxygenation. - A **delayed drop in saturation** might indicate esophageal intubation, but it's not immediate and therefore not the most reliable early indicator. *Direct visualization of passing tube beneath vocal cords* - While helpful, **direct visualization** can sometimes be misleading due to difficult airways or poor visibility, where the tube might appear to pass correctly but enter the esophagus. - This method is **operator-dependent** and its reliability can vary based on the intubator's experience and the patient's anatomy. *Auscultation over chest* - **Auscultation** can detect breath sounds; however, sounds can be transmitted from the stomach or surrounding tissues, leading to false positives. - It is also very difficult to reliably distinguish between **esophageal and tracheal sounds**, especially in noisy environments or with inexperienced personnel, making it less reliable than EtCO2.
Question 18: What is a significant disadvantage of ketamine?
- A. Increased heart rate
- B. Increased ICT
- C. Delirium (Correct Answer)
- D. All of the options
Explanation: ***Delirium*** - Ketamine is known to cause **emergence phenomena**, which include **vivid dreams, hallucinations**, and **delirium**, particularly during recovery from anesthesia. - This psychotomimetic effect can be distressing for patients and may necessitate the co-administration of a **benzodiazepine** to mitigate these symptoms. *Increased heart rate* - While ketamine does cause an **increase in heart rate** and **blood pressure** due to sympathetic stimulation, this is often considered a disadvantage but not the *most significant* when compared to the unique cognitive side effects. - This effect can be beneficial in patients with **hemodynamic instability**, but can be problematic in those with **cardiovascular disease**. *Increased ICT* - It is often considered a contraindication in patients with **elevated intracranial pressure (ICP)** as it can potentially increase **cerebral blood flow** and thus ICP. - However, recent studies suggest that in adequately ventilated patients, the effect on ICP may be less pronounced than previously thought, making delirium a more consistent and prominent disadvantage for many patients. *All of the options* - While ketamine can cause an **increased heart rate** and potentially affect **intracranial pressure**, **delirium** and other emergence phenomena are often highlighted as a unique and significant disadvantage because they are highly distressing and difficult to manage. - The psychotomimetic effects are a hallmark side effect that often governs its cautious use without concurrent medication.
Question 19: What is the maximum concentration allowed for epidural block?
- A. Chlorprocaine (Correct Answer)
- B. Lidocaine
- C. Ropivacaine
- D. Bupivacaine
Explanation: ***Chlorprocaine*** - **Chlorprocaine** is an ester-type local anesthetic that can be safely used in higher concentrations for epidural blocks up to **3%**, due to its rapid hydrolysis by plasma pseudocholinesterase, leading to a very short half-life and reduced systemic toxicity. - Its rapid metabolism minimizes the risk of accumulation and systemic toxicity, making it a suitable choice when a dense block is needed and a short duration of action is acceptable. *Lidocaine* - **Lidocaine** is an amide-type local anesthetic commonly used in epidural blocks, but its maximum concentration for this application is typically limited to **2%** to avoid systemic toxicity. - Higher concentrations of lidocaine are associated with an increased risk of neurological and cardiovascular adverse effects. *Ropivacaine* - **Ropivacaine** is an amide-type local anesthetic that is less cardiotoxic than bupivacaine, with common concentrations for epidural use ranging from **0.2% to 1%**. - Its maximum concentration is significantly lower than chlorprocaine due to its longer duration of action and potential for systemic toxicity at higher doses. *Bupivacaine* - **Bupivacaine** is a potent amide-type local anesthetic with a high risk of cardiotoxicity, and its maximum concentration for epidural use is generally restricted to **0.5%** or even less for continuous infusions. - Using concentrations above this limit significantly increases the risk of severe cardiovascular complications, including arrhythmias and cardiac arrest.
Question 20: The inducing agent of choice in shock -
- A. Isoflurane
- B. Ketamine (Correct Answer)
- C. Desflurane
- D. Thiopentone
Explanation: **Ketamine** * **Ketamine** is preferred in shock due to its sympathomimetic properties, which maintain or increase blood pressure and heart rate, thus preserving **cardiovascular stability**. * It also has minimal respiratory depression and bronchodilatory effects, making it safer for patients with compromised respiratory function. * The cardiovascular stimulating effects of ketamine helps maintain haemodynamic stability in shocked patients. It maintains cerebral autoregulation and perfusion of vital organs. *Isoflurane* * **Isoflurane** is an inhaled anesthetic that typically causes **dose-dependent myocardial depression** and **vasodilation**, which can worsen hypotension in a shock state. * It can significantly decrease systemic vascular resistance, thereby exacerbating the already compromised cardiovascular status of a shock patient. *Desflurane* * **Desflurane** is an inhaled anesthetic known for its rapid onset and offset but can cause a **significant increase in heart rate and blood pressure** upon rapid concentration changes, which may be detrimental in an unstable patient. * Like isoflurane, it also causes dose-dependent peripheral vasodilation and myocardial depression, which can worsen hypotension in patients in shock. *Thiopentone* * **Thiopentone** is a barbiturate that causes significant **myocardial depression** and **peripheral vasodilation**, leading to a substantial drop in blood pressure. * Its use in shock would further compromise cardiovascular stability and is generally contraindicated due to its potent hemodynamic depressant effects.