TIVA can reduce the need for volatile anesthetics.
It can provide improved control over depth of anesthesia.
Decreased risk of postoperative nausea and vomiting.
Quicker recovery times compared to inhalation agents.
Reduced cardiovascular depression during maintenance phase.
Pharmacokinetics:
Children have higher body water and lower body fat. This can lead to a larger central compartment (V1). Higher doses may be needed to reach the target plasma concentration. Neonates and infants may have immature organ function, affecting clearance.
Clearance is usually higher per kilogram in children. This is due to faster metabolic rates in school-age children. Neonates and infants exhibit slower clearance and prolonged half-life.
The active duration after infusion varies by age. In older children, it may be shorter versus adults. In neonates/infants, the drug may linger longer due to enzyme immaturity.
Pharmacodynamics:
Children may show sensitivity differences in GABA or opioid receptors. Dose-response curves can therefore differ. Propofol’s dose-response curve in adults may be more pronounced in young children.
Rapid anesthesia is desired in pediatric patients. However, overshooting is a risk, resulting in excessive sedation. Prolonged recovery may also occur.
Greater interpatient variability is common in neonates and infants. Close monitoring and frequent adjustments are required.
TIVA provides smooth recovery, a key benefit in pediatric anesthesia.
It's useful when volatile agents are not ideal.
Manual dosing can be difficult in pediatrics. PK changes with age/size.
Monitoring limitations persist in younger children. Clinical judgment remains key.
Determine the correct induction dose. Refer to age-specific guidelines for dosing.
Begin infusion at the initial rate. Closely monitor sedation depth and hemodynamics.
Progress through time intervals, reducing rate as recommended. Follow the schedule diligently.
Monitor depth and adjust rate. Maintain cardiorespiratory surveillance during the infusion.
This is an example of how to administer TIVA in a 2-year-old child (10 kg) undergoing a procedure.
Administer a propofol bolus of 30 mg IV slowly (3 mg/kg × 10 kg).
Start infusion at 120 mg/h (12 mg/kg/h × 10 kg). Reassess depth and vitals at ~5 minutes.
Decrease to 90 mg/h (9 mg/kg/h × 10 kg). Adjust if needed.
Lower to 60 mg/h (6 mg/kg/h).
Maintain 6 mg/kg/h or further reduce to 5 mg/kg/h if appropriate.
Weight-based dosing may overestimate required dose in obese patients. Consider lean body mass for calculations. Adjust based on clinical response and monitoring.
Adipose tissue leads to altered drug distribution and clearance. This can result in prolonged drug effects.
Use a smaller loading dose initially. Titrate carefully to avoid oversedation.
Reduce maintenance infusion rates. Regularly assess sedation depth and adjust accordingly.
Increased fat mass leads to a larger volume of distribution for lipophilic drugs.
This can cause prolonged drug effects if dosing is not properly adjusted.
Obese patients often have altered hepatic blood flow and enzyme activity.
Use lean body weight during bolus for a more accurate dosing basis to avoid overdosing.
Drugs may take longer to eliminate due to the larger adipose-rich compartment.
Prolonged infusions may delay recovery, so carefully monitor obese patients.
Doses are based on adjusted or lean body weight. Start with a higher infusion rate, then gradually reduce. Frequent reassessment is required.
Limitations: Challenging due to variability.
TCI allows precise dosing via individualized data and automatic corrections. It reduces the risk of oversedation or delayed recovery.
Limitations: Models have less validation.
Input lean body weight, age, height, and gender into the TCI pump.
Use for effect-site targeting. It adjusts for age and lean body mass.
An alternative across a wide spectrum, including obese patients.
Set effect-site concentration of Propofol to 3–4 µg/ml.
*Values are starting points using weight adjustments. Adjust based on clinical monitoring.
LBW formulas estimate body mass, excluding excess fat. The James and Janmahasatian formulas are common. Choose Janmahasatian for obese patients. Accurate dosing ensures optimal drug effect and minimizes the risk of toxicity. LBW provides a more reliable estimate of metabolically active tissue compared to total body weight, especially in individuals with a high proportion of adipose tissue.
Separate formulas for men and women, incorporating TBW and height. Less accurate in extremely obese patients. The James formula, while widely used, may overestimate LBW in obese individuals, potentially leading to excessive drug administration. It is essential to consider the limitations of this formula, especially when dealing with patients at the extremes of the weight spectrum. The James formula is as follows:
Uses TBW and BMI. More robust across a wider range of BMI values. Use this to dose obese patients. The Janmahasatian formula incorporates body mass index (BMI) to improve accuracy across diverse body compositions. This is particularly useful in obese patients where the relationship between weight, height, and lean mass is less predictable. It is also useful for calculating the dose required.
TIVA provides benefits. These include smooth induction and rapid recovery.
They have comorbidities. There is decreased organ reserve and altered body composition.
Safe, effective anesthesia is required. Optimize drug choices and dosing.
Reduced total body water decreases distribution volume for hydrophilic drugs. Increased fat leads to a larger volume for lipophilic drugs like propofol.
Reduced liver and kidney function slow drug clearance. This necessitates lower doses to avoid oversedation and delayed emergence.
Reduced clearance prolongs the context-sensitive half-time. It is important to carefully reduce the infusion rate towards the end of surgery.
Elderly patients have greater sensitivity to anesthetics. Changes in receptor density and function cause this.
The elderly often show a blunted cardiovascular response. Small dose increases may cause hypotension.
The elderly are at higher risk of POCD. Monitor depth of anesthesia to avoid deep sedation.
Reduce the induction bolus to 1–1.5 mg/kg of propofol. Use ideal or adjusted body weight.
Modify the "12-10-6 rule." Start at lower rates. Reduce by 20–30% compared to younger adults.
Start with a lower infusion rate. Use BIS to monitor. Adjust infusion rates in small increments.
Use models like Schnider or Eleveld. They adjust for age and lean body mass.
Carefully enter age, height, weight, and gender. Set lower target concentrations.
TCI automates titration and provides gradual changes. It reduces overdosage risk. Manual adjustments may be needed.
Use depth-of-anesthesia monitors and blood pressure monitoring.
Begin with lower doses than younger patients. Increase cautiously.
Prepare to use fluids, vasopressors if blood pressure drops.
Anticipate a prolonged recovery. Avoid over-sedation. Reduce POCD risk.
Elderly patients require special consideration when administering TIVA due to altered pharmacokinetics and increased sensitivity.
Evaluate cardiac function, renal status, and cognitive baseline. Consider reduced doses for patients >75 years.
Start propofol at 1-2 μg/ml effect-site concentration (30-40% reduction from standard adult dose).
Reduce remifentanil to 0.05-0.1 μg/kg/min or target 1-2 ng/ml if using TCI (50% reduction).
Maintain BIS between 50-65 (higher than younger adults). Increase in 0.2-0.5 μg/ml increments.
Maintain MAP within 20% of baseline. Reduce propofol if hypotension occurs.
Balance maternal safety and fetal well-being is key. Minimize drug transfer to the fetus.
Inhalational agents may cause uterine relaxation. They could affect fetal oxygenation.
TIVA provides precise control over anesthesia depth. This is important during C-sections.
Faster recovery aids maternal-fetal bonding. It supports immediate post-operative care.

Administer 1.5–2 mg/kg based on ideal body weight. Adjust for increased cardiac output.
Use a step-down approach, like 12-10-6 mg/kg/h, adjusted to maternal response.
Remifentanil at 0.05–0.1 µg/kg/min for analgesia. Titrate carefully.
Use Schnider or Eleveld for propofol. Account for maternal changes.
Propofol target around 3–4 µg/ml. Remifentanil around 2–3 ng/ml.
TCI offers precise control. It helps quickly achieve desired anesthesia depth.
It reduces dosing errors versus manual infusion. Automated systems enhance safety.
TCI allows for smooth emergence. This is vital for maternal recovery and fetal safety.

Monitor heart rate and blood pressure continuously. Invasive monitoring for high-risk cases.
Use BIS to maintain optimal anesthesia depth. Avoid over-sedation.
Monitor fetal heart rate if possible. Especially during C-sections.
Expect rapid recovery due to drug clearance. Ensure maternal and neonatal stability.
TIVA allows fine control of sedative and analgesic agents during MAC.
BIS helps quantify sedation depth, ensuring optimal patient comfort and safety.
The goal is to maintain patient comfort while preserving airway reflexes.
Sedation during MAC should reach specific levels. These include minimal, moderate, and deep sedation.
During minimal sedation, patients are relaxed and cooperative. Moderate sedation means the patient is sedated but responsive.
Deep sedation involves the patient being asleep with minimal response. Airway assistance may be needed.
BIS values from EEG help monitor the sedation level. This helps ensure patient comfort and safety.

The table below lists typical infusion rates. It includes propofol and remifentanil during MAC. Propofol values are shown in µg/kg/min and mg/kg/h.
TCI pumps use models and patient data. Infusion is smoother, with fewer changes.
TCI maintains target effect-site concentration. It correlates with the sedation level better.
Automated adjustments reduce manual changes. This minimizes dosing errors and enhances safety.
TCI adjusts for changes in drug distribution. It offers safety and comfort to the patient.
Manual infusion is an option if TCI is not available. Vigilant monitoring is still needed.
Start propofol at lower effect-site concentration (0.5-1.0 μg/ml) for conscious sedation.
Increase in 0.2 μg/ml increments. Allow 2-3 minutes between adjustments for equilibration.
Maintain BIS between 65-80 for sedation. Ensure patient remains responsive to verbal commands.
Add low-dose remifentanil (0.025-0.05 μg/kg/min) for painful procedures.
Reduce target concentration gradually. Expect prompt emergence with minimal residual sedation.
TIVA can be given to seriously ill patients whose systemic disease is not a constant threat to life (ASA III).
Pharmacokinetics and pharmacodynamics will be affected; ill patients are more sensitive to anaesthetic medication.
No specific protocols exist, but the algorithm for elderly patients can be adopted as both describe reduced drug concentration and dosage.
BIS may decrease during hypotensive episodes due to hypo-perfusion of the brain. Always keep BIS < 65 and propofol concentration > 1.2 µg/ml.
Relevance of TIVA in Pediatrics