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Time Constant
Last updated: 02/25/2026
Key Points
- The time constant (τ) is defined as the time required for the concentration of an anesthetic gas in the breathing circuit to reach approximately 63% of its new equilibrium value after a step change in fresh gas concentration.
- τ = Volume of the Breathing System (VBS)/Fresh Gas Flow (FGF)
- Increasing FGF or reducing VBS shortens the time constant, allowing for faster equilibration. Conversely, low-flow anesthesia prolongs equilibration, potentially delaying clinical responses to changes in vaporizer settings.
- The time constant in low-flow anesthesia can be overcome by the concentration effect, whereby increasing the concentration of volatile anesthetics accelerates induction.
Definition and Formula
- The time constant of the anesthesia breathing circuit (τ_”circuit” ) is defined as the time required for the concentration of an anesthetic gas within the circuit to reach approximately 63% of its new target or equilibrium value after a step change in the fresh gas concentration.1
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- VBS: The internal volume of the breathing systemVBS, including all hoses, the reservoir bag, the CO2 absorber, and the internal components of the machine. This volume typically ranges from 4 to 6 liters in an adult circle system.2
- FGF: The rate at which fresh is delivered into the circuit, measured in liters per minute (L/min).2
- The resulting time constant (τcircuit) is expressed in units of time.
Figure 1. Volume of breathing system of a traditional circle system. Source: Tsim P, Howatson A. Breathing systems in anesthesia. WFSA Anaesthesia Tutorial of the Week. 2016. CC BYNC ND 4.0.3
The Exponential Process of Wash-In and Wash-Out
- The change in anesthetic concentration in the circuit, whether increasing (wash-in) or decreasing (wash-out), follows an exponential curve. This is a first-order kinetic process where the rate of change is proportional to the difference between the current concentration and the target concentration.1
- τ: 63% complete
- τ: 86% complete
- τ: 95% complete (sufficient equilibration for the brain)
- τ: 98% complete
- τ: Approximately 99% (considered full equilibration for the breathing circuit)
- As fresh gas carrying the anesthetic begins to flow into the air-filled circuit (assuming complete mixing), the concentration in the circuit (FI) will rise according to first-order kinetics:
The specific equation that models this behavior is:4
FI: The fraction of inspired anesthetic in the circuit at time T.
FFGO: The fraction of inspired anesthetic in the gas leaving the fresh gas outlet (vaporizer setting), which is the maximum or final concentration achieved.
T: The time elapsed since the flow began.
τ: The time constant
Figure 2. Concentration of anesthetic gas in the circuit over time
Clinical Implications and Examples
The time constant is a practical tool for the anesthesiologist to manage the speed of induction and emergence.5
Rapid Induction and Emergence (High Flow)5
- During the initial phase of anesthesia (preoxygenation and induction) or at the end of the procedure (emergence), a high FGF rate (e.g., 6-8 L/min for an adult patient) is used.
- This high flow rate minimizes the time constant, allowing the inspired concentration to quickly match the vaporizer setting and facilitating a rapid change in patient anesthetic depth.
Maintenance (Low Flow)5
- Once the desired depth is reached, the clinician may reduce the FGF to low-flow anesthesia (e.g., 0.5-2 L/min) to conserve anesthetic agent, maintain patient heat and humidity, and minimize environmental pollution.
- The time constant increases, and any changes in the vaporizer setting will take several minutes to be reflected in the inspired gas and, subsequently, in the patient’s brain concentration.
Patient Factors5
- The patient is an integral part of the breathing system volume, specifically their functional residual capacity (FRC). The total VBS to consider for the time constant calculation can actually be considered:
- This means that a patient with a large FRC or a large circuit volume (e.g., an adult circuit on a pediatric patient) will have a longer time constant, slowing the control of anesthesia depth.
Below are some examples to illustrate some common clinical scenarios:
Table 1. Examples of different circuit systems and clinical scenarios with varying time constants on the time it takes to achieve brain equilibration (≈3τ)
The Role of Low-Flow Anesthesia
- Low-flow anesthesia is defined as the practice of using a fresh gas flow (FGF) of less than 3 L/min, often as low as 0.5 L/min during maintenance.6
- This technique offers economic benefits (reduced agent consumption), ecological benefits (less environmental pollution), and physiological benefits (better preservation of patient heat and humidity in the circuit).6
- A reduced FGF rate directly increases the time constant of the breathing system.
Clinical Implications of Long-Time Constants
- Slower Equilibration: Changes in vaporizer settings or flow rates take much longer to reach the desired inspired concentration (FI). It may take longer than desired to reach the target minimum alveolar concentration (MAC).
- Potential for Accumulation: With less gas washout, there is a potential for the accumulation of undesired trace gases degradation products, although this is largely mitigated by modern absorbents and monitoring.
Figure 3. Wash-in of the breathing circuit depending on the fresh gas flow (FGF), with presumed VBS of 6L. Higher FGF results in more rapid equilibration of the circuit.5
Overcoming the Time Constant in Low-Flow Anesthesia with the Concentration Effect
- While the time constant dictates how quickly a percentage of the final concentration is reached in the breathing circuit, the actual speed of induction is also dependent on the concentration effect.7
- The Concentration Effect states that the increase in the rate of rise for FA (alveolar concentration)/FI (inspired concentration) as the alveolar concentration is increased, and results subsequently in a more rapid induction.8
A clinician can leverage the concentration effect to achieve rapid induction even with relatively low flow rates by using a high concentration/percentage of volatile anesthetic.
- Vaporizer “Overshoot”: Instead of setting the vaporizer to the desired maintenance concentration (e.g., 1 MAC), the anesthesia provider can temporarily set the vaporizer to a much higher concentration (e.g., 2 MAC or 4% sevoflurane).
- Rapid FI and FA rise: This high fresh gas outlet concentration rapidly increases the inspired concentration (FI) and immediately creates a high partial pressure gradient that drives the agent into the patient’s blood and brain, counteracting the patient’s initial large uptake.
- Monitoring is essential: Because the clinician is intentionally pushing concentrations higher than needed for maintenance, continuous real-time monitoring of inspired (FI) and end-tidal (FA) agent concentrations is essential to guide the safe reduction of the vaporizer setting once the desired anesthetic depth is achieved.
- This technique effectively accelerates the initial “wash-in” phase, allowing the clinician to transition to a truly low-flow (e.g., 1 L/min) maintenance phase sooner and more safely, using the time constant principle for stable maintenance.
References
- Dosch MP, Loeb RG, Brainerd TL, et al. Time to a 90% change in gas concentration: a comparison of three semi-closed anesthesia breathing systems. Anesthesia & Analgesia. 2009 Apr;108(4):1193-7. PubMed
- Jones K. Time constant or half time of a breathing system? Anaesthesia. 2003. 58: 385-402. Link
- Tsim P, Howatson A. Breathing systems in anaesthesia. WFSA Anaesthesia Tutorial of the Week. Published 2016. Accessed 2025. Link
- Ebert TJ, Lindenbaum L. Inhaled anesthetics. Anesthesia Key. Published 2016. Accessed 2025. Link
- Shin HW, Yu HN, Bae GE, et al. The effect of fresh gas flow rate and type of anesthesia machine on time to reach target sevoflurane concentration. BMC Anesthesiology. 2017;17(1):10. PubMed
- Hönemann C, Hagemann O, Doll D. Inhalational anaesthesia with low fresh gas flow. Indian J Anaesth. 2013 Jul;57(4):345-50. Link
- Upadya M, Saneesh PJ. Low-flow anaesthesia—underused mode towards “sustainable anaesthesia.” Indian J Anaesth. 2018;62(3):166-172. Link
- Hannallah M. Chapter 10: Concentration and Second Gas Effects. In: Freeman B, Berger JS. Anesthesiology Core Review: Part One Basic Exam. USA; McGraw-Hill Education; 2014.
Other References
- Gamboa J, Romano O. Inhaled anesthetic agents: Mechanism of action, uptake, and distribution. OA summary. 2023. Link
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