End Tidal Carbon Dioxide Concentration and Depth of Anesthesia in Children

NCT ID: NCT06303518

Last Updated: 2025-03-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-25

Study Completion Date

2026-12-31

Brief Summary

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Carbon Dioxide (CO2) is a by-product of metabolism and is removed from the body when we breathe out. High levels of CO2 can affect the nervous system and cause us to be sleepy or sedated. Research suggests that high levels of CO2 may benefit patients who are asleep under anesthesia, such as by reducing infection rates, nausea, or recovery from anesthesia . CO2 may also reduce pain signals or the medication required to keep patients asleep during anesthesia; this has not been researched in children.

During general anesthesia, anesthesiologists keep patients asleep with anesthetic gases or by giving medications into a vein. These drugs can depress breathing; therefore, an anesthesiologist will control breathing (ventilation) with an artificial airway such as an endotracheal tube. Changes in ventilation can alter the amount of CO2 removed from the body. The anesthesiologist may also monitor a patient's level of consciousness using a 'Depth of Anesthesia Monitor' such as the Bispectral Index (BIS), which analyzes a patient's brain activity and generates a number to tell the anesthesiologist how asleep they are.

The investigator's study will test if different levels of CO2 during intravenous anesthesia are linked with different levels of sedation or sleepiness in children, as measured by BIS. If so, this could reduce the amount of anesthetic medication the child receives. Other benefits may be decreased medication costs, fewer side effects, and a positive environmental impact by using less disposable anesthesia equipment.

Detailed Description

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Purpose: Carbon dioxide (CO2) is a major end-product of metabolism and can have marked effects on central nervous system function. It can also be easily manipulated during general anesthesia via controlled ventilation. High levels of carbon dioxide (hypercapnia) are associated with sedation and have been shown to produce selective suppression of thermal and ischaemic pain in animals and humans. This effect was attenuated by dexamethasone and naloxone, indicating that stress pathways and endogenous opioids may be implicated. Hypercapnia during anesthesia may have additional benefits, including reduced levels of wound infection due to improved tissue oxygenation reduced incidence of postoperative nausea and vomiting and reduced recovery time from volatile anesthetic.

It is a known phenomenon for high levels of CO2 to be associated with reduced levels of consciousness in humans, known as CO2 narcosis. A 1927 paper described narcosis of animals when breathing 30-40% CO2 in oxygen, with prompt recovery upon removal. The authors described a 'sharp sour taste' and associated hypertension when the same solution was administered to humans. However, few studies investigate the impact of carbon dioxide on anesthetic requirements. An animal study from 1967 demonstrated that very high levels of CO2 (\>95 mmHg) offset halothane requirements in dogs. Most recently, increased carbon dioxide levels during surgery (40 - 45 mmHg) were shown to reduce the Minimal Alveolar Concentration to Blunt Adrenergic Response (skin incision; MAC-BAR) of sevoflurane in adult patients undergoing gastric carcinoma resection.

Total intravenous anesthesia (TIVA), an alternative to inhalational anesthesia, is a commonly used anesthetic technique in the investigator's institution. This is due to its many benefits, including reduced emergence delirium, reduced environmental impact and reduced post-operative nausea and vomiting. Administration can be guided by depth of anesthesia monitoring such as the Bispectral Index (BIS), which measures the patient's level of consciousness derived from electroencephalogram readings. BIS has been shown to help guide propofol dosing in children regardless of whether the TIVA technique was target controlled or a manual infusion regimen, and to correlate well with both modelled and measured propofol levels in children.

The investigator's study aims to determine whether differing levels of CO2 affect the anesthetic depth in anesthetized children, as measured by BIS.

Hypothesis: Hypercarbia is associated with a reduction in BIS readings, in anesthetized children.

Justification: The impact of EtCO2 on BIS has not been studied in children. If discovered, a correlation between the two could significantly change anesthetic practice. It is straightforward to increase EtCO2 levels in anesthetized patients, and if this was found to reduce their anesthetic requirements it could enable lower rates of anesthetic drug administration. This would benefit the patient by exposing them to less medication and fewer associated side effects, as well as benefitting the hospital and wider environment by reducing cost and use of disposable equipment such as ampoules, packaging and syringes.

Objectives: (1) To determine the effect of EtCO2 on the depth of anesthesia in children, as measured by BIS.

(2) Patient movement as detected clinically by the surgical or anesthetic team.

Research Design: The investigators plan to conduct a randomized, prospective, crossover trial. The within-subject design allows patients to act as their own controls. The order in which the EtCO2 levels are tested will be randomized between patients using sealed envelopes. The anesthesiologist in the room will be blinded to the BIS reading but will be informed by a research assistant if it reads persistently high (\>60) for over one minute.

Statistical analysis: Physiological data will be collected in real-time using purpose-built software. Patient demographics and characteristics will be collected by a research assistant. Time-series plots of BIS and EtCO2 for each participant will be made in R (R Foundation for Statistical Computing, Vienna, Austria). Generalized estimating equations (GEE), using the geepack package, will be applied to estimate the effect of changes in target EtCO2 on serial BIS measurements during the anesthesia maintenance phase. Each participant will be considered their own data cluster to provide an appropriate grouping structure for the analysis. An independent correlation structure will be applied, and a robust (sandwich) estimator method will be used to obtain standard errors.

Conditions

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Anesthesia Hypercapnia Hypocapnia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

The investigators plan to conduct a randomized, prospective, crossover trial. The six arms will be as below:

1. Normal ETCO2 -\> High Normal ETCO2 -\> Low Normal ETCO2
2. Normal ETCO2 -\> Low Normal ETCO2 -\> High Normal ETCO2
3. High Normal ETCO2 -\> Low Normal ETCO2 -\> Normal ETCO2
4. High Normal ETCO2 -\> Normal ETCO2 -\> Low Normal ETCO2
5. Low Normal ETCO2 -\> High Normal ETCO2 -\> Normal ETCO2
6. Low Normal ETCO2 -\> Normal ETCO2 -\> High Normal ETCO2
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Caregivers
The anesthesiologist will be blinded to the BIS reading and will continue to provide anesthesia according to the protocol. The BIS numerical value in the OR will be covered, but the waveform will be visible to assess signal quality. The anesthesiologist providing care to the patient will not be involved in data collection or analysis

Study Groups

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High normal ETCO2, Normal ETCO2, Low normal ETCO2

All patients will receive same interventions, in a randomised order.

Group Type EXPERIMENTAL

High normal ETCO2: ETCO2 50 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'High Normal ETCO2' (50 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2: ETCO2 40 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Normal ETCO2' (40 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low Normal ETCO2: ETCO2 30 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Low Normal ETCO2' (30 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

High normal ETCO2, Low normal ETCO2, Normal ETCO2

All patients will receive same interventions, in a randomised order.

Group Type EXPERIMENTAL

High normal ETCO2: ETCO2 50 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'High Normal ETCO2' (50 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2: ETCO2 40 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Normal ETCO2' (40 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low Normal ETCO2: ETCO2 30 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Low Normal ETCO2' (30 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low normal ETCO2, Normal ETCO2, High normal ETCO2

All patients will receive same interventions, in a randomised order.

Group Type EXPERIMENTAL

High normal ETCO2: ETCO2 50 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'High Normal ETCO2' (50 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2: ETCO2 40 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Normal ETCO2' (40 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low Normal ETCO2: ETCO2 30 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Low Normal ETCO2' (30 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low normal ETCO2, High normal ETCO2, Normal ETCO2

All patients will receive same interventions, in a randomised order.

Group Type EXPERIMENTAL

High normal ETCO2: ETCO2 50 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'High Normal ETCO2' (50 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2: ETCO2 40 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Normal ETCO2' (40 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low Normal ETCO2: ETCO2 30 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Low Normal ETCO2' (30 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2, Low normal ETCO2, High normal ETCO2

All patients will receive same interventions, in a randomised order.

Group Type EXPERIMENTAL

High normal ETCO2: ETCO2 50 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'High Normal ETCO2' (50 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2: ETCO2 40 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Normal ETCO2' (40 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low Normal ETCO2: ETCO2 30 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Low Normal ETCO2' (30 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2, High normal ETCO2, Low normal ETCO2

All patients will receive same interventions, in a randomised order.

Group Type EXPERIMENTAL

High normal ETCO2: ETCO2 50 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'High Normal ETCO2' (50 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Normal ETCO2: ETCO2 40 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Normal ETCO2' (40 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Low Normal ETCO2: ETCO2 30 mmHg (+/- 3mmHg)

Intervention Type OTHER

BIS readings will be recorded continuously at 'Low Normal ETCO2' (30 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Interventions

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High normal ETCO2: ETCO2 50 mmHg (+/- 3mmHg)

BIS readings will be recorded continuously at 'High Normal ETCO2' (50 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Intervention Type OTHER

Normal ETCO2: ETCO2 40 mmHg (+/- 3mmHg)

BIS readings will be recorded continuously at 'Normal ETCO2' (40 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Intervention Type OTHER

Low Normal ETCO2: ETCO2 30 mmHg (+/- 3mmHg)

BIS readings will be recorded continuously at 'Low Normal ETCO2' (30 mmHg +/- 3 mmHg). Each patient will be tested at High normal, normal, and low normal ETCO2 levels in a randomized order.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Children aged 3 - 11 years undergoing non- or minimally-stimulating elective procedures, defined as anesthesia without skin incision or painful manipulation (e.g., non-invasive imaging, auditory brainstem response testing), middle ear surgery, surgery with effective local or regional anesthesia before surgical incision (e.g dental procedures with local anesthetic infiltration, urology with regional block).
* American Society of Anesthesiologists (ASA) physical status I and II
* TIVA technique appropriate throughout induction and maintenance of anesthesia
* Controlled ventilation via endotracheal tube
* Anticipated surgical time ≥ 90 minutes: to allow time for anesthetic induction and subsequent testing and washout periods at all three EtCO2 levels.

Exclusion Criteria

* Need for inhalational induction of anesthesia
* Sedative premedication
* Use of ketamine intraoperatively
* Unable to place BIS electrodes due to surgical site or other contraindications (e.g., MRI)
* Allergy to study drugs (propofol, remifentanil, lidocaine)
* Depression of conscious level for any reason
* BMI \<5th or \>95th centile for age
* History of obstructive or central sleep apnea
* Known or suspected raised intracranial pressure
* Recent or historical traumatic brain injury
Minimum Eligible Age

3 Years

Maximum Eligible Age

11 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of British Columbia

OTHER

Sponsor Role lead

Responsible Party

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Christopher Chin

Clinical Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Christopher A Chin, MBBS, FRCA, FRCP, MA

Role: PRINCIPAL_INVESTIGATOR

University of British Columbia

Locations

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BC Children's Hospital

Vancouver, British Columbia, Canada

Site Status RECRUITING

Countries

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Canada

Central Contacts

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Victoria Buswell

Role: CONTACT

604-875-1989

Steffanie Fisher

Role: CONTACT

604-875-1989

Facility Contacts

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Steffanie Fisher

Role: primary

604 875 2000 ext. 1989

References

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WOODBURY DM, KARLER R. The role of carbon dioxide in the nervous system. Anesthesiology. 1960 Nov-Dec;21:686-703. doi: 10.1097/00000542-196011000-00012. No abstract available.

Reference Type BACKGROUND
PMID: 13786527 (View on PubMed)

Fukuda T, Hisano S, Toyooka H. Moderate hypercapnia-induced anesthetic effects and endogenous opioids. Neurosci Lett. 2006 Jul 31;403(1-2):20-3. doi: 10.1016/j.neulet.2006.04.026. Epub 2006 May 15.

Reference Type BACKGROUND
PMID: 16701947 (View on PubMed)

Gronroos M, Pertovaara A. A selective suppression of human pain sensitivity by carbon dioxide: central mechanisms implicated. Eur J Appl Physiol Occup Physiol. 1994;68(1):74-9. doi: 10.1007/BF00599245.

Reference Type BACKGROUND
PMID: 8162926 (View on PubMed)

Akca O, Liem E, Suleman MI, Doufas AG, Galandiuk S, Sessler DI. Effect of intra-operative end-tidal carbon dioxide partial pressure on tissue oxygenation. Anaesthesia. 2003 Jun;58(6):536-42. doi: 10.1046/j.1365-2044.2003.03193.x.

Reference Type BACKGROUND
PMID: 12846617 (View on PubMed)

Saghaei M, Matin G, Golparvar M. Effects of intra-operative end-tidal carbon dioxide levels on the rates of post-operative complications in adults undergoing general anesthesia for percutaneous nephrolithotomy: A clinical trial. Adv Biomed Res. 2014 Feb 28;3:84. doi: 10.4103/2277-9175.127997. eCollection 2014.

Reference Type BACKGROUND
PMID: 24761392 (View on PubMed)

Katznelson R, Djaiani G, Naughton F, Wasowicz M, Ragoonanan T, Duffin J, Fedorko L, Murphy J, Fisher JA. Post-operative hypercapnia-induced hyperpnoea accelerates recovery from sevoflurane anaesthesia: a prospective randomised controlled trial. Acta Anaesthesiol Scand. 2013 May;57(5):623-30. doi: 10.1111/aas.12093. Epub 2013 Mar 3.

Reference Type BACKGROUND
PMID: 23452265 (View on PubMed)

Yamaguchi J, Kinoshita K, Hosokawa T, Ihara S. "The eyes are the windows of the soul": Portable automated pupillometry to monitor autonomic nervous activity in CO2 narcosis: A case report. Medicine (Baltimore). 2023 May 12;102(19):e33768. doi: 10.1097/MD.0000000000033768.

Reference Type BACKGROUND
PMID: 37171322 (View on PubMed)

Leake CD, Waters RM. Leake CD, Waters RM (1928) The anaesthetic properties of carbon dioxide. J Pharmacol Exp Ther 33:280-281. In.

Reference Type BACKGROUND

Eisele JH, Eger EI 2nd, Muallem M. Narcotic properties of carbon dioxide in the dog. Anesthesiology. 1967 Sep-Oct;28(5):856-65. doi: 10.1097/00000542-196709000-00019. No abstract available.

Reference Type BACKGROUND
PMID: 6035017 (View on PubMed)

Wu Z, Yu J, Zhang T, Tan H, Li H, Xie L, Lin W, Shen D, Cao L. Effects of Etco2 on the Minimum Alveolar Concentration of Sevoflurane that Blunts the Adrenergic Response to Surgical Incision: A Prospective, Randomized, Double-Blinded Trial. Anesth Analg. 2022 Jul 1;135(1):62-70. doi: 10.1213/ANE.0000000000005784. Epub 2022 Jun 16.

Reference Type BACKGROUND
PMID: 34744156 (View on PubMed)

Chandler JR, Myers D, Mehta D, Whyte E, Groberman MK, Montgomery CJ, Ansermino JM. Emergence delirium in children: a randomized trial to compare total intravenous anesthesia with propofol and remifentanil to inhalational sevoflurane anesthesia. Paediatr Anaesth. 2013 Apr;23(4):309-15. doi: 10.1111/pan.12090.

Reference Type BACKGROUND
PMID: 23464658 (View on PubMed)

Narayanan H, Raistrick C, Tom Pierce JM, Shelton C. Carbon footprint of inhalational and total intravenous anaesthesia for paediatric anaesthesia: a modelling study. Br J Anaesth. 2022 Aug;129(2):231-243. doi: 10.1016/j.bja.2022.04.022. Epub 2022 Jun 18.

Reference Type BACKGROUND
PMID: 35729012 (View on PubMed)

Biallas R, Rusch D, de Decker W, Wulf H, Siebrecht D, Scholz J. [Prophylaxis of postoperative nausea and vomiting (PONV) in children undergoing strabismus surgery. Sevoflurane/N2O plus dimenhydrinate vs.propofol/remifentanil plus dimenhydrinate]. Anaesthesist. 2003 Jul;52(7):586-95. doi: 10.1007/s00101-003-0516-9. Epub 2003 Jun 18. German.

Reference Type BACKGROUND
PMID: 12898043 (View on PubMed)

Marchant N, Sanders R, Sleigh J, Vanhaudenhuyse A, Bruno MA, Brichant JF, Laureys S, Bonhomme V. How electroencephalography serves the anesthesiologist. Clin EEG Neurosci. 2014 Jan;45(1):22-32. doi: 10.1177/1550059413509801. Epub 2014 Jan 10.

Reference Type BACKGROUND
PMID: 24415399 (View on PubMed)

Louvet N, Rigouzzo A, Sabourdin N, Constant I. Bispectral index under propofol anesthesia in children: a comparative randomized study between TIVA and TCI. Paediatr Anaesth. 2016 Sep;26(9):899-908. doi: 10.1111/pan.12957.

Reference Type BACKGROUND
PMID: 27461767 (View on PubMed)

Rigouzzo A, Khoy-Ear L, Laude D, Louvet N, Moutard ML, Sabourdin N, Constant I. EEG profiles during general anesthesia in children: A comparative study between sevoflurane and propofol. Paediatr Anaesth. 2019 Mar;29(3):250-257. doi: 10.1111/pan.13579. Epub 2019 Feb 12.

Reference Type BACKGROUND
PMID: 30614153 (View on PubMed)

Rigouzzo A, Girault L, Louvet N, Servin F, De-Smet T, Piat V, Seeman R, Murat I, Constant I. The relationship between bispectral index and propofol during target-controlled infusion anesthesia: a comparative study between children and young adults. Anesth Analg. 2008 Apr;106(4):1109-16, table of contents. doi: 10.1213/ane.0b013e318164f388.

Reference Type BACKGROUND
PMID: 18349180 (View on PubMed)

Jeleazcov C, Ihmsen H, Schmidt J, Ammon C, Schwilden H, Schuttler J, Fechner J. Pharmacodynamic modelling of the bispectral index response to propofol-based anaesthesia during general surgery in children. Br J Anaesth. 2008 Apr;100(4):509-16. doi: 10.1093/bja/aem408. Epub 2008 Feb 12.

Reference Type BACKGROUND
PMID: 18270231 (View on PubMed)

McFarlan CS, Anderson BJ, Short TG. The use of propofol infusions in paediatric anaesthesia: a practical guide. Paediatr Anaesth. 1999;9(3):209-16.

Reference Type BACKGROUND
PMID: 10320599 (View on PubMed)

Habre W, Disma N, Virag K, Becke K, Hansen TG, Johr M, Leva B, Morton NS, Vermeulen PM, Zielinska M, Boda K, Veyckemans F; APRICOT Group of the European Society of Anaesthesiology Clinical Trial Network. Incidence of severe critical events in paediatric anaesthesia (APRICOT): a prospective multicentre observational study in 261 hospitals in Europe. Lancet Respir Med. 2017 May;5(5):412-425. doi: 10.1016/S2213-2600(17)30116-9. Epub 2017 Mar 28.

Reference Type BACKGROUND
PMID: 28363725 (View on PubMed)

Whitesell R, Asiddao C, Gollman D, Jablonski J. Relationship between arterial and peak expired carbon dioxide pressure during anesthesia and factors influencing the difference. Anesth Analg. 1981 Jul;60(7):508-12.

Reference Type BACKGROUND
PMID: 6787952 (View on PubMed)

Wang F, Zhang J, Yu J, Tian M, Cui X, Wu A. Variation of bispectral index in children aged 1-12 years under propofol anesthesia: an observational study. BMC Anesthesiol. 2019 Aug 7;19(1):145. doi: 10.1186/s12871-019-0815-6.

Reference Type BACKGROUND
PMID: 31390975 (View on PubMed)

Davidson A, Skowno J. Neuromonitoring in paediatric anaesthesia. Curr Opin Anaesthesiol. 2019 Jun;32(3):370-376. doi: 10.1097/ACO.0000000000000732.

Reference Type BACKGROUND
PMID: 30893116 (View on PubMed)

Other Identifiers

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H23-03546

Identifier Type: -

Identifier Source: org_study_id

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