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Capnography

Capnography is a non-invasive technique that measures the concentration of carbon dioxide (CO2) in exhaled breath.
It provides valuable information about respiratory function and is widely used in clinical settings, such as anesthesia and critical care, to monitor patient status.
Capnography can detect changes in ventilation, perfusion, and metabolism, making it a crucial tool for the assessment and management of respiratory disorders.
The measurement of end-tidal CO2 (etCO2), the CO2 concentration at the end of exhalation, is a key parameter in capnography and can help clinicians identify respiratory distress, ventilation-perfusion mismatches, and other respiratory abnormalities.
This MeSH term describes the prnciples, applications, and interpretation of capnography, a vital monitoring technique in healthcare.

Most cited protocols related to «Capnography»

In preparation for fMRI procedures, rats were endotracheally intubated and mechanically ventilated using a small animal MR-compatible ventilator (CWE Inc., MRI-1, Ardmore, PA). Anesthesia was initially maintained under constant isoflurane (1.5–2%) mixed with medical air. Next, tail vein catheterization was performed for intravenous drug and contrast agent injections (see below). Immediately following intubation and tail vein catheterization, animals were placed within a head-holder, and harnessed to a small animal cradle (both plastic and custom-made). The cradle was lined with a circulating water blanket connected to a temperature-adjustable water bath located outside the scanner room (Thermo Scientific, Waltham, MA). A rectal probe was employed and core body temperature was maintained at 37 ± 0.5 °C. Mechanical ventilation volume and rate were adjusted to maintain EtCO2 of 2.8–3.2% and SpO2 above 96%, using capnometry (Surgivet, Smith Medical, Waukesha, WI) and pulse oximetry (MouseOx Plus, STARR Life Science Corp., Oakmont, PA). EtCO2 values from the capnometry system were previously calibrated against invasive sampling of arterial blood gas, reflecting a pCO2 level of 30–40 mm Hg22 (link)23 (link).
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Publication 2016
Anesthesia Animals Arteries Bath Body Temperature Capnography Catheterization Contrast Media fMRI Head Intubation Isoflurane Mechanical Ventilation Oximetry, Pulse Pharmaceutical Preparations Rattus Rectum Saturation of Peripheral Oxygen Tail Veins
While there is no limit to the number of devices that can be connected to the Vital Recorder at the same time, two to six devices are generally used simultaneously during routine patient care. Currently, more than 20 anaesthetic devices from 10 major companies are supported, and the number of devices on the list is increasing constantly (Table 2). Communication between the various medical devices and the computer is established via an RS-232C serial connection. Analog-to-digital converters may be required to obtain waveform signals from the analog port of the patient monitor (Tram module of SolarTM 8000 patient monitor, GE healthcare, Wauwatosa, WI, USA). After connecting serial cables, serial protocol setups are required on the device side for some equipment such as the patient monitor (IntelliVue MP and MX series, Phillips North America Corporation, Andover, MA, USA), cardiac output monitors (FloTrac/Vigileo system and Vigilance monitor, Edwards Lifesciences, Irvine, CA, USA; CardioQ-ODM, Deltex Medical, Chichester, UK), bispectral index monitor (BIS Vista, Covidien, Dublin, Ireland), and target-controlled infusion pump (Orchestra® Base Primea with module DPS, Fresenius Kabi AG, Bad Homburg, Germany).

Supported devices and parameters.

DeviceTypeCompanyParametersNumber of parametersData typeAcquisition interval (sec)
Solar 8000, Dash, MPSPatient monitorGE healthcareHeart rate, blood pressures, oxygen saturation, temperature, gas concentrations, etc.24numeric2
TramRac-4AExternal module for patient monitorGE healthcareECG, capnography, plethysmography, respiration, blood pressures11wavedependent on the performance of analog-to-digital converter
IntelliVue MP and MX seriesPatient monitorPhillipsECG, plethysmography, heart rate, blood pressures, oxygen saturation, temperature, gas concentrations, etc.<100wave and numeric1/500 for ECG; 1/125 for pressure waves and EEG; 1 for numeric data
Primus, Fabius, Vamos, ZeusAnaesthesia machineDrägerGas concentrations, ventilatory volumes, flows, airway pressures<90wave and numeric1/62.5 for waves, 7 for numeric data
Avance, Aestiva, AespireAnaesthesia machineGE healthcareGas concentrations, ventilatory volumes, flows, airway pressures<90wave and numeric1/25 for waves, 5 for numeric data
BIS VistaTMEEG monitorCovidienEEG waves, bispectral index and related parameters13wave and numeric1/128 for EEG wave, 1 for numeric data
Orchestra®Target-controlled infusion pumpFresenius KabiTarget, plasma and effect-site concentrations; infused, residual, and total volumes; infusion rate and pressure; drug name and concentration<10numeric1
Vigileo, EV 1000, Vigilance IICardiac output monitorEdwards LifesciencesCardiac output and derived parameters, temperature, oxygen saturation,<35numeric2
CardioQ-ODM+Cardiac output monitorDeltexStroke volume, cardiac output and related parameters13wave and numeric1/180 for flow and arterial pressure waves; 1 for numeric data
INVOSTMCerebral/somatic oximetryCovidienRegional oxygen saturation2numeric5
Belmont® Rapid InfuserRapid infusion systemBelmont InstrumentInfused volume, infusion rate, temperature, pressure7numericevery 2.875 mL infused
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Publication 2018
Anesthetics Bispectral Index Monitor BLOOD Capnography Cardiac Output Cardiac Volume Diploid Cell Infusion Pump Medical Devices Oxygen Oxygen Saturation Patient Monitoring Patients Pharmaceutical Preparations Plasma Plethysmography Pressure Rate, Heart Respiration Wakefulness
Following each intubation, the operator completed a data collection form, which included the following information: patient demographics, occurrence of a failed prehospital intubation attempt, operator specialty, operator postgraduate year (PGY), indication for intubation, method of intubation, paralytic agent, sedative agent, reason for device selection, device(s) used, presence of difficult airway characteristics (DACs), number of attempts at intubation, outcome of each attempt, and occurrence of AEs.
Only patients undergoing orotracheal intubation in the ED were included in this study. This included patients who underwent unsuccessful attempts at intubation in the field. Methods of intubation included rapid sequence intubation (RSI), in which a paralytic agent was used; oral intubation, in which a sedative agent was used (SED); and oral intubation, in which no medications were used (OTI).
The operator had three options to choose from for the reason for device selection. If the intubation was a routine airway with no anticipated difficulty, then the device selection was marked “standard.” If the device was selected with the expectation of a difficult airway, the reason for device selection was “difficult.” If the operator was using the device to gain educational experience with the device, then it would be classified as “education.”
Standard preoperative difficult airway predictors have been shown to be challenging to apply in the emergency setting.8 (link),9 (link) Thus, we developed a list of DACs that were feasible for the operator to determine prior to intubation in an emergent setting by brief examination of the patient. These include the presence of cervical immobility, obesity, large tongue, short neck, small mandible, facial or neck trauma, airway edema, blood in the airway, and vomit in the airway.
An attempt at orotracheal intubation was defined as insertion of the laryngoscope blade into the oropharynx, regardless of whether an attempt was made to pass the endotracheal tube. Each attempt was documented with one of three possible outcomes: 1) successful tracheal intubation with no additional attempts required, 2) inability to intubate with additional attempt (s) required, or 3) inadvertent esophageal intubation with additional attempt(s) required. Successful intubation was defined as correct placement of the endotracheal tube in the trachea as confirmed by end-tidal CO2 capnometry, pulse oximetry, chest auscultation, observation of chest excursion, absence of epigastric sounds, and misting of the endotracheal tube.
Adverse events tracked in this study include the following: esophageal intubation, oxygen desaturation, witnessed aspiration, mainstem intubation, accidental extubation, cuff leak, dental trauma, laryngospasm, pneumothorax, hypotension, dysrhythmia, and cardiac arrest. Cricothyrotomy was not considered an AE as we considered it an alternative way to secure the airway (see Table 1 for definitions of these AEs).
The data forms were reviewed by the senior author (JCS). If the form had any missing data, it was returned to the operator for completion. If information on the form contained inconsistencies, the operator was interviewed by the senior author for clarification. The data forms were cross-referenced to professional billing and pharmacy records to identify any intubations performed without a corresponding data form. If an intubation was identified without a data form, the operator was given a data form to complete as soon as possible to ensure a maximal capture rate. During the study period, 93.8% of the airway forms were turned in at the time of intubation, and the remaining 6.2% were captured by cross-referencing, for an overall 100% capture rate.
The data were then entered into the electronic data-base program HanDBase 4.0 (DDH Software, Wellington, FL, www.ddhsoftware.com) for the Palm Pilot and iPad and were subsequently transferred to Excel for Windows 2010 (Microsoft, Redmond, WA). The primary outcome measures were the incidence of one or more AEs and the incidence of specific AEs.
Publication 2013
Accidents Auscultation Blade Implantation Blood Capnography Cardiac Arrest Cardiac Arrhythmia Chest Dental Health Services Edema Emergencies Experiential Learning Face Intubation Intubation, Intratracheal Laryngoscopes Laryngospasm Macroglossia Medical Devices Micrognathism Neck Neck Injuries Obesity Oropharynxs Oximetry, Pulse Oxygen Patients Pharmaceutical Preparations Physical Examination Pneumothorax Rapid Sequence Intubation Sedatives Sound Trachea Tracheal Extubation Vomiting Wounds and Injuries

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Publication 2017
Adult Capnography Childbirth Determination, Blood Pressure Diagnosis Emergencies Ethics Committees, Research Face Hospital Administration Inpatient Medical Devices Negroid Races Operative Surgical Procedures Oximetry, Pulse Patients Physicians Resuscitation SAT1 protein, human Southern African People Tuberculosis Ventilators
The Central Denmark Region covers a mixed urban and rural area of approximately 13000 km2with a population of 1.27 million. The overall population density is 97.7 inhabitants pr. km2.
The standard EU emergency telephone number (1-1-2) covers all Denmark and there is an Emergency Medical Dispatch Centre in each of the five Danish regions. Emergency Medical Dispatch is criteria based.
The Central Denmark Region has a two-tiered EMS system. The first tier consists of 64 ground ambulances staffed with Emergency Medical Technicians (EMTs) on an intermediate or paramedic level (EMT-I / EMT-P). EMTs in The Central Denmark Region do not perform PHETI, nor do they use supraglottic airway devices (SADs).
The second tier consists of ten pre-hospital critical care teams staffed with an anaesthesiologist (with at least 4½ years’ experience in anaesthesia) and a specially trained EMT. Nine of the pre-hospital critical care teams are deployed by rapid response vehicles; the tenth team staffs a HEMS helicopter.
In the most rural parts of the region there are three rapid response vehicles staffed with an EMT and an anaesthetic nurse. The anaesthetic nurses do not use SADs nor do they perform Rapid Sequence Intubation (RSI) or other forms of drug-assisted PHAAM in the pre-hospital setting. These rapid response vehicles were not part of this study.
The pre-hospital critical care teams covered by this study employ approximately 90 anaesthesiologists as part time pre-hospital physicians. There are no full-time pre-hospital critical care physicians in the region – all physicians primarily work in one of the five regional emergency hospitals or at the university hospital. All pre-hospital critical care physicians have in-hospital emergency anaesthesia and advanced airway management both in- and outside the operating theatre as part of their daily work. Intensive care is part of the Danish anaesthesiological curriculum.
All pre-hospital critical care teams carry the same equipment for airway management. This includes equipment for bag-mask-ventilation (BMV), endotracheal tubes and standard laryngoscopes with Macintosh blades (and Miller blades for infants and neonates), intubation stylets, AirTraq™ laryngoscopes, Gum-Elastic Bougies, standard laryngeal masks (LMAs), intubating laryngeal masks (ILMAs) and equipment for establishing a surgical airway. All units are equipped with a capnograph and an automated ventilator. The pre-hospital critical care teams carry a standardised set-up of medications including thiopental, propofol, midazolam and s-ketamine for anaesthesia and sedation, alfentanil, fentanyl and morphine for analgesia and suxametonium and rocuronium as neuro-muscular blocking agents (NMBAs). Lidocain is available for topical anaesthesia.
Our system has no airway management protocols or standard operating procedures (SOPs) regarding PHAAM or pre-hospital RSI [22 (link)] and the physicians use the available drugs and equipment at their own discretion.
The pre-hospital critical care anaesthesiologists in our region have an average of 17.6 years of experience in anaesthesia and on average 7.2 years of experience with pre-hospital critical care. The average pre-hospital critical care physician performs 14.5 endotracheal intubations per month, 1 of them in the pre-hospital setting.
We have previously reported details of the pre-hospital critical care physicians’ education, training, level of experience and equipment-awareness in our region [22 (link)].
We collected data from February 1st 2011 until November 1st 2012.
Follow-up data regarding 30-days mortality were collected in January and February 2013.
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Publication 2013
Airway Management Alfentanil Ambulances Anesthesia Anesthesiologist Anesthetics Awareness Capnography Cardiac Arrest Critical Care Emergencies Emergency Medical Dispatch Emergency Medical Technicians Fentanyl Hemorrhage Infant Infant, Newborn Intensive Care Intubation Intubation, Intratracheal Ketamine Laryngeal Masks Laryngoscopes Lidocaine Management, Pain Medical Devices Midazolam Morphine Muscle Tissue Nurses Operative Surgical Procedures Paramedical Personnel Pharmaceutical Preparations Physicians Propofol Rapid Sequence Intubation Rocuronium Sedatives Temporal Lobe Thiopental Topical Anesthetics

Most recents protocols related to «Capnography»

All patients included in this study were aged >18 years and had a polymerase chain reaction (PCR) confirmed diagnosis of COVID-19.
As is standard practice in our institution, the size and type of tracheostomy selected for insertion remained at the discretion of the senior ICU physician and/or Ear, Nose and Throat (ENT) surgeon. Percutaneous tracheostomy consisted of a small 1–2 cm horizontal incision in the anterior neck, just below the level of the cricoid cartilage. Blunt dissection was performed to the level of the pre-tracheal fascia, followed by cannulation of the trachea under bronchoscope guidance. The “Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set” was used for all patients (COOK MEDICAL EUROPE LTD. Europe Shared Service Centre, O’Halloran Road National Technology Park Limerick, IRELAND).
The two patients who required surgical tracheostomies had these performed in the operating theatres. A horizontal incision was followed by dissection of the strap muscles and division of the thyroid isthmus to expose tracheal rings 2–4. Tracheal stay-sutures were applied to the tracheal rings above and below the tracheal incision. The endotracheal tube was then withdrawn with the ventilator placed in apnoea mode, the tracheostomy was inserted and the cuff immediately inflated to minimise aerosolisation. PEEP was maintained as far as possible throughout and apnoeic times, although not recorded, were kept to a minimum.
Staffing for percutaneous tracheostomy insertion comprised the minimum number of staff (three) required to safely perform the procedure (40 (link),60 (link)). This included an experienced ICU nurse, and either two Consultants, or a Consultant and a Fellow. All staff wore full personal protective equipment (PPE) including; FFP3 (N95) mask, full gown, gloves, goggles and hooded face shields (61 (link)-63 ). This complied with local infection control policies and conformed to World Health Organisation and Centre for Disease Control recommendations (44 (link),64 ,65 ). All patients were preoxygenated, sedated and muscle relaxed (62 (link),63 ). Ventilation was ceased prior to tracheal dilatation to minimise aerosolization, and correct positioning was confirmed with bronchoscopy, end-tidal capnography and chest X-ray (30 (link),31 (link),44 (link),48 (link),49 (link),60 (link)-63 ). The apnoea time was not recorded but kept at a minimum to reduce the risk of clinical harm and patient desaturation. Following insertion, cuff pressures were monitored and recorded four hourly and kept in the green zone of the manometer 20–30 cmH2O. Where leaks were apparent, cuffs were inflated to higher pressures to maintain tidal volumes.
We wished to determine the incidence of unplanned tracheostomy change, the reason for the change, and the tracheostomy inserted during the change. Unplanned tracheostomy change was defined as a change in the size or type of tracheostomy necessitated by clinical need, such as persistent leak or patient-ventilator dyssynchrony. Persistent leak and ventilator dyssnychrony was assessed clinically by the Consultant ICU physician. The requirement for tracheostomy change was determined clinically on a case-by-case basis. It did not include tracheostomy changes to facilitate respiratory weaning such as downsizing, or changing a cuffed to an uncuffed tracheostomy.
Each time an unplanned tracheostomy change was undertaken (outside of downsizing for weaning) the patient was deeply sedated and muscle relaxed. The tracheostomy was changed by mounting the introducer over a guidewire from the new sterile insertion set. This is standard practice in our institution. Where upsizing was required, the Blue Rhino dilator was used as described previously.
We also sought to assess time from intubation to tracheostomy insertion, time from ICU admission to tracheostomy, ICU LOS and time to decannulation, and to examine the changes, if any, in FiO2, PEEP and PP at the time of tracheostomy insertion and at days 1, 3 and 5 post insertion. The follow-up time to determine time to decannulation, overall outcome of mortality rate was 6 months post tracheostomy insertion.
Publication 2023
Apnea Bronchoscopes Bronchoscopy Cannulation Capnography Consultant COVID 19 Cricoid Cartilage Diagnosis Dilatation Dissection Face Fascia Infection Control Institutional Practice Intubation Manometry Muscle Tissue Neck Nose Nurses Operative Surgical Procedures Patients Pharynx Physicians Polymerase Chain Reaction Positive End-Expiratory Pressure Radiography, Thoracic Respiratory Rate Sterility, Reproductive Surgeons Sutures Thyroid Gland Tidal Volume Trachea Tracheostomy
The obtained vital parameters from the PPG wristband and the reference monitors were synchronized using a means of cross-correlation on the HR signals, and synchronized signals were visually inspected and corrected if necessary. Patients with a reference recording length shorter than 15 minutes were excluded from the analysis.
Low-quality measurements were excluded from both the PPG and monitor data. For the PPG wristband vitals, a low quality index can originate from motion artefacts or a low signal-to-noise ratio. For HR and RR, detection of arrhythmia using an arrhythmia detection algorithm would also lead to a low quality score [21 (link)]. For the reference monitor, the logged ECG and capnography signals were visually inspected to identify low-quality measurements, based on assessment of the temporal sequence.
Baseline characteristics are expressed as mean (SD) or, in case of nonnormally distributed values, as median (IQR) values. Agreement between the PPG wristband and reference monitor measurements on a second-to-second basis was visualized using Bland-Altman plots [22 (link)]. As multiple observations from the same patients were analyzed, the bias and limits of agreement were calculated using the method for repeated measures of Zou et al [23 (link)]. Additionally, the 95% CIs around the limits of agreement were assessed using MOVER [23 (link)].
According to the American National Standards Institute consensus standard, the error for HR measurements should be ≤10% or ≤5 bpm. In this analysis, an error of ≤5 bpm for HR and ≤3 rpm for RR was considered clinically acceptable. Additionally, Clarke error grid analysis was performed to quantify the implications of the difference between the vitals measured by the reference monitor and the PPG wristband. Clarke error grid analysis was originally developed for blood glucose measurements, and the boundaries of the different zones were adapted on the basis of the Modified Early Warning Score protocol used in our hospital [8 (link),17 (link),24 (link),25 (link)].
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Publication 2023
Base Sequence Blood Glucose Capnography Cardiac Arrhythmia Early Warning Score
The wearable PPG wristband device, ELAN, was equipped with a Philips Cardio and Motion Monitoring Module (CM3, Philips Electronic Nederland BV), which contains a PPG and 3-axial accelerometer sensor. The PPG sensor measures the intensity of the green light scatter-reflected from the skin to determine changes in blood volume in the peripheral circulation with a sampling frequency of 32 Hz [19 (link)]. From the obtained PPG signal, HR and RR were determined using previously published algorithms, the RR measurements are derived from interbeat interval variability and PPG amplitude [20 (link)]. Additionally, the device reports a quality index with each measured vital value, which mostly captures the signal-to-noise ratio [15 (link)]. Only vitals with a quality index of 4 (range 0-4), are considered to be of high quality and can be included in further analysis.
Shortly after surgery, the PPG wristband was applied to the patient’s wrist in the postanesthesia care unit (PACU) or intensive care unit (ICU), depending on where the patient was recovering immediately after surgery. The wristband then continuously collected both HR and RR.
As a ground truth, the electrocardiogram (ECG)-based HR and capnography-based RR signals of 68 patients were extracted from the bedside monitor in the PACU or ICU. These signals were saved in real time for offline processing, allowing comparison between the HR and RR measured by the PPG wristband and the reference monitor. In the PACU, vital parameters from the CAR-ESCAPE monitor B650 (GE Healthcare) were extracted using iCollect software (GE Healthcare) with a sampling frequency of 250 Hz for ECG and 1 Hz for RR. In the ICU, vital parameters were extracted from the Philips IntelliVue MP70 monitor using IntelliVue software (Philips) with a sampling frequency of 100 Hz for ECG and 0.1 Hz for RR. HR was derived from the ECG on second-to-second bases using QRS detection algorithms, RR was obtained using the patient monitors’ algorithms.
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Publication 2023
Blood Volume Capnography Electrocardiogram Medical Devices Methyl Green Operative Surgical Procedures Patient Monitoring Patients Skin Wrist
General anesthesia induction to all participants was accomplished by injection of intravenous 1–2 mg/kg propofol, 0.5–1 mcg/kg sufentanil, and 0.1 mg/kg vecuronium, followed by insertion of endotracheal tube, fixed after confirmation of its place by capnography and auscultation. Anesthesia was maintained using inhaled sevoflurane at 1–2%, intravenous 0.1–0.3 mcg/kg/min sufentanil, and 0.04–0.06 mg/kg/min vecuronium continuously. A central venous catheter (Arrow®/Teleflex®, Wayne, USA) was inserted, then followed by pulmonary artery catheter insertion (Arrow®/Teleflex®, Wayne, USA).
Publication 2023
Anesthesia Auscultation Capnography Catheterization General Anesthesia Intubation, Intratracheal Propofol Pulmonary Artery Sevoflurane Sufentanil Vecuronium Venous Catheter, Central
All patients fasted for 8 h with an opportunity to drink clear fluids up to 2 h before the operation. The subjects were allowed to stay with one of the caregivers in the holding area until entering the operating room. The preoperative anxiety at separation from the caregiver was assessed using a four-point behavior score: 1 = calm and cooperative, 2 = anxious but reassurable, 3 = anxious and not reassurable, and 4 = crying or resisting (Yuen et al., 2008 (link); Cho et al., 2020 (link)). Subjects were taken to the operating theatre without premedication; upon arrival, they were monitored using non-invasive arterial pressure, pulse oximetry, capnography, and electrocardiography throughout the surgery. Anesthesia was induced via the inhalation of 8% sevoflurane with an oxygen inflow of 8 L/min using a face mask. Induction quality was briefly evaluated according to a four-point scale: 1 = crying and needing restraint; 2 = moderate fear that was assuaged with difficulty, 3 = slight fear but could be reassured easily, and 4 = asleep, calm, awake, and/or cooperative when accepting the mask (Köner et al., 2011 (link); Kim et al., 2013 (link)). Once consciousness was lost, sevoflurane was adjusted to 3%–4% with an oxygen inflow of 2 L/min, and intravenous access was established. All patients received antiemetics with dexamethasone 0.15 mg/kg intravenously to prevent postoperative nausea and vomiting (PONV). Endotracheal intubation was then facilitated with intravenous sufentanil 0.2 μg/kg and cisatracurium 0.1 mg/kg–0.2 mg/kg.
After intubation, children were mechanically ventilated using the volume-controlled ventilation mode. The tidal volume was set to 6 mL/kg–8 mL/kg while the respiratory rate was set to 16 beats/min and further adjusted to maintain end-tidal carbon dioxide pressure between 35 mmHg and 45 mmHg. Anesthesia was maintained with inhalation of sevoflurane 2%–3%, which was discontinued approximately 5 min before the completion of surgery. Additionally, intravenous propofol (2 mg/kg/h–4 mg/kg/h) and remifentanil (0.2 μg/kg/min–0.3 μg/kg/min) were infused continuously until the end of surgery.
Upon the completion of the surgery, the oxygen flow was increased to 6 L/min to wash out residual sevoflurane in the alveoli. The study drug according to group allocation (either S-ketamine 0.2 mg/kg which was diluted in 0.9% NaCl or the 0.9% NaCl alone) was slowly administered intravenously using a 2 mL syringe. Extubation was performed after confirming regular breathing with sufficient tidal volume (> 5 mL/kg) and purposeful movement. After extubation, the patients were transferred to the post-anesthesia care unit (PACU).
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Publication 2023
Anesthesia Antiemetics Capnography Carbon dioxide Child cisatracurium Consciousness Dexamethasone Electrocardiography Face Fear Inhalation Intubation Intubation, Intratracheal Ketamine Movement Normal Saline Operative Surgical Procedures Oximetry, Pulse Oxygen Patients Premedication Pressure Propofol Remifentanil Respiratory Rate Separation Anxiety Disorder Sevoflurane Sufentanil Syringes Tidal Volume Tooth Socket Tracheal Extubation

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More about "Capnography"

Capnography is a vital non-invasive monitoring technique that measures the concentration of carbon dioxide (CO2) in exhaled breath.
This crucial medical tool, also known as end-tidal CO2 (etCO2) monitoring, provides valuable insights into a patient's respiratory function, making it indispensable in clinical settings like anesthesia, critical care, and emergency medicine.
Capnography can detect changes in ventilation, perfusion, and metabolism, enabling healthcare professionals to identify respiratory distress, ventilation-perfusion mismatches, and other respiratory abnormalities.
The measurement of etCO2, the CO2 concentration at the end of exhalation, is a key parameter in capnography and can help clinicians assess and manage respiratory disorders.
Beyond its use in anesthesia and critical care, capnography has a wide range of applications.
It is commonly used with devices like the PowerLab, Dinamap Non-Invasive Patient Monitor, Meloxicam, Finometer, Vigilance II, HP Patient Monitor, Metacam, Monitor Life Scope TR, TruWave, and Voluven to provide comprehensive patient monitoring and support.
By leveraging the insights from capnography, clinicians can make informed decisions, optimize patient care, and improve outcomes.
To enhance the reliability and validity of capnography research, tools like PubCompare.ai can be utilized to identify the best protocols and products from the literature, preprints, and patents.
This can help researchers streamline their studies, ensure reproducibility, and ultimately advance the field of capnography and respiratory monitoring.