Verification of Endotracheal Tube Placement
This Policy Resource and Education Paper is an explication of the Policy Statement Verification of Endotracheal Tube Placement.
Introduction
The purpose of this paper is to identify the medical literature that pertains to verification of endotracheal tube placement in the emergency department and out-of-hospital settings.
This PREP is an update of a previous PREP from 2001 with the same title, Verification of Endotracheal Tube Placement.
There have been additional publications on this topic since the 2001 policy statement and PREP. For this update, a literature search was performed and articles were systematically graded. Articles used for the formulation of the policy statement are included in the Evidentiary Table that appears later in this document.
All articles were graded by at least 2 subcommittee members for strength of evidence and classified by the subcommittee members into 3 classes of evidence on the basis of the design of the study, with design 1 representing the strongest evidence and design 3 representing the weakest evidence for therapeutic, diagnostic, and prognostic clinical reports, respectively (Appendix A). Articles were then graded on 6 dimensions thought to be most relevant: blinded versus nonblinded outcome assessment, blinded or randomized allocation, direct or indirect outcome measures (reliability and validity), biases (eg, selection, detection, transfer), external validity (ie, generalizability), and sufficient sample size. Articles received a final grade (Class I, II, III) on the basis of a predetermined formula taking into account design and quality of study (Appendix B). Articles with fatal flaws were given an "X" grade.
In the course of reviewing the body of literature for this question, the committee reviewed a large number of investigations that tested various devices and techniques in the setting of the operating room (anesthetized, paralyzed, fasted adults) or the delivery room (neonatal resuscitation). Although these studies tended to have good intrinsic quality, the committee did not consider these studies (were assigned "X" grade) because of problems generalizing the results of these studies to the emergency department and out-of-hospital settings.
Discussion
Improper placement of endotracheal tubes into the esophagus ("esophageal intubation"), can remain undetected despite physical examination, chest radiography, and pulse oximetry methods that seem to confirm proper tube placement.1-7 For this reason, an additional method should be used to verify correct initial placement of the endotracheal tube.
No single technique used for confirmation of endotracheal tube placement has been proven to be 100% accurate.1-7 While visualization of the endotracheal tube passing through the vocal cords represents the primary method for assessing initial endotracheal tube placement, objective confirmation of proper placement is necessary.
Methods of endotracheal tube position assessment include repeat direct laryngoscopy, qualitative and quantitative end-tidal carbon dioxide detection, esophageal detector devices, and more recently, ultrasound utilization and transthoracic impedance.8-21
End-tidal carbon dioxide detection, using either qualitative or quantitative methods, approaches 100% sensitivity and specificity in the patient with spontaneous circulation.3,5,7,10,11
Assessment of endotracheal tube position by detection of exhaled carbon dioxide is less reliable in patients with poor circulatory perfusion conditions, particularly cardiac arrest patients. In these patients, delivery of carbon dioxide to the lungs may be insufficient to produce a reliable confirmation of tube placement. Essentially all reported false negative (endotracheal tube in the trachea with no detection of exhaled carbon dioxide) events of carbon dioxide detection in intubated patients have been observed in the setting of a low perfusion state, including cardiac arrest patients or those in extensive pulmonary edema.8-13 In these patients, an alternative method of confirming endotracheal tube placement may be required.
Esophageal detector devices have some utility as a technique for endotracheal tube position assessment. While these devices are often inexpensive and have generally demonstrated good utility in detecting esophageal intubations, inaccurate findings can result in obese patients, those with a large amount of air in the esophagus or stomach, and in patients with copious pulmonary secretions.14-16 In addition, esophageal detector devices do not provide the possibility for ongoing assessment of continued proper tube location.
Ultrasound imaging and transthoracic impedance methods offer potential as techniques that may prove to be helpful as adjuncts to detect and monitor the proper location of endotracheal tubes.17-21 The evidence is currently insufficient to endorse widespread implementation of these technologies for this purpose.
Endotracheal tubes that are initially placed into the trachea may be dislodged during patient movement or patient transport. Given the frequency of movements and transport, particularly in the emergency setting, tube position should be frequently reassessed. Continuous endotracheal tube monitoring is recommended to assure prompt detection of endotracheal tube dislodgement from the trachea. If equipment to continuously monitor endotracheal tube position is not available, at a minimum, endotracheal tube placement should be reconfirmed promptly if the patient’s condition deteriorates.
Summary
Verification of proper endotracheal tube location should be performed for all patients at the time of the initial intubation effort(s). Chest and abdomen auscultation, pulse oximetry, chest radiography and esophageal detector devices are not comparable to end-tidal carbon dioxide assessment for the verification of endotracheal tube placement in patients who have adequate tissue perfusion. Endotracheal tube location re-assessment should be performed whenever patient movement, clinical interventions, or clinical conditions suggest the possibility of tracheal tube dislodgement.
Revised by a subcommittee of the Clinical Policies Committee
John H. Burton, MD, FACEP
J. Stephen Huff, MD, FACEP
Eric J. Lavonas, MD, FACEP, FACMT, Chair
References
American Heart Association. 2005 American Heart Association (AHA) Guidelines Cardiopulmonary Resuscitation (CPR) and Emergency Cardiovascular Care (ECC) of Pediatric and Neonatal Patients: Pediatric Basic Life Support. Pediatrics. 2006;117:e989-1004.
The International Liaison Committee on Resuscitation. The International Liaison Committee on Resuscitation (ILCOR) consensus on science with treatment recommendations for pediatric and neonatal patients: pediatric basic and advanced life support. Pediatrics. 2006;117:e955-e977.
Salem MR. Verification of endotracheal tube position. Anesthesiol Clin North America. 2001;19:813-839.
Wagner CM. Verification of pediatric endotracheal tube placement. Air Med J. 2003;23:10-12.
Grmec S. Comparison of three different methods to confirm tracheal tube placement in emergency intubation. Intensive Care Med. 2002;28:701-704.
Grmec S, Mally S. Prehospital determination of tracheal tube placement in severe head injury. Emerg Med J. 2004;21:518-520.
Takeda T, Tanigawa K, Tanaka H, et al. The assessment of three methods to confirm tracheal tube placement in the emergency setting. Resuscitation. 2003;56:156-157.
Bhende MS, LaCovey DC. End-tidal carbon dioxide monitoring in the prehospital setting. Prehosp Emerg Care. 2001;5:208-213.
Bhende MS. End-tidal carbon dioxide monitoring in Pediatrics – Clinical Applications. J Postgrad Med 2001;47:215-218.
Donald MJ, Paterson B. End tidal carbon dioxide monitoring in prehospital and retrieval medicine: a review. Emerg Med J. 2006;23:728-730.
George S, Macnab AJ. Evaluation of a semiquantitative CO2 monitor with pulse oximetry for prehospital endotracheal tube placement and monitoring. Prehosp Disast Med. 2002;17:38-41.
Zar HA, Wu WW. The inability to detect carbon dioxide after endotracheal intubation as a result of one-way valve obstruction of the endotracheal tube. Anesth Analg. 2001;93:971-972.
Li J. Capnography alone is imperfect for endotracheal tube placement confirmation in emergency intubation. J Emerg Med. 2001;20:223-229.
Hendey GW, Shubert GS, Shalit M, Hogue B. The esophageal detector bulb in the aeromedical setting. J Emerg Med. 2002;23:51-55.
Tanigawa K, Takeda T, Goto E, et al. The efficacy of esophageal detector devices in verifying tracheal tube placement: a randomized cross-over study of out-of-hospital cardiac arrest patients. Anest Analg. 2001;92:375-378.
Li J. A prospective multicenter trial testing the scoti device for confirmation of endotracheal tube placement. J Emerg Med. 2001;20:231-239.
Sustic A. Role of ultrasound in the airway management of critically ill patients. Crit Care Med. 2007;35:s173-s177.
Galicinao J, Bush AJ, Godambe SA. Use of bedside ultrasonography for endotracheal tube placement in pediatric patients – a feasibility study. Pediatrics. 2007;120:1297-1303.
Hsieh KS, Lee C, Lin C, et al. Secondary confirmation of endotracheal tube position by ultrasound image. Crit Care Med. 2004;32:s374-s377.
Kramer-Johansen J, Eilevstjonn J, Olasveengen TM, et al. Transthoracic impedance as a tool to detect malpositioned tracheal tubes. Resuscitation. 2008;76:11-16.
Pytte M, Olasveengen TM, Steen PA, et al. Misplaced and dislodged endotracheal tubes may be detected by the defibrillator during cardiopulmonary resuscitation. Acta Anaesthiol Scand. 2007;51:770-772.
EVIDENTIARY TABLE
Study
|
Year
|
Design
|
Intervention(s)/Test(s)/Modality
|
Outcome Measure/Criterion Standard
|
Results
|
Limitations/Comments
|
Class
|
AHA guidelines1
|
2005
|
Consensus statement
|
|
|
Consensus statement from the AHA promoting the use of tube verification methods, particularly exhaled CO2, beyond clinical observation in pediatric patients
|
Consensus statement
|
III
|
ILCOR2
|
2006
|
Consensus statement
|
|
|
Consensus statement from ILCOR for Pediatric Basic and Advance Life Support; recommended exhaled CO2 for confirmation of tracheal tube placement and during transport; EDD may be considered for children >20 kg to confirm tracheal tube placement
|
Consensus statement
|
III
|
Salem3
|
2001
|
Review article
|
|
|
Review article discussing commonly prescribed methods of confirming ET placement
|
Review article
|
III
|
Wagner4
|
2004
|
Review article
|
|
|
Review article discussing commonly prescribed methods of confirming ET placement in pediatric patients
|
Review article
|
III
|
Grmec5
|
2002
|
Prospective observational study in adult prehospital patients
|
Capnometry – immediate; capnography; auscultation
|
Repeat laryngoscopy
|
Cardiac arrest patients: capnometry:
88% sensitivity/100% specificity; capnography:
100% sensitivity/100% specificity; auscultation: 100% sensitivity/80% specificity;
Noncardiac arrest patients: capnometry: 100% sensitivity/100% specificity; capnography: 100% sensitivity/100% specificity; auscultation:
94% sensitivity/83% specificity
|
Physicians performed test; intubator read the ETCO2 device – not fully blinded
|
I
|
Grmec and Mally6
|
2004
|
Prospective observational study in adult head injured patients
|
Capnometry – immediate;
capnometry – 6th breath;
capnography;
auscultation
|
Repeat laryngoscopy
|
Head injured patients: capnometry immediate: 100% sensitivity/100% specificity;
capnography 6th breath: 100% sensitivity/100% specificity;
capnography: 100% sensitivity/100% specificity;
auscultation: 94% sensitivity/66% specificity
|
Setting: prehospital (ground), but physicians performed test; intubator read the ETCO2 device – not fully blinded; probably a subset of Grmec 2002
|
I
|
Takeda et al7
|
2003
|
Prospective, observational study in out-of-hospital cardiac arrest patients
|
Bulb EDD, ETCO2, auscultation
|
Clinical assessment
|
ETCO2 superior to EDD in patients with circulation;
auscultation superior in cardiac arrest patients
|
Patients intubated in the ED; criterion standard flawed
|
III
|
Bhende and LaCovey8
|
2001
|
Review article
|
|
|
Review article discussing ETCO2 monitoring in the prehospital setting
|
Review article
|
III
|
Bhende9
|
2001
|
Review article
|
|
|
Review article discussing ETCO2 monitoring in pediatric patients
|
Review article
|
III
|
Donald and Paterson10
|
2006
|
Review article
|
|
|
Review article discussing ETCO2 monitoring in the prehospital setting
|
Review article
|
III
|
George and Macnab11
|
2002
|
Prospective observational case series in out-of-hospital patients
|
Capnometry
|
Clinical assessment
|
Descriptive report on a semiquantitative ETCO2 device used in transport patients for continuous monitoring as well as initial ET placement assessment
|
Design; small numbers; criterion standard not independent
|
III
|
Zar and Wu12
|
2001
|
Case report of a single patient
|
Continuous ETCO2 analyzer
|
Clinical assessment
|
Patient with continuous ETCO2 analyzer in whom mucus plug made ETCO2 unreliable
|
Single case report
|
III
|
Li J13
|
2001
|
Meta-analysis of capnography trials in ED populations; retrospective analysis of a large emergency intubation database
|
Assessment of ETCO2 for confirmation of ET placement in the ED population as published in previous trials
|
Multiple methods used in each study to assess ET placement
|
Assessment of ETCO2 for confirmation of ET placement in the ED population as published in previous trials; 10 trials met inclusion criteria for analysis; capnography calculated to have aggregate sensitivity of 93% and specificity of 97%
|
Design; multiple methods used in each study to assess ED placements
|
III
|
Hendey et al14
|
2002
|
Prospective observational study of aeromedical patients
|
EDD
|
Capnometry, oxygen saturation, clinical assessment
|
EDD found to have 80 sensitivity/97 specificity in the detection of esophageal intubation
|
Design; criterion standard not blinded
|
II
|
Tanigawa et al15
|
2001
|
Prospective, observational crossover study of out-of-hospital cardiac arrest patients
|
Syringe EDD, bulb EDD, ETCO2
|
Clinical assessment
|
Syringe EDD and bulb EDD found to have sensitivity of 73% and 71% respectively, for detection of tracheal intubation
|
Small sample size;
criterion standard flawed
|
III
|
Li J16
|
2001
|
2 phase prospective descriptive study: initial feasibility phase in a prospective series of elective surgical patients; second phase in a prospective convenience sample of intubated ED patients
|
SCOTI evaluated for ET in emergency and elective surgical intubated patients; this device is an EDD with a variety of LED displays
|
Anesthesiologist or emergency physician assessment of ET by one or many of multiple methods, including ETCO2, auscultation, direct visualization, EDD, and chest radiograph findings
|
SCOTI correctly identified 205 of 220 tracheal placements and 102 of 103 esophageal placements for sensitivity of 93% and specificity of 98%
|
Population limited to older children and adults due to less reliability in SCOTI device in endotracheal tubes less than size 6; no standardized assessment routine used for ET placement assessment; nonblinded data collection
|
III
|
Sustic17
|
2007
|
Review article
|
|
|
Review of ultrasound potential use in airway emergencies
|
Review article
|
III
|
Galicinao et al18
|
2007
|
Prospective observational study, pediatric ICU patients in phase 1, ED patients in phase 2
|
Ultrasound – cricothyroid membrane, capnometry
|
Clinical assessment, chest radiograph
|
Utility of bedside ultrasonography in a pediatric population assessed. 49 patients in phase 1, 50 in phase 2; ultrasound images found to yield accurate and rapid assessment
|
Design; nonblinded; chest x-ray utilized as criterion standard
|
Phase I: X
Phase 2: II
|
Hsieh et al19
|
2004
|
Prospective observational case series of pediatric patients in the pediatric ICU
|
Assessment of ET placement by ultrasound imaging of diaphragm movement;
|
Clinical assessment; all placements confirmed with auscultation; only initial placements confirmed with ETCO2
|
Pediatric patients newborn to 17 y enrolled and intubated; ultrasound identified 2 of 2 esophageal intubations and 8 of 8 right mainstem intubations; all correct endotracheal placements demonstrated normal ultrasound imaging
|
Pediatric patients only; patients with comorbid disease(s) affecting diaphragm motion not included and may limit this technology application to all patients
|
III
|
Kramer-Johansen et al20
|
2008
|
Prospective observational feasibility study in out-of-hospital cardiac arrest patients in whom resuscitation efforts had been ceased due to futility of further efforts
|
Transthoracic impedance changes were measured across the chest with standard defibrillation pads in order to surmise the difference in impedance between tracheal and esophageal ETs
|
Direct visualization of ET placement by investigator; capnography used in many patients
|
123 esophageal and 178 tracheal ETs were evaluated in 9 patients; impedance changes above 1.2 ohms were 100% specific and 69% sensitive for tracheal intubation
|
A derivation dataset limited to recently deceased cardiac arrest patients; application to the ED population at large as well as validation remain issues
|
III
|
Pytte et al21
|
2007
|
Case reports from 2 adult cardiac arrest patients
|
Report of continuous monitoring of transthoracic impedance during cardiopulmonary resuscitation;
|
ET placement confirmed by auscultation
|
Absence of ventilation-induced changes in transthoracic impedance suggest complications or misplacement of the ET
|
Design; small number of patients
|
III
|
AHA, American Heart Association; CO2, carbon dioxide; ED, emergency department; EDD, esophageal detector device; EMS, emergency medical services; ET, endotracheal tube; ETCO2, end-tidal carbon dioxide; ICU, intensive care unit; ILCOR, International Liaison Committee on Resuscitation; LED, light-emitting diode; SCOTI, sonomatic confirmation of tracheal intubation; y, year;
Appendix A. Literature classification schema.*
Design/Class
|
Therapy†
|
Diagnosis‡
|
Prognosis§
|
1
|
Randomized, controlled trial or meta-analyses of randomized trials
|
Prospective cohort using a criterion standard
|
Population prospective cohort
|
2
|
Nonrandomized trial
|
Retrospective observational
|
Retrospective cohort
Case control
|
3
|
Case series
Case report
Other (eg, consensus, review)
|
Case series
Case report
Other (eg, consensus, review)
|
Case series
Case report
Other (eg, consensus, review)
|
*Some designs (eg, surveys) will not fit this schema and should be assessed individually.
†Objective is to measure therapeutic efficacy comparing >2 interventions.
‡Objective is to determine the sensitivity and specificity of diagnostic tests.
§Objective is to predict outcome including mortality and morbidity.
Appendix B. Approach to downgrading strength of evidence.
Downgrading
|
1
|
2
|
3
|
| None |
I |
II |
III |
| 1 level |
II
|
III
|
X
|
| 2 levels |
III |
X |
X |
| Fatally flawed |
X |
X |
X |
| |
|
|
|