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Tip en El Manejo de La Dificultad y La Falla Ventilatoria
Tip en El Manejo de La Dificultad y La Falla Ventilatoria
Tip en El Manejo de La Dificultad y La Falla Ventilatoria
KEYWORDS
Pediatric Airway Intubation Supraglottic airway Laryngoscopy
Noninvasive ventilation
KEY POINTS
The pediatric airway is more anterior and superior, with the subglottic region being most
narrow, and these differences are pronounced until at least age 8 years, when proportions
begin to resemble more closely those of adults.
Video laryngoscopy has become a common and successful technique used in several
airway management scenarios owing to improved glottic views and ease of training.
Noninvasive ventilation, including continuous positive airway pressure, bilevel positive
airway pressure, and high-flow nasal canula, is highly effective in treating pediatric respi-
ratory failure but does not replace intubation if needed.
When properly adjusted for size, cuffed tracheal tubes are safe to use with pediatric air-
ways, except in neonates, with fewer air leaks during assisted ventilation and less post-
extubation stridor than uncuffed tubes.
INTRODUCTION
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494 Cobb
to remember that the pediatric airway is different, not alien, and can be challenging,
but is not impossible.
ANATOMIC CONSIDERATIONS
The first, most glaring difference of the pediatric airway from that of the adult is size.
This size range can create anxiety given the margin of error in technique is also smaller
when intubating. The range of equipment sizes is larger and requires more forethought
as well. The larger omega-shaped epiglottis is longer, floppier, and more prone to
obscuring the view of the glottic opening. This difference in particular highlights the
benefit of using a straight laryngoscope blade, which can lift the epiglottis from view
and allow more direct visualization of the pediatric glottis when anatomic axes are
appropriately aligned. A list of available straight blades can be found in Box 1. Curved
blades, which can also be used to optimize glottic views, can be found in Box 2. Other
types of laryngoscope blades are listed in Box 3.
In the neonatal period, laryngeal structures are the most superior, aligned near the
second cervical vertebral body (C2). By adolescence, the larynx has dropped to near
the C5-C6 level. This change means that the angle from the base of the tongue to the
glottic opening is most acute with the youngest patients.2 The infant airway also has a
lower-lying posterior palate, and, with the proportionally larger epiglottis, the naso-
pharynx and hypopharynx are in closer proximity, which encourages obligate nasal
breathing that decreases risk of aspiration. These features, in addition to a more ante-
rior airway and smaller glottic opening, can increase the challenge of proper alignment
of anatomic axes and optimal intubating positioning.3
The next significant difference is the location of the narrowest point of the airway. In
a normal adult, the glottic opening is the narrowest, such that, once the tracheal tube
has been passed through the vocal cords, there should be no other restriction to
placement. However, in children up to 8 years of age, the subglottic area has the
most narrow dimensions, at the level of the cricoid.4 This narrowing can be even
more exaggerated in children with history of laryngotracheomalacia or tracheomalacia
(Fig. 1).
Box 1
Straight laryngoscope blades
Blade name:
Cranwall
Jackson
Janeway
Magill
Miller
Phillips
Robertshaw
Seward
Soper
Wis-Hipple
Wisconsin
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Managing Pediatric Respiratory Distress 495
Box 2
Curved laryngoscope blades
Blade name:
Macintosh
Reduced Flange Macintosh
Parrott
Siker
Box 3
Other laryngoscope blades
Blade name:
McCoy
Vie Scope
Fig. 1. An adult airway (left) and pediatric airway (right). Note the cone-shaped narrowing
of the pediatric airway caused by inherent subglottic configuration. (Drawing used with
permission from Carlos Lugaro, Jr.)
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496 Cobb
DIFFERENCES IN PHYSIOLOGY
Infants and children have higher diaphragms with proportionally larger abdominal con-
tents causing reduced lung volumes.4 Developing alveoli, smaller thoraces, and differ-
ences in tissue recoil are causes for a lower functional residual capacity (FRC) in
infants and children. Because FRC is the gas still in lungs at the end of normal tidal
expiration, it is also responsible for gas exchange.7 The smaller FRC in combination
with children’s higher metabolic rates and oxygen demand shortens the window dur-
ing which intubation can be performed with optimized oxygenation. Oxygen demand
is estimated at twice that of adults, and highlights the rationale for performing apneic
oxygenation during intubation.8 Data on apneic oxygenation for pediatric patients un-
dergoing emergent intubation in the pediatric emergency department are slightly
mixed; however, 2 recent studies, Vukovic and colleagues8 and Overmann and col-
leagues,9 used alternative methods, which likely account for the opposing findings.
Results supporting use of apneic oxygenation from Vukovic and colleagues8 in 2018
used standard nasal canula, 4 L/min for patients up to 2 years of age, 6 L/min between
2 and 12 years old, and 8 L/min for those greater than 12 years old.
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Managing Pediatric Respiratory Distress 497
to consent, they can provide the much-needed emotional support, assist in calming
the child during anxiety-provoking procedures, and aid in redirection from attempts
at removing support lines and devices, such as high-flow nasal canula (HFNC) and
continuous positive airway pressure (CPAP).
The benefits of NIV are numerous for both adults and children. Specifically, NIV sup-
ports patency of the upper airway, increases FRC, reverses hypoventilation, de-
creases work of breathing, and decreases oxygen consumption while improving
cardiac output.10 Simply stated, NIV has been an undeniable game changer in the
management of respiratory distress and failure for adults, children, and infants. NIV
can be considered before tracheal intubation in children with acute respiratory failure,
but, regardless of modality, it should not delay intubation if an invasive airway is
indicated.11
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498 Cobb
pediatric patients,14 as it is also used in adults with severe asthma, chronic obstructive
pulmonary disease, pneumonia, and heart failure.
Table 1
Considerations of noninvasive modality
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Managing Pediatric Respiratory Distress 499
BiPAP or CPAP. Subjects ranged from 1 month to 2 years of age, and those patients
placed on HFNC as the initial modality of choice tended to be older than those who
started on BiPAP or CPAP.16
Starting severe asthmatics on HFNC has shown a reduction in respiratory distress
early in treatment in the emergency department.17
Ideally, patients are at least partially resuscitated to optimize conditions for intubation.
Pokrajac and colleagues18 found that pediatric patients less than the age of 1 year,
with persistent hypoxemia, or in whom clinicians were unable to obtain a pulse oxim-
etry reading before intubation, were more likely to experience peri-intubation cardiac
arrest in the pediatric emergency department.
Table 2
Mnemonic for preparing to intubate
Abbreviations: OPA, oropharyngeal airway; NPA, nasopharyngeal airway; TT, tracheal tube.
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500 Cobb
found that failure of placement of invasive airway on the first attempt was associated
with increased risk of progression to cardiopulmonary arrest, adjusted odds ratio of
1.8 (95% confidence interval, 1.2–2.6).19 There were factors with greater odds ratios;
however, this finding still highlights the importance of making the first attempt the best
attempt. There is a direct correlation between number of attempts to obtain the airway
and adverse events, including aspiration, desaturation, esophageal intubation, hypo-
tension, dysrhythmia, and cardiac arrest.20 Studies have shown that female pediatric
patients are at increased risk for failed first attempts and inappropriate insertion
depths.21 It is important to be mindful that the first attempt should be the best attempt.
Underestimating the potential difficulty of the airway can prove disastrous.
Predicting the appropriate endotracheal tube size based on its internal diameter has
long been determined by the equation [(age/4) 1 4] for uncuffed tubes, and subtract-
ing 0.5 for cuffed tubes.25 There have been proposals for estimation of tube size based
on anthropometric characteristics as well. Use of the length of the middle finger in cen-
timeters, rounded up to the nearest 0.5, may estimate the appropriate tube size inter-
nal diameter in millimeters. This estimation has been shown to have a linear
relationship with best-fit tube size, as opposed to the age formula, which is nonlinear
and begins to show greatest variation at age 6 years old.25 The diameters of the distal
phalanx of the small and index fingers were also shown to have poor accuracy in pre-
dicting the tube of best fit for children aged 1 to 10 years.26
Each of these equations is incapable of predicting the perfect-fit tube size given the
endless variety of airway dimensions in pediatric development, nor do the equations
approximate the external diameter, which is the dimension of greatest concern
when attempting to avoid postintubation subglottic stenosis or poor fit leading to inad-
equate tidal volumes and ventilation. In every preparation to place an invasive airway,
a variety of tube sizes must be available with the clinician being able to quickly assess
the size of the glottic opening and choose the tube most likely to pass on first attempt
and optimize future function, while also limiting risk of injury (Table 3).
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Managing Pediatric Respiratory Distress 501
Table 3
Equations for tube size approximation
Tube
Source Type Equation Notes
Cole Uncuffed (age in years/4) 1 4 5 ID (mm) First published in 1957
Motoyama Cuffed (age in years /4) 1 3.5 5 ID (mm) For children older than 2 y
Khine Cuffed (age in years /4) 1 3 5 ID (mm) For children less than 2 y
Ritchie- Cuffed Length of middle Derived from equations that
McLeana finger (cm) 5 ID (mm) equate TT depth to 3 ID and
3 length of the middle finger
is sized for the approximate depth of the epiglottis or vallecula, respectively, and when
the pharyngeal and laryngeal axes align, the glottic opening comes into view. The tra-
chea tube is then passed directly through the vocal cords, with estimated insertion
depth to be 3 times that of tube size. Video laryngoscopy (VL) has the benefit of
providing full views of the glottic opening without necessary alignment of the pharyn-
geal and laryngeal axes.29 A review of datasets from the National Emergency Airway
Registry for children (NEAR4KIDS) published in 2016 showed increasing trends for VL
use with first-pass success rates of 97%.21
In simulation training for pediatric residents, GlideScope VL did not improve perfor-
mance of mannequin endotracheal intubation compared with DL for normal airway,
but it may prove the safer option to avoid upper jaw injury or with more
complex airways.27 Several other studies have found the opposite, and suggest that
the only clinically significant differences to be view of glottis, which is more complete
with VL, but longer time to intubation compared with DL.2 The increase in time to intu-
bation may be related to manipulation of the tube around the tongue and teeth, and
into the trachea, as opposed to direct line of sight and passage as is achieved with DL.
BOUGIE TALK
Use of a semirigid, flexible bougie adjunct has become more popular in recent years,
particularly in the emergency department. Although once considered primarily for
salvage or rescue in difficulty airway attempts, a 2018 randomized study by Driver
and colleagues28 showed increased first-pass success rate when used in the emer-
gency department for endotracheal intubation rather than tracheal tube plus standard
stylet. This benefit held true for groups of patients deemed to have at least 1 difficult
airway characteristic, as well as all comers requiring emergent intubation. This study
was specific to patients 18 years of age and older, and excluded those with upper
airway obstruction such as angioedema or epiglottitis.
There is not yet a comparable study of size and randomization in pediatric emer-
gency airway management. Limitations to use of pediatric-sized bougie may include
the less frequent opportunities for pediatric tracheal intubation in both training and
practice compared with adults. Learning proficiency in tracheal intubation can be
challenging, and use of a bougie, be it successful in first pass attempt or rescue tech-
nique, does require instruction and practice. With pediatric intubations occurring less
frequently than with adults, emergency medicine residents and attending physicians
alike may not be comfortable adding an additional piece of equipment to the milieu.
Although several airway management techniques are transferrable between pediatrics
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502 Cobb
and adults, operator comfort does play a large role in how and when those tools are
used. Ideally, future emergency medicine research will address this topic and provide
further recommendations for bougie use, which may also support first-pass success in
infants and children, as in adults.
SUPRAGLOTTIC AIRWAYS
Supraglottic airways (SGAs) have been widely used in adult resuscitations as rescue
devices when tracheal intubation is not feasible or as the primary airway device in
select patients. SGAs include laryngeal mask airways (LMAs), which are the primary
reference of this article. They are highly popular in pediatric airway management as
well. Of particular benefit, SGAs can remove the obstruction caused by the tongue
and posterior pharyngeal tissues.29 In a 2017 study of pediatric anesthesia cases, Bur-
jek and colleagues found that there were similar rates of first-pass success between
VL and fiber-optic intubation via supraglottic airway. The first-pass rate was higher in
cases of difficult airways. Fiber-optic intubation via SGA also provides the additional
benefits of ongoing oxygenation and ventilation while the definitive airway is placed,
presumably thereby decreasing rates of peri-intubation hypoxemia.30
The research regarding the most effective or easiest-to-use LMA is ongoing, and the
landscape will continue to change with new medical technologies. For instance, the
i-gel, Pro-seal, and Classic LMAs were found to have no statistically significant differ-
ence in ease of insertion, air leak, or passage of gastric tube in a meta-analysis with
pediatric anesthesiologists.31 Another prospective study found no particular benefit
between the air-Q and i-Gel SGAs with respect to time to insertion, bronchoscope
insertion, or bronchoscopic glottic views.29
Even though some of these devices have shown up to 100% first-attempt success
with pediatric anesthesiologists, the unruly conditions of the emergency department
may not allow the same guaranteed performance. The operating room allows metic-
ulously controlled circumstances (eg, last meal, medical history, need for intubation,
hemodynamic stability), which are not applicable in the emergency department.
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Managing Pediatric Respiratory Distress 503
PHARMACOLOGY
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504 Cobb
SPECIAL POPULATIONS
Cardiac Arrest
The airway management in pediatric cardiac arrest varies widely and is largely influ-
enced by in-hospital cardiac arrest (IHCA) or out-of-hospital cardiac arrest (OHCA).
Up to 80% of pediatric patients with IHCA had an airway in place at the time of ar-
rest.37 For nontraumatic OHCA in patients less than 18 years of age, a recently pub-
lished prospective observational study found that tracheal intubation was successful
in slightly less than 60% on first-pass attempt, whereas placement of SGA (namely the
i-gel and King laryngeal tube) was successful in nearly 95% of first attempts.38
Regardless of airway management device, attempts at monitoring end-tidal cap-
nography (EtCO2) should be made. Those pediatric cardiopulmonary resuscitation
events that were conducted with EtCO2 (which can indicate adequacy of compres-
sions, as well as rapidly increase before return of spontaneous circulation) were asso-
ciated with increased occurrence of return of spontaneous circulation. Resuscitative
efforts also tended to last longer than those that did not use EtCO2.39
Neuromuscular Disease
The most common neuromuscular diseases (NMDs) requiring NIV are Duchenne
muscular dystrophy and spinal muscular atrophy.42 Other NMDs include Guillain-
Barré syndrome (GBS), amyotrophic lateral sclerosis, myasthenia gravis, polymyosi-
tis, and dermatomyositis.43 Given the progressive nature of the chronic
diseases, fatigue and alveolar hypoventilation can have insidious onsets such that,
when ill, there may be a rapid decline in respiratory function in what may initially
seem to be a minor illness. The patient may or may not already have been started
on NIV for sleeping or intermittent daytime alveolar maintenance depending on the
severity of the chronic illness, such that escalation of support may require starting
with more advanced modalities than standard-flow nasal canula. For the acute dis-
eases, such as GBS, the rapid decline in strength of respiratory muscles can create
precipitous respiratory failure and airway compromise. If an invasive airway is indi-
cated, it is important to remember that succinylcholine is generally contraindicated
because of risk of hyperkalemia from acetylcholine receptor upregulation in chronic
denervating diseases or acute disease after 48 to 72 hours.44
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Managing Pediatric Respiratory Distress 505
childhood injuries. Although resultant injury patterns can be unpredictable, the identifica-
tion of several congenital syndromes and associations can provide guidance regarding
the expected abnormalities. For instance, Goldenhar syndrome, or oculoauricular skel-
etal dysplasia, which occurs every 1 in 3000 to 7000 live births, is often associated with
hemifacial microsomia and micrognathia. In addition to the complex positioning and
configuration of the airway, they are also prone to odontoid hypoplasia and atlantoaxial
instability, which increase the risk of cervical spine injury during typical positioning and
manipulation of intubation.45,46 Down syndrome is associated with atlantoaxial insta-
bility, and should also inspire caution with spinal manipulation during intubation.
Other craniofacial dysplasias, particularly craniosynostoses causing midface hypo-
plasia, necessitate an alternative set of special precautions and considerations. The
most common craniosynostosis are Apert syndrome, Crouzon syndrome, Pfeiffer syn-
drome, Saethre-Chotzen syndrome, and Carpenter syndrome.47 Most are autosomal
dominant and have variable expression, and, despite several differences, they are all
associated with unusual cranial shape, often oblique and/or asymmetric, and midface
hypoplasia, which reduces or eliminates the nasopharynx and hypopharynx.47 The
resultant upper airway configuration causes significant obstructive sleep apnea and
chronic respiratory problems. Achondroplasia often features atypical facies accompa-
nied by a large occiput, narrow foramen magnum, and hypoplastic ribs.48 For all of
these patients, emergency physicians should anticipate difficulty with alignment of
anatomic axes, challenges with bag-valve-mask ventilation, and equipment sizes
that are difficult to estimate.
DISCLOSURE
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506 Cobb
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508 Cobb
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