Risk of pulmonary aspiration with laryngeal mask airway and tracheal tube
Risk of pulmonary aspiration with laryngeal mask airway and tracheal tube: analysis on 65,712 procedures with positive pressure ventilation
Anaesthesia 2009;64:1289-1294
Bernardini A, Natalini G
Abstract
Purpose
The purpose of this study was to test the hypothesis that
pulmonary aspiration of gastric contents was more likely when the
airway was managed with an LMA than an endotracheal tube when patients
were mechanically ventilated.
Background The
Laryngeal Mask Airway (LMA) has a number of advantages over an
endotracheal tube and it can be useful in the management of a difficult
airway when ventilation through a facemask is difficult. Nevertheless,
the LMA does not seal the trachea against entry of gastric contents as
well as an endotracheal tube (ETT). Positive pressure ventilation may
result in gastric inflation and increase the risk of regurgitation and
aspiration during LMA use. There is, however, little evidence about the
actual risk of pulmonary aspiration with an LMA vs. an ETT during
mechanical ventilation. Criteria considered to contraindicate the use
of an LMA are based primarily on opinion and not on evidence.
The
overall incidence of pulmonary aspiration (all types of airway
management) has been reported to be between 1 in 3,216 and 1 in 14,139
general anesthetics.
Methodology This retrospective
study examined data in a preexisting quality improvement database. Data
had been collected over a 10+ year period. Records were included in the
analysis if either an LMA or ETT was used during a general anesthetic
with mechanical ventilation. The selection of an LMA for airway
management was driven by locally accepted contraindications to LMA use
including: patients who were not NPO, intestinal obstruction,
pregnancy, procedures involving the airway, and prone position. An LMA
was occasionally used when one or more of these contraindications were
present in a difficult airway situation.
Default volume
controlled ventilator settings were tidal volume 8 – 10 mL / kg with
respiratory rate adjusted according to the end tidal CO2. Surgical
procedures included major abdominal, urologic, gynecologic,
retroperitoneal, and laparoscopic surgery. Pulmonary aspiration of
gastric contents was defined as the presence of gastric contents or
bilious fluid in tracheal aspirate; bilious fluid on the LMA or in the
oropharynx; or postoperative dyspnea, hypoxia, or “auscultatory
abnormalities.” When a case of aspiration was identified in the quality
improvement database the original chart was reviewed to verify the data.
Result
Slightly over 1,000,000 cases were contained in the
database. Of those, 65,712 met the criteria for inclusion; general
anesthesia and mechanical ventilation with either an LMA or ETT. Of
those, 2,517 were major abdominal surgery or laparoscopy performed with
an LMA. The airway was managed with an LMA in 1.7% of cases in which a
contraindication to LMA use was present.
Aspiration occurred in
10 cases. Of these, 4 occurred during an elective procedure; 2 with an
LMA and 2 with an ETT. The other 6 occurred during a non-elective
procedure; 1 with an LMA. Only 2 of these patients were admitted to
intensive care due to aspiration related problems; 1 of the ICU
admissions was an LMA patient and 1 was an ETT patient. The occurrence
of pulmonary aspiration in patients whose airway was managed with an
LMA and mechanical ventilation was no different than those whose airway
was managed with an ETT (odds ratio 95% confidence interval 0.09-1.4;
P=0.141). The power of the study (the probability of rejecting the
hypothesis when it is false) was calculated after the fact to be 0.69.
The
primary factor associated with pulmonary aspiration was emergency
surgery, not the airway management device. The overall incidence of
aspiration was 1 in 6,571 anesthetics.
Conclusion The
incidence of pulmonary aspiration was no greater when an LMA was used
than when an ETT was used during general anesthesia with mechanical
ventilation. Institutional contraindications to LMA use may have
influenced the results.
Comment
The focus of this
study was the risk of aspiration when mechanical ventilation was used
with an LMA. Accepted contraindications to LMA use were observed. The
study was not about the risk of using an LMA for any and every case. It
was about the added risk (if there is any) of using mechanical
ventilation with an LMA. I’m glad to see this question addressed. Many
of my colleagues are hesitant to use a ventilator with an LMA, yet
manually bagging with an LMA is fine. Both are positive pressure
ventilation. If our concern is insufflating the stomach with air it can
happen with either method of ventilation. In my view, it is all about
technique. I sometimes use mechanical ventilation with an LMA but I
don’t use the ventilator the same way I’d use it with an ETT. I take
care, for example, to keep peak pressures below 20 cm H2O. This study
indicated that there may not be any increased risk of aspiration when
mechanical ventilation is used with an LMA (see limitations in the
following paragraphs). While I’m not ready to use an LMA as widely as
this group apparently did, I do believe that with proper technique
mechanical ventilation can safely be used with an LMA.
While the
study is retrospective, it is unlikely it could have been conducted any
other way, and, as such, it is probably nearly the best we are going to
get. As retrospective studies go, this was a good one. Most
retrospective studies are not based upon a detailed quality improvement
database. The authors also took the wise step of reviewing the charts
of all patients identified by the QI database as having experienced
pulmonary aspiration. And, it has the advantage of including a large
number of patients, especially important for a relatively low frequency
event such as aspiration. Still, few aspirations were detected and
there may have been a true difference in the aspiration rate that was
undetectable as a result. Based upon the detailed statistical tests
they reported and, in my judgment, one error in analysis, I believe
there is a reasonable chance that the actual incidence of pulmonary
aspiration may have been greater with the LMA than with an ETT (see
note following).
The investigators rightly point out that the QI
database may not have detected all cases of aspiration because
complications were reported to the database by the anesthesiologist
caring for the patient. Self reporting tends to underestimate the
incidence of a complication because the clinician unconsciously gives
themself the benefit of the doubt and because reporting can get put off
until later and forgotten.
While it has a couple limitations,
this study is important and enlightening because it is generally well
done and encompasses a very large group of patients. The institution
where this study was conducted does a great service by taking the time
and effort to maintain a detailed quality improvement (QI) database for
over a decade. Without it, this study would not have been possible.
Michael Fiedler, PhD, CRNA
NOTE:
The upper boundary of the adjusted odds ratio 95% CI of the risk of
aspiration with an LMA was 5.62 times greater than an ETT. A one sided
test was used to calculate the power of the study.
© Copyright 2009 Anesthesia Abstracts · Volume 3 Number 12, December 31, 2009
