Autor : Luna, Carlos1
1Consultant, Pulmonology Division, Hospital de Clínicas, Full Professor of Pulmonology, University of Buenos Aires, Argentina.
https://doi.org/10.56538/ramr.WCGC8127
Correspondencia : Dr. Carlos M. Luna. E-mail: dr.cm.luna@gmail.com
The bacteriological diagnosis of invasive mechanical
ventilation-associated nosocomial pneumonia (VAP) is a serious concern for
physicians who treat patients sick enough to require tracheal intubation and
invasive mechanical ventilation. These pneumonias occur in patients who are
critically ill, requiring admission to the Intensive Care Unit, endotracheal
intubation, and connection to a ventilator. Under these conditions, patients
are inevitably colonized by hospital-acquired microorganisms, usually
multi-drug resistant, even more so in countries like ours compared to what is observed
in the United States or Europe.1 Depending on the effectiveness
and integrity of defense mechanisms, the pathogenic power, and the number of
microorganisms present in the airway, patients often develop pneumonia that
further worsens their condition. These pneumonias usually lead to increasing
respiratory failure, disease progression, high virulence of the colonizing
microorganisms, the ability of the defense mechanisms to remain intact, their
sensitivity to antimicrobials, and the efficacy of the antibiotic treatment
applied. Given this serious complication, it is mandatory to obtain pulmonary
secretion samples before prescribing broad-spectrum empirical antibiotics and
to de-escalate such treatment once the diagnosis, etiology, and antimicrobial sensitivity
have been confirmed.2 A controversial aspect is
finding a balance that allows attending physicians to discover “the best fit.”
Karina Otero and Tatiana Días de Carvalho carried out a
retrospective observational study, collecting data from patients with VAP
treated in the Intensive Care Unit, along with the results of bacteriological
studies of airway samples obtained since 2018, and including the years 2020 and
2021 (the peak of SARS-CoV-2 activity).3
The authors concluded that their findings show that, compared with
the mini-bronchoalveolar lavage method, endotracheal aspiration (which consists
of obtaining tracheal secretion samples through a PVC tube once the artificial
airway has been bypassed) is “optimal for routine analysis, since it is more
cost-effective and safer.”
It is encouraging to see colleagues treating critically ill
patients on invasive mechanical ventilation and conducting daily screening for
the possible presence of VAP. Even more so during such difficult times as
those experienced since the onset of the COVID-19 pandemic in 2020, which
limited the ability to manage critically ill patients with suspected VAP.
The authors put forward a proposal regarding a debate that began
more than 30 years ago and has yet to be settled, concerning the diagnostic
approach to mechanically ventilated patients who are severely complicated by
invasive ventilator-associated pneumonia.
In 1993, the diagnostic and therapeutic approach to VAP sparked a
public controversy reflected in several editorials, which were avidly followed
by intensive care physicians who took sides for one position or another
regarding how to manage VAP and the role of microbiological studies in these
patients. Chastre et al4 emphasized the bronchoalveolar
lavage culture as a measure that would allow confirmation of the diagnosis and
identification of the etiology, while Niederman et al4 highlighted the importance of
indicating an initial broad-spectrum treatment and then, at 48 hours, once
bacteriological results are available, de-escalating that treatment to minimize
antibiotic exposure. Over time, the historic controversy was resolved, and
both groups went on to collaborate and publish together on the management of
this and other types of pneumonia.
Although both bronchoalveolar lavage and the use of the protected
specimen brush eventually became established as the best bacteriological
methods to identify etiology and manage severe pneumonias, it also became clear
that performing an invasive study-one that represents only minor harm in
healthy individuals, such as a bronchoscopic examination-is not as harmless in
a critically ill patient. This, together with the conviction of experts who
generate consensus, underscores that what is best for patients should be
something readily available. Even in countries with a solid healthcare system,
access to a fiberoptic bronchoscope, protected specimen brush, and proper
performance of BAL is not always guaranteed. This has led the latest North
American and European/ALAT (Latin American Thoracic Association) guidelines to
recommend always carrying out a bacteriological study before initiating
treatment for VAP, but to favor less complex and costly techniques6,7
–including tracheal aspirate with semiquantitative culture–
clearly in line with what the authors of this study propose.
That said, and acknowledging my own adherence to the use of
invasive studies (particularly BAL) in these patients, it must be taken into
account that although the authors of the article in question correctly describe
that the sensitivity (S) of tracheal aspirate, 75.5%, is similar to that of
BAL, 75.6%, in the comparison of 22 studies,8 the specificity of tracheal
aspirate is 61%, far lower than that of BAL, 78.9%, in 22 studies.9
This latter point, in the reality of today’s world, and even more so in
countries like ours, with regard to antimicrobial resistance, makes it all the
more urgent to be prudent when administering unnecessary antibiotics, given
their impact on worsening resistance in severe infections. The Pan American
Health Organization and World Health Organization estimate that antimicrobial
resistance has become a serious public health problem worldwide and affirm that
by 2050 it will be the leading cause of death, with losses exceeding 100
trillion dollars.10 Some questions still remain: if
molecular studies that confirm pneumonia, its etiology, and resistance profile
within one hour were to become universally accessible, would it then be
necessary to obtain the best invasive sample to reach the true pathogen and
prescribe a definitive early treatment? That would certainly be highly
desirable.
Conflict
of interest
The
author declares no conflict of interest related to this editorial.
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