Justification for the research. Interstial lung disease (ILD) is characterized by a diffuse affection of the lung
interstitial tissue. It can be secondary to acute conditions such as pneumonia or pulmonary
oedema either of haemodynamic aetiology either permeability induced. ILD can also result from
chronic diffuse parenchymal lung disease (DPLD). It is admitted that acute ILD leads to
decreased pulmonary aeration and therefore to hypoxemia.
In front of a patient presenting in Emergency Department (ED) with altered oxygen saturation,
arterial blood is classically sampled. Arterial Blood Gases (ABG) procedure, in addition to
be painful for the patient, is invasive. ABG however gives access, among other results, to
the Arterial Pressure in Oxygen (PaO2), which evaluates the level of hypoxemia. Although the
correlation between ABG results and prognosis hasn't been widely evaluated, a rather recent
study supported the absence of correlation between those for Acute Heart Failure (AHF).
Authors however did not report the correlation between severity of symptoms at patient's
hospital admission and hypoxemia. Yet, according to the Berlin definition, hypoxemia
represented by the ratio PaO2/FiO2 is a severity indicator in Acute Respiratory Distress
Syndrome (ARDS).
Lung ultrasound is a simple tool, non-invasive, non-irradiating, low cost and easily
available at the patient's bedside. In addition, ultrasound equipment has become wildly
available in the ED and more and more portable. Simultaneously, the interest of lung
ultrasound for critically ill patient has been demonstrated. The ILD ultrasonographic
diagnosis is based on the presence of multiple ultrasound artefacts called B-lines. B-lines
appear when the ratio between air and water is abnormal. Different anatomic substrates have
been recognized as being at the origin of this ultrasound pattern. In acute pulmonary oedema
the presence of B-lines is related to the presence of extra-vascular water. B-lines presence
is also attributed to the thickening of sub-pleural interlobular septa. B-lines are therefore
a representation of ILD and accessible using ultrasound. Additionally, more and more
ultrasound machines are provided with options to quantify the number of B-lines.
Regarding the importance of B-lines and their interconnection to ILD, a score has been
created to evaluate ILD. The Lung Ultrasound Score (LUSS) is based on B-lines quantitative
assessment. The B-lines detection is performed in six thoracic zones bilaterally. In each
zone, ultrasound lung aeration status is determined scoring from zero to four. A normal
aeration of the lung with presence of A lines, persistent pleural sliding and less than three
B-lines scores zero point. An ILD, resulting in moderate loss of aeration with more than
three spaced B-lines, 7mm apart, scores one point. An alveolar-interstitial syndrome meaning
a severe loss of aeration with coalescent B-lines, less then 3mm apart, scores two. An
alveolar consolidation leading to a complete loss of aeration with an ultrasonographic tissue
like pattern, scores three. A total score over thirty-six can be calculated using this
method. Initially developed on an experimental model resembling various pathological
conditions encountered in the critically ill, LLUS proved to be correlated to the different
states of aeration of the lung. Literature findings are consistent with LUSS being an
efficient tool to measure lung aeration in different intensive care situations: re-aeration
antibiotics-induced in Ventilator Associated Pneumonia, assessment of PEEP-induced lung
recruitment. LUSS realized during weaning trial has been showed to be able to predict of
post-extubation distress. In the Intensive Care Unit (ICU), LUSS is efficient to quantify
lesions and predict mortality associated with ARDS.
Knowing LUSS has a good correlation to the lung aeration, the present physiological study is
meant to highlight a potential negative linear correlation between PaO2/FiO2 values and LUSS.
If this hypothesis is confirmed, the LUSS could eventually be a tooltool indirectly assessing
the impact of an ILD on haematosis and correlating the potential degree of hypoxemia in the
emergency room for patients with this acute pathology. This could secondary increase
patient's comfort by reducing ABG realization for follow up.
Study procedure:
Intervention description. A LUSS will be realized by an investigator trained for lung ultrasound (LUS) and considering
him/herself confident for its use. A five-point Likert scale will be filled. To the statement
"I am qualified to realize a LUSS", only emergency doctors answering "I strongly agree" or "I
agree" will be eligible for inclusion and added to investigators list using an amendment to
this protocol. The ultrasound machines operated for LUS belong to each ED meaning the
investigators are familiar to its use. To standardize the results, settings of the ultrasound
machines will be standardized. To allow the exploration of the pulmonary parenchyma a low
frequency curvilinear transducer will be used and evaluation of B-lines will be performed
using a depth of at least 12cm as commonly recommended1. In this SARS-COV-2 pandemic context,
patients affected with this condition having a pulmonary involvement could reach our
eligibility criteria. Therefore, special precautions, such as a single protection cover of
the ultrasound machine and proper use of disinfectant for probes will be recommended between
patients. Those measures will follow institutional procedures of ultrasound use during
COVID19 pandemic. LUS will take place within 10 minutes of ABG analysis. LUS will be
performed at the patient's bedside. The investigator will be blinded to any other procedure
made by treating physician for diagnostic purpose. The LUSS procedure will be used as
validated for ARDS15. For that matter, the thorax is virtually divided in six thoracic zones
bilaterally, comporting two anterior zones, two lateral zones and two posterior zones. The
anterior and lateral zones will be evaluated in strict dorsal decubitus and the posterior
zones will be evaluated with a light contro-lateral decubitus allowed, if necessary because
of patient morphotype. For each zone a score from zero to three will be determined:
- - 0: A normal aeration of the lung with presence of A lines, persistent pleural sliding
and less than three B-lines.
- - 1: Interstitial syndrome, resulting in moderate loss of aeration with more than three
spaced B-lines, 7mm apart, scores one point.
- - 2: Alveolar-interstitial syndrome meaning a severe loss of aeration with coalescent
B-lines, less then 3mm apart, scores two.
- - 3: An alveolar consolidation leading to a complete loss of aeration with an
ultrasonographic tissue like pattern.
LUSS will be calculated by adding the score given to each 12 zones, with a maximum of
thirty-six. Patients scoring less than two, will be considered empirically with no
interstitial syndrome and will be secondary excluded of the study. Investigators will also
report the presence of pleural effusion allowing to classify the patient in one of these
three subgroups:
- - Absence of pleural effusion.
- - Unilateral pleural effusion.
- - Bilateral pleural effusion In order to collect those results, a template with a reminder
about how to calculate the LUSS will be joined to the Case Report Form (CRF).
The result
of LUSS won't be communicated to the treating physician.
Study conduction. The study flow chart is displayed in Figure 3.
Study Setting. Before the study launching, the investigator will be recruited using a five-point Likert
scale as previously described. A presentation of the study and the procedure will be
organized by the coordinating investigators in each including ED.
Patients' recruitment. The eligible patients will be identified by the treating ED physician. Patients admitted to
ED with dyspnea, without taking account of any dyspnea classification, and for which the ED
physician decide on the basis of his clinical judgment the realization of an ABG, will be
considered for inclusion. The decision of the realization of an ABG being left to the ED
physician, ABG is not considered as an intervention. Patients less than eighteen years old,
patients presenting with a known chronic IS, COPD or patients for which LUS is not feasible
will be discarded.
Inclusion. All eligible patients will undergo a LUSS after having given an informed consent to the
investigator. The target population will include patients temporary not able to give a
written and informed consent due to their acute condition. Therefore, the consent will either
be written or verbal with secondary signature as soon as possible. Any legal representative
will also be given the possibility to sign consent. Only patients with written consent will
be included for data analysis. In Belgium, LUS isn't recognized as standard of care giving to
this study an interventional character. The result of the LUSS will not be communicated to
the treating physician.
Secondary exclusion Patients with a LUSS of less than 2 will not be considered as affected
with IS and be secondary excluded.
Data collection and Data treatment. The LUSS will be reported on a template included in the CFR. It will be filled out by the
investigator and joined to the signed consent. Name, first name, date of birth and hospital
administrative number of the included patients will be recorded on the CFR. Investigators
will only access personal data of the patient they have personally included; principal
investigators will have access to all personal data in order to be able to collect missing
data. Data will secondary be replaced by neutral identifier for analysis.
Follow up. There will be no follow up.
Statistics. The software IBM SPSS statistics 23.0 (SPSS Inc., Chicago, IL, USA) will be used to analyse
our data. Since LUSS will be considered as a continuous value for all of our analysis,
Pearson formula was used to calculate the patient sample. For the description of our
population, the continuous values will be expressed in mean with a minimal and maximal values
and standard deviations while discrete values will be reported by categories and expressed in
numbers and percentage. Comparison between quantitative data will be realized with a
Chi2-test and comparison between continuous data with a Wilcoxon-Mann-Whitney test.
Significance threshold will be set with a p-value at <0.05. Confidence intervals will be 95%
and calculate using " Mid-P exact value ".
Data Management. Data circuit and confidentiality. The paper CRFs will be collected in each centre by the principal investigators and
hand-delivered to the study promoter. Patients will initially be identified on the CRF by
their last name, first name, date of birth, file's number from the institution where they
have been included and an identification's number from the study. This identification's
number will include a reference for the inclusion centre, a number of inclusions, the first
letter of the patient name and month and year of birth. After completion of the collection of
missing data by principal investigators, patients will only be identified by their study
identification number in order to be anonymised. A list of correspondence between study
identification number and the other identifying data initially collected will be kept under
the responsibility of the promoter. This list is kept for the statutory period of time
provided for this type of research. The protection of the patient's personal data will be
guaranteed according to the European General Data Protection Regulation of 27 April 2016 (in
application since 25 May 2018), to the Belgian Law of 30 July 2018 on the protection of
privacy with regard to the processing of personal data and to the Belgian Law of 22 August
2002 on the rights of the patient.
