Thirst was reported in 70% of symptom assessments of intensive care patients. Thirst is a
major source of physical discomfort. This should make it a concern for clinicians and ICU
nurses whose mission is to alleviate symptoms in addition to treating pathology.
Balancing extracellular and intracellular volume is a goal in the poorly communicating
patient with no spontaneous access to water. Thirst may exist, persist, reappear, or
increase again after the institution of water intake; it may reveal changes in the
intra/extra sector or inappropriate intakes. Thirst could therefore be useful as a
clinical management tool. However, it has not been studied to any great extent in
mechanically ventilated patients.
Neglecting thirst in these circumstances is bound to cause suffering. This neglect may
also offset the physiological benefits in terms of clinical outcomes. It could also have
a negative impact at a distance through negative memories. Nevertheless, thirst is not
routinely assessed in ICU patients, except after extubation when the patient has access
to spontaneous hydration.
Mechanically ventilated patients have multiple causes of thirst and dry mouth and at the
same time have difficulty communicating and limited access to water. It is essential to
study thirst in this population. In particular, determining the prevalence of thirst in
this population would raise awareness of its screening. Finally, understanding the main
mechanisms involved in thirst in patients undergoing invasive mechanical ventilation
would allow the development of therapeutic solutions to minimize it.
In this context, the investigators wish to conduct a prospective observational study in
mechanically ventilated patients able to communicate in order to better understand the
prevalence, intensity, mechanisms and prognostic value of thirst as well as the sensation
of dry mouth. They will also focus on the relationship of thirst with dyspnea, anxiety
and pain.
Description of the study population and rationale for its selection The management of
thirst is usually ensured by free access to water and balancing the patient's
extracellular volume.
In the mechanically ventilated patient, this management is made more difficult by many
factors: lack of free access to water, difficulty in communication, sensation of dry
mouth induced by the mechanical ventilation device.
The population studied corresponds to patients under invasive mechanical ventilation in
three intensive care units of university hospitals:
Pitié Salpêtrière intensive care medicine unit, Avicenne hospital intensive care medicine
unit, and Saint-Louis hospital intensive care medicine unit.
Justification of the duration of the research The objective would be to include 200
patients at a rate of approximately 66 patients per service.
Eligibility criteria Recruitment will consist in considering any patient under mechanical
ventilation and communicating as potentially eligible, provided that they meet the
inclusion/non-inclusion criteria.
Conduct of the research During the study period, patients from the 3 resuscitation sites
are systematically screened for inclusion in the study on a daily basis, between 9:00 am
and 12:00 pm.
Subjects meeting the inclusion and non-inclusion criteria will be informed of the study
by the principal investigator or any other investigator trained and declared in the
research. The oral information will be supplemented by an information note. Patients who
wish to participate in the study will be given up to 24 hours to consider their decision.
If the patient agrees to participate in the study, his or her non-opposition is collected
by the investigator on a dedicated form in duplicate. One copy will be given to the
patient, and the other will be kept in the department with the research documents.
In case of suspected confusion, a delirium screening test (CAM-ICU) will be performed to
verify the patient's eligibility. If the test confirms the presence of confusion, the
patient will be excluded from the study.
The information and the collection of the non-opposition will be notified in the
patient's medical file.
Once recruited, patients are asked to rate the intensity of thirst by placing a cursor on
a 100 mm visual analog scale (VAS) bounded on the left by "not thirsty" and on the right
by "intolerably thirsty".
If a patient understands the principle of the assessment but is unable to move the VAS
cursor himself, the observer assists the patient by holding the scale and supporting the
patient's forearm. If the subject is unable to move his or her arms (as in some cases of
severe neuromuscular impairment), the observers are allowed to manipulate the VAS slider
by following the patient's instructions. However, this is not recommended and should be
avoided whenever possible. The slider should never be adjusted directly or solely by the
investigator.
Visual analog scales for dry mouth, anxiety, pain, and dyspnea will be performed as part
of the protocol after the thirst assessment. The oral status, the search for edema or
skin folds and the Revised Oral Assessment Guide (ROAG) score for intubated patients will
also be performed at the same time.
Follow-up of the population The included patients are evaluated only once during their
stay in the ICU: the day of inclusion. The duration of their participation is estimated
at 20 minutes.
Conduct in the presence of thirst in the patient In the event that the patient is
thirsty, the investigator will immediately inform the patient's physician.
