Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care (MEOPanx)

Toulouse University Hospital

Status: Unknown

Conditions: Anxiety; Pain

Treatments: Other: Administration of MEOPA as part of the care

Study type: Observational

Funder types: Other

Identifiers

NCT03613155

RC31/18/0222

2018-A01687-48 (Other Identifier)

Details and patient eligibility

About

The emergency setting, frequently associated with pain and the feeling of loss of control, can cause anxiety in patients.

Reaction anxiety may be an appropriate response to an emergency; Nevertheless, attention must be paid to the evaluation and management of the latter especially as anxiety and pain are closely linked.

Full description

There is a definite interest in the management of patients' pre-hospital anxiety. The literature reports a strong association between anxiety, post-traumatic stress and chronic pain. A study conducted at SAMU 31 also found that anxiety on arrival at the emergency department was a negative factor in the treatment of pain. Anxiety can reduce the pain threshold and promote hyperalgesia.

The management of patient anxiety in pre-hospital offers interesting results in terms of analgesia and satisfaction of users of care and should not be neglected.

MEOPA has recently been available in SMUR vehicles (emergency and resuscitation mobile service) at SAMU 31 (urgent medical assistance service); its availability can lead teams to change their practices. More and more emphasis is placed on the importance of positive communication and comfort for which MEOPA, with its conscious sedating effect, could be a facilitating factor.

The aim of our study is to evaluate the level of anxiety of patients treated by SMUR teams in Toulouse and receiving MEOPA following the usual indications for pain-induced pain or pain alleviation.

This is a pilot study, which focuses on the assessment of anxiety in patients treated in pre-hospital care by SMUR Toulouse and receiving MEOPA as part of their care. No data exists in the literature on this subject.

This descriptive study based on qualitative data collected by the FAS1 scale will provide us with the first data on this population. It does not change the usual management of the patient since only patients who must receive MEOPA following the usual indications for pain relief or pain-induced care will be included in the study

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient over 18
• Patient supported by a SMUR team from Toulouse
• Patient receiving MEOPA during pre-hospital care (in the usual indications for pain relief or pain-induced care)
• Patient having given his non-opposition to participate in the study

Exclusion criteria

• Any patient with a contraindication to MEOPA:
• Patient requiring pure oxygen ventilation
• Intracranial hypertension
• Any alteration of the state of consciousness preventing the patient's cooperation
• Traumatic brain injury
• Pneumothorax
• Emphysema bubbles
• Gas embolism
• Diving accident
• Abdominal gas distension
• Patient who received an ophthalmic gas for ocular surgery less than three months old
• Known and unsubstituted vitamin B12 deficiency
• Patient under legal protection
• Refusal of the patient to participate in the study
• Barrier of the language or alteration of the communication
• Patient in vital distress