Prevalence and Kinetics of Diaphragmatic Dysfunction in Elderly Patients With Acute Respiratory Distress

NCT ID: NCT04520815

Last Updated: 2021-10-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-06-24

Study Completion Date

2022-06-30

Brief Summary

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Acute respiratory distress (ARD) is one of the most frequent reasons for consultation and hospitalization in emergency medicine. The use of ultrasound methods as a diagnostic and clinical assessment tool in emergency medicine is increasingly important. As such, ultrasound is a simple, non-invasive means of assessing diaphragmatic function in the patient's bed. Several methods of ultrasound assessment of diaphragm function have been described. Among these different methods, the diaphragmatic excursion seems to have a better intra and interobserver reproducibility as well as a greater feasibility, in particular because of its speed of realization and its learning curve seeming faster in comparison with the measurement. of the thickening fraction. Measuring the diaphragmatic excursion could therefore ultimately represent a simple means of assessing respiratory function, both diagnostic and prognostic, in patients with acute respiratory distress in the emergency departments. The etiologies of acute respiratory distress in very elderly patients (i.e.\> 75 years) admitted to the emergency reception service are multiple.

To our knowledge, there is no data available in the literature on the prevalence of diaphragmatic dysfunction and its short- and long-term course in this category of patients. The main objective of this study is therefore to assess the prevalence of diaphragmatic dysfunction and its evolutionary kinetics in patients over the age of 75 admitted for acute respiratory distress in the emergency medicine department.

Detailed Description

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Conditions

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Respiratory Distress Syndrome, Adult

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient in spontaneous ventilation at the admission on emergency room
* Presence of acute respiratory distress defined by at least 1 of the following criteria:

* Respiratory rate \> 25/min and/or clinical signs of acute respiratory distress,
* Hypoxia defined by Sp02 \< 90 %,
* Hypercapnia defined by PaC02 \> 45 mmHg with respiratory acidosis defined by a pH value \<7.35.
* Absence of opposition of the patient to his participation in the study and the use of his data or the trusted person if the state of the patient does not allow it.

Exclusion Criteria

* Presence of a preexisting diaphragmatic dysfunction appearing in the history or the medical file of the patient and explored on the electro-physiological level,
* Patient with acute respiratory distress on arrival at the SAU with clinical criteria justifying immediate use of invasive mechanical ventilation and not allowing ultrasound measurements to be carried out or patient admitted to the SAU with mechanical ventilatory support from the outset,
* Poor command of the French language or state incompatible with the patient's understanding and / or informed adherence to the study protocol,
* History of surgery involving the integrity of the diaphragmatic muscle (diaphragm plication or diaphragmatic lumpectomy or placement of diaphragmatic pacemaker),
* Criteria for shock or severe hemodynamic instability,
* Intra-cranial hypertension.
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de la Réunion

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Thomas GROSEIL, Dr

Role: PRINCIPAL_INVESTIGATOR

CHU de La Réunion

Locations

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Centre Hospitalier Universitaire de la Réunion

Saint-Denis, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Emilie TECHER

Role: CONTACT

+2 62 262 90 62 89

Thomas GROSEIL, Dr

Role: CONTACT

+262 262 90 60 70

Facility Contacts

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Emilie TECHER

Role: primary

0262946289 ext. +262

Other Identifiers

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2020/CHU/10

Identifier Type: -

Identifier Source: org_study_id

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