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An observational study was conducted in many countries to collect data regarding the current treatment practices and their outcomes in a patient with weak immunity who was admitted to the intensive care unit with severe difficulty in breathing for improvement in future treatment practices.

Not Applicable
Conditions
Health Condition 1: J960- Acute respiratory failureHealth Condition 2: D849- Immunodeficiency, unspecified
Registration Number
CTRI/2024/01/061901
Lead Sponsor
Groupe de Recherche respiratoire en Réanimation Onco Hématologique
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1 adult patients

2 admitted to the ICU between 1 Jan 2017 to 31 Dec 2022

3. with acute respiratory failure oxygen dependance more than 6 liter per min to achieve SPO2 more than 92 percentage and or respiratory rate more than 30 per minute and or labored breathing and or the need for non invasive or invasive mechanical ventilation or high flow nasal cannula

4 with a known immunodepression hematological malignancy including autologous and allogeneic stem cell transplant, solid tumor requiring treatments over the last five years, solid organ transplant, immunosuppressive drugs for auto-immune or auto inflammatory disease and primary immunodeficeincy

Exclusion Criteria

1. Patients with isolated HIV infection are not eligible for this study

2. Patients already included in the cohort

3. Patient refuse for consent and data collection

4. Patients deprived of liberty under guardianship or curatorship

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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