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Cardiopulmonary Effects of Prone Position in CARDS

B

Bakirkoy Dr. Sadi Konuk Training and Research Hospital

Status

Completed

Conditions

ARDS Due to Disease Caused by SARS Co-V-2
Right Ventricular Dysfunction

Treatments

Procedure: the first hour of prone position
Procedure: the first hour of returning to the supine position
Procedure: before prone position

Study type

Observational

Funder types

Other

Identifiers

NCT06456606
2022/40

Details and patient eligibility

About

In coronavirus disease-2019 (COVID-19)-related ARDS (C-ARDS), especially in the severe form, increased shunt rate, impaired ventilation/perfusion ratio (V/Q), hypoxic pulmonary vasoconstriction inhibition, and increased immune microthrombosis may have similar effects on the right ventricle .The cardiopulmonary pathophysiology and outcomes of C-ARDS vary, and this variability requires monitoring to follow the diagnosis and treatment process. This study aimed to increase the treatment success of the prone position in C-ARDS and to provide a prognostic factor for survival by analyzing and monitoring heart-lung interactions. Therefore, we used transesophageal echocardiography (TEE) to evaluate the cardiopulmonary effects of prone position.

Full description

This prospective study included 30 moderate-to-severe C-ARDS patients who were treated with prone position in the first 48 hours of invasive mechanical ventilation support. It was evaluated with transesophageal echocardiography three times: before prone position (PP) (T0), the first hour of PP (T1), and the first hour of returning to the supine position (T0 + 24 hours) (T2) after 23 hours prone position treatment. Right ventricular end-diastolic area/left ventricular end-diastolic area (RVEDA/LVEDA) was preferred right ventricular evaluations as primer outcome. Static compliance (C-stat) was examined in the evaluation of the pulmonary effect of prone position as secondary outcome.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • >18 years
  • Patients diagnosed with polymerase chain reaction/computed tomography results
  • Moderate/severe severity class according to the Berlin ARDS classification
  • Prone position applied in the first 48 h after orotracheal intubation in treatment
  • Obtaining an informed consent form

Exclusion criteria

  • Pulmonary embolism
  • Pneumothorax
  • Heart valve disease
  • Pregnancy
  • Perforated esophageal varices
  • Coagulopathy
  • Esophageal stricture
  • Esophageal tumor
  • Neck fracture
  • Thrombocytopenia
  • Gastrointestinal bleeding
  • Previous stomach surgery
  • Previous esophageal surgery
  • Esophageal perforation

Trial design

30 participants in 1 patient group

group a
Description:
30 moderate-to-severe C-ARDS patients who were treated with prone position in the first 48 hours of invasive mechanical ventilation support. It was evaluated with transesophageal echocardiography three times: before prone position (T0), the first hour of prone position (T1), and the first hour of returning to the supine position (T0 + 24 hours) (T2) after 23 hours prone position treatment.
Treatment:
Procedure: before prone position
Procedure: the first hour of returning to the supine position
Procedure: the first hour of prone position

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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