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Ultrasonographic Assessment of the Effect of CPB Acute Lung Injury (CBP)

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Lung Ultrasound

Treatments

Procedure: lung recruitment

Study type

Interventional

Funder types

Other

Identifiers

NCT03619525
lung ultrasound after CPB

Details and patient eligibility

About

The study is designed to use the lung ultrasound to assess the effect of intermittent lung recruitment during cardiopulmonary bypass in cardiac surgeries on extra vascular lung water.

Full description

Significant respiratory dysfunction is a common problem after cardiac surgery, with an incidence of about 25%. the formation of atelectasis appears to be the primary factor responsible for increased intrapulmonary shunt after cardiac surgery with CPB. The investigators will use the lung ultrasound to evaluate the effects of intermittent recruitment of the lungs during CPB on extra vascular lung water (EVLW).

Objectives :

To evaluate the effect of intermittent lung recruitment during CPB in cardiac surgery on:

Lung ultrasound score (LUS),Oxygenation at different times postoperatively,Time for extubation and length of ICU stay

sixty patients aged from 18-60 years old, scheduled for elective cardiac surgery with CPB will be included in the study. Patients will be randomly allocated into one of two groups: Group A (n=30): will receive intermittent lung recruitment during CPB.Group B (n=30): control group.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult patients aged (18-60 years),
  • elective valvular cardiac surgery with cardiopulmonary bypass (CPB).

Exclusion criteria

  • • Emergency surgeries.

    • coronary artery bypass graft surgery
    • patients requiring re-exploration in the immediate postoperative period (within 2hours)
    • left Ventricular ejection fraction less than 40%
    • patients with preoperative congestive heart failure, cardiogenic shock , preoperative pulmonary edema
    • pre-existing severe chronic pulmonary dysfunction (defined as pulmonary disease requiring home oxygen therapy or causing shortness of breath after 1 to 2 flights of stairs)
    • Morbid obesity
    • Renally impaired patients with creatinine more than 2 mg/dl

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

recruitment group
Active Comparator group
Description:
will receive intermittent lung recruitment during CPB
Treatment:
Procedure: lung recruitment
control group
No Intervention group
Description:
will recieve no intervention

Trial contacts and locations

1

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Central trial contact

Mohammed Hamza, lecturer; Maged el gendy, assiststant lecturer

Data sourced from clinicaltrials.gov

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