Does Fluid Requirement Decrease With the Use of Pneumatic Compression Device on Lower Limbs

All India Institute of Medical Sciences, Rishikesh

Status: Completed

Conditions: Fluid Overload

Treatments: Device: HUNTLEIGH FLOWTRON ACS900

Study type: Interventional

Funder types: Other

Identifiers

NCT03789474

AIIMSRishikesh

Details and patient eligibility

About

Impact of intraoperative use of pneumatic peristaltic compression device on hemodynamics vis a vis on fluid requirement during general anaesthesia and surgery.

Full description

Induction of general anaesthesia is associated with cardiac depression and peripheral vasodilatation resulting in hypotension .This hypotension can be corrected by giving intravenous fluid, or the vasoconstrictor. While optimum fluid balances in the perioperative period is of vital importance in overnight fasting patients to correct the fluid deficit, any fluid overload is not only counterproductive to the heart function but is associated with fluid retention in body and edema in postoperative period.

Peristaltic pneumatic compression device, a variant of intermittent sequential compression of legs, uses higher pressure and longer compression cycles to avoid venous stasis in immobilized patients. Sequential compression devices have sleeves with pockets of inflation, which works to squeeze on the appendage in a milking action .The most distal areas will inflate initially, and the subsequent pockets will follow in the same manner. The primary aim of the device is to squeeze blood from the underlying deep veins to proximal side. When the inflatable sleeves deflate, the veins will replenish with blood. The intermittent compressions of the sleeves will ensure the movement of venous blood . Peristaltic Pneumatic Compression of the legs significantly reduces fluid demand and enhances stability during minor ear, nose, and throat surgery. Peristaltic Pneumatic Compression has the potential to support fluid restriction regimens during surgery .

Enrollment: 60 patients

Sex: All

Ages: 25 to 50 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• ASA(American Society of Anaesthesiologists) grade I or II, of both genders
• Age group of 25 to 50 years
• Patients undergoing surgeries under GA(General Anaesthesia) for 2-3 hours

Exclusion criteria

• Patients expected to get major blood loss
• Burns patients.
• Patients with significant cardiac diseases.
• Patients with pulmonary diseases and impaired renal function.
• Lower limb surgeries and abdominal surgeries

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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60 participants in 2 patient groups

Group A

No Intervention group

Description:

No intervention was done ,served as a control group.

Group B

Experimental group

Description:

Intervention:peristaltic pneumatic compression device was placed on the legs of the patient and was active. HUNTLEIGH FLOWTRON ACS900 calf length device was used.

Treatment:

Device: HUNTLEIGH FLOWTRON ACS900