> Skip repeated content

Peripheral versus Central Venous Pressure Monitoring in the Perioperative Period

IRB Number: 29097
inactive

May 11, 2010

Institutional Review Board, Hospital for Special Surgery

The safety of our participants is our top priority. The trial/study is approved and periodically reviewed by the Institutional Review Board (IRB), which includes doctors, administrators, ethicists, and members of the general public. The safety of clinical trials is reviewed by the U.S. Food and Drug Administration.

Before enrolling in a clinical trial or research study, the investigator will explain the purpose of the trial/study, its expected benefits, any possible risks or side effects, and what your role will be. If you want to join the trial/study, you must sign informed consent documents. You can leave a trial/study at any time without penalty.

For further information, see Understanding Clinical Trials/Research Studies.

Principal Investigator

Stavros G. Memtsoudis, MD, PhD

Co-Investigators

 

Gregory A. Liguori, MD
Michael K. Urban, MD, PhD
Michael C. Ho, MD
Jonathan C. Beathe, MD
Matthew C. Rade
Cheryl A. Conwell

Summary

Measuring central venous pressure (CVP) is widely considered a useful aid in the management of a patient’s fluid status during surgery. Usually, the placement of a central venous line is required, which is associated with a number of risks including line infection, vessel injury, accidental carotid puncture and pneumothorax. In addition, placing a central line can be technically difficult or impossible, especially intraoperatively, when patient access is limited by surgical drapes. A number of studies have suggested that peripherally transduced venous pressures (PVP) correlate well with centrally derived values and thus could be used interchangeably. However, information on the feasibility of this technique in the perioperative period, effect on patient comfort, cost and complications is extremely limited. In view of the usefulness of information provided by the measurement of venous pressure in large blood loss/fluid shift cases, such as spine surgical procedures, it seems prudent to study the correlation between CVP and PVP in this population. We propose to measure centrally and peripherally transduced venous pressure in 220 patients undergoing spine surgery in the prone position. The patients would be enrolled in the study for the duration of the surgery and for 6 hours post operatively, during which pressures would be transduced and recorded form a central line and a peripherally placed intravenous catheter.

Inclusion/Exclusion Criteria

Inclusion criteria:

• All patients ages 18-99 presenting for spine surgery in the prone position and deemed to require a central line for monitoring are eligible for the study.

Exclusion criteria:

• Patients younger than 18 years old and older than 99
• Patients having contraindications for central line or peripheral line placements such as infection of the skin at the intended site of insertion and known vascular abnormalities of the central venous system (i.e., blood clots, vascular occlusions, etc.)
• Patients having poor peripheral venous access site availability

Contact Information

Stavros G. Memtsoudis, MD
memtsoudiss@hss.edu
212.606.1036