Percutaneous Catheter Decompression in the Treatment of Elevated Intra-abdominal Pressure

Sponsor
Orlando Regional Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT01230255
Collaborator
(none)
62
1
2
43
1.4

Study Details

Study Description

Brief Summary

Intra-abdominal hypertension (IAH) and abdominal compartment syndrome (ACS) have traditionally been treated surgically through emergent laparotomy. Intensivist-performed bedside drainage of free intra-peritoneal fluid or blood [percutaneous catheter decompression (PCD)] has been suggested as a less-invasive alternative to traditional open abdominal decompression (OAD). This study assesses the relative efficacy of PCD vs. OAD in reducing elevated intra-abdominal pressure (IAP).

Condition or Disease Intervention/Treatment Phase
  • Procedure: Percutaneous catheter drainage
Phase 3

Detailed Description

Intra-abdominal hypertension (IAH), the presence of elevated intra-abdominal pressure (IAP), and abdominal compartment syndrome (ACS), the development of IAH-induced organ-dysfunction and failure, are both associated with significant morbidity and mortality when appropriate and expedient treatment is not rendered. Elevated IAP is an independent predictor of mortality during critical illness and serial IAP measurements are increasingly being performed in the intensive care unit (ICU) setting.

Despite growing evidence demonstrating the survival benefit of serial IAP monitoring and abdominal decompression in patients with IAH / ACS, some physicians are reluctant to consider decompression or unable to convince a surgeon to open the abdomen of patients manifesting IAH-related organ failure. Percutaneous catheter drainage (PCD) of free intra-abdominal fluid, air, abscess, or blood has been suggested in several case reports and small clinical trials to be a less invasive technique for reducing IAP and potentially correcting IAH-induced organ dysfunction. PCD, performed under ultrasound or computed tomography guidance, is described in the current World Society of the Abdominal Compartment Syndrome (WSACS) consensus recommendations as a therapeutic option, but insufficient data currently exist to support a strong evidence-based recommendation for the percutaneous treatment of IAH / ACS (10,12). Since 2007, we have employed PCD in the treatment of patients with IAH due to free intraperitoneal fluid and blood. This study describes our experience with the less invasive PCD technique compared to contemporaneous matched control patients who received traditional open abdominal decompression (OAD) for the treatment of IAH / ACS.

Study Design

Study Type:
Interventional
Actual Enrollment :
62 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Percutaneous Catheter Decompression in the Treatment of Elevated Intra-abdominal Pressure
Study Start Date :
Jan 1, 2007
Actual Primary Completion Date :
Jun 1, 2010
Actual Study Completion Date :
Aug 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: Percutaneous catheter decompression

Ultrasound guided percutaneous catheter drainage of free intra-peritoneal fluid or blood

Procedure: Percutaneous catheter drainage
Ultrasound guided insertion of a 14 French pigtail catheter to drain free intra-peritoneal fluid or blood and thereby reduce elevated intra-abdominal pressure

Active Comparator: Open abdominal decompression

Surgical treatment of elevated intra-abdominal pressure through traditional open abdominal decompression

Procedure: Percutaneous catheter drainage
Ultrasound guided insertion of a 14 French pigtail catheter to drain free intra-peritoneal fluid or blood and thereby reduce elevated intra-abdominal pressure

Outcome Measures

Primary Outcome Measures

  1. Reduction in intra-abdominal pressure [4 hours]

Secondary Outcome Measures

  1. Increased abdominal perfusion pressure [4 hours]

  2. Percutaneous drainage failure rate [7 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Elevated intra-abdominal pressure
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Orlando Regional Medical Center Orlando Florida United States 32806

Sponsors and Collaborators

  • Orlando Regional Medical Center

Investigators

  • Principal Investigator: Michael L Cheatham, MD, Orlando Regional Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01230255
Other Study ID Numbers:
  • OH09.068.04
First Posted:
Oct 29, 2010
Last Update Posted:
Oct 29, 2010
Last Verified:
Oct 1, 2010

Study Results

No Results Posted as of Oct 29, 2010