Peritoneal/ Serum Lactate Ratio in Relaparotomy (lactate)

This study has been completed.
Sponsor:
Information provided by:
Ospedale S. Giovanni Bosco
ClinicalTrials.gov Identifier:
NCT01161849
First received: June 21, 2010
Last updated: January 3, 2011
Last verified: July 2010
  Purpose

Laparotomy performed for both emergency of elective surgery may by complicated by intrabdominal collection, anastomotic leakage, infarction and others. This conditions are able to induce peritoneal inflammation. Inflamed peritoneum are able to produce excess of lactate that the investigators can measure by collecting fluid from peritoneal drainage.

Drainage were left in abdomen for monitoring intrabdominal condition until the passage of stool or flatus. Minimum drainage of serum is present daily also in uncomplicated post operative period.

Serum lactate relates with increased systemic anaerobic metabolism such as SIRS, sepsis and systemic hypoperfusion and it is easy to measure with a blood gas analysis.

The investigators hypothesized that the increases of peritoneal/ serum lactate ratio could be an earlier, sensible, non-invasive, and economical marker of post surgical complications. The decision whether and when to perform a relaparotomy in secondary peritonitis is largely subjective and based on professional experience. Actually no existing scoring system aids in this decision.

The aim of this study is to demonstrate that this ratio could be and useful tool for the surgeon in this decisional process.


Condition
Surgical Complications
Relaparotomy

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Peritoneal/Serum Lactate Ratio in Relaparotomy

Resource links provided by NLM:


Further study details as provided by Ospedale S. Giovanni Bosco:

Estimated Enrollment: 60
Study Start Date: August 2010
Study Completion Date: December 2010
Primary Completion Date: October 2010 (Final data collection date for primary outcome measure)
Detailed Description:

Post operative intraabdominal sepsis due to surgical complications is associated with an important mortality and morbidity. Early diagnosis is crucial to improve outcome. Relaparotomy could be necessary to eradicate the intraabdominal focus of sepsis or hypoperfusion. The relaparotomy must be performed early after the diagnosis of surgical complications before the onset of multi organ failure.

This prospective observational study includes the post operative period of consecutive patients requiring both major elective surgery and urgent laparotomy.

Demographic data, presence and nature of underlying disease and surgical diagnosis will be recorded on admission and study inclusion.

Daily after study inclusion, the investigators measure: venous blood gases, blood lactate and lactate presents in the fluid collected from the abdomen. Possum and SAPSII scores will be calculated daily or when a patient develops a rapid clinical deterioration.

The investigators follow patients with complicated or uncomplicated post operative period.

Post operative complications are defined as: mesenteric ischemia, need for reintervention, anastomotic leakage or fistula, secondary peritonitis and death.

The primary end point is to demonstrate the correlation between surgical complications and serum/abdominal lactate ratio.

The second end point is to verify the correlation between need to relaparotomy and Possum an SAPSII scores.

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients admitted to our surgery department for the post operative period after major abdominal surgery (neoplastic and non neoplastic) or urgent laparotomy for traumatic or non traumatic acute abdomen.

Criteria

Inclusion Criteria:

  • Post operative period of abdominal surgery (elective surgery of:colon-rectum, ileum, stomach and, pancreas)
  • Post operative period after Urgent laparotomy for both traumatic and/or non traumatic acute abdomen
  • Patients with signs of sepsis in the post operative period
  • Patients with signs of systemic hypoperfusion in the post operative

Exclusion Criteria:

  • Liver surgery
  • Drainage of bile, blood and dejection from abdominal drainage
  • Sepsis/ systemic hypoperfusion due to extraabdominal infection site
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01161849

Locations
Italy
Chirurgia Generale e d'Urgenza; Ospedale SG Bosco: aslTO2
Torino, Italy, 10153
Medicina D'Urgenza; Ospedale SG Bosco; ASLTO2
Torino, Italy, 10153
Sponsors and Collaborators
Ospedale S. Giovanni Bosco
Investigators
Principal Investigator: roberto bini, md Chirurgia d'urgenza
Principal Investigator: Giovanni Ferrari, MD Medicina d'urgenza
Study Chair: Renzo Leli, MD Chirurgia d'urgenza
  More Information

Publications:

Responsible Party: Roberto Bini MD, Chirurgia d'urgenza
ClinicalTrials.gov Identifier: NCT01161849     History of Changes
Other Study ID Numbers: Lali2010
Study First Received: June 21, 2010
Last Updated: January 3, 2011
Health Authority: Italy: Ministry of Health

Keywords provided by Ospedale S. Giovanni Bosco:
lactate
urgent surgery
major surgery
surgical complications
possum
sapsII
relaparotomy

ClinicalTrials.gov processed this record on September 18, 2014