Pathophysiology of Perioperative Fluid Management in Emergency Laparotomy

Fluid Overload Clinical Trial

Official title:

Pathophysiology of Perioperative Fluid Management in Patients Un-dergoing High Risk Emergency Laparotomy, a Prospective Descriptive Cohort Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03997721
• Other study ID #: H-19010653
• Status: Completed
• Start date: May 23, 2019
• Est. completion date: May 1, 2021

Study information

• Verified date: September 2022
• Source: Copenhagen University Hospital, Hvidovre
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Pathophysiology of perioperative fluid management in patients undergoing emergency laparotomy.

Description:

In critically ill patients and patients undergoing major surgery, the combination of internal fluid shifts and fluid retention resulting in extravascular fluid accumulation and postoperative organ dysfunctions, complicates perioperative fluid management and influences patient outcome.

Changes in extravascular volume after surgery have been much debated, studies in major surgery suggest that extracellular volume expansion may correlate with intraoperative fluid administration, while other studies show the intravascular volume to be decreased after surgery.

Difficulty in obtaining accurate measurements of the fluid phases is recognized and despite years of research, perioperative extravascular volume changes have not been clarified in acute high-risk abdominal (AHA) surgery. It is essential to be able to identify and characterize the transition from necessary fluid resuscitation to harmful fluid volume accumulation, intra- as well as extravascular.

The present study seeks to investigate the perioperative fluid status and fluid shifts in patients undergoing AHA surgery, specifically focusing on intra- versus extra-vascular fluid status in patients with intestinal obstruction versus intestinal perforation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 73
• Est. completion date: May 1, 2021
• Est. primary completion date: March 2, 2021
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Adults (18 years or over) undergoing emergency high-risk abdominal surgery for following abdominal pathology:

1. Perforated small intestine

2. Perforated large intestine

3. Perforated ulcer

4. Intestinal obstruction

5. Anastomotic leakage following elective surgery

2. Provided verbal and written informed consent

3. Must speak and understand the Danish language

Exclusion Criteria:

1. Appendectomies, cholecystectomies, negative diagnostic laparoscopies/laparotomies, herniotomies without bowel resections, sub-acute internal hernias after gastric bypass surgery, sub-acute surgery for inflammatory bowel diseases.

2. Primary surgery for intestinal ischemia, abdominal bleed

3. Emergency re-operations after elective surgery owing to intraabdominal bleeding, paralytic/obstructive ileus, intestinal ischemia

4. Reoperation owing to fascial separation with no other abdominal pathology identified and sub-acute colorectal cancer-surgery were excluded from the cohort. Sub-acute surgery was defined as surgery planned within 48 hours.

5. Traumas, gynecological, urogenital and other vascular pathology, pregnant patients.

6. Dementia and/or cognitive dysfunction (diagnosed).

Related Conditions & MeSH terms

• Anastomotic Leak
• Emergencies
• Fluid Overload
• Intestinal Obstruction
• Intestinal Perforation
• Pathophysiology

Locations

Country	Name	City	State
Denmark	Copenhagen University Hospital Hvidovre	Hvidovre

Sponsors (1)

Lead Sponsor	Collaborator
Copenhagen University Hospital, Hvidovre

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The fluid distribution, during the early perioperative period (= 5 days), in patients with intestinal perforation versus intestinal obstruction versus postoperative complications with peritonitis.	Intra vs. extra vascular. Stroke volume assessment, Bioimpedance measurements	perioperative period
Secondary	Impact of fluid distribution/fluid overload on preload dependency.		Preoperatively, 6 hours postoperatively and on first, third and fifth postoperative day
Secondary	Impact of fluid distribution/fluid overload on peripheral perfusion.		Preoperatively, 6 hours postoperatively and on first, third and fifth postoperative day
Secondary	Correlation between fluid balance just prior to surgery and intraoperative need for vasopressor/inotropes administration.		Preoperatively, 6 hours postoperatively and on first, third and fifth postoperative day
Secondary	Evaluate the relationship between fluid overload and mortality rate in patients undergoing emergency laparotomy.		Preoperatively, 6 hours postoperatively and on first, third and fifth postoperative day
Secondary	Association between pre- to postoperative changes in volume status and perioperative fluid volume administration, in patients with intestinal perforation versus intestinal obstruction versus postoperative complications with peritonitis.		Preoperatively, 6 hours postoperatively and on first, third and fifth postoperative day