Randomized Clinical Trial to Test the Efficacy and Safety of Outpatient Clinical Management of Urgent Laparoscopic Appendectomy in Uncomplicated Acute Appendicitis
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Appendicitis Acute
- Sponsor
- HJ23
- Enrollment
- 120
- Locations
- 1
- Primary Endpoint
- length of hospital stay (LHS)
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
The aim of this study is to evaluate the safety and efficacy of outpatient management of uncomplicated acute appendicitis. For this purpose, a randomized clinical trial was designed. Selected patients who have undergone surgery for acute appendicitis are randomized into two groups. One group with hospitalization and another group without admission.
Detailed Description
The aim of this study is to evaluate the efficacy and safety of outpatient management of laparoscopic appendicectomy in uncomplicated acute appendicitis. This was a single center randomized controlled clinical trial consisting in 2 treatment groups. Patients were recruited in University Hospital of Tarragona Joan XXIII of Spain. All patients admitted in the emergency department at University Hospital of Tarragona Joan XXIII with acute appendicitis diagnosis were likely to enter in the study. All patients who accomplished at least 4 over 5 of the Saint-Antoine criteria were included. The 5 criteria were: Leukocytosis lower than 15.000; C-Reactive protein lower than 30mg; Body mass index lower than 30kg/m2; appendicular diameter lower than 10mm and no radiological sign of complication. All patients who met the inclusion criteria and none of the exclusion criteria were admitted to the study for emergency surgery. In order to avoid the biases a unique anesthetic and surgical protocol were established for both groups. Once Laparoscopic appendicectomy was performed the patients were randomly assigned to the hospitalization group or outpatient group. Patients in the hospitalization group were admitted in the hospitalization ward. Patients in the outpatient group were referred to the day-surgery unit where they were discharged according to ALDRETE criteria. The primary endpoint was the length of hospital stay (LHS). The length of hospital stay was calculated from the day and hour of admission in the surgical area to the day and hour of discharge, based on the hours of hospital stay. Secondary endpoints included the failures of the outpatient management, readmissions and the hospitals cost.
Investigators
Jordi Elvira Lopez
Principal Investigator
HJ23
Eligibility Criteria
Inclusion Criteria
- •patients over 18 years old
- •meet at least 4 over 5 Saint Antoine criteria
- •ASA classification (American Society of Anesthesiologists) less than or equal to 3
- •patients who live accompanied in a home at a maximum distance of 30 minutes from the hospital and an adequate cognitive capacity.
Exclusion Criteria
- •pregnancy or breastfeeding
- •complicated Acute Appendicitis
- •surgical management performed in more 90 minutes.
Outcomes
Primary Outcomes
length of hospital stay (LHS)
Time Frame: up to 5 days
The length of hospital stay (LHS) was calculated from the date and time of urgent appendectomy surgery to the date and time of hospital discharge, based on the hours of hospital stay (assessed up to 5 days)
Secondary Outcomes
- failures of the outpatient management(assessed up to 30 days)
- readmissions(assessed up to 30 days)
- hospitals cost(through study completion, an average of 1 year)