Appendectomy: Robotic-assisted or laparoscopic appendectomy for acute appendicitis.
Study summary
The purpose of this retrospective study is to compare perioperative data for subjects who have undergone an emergent or urgent robotic-assisted or laparoscopic appendectomy for acute appendicitis.
Eligibility
Sex
ALL
Min age
22 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Subject is 22 years of age or older at time of procedure
* Subject has undergone robotic-assisted or laparoscopic emergent or urgent appendectomy for acute appendicitis between 2018 and 30 days prior to IRB approval
Exclusion Criteria:
* Subject with appendiceal neoplasms
* Subject who underwent a single-port appendectomy
* Subject who was pregnant or breastfeeding at the time of the procedure
Primary outcome measure(s)
Operative time — Intraoperative
Procedure time — Intraoperative
Conversion — Intraoperative
Adverse events — Intraoperative and postoperative out to 30 days from procedure date
Mortality rate through 30 days — Intraoperative and postoperative out to 30 days from procedure date All cause
Unplanned procedure-related readmission rate through 30 days — Discharge through 30 days
Concomitant procedures — Intraoperative
Estimated blood loss — Intraoperative
Severity of appendicitis — Preoperative
Unplanned procedure-related reoperation rate through 30 days — Postoperative through 30 days
Length of stay — Start of procedure to discharge from the hospital (check-out time), up to approximately one week Total number of days the subject stayed in the hospital after the index procedure prior to being discharged.
Discharge disposition — Discharge from the hospital (check-out time), up to approximately one week. Where the subject was discharged to when released from the hospital
Blood Transfusion — Intraoperative and discharge from the hospital (check-out time), up to approximately one week. Any occurrence of blood transfusion either at the time of the procedure or at any point during the post-procedure hospitalization until the participant is discharged.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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