Skip to content

Impact of Functional Status on 30-day Resource Utilization and Organ System Complications Following Bariatric Surgery

Impact of Functional Status on 30-day Resource Utilization and Organ System Complications Following Index Bariatric Surgery: a Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05917691
Enrollment
65627
Registered
2023-06-26
Start date
2015-01-01
Completion date
2019-12-31
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dependence, Frailty, Perioperative/Postoperative Complications

Brief summary

The goal of this observational study is to assess the effect of functional status on bariatric surgical thirty-day outcomes. The main questions it aims to answer are: * Is functional status associated with higher incidence of 30-day unplanned resource utilization? * Is functional status associated with higher incidences of secondary adverse events? Participants will be sampled from the 2015-2019 American College of Surgeons National Surgical Quality Improvement Program

Interventions

PROCEDUREBariatric surgery

Current Procedural Terminology (CPT) codes: 43644, 43645, 43770, 43775, 43842, 43843, 43845, 43846, 43847.

DRUGGeneral anesthetic

Cases were required to have a documented general anesthesia anesthetic technique. Administered drugs were otherwise indeterminate under the current study design (observational study of a deidentified database).

DEVICEIndeterminate

Devices were indeterminate under the current study design (observational study of a deidentified database).

Sponsors

University of Virginia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Current Procedural Terminology (CPT) codes: 43644, 43645, 43770, 43775, 43842, 43843, 43845, 43846, 43847 * Elective, non-emergent cases * General surgery surgical specialty * General anesthesia anesthetic technique

Exclusion criteria

* Documented concurrent or other procedures * Patients admitted to the hospital for greater than one day preceding surgery * Acute kidney injury (preoperative) * End-stage renal disease (preoperative) * Metastatic disease (preoperative) * Wound infection (preoperative) * Sepsis (preoperative)

Design outcomes

Primary

MeasureTime frameDescription
Unplanned resource utilization (composite)30 daysA composite binary outcome comprising unplanned readmission, return to the operating room, or prolonged (≥ 30 day) length of stay.

Secondary

MeasureTime frameDescription
Composite organ system complications30 daysCardiac complications included cardiac arrest and myocardial infarction. The only neurologic complication that was captured was stroke/cerebrovascular accident. Respiratory complications included reintubation, prolonged ventilatory wean, and pneumonia. Hematologic/infectious complications included superficial surgical site infection (SSI), deep incisional SSI, organ space SSI, wound dehiscence, bleeding, sepsis, septic shock, deep venous thrombosis, and pulmonary embolism. Renal complications included progressive renal insufficiency and acute kidney injury.
Mortality30 daysMortality

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026