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

NCT ID: NCT05917691

Last Updated: 2023-06-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

65627 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-01-01

Study Completion Date

2019-12-31

Brief Summary

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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

Detailed Description

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Conditions

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Dependence Perioperative/Postoperative Complications Frailty

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Dependent functional status

223 patients; "dependent" for those documented as "partially dependent" or "totally dependent."

Bariatric surgery

Intervention Type PROCEDURE

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

General anesthetic

Intervention Type DRUG

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).

Indeterminate

Intervention Type DEVICE

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

Independent functional status

65404 patients; "independent" for those documented as such.

Bariatric surgery

Intervention Type PROCEDURE

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

General anesthetic

Intervention Type DRUG

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).

Indeterminate

Intervention Type DEVICE

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

Interventions

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Bariatric surgery

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

Intervention Type PROCEDURE

General 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).

Intervention Type DRUG

Indeterminate

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

Intervention Type DEVICE

Eligibility Criteria

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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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Virginia

OTHER

Sponsor Role lead

Responsible Party

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Zhiyi Zuo, MD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Study Documents

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Document Type: Individual Participant Data Set

View Document

Other Identifiers

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HSRZOKZZ2

Identifier Type: -

Identifier Source: org_study_id

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