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POCUS for Small Bowel Obstruction in the ED: a Retrospective Study

The Impact of Point-of-care Ultrasound on the Diagnosis and Management of Small Bowel Obstruction in the Emergency Department: a Retrospective Observational Single-center Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05864378
Acronym
SBOCUS
Enrollment
230
Registered
2023-05-18
Start date
2023-09-01
Completion date
2024-02-01
Last updated
2023-05-18

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

Conditions

Point of Care Ultrasound, Small Bowel Obstruction

Keywords

POCUS, SBO

Brief summary

This study protocol aims to evaluate the impact of point-of-care ultrasound (POCUS) on the diagnosis and management of small bowel obstruction (SBO) in the emergency department (ED). SBO is a potentially life-threatening condition that requires prompt diagnosis and management. Currently, the diagnosis of SBO is based on clinical evaluation and imaging tests, including plain abdominal radiography and computed tomography (CT) scan. POCUS is a bedside imaging technique that is rapid, non-invasive, repeatable, cost-effective and radiation-free, and can provide valuable information for the diagnosis and management of SBO. The primary objective of this study is to compare the time to diagnosis of SBO between patients who undergo POCUS intestinal loops examination and those who do not undergo POCUS in the ED. The secondary objectives include comparing the hospital length of stay, the rate of surgical intervention, the rate of complications, and the mortality rate between the two groups. This is a monocentric retrospective cohort study that will include all adult patients (\> 18 years old) who presented to the ED with suspected SBO. The study population will be divided into two groups: the POCUS group and the non-POCUS group. The sample size calculation will be based on the assumption of a 30% reduction in the time to diagnosis of SBO in the POCUS group compared to the non-POCUS group, with a power of 80%. The results of this study may provide more robust evidence on the diagnostic accuracy and impact of POCUS for SBO in the ED.

Interventions

None listed

Sponsors

Azienda Ospedaliero-Universitaria di Modena
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Age \> 18 years old * Clinical suspicion of SBO based on history and physical examination * Plain abdominal radiography (AXR) or CT scan performed in the ED

Exclusion criteria

* Pregnancy * Known bowel obstruction * Previous abdominal surgery within 30 days * Refusal or inability to consent

Design outcomes

Primary

MeasureTime frameDescription
Time to diagnosis of SBO by POCUS or CT scanAll patients will be seen by the emergency physician within 6 hours of admission to the emergency department.The primary outcome will be the time to diagnosis of SBO by POCUS or CT scan, defined as the interval between the ED arrival and the confirmation of SBO by either imaging modality, comparing the two groups.

Secondary

MeasureTime frameDescription
The hospital length of stayPatients will be followed up for a maximum of 2 months from admission to the emergency department, until discharge or death.The interval between the ED arrival and the hospital discharge
The rate of surgical interventionPatients will be followed up for a maximum of 2 months from admission to the emergency department, until discharge or death.The proportion of patients who underwent laparotomy or laparoscopy for SBO
The rate of complicationsPatients will be followed up for a maximum of 2 months from admission to the emergency department, until discharge or death.The proportion of patients who developed bowel ischemia, perforation, peritonitis or sepsis during their hospitalization
The mortality ratePatients will be followed up for a maximum of 2 months from admission to the emergency department, until discharge or death.The proportion of patients who died during their hospitalization or within 30 days after their ED arrival

Contacts

Primary ContactCarmine Cristiano Di Gioia
cristianodigioia@icloud.com+39 3493812503

Outcome results

None listed

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