Skip to main content
OpenTrials
Completed

NCT Number: NCT02682368

Multicentric Point of Care UltraSound by Surgeons Trial

Acute gallbladder pathology and acute diverticulitis are common conditions met in emergency departments and comprise the bulk of admissions throughout general surgical calls. Both entities need imagistic description to tailor further management, which may be not readily available at the moment of patient's presentation. These delays may lose the window of opportunity for timed, quality decision making and may induce increased length of stay and subsequent increased costs.

Ultrasound scanning has become very popular over the last half century and the equipment has become more compact, of a higher quality and less expensive, which has facilitated the growth of point-of-care ultrasonography - POCUS - that is, ultrasound performed and interpreted by the clinician at the bedside. The concept of an 'ultrasound stethoscope' is rapidly moving from theory to reality.

There are a number of studies and case reports that are highlighting the advantages of POCUS, but still common grounds need to be sought after. Some countries, like USA and Germany, incorporate basic ultrasound in their resident's curriculum among different specialties.

In the author's knowledge and based on the literature, there are a few-second-to-none studies regarding POCUS involving strictly the surgeons. The hypothesis of this study is that, surgeon performed ultrasound can be as accurate as the radiologists' findings for basic diagnostics in the aforementioned pathology, leading to real time decision making in the benefit of the patient.

The closing remark is that by learning and doing these procedures the surgeon performing POCUS doesn't undermine his/her radiologist colleague's authority and skill. The big picture is that some basic tasks are transferrable and if used in an appropriate and methodical manner the final common goal - the benefit of the patient - is readily achieved.

Completed

Looking for future studies?

Notify Me

Key information

About this study

The study was accepted as a Master of Surgery Thesis by Research (MCh) at the Royal College of Surgeons in Ireland (RCSI)

There will be two parallel studies done at the same time:

  • POCUSS-1 for acute biliary disease
  • POCUSS-2 for suspected diverticulitis

STUDY DESIGN

  • Patients with suspected acute biliary disease or acute diverticulitis will undergo POCUS performed by the surgeons enrolled in the study.

These patients are recruited from either

  • emergency department
  • outpatients clinic
  • ward consults
  • Patients will have the procedure explained to them and then will receive a leaflet with the same information will be handed over. Consent will be obtained (verbal and written) from the patients that wish to be enrolled in the study.
  • POCUS is performed and data recorded on REDCap®.

4a. The same patients will have a departmental imagistic investigation (ultrasound, CT) reported by qualified radiologists.

4b. In the event of emergency surgery without prior departmental imaging, POCUS will be compared to the intra-operative findings.

  • Data will be collected and stored anonymously and processed with REDCap, Microsoft Excel, IMB SPSS, R-studio

DISCLAIMER:

Specific for this study, patient data will be anonymous and in line with General Data Protection Regulation (GDPR) (EU) 2016/679 law. Data protection is designed by default. There will be NO patients' personal name, surname, home address or date of birth needed or uploaded. Each patient will be represented by an unique identification number provided by the hospital. Only gender and age will be recorded as these will be necessary for the final data analysis and results. Once the study has finished, the data will be erased.

The same rules will be applied in hospitals from other countries that will get involved in the study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

POCUS-1 Inclusion Criteria - adapted after Tokyo Guidelines 2018

  • RUQ mass/pain/tenderness
  • Murphy's Sign
  • Fever
  • Elevated WBC
  • Elevated CRP
  • Deranged liver function tests
  • Jaundice

POCUS-2 Inclusion Criteria

  • Left iliac fossa tenderness and/or palpable mass
  • Fever
  • Elevated WBC
  • Elevated CRP
  • Peritonism - Left lower quadrant / hypogastrium
  • Per rectum bleeding/mucus discharge

POCUSS-1 and 2 Exclusion Criteria:

  • Age under 18 (ethical and consent issues)
  • Pregnancy
  • Obesity (BMI ≥ 30)-difficulty in performing USS
  • Previously documented gallstones within the last 2 months for non-critical presentations
  • Previously documented diverticulitis within the last 2 months for non-critical presentations
  • POCUS performed after official report (for training purposes)
  • Previous colonic resection, particularly left sided or sigmoid colon.
  • Previous cholecystectomy

Treatment and study plan

Point of Care Ultrasound by Surgeons (POCUSS)

Diagnostic Test

POCUSS-1. To identify the gallbladder and it's contents, complications and perform measurements, elicit sonographic Murphy.

POCUSS-2: To perform focused left lower quadrant sonography and identify bowel wall thickness, diverticulae, measure the colonic wall thickness, assess pericolic fat and detect possible complications; evaluate sensibility on graded compression.

Other names: Sonos®, BK Ultrasound®

Radiology report

Diagnostic Test

Radiologist report compared to the point of care ultrasound impression.

Other names: NIMIS: The National Integrated Medical Imaging System

Surgery-Intra-operative findings

Procedure

Intra-operative findings compared to the previously performed point of care ultrasound.

Primary outcomes

  1. Sensitivity POCUS

    Time frame: Up to 3 years, after the all the patients are included

    Sensitivity was defined as the number of patients with a positive detection at POCUS of acute biliary disease or acute diverticulitis divided by the number of patients with pathological findings of the gallbladder or bowel as a final diagnosis.

  2. Specificity POCUS

    Time frame: Up to 3 years, after the all the patients are included

    Specificity was defined as the number of patients with a negative POCUS for cholecystitis or diverticulitis, divided by the number of patients without pathological findings.

  3. Positive predictive value

    Time frame: Up to 3 years, after the all the patients are included

    The number of patients with a true-positive detection at POCUS of gallbladder or bowel alteration divided by the total number of patients with a positive detection at POCUS.

  4. Negative predictive value

    Time frame: Up to 3 years, after the all the patients are included

    The number of patients with a true-negative detection at POCUS of gallbladder or bowel alteration divided by the total number of patients with a negative detection at ultrasound.

  5. POCUS and radiology/surgery correlation

    Time frame: Up to 3 years, after the all the patients are included

    Cohen's Kappa for agreement between POCUS and radiology

Secondary outcomes

  1. Radiology turnaround time

    Time frame: Up to 1 week

    Time difference (in hours) between radiologist report and POCUS. For each participant date and time will be recorded in REDCap for both POCUS and radiology report. Simple arithmetic subtraction will be used as an equation cell (datediff). Then mean and median will be calculated to include all patients in the study.

  2. Surgery turnaround time

    Time frame: Between 6 and 48 hours, when emergency surgery would be expected

    Time difference (in hours) between the start of surgery and POCUS. For each participant date and time will be recorded in REDCap for both POCUS and surgical intervention. Simple arithmetic subtraction will be used in a calculation cell (datediff). Then mean and median will be calculated to include all patients in the study.

  3. Likelihood ratio

    Time frame: Up to 3 years

    Likelihood ratio for a positive test result = sensitivity/(1 - specificity)

    Likelihood ratio for a negative test result = (1 - sensitivity)/specificity

Sponsors and collaborators

Lead sponsor

Connolly Hospital Blanchardstown

Other

Collaborators

  • European Society for Trauma and Emergency Surgery
  • Modular UltraSound ESTES Course (MUSEC)
  • Royal College of Surgeons, Ireland

Registry information

Acronym: POCUSS

Important dates

Study start
2015
Primary completion
2019
Study completion
2019
First posted
Feb 15, 2016
Registry last updated
Jul 25, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.