SPES: Accuracy of Multi-organ Ultrasound for the Diagnosis of Pulmonary Embolism

Sponsor
Azienda Ospedaliero-Universitaria Careggi (Other)
Overall Status
Completed
CT.gov ID
NCT01635257
Collaborator
(none)
357
3
6
119
19.8

Study Details

Study Description

Brief Summary

Patients with suspected Pulmonary Embolism (PE) and a high clinical probability or a high D-dimer level should undergo a second level diagnostic test such as Multidetector Computed Tomography Angiography (MCTPA). Unfortunately MCTPA involves radiation exposure, is expensive, is not feasible in unstable patients and has contraindications. UltraSound (US) is safe and rapidly available even in unstable patients. Many authors evaluated the diagnostic role of Compression Ultrasound Scan (CUS) for detecting limbs Deep Vein Thrombosis (DVT), TransThoracic Echocardiography (TTE) for detecting Right Ventricular Dysfunction (RVD) or Thoracic UltraSound (TUS) for detecting subpleural infarcts in patients with suspected PE. No previous studies have investigated the diagnostic accuracy of CUS, TTE and TUS combined (multiorgan US) for the diagnosis of PE. This study evaluates the diagnostic accuracy of multiorgan US.

Methods. Consecutive patients that underwent MCTPA in the Emergency Department for clinical suspicion of PE and with a simplified Well's score>4 (PE likely) or with a D-dimer value ≥500ng/ml were enrolled in the study. MCTPA was considered the gold standard for PE diagnosis. A multiorgan US was performed by an emergency physician sonographer before MCTPA. PE was considered echographically present if CUS was positive for DVT or TTE was positive for RVD or at least one pulmonary subpleural infarct was detected with TUS. The accuracy of the single and multiorgan US was calculated.

Condition or Disease Intervention/Treatment Phase
  • Other: Ultrasound scan

Study Design

Study Type:
Observational
Actual Enrollment :
357 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Accuracy of Multi-organ Ultrasound (Venous, Cardiac and Thoracic) for the Diagnosis of Pulmonary Embolism: Suspected Pulmonary Embolism Sonographic Assessment (SPES) Multicenter Prospective Study
Study Start Date :
Jun 1, 2012
Actual Primary Completion Date :
Dec 1, 2012
Actual Study Completion Date :
Dec 1, 2012

Arms and Interventions

Arm Intervention/Treatment
suspected pulmonary embolism patients

patients with clinical suspicion of PE and with a simplified Well's score>4 (PE likely) or with a D-dimer value ≥500ng/ml presenting to the emergency departments of Careggi University Hospital (Firenze), of San Luigi Gonzaga University Hospital (Torino) of Ospedale Pierantoni-Morgagni (Forlì)

Other: Ultrasound scan
A multiorgan ultrasound was performed by an emergency physician sonographer before MCTPA. Pulmonary embolism was considered echographically present if compression ultrasound was positive for deep vein thrombosis or transthoracic-echocardiography was positive for right ventricular dysfunction or at least one pulmonary subpleural infarct was detected with thoracic ultrasound.

Outcome Measures

Primary Outcome Measures

  1. Accuracy of ultrasound for the diagnosis of pulmonary embolism [The goldstandard for PE diagnosis is the MCTPA performed within 24 hours from ED presentation. The recruiting period is 5 months. There is not a follow-up for the included patients.]

    Sensitivity, specificity, negative and positive predictive value, negative and positive likelihood ratio of limb, cardiac, thoracic and multi-organ ultrasound for the diagnosis of pulmonary embolism in the emergency department considering as gold standard the Multidetector Computed Tomography Angiography (MCTPA)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients with clinical suspected pulmonary embolism

  • Simplified Well's score>4 (PE likely) or D-dimer value ≥500ng/ml

  • Patients that undergo MCTPA in the Emergency Department for suspected pulmonary embolism

Exclusion Criteria:
  • Refused consent

  • Less than 18 years old

  • Not possible to perform ultrasound scan within 3 hours before MCTPA

Contacts and Locations

Locations

Site City State Country Postal Code
1 Emergency Department Azienda Ospedaliera Universitaria Careggi Firenze Tuscany Italy 50134
2 Department of Emergency Medicine, Pierantoni Morgagni Hospital Forlì Italy 47121
3 Department of Emergency Medicine, San Luigi Gonzaga University Hospital Torino Italy 10043

Sponsors and Collaborators

  • Azienda Ospedaliero-Universitaria Careggi

Investigators

  • Study Chair: Stefano Grifoni, MD, Director of Pronto Soccorso generale of AUO Careggi

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Peiman Nazerian, Medical Doctor Emergency Medicine, Azienda Ospedaliero-Universitaria Careggi
ClinicalTrials.gov Identifier:
NCT01635257
Other Study ID Numbers:
  • 080974
First Posted:
Jul 9, 2012
Last Update Posted:
Mar 18, 2013
Last Verified:
Mar 1, 2013
Keywords provided by Peiman Nazerian, Medical Doctor Emergency Medicine, Azienda Ospedaliero-Universitaria Careggi
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 18, 2013