Ruling Out Pulmonary Embolism During Pregnancy:a Multicenter Outcome Study
2 other identifiers
observational
402
2 countries
9
Brief Summary
Venous thromboembolism (VTE) remains a major cause of maternal morbidity and mortality in developed countries. Objective diagnosis of pulmonary embolism (PE) and/or deep vein thrombosis (DVT) in pregnancy is crucial. Failure to identify PE or/or DVT will place the mother's life at risk, and unnecessary treatment will not only expose her to anticoagulants but will also label her as having had VTE. Thus, this diagnosis has serious implications for the management of her present pregnancy, and for other aspects of her life ranging from contraception to thromboprophylaxis in future pregnancies and hormone replacement therapy in later life. It is therefore critical that all women with symptoms or signs that suggest venous thromboembolism have appropriate investigation and diagnosis based on objective diagnostic tests. The current diagnostic approach in suspected PE is based on sequential diagnostic tests: 1) assessment of clinical probability, 2) fibrin D-dimer measurement, 3) compression ultrasonography of lower limb veins and 4) multi-slice computed tomography (MSCT). However, physicians are reluctant to perform MSCT in pregnant women because of potential adverse effect of radiation exposure to the fetus. For this reason, ventilation/perfusion or perfusion-only lung scan has been the cornerstone of PE diagnosis in pregnant women. Indeed, perfusion lung scan was assumed to be associated with less radiation than computed tomography (CT). However, this technique is now widely abandoned in the usual diagnostic strategy of PE for the following reasons: it is not widely available; its interpretation may be difficult and the test may be inconclusive in the presence of other chest abnormalities. Moreover, recent data convincingly show that the radiation exposure associated with single-slice or multi-slice CT exposes the fetus to less radiation than perfusion lung scan. However, the use of CT has never been adequately validated in pregnant women with clinically suspected PE. The investigators, therefore, plan to set up a prospective management study in which pregnant women with suspected PE will undergo a sequential diagnostic strategy based on 1) assessment of clinical probability 2) D-dimer measurement 3) compression ultrasonography, and 4) MSCT. Nowadays, the overestimated fear of radiation exposure for the fetus leads to an irrational attitude and inadequate investigations in pregnant women with suspected PE, even though both European \[3, 4\] and North-American guidelines \[5\] suggest that only objective testing may accurately rule out the disease. The proposed study should lead to an increased awareness of the risks and benefits of appropriate imaging in pregnant women suspected of PE and should result in a more rational management of this under-studied patient group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2008
Longer than P75 for all trials
9 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2008
CompletedFirst Submitted
Initial submission to the registry
October 10, 2008
CompletedFirst Posted
Study publicly available on registry
October 13, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2017
CompletedMay 9, 2018
May 1, 2018
8.9 years
October 10, 2008
May 3, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Proportion of patients with a symptomatic thromboembolic event in the three month follow-up among those in whom PE was ruled out by the diagnostic strategy and who were left untreated by anticoagulants.
3 months
Secondary Outcomes (3)
Efficacy of non invasive testing
3 months
Proportion of patients with a negative D-dimer result
3 months
Proportion of patients with a lower limb venous ultrasound showing a proximal DVT
3 months
Study Arms (1)
Ct scan
Pregnant patients with suspected PE will undergo a strategy based on clinical probability assessment, D-dimer measurement, lower limb compression ultrasonography and multi-slice computed tomography.
Interventions
Eligibility Criteria
Pregnant women with suspected PE.
You may not qualify if:
- Age less than 18 years
- Absence of informed consent
- Patients allergic to contrast medium
- Impaired renal function (creatine clearance less than 30 ml/min as estimated by the Cockroft formula)
- Geographic inaccessibility for follow-up
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital, Genevalead
- Swiss National Science Foundationcollaborator
- University Hospital, Brestcollaborator
Study Sites (9)
Pierre-Marie ROY
Angers, 49933, France
Grégoire LE GAL
Brest, 29609, France
Florence PARENT
Clamart, 92141, France
Isabelle QUERE
Montpellier, 34295, France
Jean-Christophe GRIS
Nîmes, 30029, France
Guy MEYER
Paris, 75015, France
Caroline BOHEC
Pau, 64000, France
Antoine ELIAS
Toulon, 83056, France
Marc Righini
Geneva, 1205, Switzerland
Biospecimen
Nt-pro BNP measurement
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof
Study Record Dates
First Submitted
October 10, 2008
First Posted
October 13, 2008
Study Start
September 1, 2008
Primary Completion
August 1, 2017
Study Completion
August 1, 2017
Last Updated
May 9, 2018
Record last verified: 2018-05