The primary hypothesis is that a novel clinical decision rule for pulmonary embolism (the YEARS strategy) is at least as safe as previous studies, yet with an increased proportion of patients safely not referred for CTPA, thus fewer false-positive D…
ID
Bron
Verkorte titel
Aandoening
Pulmonary embolism, clinical decision rule, YEARS strategy, primary care /
Longembolie, beslisregel, YEARS strategie, eerstelijnszorg
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary outcomes of this study will be both the safety and efficiency of the YEARS-strategy in primary care.
Achtergrond van het onderzoek
Rationale: Clinical decision rules and D-dimer testing are available for general practitioners to distinguish pulmonary embolism (PE) from common alternative cardiopulmonary diagnoses in patients with a suspicion of PE. However, D-dimer testing is often falsely elevated, leading to unneeded, costly and potential harmful referrals for CT pulmonary angiography (CTPA). To alleviate this problem, a risk-tailored diagnostic approach was recently tested and validated with good results in secondary care: the YEARS-strategy. In secondary care, this algorithm leads to an absolute reduction of 14% of CTPAs with a completely similar safety (only 0.4% missed PE cases), as compared to a fixed D-dimer threshold of 500 mcg/L. This strategy however is not yet implemented in primary care, and awaits validation in this healthcare setting.
Objective: Our primary objective is to prospectively implement and validate the YEARS strategy in primary care. Secondary objectives are, (i) to quantify the added diagnostic value of C-reactive protein (CRP) to a clinical assessment and D-dimer testing in order to enhance distinguishing PE from a pneumonia, (ii) to develop a polytomous logistic model for estimating the diagnostic probability of both PE and pneumonia, and (iii) to statistically quantify predictors for assessing PE as most likely diagnosis by GPs.
Study design: prospective diagnostic cohort study.
Study population: this study will include 750 patients with subacute new onset or worsening of existing shortness of breath with or without chest symptoms, which makes them suspected of having PE.
Intervention: participants will be managed by their GP according to the YEARS-strategy. Furthermore, additional blood will be drawn for CRP. There will be a clinical follow-up in primary care for 3 months in all patients to establish the final diagnosis.
Doel van het onderzoek
The primary hypothesis is that a novel clinical decision rule for pulmonary embolism (the YEARS strategy) is at least as safe as previous studies, yet with an increased proportion of patients safely not referred for CTPA, thus fewer false-positive D-dimer tests
Onderzoeksopzet
There will be a clinical follow-up in primary care for 3 months in all patients to establish the final diagnosis.
Onderzoeksproduct en/of interventie
The intervention is a novel clinical decision rule for patients with a suspected pulmonary embolism: the YEARS-strategy. In this strategy, the physician scores three clinical items: (i) haemoptysis, (ii) clinical signs suggestive of deep venous thrombosis, and (iii) PE considered the most likely diagnosis. If none of these items is present, a D-dimer threshold of 1000 mcg/L is applied, while if one or more items are present, the classical threshold of 500 mcg/L is used. If a suspected patient has a D-dimer below either threshold, PE is safely ruled out. Furthermore, additional blood will be drawn for CRP in order to quantify the added diagnostic value of CRP in the diagnostic management of PE.
Algemeen / deelnemers
R. Maanen, van
Postbus 85500
Utrecht 3508 GA
The Netherlands
+31 088 7569237
r.vanmaanen@umcutrecht.nl
Wetenschappers
R. Maanen, van
Postbus 85500
Utrecht 3508 GA
The Netherlands
+31 088 7569237
r.vanmaanen@umcutrecht.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Clinical suspicion of pulmonary embolism (PE), with complaints such as subacute new onset or worsening of existing shortness of breath or chest symptoms;
- Aged 18 years or older
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Pregnant;
- Already using anticoagulants (i.e. a vitamin K antagonist, low-molecular weight heparine or a direct oral anticoagulant);
- Life expectancy < 1 month
- Haemodynamic instability
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL7232 |
NTR-old | NTR7431 |
CCMO | NL64357.041.18 |
OMON | NL-OMON52757 |