Effect of a Pulmonary Embolism Diagnostic Strategy on Clinical Outcomes in Patients Hospitalized for COPD Exacerbation: A Randomized Clinical Trial.

dc.contributor.authorJiménez, David
dc.contributor.authorAgustí, Alvar
dc.contributor.authorTabernero, Eva
dc.contributor.authorJara-Palomares, Luis
dc.contributor.authorHernando, Ascensión
dc.contributor.authorRuiz-Artacho, Pedro
dc.contributor.authorPérez-Peñate, Gregorio
dc.contributor.authorRivas-Guerrero, Agustina
dc.contributor.authorRodríguez-Nieto, María Jesús
dc.contributor.authorBallaz, Aitor
dc.contributor.authorAgüero, Ramón
dc.contributor.authorJiménez, Sonia
dc.contributor.authorCalle-Rubio, Myriam
dc.contributor.authorLópez-Reyes, Raquel
dc.contributor.authorMarcos-Rodríguez, Pedro
dc.contributor.authorBarrios, Deisy
dc.contributor.authorRodríguez, Carmen
dc.contributor.authorMuriel, Alfonso
dc.contributor.authorBertoletti, Laurent
dc.contributor.authorCouturaud, Francis
dc.contributor.authorHuisman, Menno
dc.contributor.authorLobo, José Luis
dc.contributor.authorYusen, Roger D
dc.contributor.authorBikdeli, Behnood
dc.contributor.authorMonreal, Manuel
dc.contributor.authorOtero, Remedios
dc.contributor.authorSLICE Trial Group
dc.date.accessioned2025-01-07T15:41:25Z
dc.date.available2025-01-07T15:41:25Z
dc.date.issued2021
dc.description.abstractActive search for pulmonary embolism (PE) may improve outcomes in patients hospitalized for exacerbations of chronic obstructive pulmonary disease (COPD). To compare usual care plus an active strategy for diagnosing PE with usual care alone in patients hospitalized for COPD exacerbation. Randomized clinical trial conducted across 18 hospitals in Spain. A total of 746 patients were randomized from September 2014 to July 2020 (final follow-up was November 2020). Usual care plus an active strategy for diagnosing PE (D-dimer testing and, if positive, computed tomography pulmonary angiogram) (n = 370) vs usual care (n = 367). The primary outcome was a composite of nonfatal symptomatic venous thromboembolism (VTE), readmission for COPD, or death within 90 days after randomization. There were 4 secondary outcomes, including nonfatal new or recurrent VTE, readmission for COPD, and death from any cause within 90 days. Adverse events were also collected. Among the 746 patients who were randomized, 737 (98.8%) completed the trial (mean age, 70 years; 195 [26%] women). The primary outcome occurred in 110 patients (29.7%) in the intervention group and 107 patients (29.2%) in the control group (absolute risk difference, 0.5% [95% CI, -6.2% to 7.3%]; relative risk, 1.02 [95% CI, 0.82-1.28]; P = .86). Nonfatal new or recurrent VTE was not significantly different in the 2 groups (0.5% vs 2.5%; risk difference, -2.0% [95% CI, -4.3% to 0.1%]). By day 90, a total of 94 patients (25.4%) in the intervention group and 84 (22.9%) in the control group had been readmitted for exacerbation of COPD (risk difference, 2.5% [95% CI, -3.9% to 8.9%]). Death from any cause occurred in 23 patients (6.2%) in the intervention group and 29 (7.9%) in the control group (risk difference, -1.7% [95% CI, -5.7% to 2.3%]). Major bleeding occurred in 3 patients (0.8%) in the intervention group and 3 patients (0.8%) in the control group (risk difference, 0% [95% CI, -1.9% to 1.8%]; P = .99). Among patients hospitalized for an exacerbation of COPD, the addition of an active strategy for the diagnosis of PE to usual care, compared with usual care alone, did not significantly improve a composite health outcome. The study may not have had adequate power to assess individual components of the composite outcome. ClinicalTrials.gov Identifier: NCT02238639.
dc.identifier.doi10.1001/jama.2021.14846
dc.identifier.essn1538-3598
dc.identifier.pmcPMC8493436
dc.identifier.pmid34609451
dc.identifier.unpaywallURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493436
dc.identifier.urihttps://hdl.handle.net/10668/27333
dc.issue.number13
dc.journal.titleJAMA
dc.journal.titleabbreviationJAMA
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Sevilla (IBIS)
dc.organizationSAS - Hospital Universitario Virgen del Rocío
dc.page.number1277-1285
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeRandomized Controlled Trial
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subject.meshAged
dc.subject.meshCause of Death
dc.subject.meshComputed Tomography Angiography
dc.subject.meshConfidence Intervals
dc.subject.meshDisease Progression
dc.subject.meshFemale
dc.subject.meshFibrin Fibrinogen Degradation Products
dc.subject.meshHemorrhage
dc.subject.meshHospitalization
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshPatient Readmission
dc.subject.meshPulmonary Disease, Chronic Obstructive
dc.subject.meshPulmonary Embolism
dc.subject.meshRecurrence
dc.subject.meshSpain
dc.subject.meshTreatment Outcome
dc.subject.meshVenous Thromboembolism
dc.titleEffect of a Pulmonary Embolism Diagnostic Strategy on Clinical Outcomes in Patients Hospitalized for COPD Exacerbation: A Randomized Clinical Trial.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number326

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