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Pediatric pulmonary thromboembolism: a 3-year Canadian Pediatric Surveillance Program study
Author(s): ,
Paul Moorehead
Affiliations:
Discipline of Pediatrics, Memorial University, St. John’s, Newfoundland and Labrador, Canada
,
Amy C. Plint
Affiliations:
Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada
,
Anthony K.C. Chan
Affiliations:
Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada
,
Sarah McMullen
Affiliations:
Department of Critical Care, Nova Scotia Health, Halifax, Nova Scotia, Canada
,
Lily Ramsay
Affiliations:
Department of Pediatric Critical Care, IWK Health, Halifax, Nova Scotia, Canada
Kristina Krmpotic
Affiliations:
Department of Critical Care, Dalhousie University, Halifax, Nova Scotia, Canada
Kristina Krmpotic, IWK Health, Box 9700, 5850/5980 University Ave, Halifax, NS, B3K 6R8, Canada.
ISTH Academy. Presenters F. 05/01/24; 422460
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Faculty /  Presenters
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Journal Abstract
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Background

Pediatric pulmonary embolism (PE) is a rare event associated with significant morbidity and mortality. Awareness of clinical presentation and practices unique to children may aid clinicians in prompt identification and treatment.

Objectives

To describe the incidence, risk factors, clinical presentation, diagnostic and therapeutic practices, and short-term outcomes of pediatric PE.

Methods

We conducted a 3-year national surveillance study through the Canadian Pediatric Surveillance Program. Over 2800 pediatric specialists and subspecialists were contacted monthly from 2020 to 2022 and requested to report all new cases of PE in patients up to 18 years of age. Case-specific data were obtained through voluntary completion of a detailed questionnaire.

Results

Fifty-eight cases (78% female, n = 45) were reported (2.4 cases per million children), with rates highest in adolescents 15 to 18 years (6.6 cases per million). Detailed information, available for 31 (53%) cases, documented at least 1 risk factor in 28 (90%) cases; 24 (77%) patients presented with 2 or more symptoms. Computed tomography pulmonary angiography was used for diagnostic confirmation in 25 (81%) cases. Anticoagulation was initiated in 24 (77%) of 31 cases; fewer than 5 patients underwent thrombolysis or surgical interventions. Of 28 patients who received therapeutic interventions, 8 (29%) experienced treatment-related complications. Fewer than 5 mortalities were reported.

Conclusion

Pediatric PE is a rare event, with female adolescents at the highest risk. Although the presentation is often nonspecific, clinicians should maintain a high index of suspicion, particularly in patients with risk factors and when other diagnoses that may explain symptoms have been excluded.

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