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Bleeding Risk With Combination Intrapleural Fibrinolytic and Enzyme Therapy in Pleural Infection: An International, Multicenter, Retrospective Cohort Study

Authors :
Jason, Akulian
Eihab O, Bedawi
Hawazin, Abbas
Christine, Argento
David T, Arnold
Akshu, Balwan
Hitesh, Batra
Juan Pablo, Uribe Becerra
Adam, Belanger
Kristin, Berger
Allen Cole, Burks
Jiwoon, Chang
Ara A, Chrissian
David M, DiBardino
Xavier Fonseca, Fuentes
Yaron B, Gesthalter
Christopher R, Gilbert
Kristen, Glisinski
Mark, Godfrey
Jed A, Gorden
Horiana, Grosu
Mridul, Gupta
Fayez, Kheir
Kevin C, Ma
Adnan, Majid
Fabien, Maldonado
Nick A, Maskell
Hiren, Mehta
Joshua, Mercer
John, Mullon
Darlene, Nelson
Elaine, Nguyen
Edward M, Pickering
Jonathan, Puchalski
Chakravarthy, Reddy
Alberto E, Revelo
Lance, Roller
Ashutosh, Sachdeva
Trinidad, Sanchez
Priya, Sathyanarayan
Roy, Semaan
Michal, Senitko
Samira, Shojaee
Ryan, Story
Jeffrey, Thiboutot
Momen, Wahidi
Candice L, Wilshire
Diana, Yu
Aline, Zouk
Najib M, Rahman
Lonny, Yarmus
Source :
Chest. 162(6)
Publication Year :
2022

Abstract

Combination intrapleural fibrinolytic and enzyme therapy (IET) has been established as a therapeutic option in pleural infection. Despite demonstrated efficacy, studies specifically designed and adequately powered to address complications are sparse. The safety profile, the effects of concurrent therapeutic anticoagulation, and the nature and extent of nonbleeding complications remain poorly defined.What is the bleeding complication risk associated with IET use in pleural infection?This was a multicenter, retrospective observational study conducted in 24 centers across the United States and the United Kingdom. Protocolized data collection for 1,851 patients treated with at least one dose of combination IET for pleural infection between January 2012 and May 2019 was undertaken. The primary outcome was the overall incidence of pleural bleeding defined using pre hoc criteria.Overall, pleural bleeding occurred in 76 of 1,833 patients (4.1%; 95% CI, 3.0%-5.0%). Using a half-dose regimen (tissue plasminogen activator, 5 mg) did not change this risk significantly (6/172 [3.5%]; P = .68). Therapeutic anticoagulation alongside IET was associated with increased bleeding rates (19/197 [9.6%]) compared with temporarily withholding anticoagulation before administration of IET (3/118 [2.6%]; P = .017). As well as systemic anticoagulation, increasing RAPID score, elevated serum urea, and platelets of 100 × 10IET use in pleural infection confers a low overall bleeding risk. Increased rates of pleural bleeding are associated with concurrent use of anticoagulation but can be mitigated by withholding anticoagulation before IET. Concomitant administration of IET and therapeutic anticoagulation should be avoided. Parameters related to higher IET-related bleeding have been identified that may lead to altered risk thresholds for treatment.

Details

ISSN :
19313543
Volume :
162
Issue :
6
Database :
OpenAIRE
Journal :
Chest
Accession number :
edsair.pmid..........a6d927541d957ce4300a22a971b7f345