Chest Journal: Published on November, 2022
TAKE-HOME MESSAGE
In this single-center, open-label, randomized trial,
hemodynamically stable patients presenting to an emergency department with
hemoptysis were assigned to receive different formulations of tranexamic acid
(TA).
The 55 patients randomized to receive nebulized TA were found
to have a significantly higher rate of cessation of bleeding at 30 minutes and
significantly less hemoptysis up to 24 hours after presentation compared with
the 55 patients receiving intravenous TA.
Compared with the intravenous TA group, fewer patients in the
nebulized TA group required bronchial artery embolization.
This study offers the first prospective comparison of TA formulations in patients with hemoptysis. Nebulized TA may be more efficacious than IV TA in reducing the amount of hemoptysis and need for ED interventional procedures.
Background: Tranexamic acid (TA) is used to control bleeding in patients
with hemoptysis. However, the effectiveness of the different routes of TA
administration has not been studied.
Research question: Does the nebulized route of TA administration reduce
the amount of hemoptysis compared with the IV route in patients presenting to
the ED with hemoptysis?
Study design and methods: This was a pragmatic, open-label,
cluster randomized, parallel, single-center, pilot trial of nebulized TA (500
mg tid) vs IV TA (500 mg tid) in adult patients presenting to the ED with active
hemoptysis. The primary outcome was cessation of bleeding at 30 min. Secondary
outcomes included amount of hemoptysis at 6, 12, and 24 h; interventional
procedures; and side effects of TA. Patients who were hemodynamically unstable
or requiring immediate interventional procedure or mechanical ventilation were
excluded from the study.
Results: Of the 55 patients in each arm, hemoptysis cessation at 30
min following TA administration was significantly higher in the nebulization
arm (n = 40) compared with the IV arm (n = 28). Also, hemoptysis amount was
reduced significantly in the nebulization arm at all time periods of
observation. Fewer patients in the nebulization arm required bronchial artery
embolization and thereby had higher discharge rates from the ED. Two patients
in the nebulization arm had asymptomatic bronchoconstriction that resolved after
short-acting beta-agonist nebulization. No patient discharged from the ED
underwent any interventional procedure or revisited the ED with rebleed during
the 72 h follow-up period.
Interpretation: Nebulized TA may be more efficacious than IV TA in reducing
the amount of hemoptysis and need for ED interventional procedures. Future
larger studies are needed to further explore the potential of nebulized TA
compared with IV TA in patients with mild hemoptysis.
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