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A Randomized Controlled Trial of Thoracentesis in Acute Heart Failure

  • Signe Glargaard*
  • , Jakob Hartvig Thomsen
  • , Christian Tuxen
  • , Matias Greve Lindholm
  • , Christian Axel Bang
  • , Morten Schou
  • , Kasper Iversen
  • , Rasmus Vedby Rasmussen
  • , Brian Bridal Løgstrup
  • , Søren Vraa
  • , Nis Stride
  • , Ekim Seven
  • , Anders Barasa
  • , Marlene Tofterup
  • , Dan Eik Høfsten
  • , Kasper Rossing
  • , Lars Køber
  • , Finn Gustafsson
  • , Jens Jakob Thune
  • *Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftArtikelForskningpeer review

Abstract

BACKGROUND: TAP-IT (Thoracentesis to Alleviate Cardiac Pleural Effusion-Interventional Trial) investigated the effect of therapeutic thoracentesis in addition to standard medical therapy in patients with acute heart failure and sizeable pleural effusion.

METHODS: This multicenter, unblinded, randomized controlled trial, conducted between August 31, 2021, and March 22, 2024, included patients with acute heart failure, left ventricular ejection fraction ≤45%, and non-negligible pleural effusion. Patients with very large effusions (more than two-thirds of the hemithorax) were excluded. Participants were randomly assigned 1:1 to upfront ultrasound-guided pleural pigtail catheter thoracentesis in addition to standard medical therapy or standard medical therapy alone. The primary outcome was days alive out of the hospital over the following 90 days; key secondary outcomes included length of admission and 90-day all-cause mortality. All outcomes were analyzed according to the intention-to-treat principle.

RESULTS: A total of 135 patients (median age, 81 years [25th; 75th percentile, 75; 83]; 33% female; median left ventricular ejection fraction, 25% [25th; 75th percentile, 20%; 35%]) were randomized to either thoracentesis (n=68) or standard medical therapy (n=67). The thoracentesis group had a median of 84 days (77; 86) alive out of the hospital over the following 90 days compared with 82 days (73; 86) in the control group (P=0.42). The mortality rate was 13% in both groups, with no difference in survival probability (P=0.90). There were no differences in the duration of the index admission (control group median, 5 days [3; 8]; thoracentesis group median, 5 days [3; 7; P=0.69]). Major complications occurred in 1% of thoracenteses performed during the study period.

CONCLUSIONS: For patients with acute heart failure and pleural effusion, a strategy of upfront routine thoracentesis in addition to standard medical therapy did not increase days alive out of the hospital for 90 days, all-cause mortality, or duration of index admission. The current findings lay the groundwork for future research to confirm the results.

REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT05017753.

OriginalsprogEngelsk
Sider (fra-til)1150-1161
Antal sider12
TidsskriftCirculation
Vol/bind151
Udgave nummer16
Tidlig onlinedato1 apr. 2025
DOI
StatusUdgivet - 22 apr. 2025

Finansiering

BevillingsgivereBevillingsgivernummer
Danmarks Frie Forskningsfond1030-00131B
Brødrene Hartmanns FondA36846
Skibsreder Per Henriksen, R og Hustrus Fond
Københavns Universitetshospital

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