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Pleural Effusions After Cardiac Surgery

Charité University Medicine Berlin logo

Charité University Medicine Berlin

Status

Completed

Conditions

Pleura; Effusion

Study type

Observational

Funder types

Other

Identifiers

NCT03409055
PONTOS-Effusions

Details and patient eligibility

About

Pleural effusions occur commonly in patients recovering from cardiac surgery, however, the impact on outcomes is not well characterized. The purpose of this study is to characterize the outcomes of cardiac surgery patients with pleural effusions.

All patients undergoing cardiac surgery between 2006 and 2019 were included in this observational, cross-sectional analysis using propensity matching.

Full description

Pleural effusions are common in patients recovering from cardiac surgery. Symptomatic patients with pleural effusions complain of shortness of breath, cough, chest pain and are more hypoxic and tachypneic. Clinically significant effusions can slow recovery in the hospital and beyond, and are a critical source of hospital readmissions after discharge. It is not well characterized how this impacts hospital outcomes. Further it is unknown if the effusions themselves are associated with impaired outcomes, or if pleural effusions simply arise in more complicated, older patients, thus suggesting the impaired outcomes are the result of coexisting morbidities. To better understand the impact of this complication and to address the question mentioned before, this study was carried out to determine the clinical and economic outcomes of pleural effusions in propensity-matched patients during early recovery from cardiac surgery. To compare patient groups with and without pleural effusion, the following baseline characteristics were used: e.g. age, sex, body-mass-index, priority of surgery, type of surgery, duration of surgery, APACHE II Score of patients on admission in the ICU.

Enrollment

11,198 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • In-patients of the Charité Universitätsmedizin Berlin
  • at least 18 years old
  • female or male sex
  • cardiosurgical intervention (OPS 5.35 and 5.36) between 01/06 and 12/19
  • post-operative monitoring in the intensive care unit

Exclusion criteria

  • previous cardiosurgical interventions during the same hospital stay
  • incomplete documentation.

Trial design

11,198 participants in 3 patient groups

Group 0
Description:
patients without pleural effusion
Group 1
Description:
patients with pleural effusion
Group 2
Description:
patients with pleural Effusion and need of drainage

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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