The return of a disappearing entity: Dressler's syndrome after transvenous pacemaker implantation

António Tralhão1, Diogo Cavaco, Marisa Trabulo

  • 1Department of Cardiology, Hospital de Santa Cruz, Centro Hospitalar de Lisboa Ocidental, Carnaxide, Portugal.

BMJ Case Reports
|March 22, 2014
PubMed

Insights

A rare Dressler-like syndrome developed in a patient after biventricular pacemaker implantation complicated by coronary sinus vein perforation. Steroid and colchicine therapy led to remission of pericardial and pleural effusions.

Area of Science:

  • Cardiology
  • Internal Medicine
  • Medical Complications

Background:

  • A 76-year-old woman with idiopathic dilated cardiomyopathy and left bundle branch block underwent biventricular pacemaker implantation.
  • The procedure was complicated by coronary sinus tributary vein perforation, leading to pericardial effusion without tamponade.

Observation:

  • Three months post-procedure, the patient presented with fever, pleuritic chest pain, and worsening functional class.
  • Clinical examination revealed new pericardial and pleural effusions.
  • Blood and pleural fluid cultures were sterile, and the patient did not respond to antibiotic therapy.

Findings:

  • A Dressler-like syndrome was hypothesized as the cause of the effusions.
  • The patient showed clinical improvement following a short course of steroid therapy.
  • Discharge on colchicine resulted in complete remission of pleural effusion within two months, as confirmed by chest X-ray.

Implications:

  • This case highlights a rare post-procedural complication mimicking Dressler's syndrome.
  • It underscores the importance of considering inflammatory post-pericardiotomy syndromes in patients with unexplained effusions after cardiac procedures.
  • Successful management with steroids and colchicine suggests these agents may be effective in similar cases.

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