Why the study?
Is transatrial pericardial access safe and free from significant bleeding in the presence of aspirin therapy or pulmonary artery hypertension?
Is transatrial pericardial access safe and free from significant bleeding in the presence of aspirin therapy or pulmonary artery hypertension?
Transatrial pericardial access does not cause significant bleeding in preclinical models despite aspirin use or pulmonary artery hypertension, supporting its safety for local cardiac drug delivery.
Transatrial pericardial access shows low bleeding risk in animals despite aspirin or PAH; leaves open human safety confirmation before clinical use.
The reliability, rapidity, and safety of nonsurgical, transatrial pericardial access for local cardiac therapy have been demonstrated in healthy animals. Since many patients take aspirin or have increased right-sided pressures, we evaluated the procedure's safety under these conditions. Transatrial pericardial access was performed in anesthetized pigs following aspirin administration (162 mg p.o., n = 6) or during experimental pulmonary artery hypertension (n = 4 different animals) and required only 3 minutes following guide catheter positioning. Platelet aggregability testing with arachidonic acid confirmed aspirin effectiveness. Mean pericardial fluid hematocrit was 0.1 +/- 0.1% after 2 days of aspirin therapy and 1.9 +/- 1.1% at sacrifice 24 hours later (NS). Mean pericardial fluid hematocrit was 1.0 +/- 0.5% after 45 minutes of pulmonary artery hypertension and 4.3 +/- 0.8% at sacrifice 30 minutes later (NS). Histologic analysis in both groups revealed a small thrombus and localized inflammation at the site of puncture. Neither aspirin use nor pulmonary artery hypertension causes significant bleeding into the pericardial space following transatrial access and thus does not preclude this route for local cardiac drug delivery.
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Pulerwitz et al. (2001) studied this question.
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