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Background: Acute pericardial tamponade (APT) is one of the most serious complications of catheter ablation for atrial fibrillation (AF-CA). Direct autotransfusion (DAT) is a method of reinjecting pericardial blood directly into patients through vein access without a cell-salvage system. Data regarding DAT for APT are rare and provide limited information. Our present study aims to further investigate the safety and feasibility of DAT in the management of APT during the AF-CA procedure.
Methods And Results: We retrospectively reviewed 73 cases of APT in the perioperative period of AF-CA from January 2014 to October 2021 at our institution, among whom 46 were treated with DAT. All included patients successfully received emergency pericardiocentesis through subxiphoid access guided by X-ray. Larger volumes of aspirated pericardial blood (658.4 ± 545.2 vs. 521.2 ± 464.9 ml), higher rates of bridging anticoagulation (67.4 vs. 37.0%), and surgical repair (6 vs. 0) were observed in patients with DAT than without. Moreover, patients with DAT were less likely to complete AF-CA procedures (32/46 vs. 25/27) and had a lower incidence of APT first presented in the ward (delayed presentation) (8/46 vs. 9/27). There was no difference in major adverse events (death/disseminated intravascular coagulation/multiple organ dysfunction syndrome and clinical thrombosis) (0/0/1/0 vs. 1/0/0/0), other potential DAT-related complications (fever/infection and deep venous thrombosis) (8/5/2 vs. 5/3/1), and length of hospital stay (11.4 ± 11.6 vs. 8.3 ± 4.7 d) between two groups.
Conclusion: DAT could be a feasible and safe method to deal with APT during AF-CA procedure.
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http://dx.doi.org/10.3389/fcvm.2022.984251 | DOI Listing |
Perfusion
September 2025
Department of Critical Care, King Fahad Medical City, Riyadh, Saudi Arabia.
Extracorporeal membrane oxygenation (ECMO) supports patients with severe refractory cardiac or respiratory failure but managing residual circuit blood after weaning lacks consensus. After decannulation, the oxygenator and circuit retain approximately 500-700 mL of blood, depending on tubing length, cannula size, and circuit configuration. Clinicians usually choose among direct reinfusion, cell-salvage processing, or disposal.
View Article and Find Full Text PDFStem Cell Res Ther
August 2025
Sorbonne Université, INSERM, Institut de Myologie, GH Pitié-Salpêtrière, Centre de Recherche en Myologie, Paris, F-75013, France.
Background: Mesenchymal Stromal Cells (MSC) possess innate immunomodulatory properties, which can be significantly enhanced through co-culture with peripheral blood mononuclear cells (PBMC), making them attractive tools for the treatment of autoimmune and inflammatory diseases.
Methods: Leveraging a multi-omics approach encompassing RNA sequencing, flow and mass cytometry, secretome analysis, completed by functional evaluations, we investigated the mechanisms underpinning PBMC conditioning of MSC in vitro and their benefits in an animal model of Myasthenia gravis. MSC derived from human adipose tissue were left untreated in resting state (rMSC), conditioned by PBMC (cMSC), or activated by the pro-inflammatory molecule interferon (IFN)-γ (γMSC), then compared for their gene expression profiles, phenotypes and functional capacities.
Clin Chem
September 2025
Biotechnology Unit, Department of Life Technologies, University of Turku, Turku, Finland.
Background: High-sensitivity cardiac troponin (hs-cTn) assays are prone to negative and positive interferences caused by endogenous cardiac troponin-specific autoantibodies (cTnAAbs). Large macrotroponin complexes formed of cardiac troponin (cTn) and cTnAAbs may result in falsely elevated hs-cTn results. This is potentially due to reduced clearance of macrotroponin, but direct evidence is still lacking.
View Article and Find Full Text PDFBMJ Case Rep
June 2025
Hematology, Unidade Local de Saúde de Coimbra, Coimbra, Portugal.
This report presents a case of mediastinal grey zone lymphoma (GZL) in a young man, a rare subtype of B-cell lymphoma, unclassifiable, with intermediate features between diffuse large B-cell lymphoma and classic Hodgkin lymphoma (CHL). Being refractory to first-line treatment, a second biopsy revealed involvement by CHL, nodular sclerosis variant, requiring CHL-directed second-line therapy and autologous stem cell haematopoietic transplantation. This case highlights the diagnostic intricacies of GZL and the challenges in choosing optimal therapies, particularly in refractory/relapsing cases.
View Article and Find Full Text PDFBlood Adv
August 2025
Division of Hematology, Oncology, and Stem Cell Transplantation, Department of Pediatrics, Stanford University, Palo Alto, CA.
Two autologous hematopoietic stem cell (HSC)-based gene therapies (GTs) are now commercially available for severe sickle cell disease and transfusion-dependent β-thalassemia. However, the safety and efficacy of a subsequent autologous HSC-based GT after graft failure with a previous allogeneic hematopoietic cell transplant (HCT) remains unclear. Some individuals who have experienced a failed first attempt at a potentially curative therapy might seek a second opportunity for cure via GT.
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