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1.
JACC Cardiovasc Interv ; 13(18): 2112-2120, 2020 09 28.
Article in English | MEDLINE | ID: mdl-32972572

ABSTRACT

OBJECTIVES: This study sought to assess patent fossa ovalis (PFO) anatomy by transesophageal echocardiography (TEE) in patients undergoing percutaneous suture-mediated PFO closure to identify predictors of post-procedural residual atrial right-to-left shunt (RLS). BACKGROUND: Percutaneous suture-mediated PFO closure has been proven to be a safe and effective technique in most PFO patients. METHODS: From June 2016 to October 2019, 247 consecutive patients underwent percutaneous suture-mediated PFO closure at our institution. Of them, 230 (46 ± 13 years of age, 146 women) had complete and technically evaluable pre-procedural TEE. The following parameters in short-axis view were assessed: presence and grade of spontaneous RLS, PFO length and width, presence of atrial septal aneurysm and its maximal bulge, and presence of an embryonic or fetal remnant (Chiari network or Eustachian valve). RESULTS: At the first follow-up transthoracic echocardiography performed between 3 and 6 months from the closure procedure, a residual RLS ≥2 grade was found in 37 (16%) patients. Grade of pre-procedural spontaneous RLS (hazard ratio: 1.99; 95% confidence interval: 1.14 to 3.48; p = 0.016) shunt and PFO width (hazard ratio: 2.52; 95% confidence interval: 1.85 to 3.43; p < 0.001) were both found to be significantly associated with significant residual RLS at multivariable analysis. The presence of atrial septal aneurysm and its maximal bulge and of congenital remnants was not associated with significant residual RLS. CONCLUSIONS: Percutaneous suture-mediated PFO closure is feasible in the majority of septal anatomies; however, PFO >5 mm in width and spontaneous large RLS are less likely to be closed with 1 stitch only.


Subject(s)
Foramen Ovale, Patent , Heart Aneurysm , Adult , Cardiac Catheterization , Echocardiography, Transesophageal , Female , Follow-Up Studies , Humans , Male , Middle Aged , Sutures , Treatment Outcome
2.
J Pediatr Hematol Oncol ; 42(6): e469-e471, 2020 08.
Article in English | MEDLINE | ID: mdl-31094909

ABSTRACT

Invasive aspergillosis in hematologic pediatric patients is an opportunistic infection that is difficult to treat, with a high mortality rate when localized in the central nervous system. We are describing a 3-year-old girl who was affected by acute lymphoblastic leukemia who developed cerebral and pulmonary aspergillosis during induction chemotherapy. The patient failed first-line voriconazole treatment because of being a CYP2C19 ultrarapid metabolizer and received effective isavuconazole therapy with no notable side effects.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Aspergillus/drug effects , Neuroaspergillosis/drug therapy , Nitriles/therapeutic use , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Pulmonary Aspergillosis/drug therapy , Pyridines/therapeutic use , Triazoles/therapeutic use , Antifungal Agents/therapeutic use , Aspergillus/isolation & purification , Child, Preschool , Female , Humans , Neuroaspergillosis/chemically induced , Neuroaspergillosis/pathology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology , Prognosis , Pulmonary Aspergillosis/chemically induced , Pulmonary Aspergillosis/pathology
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