Résumé
We aimed to determine the characteristic adverse events (AEs) of iodinated contrast media (IOCM) and to compare the safety profiles of different IOCM. This study used the database of AEs reports submitted by healthcare professionals from 15 Regional Pharmacovigilance Centers between June 24, 2009 and December 31, 2010 in Korea. All reports of IOCM, including iopromide, iohexol, iopamidol, iomeprol, ioversol, iobitridol and iodixanol, were analyzed. Safety profiles were compared between different IOCM at the system organ level using the proportional reporting ratio (PRR) and 95% confidence interval (95% CI). Among a total of 48,261 reports, 6,524 (13.5%) reports were related to the use of IOCM. Iopromide (45.5%), iohexol (16.9%), iopamidol (14.3%) and iomeprol (10.3%) were identified as frequently reported media. 'Platelet, bleeding & clotting disorders' (PRR, 29.6; 95%CI, 1.9-472.6) and 'urinary system disorders' (PRR, 22.3; 95% CI, 17.1-29.1) were more frequently reported for iodixanol than the other IOCM. In conclusion, the frequency of AEs by organ class was significantly different between individual media. These differences among different IOCM should be considered when selecting a medium among various IOCM and when monitoring patients during and after its use to ensure optimum usage and patient safety.
Sujets)
Adolescent , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Nouveau-né , Mâle , Adulte d'âge moyen , Jeune adulte , Anomalies des plaquettes/induit chimiquement , Produits de contraste/effets indésirables , Bases de données factuelles , Radio-isotopes de l'iode/composition chimique , Tumeurs/imagerie diagnostique , Radiopharmaceutiques/effets indésirables , Maladies urologiques/induit chimiquementRésumé
Se presenta el caso de un adolescente de 14 años de edad que ingresó al hospital por fístula estercorácea como complicación de una apendicectomía. Diecinueve días después de su ingreso, se llevó a cabo la resección de la fístula sin complicaciones transquirúrgicas. Se administró carbenicilina a 400 mg/kg/día; dos horas después de la primera dosis, presentó sangrado masivo que ameritó reintervención encontrándose 500 ml de sangre libre en cavidad. Se demostró disfución plaquetaria. Se suspendió la carbenicilina y se manejó con plasma rico en plaquetas, con lo que se controló el episodio hemorrágico. Se discute la fisipatología y se revisa la literatura al respecto