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10.1097/PEC.0000000000000108 http://scihub22266oqcxt.onion/10.1097/PEC.0000000000000108 24694881!ä!24694881 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Pediatr+Emerg+Care 2014 ; 30 (4): 257-61 Nephropedia Template TP {{tp|p=24694881|t=2014. Acquired long QT syndrome: a focus for the general pediatrician |pdf=|usr=}}{{24694881}} gab.com Text Acquired long QT syndrome: a focus for the general pediatrician JO: Pediatr Emerg Care http://www.kidney.de/pget.php?&tw=1&pmid=24694881 #FOAvip Acquired long QT syndrome (LQTS) is a disorder of cardiac repolarization most often due to specific drugs, hypokalemia, or hypomagnesemia that may precipitate torsade de pointes and cause sudden cardiac death. Common presentations of the LQTS are palpitations, presyncope, syncope, cardiac arrest, and seizures. An abnormal 12-lead electrocardiogram obtained while the patient is at rest is the key to diagnosis. The occurrence of drug-induced LQTS is unpredictable in any given individual, but a common observation is that most patients have at least 1 identifiable risk factor in addition to drug exposure. The cornerstone of the management of acquired LQTS includes the identification and discontinuation of any precipitating drug and the correction of metabolic abnormalities, such as hypokalemia or hypomagnesemia. Most of the episodes of torsade de pointes are short-lived and terminate spontaneously. We propose a management protocol that could be useful for the daily practice in the emergency pediatric department to reduce the risk of acquired QT prolongation. Twit Text FOAVip Acquired long QT syndrome: a focus for the general pediatrician ????Pediatr Emerg Care http://www.kidney.de/pget.php?&tw=1&pmid=24694881 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24694881 #FOAvip English Wikipedia <ref>{{Cite pmid|24694881}}</ref> Acquired long QT syndrome: a focus for the general pediatrician #MMPMID24694881 Marzuillo P; Benettoni A; Germani C; Ferrara G; D'Agata B; Barbi E Pediatr Emerg Care 2014[Apr]; 30 (4): 257-61 PMID24694881show ga Acquired long QT syndrome (LQTS) is a disorder of cardiac repolarization most often due to specific drugs, hypokalemia, or hypomagnesemia that may precipitate torsade de pointes and cause sudden cardiac death. Common presentations of the LQTS are palpitations, presyncope, syncope, cardiac arrest, and seizures. An abnormal 12-lead electrocardiogram obtained while the patient is at rest is the key to diagnosis. The occurrence of drug-induced LQTS is unpredictable in any given individual, but a common observation is that most patients have at least 1 identifiable risk factor in addition to drug exposure. The cornerstone of the management of acquired LQTS includes the identification and discontinuation of any precipitating drug and the correction of metabolic abnormalities, such as hypokalemia or hypomagnesemia. Most of the episodes of torsade de pointes are short-lived and terminate spontaneously. We propose a management protocol that could be useful for the daily practice in the emergency pediatric department to reduce the risk of acquired QT prolongation. |Adolescent[MESH] |Death, Sudden, Cardiac/etiology[MESH] |Electrocardiography[MESH] |Female[MESH] |General Practitioners[MESH] |Humans[MESH] |Long QT Syndrome/*diagnosis/drug therapy/etiology[MESH] |Ondansetron/adverse effects/therapeutic use[MESH] |Risk Factors[MESH]Acquired long QT syndrome: a focus for the general pediatrician (epmc).pdf DeepDyve Pubget Overpricing