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http://scihub22266oqcxt.onion/ 8854446!ä!8854446 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Zhonghua+Yi+Xue+Za+Zhi+(Taipei) 1995 ; 56 (3): 215-9 Nephropedia Template TP {{tp|p=8854446|t=1995. Acquired long QT syndrome in a child undergoing craniotomy: a case report |pdf=|usr=}}{{8854446}} gab.com Text Acquired long QT syndrome in a child undergoing craniotomy: a case report JO: Zhonghua Yi Xue Za Zhi (Taipei) http://www.kidney.de/pget.php?&tw=1&pmid=8854446 #FOAvip The long QT syndrome (LQTS) is a rare disorder of cardiac conduction in children. It may lead to severe arrhythmia, syncope or sudden death. Electrolyte disturbance and the use of procainamide are closely related to the acquired LQTS. This report concerns a fatality of acquired LQTS in a boy undergoing craniotomy. After induction of anesthesia, his electrocardiogram displayed a frequent torsade de pointes type of ventricular tachycardia with prolonged QT interval. Therefore, congenital LQTS was impressed. However, the arrhythmia was aggravated by intravenous propranolol. Isoproterenol infusion was given under the diagnosis of acquired LQTS. The arrhythmia was successfully abolished and a stable hemodynamic status was maintained. However, the child could not tolerate the anesthesia which lasted for 30 hours, and eventually succumbed, despite aggressive treatment and resuscitation attempts. Differential diagnosis between the types of LQTS should be made promptly. This may be of paramount importance in the outcome since prognosis depends upon proper treatment. This case report discusses the etiology and management of this rare abnormality. Twit Text FOAVip Acquired long QT syndrome in a child undergoing craniotomy: a case report ????Zhonghua Yi Xue Za Zhi (Taipei) http://www.kidney.de/pget.php?&tw=1&pmid=8854446 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=8854446 #FOAvip English Wikipedia <ref>{{Cite pmid|8854446}}</ref> Acquired long QT syndrome in a child undergoing craniotomy: a case report #MMPMID8854446 Hsieh YC; Chow LH; Wong TD; Jeng KN; Lui PW; Lee TY Zhonghua Yi Xue Za Zhi (Taipei) 1995[Sep]; 56 (3): 215-9 PMID8854446show ga The long QT syndrome (LQTS) is a rare disorder of cardiac conduction in children. It may lead to severe arrhythmia, syncope or sudden death. Electrolyte disturbance and the use of procainamide are closely related to the acquired LQTS. This report concerns a fatality of acquired LQTS in a boy undergoing craniotomy. After induction of anesthesia, his electrocardiogram displayed a frequent torsade de pointes type of ventricular tachycardia with prolonged QT interval. Therefore, congenital LQTS was impressed. However, the arrhythmia was aggravated by intravenous propranolol. Isoproterenol infusion was given under the diagnosis of acquired LQTS. The arrhythmia was successfully abolished and a stable hemodynamic status was maintained. However, the child could not tolerate the anesthesia which lasted for 30 hours, and eventually succumbed, despite aggressive treatment and resuscitation attempts. Differential diagnosis between the types of LQTS should be made promptly. This may be of paramount importance in the outcome since prognosis depends upon proper treatment. This case report discusses the etiology and management of this rare abnormality. |Child[MESH] |Craniotomy[MESH] |Humans[MESH] |Long QT Syndrome/*etiology/therapy[MESH] |Magnesium/therapeutic use[MESH]Acquired long QT syndrome in a child undergoing craniotomy: a case rep(epmc).pdf DeepDyve Pubget Overpricing