Valproic acid—induced hyperammonemic encephalopathy in a full-term neonate: a brief review and case report

2017 ◽  
Vol 73 (5) ◽  
pp. 647-649 ◽  
Author(s):  
Pavla Pokorná ◽  
Karolina Hronová ◽  
Martin Šíma ◽  
Ondřej Slanař ◽  
Petr Klement ◽  
...  
2003 ◽  
Vol 38 (11) ◽  
pp. 1665-1666 ◽  
Author(s):  
Jeroen Heemskerk ◽  
George H Sie ◽  
Anita M Van den Neucker ◽  
Pierre-Philippe Forget ◽  
Erik Heineman ◽  
...  

2018 ◽  
Vol 21 (1) ◽  
pp. 102-106
Author(s):  
Ferda Apa ◽  
Figen Çulha Ateşci ◽  
Gülfizar Sözeri Varma

2020 ◽  
Vol 7 ◽  
pp. 2329048X2096788 ◽  
Author(s):  
Jennifer Bennett ◽  
Christy Gilkes ◽  
Karin Klassen ◽  
Marina Kerr ◽  
Aneal Khan

This case report describes 2 siblings with myoclonic epilepsy who had novel mutations in the glutamine synthetase ( GLUL) gene: c.316C>T, p.(Arg106*) and c.42G>C, p.(Lys14Asn). Valproic acid improved seizure control, but was associated with hyperammonemic encephalopathy. Addition of carglumic acid reduced ammonia levels but drug coverage was declined. We therefore designed a protocol to measure the reduction in plasma ammonia in response to carglumic acid therapy. After the first dose of carglumic acid, Patient 1 showed a reduction in plasma ammonia levels within 3 hours, from 114 umol/L to 68 umol/L (reference 12-47 umol/L), and Patient 2 from 108 umol/L to 80 umol/L, which was sustained over a 2 week period. Overall, there was a strong negative correlation between plasma ammonia levels and carglumic acid levels (r = −0.86, p = 0.0013), and recurrence of hyperammonemic encephalopathy was not observed while the patients were taking carglumic acid.


Author(s):  
Karthika Ashok Kumar ◽  
Chanshi Chandran ◽  
Remya Reghu

Valproic acid is commonly used in the treatment of both focal and generalized epilepsies and is often tolerated well.Valproic acid is usually tolerated well, but serious complications, including hepatotoxicity and hyperammonemic encephalopathy, may occur. Here we report a case of valproic acid induced hyperammonemic encephalopathy on concomitant use with lacosamide. 


2018 ◽  
Vol 2018 ◽  
pp. 1-3 ◽  
Author(s):  
Judy Ibrahim ◽  
Nadia Hamwi ◽  
Hala Rabei ◽  
Mohamed Abdelghafar ◽  
Zahraa Al-Dulaimi ◽  
...  

Stenotrophomonas maltophilia is an environmental bacterium of growing concern due to its multidrug resistance and pathogenic potential. It is considered an opportunistic pathogen of nosocomial origin most of the time, targeting a specific patients' population. We describe a case of a previously healthy full-term neonate who was found to have S. maltophilia meningitis and was successfully treated with a combination of Trimethoprim-Sulfamethoxazole and Ciprofloxacin.


2012 ◽  
Vol 03 (02) ◽  
pp. 151-153
Author(s):  
Hélio A. Guimarães Filho ◽  
Janett J. Liberalino ◽  
Ana T. P. Mendonça ◽  
Carlos V. S. B. Leite Filho ◽  
Leonardo F. Felipe ◽  
...  

Perfusion ◽  
2020 ◽  
pp. 026765912097359
Author(s):  
Pavla Pokorná ◽  
Martin Šíma ◽  
Dick Tibboel ◽  
Ondřej Slanař

Introduction: Extracorporeal membrane oxygenation (ECMO) is a lifesaving support technology for potentially reversible neonatal cardiac and/or respiratory failure. Pharmacological consequences of ECMO-induced haemolysis in neonates are not well understood. Case report: We report a case report of a full-term neonate treated for congenital diaphragmatic hernia and sepsis with ECMO and with vancomycin. While the population elimination half-life of 7 h was estimated, fitting of the simulated population pharmacokinetic profile to truly observed drug concentration points resulted in the personalized value of 41 h. Discussion: The neonate developed ECMO-induced haemolysis with subsequent acute kidney injury resulting in prolonged drug elimination. Whole blood/serum ratio of 0.79 excluded possibility of direct increase of vancomycin serum concentration during haemolysis. Conclusion: Vancomycin elimination may be severely prolonged due to ECMO-induced haemolysis and acute kidney injury, while hypothesis of direct increase of vancomycin levels by releasing the drug from blood cells during haemolysis has been disproved.


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