scholarly journals WPW syndrome, PPHN with large PFO- in a full-term neonate presenting with decompensated heart failure - A case report

2021 ◽  
Vol 73 ◽  
pp. S10-S11
Author(s):  
Ashish Sharma ◽  
Cinosh Mathew ◽  
Jayesh Rawal
2011 ◽  
Vol 22 (2) ◽  
pp. 13-18 ◽  
Author(s):  
Paul E. H. Ricard ◽  
Robert Camarda ◽  
Laura Little Foley ◽  
Michael M. Givertz ◽  
Lawrence P. Cahalin

2003 ◽  
Vol 38 (11) ◽  
pp. 1665-1666 ◽  
Author(s):  
Jeroen Heemskerk ◽  
George H Sie ◽  
Anita M Van den Neucker ◽  
Pierre-Philippe Forget ◽  
Erik Heineman ◽  
...  

2019 ◽  
Vol 12 (5) ◽  
pp. e229237
Author(s):  
Siv Steinsmo Ødegård ◽  
Birgitte Kahrs ◽  
Astri Maria Lang ◽  
Siri Ann Nyrnes

We present a case report of anomalous mitral arcade in a live born former recipient of twin–twin transfusion syndrome. At 33+0 week of gestation fetal ultrasound demonstrated that she had a large mitral insufficiency, decreased movement of the lateral cusp of the mitral valve and dilated left atrium. The twins were delivered by caesarean section at week 33+1 due to fetal distress. The former recipient twin developed decompensated heart failure during her first day of life and was transferred to a surgical paediatric heart centre. Her clinical condition rapidly deteriorated, and she died of congestive heart failure 3 days old. Prenatal signs of anomalous mitral arcade in a recipient of twin–twin transfusion syndrome should warrant preparation of a critically ill neonate, including parental counselling and in utero transfer to surgical paediatric heart centre. There is a surgical treatment option available for neonates, but the experience with this technique is still very limited with a high risk of morbidity and mortality.


2017 ◽  
Vol 73 (5) ◽  
pp. 647-649 ◽  
Author(s):  
Pavla Pokorná ◽  
Karolina Hronová ◽  
Martin Šíma ◽  
Ondřej Slanař ◽  
Petr Klement ◽  
...  

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.


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