Persistent Pulmonary Hypertension of the Newborn: Pathophysiology by A. Moscatelli | OPENPediatrics
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- เผยแพร่เมื่อ 9 ก.ค. 2024
- In this video, Dr. Andrea Moscatelli discusses the pathophysiology of persistent pulmonary hypertension of the newborn, PPHN.
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This was the toughest case I have personally encountered so far. My son had severe MAS, resuscitated at birth. Anemia. PPHN. Had a TRALI.
3 cardiac arrests.
For pphn they tried iloprost (it did not work)
Sildenafil made a significant improvement. The first 2 years of his life was really challenging because of reccurent pneumonia.
On his 7th year of life he was found to have a genetic condition, distal deletion on his chromosome 18. He is now 10 ang thriving. There are some delays in his physical growth but overall he is doing well.
Dr. Kho, a neonatologist and her team in UST Hospital was amazing in managing my son's condition during his first month of life.
If you are reading this and you are a doctor or nurse, I want to thank you in advance because you will be saving lives.
Excellent reminders. Touched most of the main points. Thank you
That was a perfect lesson! I couldn't really understand PPHN but after this video I am ready to go, thanks!
It was brilliant. I love that the basics were also touched upon first. I would like to know more about the pre and post ductal
Excellent ppt
Great video, thank you so much!
excellent work , i really loved this one
Wonderful! Thank you for the lecture 😊
Thanks for the video. I always like a few examples with different scenarios if you were to make similar videos again.
Thanks alot. Amazing topic
amazing video, thank you
i found this channel amazing as an intern !
Thanks a lot!
Excellent
Hi
It’s a very good topic and very important topic to understand the basics of pphn
Interesting lecture
Thanks💓
Very educational and practically explained! Thank u for this video!
Amezing
Sir great talk, could you please tell me where to get those animated images? it is great fir teaching.
kindly reply to prathap_c@yahoo.com
My new born baby boy is affected by this and admitted now.Please pray for my kid ..could not control my tears ..breaking my heart seeing the little one suffer
Hi Kamala...I'm in NY, USA and my son went through a severe bout with PPHN
I will pray for your son....God saved my child and I believe He can do the same for you....maybe he's already recovering...🙏🙏🙏
My boy was in the NICU for 4 weeks, at Cohen's children's hospital.
Will you share an update please.
@@B.Mega.D My son has recovered from severe pphn after 3 weeks of NICU treatment. He had still mild ph as per the scan report which was taken couple of week ago but doctors believe that will eventually go away when baby grows. Further he not got any symptoms of pphn anymore . My son and your kid are born champions. Thanks to God’s blessing ,the one who is above all , Dr. Hari Priya from PHC hospital, Chennai and well wishers like you 🙏🏿👍🏼👍🏼
That's excellent news Kamala! I know now you are just catching up on holding, and loving him like you couldn't when he was getting treated at the hospital... May God continue to bless you🙏😊👶.Be well !
Bye,bye🙂🙂🙂...(I am happy because of this tonight, thank you).
@@B.Mega.D thanks a lot for the kind words 😀
What are the suitable foods for can give to pphn baby's mother ?
What is the future life period of PPHN recover baby?
my baby have it pphn and he didnt make it 😢 main cause is disseminated intravascular coagulation 2nd is severe pphn and 3rd is meconium aspiration he only live 2 days
Which vasodilatator are used? NO?
Yes
The therapy is very agressive
My daughter was born at 34 weeks with idiopathic pulmonary hypertension on October 25th 2022 at 4 days old she was put on ECMO after 2 1/2 weeks she came off better than she was she had coded twice before ECMO and once on ECMO for 20 minutes after ECMO she was still having trouble on and off the regular vent and non invasive well finally she was on bubble CPAP for a week was doing good then had to do a heart Cath procedure that put her back on the non invasive vent due to the pulmonary hypertension acting up they said babies and people with pulmonary don't do well with surgeries or anything stressful well fast forward to today may 5th finally went down to 29 or 30 on her PIP peep still at 30 on FiO2 peep is 34 or 40 but in the results of having to stay on oxygen she contracted bronchial pulmonary dysplasia as well plus she has underdeveloped lungs they upped her protein in the formula so hopefully that starts helping her lungs grow I don't know if anything is working honestly she is on bosentan sildenafil and steroids and Albuterol steroids my poor baby just can't get back off the vent 😭
How is she doing now? 😔
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