If someone was born with congenital hydrocephalus and it was treated right after birth, with the implantation of a shunt, life expectancy is within the "normal" range. That is, also dependant on if the person who has hydrocephalus is aware of the symptoms and seeks out a neurosurgeon... when needed. However, if you have "acquired" hydrocephalus, your life expectancy may be decreased. Also, people with NPH or "normal pressure hydrocephalus" can have a decreased life expectancy. For instance, former Rep. Gabrielle Giffords (D-AZ) has acquired hydrocephalus, due to the trauma of getting shot in the head. Her life expectancy may be decreaded by that. How long is anyone's guess.
You have to remember, congenital hydrocephalus is quite complex. Most of the time, the deaths in early childhood, may be due to the infant not able to tell people what is wrong, a neurosurgeon draining too much or too little CSF (cerebrospinal fluid) can cause a systemic breakdown that tiny bodies don't know how to handle and they have a "cascade failure" with the heart and brain stopping. But, that is a *worst case* scenerio.
I was shunted at one month. Have had numerous operations. Was told I would not live past age 16, I'm now in my 50's. Living near a "teaching hospital" is a good idea. They teach the newest skills. Yet, having staff that follows you for 20+ yrs is also a plus;-) Hope that info helps.
50 plus years is an encouragement to me. My daughter is 4yrs with vp shunt inserted at 8 months old. Please let me know how i can handle seizures as we undertake this journey. Regards.
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