My father, aged 74, has been suffering from NPH for at least 6 years. His symptoms have been textbook: gait problems, short term
memoryMemory loss
Mental status tests loss and other
cognitiveMental status tests problems, etc. Four years ago he had a
shuntCyanotic heart disease
Transjugular intrahepatic portosystemic shunt (tips) inserted. This alleviated the symptoms somewhat, for a brief period, but gradually they have worsened again. Currently they seem fairly severe to me. My father is now experiencing spells in which he loses
completeComplete
Complete a-z
Complete allergy
Complete natal
Complete premium
Complete senior
Complete-rf controlControl
Control rx of his legs. On such occasions he has collapsed to the ground, or found it impossible to get out of bed. His
handHand or foot spasms
Hand tremor control/coordination is so bad that he can no longer sign his name. Short term memory loss and problems reasoning are worsening. He has moments in which he 'spaces out' and clearly has no idea who or where he is.
Ever since the shunt was inserted he has been monitored on an ongoing basis by a variety of medical professionals (though not -- I think -- the specialist who inserted the shunt). Despite his persistent decline, they have continued to give him a clean bill of health until recently. As of a week ago, his GP indicated that a check-up with the specialist who inserted the shunt is in order.
I would very much appreciate any information you could provide to help my family formulate questions to ask the specialist.I have found all sorts of valuable information about NPH on the Internet (including messages on this site), so I think I have some idea about its causes, symptoms, treatment, etc., but I haven't found much about what to expect once a patient has received treatment. What is the long-term prognosis for NPH patients who have had a shunt inserted? So far, the family has assumed that my father's rapid deterioration is inevitable, but I am starting to question this. What is the rate of shunt failure? I understand that there are a variety of shunts, is any particular type more helpful to NPH patients (eg a programable shunt)? What sorts of tests are recommended for post-surgery NPH patients? MRI? Something else? Should the specialist be searching for additional problems? Are there any other common underlying causes of textbook NPH symptoms?
I apologise for the barrage of questions, but I understand that multiple postings to this site are expensive and drain valuable resources, so I've tried to cover everything in this one message!
Thanking you in anticipation for any feedback you can provide,
Susan