Nutrition Health Chat: Tuesday, Dec. 8th, 5-6 PM Eastern. Learn how vitamins, minerals, and phytonutrients affect your health. Free live Q&A. Join us!
Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum.  ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
Neurology  (Expert Forum)
 | 
Re: POTS
This forum is for questions and support regarding neurology issues such as: Alzheimer's Disease, ALS, Autism, Brain Cancer, Cerebral Palsy, Chronic Pain, Epilepsy, Fibromyalgia, Headaches, MS, Neuralgia, Neuropathy, Parkinson's Disease, RSD, Sleep Disorders, Stroke, Traumatic Brain Injury.

Re: POTS

by CF-Neuro-MD-, Jan 01, 1995 12:00AM
Posted By CCF Neuro MD *!* on December 04, 1997 at 21:55:33:

In Reply to: POTS posted by Phillips on November 11, 1997 at 20:00:28:







: I was recently diagnosed with postural orthostatic tachycardia syndrome via
tilt table. My symptoms at the time were resting and standing tachycardia.
I also had tremors, flushing, voice sounding "shakey", palpitations and
shortness of breath. However I was also extremely hypertensive (160/120)
Standing, active heart rates 140-160. I realize that hypertension is unusual
with POTS and the explanation I received was that I was having a sympothetic over
response to the cerebral hypotension. Does this seem likely? I was started on
clonidine for these symptoms, which did improve. However I did go on to develop
hypotension and am know on midodrine and florinef. The clonidine was recently
stopped and the sympothetic sxs are returning with minimal change in blood pressure.
I'm under the impression that POTS doesn't progress, but this seems to be progression.
What is your opinion?




The normal physiological response to hypoperfusion of the brain by means
of increased heart rate or tachycardia, which pumps blood  more rapidly to the brain ,maintaining perfusion. Since control of the sympathetic nervous system is abnormal  in POTS an overshoot  of the response sounds like a very plausible explanation.
The response  to Clonidine and reappearance of symptoms after stopping clonidine  would tend to support this hypothesis.
The symptoms of  tremulousness palpitations etc. certainly sound very compatible with POTS.
Regarding the natural history and progression of POTS I have traced a review article on the subject, I is nit currently to hand however I will obtain it and Attempt to answer the last part of your question in a follow -up.
This information is provided for general medical education purposes only.
Please consult your physician for diagnostic and treatment options of your specific medical condition.


Continue discussion
RSS Expert Activity
In the ER: Coffee, anyone?
11 hrs ago by Jon Geller, D.V.M.
My animal blogs! 
13 hrs ago by Justine Lee, D.V.M., DACVECC
Prevention Gains Momentum: Your Gui... 
Nov 29 by Lee Kirksey, MD