Category Archives: Uncategorized

Research Update: more proof POTS is not “all in your head”

Many physicians mistake the physical symptoms of POTS, such as tachycardia, palpitations, and shortness of breath, as the signs of an anxiety disorder or some other psychological problem.  Prior research has documented that POTS is not associated with increased levels of anxiety or psychiatric disorders, that POTS symptoms are phenomenologically different and clinically distinguishable from panic disorder, and that the upright tachycardia seen POTS patients is not caused by anxiety.

Despite publication of this research, many physicians continue to misdiagnose POTS patients as having anxiety disorders or other psychiatric conditions.   While psychiatric disorders are serious health problems that require proper treatment, the treatment for these conditions is not the same as the treatment for POTS, and can sometimes make POTS symptoms worse.

New research provides additional proof that POTS is not “all in your head.”  A study recently published in Clinical Autonomic Research, Visceral sensitization in postural tachycardia syndrome, examined whether palpitations frequently reported by POTS patients were psychological or organic in origin.  Palpitations are those thumping, fluttering, pounding sensations everyone feels from time to time in their heart, but many POTS patients experienced palpitations on a regular basis, and much more so than healthy individuals.

This study found that POTS patients “did not amplify their somatic and visceral sensations compared with control subjects, indicating that they are not predisposed to exaggerating every symptom and militating against psychologic origin.”  After analyzing the data collected, the study’s author, Dr. Ramesh Khurana, concludes that the palpitations in POTS “are of an organic origin.”

However, Dr. Khurana notes that POTS patients had greater ability to discriminate the type of palpitation compared with healthy subjects, “favoring visceral hypersensitivity and a central origin of POTS symptoms.”  Visceral sensitivity is a medical term used to describe an increased sensation of pain and sensations coming from your own internal organs, more so than a normal person would experience.  By “a central origin” Dr. Khurana is referring to the central nervous system, which includes the brain and spinal cord.  He explains, “potential locations for visceral hypersensitivity include sensory receptors in the cardiovascular system, extrinsic sensory afferent neurons, spinal nociceptive neurons, medulla, midbrain raphe, hypothalamus, and cortex.”

Dr. Khurana also reminds us that POTS is heterogeneuous condition, and that the concept of visceral sensitization may not apply to every POTS patient.  He notes that palpitations did not occur in all of the POTS patients who participated in the study.

 

DysautonomiaAdvancementDysautonomia International is actively raising funds to support additional research on POTS.  If you would like to support POTS research, please visit our donation page today.

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Thanks For The Memories 2013, Hello 2014!

2013 Recap
2013 was a year of tremendous growth and many firsts for Dysautonomia International. With the help of hundreds of amazing volunteers and generous donors, we held our first Dysautonomia Lobby Day on Capitol Hill (and a second lobby day), hosted our first national conference, battled insurance companies that are denying coverage for autonomic testing, launched the first POTS Research Registry, helped researchers recruit patients for groundbreaking dysautonomia research projects, presented a patient friendly research update from the 24th Symposium on the Autonomic Nervous System, and gave out our first four research grants.  Our volunteers also organized the second annual Dysautonomia Awareness Month in October, held the second annual Dysautonomia Awareness Tweet-A-Thon, increased press coverage on dysautonomia, obtained proclamations from state and local governments, distributed newly diagnosed patient brochures to medical offices, and held fundraisers, large and small, all year long.  Of course, we continued to provide patients and caregivers with educational resources, videos, resources, and connections to support groups that can help make life with dysautonomia a little bit more manageable.

A New Blog for a New Year
What better way to kick off the New Year than with another first – our first blog post on our new blog!  Through this blog, we’ll be bringing you the latest dysautonomia news, events, and research, as well as guests posts from physicians, researchers and other experts.

When we have a new blog post, we will announce it on our Facebook and Twitter pages, so be sure to follow us on one or both of those sites.  The blog will allow us to bring you more in-depth information that just a simple Facebook or Twitter post.

Our blog team is excited to offer “Dysautonomia Q&A” posts.  A few times per year, we will reach out to our network of dysautonomia savvy physicians, physical therapists, psychologists, school social workers, lawyers and other experts to answer 10 questions submitted by patients and caregivers.  The questions can be on any topic related to dysautonomia.  If you would like to submit a question, please send your question to blog@dysautonomiainternational.org.   We will select 10 questions that are applicable to a broad audience of patients, find an expert to answer each question, and publish their response on this blog .   If your question is selected, your name and e-mail will not be published.

Dysautonomia International wishes you all a Happy Healthy New Year!  We’re looking forward to new adventures in dysautonomia awareness, advocacy, and research in 2014.

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