Postural orthostatic tachycardia syndrome & LD
Posted: Mon 21 Apr 2014 8:03
http://www.ncbi.nlm.nih.gov/pubmed/21305487
What has POTS to do with Lyme Disease
http://www.lymeneteurope.org/forum/view ... f=6&t=2762
http://www.ctvnews.ca/health/proper-dia ... -1.1784370Cardiol J. 2011;18(1):63-6.
Postural orthostatic tachycardia syndrome following Lyme disease.
Kanjwal K1, Karabin B, Kanjwal Y, Grubb BP.
Author information
1Section of Electrophysiology, Division of Cardiology, Department of Medicine,The University of Toledo Medical
Center, Toledo, USA.
Abstract
BACKGROUND:
A subgroup of patients suffering from Lyme disease (LD) may initially respond to antibiotics only to later develop a syndrome of fatigue, joint pain and cognitive dysfunction referred to as 'post treatment LD syndrome'. We report on a series of patients who developed autonomic dysfunction in the form of postural orthostatic tachycardia syndrome (POTS).
METHODS:
All of the patients in this report had suffered from LD in the past and were successfully treated with antibiotics. All patients were apparently well, until years later when they presented with fatigue, cognitive dysfunction and orthostatic intolerance. These patients were diagnosed with POTS on the basis of clinical features and results of the tilt table (HUTT) testing.
RESULTS:
Five patients (all women), aged 22-44 years, were identified for inclusion in this study. These patients developed symptoms of fatigue, cognitive dysfunction, orthostatic palpitations and either near syncope or frank syncope. The debilitating nature of these symptoms had resulted in lost of the employment or inability to attend school. Three patients were also suffering from migraine, two from anxiety and depression and one from hypertension. All patients demonstrated a good response to the employed treatment. Four of the five were able to engage in their activities of daily living and either resumed employment or returned to school.
CONCLUSIONS:
In an appropriate clinical setting, evaluation for POTS in patients suffering from post LD syndrome may lead to early recognition and treatment, with subsequent improvement in symptoms of orthostatic intolerance.
PMID:
21305487
[PubMed - indexed for MEDLINE]
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Yvonne and Fin24 were discussing the relationship between POTS and Lyme disease in 2009:Proper diagnosis of rare disorder can greatly improve quality of life
Karolyn Coorsh, CTVNews.ca
Published Sunday, April 20, 2014 10:00PM EDT
Canadian doctors are trying to shed light on a mysterious illness in the hopes of prompting earlier diagnosis and treatment for those affected by the rare nervous-system disorder.
Postural Tachycardia Syndrome, or POTS, has likely existed for centuries but was only well-defined less than 25 years ago. There is no known cause or cure for POTS, which is an unusual heart rate increase experienced when someone is in an upright position. It's caused by a malfunction of the automatic nervous system that regulates heartbeat and blood pressure as we move.
Dr. Carlos Morilla , a cardiologist with Hamilton Health Sciences, said the disorder can “markedly” impair quality of life, especially because it is not widely understood in the medical world.
[The rest of the article follows, and there is also a short video clip.]
What has POTS to do with Lyme Disease
http://www.lymeneteurope.org/forum/view ... f=6&t=2762