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Pract Neurol. 2016 Dec;16(6):431-438. doi: 10.1136/practneurol-2016-001405. Epub 2016 Sep 22.

Clinical challenges in the diagnosis and management of postural tachycardia syndrome.

Author information

1
Department of Neurology, UT Health Science Center San Antonio, San Antonio, Texas, USA.
2
Cumming School of Medicine, University of Calgary, Calgary, Canada.
3
Department of Cardiac Sciences, Libin Cardiovascular Institute of Alberta, Cumming School of Medicine, University of Calgary.

Abstract

Postural tachycardia syndrome (POTS) is a multifactorial clinical syndrome defined by an increase in heart rate of ≥30 bpm on standing from supine position (or ≥40 bpm in children). It is associated with symptoms of cerebral hypoperfusion that are worse when upright and improve when in supine position. Patients often have additional symptoms including severe fatigue and difficulty concentrating. There are several possible pathophysiologic mechanisms including hypovolaemia, small-fibre peripheral neuropathy and hyperadrenergic states. POTS can also be associated with several disorders including mastocytosis, Ehlers-Danlos syndrome (hypermobility type) and autoimmune disorders. The treatment is focused on symptom relief and not solely on reducing tachycardia. Given its varying presentations, it is important to employ a practical, mechanism-focused approach to the diagnosis and management of POTS.

KEYWORDS:

AUTONOMIC; POTS; orthostatic intolerance; postural tachycardia syndrome; tachycardia

PMID:
27660311
DOI:
10.1136/practneurol-2016-001405
[Indexed for MEDLINE]

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