Definition, Diagnosis and Clinical Presentation
Diagnosis

Mechanism-Based Herbal Approaches to POTS (Pt. 1)

Definition, Diagnosis and Clinical Presentation
Ayla Wolf, DAOM, LAc, Dipl. OM
WHAT YOU NEED TO KNOW
  • Over the past several years, and particularly since the COVID-19 pandemic, POTS has moved from the periphery of clinical awareness into the mainstream of both conventional and integrative medicine.
  • Patients with POTS are often misdiagnosed – or dismissed entirely – as having anxiety, deconditioning or psychosomatic illness.
  • A clear grasp of diagnostic criteria and pathophysiology allows clinicians to validate patients’ experiences and design more effective, individualized treatment strategies.

Postural orthostatic tachycardia syndrome (POTS) was once considered a relatively uncommon condition – one that even seasoned practitioners might encounter only occasionally in clinical practice. That reality has changed dramatically. Over the past several years, and particularly since the COVID-19 pandemic, POTS has moved from the periphery of clinical awareness into the mainstream of both conventional and integrative medicine.

This heightened attention is due in large part to the effects of SARS-CoV-2 infection on the autonomic nervous system (ANS). As a result, clinicians across disciplines are now encountering increasing numbers of patients presenting with symptoms of orthostatic intolerance, exercise intolerance, tachycardia, dizziness, fatigue, and cognitive dysfunction. Many of these patients ultimately meet diagnostic criteria for POTS.

POTS falls under the broader category of dysautonomia, a term used to describe dysfunction of the autonomic nervous system. The ANS governs a vast range of involuntary physiological processes, including heart rate, blood pressure regulation, digestion, thermoregulation, pupillary reflexes, and aspects of immune and inflammatory control. Given the breadth of these functions, dysautonomia can manifest in a wide variety of clinical presentations – often involving multiple organ systems and fluctuating symptom patterns.

Dysautonomia vs. Autonomic Dysregulation

It is essential to delineate an important clinical distinction: Not all autonomic symptoms constitute dysautonomia in the medical sense. Many individuals experience milder forms of autonomic dysregulation during periods of high stress, anxiety, depression, trauma exposure, or post-traumatic stress. In these cases, symptoms such as palpitations, lightheadedness, gastrointestinal upset, headaches or dizziness may arise from heightened sympathetic tone or impaired parasympathetic regulation. While these presentations can be clinically significant and deserve thoughtful treatment, they do not necessarily meet criteria for a diagnosable autonomic disorder.

In contrast, dysautonomia as a medical diagnosis refers to a persistent, pathological failure of autonomic regulation, often measurable through objective testing and associated with predictable physiological abnormalities. POTS represents one such subtype, characterized by a reproducible abnormal cardiovascular response to upright posture.

Understanding this distinction is critical for acupuncturists. Patients with POTS are often misdiagnosed – or dismissed entirely – as having anxiety, deconditioning or psychosomatic illness. A clear grasp of diagnostic criteria and pathophysiology allows clinicians to validate patients’ experiences and design more effective, individualized treatment strategies.

Understanding POTS: Current Diagnostic Criteria

Postural orthostatic tachycardia syndrome is defined by an excessive increase in heart rate upon assuming an upright posture, in the absence of significant orthostatic hypotension. Current diagnostic criteria generally include:

  • A sustained increase in heart rate of ≥30 beats per minute within 10 minutes of maintaining an upright posture (or ≥40 beats per minute in adolescents ages 12-19).
  • Symptoms must be chronic, typically present for at least 3-6 months.
  • Blood pressure does not fall sufficiently to meet criteria for orthostatic hypotension.
  • Symptoms are provoked or worsened by standing and often quickly improve with recumbency.

Importantly, POTS is not a single disease entity, but rather a clinical syndrome with multiple underlying mechanisms. This heterogeneity explains why patients with the same diagnosis may present very differently; and why a one-size-fits-all treatment approach is rarely effective.

Common Clinical Features

Patients with POTS may report a wide constellation of symptoms, including:

  • Palpitations or increased awareness of heartbeat
  • Lightheadedness, dizziness or near-syncope
  • Fatigue and post-exertional symptom flares
  • Exercise intolerance
  • Cognitive dysfunction and brain fog
  • Headaches or migraines
  • Gastrointestinal dysmotility
  • Temperature dysregulation
  • Sleep disturbances

Many patients also report symptom onset following a triggering event, such as viral illness, traumatic brain injury, surgery, pregnancy, or prolonged immobilization. In clinical practice, it is not uncommon to see POTS emerge as part of a broader post-viral or post-concussive syndrome.

Overlap With Autoimmune and Connective-Tissue Disorders

Another clinically significant – and often underappreciated – aspect of POTS is its frequent overlap with autoimmune and connective-tissue disorders, particularly Ehlers-Danlos syndrome (EDS) and related hypermobility spectrum disorders. A substantial subset of POTS patients demonstrate joint hypermobility, tissue fragility, or a history of frequent sprains, dislocations, and chronic pain.

In these individuals, impaired connective-tissue integrity may contribute to excessive venous pooling in the lower extremities when upright, placing greater demand on autonomic reflexes to maintain cerebral perfusion. Over time, this increased compensatory burden may exacerbate or unmask autonomic dysfunction.

Additionally, immune dysregulation, whether autoimmune or mast cell-mediated, appears to play a contributory role in many patients, further complicating the clinical picture.

For acupuncturists, recognizing these overlaps is critical. Patients with POTS and comorbid hypermobility or autoimmune features often present with heightened sensitivity to treatment, slower recovery timelines, and complex mixed-pattern presentations. A narrow or overly aggressive approach may fail to address the underlying terrain contributing to autonomic instability.

Why This Matters for Acupuncturists

From a traditional East Asian medicine perspective, POTS patients often present with complex, overlapping patterns that do not fit neatly into a single diagnostic category. Symptoms may fluctuate day to day, worsen with exertion, heat, or stress, and involve both excess and deficiency presentations. Without a clear understanding of the biomedical framework of POTS, clinicians risk undertreating the condition – or inadvertently exacerbating symptoms by applying strategies better suited for stress-induced autonomic imbalance rather than true dysautonomia.


Author’s Note: Part 2 of this article will explore distinct phenotypes of POTS based on underlying mechanisms, and translate these patterns into traditional Chinese medicine differential diagnoses, allowing practitioners to select more precise and supportive herbal strategies.


Resource

  • Lau DH, Fedorowski A, Raj SR, et al. Postural orthostatic tachycardia syndrome: a state-of-the-art review. Heart Lung Circ, 2026;35(2):171-185.
October 2026