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. Author manuscript; available in PMC: 2024 Jul 18.
Published in final edited form as: J Am Coll Cardiol. 2023 Jul 18;82(3):245–264. doi: 10.1016/j.jacc.2023.04.054

TABLE 1.

Differential Diagnosis and Recommended Testing to Consider for Abnormal Health Metrics From Consumer Wearable Devices

Metric Differential Diagnosis Confirmatory Diagnostic
Testing to Be Considered
Additional Testing Considerationsa
Low heart rate (resting conditions) Wearable device heart rate measurement failure
Bradyarrhythmia
 Sinoatrial node dysfunction, high grade atrioventricular block
Sinus bradycardia
 Anorexia/malnutrition, CNS disease, hypothermia, hypothyroidism, exercise training, medication effect, sleep apnea, increased vagal tone
  • 12-lead ECG

  • Clinically approved ambulatory rhythm monitor

Bradyarrhythmia
 Refer to AHA/ACC guidelines following arrhythmia confirmationb
Sinus bradycardia
  • Careful medication history

  • Laboratory studies (BMP, TSH)

  • Sleep study

High heart rate (resting conditions) Wearable device heart rate motion artifact
Tachyarrhythmia
 Paroxysmal supraventricular tachycardia, ventricular tachycardia
Sinus tachycardia
 Anxiety, dehydration, anemia, medication effect (eg, beta-blocker withdrawal, beta agonist), infection, heart failure, hyperthyroidism, pain, POTS, pregnancy, PE, shock, stimulant use, inappropriate sinus tachycardia
  • 12-lead ECG

  • Clinically approved ambulatory rhythm monitor

Tachyarrhythmia
 Refer to AHA/ACC guidelines following arrhythmia confirmationb
Sinus tachycardia
  • Careful medication history

  • Laboratory studies (BMP, CBC, D-dimer, TSH, iron studies)

  • TTE

Low SpO2 (resting conditions) Wearable device SpO2 measurement failure
High altitude
Hypoventilation
 Chest wall pathology (eg, kyphoscoliosis), CNS disease, sedatives, hypothyroidism, metabolic alkalosis, OSA, respiratory muscular weakness (eg, ALS)
V/Q mismatch or shunt
 ARDS, asthma, atelectasis, pulmonary AVM, bronchiectasis, COPD, pulmonary edema (cardiac and noncardiac), ILD, intracardiac shunt, mucus plugging, PE, PNA
  • Clinically approved pulse oximetry

  • Arterial blood gas

  • Careful medication history

  • Chest radiography

  • Laboratory studies (D-dimer)

  • PFTs

  • TTE with bubble study

Irregular heart rhythm (resting conditions and during exercise) Wearable device heart rate measurement failure
Wearable device heart rate motion artifact
Arrhythmia
Respiratory sinus arrhythmia
  • 12-lead ECG

  • Clinically approved ambulatory rhythm monitor

Arrhythmia
 Refer to AHA/ACC guidelines following arrhythmia confirmationb
Sinus arrhythmia
 No further testing recommended
HRV (low) Wearable device heart rate measurement failure
aging
Physical deconditioning
inadequate recovery/overtraining
infection
Medication effect
Mental stress
Poor sleep
Systemic illness
Toxins (eg, EtOH)
Thermal stress (warmer temperatures)
  • Detailed medical and social history

No further testing recommended
HRR (low) Wearable device heart rate measurement failure
Physical deconditioning
Medication effect
Systemic illness
Tachyarrhythmia
  • Detailed medical and social history

  • Exercise ECG with postrecovery monitoring

Peak V.O2 (low) Wearable device V.O2 algorithm inaccuracy
Physical deconditioning
Cardiopulmonary disease
Anemia
Skeletal muscular disease (myopathy)
  • CPET

  • Laboratory studies (CBC)

High respiratory rate (resting conditions and during exercise) Wearable device RR motion artifact
Anxiety
Cardiac disease (arrhythmia, ischemia, heart failure)
Diabetic ketoacidosis
Anemia
Exercise
Fever/sepsis
Pulmonary disease (asthma, COPD, effusion, ILD, PE)
Toxins
  • Visual assessment and manual assessment of respiratory rate

  • Chest radiography

  • Laboratory studies (ABG, CBC, CMP, toxicology)

  • PFTs

Low respiratory rate (resting conditions and during exercise) Wearable device RR measurement failure
CNS disease
Hypothyroidism
Medication effect
Sleep apnea
Toxins (eg, opiates)
  • Visual assessment and manual assessment of respiratory rate

  • Laboratory studies (TSH, toxicology)

  • Sleep study

Sleep (poor sleep) Wearable device heart rate and/or RR measurement failure
Dehydration
Medication effect (eg, stimulants)
Sleep disorder (eg, restless leg, syndrome, sleep apnea)
Stress/anxiety
Toxins (eg, EtOH)
  • Detailed medical and social history

  • Laboratory studies (iron studies)

  • Sleep study

a

A thorough history and physical examination is recommended as the starting point in the evaluation of all abnormal testing.

b

For confirmed bradyarrhythmia, refer to the 2018 AHA/ACC/HRS guideline on the evaluation and management of patients with bradycardia and cardiac conduction delay.102 For confirmed tachyarrhythmia, refer to the 2015 AHA/ACC/HRS guideline for the management of adult patients with supraventricular tachycardia103 or the 2017 AHA/ACC/HRS guideline for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death104 or the 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation105/2019 AHA/ACC/HRS focused update of the 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation.106

ABG = arterial blood gas; ARDS = acute respiratory distress syndrome; AVM = arteriovenous malformation; BMP = basic metabolic panel; CMP = comprehensive metabolic panel; CNS = central nervous system; COPD = chronic obstructive pulmonary disease; EtOH = alcohol; ILD = interstitial lung disease; OSA = obstructive sleep apnea; PE = pulmonary embolism; PFT = pulmonary function test; PNA = pneumonia; POTS = postural orthostatic tachycardiac syndrome; RR = respiratory rate; TSH = thyroid stimulating hormone; TTE = transthoracic echocardiography.