# Dental drugs with proarrhythmic risk in patients with Brugada syndrome: precaution instructions for practices in the field of orofacial pain

**Authors:** Dawool Han, Na Yeong Cho, Eunae Sandra Cho, Seung-Young Roh

PMC · DOI: 10.3389/fcvm.2026.1754683 · Frontiers in Cardiovascular Medicine · 2026-02-04

## TL;DR

This paper reviews how certain dental drugs used for orofacial pain can increase heart risks in patients with Brugada syndrome and suggests precautions to reduce these dangers.

## Contribution

The paper introduces a risk-stratified approach for orofacial pain specialists to manage drug-induced arrhythmias in Brugada syndrome patients.

## Key findings

- Drugs for orofacial pain can unmask Brugada electrocardiographic patterns or trigger arrhythmias.
- Current dental guidelines often overlook long-term drug risks in Brugada syndrome patients.
- A precaution-based approach may reduce cardiac events while maintaining pain control.

## Abstract

Orofacial pain, diagnosed and treated in a subfield of dentistry, highly relies on long-term psychotropic, neuromodulating, and analgesic regimens that have the potential to alter cardiac ion channels and autonomic tone. In patients with inherited arrhythmia syndromes such as Brugada syndrome (BrS), these drugs may unmask a type 1 Brugada electrocardiographic pattern or trigger malignant ventricular arrhythmias and sudden cardiac death, yet most dental guidance addresses only short-term use of local anesthetics. In this narrative review, we synthesize evidence on the arrhythmogenic potential of medications used for orofacial pain—non-steroidal anti-inflammatory drugs, tricyclic antidepressants, anticonvulsants, and primary headache therapies. Finally, we propose a pragmatic risk-stratified approach for orofacial pain specialists. Incorporating channelopathy-specific precautions into orofacial pain pharmacotherapy may reduce drug-induced ventricular arrhythmias and sudden cardiac death while preserving effective long-term pain control.

## Linked entities

- **Diseases:** Brugada syndrome (MONDO:0015263)

## Full-text entities

- **Genes:** SCN5A (sodium voltage-gated channel alpha subunit 5) [NCBI Gene 6331] {aka CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD}, TRPM7 (transient receptor potential cation channel subfamily M member 7) [NCBI Gene 54822] {aka ALSPDC, CHAK, CHAK1, LTRPC7, LTrpC-7, TRP-PLIK}, KCNH2 (potassium voltage-gated channel subfamily H member 2) [NCBI Gene 3757] {aka ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}
- **Diseases:** heart failure (MESH:D006333), neuralgia (MESH:D009437), depression (MESH:D003866), Chronic pain (MESH:D059350), trigeminal neuralgia (MESH:D014277), musculoskeletal disorders (MESH:D009140), cardiac sodium channel blockage (MESH:D020513), cardiac disorders (MESH:D006331), migraine (MESH:D008881), ventricular fibrillation (MESH:D014693), neuropathies (MESH:D009422), overdose (MESH:D062787), thrombotic (MESH:D013927), hypertension (MESH:D006973), atrial fibrillation (MESH:D001281), myocardial infarction (MESH:D009203), sudden death (MESH:D003645), cluster headache (MESH:D003027), nociceptive pain (MESH:D059226), cardiac side effects (MESH:D064420), Cardiac arrhythmias (MESH:D001145), masticatory and musculoskeletal pains (MESH:D059352), cardiac structural abnormalities (MESH:C566527), strokes (MESH:D020521), postherpetic neuralgia (MESH:D051474), sudden cardiac death (MESH:D016757), Orofacial Pain (MESH:D005157), Fever (MESH:D005334), burning mouth syndrome (MESH:D002054), arrhythmic (OMIM:212500), Primary headaches (MESH:D051270), seizure (MESH:D012640), trigeminal autonomic cephalalgias (MESH:D051303), systemic diseases (MESH:D034721), temporomandibular disorders (MESH:D013705), acute and chronic pain (MESH:D059787), syncope (MESH:D013575), craniofacial traumas (MESH:D014947), tension-type headaches (MESH:D018781), Headache (MESH:D006261), inflammation (MESH:D007249), joint diseases of the jaw (MESH:D007571), sleep disorders (MESH:D012893), pain (MESH:D010146), hereditary channelopathies (MESH:D009386), BrS (MESH:D053840), poisoning (MESH:D011041), aberrant heart rhythms (MESH:D002869), myofascial pain syndrome (MESH:D009209), psychiatric (MESH:D001523), SCD (MESH:C536778), Channelopathies (MESH:D053447), anxiety (MESH:D001007), cardiac arrest (MESH:D006323), angina (MESH:D000787)
- **Chemicals:** Carbamazepine (MESH:D002220), Amitriptyline (MESH:D000639), Verapamil (MESH:D014700), Gabapentin (MESH:D000077206), calcium (MESH:D002118), lidocaine (MESH:D008012), naproxen (MESH:D009288), propafenone (MESH:D011405), SUNA (-), flecainide (MESH:D005424), Sodium (MESH:D012964), procaine (MESH:D011343), lamotrigine (MESH:D000077213), phenytoin (MESH:D010672), Oxcarbazepine (MESH:D000078330), nortriptyline (MESH:D009661), acetaminophen (MESH:D000082), sumatriptan (MESH:D018170), epinephrine (MESH:D004837)
- **Species:** Enterovirus C (no rank) [taxon 138950], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

94 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913552/full.md

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Source: https://tomesphere.com/paper/PMC12913552