Letters to the Editor

Office Electrocautery Is Safe for Patients With Pacemakers

American Family Physician. 2026;114(4):332.

To the Editor: As family physicians practicing and teaching electrosurgery and electrocautery for decades, we write to clarify appropriate practice in response to the article by Lanney and colleagues on pacemaker therapy.1 Although the authors provide a helpful overview, their broad caution about all electrocautery performed above the waist may be appropriate for high-powered operating room devices but perpetuates unfounded concerns about modern office-based practice and contemporary devices.

In the 2024 American Heart Association scientific statement, the authors cite the 2011 Heart Rhythm Society/American Society of Anesthesiologists expert consensus statement without considering technological advances.2,3 Current evidence shows that electromagnetic interference risk is determined primarily by proximity of the electrosurgical tool to the pulse generator and the type of current.4,5 Modern cardiac implantable electronic devices incorporate filtering components, including feedthrough capacitors and band-pass filters, designed to minimize effects of external electrical fields.5

The literature supports a more nuanced approach. The devices most used in family medicine and dermatology, such as the Conmed Hyfrecator, are low-powered monopolar units that do not cycle current through the body to a grounding pad. In vivo data on monopolar hyfrecation show that procedures on the head, neck, and extremities are safe.6 A retrospective study of 45 patients undergoing Mohs surgery and electrodesiccation found no adverse perioperative effects, device malfunction, inappropriate firing, or loss of capture on interrogation.2 This suggests outpatient procedures can generally be performed without excessive monitoring or specialist referral outside a 3 to 15 cm safety margin.6

A 2012 study used a collagen-based gel model implanted with pacemakers and defibrillators to test for interference and found none until the cautery was within 1 cm of the devices at usual clinical power settings or until within 3 cm at the highest power settings. It conservatively recommended avoiding hyfrecator use within approximately 5 cm of pacemakers or defibrillators, an area rarely involved in skin cancers and procedures typically managed in family medicine.4

The above the umbilicus rule may be useful in the operating room for major surgery, but invoking it indiscriminately perpetuates the myth that office electrocautery cannot be used safely in patients with pacemakers.

Daniel Stulberg, MD, FAAFP

Albuquerque, New Mexico

danstulberg@gmail.com

Ricardo Galicia, MD

Albuquerque, New Mexico

Author Disclosure: No relevant financial relationships.

Editor’s Note: This letter was sent to the authors of “Pacemaker Therapy: Indications and Recommendations,” who declined to reply.

  1. 1.Lanney H, Hu Y, Karnovsky SC. Pacemaker therapy: indications and recommendations. Am Fam Physician. 2026;113(6):551-558.
  2. 2.Wan EY, Rogers AJ, Lavelle M, et al.; American Heart Association Electrocardiography and Arrhythmias Committee of the Council on Clinical Cardiology; Council on Cardiovascular and Stroke Nursing; Council on Cardiovascular Surgery and Anesthesia; Council on Peripheral Vascular Disease. Periprocedural management and multidisciplinary care pathways for patients with cardiac implantable electronic devices: a scientific statement from the American Heart Association. Circulation. 2024;150(8):e183-e196.
  3. 3.Crossley GH, Poole JE, Rozner MA, et al. The Heart Rhythm Society (HRS)/American Society of Anesthesiologists (ASA) Expert Consensus Statement on the perioperative management of patients with implantable defibrillators, pacemakers and arrhythmia monitors: facilities and patient management. Heart Rhythm. 2011;8(7):1114-1154.
  4. 4.Weyer C, Siegle RJ, Eng GG. Investigation of hyfrecators and their in vitro interference with implantable cardiac devices. Dermatol Surg. 2012;38(11):1843-1848.
  5. 5.James ML, Wright B, Thomas HE. Management of cardiac implantable electronic devices around the time of dermatological procedures requiring electrosurgery: an important guidance update. Clin Exp Dermatol. 2024;49(4):403-405.
  6. 6.Amin SD, Homan KB, Assar M, et al. Hyfrecation and interference with implantable cardiac devices. Dermatol Surg. 2020;46(5):612-615.

Email letter submissions to afplet@aafp.org. Letters should be fewer than 400 words and limited to six references, one table or figure, and three authors. Letters submitted for publication in AFP must not be submitted to any other publication. Letters may be edited to meet style and space requirements.

This series is coordinated by Kenny Lin, MD, MPH, deputy editor.

Copyright © 2026 by the American Academy of Family Physicians.

This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. See permissions for copyright questions and/or permission requests.