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Adverse Events Associated With 10-kHz Dorsal Column Spinal Cord Stimulation: A 5-Year Analysis of the Manufacturer and User Facility Device Experience (MAUDE) Database.
D'Souza, Ryan S; Olatoye, Oludare O; Butler, Casey S; Barman, Ross A; Ashmore, Zachary M; Hagedorn, Jonathan M.
Affiliation
  • D'Souza RS; Division of Pain Medicine Department of Anesthesiology and Perioperative Medicine.
  • Olatoye OO; Division of Pain Medicine Department of Anesthesiology and Perioperative Medicine.
  • Butler CS; Division of Pain Medicine Department of Anesthesiology and Perioperative Medicine.
  • Barman RA; Departments of Anesthesiology and Perioperative Medicine.
  • Ashmore ZM; Physical Medicine and Rehabilitation, Mayo Clinic Hospital, Rochester, MN.
  • Hagedorn JM; Division of Pain Medicine Department of Anesthesiology and Perioperative Medicine.
Clin J Pain ; 38(5): 320-327, 2022 02 08.
Article in En | MEDLINE | ID: mdl-35132023
ABSTRACT

BACKGROUND:

High-frequency (10-kHz) spinal cord stimulation (SCS) continues to be an emerging therapy in chronic pain management. The same complications that plagued earlier SCS systems may affect newer stimulation technologies, although there is limited data on the type of complications and surgical management of these complications.

OBJECTIVE:

The aim of this study was to systematically examine real-world complications associated with 10-kHz SCS reported on the Manufacturer and User Facility Device Experience (MAUDE) database. MATERIALS AND

METHODS:

The MAUDE database was queried for entries reported between January 1, 2016 and December 31, 2020. Entries were classified into procedural complications, device-related complications, patient complaints, surgically managed complications, serious adverse events, and/or other complications. Primary outcomes included type and frequency of complications, and surgical management of complications.

RESULTS:

A total of 1651 entries were analyzed. Most entries were categorized as procedural complications (72.6%), followed by serious adverse events (10.5%), device-related complications (10.5%), and patient complaints (9.9%). Most complications were managed surgically with explant (50.9%) rather than revision (5.0%) or incision/drainage (6.6%). Of procedural complications, the most common entries included non-neuraxial infection (52.9%), new neurological symptoms (14.7%), and dural puncture (9.5%). Of device-related complications, the most common entries included lead damage (41.6%), erosion (18.5%), and difficult insertion (11.5%).

CONCLUSION:

This retrospective 5-year analysis of complications from10-kHz SCS provides a real-world assessment of safety data unique for this stimulation modality. This analysis may help inform future clinical decisions, lead to device enhancement and optimization, and improve mitigation of risks to provide safe and efficacious use of 10-kHz SCS.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord Stimulation Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Clin J Pain Journal subject: NEUROLOGIA / PSICOFISIOLOGIA Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord Stimulation Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Clin J Pain Journal subject: NEUROLOGIA / PSICOFISIOLOGIA Year: 2022 Type: Article