The use of transcutaneous electrical nerve stimulation (TENS) in a major cancer center for the treatment of severe cancer-related pain and associated disability. Academic Article uri icon

Overview

abstract

  • BACKGROUND: Cancer pain is difficult to treat, often requiring a multimodal approach. While medication management remains the mainstay for the treatment of cancer pain, medications are often associated with undesired side effects. Transcutaneous electrical nerve stimulation (TENS) provides a potential adjunctive method for treating cancer pain with minimal side effects. OBJECTIVE: Few studies have been performed evaluating the efficacy of TENS on cancer pain. We sought to examine the usefulness of TENS on all cancer patients and to specifically look at the use of TENS as a goal-directed therapy to improve functionality. DESIGN: Retrospective cohort study. METHODS: Since 2008, patients with chronic cancer pain and on multimodal pain regimens were trialed with TENS. Those patients who showed an improvement in pain symptoms or severity were educated about and provided with a TENS unit for use at home. Pain symptoms and scores were monitored with the visual analog scale (VAS), the numerical rating pain (NRP) scale, and Short-Form McGill Questionnaire at the start of TENS treatment and at 2 months follow-up. RESULTS: TENS proved beneficial in 69.7% of patients over the course of 2 months. In TENS responsive patients, VAS scores decreased by 9.8 on a 0-100 mm scale (P < 0.001), and NRP scores decreased by 0.8 on a 1-10 scale (P < 0.001). LIMITATIONS: Lack of placebo and lack of blinding of physician and patient. CONCLUSIONS: TENS provides a beneficial adjunct for the treatment of cancer pain, especially when utilized as a goal-directed therapy.

publication date

  • February 25, 2013

Research

keywords

  • Disabled Persons
  • Neoplasms
  • Pain Management
  • Severity of Illness Index
  • Transcutaneous Electric Nerve Stimulation

Identity

Scopus Document Identifier

  • 84932197128

Digital Object Identifier (DOI)

  • 10.1111/pme.12038

PubMed ID

  • 23438255

Additional Document Info

volume

  • 16

issue

  • 6