The Effectiveness of a Non-Invasive Shot Blocking Device for Reducing Pain of In-office Injections in Hand Surgery.
Brian D RinkerDavid A AtashrooMegan A StoutF Ryan WermelingPublished in: Hand (New York, N.Y.) (2019)
Background: The gate control theory asserts that non-painful stimuli can block pain perception. The ShotBlockerâ„¢ device is a plastic disk with blunt projections that rests on the skin, and we hypothesize that it will reduce pain during hand injections. Methods: This is a prospective randomized trial of 117 patients undergoing injections for common hand conditions. Patients were randomized into 3 groups: device, placebo (device with projections removed), and control. Patients recorded on an analog pain scale the pain severity of the injection, as well as their most recent tetanus shot. A normalized pain score was obtained from the difference between the injection and tetanus shot pain scores. The mean non-normalized and normalized scores for each treatment group were compared to the control group using the Wilcoxon signed rank test. Results: There were 91 women and 26 men. Common diagnoses included trigger finger (n = 53), DeQuervain's tendonitis (n = 33), and basal joint arthritis (n = 22). The groups did not differ significantly in age, gender, or diagnosis. Mean pain score in the device group was 5.2 out of 10, and it was 5.7 for the control group. The normalized pain score in the device group was significantly lower than the control group. Normalized and non-normalized pain scores for the placebo group were not significantly lower than the control group. Conclusions: The shot blocking device effectively reduced pain of injection versus controls when pain scores were normalized for pain tolerance. The modified device did not reduce the pain of injection, suggesting that gate control is the mechanism of action.
Keyphrases
- chronic pain
- pain management
- neuropathic pain
- patients undergoing
- type diabetes
- rheumatoid arthritis
- ejection fraction
- mental health
- acute coronary syndrome
- pregnant women
- chronic kidney disease
- percutaneous coronary intervention
- study protocol
- polycystic ovary syndrome
- patient reported outcomes
- placebo controlled
- wound healing