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Virtual Reality Analgesia for Children With Large Severe Burn Wounds During Burn Wound Debridement
被引:32
|作者:
Hoffman, Hunter G.
[1
,2
,3
]
Patterson, David R.
[4
]
Rodriguez, Robert A.
[5
,6
]
Pena, Raquel
[5
,6
]
Beck, Wanda
[6
]
Meyer, Walter J.
[3
,5
,6
]
机构:
[1] Univ Washington, Coll Engn, Dept Mech Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Psychol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Radiol, Seattle, WA 98195 USA
[4] Univ Washington, Dept Rehabil Med, Seattle, WA USA
[5] Univ Texas Med Branch Galveston, Galveston, TX USA
[6] Shriners Hosp Children Galveston, Galveston, TX USA
来源:
关键词:
virtual reality;
pain;
pediatric burn injuries;
analgesia;
burn;
opioid;
ADJUNCTIVE PAIN-CONTROL;
PHYSICAL-THERAPY;
DISTRACTION;
MECHANISMS;
MANAGEMENT;
MAGNITUDE;
PATIENT;
HELMET;
TRIALS;
MOTION;
D O I:
10.3389/frvir.2020.602299
中图分类号:
TP31 [计算机软件];
学科分类号:
081202 ;
0835 ;
摘要:
The objective of this study was to compare the effect of adjunctive virtual reality vs. standard analgesic pain medications during burn wound cleaning/debridement. Participants were predominantly Hispanic children aged 6-17 years of age, with large severe burn injuries (TBSA = 44%) reporting moderate or higher baseline pain during burn wound care. Using a randomized between-groups design, participants were randomly assigned to one of two groups, (a) the Control Group = pain medications only or (b) the VR Group = pain medications + virtual reality. A total of 50 children (88% Hispanic) with large severe burns (mean TBSA > 10%) received severe burn wound cleaning sessions. For the primary outcome measure of worst pain (intensity) on Study Day 1, using a between groups ANOVA, burn injured children in the group that received virtual reality during wound care showed significantly less pain intensity than the No VR control group, [mean worst pain ratings for the No VR group = 7.46 (SD = 2.93) vs. 5.54 (SD = 3.56), F-(1,F-48) = 4.29, < 0.05, MSE = 46.00]. Similarly, one of the secondary pain measures, "lowest pain during wound care" was significantly lower in the VR group, No VR = 4.29 (SD = 3.75) vs. 1.68 (2.04) for the VR group, F-(1,F-47) = 9.29, <0.005, MSE = 83.52 for Study Day 1. The other secondary pain measures showed the predicted pattern on Study Day 1, but were non-significant. Regarding whether VR reduced pain beyond Study Day 1, absolute change in pain intensity (analgesia = baseline pain minus the mean of the worst pain scores on Study days 1-10) was significantly greater for the VR group, F-(1,F-48) = 4.88, p < 0.05, MSE = 34.26, partial eta squared = 0.09, but contrary to predictions, absolute change scores were non-significant for all secondary measures.
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