Use of an adaptive sensory environment in patients with autism spectrum disorder (ASD) in the perioperative environment: a parallel, randomized controlled trial

被引:0
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作者
Antosh, Sean [1 ,2 ]
Drennan, Chelsea [3 ]
Stolfi, Adrienne [2 ]
Lawson, Robin [3 ]
Huntley, Elise [4 ]
McCullough-Roach, Reaundra [5 ]
Hill, Madelyn [3 ]
Adelekan, Tahira [2 ,6 ]
Vachhrajani, Shobhan [2 ,3 ,7 ]
机构
[1] Dayton Childrens Hosp, Dept Anesthesia, One Childrens Plaza, Dayton, OH 45404 USA
[2] Wright State Univ, Boonshoft Sch Med, Dayton Childrens Hosp, Dept Pediat, One Childrens Plaza, Dayton, OH 45404 USA
[3] Dayton Childrens Hosp, Dept Surg, One Childrens Plaza, Dayton, OH 45404 USA
[4] Dayton Children s Hosp, Dept Child Life, One Childrens Plaza, Dayton, OH 45404 USA
[5] Wright State Univ, Boonshoft Sch Med, 3640 Colonel Glenn Hwy, Dayton, OH 45435 USA
[6] Dayton Childrens Hosp, Div Dev Pediat, One Childrens Plaza, Dayton, OH 45404 USA
[7] Dayton Childrens Hosp, Dept Neurosurg, One Childrens Plaza, Dayton, OH 45404 USA
来源
关键词
Autism spectrum disorder (ASD); Perioperative anxiety; Adaptive sensory environment; Randomized controlled trial (RCT); ORAL CARE; PREOPERATIVE ANXIETY; CHILDREN; ANESTHESIA; MANAGEMENT; EXPERIENCES; INDUCTION; SCALE;
D O I
10.1016/j.lana.2024.100736
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background Patients with autism spectrum disorders (ASD) experience higher rates of perioperative anxiety and are likely to receive premedication. Little is known about nonpharmaceutical interventions which may decrease anxiety. This study aims to evaluate the use of an adaptive sensory environment (ASE) to reduce ASD patient anxiety during the perioperative process. Methods Our feasibility study (ClinicalTrials.gov NCT04994613) enrolled 60 patients in two parallel groups randomized to a control (no ASE) or intervention group (ASE). We included all surgical patients aged three to twelve years, with a formal diagnosis of ASD, Asperger's ' s Syndrome, or pervasive developmental disorder not otherwise specified. fi ed. Preoperative behaviors were recorded by an unblinded nurse utilizing the validated Modified fi ed Yale Preoperative Anxiety Scale (mYPAS). The difference in score on the mYPAS was the primary outcome, and an intention-to-treat analysis was employed. A generalized estimating equations model was used to compare mYPAS scores controlling for significant fi cant independent variables. Findings 58 patients were analyzed after 1:1 randomization of 30 patients to each group. Groups were balanced except the median number of intra operative pain medications was significantly fi cantly lower in the ASE group (1 vs. 3, p = 0.012). Mean (SD) age for all patients was 7.2 (2.9) years, range 2.6-12.7. - 12.7. 72.4% (42/58) were White and all were Non-Hispanic or Latino. 74% were Male (21/30 ASE and 22/28 Control) and 26% were Female (9/30 ASE and 6/28 Control). No differences were found in mYPAS scores between groups at three time periods (43.5 vs. 42, p = 0.88, 47.8 vs. 48.4, p = 0.76, and 36.4 vs. 43.8, p = 0.15, ASE vs. control group, respectively). The ASE group had a significant fi cant within-group decrease in mY PAS scores from nursing intake to transition (p = 0.030). Interpretation An ASE did not significantly fi cantly reduce perioperative anxiety. However, the promising results deserve further investigation.
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页数:10
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