Pertschuk M J, Whitaker L A
Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia.
Plast Reconstr Surg. 1988 Nov;82(5):741-6. doi: 10.1097/00006534-198811000-00001.
Thirty-four children between the ages of 7 and 15 years with congenital craniofacial anomalies underwent psychosocial evaluation before and 12 to 18 months after surgery. Also evaluated were healthy children matched to the craniofacial subjects by sex, age, intelligence, and economic background. Preoperative assessment revealed the craniofacial group to have multiple but not severe psychosocial limitations. At follow-up, only a measure of social functioning still differentiated the groups, with the craniofacial subjects experiencing more negative social encounters. Comparison of initial and follow-up scores for the craniofacial group revealed a significant reduction in trait anxiety and trends toward reduction in parent-reported inhibited and hyperactive behavior. Scores on measures of extraversion and social functioning tended to be positively correlated with age for the comparison subjects only. Results suggest a modest improvement in psychological adjustment following surgery with a residual, possibly increasing, deficit in social functioning.
34名年龄在7至15岁之间患有先天性颅面畸形的儿童在手术前以及手术后12至18个月接受了社会心理评估。还对在性别、年龄、智力和经济背景方面与颅面畸形患儿相匹配的健康儿童进行了评估。术前评估显示,颅面畸形组存在多种但并不严重的社会心理限制。在随访时,只有一项社会功能指标仍能区分两组,颅面畸形患儿经历了更多负面的社交遭遇。颅面畸形组初始分数与随访分数的比较显示,特质焦虑显著降低,且家长报告的抑制和多动行为有减少趋势。仅在对照组中,外向性和社会功能指标的分数往往与年龄呈正相关。结果表明,手术后心理调适有适度改善,但社会功能仍有残余缺陷,且可能在加重。