Vitale Michael G, Matsumoto Hiroko, Roye David P, Gomez Jaime A, Betz Randal R, Emans John B, Skaggs David L, Smith John T, Song Kit M, Campbell Robert M
Division of Pediatric Orthopaedics, Department of Orthopaedic Surgery, College of Physicians and Surgeons, Columbia University, 600 West 168th Street, New York, NY 10032, USA.
J Pediatr Orthop. 2008 Mar;28(2):239-43. doi: 10.1097/BPO.0b013e31816521bb.
The traditional techniques to treat thoracic insufficiency syndrome (TIS) are not able to stabilize or improve chest wall size or pulmonary function while allowing spine growth. To this end, vertical expandable prosthetic titanium rib (VEPTR) was specifically designed to treat TIS by allowing growth of the thoracic cavity and control/correction of spine deformity. The purpose of this study was to determine quality of life (QOL) of children with TIS and its impact on their parents before and after implantation of the VEPTR and also compare these results to those of healthy children.
As part of the original multicenter evaluation of the VEPTR, a Child Health Questionnaire (CHQ) was collected preoperatively on 45 patients who were subsequently treated with expansion thoracoplasty using the VEPTR. The average age was 8.2 +/- 2.6 years, and the parent form of the CHQ was filled out by the primary caretaker. Patients were divided into 3 diagnostic categories: rib fusion (n = 15), hypoplastic thorax syndromes (n = 17), and progressive spinal deformity (n = 13).
There were significant differences between the study patients and healthy children in physical domains. Compared with parents of healthy children, parents of children with TIS experienced more limitations on their time and emotional lives due to their children's health problems. There were no significant differences in CHQ before and after the surgery except for a significant decrease in the self-esteem among a subgroup of patients with hypoplastic thorax syndromes. There were no significant differences in postoperative QOL between patients who had VEPTR-related complications and patients who did not have the complications.
The children with TIS had lower physical scores and higher caregiver burden scores than healthy children. However, the scores in psychosocial domains were similar to those in healthy children. Our study demonstrated that QOL of children and burden of care in their parents remained the same after VEPTR instrumentation. Children's QOL seemed to be not affected by whether they had VEPTR-related complications or not.
治疗胸廓发育不全综合征(TIS)的传统技术无法在允许脊柱生长的同时稳定或改善胸壁尺寸或肺功能。为此,专门设计了垂直可扩张人工钛肋(VEPTR)来治疗TIS,通过扩大胸腔并控制/矫正脊柱畸形来实现。本研究的目的是确定TIS患儿在植入VEPTR前后的生活质量(QOL)及其对父母的影响,并将这些结果与健康儿童的结果进行比较。
作为VEPTR原始多中心评估的一部分,术前收集了45例随后接受VEPTR扩张胸廓成形术治疗患者的儿童健康问卷(CHQ)。平均年龄为8.2±2.6岁,CHQ的家长版由主要照顾者填写。患者分为3个诊断类别:肋骨融合(n = 15)、胸廓发育不全综合征(n = 17)和进行性脊柱畸形(n = 13)。
研究患者与健康儿童在身体领域存在显著差异。与健康儿童的父母相比,TIS患儿的父母因孩子的健康问题在时间和情感生活上受到更多限制。除了胸廓发育不全综合征亚组患者的自尊显著下降外,手术前后CHQ无显著差异。发生VEPTR相关并发症的患者与未发生并发症的患者术后生活质量无显著差异。
TIS患儿的身体得分低于健康儿童,照顾者负担得分高于健康儿童。然而,心理社会领域的得分与健康儿童相似。我们的研究表明,VEPTR植入术后儿童的生活质量和父母的照顾负担保持不变。儿童的生活质量似乎不受是否发生VEPTR相关并发症的影响。