Takeoka Yoshiki, Kakutani Kenichiro, Miyamoto Hiroshi, Suzuki Teppei, Yurube Takashi, Komoto Izumi, Ryu Masao, Satsuma Shinichi, Uno Koki
Department of Orthopaedic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Department of Orthopaedic Surgery, National Hospital Organization Kobe Medical Center, Kobe, Japan.
Neurospine. 2021 Dec;18(4):778-785. doi: 10.14245/ns.2142720.360. Epub 2021 Dec 31.
To clarify the complications of posterior fusion for atlantoaxial instability (AAI) in children with Down syndrome and to discuss the significance of surgical intervention.
Twenty pediatric patients with Down syndrome underwent posterior fusion for AAI between February 2000 and September 2018 (age, 6.1 ± 1.9 years). C1-2 or C1-3 fusion and occipitocervical fusion were performed in 14 and 6 patients, respectively. The past medical history, operation time, estimated blood loss (EBL), duration of Halo vest immobilization, postoperative follow-up period, and intra- and perioperative complications were examined.
The operation time was 257.9 ± 55.6 minutes, and the EBL was 101.6 ± 77.9 mL. Complications related to the operation occurred in 6 patients (30.0%). They included 1 major complication (5.0%): hydrocephalus at 3 months postoperatively, possibly related to an intraoperative dural tear. Other surgery-related complications included 3 cases of superficial infections, 1 case of bone graft donor site deep infection, 1 case of C2 pedicle fracture, 1 case of Halo ring dislocation, 1 case of pseudoarthrosis that required revision surgery, and 1 case of temporary neurological deficit after Halo removal at 2 months postoperatively. Complications unrelated to the operation included 2 cases of respiratory infections and 1 case of implant loosening due to a fall at 9 months postoperatively.
The complication rate of upper cervical fusion in patients with Down syndrome remained high; however, major complications decreased substantially. Improved intra- and perioperative management facilitates successful surgical intervention for upper cervical instability in pediatric patients with Down syndrome.
阐明唐氏综合征患儿寰枢椎不稳(AAI)后路融合术的并发症,并探讨手术干预的意义。
2000年2月至2018年9月期间,20例唐氏综合征患儿因AAI接受了后路融合术(年龄6.1±1.9岁)。其中14例患者进行了C1-2或C1-3融合术,6例患者进行了枕颈融合术。对既往病史、手术时间、估计失血量(EBL)、头环背心固定时间、术后随访时间以及术中和围手术期并发症进行了检查。
手术时间为257.9±55.6分钟,EBL为101.6±77.9毫升。6例患者(30.0%)发生了与手术相关的并发症。其中包括1例严重并发症(5.0%):术后3个月出现脑积水,可能与术中硬脑膜撕裂有关。其他与手术相关的并发症包括3例浅表感染、1例骨移植供区深部感染、1例C2椎弓根骨折、1例头环脱位、1例需要翻修手术的假关节形成以及1例术后2个月拆除头环后出现的短暂神经功能缺损。与手术无关的并发症包括2例呼吸道感染和1例术后9个月因跌倒导致的植入物松动。
唐氏综合征患者上颈椎融合术的并发症发生率仍然很高;然而,严重并发症大幅减少。术中和围手术期管理的改善有助于唐氏综合征小儿患者上颈椎不稳的成功手术干预。