Logan James, Peters Susan E, Strauss Ruby, Manzanero Silvia, Couzens Gregory B, Ross Mark
Brisbane Hand and Upper Limb Research Institute, Brisbane Private Hospital, Wickham Terrace, Brisbane, Queensland, Australia.
Orthopaedic Department, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia.
J Wrist Surg. 2020 Dec;9(6):509-517. doi: 10.1055/s-0040-1714685. Epub 2020 Aug 21.
Pyrocardan trapeziometacarpal interposition implant is a free intra-articular spacer composed of pyrocarbon. This biconcave resurfacing implant, both ligament and bone-stock sparing, is indicated for use in early-to-moderate stage trapeziometacarpal osteoarthritis. It was hypothesized that the postoperative outcome measures of the Pyrocardan implant would be comparable to those seen with ligament reconstruction and tendon interposition (LRTI) surgeries and those reported by the designer of the implant, Phillipe Bellemère, but that strength would be greater than for LRTI. In this prospective case series, 40 Pyrocardan implants were performed in 37 patients. Average age was 58 years (range: 46-71). Patients were assessed preoperatively, 3 months, 6 months, 1 year, 2 years, and beyond (long term) wherever possible. There have been no major complications or revision surgeries for the series. Average follow-up was 29 months (range: 12 months-7 years). Twenty-eight joints were assessed at over 2 years post index surgery. Outcome measure scores improved from preoperative assessment to the most recent follow-up equal or greater than 2 years. Average grip strength at 2 years was 30 kg, as compared with 19.6 kg in an age-matched cohort who underwent trapeziectomy and 25 kg in Bellemère's original series of Pyrocardan implants. Pyrocardan interposition arthroplasty appears to be a safe, effective treatment for trapeziometacarpal arthritis. Patient-reported clinical outcomes were at least equivalent to LRTI and are comparable to Bellemère's original series. Grip and pinch strength appear to be better than LRTI. This is a Level III, prospective observational cohort study.
派罗卡丹大多角骨-第一掌骨间置入植入物是一种由热解碳制成的游离关节内间隔物。这种双凹面表面置换植入物,既能保留韧带又能保留骨量,适用于早中期大多角骨-第一掌骨骨关节炎。研究假设派罗卡丹植入物的术后结果指标将与韧带重建和肌腱置入(LRTI)手术的结果指标以及该植入物设计者菲利普·贝勒梅尔报告的结果指标相当,但强度会大于LRTI。在这个前瞻性病例系列中,对37例患者进行了40次派罗卡丹植入手术。平均年龄为58岁(范围:46 - 71岁)。尽可能在术前、术后3个月、6个月、1年、2年及以后(长期)对患者进行评估。该系列未出现重大并发症或翻修手术。平均随访时间为29个月(范围:12个月 - 7年)。在索引手术后超过2年对28个关节进行了评估。结果指标评分从术前评估到最近一次随访(等于或大于2年)有所改善。2年时的平均握力为30千克,相比之下,接受大多角骨切除术的年龄匹配队列中的平均握力为19.6千克,在贝勒梅尔最初的派罗卡丹植入物系列中为25千克。派罗卡丹置入关节成形术似乎是治疗大多角骨-第一掌骨关节炎的一种安全、有效的方法。患者报告的临床结果至少与LRTI相当,并且与贝勒梅尔最初的系列相当。握力和捏力似乎比LRTI更好。这是一项III级前瞻性观察队列研究。