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大多数纤维性骨发育不良性骨化性肌炎患者的骨折经非手术治疗后愈合,且很少出现发作、异位骨化和活动度丧失。

Most Fractures Treated Nonoperatively in Individuals With Fibrodysplasia Ossificans Progressiva Heal With a Paucity of Flareups, Heterotopic Ossification, and Loss of Mobility.

机构信息

Department of Orthopaedic Surgery, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA, USA.

The Center for Research in FOP and Related Disorders, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Clin Orthop Relat Res. 2023 Dec 1;481(12):2447-2458. doi: 10.1097/CORR.0000000000002672. Epub 2023 May 8.

Abstract

BACKGROUND

Fibrodysplasia ossificans progressiva (FOP) is an ultrarare genetic disorder with episodic and progressive heterotopic ossification. Tissue trauma is a major risk factor for flareups, heterotopic ossification (HO), and loss of mobility in patients with FOP. The International Clinical Council on FOP generally recommends avoiding surgery in patients with FOP unless the situation is life-threatening, because soft tissue injury can trigger an FOP flareup. Surprisingly little is known about flareups, HO formation, and loss of mobility after fractures of the normotopic (occurring in the normal place, distinct from heterotopic) skeleton when treated nonoperatively in patients with FOP.

QUESTIONS/PURPOSES: (1) What proportion of fractures had radiographic evidence of union (defined as radiographic evidence of healing at 6 weeks) or nonunion (defined as the radiographic absence of a bridging callus at 3 years after the fracture)? (2) What proportion of patients had clinical symptoms of an FOP flareup because of the fracture (defined by increased pain or swelling at the fracture site within several days after closed immobilization)? (3) What proportion of patients with fractures had radiographic evidence of HO? (4) What proportion of patients lost movement after a fracture?

METHODS

We retrospectively identified 36 patients with FOP from five continents who sustained 48 fractures of the normotopic skeleton from January 2001 to February 2021, who were treated nonoperatively, and who were followed for a minimum of 18 months after the fracture and for as long as 20 years, depending on when they sustained their fracture during the study period. Five patients (seven fractures) were excluded from the analysis to minimize cotreatment bias because these patients were enrolled in palovarotene clinical trials (NCT02190747 and NCT03312634) at the time of their fractures. Thus, we analyzed 31 patients (13 male, 18 female, median age 22 years, range 5 to 57 years) who sustained 41 fractures of the normotopic skeleton that were treated nonoperatively. Patients were analyzed at a median follow-up of 6 years (range 18 months to 20 years), and none was lost to follow-up. Clinical records for each patient were reviewed by the referring physician-author and the following data for each fracture were recorded: biological sex, ACVR1 gene pathogenic variant, age at the time of fracture, fracture mechanism, fracture location, initial treatment modality, prednisone use at the time of the fracture as indicated in the FOP Treatment Guidelines for flare prevention (2 mg/kg once daily for 4 days), patient-reported flareups (episodic inflammatory lesions of muscle and deep soft connective tissue characterized variably by swelling, escalating pain, stiffness, and immobility) after the fracture, follow-up radiographs of the fracture if available, HO formation (yes or no) as a result of the fracture determined at a minimum of 6 weeks after the fracture, and patient-reported loss of motion at least 6 months after and as long as 20 years after the fracture. Postfracture radiographs were available in 76% (31 of 41) of fractures in 25 patients and were independently reviewed by the referring physician-author and senior author for radiographic criteria of fracture healing and HO.

RESULTS

Radiographic healing was noted in 97% (30 of 31) of fractures at 6 weeks after the incident fracture. Painless nonunion was noted in one patient who sustained a displaced patellar fracture and HO. In seven percent (three of 41) of fractures, patients reported increased pain or swelling at or near the fracture site within several days after fracture immobilization that likely indicated a site-specific FOP flareup. The same three patients reported a residual loss of motion 1 year after the fracture compared with their prefracture status. HO developed in 10% (three of 31) of the fractures for which follow-up radiographs were available. Patient-reported loss of motion occurred in 10% (four of 41) of fractures. Two of the four patients reported noticeable loss of motion and the other two patients reported that the joint was completely immobile (ankylosis).

CONCLUSION

Most fractures treated nonoperatively in individuals with FOP healed with few flareups, little or no HO, and preservation of mobility, suggesting an uncoupling of fracture repair and HO, which are two inflammation-induced processes of endochondral ossification. These findings underscore the importance of considering nonoperative treatment for fractures in individuals with FOP. Physicians who treat fractures in patients with FOP should consult with a member of the International Clinical Council listed in the FOP Treatment Guidelines ( https://www.iccfop.org ).

LEVEL OF EVIDENCE

Level IV, therapeutic study.

摘要

背景

纤维性骨发育不良(FOP)是一种超罕见的遗传疾病,具有间歇性和进行性异位骨化。组织创伤是 FOP 患者发作、异位骨化(HO)和活动能力丧失的主要危险因素。国际 FOP 临床理事会通常建议 FOP 患者除非危及生命,否则避免手术,因为软组织损伤会引发 FOP 发作。令人惊讶的是,对于 FOP 患者非手术治疗的正常(发生在正常位置,与异位不同)骨骼骨折后发作、HO 形成和活动能力丧失的了解甚少。

问题/目的:(1)有多少比例的骨折有影像学证据表明愈合(定义为骨折后 6 周有愈合的影像学证据)或不愈合(定义为骨折后 3 年无桥接骨痂的影像学证据)?(2)有多少比例的患者因骨折出现 FOP 发作的临床症状(定义为骨折后几天内骨折部位疼痛或肿胀增加)?(3)有多少比例的骨折患者有影像学证据表明 HO?(4)有多少比例的患者在骨折后失去活动能力?

方法

我们从五个大陆回顾性地确定了 36 名患有 FOP 的患者,他们在 2001 年 1 月至 2021 年 2 月期间发生了 48 处正常骨骼的骨折,这些骨折均采用非手术治疗,骨折后至少随访 18 个月,最长随访 20 年,具体取决于骨折发生在研究期间的时间。为了尽量减少共同治疗的偏倚,我们将 5 名患者(7 处骨折)排除在分析之外,因为这些患者在骨折时参加了 palovarotene 临床试验(NCT02190747 和 NCT03312634)。因此,我们分析了 31 名患者(13 名男性,18 名女性,中位年龄 22 岁,年龄范围为 5 岁至 57 岁)的 41 处正常骨骼骨折,这些骨折均采用非手术治疗。患者的中位随访时间为 6 年(范围为 18 个月至 20 年),无失访患者。由转诊医生作者对每位患者的临床记录进行了回顾,并记录了每位骨折患者的以下数据:生物学性别、ACVR1 基因致病性变异、骨折时的年龄、骨折机制、骨折部位、初始治疗方式、骨折时 FOP 治疗指南中预防性使用泼尼松(每天 2mg/kg,连续 4 天)、骨折后患者报告的发作(以肌肉和深部软组织的炎症性病变为特征,表现为肿胀、疼痛加剧、僵硬和活动能力丧失)、如果有随访的骨折 X 线片、骨折后至少 6 周确定的 HO 形成(是或否)以及骨折后至少 6 个月和最长 20 年的患者报告的运动丧失。在 25 名患者中的 20 名患者中获得了 76%(31 处)骨折的随访 X 线片,由转诊医生作者和资深作者独立对骨折愈合和 HO 的放射学标准进行了回顾。

结果

在骨折后 6 周时,97%(30/31)的骨折有影像学愈合。1 名患者发生髌骨骨折移位,HO 形成和无痛性不愈合。在 7%(3/41)的骨折中,患者在骨折固定后几天内报告骨折部位或附近出现疼痛或肿胀,这可能表明存在特定于 FOP 的发作。这 3 名患者在骨折后 1 年报告了残留的运动丧失,与骨折前的状态相比。有 10%(3/31)的随访 X 线片有骨折的 HO 形成。41 处骨折中有 10%(4/41)的患者报告运动丧失。其中 2 名患者报告明显运动丧失,另外 2 名患者报告关节完全僵硬(关节强直)。

结论

在 FOP 患者中,大多数非手术治疗的骨折愈合良好,发作、HO 和活动能力丧失的发生率较低,这表明骨折修复和 HO 之间存在脱耦,HO 是两种炎症诱导的软骨内骨化过程。这些发现强调了考虑对 FOP 患者的骨折进行非手术治疗的重要性。治疗 FOP 患者骨折的医生应咨询 FOP 治疗指南中列出的国际 FOP 临床理事会成员(https://www.iccfop.org)。

证据水平

IV 级,治疗性研究。

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