German Joint Centre, ATOS Clinic Heidelberg, Bismarckstraße 9, 69115, Heidelberg, Germany.
Institution for Medical Biometrics, Heidelberg University Hospital, INF 130.3, 69120, Heidelberg, Germany.
Arch Orthop Trauma Surg. 2023 Aug;143(8):4853-4860. doi: 10.1007/s00402-023-04802-4. Epub 2023 Feb 16.
One current trend in the field of shoulder arthroplasty is a design shift to shorter and metaphyseal fixed humeral stem components. The aim of this investigation is to analyze complications resulting in revision surgery after anatomic (ASA) and reverse (RSA) short stem arthroplasty. We hypothesize that complications are influenced by the type of prosthesis and indication for arthroplasty.
A total of 279 short stem shoulder prostheses were implanted by the same surgeon (162 ASA; 117 RSA), and 223 of these prostheses were implanted as primary procedures; in 54 cases, arthroplasty was performed secondary to prior open surgery. Main indications were osteoarthritis (OA) (n = 134), cuff tear arthropathy (CTA) (n = 74) and posttraumatic deformities (PTr) (n = 59). Patients were evaluated at 6 weeks (follow-up 1; FU1), 2 years (FU2) and the time span of the last follow-up defined as FU3 with a minimum FU of 2 years. Complications were categorized into early complications (within FU1), intermediate complications (within FU2) and late complications (> 2 years; FU3).
In total, 268 prostheses (96.1%) were available for FU1; 267 prostheses (95.7%) were available for FU2 and 218 prostheses (77.8%) were available for FU3. The average time for FU3 was 53.0 months (range 24-95). A complication leading to revision occurred in 21 prostheses (7.8%), 6 (3.7%) in the ASA group and 15 (12.7%) in the RSA group (p < 0.005). The most frequent cause for revision was infection (n = 9; 42.9%). After primary implantation, 3 complications (2.2%) occurred in the ASA and 10 complications (11.0%) in the RSA group (p < 0.005). The complication rate was 2.2% in patients with OA, 13.5% in CTA and 11.9% in PTr.
Primary reverse shoulder arthroplasty had a significantly higher rate of complications and revisions than primary and secondary anatomic shoulder arthroplasty, respectively. Therefore, indications for reverse shoulder arthroplasty should be critically questioned in each individual case.
在肩关节置换领域,目前的一个趋势是设计向更短的干骺端固定肱骨干假体转变。本研究旨在分析解剖型(ASA)和反式(RSA)短柄肩关节假体置换术后导致翻修手术的并发症。我们假设并发症与假体类型和关节置换适应证有关。
由同一位医生(162 例 ASA;117 例 RSA)共植入 279 例短柄肩关节假体,其中 223 例为初次手术植入;54 例为初次手术后翻修。主要适应证为骨关节炎(OA)(n=134)、肩袖撕裂性关节炎(CTA)(n=74)和创伤后畸形(PTr)(n=59)。患者在术后 6 周(随访 1;FU1)、2 年(FU2)和最后一次随访时间(FU3)进行评估,最后一次随访时间定义为至少 2 年的 FU3。并发症分为早期并发症(FU1 内)、中期并发症(FU2 内)和晚期并发症(>2 年;FU3)。
共有 268 例假体(96.1%)可用于 FU1;267 例假体(95.7%)可用于 FU2,218 例假体(77.8%)可用于 FU3。FU3 的平均时间为 53.0 个月(范围 24-95)。21 例(7.8%)发生导致翻修的并发症,其中 ASA 组 6 例(3.7%),RSA 组 15 例(12.7%)(p<0.005)。最常见的翻修原因是感染(n=9;42.9%)。初次植入后,ASA 组有 3 例(2.2%)和 RSA 组有 10 例(11.0%)并发症(p<0.005)。OA 患者的并发症发生率为 2.2%,CTA 为 13.5%,PTr 为 11.9%。
初次 RSA 肩关节置换的并发症和翻修率明显高于初次 ASA 和 RSA 肩关节置换。因此,在每例患者中都应严格考虑 RSA 肩关节置换的适应证。