• Hauke Horstmann, Roman Karkosch, Annika Berg, Christoph Becher, Maximilian Petri, and Tomas Smith.
• Department of Orthopaedic Surgery, Diakovere Annastift, Hannover Medical School, Anna-von-Borries-Str. 1-7, 30625, Hannover, Germany. hauke.horstmann@diakovere.de.
• Arch Orthop Trauma Surg. 2022 Aug 1; 142 (8): 201120172011-2017.

PurposeReconstruction of the medial patellofemoral ligament (MPFL) is an established procedure to restore patellar stability. Aim of this study is to evaluate the results of a dynamic MPFL reconstruction technique in a large university hospital setting.MethodsTwo hundred and thirteen consecutive patients with 221 knees were surgically treated for recurrent lateral patellar dislocation. All patients obtained dynamic reconstruction of the MPFL with detachment of the gracilis tendon at the pes anserinus while maintaining the proximal origin at the gracilis muscle. Patellar fixation was performed by oblique transpatellar tunnel transfer. Follow-up data including Kujala and BANFF score, pain level as well as recurrent patella instability were collected at a minimum follow-up of 2 years.ResultsFollow-up could be obtained from 158 patients (71%). The mean follow-up time was 5.4 years. Mean pain level was 1.9 ± 2.0 on the VAS. Mean Kujala score was 78.4 ± 15.5. Mean BANFF score was 62.4 ± 22.3. MPFL-reconstructions that were performed by surgeons with a routine of more than ten procedures had a significantly shorter surgical time 52.3 ± 17.6 min. Male patients yielded higher satisfaction rates and better clinical scores compared to females. Complications occurred in 27.2% of procedures, 20.9% requiring revision surgery of which were 9.5% related to recurrent patellar instability. 78% of all patients indicated they would undergo the procedure again.ConclusionDynamic MPFL reconstruction presents a reproducible procedure with increased complication rates, inferior to the results of static reconstruction described in the literature. Despite, it appears to be an efficient procedure to restore patellar stability in a large university hospital setting, without the necessity for intraoperative fluoroscopy.Trial RegistrationThe study was registered in ClinicalTrials.gov with the registration number NCT04438109 on June 18th 2020.© 2021. The Author(s).

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