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Operationsziel
Durchführung einer periazetabulären Osteotomie (PAO) über einen minimal-invasiven Zugang zur dreidimensionalen Korrektur der Orientierung der Hüftgelenkpfanne.
Indikationen
Symptomatische Hüftdysplasie in der Adoleszenz nach dem Schluss der Y‑Wachstumsfuge und beim Erwachsenen.
Kontraindikationen
Fortgeschrittene Arthrose (Arthrosegrad ≥ 2 nach Tönnis), präformierte Sekundärpfanne, offene Y‑Wachstumsfuge.
Operationstechnik
Über einen minimal-invasiven Zugang wird eine periazetabuläre Osteotomie durchgeführt.
Ergebnisse
Insgesamt wurden 39 Patienten über 3,5 (3 bis 4,5) Jahre nachbeobachtet. Der laterale Centrum-Erker-Winkel nach Wiberg konnte signifikant von 16,1° (7–24°) auf 30,5° (25–37°) (p < 0,0001), der Tragflächenwinkel von 13,2° (2–25,3°) auf 2,8° (−3–13°) (p < 0,0001) korrigiert werden. Die mittlere Operationszeit betrug 88 (57 bis 142) Minuten. Es traten keine schweren Komplikationen auf.
Background:
Arthroscopic treatment of femoroacetabular impingement syndrome (FAIS) has become a common procedure. However, meaningful long-term clinical outcomes have not been defined.
Purpose:
To define the minimal clinically important difference (MCID), substantial clinical benefit (SCB), and patient acceptable symptomatic state (PASS) for the modified Harris Hip Score (mHHS) at a minimum 10-year follow-up in patients undergoing arthroscopic treatment for FAIS and identify preoperative predictors for achievement of the MCID, SCB, and PASS.
Study Design:
Case-control study; Level of evidence, 3.
Methods:
A consecutive series of patients undergoing arthroscopic treatment for FAIS between 2007 and 2009 with a minimum 10-year follow-up was analyzed. Patient data included patient characteristics, radiographic parameters, and the pre- and postoperative mHHS and visual analog scale (VAS) for pain score. Paired t tests were used to compare the patient-reported outcome measures (PROMs). The MCID was determined by calculating half of the standard deviation, and SCB and PASS were calculated by the anchor method. Correlation and logistic regression analyses were conducted to identify predictors for the achievement of the MCID, SCB, and PASS.
Results:
A total of 44 patients (27 men, 17 women) were included. The mean age and body mass index were 42.2 years (range, 16-67 years) and 22.3 kg/m2 (range, 16.76-29.78 kg/m2), respectively. The MCID, absolute SCB, net change SCB, and PASS of the mHHS were calculated to be 19.6, 90.1, 31.5, and 84.4 points, respectively. Preoperative symptom duration was identified as an independent predictor for the achievement of meaningful clinical outcomes. The median symptom durations for patients who achieved the MCID, absolute SCB, net change SCB, and PASS were 11.7, 9.1, 9.0, and 10.8 months, respectively. The median symptom duration for patients who did not achieve the MCID, absolute SCB, net change SCB, and PASS were 15.8, 17.4, 17.3, and 18.4 months, respectively. No other statistically significant correlations were found.
Conclusion:
The preoperative duration of symptoms was identified as an independent predictor for achievement of the MCID, SCB, and PASS. These findings can be helpful in accelerating the transition to surgical treatment of FAIS.