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Femoroacetabular impingement surgery leads to early pain relief but minimal functional gains past 6 months: experience from the FIRST trial

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Knee Surgery, Sports Traumatology, Arthroscopy Aims and scope

Abstract

Purpose

To understand the early outcomes after hip arthroscopy and better define the trajectory of improvement in a prospective cohort of patients who have undergone hip arthroscopic osteochondroplasty for femoroacetabular impingement (FAI) syndrome.

Methods

Data were analyzed from the Femoroacetabular Impingement RandomiSed controlled Trial (FIRST) on the 108 study patients who underwent osteochondroplasty, with or without labral repair. Study outcomes included patient-reported pain (using a 100-point Visual Analogue Scale (VAS)), hip function (using the Hip Outcome Score (HOS) and International Hip Outcome Tool (iHOT-12)), and health-related quality of life (using the EuroQol 5 Dimensions (EQ-5D)) measured at baseline, 2 weeks, 3 months, 6 months, and 12 months post-operatively.

Results

There was a decrease in mean post-operative pain VAS scores from baseline. The first 2 weeks post-operative yielded the greatest reduction in pain with a mean (SD) VAS score of 37.8 (23.4), with score stabilization between 6 months (26.9 (26.9)) and 12 months (25.3 (27.6)). Mean HOS (activities of daily living) scores improved from baseline (59.7 (16.2)) starting at 6 weeks post-operative (64.1 (19.1)). The HOS (Sports) showed no improvement from baseline (41.2 (20.4)) until 3 months (49.1 (27.9)), and continued to improve at 6 months (64.1 (28.7)) and 12 months (68.6 (30.5)). The iHOT-12 scores showed functional improvement from baseline (31.3 (18.8)), as early as 6 weeks (44.9 (22.4)) up to and including 12 months (67.1 (29.7)). EQ-5D index scores showed modest steady improvement from 6 weeks to 12 months post-operative, while the EQ-5D VAS component similarly showed modest and steady improvements from 3 months onward.

Conclusion

Results from this study highlight that hip arthroscopic osteochondroplasty with or without labral repair for FAI leads to early pain relief. While all scores improved from baseline, functional gains appear to plateau from 6 months onwards. These data can be used to inform decision-making about timelines for rehabilitation and return to sport, a knowledge gap in the current FAI literature.

Level of evidence

II.

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Abbreviations

FAI:

Femoroacetabular impingement

FIRST:

Femoroacetabular Impingement RandomiSed controlled Trial

RCT:

Randomized controlled trial

VAS:

Visual analogue scale

HOS-ADL:

Hip outcome score-activities of daily living

HOS-Sports:

Hip outcome score-sports subscale

iHOT-12:

International hip outcome tool-12

MCID:

Minimum clinically important difference

EQ-5D:

Euro-Qol 5 dimensions

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Acknow̄ledgements

Writing Committee: Olufemi R. Ayeni MD, MSc, PhD, FRCSC (Chair, McMaster University), Jon Karlsson MD, PhD (University of Gothenburg), Diane Heels-Ansdell MSc (McMaster University), Lehana Thabane PhD (McMaster University), Volker Musahl MD (University of Pittsburgh), Nicole Simunovic MSc (McMaster University), Andrew Duong MSc (McMaster University), and Mohit Bhandari MD, PhD, FRCSC (McMaster University) .

Steering Committee: Olufemi R. Ayeni (Chair, McMaster University), Mohit Bhandari (Co-Chair, McMaster University), Asheesh Bedi (University of Michigan), Teppo Järvinen (University of Helsinki), Volker Musahl (University of Pittsburgh), Douglas Naudie (University of Western Ontario), Matti Seppänen MD (Turku University), Gerard Slobogean (University of Maryland, Baltimore), Lehana Thabane (McMaster University) .

Methods Centre: Olufemi R. Ayeni (Principal Investigator); Nicole Simunovic (Research Manager); Andrew Duong, Matthew Skelly, Ajay Shanmugaraj, Sarah Crouch (Project Management); Sheila Sprague (Research Methodologist); Diane Heels-Ansdell, (Statistical Analysis); Lisa Buckingham (Data Management) (McMaster University) .

Data and Safety Monitoring Committee: Tim Ramsay (Chair, Ottawa Hospital Research Institute), John Lee (University of Toronto), Petteri Kousa (Sports Clinic Hospital Dextra) .

Adjudication Committee: Sasha Carsen (Chair, University of Ottawa), Hema Choudur (Hamilton Health Sciences), Yan Sim (McMaster University), Kelly Johnston (University of Calgary) .

Participating Clinical Sites Canada: McMaster University Medical Centre (Hamilton, ON) – Olufemi R. Ayeni MD, PhD, FRCSC; Sarah Crouch BSc (Pharm); Andrew Duong MSc; Ajay Shanmugaraj BSc; Nicole Simunovic MSc; Matthew Skelly BSc; Sheila Sprague PhD. Dalhousie University (Halifax, NS) – Ivan Wong MD, FRCSC, Dip. Sports Medicine, MACM; Ryland Murphy BSc; Sara Sparavalo MASc. St. Michael’s Hospital (Toronto, ON) – Daniel Whelan MD, MSc, FRCSC; Ryan Khan BA, CCRP. Kingston Health Sciences Centre (Kingston, ON) – Gavin CA Wood MBChB, FRCS; Fiona Howells BPharm; Heather Grant MSc. London Health Sciences Centre (London, ON) – Douglas Naudie MD, MSc, FRCSC; Bryn Zomar MSc; Michael Pollock MSc. Fowler Kennedy Sport Medicine Clinic (London, ON) – Kevin Willits MD, FRCSC; Andrew Firth MSc; Stacey Wanlin; Alliya Remtulla MSc; Nicole Kaniki PhD. CHU de Québec-Université Laval (Quebec City, QC) – Etienne L. Belzile MD; Sylvie Turmel RN.

International: Odense University Hospital (Odense, Denmark) – Uffe Jørgensen MD, Dr. Med Sci; Annie Gam-Pedersen RN. Tays Hatanpää (Tampere University Hospital, Tampere, Finland) – Raine Sihvonen MD, PhD; Marko Raivio MD; Pirjo Toivonen PT. Turku University Hospital (Turku, Finland) - Matti Seppänen MD; Mari Pirjetta Routapohja RN.

Post-Trial Statement: The Methods Centre at McMaster University coordinated the trial. The Methods Centre was responsible for programming trial randomization, the maintenance of the database, data validation, data analyses, and study-centre coordination. The Steering Committee designed the trial, some members assisted with developing the statistical analysis plan, and vouch for the completeness and accuracy of the data and analyses. OR Ayeni, the first author and chair of the writing committee, wrote the first draft of the manuscript; the writing committee made revisions.

Funding

Research grants for the FIRST trial were received from the Canadian Institutes of Health Research (CIHR) (PI: ORA, MB), American Orthopaedic Society for Sports Medicine (PI: ORA), Canadian Orthopaedic Foundation (PI: ORA, MB), McMaster Surgical Associates (PI: ORA, MB), and Hamilton Health Sciences Department of Surgery (PI: ORA).

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Contributions

MA participated in data interpretation, statistical analysis, and drafted the manuscript. NS was involved in study design, data acquisition, data analysis, and revising the manuscript. DHA was involved in data acquisition and statistical analysis. OA conceived the study and participated in revision of the manuscript.

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Correspondence to Olufemi R. Ayeni.

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Conflict of interest

Dr. Ayeni serves on the speakers bureau for ConMed and Stryker, and sits on the editorial boards for The American Journal of Sports Medicine, and BMC Musculoskeletal Disorders.

Ethical approval

The FIRST trial was approved by the Hamilton Integrated Research Ethics Board (12-396) before it started. All participating centres obtained their own site-specific ethics approval before starting the trial. All participants provided written informed consent.

Informed consent

Written informed consent was obtained by study personnel from all patients enrolled in the FIRST trial.

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Almasri, M., Simunovic, N., Heels-Ansdell, D. et al. Femoroacetabular impingement surgery leads to early pain relief but minimal functional gains past 6 months: experience from the FIRST trial. Knee Surg Sports Traumatol Arthrosc 29, 1362–1369 (2021). https://doi.org/10.1007/s00167-020-06401-x

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