Haltbarkeit von Suppl. Stabkonstrukte – ergänzende Stabtechnik für langsegmentige posteriore instrumentierte Wirbelsäulenfusionen
Haltbarkeit von ergänzenden Stabkonstruktionen – SuppleMentAry Rod Technique (SMART) – für langsegmentige posteriore instrumentierte Wirbelsäulenfusionsverfahren: Eine multizentrische retrospektive Vergleichsstudie mit Doppelstabkonstruktionen
This is a multicenter retrospective comparative cohort study. The index surgery for this study is primary or revision long-segment posterior thoracolumbar (TL) instrumented fusion using either a supplementary rod construct or a dual-rod construct. Eligible patients who already had index surgery, will be identified for enrollment through a review of medical records of the participating surgeons at the study sites.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
This multicenter retrospective comparative cohort study will enroll 1244 patients, who underwent primary or revision long-segment posterior thoracolumbar (TL) instrumented fusion using either a supplementary rod construct or a dual-rod construct. By comparing two groups of patients, ie, patients treated with supplementary rod constructs vs dual-rod constructs, in the setting of long-segment posterior instrumented spinal fusion, this study aims to provide quality evidence regarding the benefits of supplementary rod constructs in reducing the risk of RFs and other mechanical complications. This study shall provide the first long-term clinical evidence on clinical outcome and benefit of supplementary rod constructs.
All participating surgeons will be asked to identify a time point, denoted as X, when they started using predominantly either supplementary rod constructs or dual-rod constructs for long-segment posterior TL instrumented spinal fusion. This time point X must be on or before December 31, 2020 (the last eligible date for the index surgery). Participating surgeons will be instructed to select the time point X to be as early within the collection window as feasible to maximize the available FU period.
Once the time point X is identified for a participating surgeon, medical records of patients treated by this surgeon will be reviewed to identify consecutive eligible patients with the index surgery done between the time point X and December 31, 2020, inclusive. In the case that an eligible patient had undergone several surgeries during this period, the first primary or revision of long-segment posterior TL instrumented fusion using either a supplementary rod construct or a dual-rod construct is defined as the index surgery.
Patients will then be grouped based on the rod constructs into either the supplementary rod construct group or dual-rod construct group.
The study has two FU periods:
- The first FU period is the first 2 years after the index surgery. The primary analysis will be done using data from the first 2 years of FU.
- The second FU period ends on December March 31, 20232024. The duration of this FU therefore ranges from 3 years and 3 months to 10 years and 3 months.
The primary study endpoint is the occurrence of the first RF within 2 years after the index surgery.
Studientyp
Einschreibung (Geschätzt)
Kontakte und Standorte
Studienkontakt
- Name: Viola Grünenfelder
- Telefonnummer: +41 79 696 33 97
- E-Mail: viola.gruenenfelder@aofoundation.org
Studieren Sie die Kontaktsicherung
- Name: Alix Frischknecht
- Telefonnummer: +41 79 606 41 48
- E-Mail: alix.frischknecht@aofoundation.org
Studienorte
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Hong Kong, China
- Abgeschlossen
- Duchess of Kent Children's Hospital
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Kolkata, Indien
- Rekrutierung
- Kothari Medical Centre
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Kontakt:
- Saumayajit Basu, MD
- E-Mail: saumyajitbasu@hotmail.com
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Hamamatsu, Japan, 431-3192
- Abgeschlossen
- Hamamatsu University School of Medicine
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Tokyo, Japan, 113-8654
- Rekrutierung
- University of Tokyo
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Kontakt:
- So Kato, Prof
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Calgary, Kanada, T2N 2T9
- Rekrutierung
- University of Calgary Spine
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Kontakt:
- Ganesh Swamy
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Toronto, Kanada, M5T 2S8
- Rekrutierung
- University of Toronto
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Kontakt:
- Stephen Lewis
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Kontakt:
- Christopher Nielsen
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Barcelona, Spanien, 08035
- Rekrutierung
- Hospital Vall d´Hebron
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Kontakt:
- Ferran Pellisé, MD
- E-Mail: 24361fpu@comb.es
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Istanbul, Türkei (türkiye)
- Rekrutierung
- Acibadem Maslak Hospital
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Kontakt:
- Caglar Yilgor, MD
- E-Mail: caglaryilgor@gmail.com
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Kontakt:
- Ahmet Alanay
- E-Mail: aalanay@gmail.com
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California
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Redwood City, California, Vereinigte Staaten, 94588
- Rekrutierung
- Stanford Spine Clinic
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Kontakt:
- Serena Hu, MD
- E-Mail: shu3@stanford.edu
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Sacramento, California, Vereinigte Staaten, 95819
- Rekrutierung
- University of California
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Kontakt:
- Yashar Javidan
- E-Mail: yjavidan@ucdavis.edu
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San Francisco, California, Vereinigte Staaten, 94144
- Beendet
- UCSF Spine Center
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Maryland
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Baltimore, Maryland, Vereinigte Staaten, 21287
- Rekrutierung
- John Hopkis Hospital
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Kontakt:
- Khaled Kebaish
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Minnesota
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Minneapolis, Minnesota, Vereinigte Staaten, 55454
- Rekrutierung
- University of Minnesota Medical Center
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Kontakt:
- David Polly, MD
- E-Mail: pollydw@umn.edu
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Missouri
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St Louis, Missouri, Vereinigte Staaten, 63110
- Rekrutierung
- Washington University in St. Louis, School of Medicine
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Kontakt:
- Brian Neuman
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St Louis, Missouri, Vereinigte Staaten, 63310
- Abgeschlossen
- Washington University in St. Louis, School of Medicine, Saint Louis, Missouri 63110
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New York
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New York, New York, Vereinigte Staaten, 10032
- Rekrutierung
- Columbia University / NYP Och Spine Hospital
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Kontakt:
- Zeeshan Sardar
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Virginia
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Charlottesville, Virginia, Vereinigte Staaten, 22908
- Rekrutierung
- University of Virginia
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Kontakt:
- Justin S Smith, MD, PhD
- Telefonnummer: 434-243-6339
- E-Mail: jss7f@virginia.edu
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Kontakt:
- Judith G Beenhakker
- E-Mail: JGB3P@uvahealth.org
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Patients who underwent long-segment posterior thoracolumbar (TL) instrumented fusion
Beschreibung
Inclusion Criteria:
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Age 45 years and older.
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Patients receiving long-segment posterior TL instrumented fusion using either supplementary rod constructs or dual-rod constructs (the index surgery).
- Long-segment is defined as the UIV at a thoracic level and the LIV at the sacrum/ilium.
- Supplementary rod constructs are defined as: in addition to the traditional two primary rods, at least one supplementary rod (eg, accessory rods or satellite rods) is used, and at least one supplementary rod and one primary rod (ie, at least two rods) together must span multiple (≥ 2) vertebral levels. The supplementary rod constructs do not include rods connected end-to-end or side-to-side that do not bridge multiple vertebral levels.
- The index surgery can be a primary surgery or a revision surgery.
- The index surgery, staged or non-staged, must use posterior spinal fusion but can be in combination with other approaches such as an anterior procedure.
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If the index surgery is a revision surgery, the primary rods must be replaced in the revision surgery, with the exception of Harrington or Luque rods which can remain in place.
o If the Harrington or Luque rods remain in situ, they must already have the UIV at the thoracic level and the LIV at the sacrum/ilium, or an extension of the existing Harrington or Luque is performed such that the UIV is at the thoracic level and the LIV at the sacrum/ilium.
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The index surgery was performed between January 1, 2014, and December 31, 2020, inclusive.
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Minimum 3 months of FU after the index surgery.
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Ability to provide informed consent according to the IRB/EC defined and approved procedures if applicable for retrospective data analysis.
Exclusion Criteria:
- Spinal fusion performed for acute trauma (ie, ≤ 1 year of trauma).
- Spinal fusion performed for tumor.
- Spinal fusion performed for infection.
- Patients with Parkinson's Disease.
- Patients with neuromuscular disorders.
- Patients with spine malignancies requiring chemo- or radiation therapy.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Beobachtungsmodelle: COHORT
- Zeitperspektiven: RETROSPECTIVE
Kohorten und Interventionen
Gruppe / Kohorte |
Intervention / Behandlung |
|---|---|
|
primary/revision long-segment posterior TL instrumented fusion with dual-rod constructs
The index surgery for this study is the primary or revision of long-segment posterior TL instrumented fusion using dual-rod construct. |
long-segment posterior TL instrumented fusion with either supplementary rod constructs or dual-rod constructs. |
|
primary/revision long-segment posterior TL instrumented fusion with supplementary rod constructs
The index surgery for this study is the primary or revision of long-segment posterior TL instrumented fusion using either a supplementary rod construct. |
long-segment posterior TL instrumented fusion with either supplementary rod constructs or dual-rod constructs. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Rod fracture (RF)
Zeitfenster: 2 years
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Incidence of rod fracture(s) |
2 years
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Time to rod fracture
Zeitfenster: 2 years
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Time to the first rod fracture after index surgery |
2 years
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Time to rod fracture
Zeitfenster: 10 years and 3 months
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Time to the first rod fracture after index surgery |
10 years and 3 months
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Configurations of supplementary rod constructs
Zeitfenster: Baseline
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Descriptions of configurations of supplementary rod constructs |
Baseline
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Treatment for rod fracture
Zeitfenster: 10 years and 3 months
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Descriptions of different treatment strategies for rod fractures |
10 years and 3 months
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Recurrent RFs
Zeitfenster: 10 years and 3 months
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Incidence of recurrent rod fractures |
10 years and 3 months
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Other mechanical failures
Zeitfenster: 10 years and 3 months
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Other mechanical failures other than rod fractures |
10 years and 3 months
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Surgical complications
Zeitfenster: 10 years and 3 months
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Selective surgical complications |
10 years and 3 months
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Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Justin S Smith, MD, PhD, Professor of Neurosurgery Chief of Spine Division, Fellowship Director University of Virginia
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- SMART
Plan für individuelle Teilnehmerdaten (IPD)
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