Long-term outcomes after removal of rib stabilization hardware in patients with blunt chest trauma.

Purpose: The study aim was to investigate the long-term outcomes after hardware removal (HR) in patients with blunt chest trauma. We hypothesized that HR might be beneficial in indicated patients to improve patient health. Methods: We performed a retrospective single-center study between 2017 and 20...

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Publicado en:European Journal of Trauma & Emergency Surgery Vol. 51; no. 1; pp. 1 - 15
Autores principales: Svec, Maria B., Bachmann, Helga, Hojski, Aljaz, Macharia-Nimietz, Eric F., Dackam, Sandrine V. C., Lardinois, Didier
Formato: Journal Article
Publicado: Springer Nature 4/29/2025
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 4/29/2025
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00068-025-02858-y
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        atl: Long-term outcomes after removal of rib stabilization hardware in patients with blunt chest trauma.
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          Svec, Maria B.
          Bachmann, Helga
          Hojski, Aljaz
          Macharia-Nimietz, Eric F.
          Dackam, Sandrine V. C.
          Lardinois, Didier
        affil: https://ror.org/04k51q396 Department of Thoracic Surgery, University Hospital Basel, Spitalstrasse 21, 4031, Basel, Switzerland
      sug:
      ab: Purpose: The study aim was to investigate the long-term outcomes after hardware removal (HR) in patients with blunt chest trauma. We hypothesized that HR might be beneficial in indicated patients to improve patient health. Methods: We performed a retrospective single-center study between 2017 and 2023. Descriptive statistics were used for the analysis. One study-specific follow-up visit was conducted, 28 months (range 3–72) after HR. The study-specific health survey used, consisted of four functional dimensions (mobility, self-care, usual activities, mental health) and two symptom dimensions (thoracic pain, chest tightness) which were rated on a numerical scale and compared to the status before HR in four categories (much better to worse). Results: Of the 28 patients, the average age was 59 years (range 29–83), 12 fractures (1–39) were fixed, and 4 implants (1–11) were used. The indications for HR were persistent thoracic pain (36%), discomfort (25%), chest tightness (21%), hardware dislocation (11%) and hardware infection (7%). HR was performed 18 months (5 days-104 months) after surgery for trauma. Patients with chest tightness and infection exhibited the greatest improvement in symptoms (75%), followed by those with hardware dislocation (61%). The improvement rate in the other 2 groups was 58%. All patients who experienced chest tightness, hardware dislocation and infection were completely satisfied and would undergo HR again. Conclusion: HR is safe and feasible, resulting in significant symptom relief and improvement in health status in approximately two-thirds of patients. In indicated patients, HR might be performed earlier and more liberally if symptoms are disabling. Clinical trial registration number: NCT06003595 registered on July 18, 2023.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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