First clinical results of a novel minimally-invasive fusion system for the sacroiliac joint.


Journal

Technology and health care : official journal of the European Society for Engineering and Medicine
ISSN: 1878-7401
Titre abrégé: Technol Health Care
Pays: Netherlands
ID NLM: 9314590

Informations de publication

Date de publication:
2022
Historique:
pubmed: 29 3 2022
medline: 21 9 2022
entrez: 28 3 2022
Statut: ppublish

Résumé

Sacroiliac joint (SIJ) painful dysfunction is a common source of low back pain (LBP). Several surgical treatment options for SIJ fusion were described. A promising treatment option with demonstrated clinical improvement is the minimally-invasive SIJ fusion. The aim of this case study was to document the effectiveness and safety of the new SIJ system (Torpedo®) over a period of 6 months after the minimally invasive implantation. Patients with failed conservative treatment of painful SIJ dysfunction were enrolled successively in two centers. The Diagnosis was made by positive response to SIJ-injection with local anesthetic and at least by two positive SIJ provocation tests. The Torpedo® Implant system was used for the implantation. This workpiece made of titanium alloy is characterized by a helical profile geometry (CST: chronical spinal turn) with a hydrophilic surface. The evaluated endpoints LBP and grade of disability were assessed using a 0-10 numerical rating scale (NRS), and Oswestry Disability Index (ODI) preoperatively and at one, three and six months postoperatively. 15 patients (10 female, 5 male; mean age 59 ± 13 years) were operated on one after the other. The pain intensity decreased in all 15 patients. After 6 months, a decrease in the median values of 70% (quartiles 1-3: 65-79%) was calculated. The median values of the Oswestry Disability Index after 6 months were 62% (quartiles 1-3: 53-67) lower than before the operation. Before surgery, 13 patients (87%) were taking opioids for pain management. Six months after the operation, opioids were only needed by 3 patients (20%). Implant malpositioning was not detected on plain radiograph. No surgical site infections or perioperative complications occurred. The clinical improvement in early follow up and the absence of surgery related complications demonstrate a high grade of device-related safety and effectiveness of the treatment with a novel minimally-invasive SIJ fusion system.

Sections du résumé

BACKGROUND BACKGROUND
Sacroiliac joint (SIJ) painful dysfunction is a common source of low back pain (LBP). Several surgical treatment options for SIJ fusion were described. A promising treatment option with demonstrated clinical improvement is the minimally-invasive SIJ fusion.
OBJECTIVE OBJECTIVE
The aim of this case study was to document the effectiveness and safety of the new SIJ system (Torpedo®) over a period of 6 months after the minimally invasive implantation.
METHODS METHODS
Patients with failed conservative treatment of painful SIJ dysfunction were enrolled successively in two centers. The Diagnosis was made by positive response to SIJ-injection with local anesthetic and at least by two positive SIJ provocation tests. The Torpedo® Implant system was used for the implantation. This workpiece made of titanium alloy is characterized by a helical profile geometry (CST: chronical spinal turn) with a hydrophilic surface. The evaluated endpoints LBP and grade of disability were assessed using a 0-10 numerical rating scale (NRS), and Oswestry Disability Index (ODI) preoperatively and at one, three and six months postoperatively.
RESULTS RESULTS
15 patients (10 female, 5 male; mean age 59 ± 13 years) were operated on one after the other. The pain intensity decreased in all 15 patients. After 6 months, a decrease in the median values of 70% (quartiles 1-3: 65-79%) was calculated. The median values of the Oswestry Disability Index after 6 months were 62% (quartiles 1-3: 53-67) lower than before the operation. Before surgery, 13 patients (87%) were taking opioids for pain management. Six months after the operation, opioids were only needed by 3 patients (20%). Implant malpositioning was not detected on plain radiograph. No surgical site infections or perioperative complications occurred.
CONCLUSIONS CONCLUSIONS
The clinical improvement in early follow up and the absence of surgery related complications demonstrate a high grade of device-related safety and effectiveness of the treatment with a novel minimally-invasive SIJ fusion system.

Identifiants

pubmed: 35342065
pii: THC213348
doi: 10.3233/THC-213348
doi:

Substances chimiques

Alloys 0
Anesthetics, Local 0
Titanium D1JT611TNE

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1139-1145

Auteurs

Adnan Kasapovic (A)

Department of Orthopedic and Trauma Surgery, University Hospital Bonn, Bonn, Germany.

Desirée Schwetje (D)

Department of Orthopedic and Trauma Surgery, University Hospital Bonn, Bonn, Germany.

Thaer Ali (T)

Department of Orthopedic and Trauma Surgery, University Hospital Bonn, Bonn, Germany.

Max Jaenisch (M)

Department of Orthopedic and Trauma Surgery, University Hospital Bonn, Bonn, Germany.

Martin Gathen (M)

Department of Orthopedic and Trauma Surgery, University Hospital Bonn, Bonn, Germany.

Rahel Bornemann (R)

Department of Orthopedic and Trauma Surgery, University Hospital Bonn, Bonn, Germany.

Hany Abdallah (H)

Department of Orthopaedic and Spine Surgery, Wadi al Neel Military, Hospital, Cairo, Egypt.

Uwe Vieweg (U)

Department of Spine Surgery, Sana Hospital Rummelsberg, Schwarzenbruck, Germany.

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Classifications MeSH