{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,26]],"date-time":"2025-12-26T07:12:55Z","timestamp":1766733175684,"version":"3.46.0"},"reference-count":45,"publisher":"Oxford University Press (OUP)","issue":"12","license":[{"start":{"date-parts":[[2025,6,26]],"date-time":"2025-06-26T00:00:00Z","timestamp":1750896000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"funder":[{"name":"SI-BONE"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,12,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Purpose<\/jats:title>\n                    <jats:p>Sacroiliac joint (SIJ) pain, a frequent contributor to low back pain, is commonly treated with minimally invasive SIJ fusion. A large body of evidence supports the safety and effectiveness of lateral transiliac SIJ fusion. Traditionally performed by surgeons, this procedure is increasing in utilization by non-surgeon interventionalists. Herein, we present early safety results from a single-arm clinical trial of participants who underwent lateral SIJ fusion using threaded titanium implants placed by interventional pain management physicians.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>STACI (NCT05870488) is a 2-year prospective study conducted at 15 US interventional pain management sites. The primary endpoint is change in SIJ pain from baseline to 6 months. Secondary endpoints include changes in function (Oswestry Disability Index), quality of life (PROMIS-29), device- or procedure-related adverse events, and evidence of fusion on CT scan at 2\u2009years.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>A total of 110 patients were enrolled. Mean (SD) participant age is 64 (14) years and 68% are female. Mean (SD) operative time was 44\u2009minutes (16) and estimated blood loss was 14\u2009cc (15). No serious or device-related adverse events have occurred. Reported perioperative adverse events include one surgical site infection and one hematoma. At 1-month follow-up, ODI improved by 18 points (P\u2009&amp;lt;\u2009.0001) and SIJ pain (NRS) decreased by 4 points (P\u2009&amp;lt;\u2009.0001) from baseline.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>Early results from this prospective multicenter study support the relative safety and early effectiveness of LTI SIJ fusion using a threaded implant when performed by interventional pain management physicians. The data are consistent with published literature with a low adverse event rate and early improvements in pain and function.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1093\/pm\/pnaf082","type":"journal-article","created":{"date-parts":[[2025,6,26]],"date-time":"2025-06-26T07:55:16Z","timestamp":1750924516000},"page":"918-923","source":"Crossref","is-referenced-by-count":1,"title":["Safety and initial effectiveness of minimally invasive sacroiliac joint fusion with metal implants using a lateral transiliac approach: a prospective trial"],"prefix":"10.1093","volume":"26","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4112-761X","authenticated-orcid":false,"given":"Jacqueline","family":"Weisbein","sequence":"first","affiliation":[{"name":"Napa Valley Orthopaedics , Napa, CA 94558,","place":["United States"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Denis","family":"Patterson","sequence":"additional","affiliation":[{"name":"Nevada Advanced Pain 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