{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,2]],"date-time":"2026-11-02T23:18:16Z","timestamp":1793661496288,"version":"4.5.1"},"reference-count":23,"publisher":"American Medical Association (AMA)","issue":"11","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Neurol"],"published-print":{"date-parts":[[2025,11,1]]},"abstract":"<jats:sec id=\"ab-noi250063-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>The Implantable Neurostimulator for the Treatment of Parkinson\u2019s Disease (INTREPID) trial was a randomized, double-blind, sham-controlled study of subthalamic nucleus (STN) deep brain stimulation (DBS) for the treatment of Parkinson disease (PD).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-noi250063-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To evaluate the long-term (5-year) outcomes and safety of STN-DBS for PD.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-noi250063-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This was a prospective, randomized (3:1), 12-week double-blind sham-controlled study at 23 movement disorder centers across the US with an open-label 5-year follow-up. Patients were implanted and followed up with the Vercise DBS system from May 2013 to December 2022. Eligibility required diagnosis of bilateral idiopathic PD with more than 5 years of motor symptoms, more than 6 hours per day of poor motor function, modified Hoehn and Yahr Scale scores higher than 2, Unified Parkinson\u2019s Disease Rating Scale (UPDRS-III) score of 30 or higher (medication-off state), and 33% or higher improvement in UPDRS-III medication-on score.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-noi250063-7\">\n                    <jats:title>Intervention<\/jats:title>\n                    <jats:p>Bilateral STN-DBS for moderate to advanced PD.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-noi250063-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Primary outcomes included changes in UPDRS and dyskinesia scores, quality-of-life measures, and safety assessments. Exploratory analyses included medication reduction and DBS association with motor signs.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-noi250063-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 313 patients were enrolled with 191 receiving the DBS system, and 137 participants (72%) completed the study. The study population had a mean (SD) age of 60 (7.9) years, with 139 (73%) male participants. Motor function without medication as measured by UPDRS-III improved from a mean (SD) of 42.8 (9.4) to 21.1 (10.6) at year 1 (51%; 95% CI, 49%-53%;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) and 27.6 (11.6) at year 5 (36%; 95% CI, 33%-38%;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). Activities of daily living without medication as measured by UPDRS-II improved from a mean (SD) of 20.6 (6.0) to 12.4 (6.1) at year 1 (41%; 95% CI, 38%-42%;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) and 16.4 (6.5) at year 5 (22%; 95% CI, 18%-23%;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). Dyskinesia scores decreased from 4.0 (5.1) to 1.0 (2.1) at year 1 (75%; 95% CI, 73%-75%;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) and to 1.2 (2.1) at year 5 (70%; 95% CI, 63%-75%;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). The levodopa equivalent dose was reduced by 28% at year 1, remaining stable at year 5 (28%; 95% CI, 26%-31%;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). The most common serious adverse event was infection (9 participants). Ten deaths were reported, none related to the study.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-noi250063-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>Although STN-DBS outcomes declined slightly, possibly due to the progressive nature of the disease, patients with PD sustained significant improvement in motor and activities of daily living scores, along with a stable reduction in anti-parkinsonian medication over the 5-year follow-up period.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamaneurol.2025.3373","type":"journal-article","created":{"date-parts":[[2025,9,15]],"date-time":"2025-09-15T15:00:38Z","timestamp":1757948438000},"page":"1181","source":"Crossref","is-referenced-by-count":31,"title":["Five-Year Outcomes from Deep Brain Stimulation of the Subthalamic Nucleus for Parkinson Disease"],"prefix":"10.1001","volume":"82","author":[{"given":"Philip A.","family":"Starr","sequence":"first","affiliation":[{"name":"Department of Neurosurgery, University of California, San Francisco"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rajat S.","family":"Shivacharan","sequence":"additional","affiliation":[{"name":"Division of Neuromodulation, Boston Scientific, Valencia, California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Edward","family":"Goldberg","sequence":"additional","affiliation":[{"name":"Division of Neuromodulation, Boston Scientific, Valencia, California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alexander I.","family":"Tr\u00f6ster","sequence":"additional","affiliation":[{"name":"Department of Clinical Neuropsychology, Barrow Neurological Institute, Phoenix, Arizona"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Paul A.","family":"House","sequence":"additional","affiliation":[{"name":"Neurosurgical Associates LLC, Murray, Utah"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Monique L.","family":"Giroux","sequence":"additional","affiliation":[{"name":"Movement and Neuroperformance Center of Colorado, Englewood"},{"name":"Now with Clinical Lead Movement Disorders, Praxis Precision Medicines Inc, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adam O.","family":"Hebb","sequence":"additional","affiliation":[{"name":"Department of Neurological Surgery, Kaiser Permanente, Denver, Colorado"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Donald M.","family":"Whiting","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Allegheny Health Network, Pittsburgh, Pennsylvania"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Timothy 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