EUROSPINE 2026 — Spine in Motion Gothenburg, 7–9 October 2026

Complications & Epidemiology

Intraoperative and Postoperative Complications After Stand-Alone L5-S1 ALIF: Retrospective Review of 176 Single-Center Cases

M. Polt1, F. Avrumova2, G. Loggia3, F. Altorfer4, F. Girardi2, F. Cammisa2, H.J. Kim2, H. Sandhu2, T.J. Albert2, D. Lebl2

  1. Hospital for Special Surgery, New York, United States of America
  2. Hospital for Special Surgery Main Hospital, New York, United States of America
  3. Hospital for Special Surgery Main Hospital, Zürich, United States of America
  4. Universitätsklinik Balgrist, zurich, Switzerland
Poster 000839: Intraoperative and Postoperative Complications After Stand-Alone L5-S1 ALIF: Retrospective Review of 176 Single-Center Cases
Abstract no.
000839
Topic
Complications & Epidemiology
Session
ePoster - Complications
Author
M. Polt
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Abstract

Stand-alone L5-S1 anterior lumbar interbody fusion (ALIF) carries vascular, neurological, urological, and bowel-related risks. However, complication data are limited, and stability-related complications remain debated. This study evaluates intraoperative and postoperative complications occurring within 12 months after isolated stand-alone L5-S1 ALIF.

A retrospective analysis was performed of patients who underwent isolated stand-alone L5-S1 ALIF within 10 years. Exclusion criteria included: combined anterior-posterior surgery, prior fusion at the level L5-S1, as well as presence of a fracture, infection or tumor at the index level. Aside from demographic data, the following were collected: indication for surgery, estimated blood loss (EBL), operative time, length of stay (LOS), intraoperative and postoperative complications through 12 months. Index-level revisions were analyzed for initial indication, revision reason, and revision procedure.

A total of 175 patients (103 F, 72 M; mean age 50.2 ± 13.2 years; BMI 26.8 ± 5.3) underwent isolated stand-alone L5-S1 ALIF. Primary indications were degenerative disc disease (DDD) (137/175, 78.3%), degenerative spondylolisthesis grade I (13/175, 7.4%), isthmic spondylolisthesis grade I (12/175, 6.9%) and II (2/175, 1.1%), junctional distal breakdown (8/175, 4.6%), degenerative scoliosis (2/175, 1.1%), and Bertolotti’s syndrome (1/175, 0.6%). Mean EBL was 57.7 ± 83.9 mL, operative time 103.6 ± 21.6 minutes, and LOS 1.8 ± 1.2 days. Intraoperative events were limited to venous bleeding (small <500 mL: 2/175, 1.1%; large >500 mL: 1/175, 0.6%), without postoperative sequelae. Postoperative complications included 1 cauda equina syndrome (0.6%), 1 S1 endplate fracture (0.6%), 1 sacral stress fracture (0.6%), 2 delayed union (1.1%), 2 paralytic ileus (1.1%), 7 constipation (4.0%), 5 urinary retention (2.9%), 1 retrograde ejaculation (0.6%), 1 wound infection (0.6%), and 1 new-onset radiculopathy (0.6%). Five revisions occurred: 1 urgent hemilaminectomy for postoperative cauda equina syndrome and 4 requiring additional posterior stabilization: 3 decompressions with posterolateral fusion L5-S1 for delayed union (n=2) and sacral stress fracture (n=1), and 1 posterior fusion L5-S1 with iliac fixation for S1 endplate fracture (n=1). Revisions requiring posterior stabilization occurred in 2/14 patients (14.3%) with isthmic spondylolisthesis grade I-II compared with 2/161 patients (1.2%) without isthmic spondylolisthesis.

To date, this is the largest single-center cohort of isolated stand-alone L5-S1 ALIF, showing a favorable safety profile with no relevant intraoperative complications, low postoperative complications, and 12-months revision rate of 2.9%. However, stability-related failures requiring additional posterior stabilization demonstrate the need for careful patient selection and preoperative counselling, particularly for isthmic spondylolisthesis.

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