Evidence map›Paper›PMID 40055240›Full record

ArticleInternational journal of implant dentistry2025

Horizontal vascular-stalked split osteotomy (HVSO): a bone augmentation technique for the atrophic jaw- a retrospective cohort study in 29 patients.

Dirk Nolte, Johannes Angermair, Heidi Bradatsch, Rolf Ewers, Michael Alfertshofer, Robert Linsenmann, Sven Otto, Karin Christine Huth

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Article in International journal of implant dentistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Dirk NoltePrivate Practice for Oral and Maxillofacial Surgery, Munich, Germany.
Johannes AngermairPrivate Practice for Oral Surgery, Wiesbaden, Germany.
Heidi BradatschPrivate Practice for Oral and Maxillofacial Surgery, Munich, Germany.
Rolf EwersUniversity Hospital for Cranio- Maxillofacial and Oral Surgery, Medical University Vienna, Vienna, Austria.
Michael AlfertshoferDepartment of Oral and Maxillofacial Surgery, Charité- Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany. michael-georg.alfertshofer@charite.de.
Robert LinsenmannPrivate Practice for Oral and Maxillofacial Surgery, Munich, Germany.
Sven OttoDepartment of Oral and Maxillofacial Surgery, University Medical Center Munich, Munich, Germany.
Karin Christine HuthDepartment of Conservative Dentistry and Periodontology, University Hospital Munich, LMU Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImplant therapy in the advanced atrophic jaw remains challenging in oral and maxillofacial surgery. Hence, a plethora of different augmentation procedures to increase bone volume in the maxilla and mandible have been published. Horizontal vascular-stalked split osteotomy (HVSO) represents a safe and effective approach for the three-dimensional jaw augmentation since it combines maximum vascularization through lingual or palatinal periosteal stalking with reduced grafting morbidity.

objectiveTo analyze the efficacy of HVSO for implantation therapy in atrophic jaws by assessing vertical bone gain and implant survival rates. MATERIALS AND

methodsA total of n = 29 patients (14 females, 15 males) with a mean age of 55.4 ± 10.0 years and reduced volume of the alveolar ridge were retrospectively analyzed after treatment with 34 HVSOs in the maxilla and mandible. After controlled clinical follow-up of six months after augmentation, enossal implantation of 79 implants (maxilla 45, mandible 34) was performed. A standardized two-dimensional radiological assessment with panoramic tomography (OPTG) of the augmented bone height and clinical evaluation of the implants was performed over a mean follow-up period of 2.3 years.

resultsHVSO resulted in a significant increase in vertical bone height by 4.4 mm ± 2.0 mm (mean vertical gain: +59.4%) with + 101% in the maxilla and + 27.5% in the mandible directly after the procedure (T1), with both p < 0.001. After a mean observation period of 2.3 years bone height remained stable with a total gain of 41.4% (maxilla: 72.6%, mandible: 18.6%), with p < 0.001 and p = 0.001, respectively. Overall implant survival rate was 91% (maxilla: 89%; mandible: 94%).

conclusionHVSO reliably supports significantly enhanced vertical bone height with long-term stable results, thereby facilitating successful implantation in atrophic jaws with high implant survival rates observed over an extended follow-up period. CLINICAL TRIAL NUMBER: Not applicable as the study was no clinical trial.

Indexed as

Alveolar Ridge AugmentationOsteotomyAdultAgedAtrophyDental Implantation, EndosseousFemaleHumansMaleMandibleMaxillaMiddle AgedRetrospective StudiesTreatment OutcomeBone augmentationDental implantsImplantologyOral surgerySplit osteotomy

Identifiers

PMID40055240
PMCPMC11889328

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.