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An advanced prediction model for postoperative complications and early implant failure

OBJECTIVES: Risk prediction in implant dentistry presents specific challenges including the dependence of observations from patients with multiple implants and rare outcome events. The aim of this study was to use advanced statistical methods based on penalized regression to assess risk factors in i...

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Autores principales: Feher, Balazs, Lettner, Stefan, Heinze, Georg, Karg, Florian, Ulm, Christian, Gruber, Reinhard, Kuchler, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589383/
https://www.ncbi.nlm.nih.gov/pubmed/32683718
http://dx.doi.org/10.1111/clr.13636
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author Feher, Balazs
Lettner, Stefan
Heinze, Georg
Karg, Florian
Ulm, Christian
Gruber, Reinhard
Kuchler, Ulrike
author_facet Feher, Balazs
Lettner, Stefan
Heinze, Georg
Karg, Florian
Ulm, Christian
Gruber, Reinhard
Kuchler, Ulrike
author_sort Feher, Balazs
collection PubMed
description OBJECTIVES: Risk prediction in implant dentistry presents specific challenges including the dependence of observations from patients with multiple implants and rare outcome events. The aim of this study was to use advanced statistical methods based on penalized regression to assess risk factors in implant dentistry. MATERIAL AND METHODS: We conducted a retrospective study from January 2016 to November 2018 recording postoperative complications including bleeding, hematoma, local infection, and nerve damage, as well as early implant failure. We further assessed patient‐ and implant‐related risk factors including smoking and diabetes, as well as treatment parameters including types of gaps and surgical procedures. Univariable and multivariable generalized estimating equation (GEE) models were estimated to assess predictor effects, and a prediction model was fitted using L1 penalized estimation (lasso). RESULTS: In a total of 1,132 patients (mean age: 50.6 ± 16.5 years, 55.4% female) and 2,413 implants, postoperative complications occurred in 71 patients. Sixteen implants were lost prior to loading. Multivariable GEE models showed a higher risk of any complication for diabetes mellitus (p = .006) and bone augmentation (p = .039). The models further revealed a higher risk of local infection for bone augmentation (p = .003), and a higher risk of hematoma formation for diabetes mellitus (p = .007) and edentulous jaws (p = .024). The lasso model did not select any risk factors into the prediction model. CONCLUSIONS: Using novel methodology well‐suited to tackle the specific challenges of risk prediction in implant dentistry, we were able to reliably estimate associations of risk factors with outcomes.
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spelling pubmed-75893832020-10-30 An advanced prediction model for postoperative complications and early implant failure Feher, Balazs Lettner, Stefan Heinze, Georg Karg, Florian Ulm, Christian Gruber, Reinhard Kuchler, Ulrike Clin Oral Implants Res Original Research OBJECTIVES: Risk prediction in implant dentistry presents specific challenges including the dependence of observations from patients with multiple implants and rare outcome events. The aim of this study was to use advanced statistical methods based on penalized regression to assess risk factors in implant dentistry. MATERIAL AND METHODS: We conducted a retrospective study from January 2016 to November 2018 recording postoperative complications including bleeding, hematoma, local infection, and nerve damage, as well as early implant failure. We further assessed patient‐ and implant‐related risk factors including smoking and diabetes, as well as treatment parameters including types of gaps and surgical procedures. Univariable and multivariable generalized estimating equation (GEE) models were estimated to assess predictor effects, and a prediction model was fitted using L1 penalized estimation (lasso). RESULTS: In a total of 1,132 patients (mean age: 50.6 ± 16.5 years, 55.4% female) and 2,413 implants, postoperative complications occurred in 71 patients. Sixteen implants were lost prior to loading. Multivariable GEE models showed a higher risk of any complication for diabetes mellitus (p = .006) and bone augmentation (p = .039). The models further revealed a higher risk of local infection for bone augmentation (p = .003), and a higher risk of hematoma formation for diabetes mellitus (p = .007) and edentulous jaws (p = .024). The lasso model did not select any risk factors into the prediction model. CONCLUSIONS: Using novel methodology well‐suited to tackle the specific challenges of risk prediction in implant dentistry, we were able to reliably estimate associations of risk factors with outcomes. John Wiley and Sons Inc. 2020-07-31 2020-10 /pmc/articles/PMC7589383/ /pubmed/32683718 http://dx.doi.org/10.1111/clr.13636 Text en © 2020 The Authors. Clinical Oral Implants Research published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Feher, Balazs
Lettner, Stefan
Heinze, Georg
Karg, Florian
Ulm, Christian
Gruber, Reinhard
Kuchler, Ulrike
An advanced prediction model for postoperative complications and early implant failure
title An advanced prediction model for postoperative complications and early implant failure
title_full An advanced prediction model for postoperative complications and early implant failure
title_fullStr An advanced prediction model for postoperative complications and early implant failure
title_full_unstemmed An advanced prediction model for postoperative complications and early implant failure
title_short An advanced prediction model for postoperative complications and early implant failure
title_sort advanced prediction model for postoperative complications and early implant failure
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589383/
https://www.ncbi.nlm.nih.gov/pubmed/32683718
http://dx.doi.org/10.1111/clr.13636
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