Prospective observational study on the clinical behaviour of dental implants in patients with haemophilia. Preliminary results

Gatti, Patricio César; Parreira, Miryam; Fillol, Agustina Gutierrez; Gualtieri, Ariel; Puia, Sebastián Ariel

doi:10.1016/j.bjoms.2021.03.014

Cited by 3 publications

(6 citation statements)

References 17 publications

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“…In the only series published, Gatti et al . ( 8 ) describe 3 cases of postoperative haemorrhage, which were controlled by the protocol described in this study, while in this study only 1 patient suffered this accident. In the aforementioned study ( 8 ), designed for 4 months, no implant loss is described, as occurred in this study during a similar period, causing the later loss of implants affected by the postoperative haematoma.…”

Section: Discussionmentioning

confidence: 90%

“…( 8 ) describe 3 cases of postoperative haemorrhage, which were controlled by the protocol described in this study, while in this study only 1 patient suffered this accident. In the aforementioned study ( 8 ), designed for 4 months, no implant loss is described, as occurred in this study during a similar period, causing the later loss of implants affected by the postoperative haematoma. Once again, the monitoring of these patients over the years is important, because although the survival rate of this study at 3 months was 100%, a survival rate of 94.6% was revealed in the group with hereditary coagulopathies after 2 years of prosthetic load, which is slightly lower than that published by Jamcoski et al .…”

Section: Discussionmentioning

confidence: 94%

“…( 19 ) may be the same as that of Rosen & Gornitsky ( 18 ), with different scientific considerations. Only one recent observational prospective study was observed, at 4 months on 10 patients (21 implants) with haemophilia A in selected patients ( 8 ). This retrospective case-control study at 2 years would be the only one with these characteristics published to date.…”

Section: Discussionmentioning

confidence: 99%

“…Neither in this study, nor in the series of 21 implants in 10 patients published by Gatti et al . ( 8 ) were these techniques used on patients with hereditary coagulopathies.…”

Section: Discussionmentioning

confidence: 99%

“…There is no long-term retrospective case-control study on the placement of implants in hereditary coagulopathies patients. Only one prospective observational study at 4 months has been published ( 8 ). Furthermore, no clinical trial has been published and there are only some isolated clinical cases.…”

Section: Introductionmentioning

confidence: 99%

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2-years retrospective observational case-control study on survival and marginal bone loss of implants in patients with hereditary coagulopathies

Pérez-Fierro¹,

Castellanos-Cosano²,

Hueto-Madrid³

et al. 2020

Med Oral

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Background Evaluating 2-years implant loss and marginal bone loss in patients with hereditary coagulopathies, comparing with a healthy control group. Material and Methods 37 implants in 13 patients (17 haemophilia A, 20 Von-Willebrand disease) versus 26 implants in 13 healthy patients. Data measured through Lagervall-Jansson index (after surgery, at prosthetic loading, at 2 years). Statistics: Chi-square, Haberman’s, ANOVA, Mann-Whitney-U. Significance p <0.05. Results Haemorrhagic accidents in 2 coagulopathies patients (non-statistical differences). Hereditary coagulopathies patients suffered more hepatitis ( p <0.05), HIV ( p <0.05) and less previous periodontitis ( p <0.01). Non-statistical differences in marginal bone loss among groups. 2 implants were lost in the hereditary coagulopathies and none in the control group (non-statistical differences). Hereditary coagulopathies patients had longer ( p <0.001), and narrower implants ( p <0.05) placed. 43.2% external prosthetic connection in hereditary coagulopathies patients ( p <0.001); change of prosthetic platform more frequent in control group ( p <0.05). 2 implants lost: external connection ( p <0.05). Survival rate 96.8% (hereditary coagulopathies 94.6%, control group 100%). Conclusions Implant and marginal bone loss at 2 years is similar in patients with hereditary coagulopathies and control group. Precautions should be taken on the treatment for hereditary coagulopathies patients, through prior haematological protocol. Implant loss only occurred in in a patient with Von-Willebrand´s disease. Key words: Dental implants, inherited coagulation disorders, haemophilia A/B, Von Willebrand disease, marginal bone loss.

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Section: Discussionmentioning

confidence: 90%

Section: Discussionmentioning

confidence: 94%

Section: Discussionmentioning

confidence: 99%

“…Neither in this study, nor in the series of 21 implants in 10 patients published by Gatti et al . ( 8 ) were these techniques used on patients with hereditary coagulopathies.…”

Section: Discussionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

See 3 more Smart Citations

2-years retrospective observational case-control study on survival and marginal bone loss of implants in patients with hereditary coagulopathies

Pérez-Fierro¹,

Castellanos-Cosano²,

Hueto-Madrid³

et al. 2020

Med Oral

View full text Add to dashboard Cite

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Systemic Factors Affecting Prognosis of Dental Implants

Thomas,

Bellani,

Piermatti

et al. 2024

Dental Clinics of North America

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Dental implant considerations in patients with systemic diseases: An updated comprehensive review

Mosaddad,

Talebi,

Keyhan

et al. 2024

J of Oral Rehabilitation

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BackgroundVarious medical conditions and the drugs used to treat them have been shown to impede or complicate dental implant surgery. It is crucial to carefully monitor the medical status and potential post‐operative complications of patients with systemic diseases, particularly elderly patients, to minimize the risk of health complications that may arise.AimThe purpose of this study was to review the existing evidence on the viability of dental implants in patients with systemic diseases and to provide practical recommendations to achieve the best possible results in the corresponding patient population.MethodsThe information for our study was compiled using data from PubMed, Scopus, Web of Science and Google Scholar databases and searched separately for each systemic disease included in our work until October 2023. An additional manual search was also performed to increase the search sensitivity. Only English‐language publications were included and assessed according to titles, abstracts and full texts.ResultsIn total, 6784 studies were found. After checking for duplicates and full‐text availability, screening for the inclusion criteria and manually searching reference lists, 570 articles remained to be considered in this study.ConclusionIn treating patients with systemic conditions, the cost–benefit analysis should consider the patient's quality of life and expected lifespan. The success of dental implants depends heavily on ensuring appropriate maintenance therapy, ideal oral hygiene standards, no smoking and avoiding other risk factors. Indications and contraindications for dental implants in cases of systemic diseases are yet to be more understood; broader and hardcore research needs to be done for a guideline foundation.

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Prospective observational study on the clinical behaviour of dental implants in patients with haemophilia. Preliminary results

Cited by 3 publications

References 17 publications

2-years retrospective observational case-control study on survival and marginal bone loss of implants in patients with hereditary coagulopathies

2-years retrospective observational case-control study on survival and marginal bone loss of implants in patients with hereditary coagulopathies

Systemic Factors Affecting Prognosis of Dental Implants

Dental implant considerations in patients with systemic diseases: An updated comprehensive review

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