Evidence map›Paper›PMID 37580431›Full record

Trial reportClinical oral investigations2023

Combination of leukocyte and platelet-rich fibrin and demineralized bovine bone graft enhanced bone formation and healing after maxillary sinus augmentation: a randomized clinical trial.

Carolina Mendonça de Almeida Malzoni, Elton Carlos Pichotano, Luiz Guilherme Freitas de Paula, Ricardo Violante de Souza, Roberta Okamoto, Rupert S Austin, Elcio Marcantonio, Rafael Scaf de Molon, Daniela Leal Zandim-Barcelos

Open access · greenAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Clinical oral investigations, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 7 pooled it
8.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 7 syntheses or guidelines pooled it, 27 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Carolina Mendonça de Almeida MalzoniDepartment of Diagnosis and Surgery, School of Dentistry at Araraquara, São Paulo State University - UNESP, Rua Humaitá, 1680, Araraquara, SP, 14801-903, Brazil.
Elton Carlos PichotanoDepartment of Diagnosis and Surgery, School of Dentistry at Araraquara, São Paulo State University - UNESP, Rua Humaitá, 1680, Araraquara, SP, 14801-903, Brazil.
Luiz Guilherme Freitas de PaulaDepartment of Diagnosis and Surgery, School of Dentistry at Araraquara, São Paulo State University - UNESP, Rua Humaitá, 1680, Araraquara, SP, 14801-903, Brazil.
Ricardo Violante de SouzaPrivate practice, School of Medicine of Ribeirão Preto, Sao Paulo University - USP, Ribeirao Preto, Sao Paulo, 14040-904, Brazil.
Roberta OkamotoDepartment of Basic Sciences, School of Dentistry at Araçatuba, São Paulo State University - UNESP, Araçatuba, SP, 16015-050, Brazil.
Rupert S AustinTissue Engineering and Biophotonics, King's College London Dental Institute, Guy's Hospital, London, UK.
Elcio MarcantonioDepartment of Diagnosis and Surgery, School of Dentistry at Araraquara, São Paulo State University - UNESP, Rua Humaitá, 1680, Araraquara, SP, 14801-903, Brazil.
Rafael Scaf de MolonDepartment of Diagnosis and Surgery, School of Dentistry at Araçatuba, Sao Paulo State University - UNESP, Rua Jose Bonifacio, 1193, Vila Mendonça, Araçatuba, SP, 16015-050, Brazil. rafael.molon@unesp.br.
Daniela Leal Zandim-BarcelosDepartment of Diagnosis and Surgery, School of Dentistry at Araraquara, São Paulo State University - UNESP, Rua Humaitá, 1680, Araraquara, SP, 14801-903, Brazil. daniela.zandim-barcelos@unesp.br.
Universidade Estadual Paulista (Unesp) · BRCentro Universitário de Araraquara · BRKing's College London · GBUniversidade de Ribeirão Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe resorption of alveolar ridge bone and maxillary sinus pneumatization are challenges to implant-supported prosthetic rehabilitation. Bone regeneration using bone substitutes and growth factors are alternatives for maxillary sinus augmentation (MSA). Therefore, we sought to evaluate the effects of the association between leukocyte and platelet-rich fibrin (L-PRF) and deproteinized bovine bone mineral (DBBM) in MSA procedures. MATERIALS AND

methodsThirty-six maxillary sinuses from 24 individuals were included in this randomized clinical trial. The maxillary sinuses were randomly grafted with LPRF and DBBM (test group) or grafted only with DBBM (positive control). Dental implants were installed in the test group following two periods of evaluation: after 4 (DBBM+LPRF4) and 8 (DBBM+LPFR8) months of sinus graft healing, while the control group received implants only after 8 months. Cone beam computed tomography (CBCT) was taken 1 week after surgery (T1) and before implant placement (T2). Bone samples were collected during implant placement for histomorphometric and immunohistochemical (IHC) analysis. The primary implant stability was assessed by resonance frequency analysis.

resultsCBCT analysis demonstrated a significant decrease in bone volume from T1 to T2 in all groups without differences among them. Histologically, the test group showed significantly increase in bone neoformation in both periods of evaluation (LPRF+DBBM4: 44.70±14.01%; LPRF+DBBM8: 46.56±12.25%) compared to the control group (32.34±9.49%). The control group showed the highest percentage of residual graft. IHC analysis showed increased staining intensity of osteocalcin (OCN), vascular endothelial growth factor (VEGF), and runt related transcription factor 2 (RUNX-2) in LPRF+DBBM4 group, and osteopontin (OPN) in the L-PRF+DBBM8. Primary implant stability was successfully achieved (above 60 in implant stability quotient) in all the evaluated groups.

conclusionCombination of L-PRF and DBBM increased and accelerated new bone formation allowing early implant placement probably due to the higher protein expression of RUNX2, VEGF, OCN, and OPN. These data suggest that the use of L-PRF might be an interesting alternative to use in combination with DBBM for augment the maxillary sinuses allowing the installation of appropriate length implants in shorter period of time. CLINICAL RELEVANCE: This study showed improvement in bone neoformation and accelerated healing when associating L-PRF and DBBM for maxillary sinus augmentation procedures.

trial registrationThis study was registered before participant recruitment in Brazilian Registry of Clinical Trials (ReBEC - RBR-95m73t).

Indexed as

Bone SubstitutesPlatelet-Rich FibrinSinus Floor AugmentationAnimalsBiological ProductsBone TransplantationCattleDental Implantation, EndosseousHumansLeukocytesMaxillary SinusMineralsOsteogenesisVascular Endothelial Growth Factor ABiological Productsbone mealBone SubstitutesMineralsVascular Endothelial Growth Factor ABone graftDemineralized bovine boneDental implantsPlatelet-rich fibrinSinus floor augmentation

Identifiers

PMID37580431
OpenAlexW4385803575

What OpenQuestion holds

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Registered trials

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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.