4 - Zimmer Dental
Transcript
4 - Zimmer Dental
Presented at the Academy of Osseointegration Annual Meeting, 2013 Valutazione dell‘assemblato Implantare Dentale 3 Background Results in Materiale Trabecular Metal in un modello canino di perimplantite. Four dogs were euthanized at 24 and 38 weeks after implantation. Histological sections (one section per dog) were obtained at necropsy at 24 & 38 weeks post implant placement (Figure 2) and were stained with Sanderson’s rapid bone stain to assess percent bone-implant-contact (%BIC), amount of bone formed and histopathological parameters (acute and chronic All implants survived, control implants sh Osseointegration (or bone ongrowth) was described by Suneel Battula, PhD, Jin fibrosis, Whan Lee, PhD, Savvas Papanicolaou, Botissue Wen, PhD, Michael Collins, MS, MBA inflammation, evidence of bacterial infectionMS, andHai soft in contact with the implant). and test implants showed osseoincorp Brånemark et al, as the process of living bone forming structural %BIC was measured along Zimmer the entire length ofCarlsbad, the implant and total amount of bone formed Dental Inc., CA histologically. All the implants in the PI gro and functional connection with a load carrying titanium implant.1 Evaluation of Trabecular Metal Material Implant a Canine Periimplantitis Model was compared due Dental to the differences in theAssembly geometries of thein implants. Effects of implant type loss of supporting tissue with progression Osseoincorporation is the combination of bone ingrowth and bone Presentato al Meeting and Annuale dell’Accademia di and Osteintegrazione, parameters probing depth were 2013 statistically on the histomorphometric histopathological the implants survived (Figure 2). PD of sha Suneel Battula, ongrowth which was demonstrated by a dental implant withPhD, Jin Whan Lee, PhD, Savvas Papanicolaou, MS, Hai Bo Wen, PhD, Michael Collins, MS, MBA analyzed. of implants was lower and statistically d Trabecular MetalTM material Evaluation (TM), 2,3 a cancellous-like of Trabecular Metal Material Dental Assembly in a Canine Periimplantitis Model Zimmer DentalImplant Inc., Carlsbad, CA Quattro cani sono stati sacrificati alle settimane 24 e 38 post-impianto. Lein sezioni group for both 24 & 38 week groups. The interconnected Prior osteoconductive structure with Evaluation Evaluationporosity. of ofSuneel Trabecular Trabecular Metal Metal Material Material Dental Dental Implant Implant Assembly Assembly insettiaaMichael Canine Canine Periimplantitis Periimplantitis Model Model Suneel Battula, Battula, PhD, PhD, Jin Jin Whan Whan Lee, Lee, PhD, PhD, Savvas Savvas Papanicolaou, Papanicolaou, MS, MS, Hai Hai Bo Bo Wen, Wen, PhD, PhD, Michael Collins, Collins, MS, MS, MBA MBA istologiche (una sezione per cane) sono state ottenute all’esame necroptico alle was significantly different from that at 30 Risultati Premessa studies conducted using a TM implant in a healed site canine Presented atWhan theLee, Academy of Osseointegration Annual Meeting, 2013 Suneel Suneel Battula, Battula, PhD, Jin Jin Lee,PhD, PhD,Savvas Savvas MS, MS, Hai Hai BoWen, Wen,PhD, PhD, MichaelCollins, Collins,MS, MS,MBA MBA mane 24Whan e 38 post-impianto (Figura 2)Papanicolaou, ePapanicolaou, sono state colorate con la Bo colorazione rapidaMichael week study group which indicated model demonstrated active bone formation inside the pores at PhD, Zimmer Zimmer Dental Dental Inc., Inc., Carlsbad, Carlsbad, CA CA di euthanized Sanderson,atper la percentuale del contatto osso-impianto (BIC%, Four per dogsosso were 24verificare and 38 weeks after implantation. Histological sections (one The mean bone-implant-con ZimmerDental DentalInc., Inc.,Carlsbad, Carlsbad,CA CA early healing stages and level of osseointegration and stability section per dog) were obtained atZimmer Tutti gli impianti sono sopravvissuti; gliperiimplantitis. impianti di controllo hanno mostrato segni necropsy at 24 & 38 weeks post implant Annual placement (Figure L’osteointegrazione (o crescita Background ossea esterna) è stata descritta da Brånemark e Presented col- bone-implant-contact), la quantità di osso neoformato e i parametri istopatologici (in-2) Results Figure 2. Histological at the Academy of Osseointegration Meeting, 2013 52.7% & 62.9%, 69.6% & 71.3%, 46.9% & di osteointegrazione e gli impianti test hanno mostrato segni di incorporazione ossea comparable clinically successful threaded and were stained with Sanderson’s rapidof bone stain to assess percent bone-implant-contact laboratori cometo il processo mediante il quale l’ossoconventional vivente forma connessioni struttufiammazione acuta eAcademy cronica, evidenza di infezione batterica e tessuto molle a contatto Presented at the Osseointegration Annual Meeting, 2013 Presented at the Academy of Osseointegration Annual Meeting, 2013 sections of 38 weeks sia dal punto di vista clinico che istologico. gli impianti del gruppo hanno forTutti control (sham & PI) PI and testesi-(sham & amount ofeuthanized bone formed and histopathological parameters (acute sections and chronic implant.2 The aim ofimpianto the study was to evaluate the performance of (%BIC), 1 Four dogs were were euthanized at 24 24 and and 38 38 weeks weeks after after l’intera implantation. implantation. Histological Histological sections (one (one rali e funzionali con un in titanio All implants survived, control implants showed osseointegration Four dogs were euthanized at 24 and 38 weeks after implantation. Histological sections (one con dogs l’impianto). La BIC% at è stata misurata lungo lunghezza dell’impianto e la Osseointegration (or bone sottoposto ongrowth) a carico. was L’incorporazione described by ossea Four group (a) Control Sham inflammation, fibrosis, evidence of bacterial infection and soft tissue in contact with the implant). bito una significativa perdita di tessuto di supporto con progressione della perimplansection section per per dog) dog) were were obtained obtained at at necropsy necropsy at at 24 24 & & 38 38 weeks weeks post post implant implant placement placement (Figure (Figure 2) 2) Four dogs were euthanized at 24 and 38 weeks after implantation. Histological sections (one weeks respectively. Four Fourdogs dogs were werewere euthanized euthanized atat24 and and 38 38weeks weeks after implantation. implantation. Histological Histological sections sections (one (one section pertotale dog) obtained at24necropsy at 24 &after 38 weeks post delle implant placement (Figure 2) a èdental with porous TMforming sleeve an showed osseoincorporation clinically andBIC values showed and test implantsResults Background Background Results Brånemarkassembled et al, as the process of living data dallaimplant combinazione di crescita ossea interna edbone esterna, che èstructural stataindimostrata quantità dialong osso formato èlength stata confrontata in and virtù differenze nella geo%BIC was measured the entire of the implant total amount of bone formed and and were were stained stained with withobtained Sanderson’s Sanderson’s rapid rapid bone bone stain stain to to assess assess percent percent bone-implant-contact bone-implant-contact section per dog) were obtained atatnecropsy necropsy at 24 &&38 38 weeks post implant placement (Figure 2) (b)ma Control PIAll(c) Test tutti gli impianti sono sopravvissuti (Figura 2). La groups profondità di threaded sondaggio del section section per per dog) dog)were were obtained at necropsy at at24 24 & 38weeks weeks post post implant implant placement placement (Figure (Figure 2) 2) tite, and were stained with Sanderson’s rapid bone stain to assess percent bone-implant-contact histologically. the implants in the PI group exhibited significant 2,3 implant.1 and functional connection with a load carrying titanium Background Background Results Results between the for Ti portions experimentally induced canine periimplantitis model by comparing con un impianto dentale con il Materiale Trabecular Metal (TM), una struttura ostemetria degli impianti. Gliformed effettiinrapid del distain impianto sui parametri istomorfometrici, was and compared due to with thebone differences thetipo geometries of the implants. Effects ofand implant type (%BIC), (%BIC), amount amount of of bone formed and and histopathological histopathological parameters parameters (acute (acute and chronic chronic and were stained with Sanderson’s rapid bone stain to assess percent bone-implant-contact and were were stained stained with Sanderson’s Sanderson’s rapid bone bone stain to to assess assess percent percent bone-implant-contact bone-implant-contact (%BIC), amount of bone formed and histopathological parameters (acute and chronic loss of supporting tissue with progression of periimplantitis but all gruppo placebo per entrambi di impianti inferiore e statisticamente diversa All All implants implants survived, survived, control controli tipi implants implants showed showedera osseointegration osseointegration Sham (d) Test PI Osseoincorporation is the combination of bone ingrowth and bone by Osseointegration Osseointegration (or (or bone bone ongrowth) ongrowth) was was described described by All implants survived, control implants showed osseointegration Osseointegration (or bone ongrowth) was described by 3). More bone and was found in area encompa oconduttiva simil-spongiosa a pori interconnessi. Studi precedenti condotti con on the histomorphometric and parameters and probing depth were statistically with conventional titanium (Ti) threaded implant with respect to l’iminflammation, inflammation, fibrosis, fibrosis, evidence evidence of ofdibacterial bacterial infection infection and soft soft tissue tissue in in contact contact with with the the implant). implant). istopatologici e la sondaggio sonoand stati analizzati statisticamente. (%BIC), amount ofofprofondità bone formed and histopathological parameters (acute and chronic (%BIC), (%BIC), amount amount of bone bonehistopathological formed formed and and histopathological histopathological parameters parameters (acute (acute and and chronic chronic inflammation, fibrosis, evidence of bacterial infection and soft tissue in contact with the implant). showed showed osseoincorporation osseoincorporation clinically clinically andtypes La profondità di and and test test implants the implants survived (Figure 2). PD ofshowed sham group for settimane. both All implants survived, control implants showed osseointegration Brånemark Brånemark et et al, al, as as the thebone process process of ofaliving living bone bone forming forming structural structural ongrowthOsseointegration which was demonstrated by dental implant with Osseointegration (or bone ongrowth) was described by All implants implants survived, survived, control control implants implants showed osseointegration osseoincorporation clinically and and test implants da All quella delimplants gruppo PIshowed per entrambi i gruppi diosseointegration 24 e 38 Osseointegration (or (or bone ongrowth) ongrowth) was was described described by by analyzed. Brånemark et al, as the process of living bone forming structural %BIC %BIC was was measured measured along along the the entire entire length length of of the the implant implant and and total total amount amount of of bone bone formed formed inflammation, fibrosis, evidence of bacterial infection and soft tissue in contact with the implant). piego di un impianto TM nel sito di un modello canino andato incontro a guarigione inflammation, inflammation, fibrosis, fibrosis, evidence evidence of of bacterial bacterial infection infection and and soft soft tissue tissue in in contact contact with with the the implant). implant). %BIC was measured along the entire length of the implant and total amount of bone formed porous regions along the length of the imp tissue response, histomorphometry and risk of infection. histologically. histologically. All All the thelower implants implants in inosseoincorporation the the PI PI group groupdifferent exhibited exhibited significant significant showed osseoincorporation clinically and and test implants of implants was statistically from that ofdaPIquella and and functional functional connection connection with with a load load carrying carrying titanium titanium implant.1 implant.1 Brånemark etetal, al, as the process of living bone forming structural Trabecular MetalTM material (TM), 2,3 a bone cancellous-like showed showed osseoincorporation clinically clinically and and and and test test implants implants histologically. All the implants in the group exhibited significant Brånemark Brånemark et al, as asthe the process process of living living bone forming formingstructural structural and functional connection with aa of load carrying titanium implant.1 alle settimane 18and e 24 eraPIsignificativamente diversa riscontrata was was compared compared due due to to along the the differences differences in in the the geometries geometries of of the the implants. implants. Effects Effects of ofbone implant implant type type sondaggio %BIC was measured along the entire length ofofthe the implant and total amount of bone formed %BIC %BIC was was measured measured along the the entire entire length length of the implant implant and and total total amount amount of bone formed formed was compared due to the differences in the geometries of the implants. Effects of implant type Figura 2: Sezioni istoloss loss of of supporting supporting tissue tissue with with progression progression of of periimplantitis periimplantitis but but all all hanno dimostrato la formazione attiva di osso all’interno dei pori nelle prime fasi della histologically. All the implants iningroups. the PI group exhibited significant Osseoincorporation Osseoincorporation is iswith the the combination combination of bone bone ingrowth ingrowth and and bone bone group for both 38with week The PD at 18 and 24and and functional connection with load carrying titanium implant.1 histologically. histologically. All All24 the the&implants implants in the thePI PIgroup group exhibited exhibited significant significant both the sham PI la groups. In the poro loss of supporting tissue progression of periimplantitis but allweeks structure interconnected porosity. Prior osteoconductive and andfunctional functional connection connection with withaaaload loadof carrying carrying titanium titanium implant.1 implant.1 Osseoincorporation is the combination of bone ingrowth and bone on on the the histomorphometric histomorphometric and and histopathological histopathological parameters parameters and and probing probing depth depth were were statistically statistically was compared due toto the the differences ininthe the geometries ofofthe the implants. Effects ofofimplant implant type was was compared compared due due to the differences differences in the geometries geometries of the implants. implants. Effects Effects of implant type type alle settimane 30 e 38 nel gruppo di studio di 38 settimane, indicando progressione on the histomorphometric and histopathological parameters and probing depth were statistically the the implants implants survived survived (Figure (Figure 2). PD PDthat of of sham sham group group for for both bothbut types types loss ofofsignificantly supporting tissue with progression ofof periimplantitis but all logiche del gruppo di 38 ongrowth ongrowth which which was demonstrated demonstrated by a dental implant with with Osseoincorporation isTM the combination of bone ingrowth and bone was different from at 30 & 38 weeks in the 38 loss loss of supporting supporting tissue tissue with with2). progression progression of periimplantitis periimplantitis but all all the implants survived (Figure 2). PD of sham group for both types guarigione e studies livelli diconducted osteintegrazione stabilità paragonabili quelli ottenibili con il analyzed. Osseoincorporation Osseoincorporation is the the combination combination of of bone bone ingrowth ingrowth and andbone bone ongrowth which was demonstrated by aa adental dental implant with using was aeis implant in aby healed site implant canine analyzed. demonstrated a mean bone ingrowth of on the histomorphometric and histopathological parameters and probing depth were statistically on onthe thehistomorphometric histomorphometricand andhistopathological histopathologicalparameters parametersand andprobing probingdepth depthwere werestatistically statistically della analyzed. of of implants implants was was lower lower and and statistically statistically different different from from that that of of PI PI (BIC) perimplantite. I valori medi relativi al contatto osso-impianto the implants survived (Figure 2). PD ofofsham sham group for both types Trabecular Trabecular MetalTM MetalTM material material (TM), 2,3 a cancellous-like ongrowth which was demonstrated by dental implant with the the implants implants survived survived (Figure (Figure 2). 2). PD PD of sham group group for for both bothtypes types of implants was lower and statistically different from that of PI 2 (TM), week study group which indicated the progression of erano 52,7% e ongrowth ongrowth which which was was demonstrated demonstrated by by2,3 aaadello dental dental implant implant with Trabecular MetalTM material (TM), 2,3 aa cancellous-like cancellous-like settimane model demonstrated active bone formation inside the pores at with successo clinico di impianti filettati convenzionali. Lo scopo studio era di valu- analyzed. analyzed. analyzed. 35.6% & that 32.7% for di sham & (plaPI groups group group for for both both 24 24lower & & 38 38mean week week groups. groups. The Thedifferent PD PD at at 18 18 and and 24 24 weeks weeks of implants was lower and statistically different from that ofofiPI PI structure with interconnected interconnected porosity. porosity. Prior Prior osteoconductive osteoconductive structure Trabecular MetalTM material (TM), 2,3 cancellous-like group for both 24 & 38 week groups. The PD at 18 and 24 weeks of of implants implants was lower and and statistically statistically different from that of PIwere (a) (b) (c) (a) Controllo(d) 62,9%; 69,6% ewas 71,3%; 46,9% e 56,2%, 68,9% efrom 64,8% per gruppi controllo Trabecular Trabecular MetalTM MetalTM material (TM), (TM), 2,3 2,3 aaand a cancellous-like cancellous-like with interconnected porosity. Prior osteoconductive structure periimplantitis. The bone-implant-contact (BIC) values Materials and early healing stages and levelmaterial of with osseointegration stability placebo tare le prestazioni di studies impianti dentali assemblati con una guaina porosa incanine TM in un was was significantly significantly different different from from that that at at 30 30 & & 38 38 weeks weeks in in the the 38 38 group for both 24 & 38 week groups. The PD at 18 and 24 weeks Figure 2. Histological studies conducted conducted using using a a TM TM implant implant in in a a healed healed site site canine structure with interconnected porosity. Prior osteoconductive group group for for both both 24 24 & & 38 38 week week groups. groups. The The PD PD at at 18 18 and and 24 24 weeks weeks was significantly different from that at 30 & 38 weeks in the 38 structure structure with with interconnected interconnected porosity. porosity. Prior Prior osteoconductive osteoconductive studies conducted using a TM implant in a healed site canine respectively. Histopathological (Fig 52.7% &test 62.9%, 69.6% & 71.3%, 46.9% &24 56.2%, & 64.8% I valori BICanalysis comparable to clinically successful conventional threaded cebo e PI) study estudy (placebo e PI) alle settimane e 38,68.9% rispettivamente. non (b) Controllo PI38 weeks week week group group which which indicated indicated the the progression progression of of was significantly different from that at 30 & 38 weeks ininthe the 38 modello canino di perimplantite indottausing sperimentalmente mediante il confronto model model demonstrated demonstrated active active bone bone formation formation inside inside the the pores pores at at con sections of studies conducted using TM implant in healed site canine was was significantly significantly different different from that thatat at30 30& && 38 38 weeks weeks in the24 38 38& 38 week study group which the progression of model demonstrated active bone formation the pores at studies conducted conducted using TM TM implant implant in inperformance aaainside healed healed site site canine Methods formostrato control (sham &differenza PI)from andindicated test (sham PI) groups at implant.2studies The aim of the study wasaaato evaluate the ofcanine to mild incidence of acute and chronic in hanno alcuna statisticamente significativa tra i gruppi rispetto alle periimplantitis. periimplantitis. The The mean mean bone-implant-contact bone-implant-contact (BIC) (BIC) values values were were week study group which indicated the progression of early early healing healing stages stages active and and level level of of osseointegration osseointegration and and stability (c) Test placebo model demonstrated active bone formation inside the pores atat week week study group group which which indicated indicated the the progression progression of of periimplantitis. The mean bone-implant-contact (BIC) values were group (a) Control Sham model demonstrated demonstrated active bone bone formation formation inside inside the the pores at early healing stages and level of osseointegration and stability impianti in titanio (Ti)model filettati convenzionali rispetto alla risposta tissutale, istability parametri weeksstudy respectively. BIC values showed no statistical difference a dental implant assembled with porous TM sleeve in pores an (a) (b) Figure Figure 2. 2. Histological Histological Figure 2. Histological 52.7% 52.7% & & 62.9%, 62.9%, 69.6% 69.6% & & 71.3%, 71.3%, 46.9% 46.9% & & 56.2%, 56.2%, 68.9% 68.9% & & 64.8% 64.8% periimplantitis. The mean bone-implant-contact (BIC) values were porzioni filettate in titanio impianti 3). Negli test, è stata rilevata comparable comparable to clinically clinically successful successful conventional conventional threaded threaded reveal any evidence early healing stages and level ofof osseointegration osseointegration and stability periimplantitis. periimplantitis. The The mean mean bone-implant-contact bone-implant-contact (BIC) (BIC) values values were were 52.7% & 62.9%, 69.6% & degli 71.3%, 46.9% &(Figura 56.2%, 68.9% & impianti 64.8% (b) Control PI (c) Test early early healing healing stages stages and and level level of osseointegration and and stability stability comparable to clinically successful conventional threaded Test (TM and andto control (Ti6Al4V) dental implants (d) Test PI 2.of istomorfometrici eTi6Al4V) il rischio di infezione. between the groups for threaded Ti portions of the implants (Figure of bacterial infect experimentally induced canine model by sections sections of 38 38 weeks weeks Figure Histological Figure Figure2. 2. Histological Histological sections of 38 weeks for for control control (sham (sham & & PI) PI) and test test (sham (sham & &56.2%, PI) PI) groups groups at at 24 & & 38 38 52.7% &&62.9%, 62.9%, 69.6% &and 71.3%, 46.9% &compresa 56.2%, 68.9% &24 64.8% implant.2 implant.2 The The to aim aim of of the theperiimplantitis study study was was to to evaluate evaluate the thecomparing performance performance of of comparable to clinically successful conventional threaded 52.7% 52.7% & 62.9%, 69.6% 69.6% & & 71.3%, 71.3%, 46.9% 46.9%& & 56.2%, 68.9% 68.9% & & 64.8% 64.8% for control (sham & PI) and test (sham & PI) groups at 24 & 38 comparable comparable to clinically clinically successful successful conventional conventional threaded threaded implant.2 The aim of the study was to evaluate the performance of una maggiore quantità di osso nell’area fra le regioni filettate e porose lun-of the gr Sham (d) Test PI tissues or inside TM in any 3).control More bone was found in area encompassing the threaded andpores group group (a) (a)of Control Control Sham Sham with conventional titanium (Ti) threaded implant with respect (4.1mm x13mm, n=32) were bilaterally placed inthe mandibular sections of 38 weeks sections sections of 38 38weeks weeks group (a) Control Sham weeks weeks respectively. respectively. BIC BIC values values showed showed no no statistical statistical difference difference for (sham &&PI) PI) and test (sham && PI) groups atat 24 &&38 38 a aimplant.2 dental dentalThe implant implant assembled assembled with with porous porous TM TM sleeve sleeve toin in of an an * The aim of the study was to evaluate the performance of for for control control (sham (sham & PI)and and test test (sham (sham & PI) PI) groups groupsat 24 24 & 38 regione porosa, gli weeks respectively. BIC values showed no statistical difference implant.2 The aim aimof of the thestudy studywas was to toevaluate evaluate theperformance performance of aimplant.2 dental implant assembled with porous TM sleeve in an go la lunghezza dell’impianto, sia nei gruppi placebo che PI. Nella (b) (b) Control Control PI PI (c) (c) Test Test porous regions along the length of the implant, for test implants in group (a) Control Sham tissue response, histomorphometry andperiimplantitis risk ofporous infection. group group (a) (a)Control Control Sham (b) Control PI *(c) Sham Test * respectively. indicated mild to minimal fibrosis and mo between between the the groups groups for for threaded threaded Ti portions portions of ofstatistical the the implants implants (Figure (Figure weeks respectively. BIC values showed no statistical difference experimentally induced induced canine canine periimplantitis model model by by comparing comparing aexperimentally dental implant assembled with TM sleeve an premolar and molar sockets of eight hound dogs (4 inintest weeks weeks respectively. BIC BIC values valuesTi showed showed no no statistical difference difference between the groups for threaded Ti portions of the implants (Figure a aextraction dental dental implant implant assembled assembled with with porous porous TM TM sleeve sleeve in an an experimentally induced canine periimplantitis model by comparing Sham Sham (d) (d) Test Test PI PI (b) Control PI (c) Test both the sham and PI groups. In the porous region, test implants impianti test hanno dimostrato una crescita interna ossea media dithe 28,4% e 36,33% (b) (b) Control Control PI PI (c) (c) Test Test Sham (d) Test PI 3). 3). More More bone bone was was found found in in area area encompassing encompassing the the threaded threaded and and between the groups for threaded Ti portions of the implants (Figure with with conventional conventional titanium titanium (Ti) (Ti) threaded threaded implant implant with with respect respect to to experimentally induced canine periimplantitis model by comparing between between the the groups groups for for threaded threaded Ti Ti portions portions of of the the implants implants (Figure (Figure 3). More bone was found in area encompassing the threaded and experimentally experimentally induced induced canine canine periimplantitis periimplantitis model model by bycomparing comparing with conventional titanium (Ti) threaded assignment. implant with respect to tissue contact withand implant for both and 4 control Materiali implants per dog) by random The e metodi Sham (d) Test PI demonstrated a mean bone ingrowth of 28.4% & 36.33% Sham Sham (d) (d) Test Test PI PI porous porous regions regions along along the the length length of of the the implant, implant, for for test test implants implants in in 3). More bone was found in area encompassing the threaded and *was tissue tissue response, response, histomorphometry histomorphometry and and risk risk of of infection. infection. e di3). 35,6% ebone 32,7% i gruppi placebo e PI alle settimane 24 with conventional titanium (Ti) threaded implant with respect toto 3). More More bone wasper found found ininarea area encompassing the the threaded threaded and and porous regions along the length ofencompassing the implant, for test implants in e 38, rispettivamente. with withconventional conventional titanium titanium(Ti) (Ti)threaded threaded implant implant with withrespect respectto tissue response, histomorphometry and risk of infection. implants. & 32.7% for sham & PI groups at 24 and 38 in 35.6% extraction sockets tissue wereresponse, filled with bone graft material (Puros® both both the the sham sham and and PI PI groups. groups. In Inof the the porous porous region, region, test test implants implants porous regions along the length ofof the implant, for test implants a) b) c) d) (a) (b) (c) (d) tissue response, histomorphometry and risk ofofinfection. infection. Materials and porous porous regions regions along along the the length length the the implant, implant, for fortest test implants implants in both the sham and PI groups. In the porous region, test implants tissue response, histomorphometry histomorphometry and andrisk risk of infection. L’analisi istopatologica (Figura 4) ha mostrato un’incidenza diinweeks infiammazione acuta e respectively. Histopathological analysis (Figure showed minimal demonstrated demonstrated mean mean bone bone ingrowth ingrowth of of 28.4% 28.4% & &4)test 36.33% 36.33% and and both the sham and PI groups. InInthe the porous region, test implants demonstrated aa mean bone ingrowth of 28.4% & 36.33% and both both the thesham shama and and PI PIgroups. groups. In theporous porous region, region, test implants implants Cancellous Particulate). 12 weeks post implantation, periimplantitis cronica da minima a lieve, ma non ha rilevato alcuna evidenza di infezione batterica Methods & 32.7% for sham &ingrowth PI PI groups groups at at 24 24 & and and 38 38 weeks weeks 35.6% 35.6% & incidence 32.7% for ofsham to mild acute and chronic inflammation but did not demonstrated mean bone ingrowth ofof 28.4% 28.4% & 36.33% and Gli impianti dentali (4,1 mm 3 13 mm, n=32) testand (TM e Ti6Al4V) e di controllo demonstrated demonstrated aaa mean mean bone bone& ingrowth of 28.4% & 36.33% 36.33% and and (a) (a) (b) (b) (c) (c) (d) (d) sham & PI groups at 24 and 38 weeks 35.6% & 32.7% for Materials Materials and (a) (b) nell’ambito was inducedTest by (TM placement of ligatures in periimplantitis (PI) group dei tessuti perimplantari o (Figure all’interno dei 38 pori TM in nessuno dei gruppi. respectively. respectively. Histopathological Histopathological analysis analysis (Figure 4) 4) showed showed minimal minimal & 32.7% for sham & PI groups at 24 and 38 weeks 35.6% reveal any evidence of bacterial infection within peri-implant & & 32.7% 32.7% for for sham sham & & PI PI groups groups at at 24 24 and and 38 weeks weeks 35.6% 35.6% respectively. Histopathological analysis (Figure 4) showed minimal (a) (b) (c) (d) and Ti6Al4V) and control (Ti6Al4V) dental implants (a) (b) (c) (d) (Ti6Al4V) sono stati inseriti bilateralmente in siti post-estrattivi Materials Materials and and premolari e molari di Methods Methods to to mild mildhaincidence incidence of of acute acute and chronic chronic inflammation inflammation but butanalysis did did not not respectively. Histopathological analysis (Figure 4) showed minimal (4 8 dogs) while the shamn=32) group (4 dogs) received regular oral I siti anche rilevato laand presenza di fibrosi da minima a lieve tissues or inside TM pores in any of(Figure the groups. The alsoe un contatto da respectively. respectively. Histopathological Histopathological analysis analysis (Figure 4) 4)showed showed minimal minimal to mild incidence of acute and chronic inflammation but did not (4.1mm were bilaterally placed in mandibular 4.0 * 100 (a) (a) (b) (b) L’analisi cani (4 impianti testx13mm, e 4 di controllo perMethods ogni cane) con assegnazione casuale. Methods Conclusion reveal reveal any any evidence evidence of of bacterial bacterial infection infection within within peri-implant peri-implant to mild incidence of acute and chronic inflammation but did not * Test Test (TM (TM and and Ti6Al4V) Ti6Al4V) and and control control (Ti6Al4V) (Ti6Al4V) dental dental implants implants to to mild mild incidence incidence of of acute acute and and chronic chronic inflammation inflammation but but did did not not soft reveal any evidence of bacterial infection within peri-implant * indicated mild to minimal fibrosis and moderate to minimal Test (TMinand Ti6Al4V) and control (Ti6Al4V) dental implants premolar and molar extraction sockets of eight hound dogs (4 test minimo a lieve del tessuto molle con l’impianto, sia per i controlli che per gli impianti prophylaxis. The dogs the PI group did not receive oral (a) (a) (b) estrattivi sono stati riempiti con materiale da and innesto osseo (Particolato diimplants Osso Spontissues tissues or or inside inside TM TM pores pores in in any any of of the the groups. groups. The The analysis analysis also alsodental Controllo(b) placebo reveal any evidence of bacterial infection within peri-implant Controllo placebo (4.1mm (4.1mm x13mm, x13mm, n=32) n=32) were were bilaterally bilaterally placed placed in in mandibular mandibular reveal reveal any any evidence evidence of of bacterial bacterial infection infection within within peri-implant peri-implant tissues or inside TM pores in any of the groups. The analysis also Test (TM and Ti6Al4V) and control (Ti6Al4V) dental implants tissue contact with the implant for both control and test Test Test (TM (TM and and Ti6Al4V) Ti6Al4V) and control control (Ti6Al4V) (Ti6Al4V) dental dental implants (4.1mm x13mm, n=32) were bilaterally placed in mandibular * * 3.0 and 4 control implants per dog) by random assignment. The 75 * dentali test. p >0.05 *** Test placebo * prophylaxis. were placed in sockets the cervical region of (4 the Test placebo *** indicated indicated mild to toTM minimal minimal fibrosis and and moderate to to analysis minimal minimal soft soft tissues or inside TM pores in any ofof the groups. The analysis also premolar premolar and and molar molar extraction extraction sockets of of eight eight hound hound dogs (4 test test gioso Puros®extraction ).The A 12ligatures settimane dall’impianto èwere stata indotta la perimplantite mediante tissues tissues or ormild inside inside TM pores poresfibrosis in inany anyof the themoderate groups. groups.The The analysisalso also indicated mild to minimal fibrosis and moderate to minimal soft (4.1mm x13mm, n=32) were bilaterally placed in mandibular implants. (4.1mm (4.1mm x13mm, n=32) n=32) were bilaterally bilaterally placed placed in indogs mandibular mandibular premolar and molar extraction sockets of eight hound dogs (4 test socketsx13mm, were filled with bone graft material (Puros® ** * <0.05 * pimplant The histopathological and histomorphome Controllo PI Controllo PI ** tissue tissue contact contact with with the the implant for for both both control control and and test test dental dental * indicated mild to minimal fibrosis and moderate to minimal soft * and and 4 4 control control implants implants per per dog) dog) by by random random assignment. assignment. The The * * indicated indicated mild mild to to minimal minimal fibrosis fibrosis and and moderate moderate to to minimal minimal soft soft tissue contact with the implant for both control and test dental premolar and molar extraction sockets of eight hound dogs (4 test implants and were held in place by a healing collar. Probing depth premolar premolar and and molar molar extraction extraction sockets sockets of of eight eight hound hound dogs dogs (4 (4 test test andParticulate). 4 control implants dog) by random il posizionamento di legature nel gruppo dellaper perimplantite (PI) periimplantitis (4 assignment. cani) mentreThe il grup2.0 Test PI *** 50 Cancellous 12 weeks post implantation, Test PI implants. implants. tissue contact with the implant for both control and test dental canine study suggest that the TM dent extraction extraction sockets sockets were were per filled filled with withby bone bone graft graft assignment. material material (Puros® (Puros® tissue tissue contactwith withthe theimplant implantfor forboth bothcontrol controland andtest testdental dental implants. and control implants per dog) by assignment. The and 444 the control control implants implants per dog) dog) by random random assignment. The The extraction sockets were filled with bone graft (Puros® Figure 3. Comparing histomorphometric parameters measured for contact different induced by placement of ligatures inorale. periimplantitis (PI) group (PD) was measured for 24 week group at 18 & 24 weeks po placebo (4was cani) haand ricevuto la normale profilassi Irandom cani delmaterial gruppo PIand non han** * implants. Cancellous Cancellous Particulate). Particulate). 12 12 weeks weeks post post implantation, implantation, periimplantitis periimplantitis implants. implants. extraction sockets were filled with bone graft material (Puros® extraction extraction sockets sockets were were filled with with bone bone graft graftregular material material (Puros® (Puros® Cancellous Particulate). 12filled weeks post implantation, periimplantitis similarly to the conventional thread 25 Conclusioni dogs) while the sham group (4 dogs) received oral ricevuto la(4profilassi orale. LeParticulate). legature sono state posizionate nella periimplantitis regione cervicale implant systems 1.0 (a) %BIC (b) total amount of bone formed. fornothe 38 week group at 18, 24, 30 &12 38 weeks. was was induced induced by by placement placement of of ligatures ligatures in in periimplantitis periimplantitis (PI) (PI) group group Cancellous Particulate). 12 weeks post implantation, periimplantitis Conclusion Cancellous Cancellous Particulate). 12 weeks weeks post postimplantation, implantation, periimplantitis was induced by placement of ligatures in periimplantitis (PI) group prophylaxis. The dogs in the PI group did not receive oral experimentally induced periimplantitis env (4 (4 dogs) dogs) while while the the sham sham group group (4 (4 dogs) dogs) received received La regular regular oral oral di degli impianti ed erano tenute in posizione da un collare diin guarigione. profondità was induced by placement of ligatures inin periimplantitis (PI) group was was induced induced by byplacement placement of ofligatures ligatures periimplantitis periimplantitis (PI) (PI)group group (4 dogs) while the sham group (4 dogs) received regular oral 0 0.0 Conclusion Conclusion p >0.05 prophylaxis. The ligatures were placed inPI the cervical region of the oral 2438 2438 prophylaxis. prophylaxis. The The dogs dogs in in the the PI group group did did not not receive receive oral (4 dogs) while the sham group (4 dogs) received regular exhibit bacterial infection. I risultati istopatologici e istomorfometrici di questo canino suggeriscono (4 (4 dogs) dogs) while while the the sham sham group group (4 (4 dogs) dogs) received received regular regular oral oral prophylaxis. The dogs in the PI group did not receive * p <0.05 The histopathological and histomorphometric findingsstudio from this sondaggio (PD) è stata misurata perinil place gruppo dia 24 settimane alle settimane 18 e 24, Post-impianto (settimane) Post-impianto (settimane) implants and were held by healing collar. Probing depthof Conclusion Conclusion p .0.05 p .0.05 p >0.05 prophylaxis. prophylaxis. The ligatures ligatures were were placed placed in in the thedid cervical cervical region of oral the the The dogs in the PI group did not receive oral pp>0.05 >0.05 prophylaxis. prophylaxis.The The The dogs dogs in in the the PI PI group group did not notregion receive receive oral The ligatures were placed in the cervical region of the canine study suggest that the TM dental implants performed 1 1 3 1 3 1 11 3 33 2 2 2 22 4 e per il gruppo di 38 alle settimane 18,group 24, 30healing e18 38.& collar. (PD) wassettimane measured theheld 24 week 24 weeks anddepth implants implants and andfor were were held in in place place by by aaat healing collar. Probing Probing depth prophylaxis. The ligatures were placed ininthe the cervical region of the prophylaxis. prophylaxis. Theligatures ligatures wereplaced placed in thecervical cervical region regionof ofthe the implants andThe were held in were place by a healing collar. Probing depth for the 38implants week group at 18,held 24, 30 & weeks. (PD) (PD) was was measured measured for for in the the 24 2438 week week group at atcollar. 18 18 & & 24 24 weeks weeks and and implants and were held in place by healing collar. Probing depth (PD) was measured for the 24 week group at 18 & 24 weeks and implants and and were were held inplace place by by aaagroup healing healing collar. Probing Probing depth depth for for the the 38 38 measured week week group group at atthe 18, 18, 24, 24, 30 30 & &group 38 38 weeks. weeks. (PD) was measured for the 24 week group atat18 18 &&24 24 weeks and (PD) (PD) was was measured for for the24 24week week group at 18& 24weeks weeksand and for the 38 week group at 18, 24, 30 & 38 weeks. for the 38 week group atat18, 18, 24, 30 &&38 38 weeks. for forthe the38 38week weekgroup groupat 18,24, 24,30 30& 38weeks. weeks. Crescita (mm2) Percentuale (%) 2 (a) <0.05 <0.05 Figure 3. Comparing histomorphometric parameters measured for different *** ppp<0.05 pp >0.05 p>0.05 >0.05 Figura 3: Figure Raffronto dei parametri istomorfometrici misurati per formed. i diversi sistemi implant systems (a) %BIC (b) totalparameters amount of bone histomorphometric parameters measured measured for for different different Figure 3. 3. Comparing Comparing histomorphometric parameters measured for different Figure 3. Comparing histomorphometric implantari (a) BIC% (b) systems quantità totale di(b) osso formato. implant implant systems systems (a) (a) %BIC %BIC (b) (b) total total amount amount of of ofmeasured bone bone formed. formed. formed. histomorphometric parameters measured for different Figure 3. Comparing histomorphometric histomorphometric parameters parameters measured for fordifferent different Figure Figure 3. 3.Comparing Comparing implant (a) %BIC total amount bone (a) (a) (a) (a) (a) (a) 3.00 or or or or orTest Controllo Figure 1: Implant placement in a canine model. Control Test Figure 1:Figure Implant placement in a canine model.model. Figure 1: 1: Implant Implant placement placement in in a canine model. Control TestTest Figure 1: Implant placement in aa canine canine model. Control Control Test Figure 1: Implant placement ininaaacanine canine model. Figure Figure1: 1:Implant Implantplacement placementin caninemodel. model. Control Control Test Test Figura 1: Inserimento degli impianti in un modello canino. © 2013 Zimmer Dental, All rights ZD1093, Rev. 04/13 © ©2013 2013 Zimmer Dental, AllInc. rights reserved. ZD1093, Rev. 04/13 © © riservati. 2013 2013Inc. Zimmer Zimmer Dental, Dental, Inc. All Allreserved. rights rights reserved. reserved. ZD1093, ZD1093, Rev. Rev. 04/13 04/13 Zimmer Dental Inc. Tutti i diritti ZD1093IT, Rev. 04/13. Inc. © 2013 Zimmer Dental, Inc. All rights reserved. ZD1093, Rev. 04/13 ©©2013 2013 Zimmer Dental, Inc. All rights reserved. ZD1093, Rev. 04/13 © 2013Zimmer ZimmerDental, Dental,Inc. Inc.All Allrights rightsreserved. reserved.ZD1093, ZD1093,Rev. Rev.04/13 04/13 p<0.05 <0.05 ** *pp <0.05 implant systems (a) %BIC (b) total amount ofofbone bone formed. implant implantsystems systems(a) (a)%BIC %BIC(b) (b)total totalamount amountof boneformed. formed. 4.00 oro 44 (b) (b) (b) (b) (b) 4.00 3.00 Controllo placebo Test placebo Controllo PI Test PI 2.00 Scala di valutazione Measurement Scale 0. Nessuna evidenza Measurement Measurement 0. Measurement 1.00 1. 0.00 (b) 2. 3. Tessuto molle Infezione a contatto con batterica l’impianto Infiamma Infiamma zione acuta zione cronica Fibrosi 4. Scale 1. MinimaScale 0.0. Scale No 0. 2. Lieve evidence Measurement No No Measurement Measurement Measurement Minimal 3. Moderata Scale No evidence evidence Scale Scale Scale Mild 0. evidence Minimal 0. 0. 0. Minimal 4. Grave Moderate Minimal 1. 1. Mild Mild No Mild SevereNo Moderate Moderate No No evidence 3. Moderate 4. 4. Severe Severe evidence evidence evidence Minimal 4.1. Severe 1. 1. 1. Minimal Minimal Minimal 2. Mild 2. 2. 2. MildMild Mild 3. Moderate 3. 3. 3. Moderate Moderate Moderate 4. Severe 4. 4. 4. Severe Severe Severe 1. 2. 2. 2. 3. 3. 2.00 1.00 Measurement Scale 0. 1. 2. 3. 4. 0.00 Controllo placebo Test placebo Controllo PI Test PI No evidence Minimal Mild Moderate Severe Scala di valutazione Measurement 0. Nessuna evidenza Scale Measurement Measurement 0. Measurement 1. Minima Scale Scale 0.0. Scale No 2. Lieve0. evidence Measurement No No 3. Moderata Measurement Measurement Measurement Minimal Scale No evidence evidence Scale Scale Scale Mild 4. Grave0.0. 0.0. evidence Minimal Minimal 1. 1. 1. Tessuto molle Infezione a contatto con batterica l’impianto Infiamma Infiamma zione acuta zione cronica Fibrosi 2. 3. 1. 2. 2. 2. 4. 3. 3. Moderate Minimal Mild Mild No Mild Severe Moderate Moderate No No No evidence Moderate Severe Severe evidence evidence evidence Minimal Severe Minimal Minimal Minimal Mild MildMild Mild Moderate Moderate Moderate Moderate Severe Severe Severe Severe 4 4 4 cheThe le prestazioni degli and impianti dentali TM sono statefrom simili (b) The histopathological histopathological and histomorphometric histomorphometric findings findings from this thisa quelle degli impianti The histopathological and histomorphometric findings from this similarly tosuggest theinand conventional threaded implants in an canine canine study studyfilettati suggest that thathistomorphometric the the TM TMdidental dental implants implants performed performed The histopathological and histomorphometric findings from this convenzionali condizioni perimplantite indotta sperimentalmente e non The The histopathological histopathological and histomorphometric findings findings from from this this canine study suggest that the TM dental implants performed experimentally induced periimplantitis environment and did similarly similarly to to the the conventional conventional threaded threaded implants implants in in an an canine study suggest that the TM dental implants performed canine canine study study suggest suggest that that the the TM TM dental dental implants implants performed performed similarly to segni the conventional threaded implants in an not hanno mostrato di infezione batterica. 55 Bibliografia implantari a (a) 24 settimane (b) 38 settimane implant systems atat(a) (a) 24 weeks (b) 38 weeks implant implant systems systems at (a)24 24weeks weeks(b) (b)38 38weeks weeks 4.1. 1. 2. 2. 3. 3. 4. 4. 1. 1. 2. 2. 3. 3. 4. 4. References Brånemark PI, Hansson BO, Adell R, Breine Öhman A.. Scand J Plast Reconstr Surg. 1977 References References 1 Brånemark PI, Hansson BO, Adell R, Breine U, Lindström J, Hallén O,2.ÖhmanKim A. Scand J Plast ReconstrS, Surg.Larsen 1977;111 (Suppl D, Huja P, 16):1-132. et. Al. Conferenc References References Brånemark PI, Hansson BO, Adell R, Breine U, Lindström J, Hallén O, 2 Kim D, Huja S, Larsen P, et. Al. Conference Proceeding of European Association for Osseointegration. Glasgow, UK, 2010 Brånemark Brånemark PI, PI,Scand Hansson Hansson BO, BO,Reconstr Adell Adell R, R, Breine Breine1977;111 U, U, Lindström Lindström J, J, Hallén Hallén O, O, Association for Osseointegration. Glasgow, UK Brånemark PI, Hansson BO, Adell R, Breine U, Lindström J, Hallén O, Öhman A.. J Plast Surg. (Suppl 16):1-132. 3 Bobyn JD, Stackpool G, Hacking SA et. al. J Bone Joint Surg Br. 1999; 81(5):907-914. Öhman Öhman A.. A..Huja Scand Scand Plast Reconstr Reconstr Surg. 1977;111 1977;111 (Suppl (Suppl 16):1-132. 16):1-132. Brånemark PI, Hansson BO, Adell R, Breine U, Lindström J, Hallén O, Öhman A.. Scand Plast Reconstr Surg. 1977;111 (Suppl 16):1-132. Kim D, S,JJJ Plast Larsen P,Adell et. Surg. Al. Conference Proceeding of European Brånemark Brånemark PI, PI,Hansson Hansson BO, BO, Adell R, R,Breine Breine U,Lindström Lindström J, J,Hallén Hallén O, O, 3. U, Bobyn JD, Stackpool G, Hacking SA et. al. J Nota: Trabecular Metal™ èScand unS, marchio registrato di Zimmer, Inc. 1977;111 Kim Kim D, D, A.. Huja Huja S, Larsen P, et. et. Al. Al. Surg. Conference Conference Proceeding Proceeding of of European European Öhman A.. Plast Reconstr Surg. (Suppl 16):1-132. Kim D, Huja S, Larsen P, et. Al. Conference Proceeding of European Association forLarsen Glasgow, UK, 201016):1-132. Öhman Öhman A..Scand Scand JJOsseointegration. JPlast PlastP, Reconstr Reconstr Surg. 1977;111 1977;111 (Suppl (Suppl 16):1-132. 81(5):907-914. Association Association for for Osseointegration. Osseointegration. Glasgow, Glasgow, UK, UK, 2010 2010 Kim D, Huja S, Larsen P, et. Al. Conference Proceeding ofofEuropean European Association forS, Osseointegration. Glasgow, UK,al.Proceeding 2010 Kim Kim D, D,Huja Huja S, Larsen LarsenP, P,et. et.Al. Al. Conference Conference Proceeding of European Bobyn JD, Stackpool G, Hacking SA et. J Bone Joint Surg Br. 1999; 1. 1.1. 1. 5 55 1. 1.2. 1. References 2. 2. 2. 3. 1. Measurement Scale 0. 2.2. 2. 1. No evidence Minimal Mild Moderate Severe Bobyn Bobyn JD, JD, Stackpool Stackpool G, G, Hacking HackingGlasgow, SA SA et. et. al. al.UK, JJUK, J Bone Bone Joint Joint Surg Surg Br. Br. 1999; 1999; Association for Osseointegration. Glasgow, UK, 2010 Bobyn JD, Stackpool G, Hacking SA et. al. Bone Joint Surg Br. 1999; Association Association for forOsseointegration. Osseointegration. Glasgow, 2010 2010 81(5):907-914. 81(5):907-914. 81(5):907-914. Bobyn JD, Stackpool G, Hacking SA et. al. Bone Joint Surg Br. 1999; 81(5):907-914. Bobyn BobynJD, JD,Stackpool StackpoolG, G,Hacking HackingSA SAet. et.al. al.JJNote: JBone BoneJoint Joint Surg Surg Br. Br. 1999; Trabecular 1999; Metal™ 81(5):907-914. 81(5):907-914. 81(5):907-914. Note: Trabecular Metal™ istrademark a trademark of Zimmer, Inc. Note: Note: Trabecular Trabecular Metal™ Metal™ is is a a trademark of of Zimmer, Zimmer, Inc. Inc. Note: Trabecular Metal™ is a trademark of Zimmer, Inc. Note: Trabecular Metal™ isisaaatrademark trademark ofofZimmer, Zimmer, Inc. Note: Note:Trabecular TrabecularMetal™ Metal™is trademarkof Zimmer,Inc. Inc. 3.3. 3. 3. 3. 3. Figure 4. Comparingparameters histopathological parameters measured for different Figure 4. Comparing histopathological for different Figure Figure 4. 4. Comparing Comparing histopathological histopathological parameters parametersmeasured measured measured for for different different Figure 4. Comparing histopathological parameters measured for different Figura 4: Raffronto dei parametri istopatologici misurati per i diversi sistemi implant systems at (a) 24 weeks (b) 38 weeks implant systems atat (a)(a) 2424 (b) weeks implant implant systems systems at (a) 24weeks weeks weeks (b) (b)38 38 38 weeks weeks for Figure 4.4.Comparing Comparing histopathological parameters measured for different Figure Figure4. Comparing histopathological histopathological parameters parameters measured measured fordifferent different implant systems at (a) 24 weeks (b) 38 weeks 3. 4. 4. 5 exhibit bacterial infection. experimentally experimentally induced induced periimplantitis periimplantitis environment environment and and did did not similarly to the conventional threaded implants inin not an similarly similarly to to the the conventional conventional threaded threaded implants implants in an an experimentally induced periimplantitis environment and did not exhibit exhibit bacterial bacterialinduced infection. infection. experimentally induced periimplantitis environment and did not exhibit bacterial infection. experimentally experimentally induced periimplantitis periimplantitis environment environment and and did did not not exhibit bacterial infection. exhibit exhibitbacterial bacterialinfection. infection. 2. 3. 4. is a trademark of Zimme