Bondbone Synthetic Bone Graft: thoughts on quick resorption?

I just wanting to get some advice, especially from Dr. Peter Fairbairn. I am a dentist in Australia and when my local supplier first brought out BondBone (biphasic calcium sulphate – MIS Implants) into the Australian market 5 years ago, I took it onboard and used it to graft my implant cases. After a few years of using it and seeing the results, I have to admit it is not what I expected. It resorbs much too quickly (within 1-2 months) and does not hold ridge profile very well (due to its quick resorption). As I like the idea of synthetics and I like the idea of grafting at the time of implant placement, I am not keen on using membranes and Bio-Oss, which seems to be very mainstream here in Australia. Does anyone know of any other synthetics similar to BondBone, but works better and actually holds volume for longer? I have heard of products like Fortoss Vital, but cannot access it in Australia. Or should I mix the BondBone with bTCP and make my own graft that way? Any thoughts?

32 Comments on Bondbone Synthetic Bone Graft: thoughts on quick resorption?

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Phil
4/4/2016
Yes, you are 100% correct. Calcium sulfate resorbs very quickly, usually in 4 to 6 weeks. For this reason, it is recommended, to mix calcium sulfate with other bone substitutes with longer resorption profiles to create a composite-type graft. This is especially the case when there is a larger lesion. The granule type that is mixed with calcium sulfate can be selected according to the clinician’s preference. Many clinicians mix calcium sulfate with allograft, and others use other synthetics like b-TCP or hydroxyapatite. With regards to b-TCP, you may want to check out the article: "Enhancing extraction socket therapy with a biphasic calcium sulfate. Horowitz RA1, Rohrer MD, Prasad HS, Tovar N, Mazor Z.Compend Contin Educ Dent. 2012 Jun;33(6):420-6, 428. Also, there is a new bone graft cement from the same company that created BondBone(or 3D Bond, the generic name). This new product is called Bond Apatite, which addresses the issues you raised with using calcium sulfate alone. Bond Apatite is a combination of biphasic calcium sulfate with a formula of hydroxyapatite (HA) granules. Calcium sulfate acts a short-range space maintainer scaffold. It completely degrades in strict relation to the bone formation rate (4-10 weeks), while the HA acts as a long term space maintainer. The amount of HA within the graft is a relatively small proportion, and is intended only to slow down the overall resorption of the graft.
andrew
4/4/2016
Hi Phil, thanks for the info. What I find interesting is Fortoss Vital does the same thing, but with bTCP, whereas Bond Apatite uses HA. I would think using bTCP makes more sense as it resorbs and is replaced by bone faster than HA, so bTCP would be a better choice to combine with biphasic calcium sulphate?
Phil
4/5/2016
Hi Andrew, Thanks for the reply. Yes, bTCP resorbs faster than HA (I think it's by several weeks at least, but I don't remember exactly). However, I don't think that makes it a "better choice" per se for mixing with CS. I think it depends on how much you mix in, and the indication. Some would prefer the slower resorption. What is resorption of mineralized allograft (which is commonly mixed with CS here in the United States) and how does it compare to HA or bTCP? The ideal bone grafting composite is, in theory, a mixture of a fast resorbing and slow resorbing materials. How slow the slow graft in the CS composite should resorb is an interesting question. Basically, there are pro/cons to each of these synthetic materials, which must be taken into consideration and my feeling is that you could be successful with both types of graft composites when it comes to CS. Really just a preference, I suppose, and depends on the clinical situation. Hopefully, Peter will chime in here, as I'm certainly not qualified enough, really to address the major issues vis a vis, what's best to mix with CS (in the United States, I think most clinicians will mix CS with allograft).
Peter Fairbairn
4/5/2016
Hi Phil and Andrew , yes what Phil has said is correct but it is not a black and white as that in reality as the basic materials can be varied a large amount in manufacture and thus HA can be made to not resorb at all or even be relatively highly resorpable ( Nano or highly porous HA ) . Likewise the nature of BTcP can be varied a lot as well and after many years we are getting to understand more about them ( can Pubmed one of my animal studies , have another two awaiting publication and just started a fourth ) . So many of the older BTcP products were like earlier cars performance wise and the time of resorption is the key to success as it must be in time with the formation of the new host bone . The product mentioned are great and developed essentially by CS manufacturers which is great but I feel that the material it is mixed with plays a greater role hence have spent more development time in this area. After 13 years only using these materials in 3,500 grafts ( Pubmed protocol ) without ever using a membrane I feel they will be the future especially in tunnel grafting techniques . Minimally invasive surgical protocols are the way forward and these materials work very well in this aspect . In the US , yes Allografts are very popular and this is what most mix CS with and have great results again following a set protocol always helps . I feel that BTcp is the ideal mix after trying many over the years due to its Osteo-inductive properties ( See many research papers in Orthopedics and Bone journals , as well as work of Pamela Habovic ) and these new biphasic ( CS and BTcP ) materials appear to be even more osteo-inductive than the BtCp and HA materials used in past research. We have just started another study to hopefully show this as we are seeing it clinically where we see 50% new host bone at as little as 8 weeks in core samples . Recently we have developed a material EthOss which appears to be a nice step in the right direction with improved handling and consistent results which was launched in October in Europe . Sadly Australia is a smaller market and possibly not on the companies priority list so mixing is the best solution at the moment but as I said early on the BTcp you mix with is a very important aspect for the end result . Not sure what you have in Australia to use , if you can give me some products available I can look into it .. Will be speaking on it in Baden Baden on Saturday , in London next Thursday ( Tesla ) and Porto next Friday . But generally early days , CS has a big future Regards Peter
Phil
4/5/2016
Thanks Peter for an amazing summary. didn't realize that nature of b-TCP and HA products has changed over the years.
Leal
4/5/2016
Peter, where in Porto are you going to be?
David Anson
4/6/2016
Peter, I have been using CS for over 25 years and have published a number of articles on it, one with Dr. John Sottosanti, who popularized it's use as a composite graft and as a barrier (about 1990),and agree with you that it is a great material, and one with Dr. Robert Horowitz. Unfortunately, as there are few barriers to manufacturers producing it, so no company has really gotten behind it to do the research that should be done. It is unfortunate as it's use should be much greater than it is. My question is that I would like to know if it is gaining popularity in Europe? Thanks, David Anson
Peter Fairbairn
4/6/2016
Yes David , Bob is a great guy and really an expert in this field and I agree this is a great material and an opportunity missed but Dentistry is taught by Business not biology sadly . We do what industry wants , we need to think a little more . Sottosanti was a leader , we know where we are going and yes in Europe hopefully we will breakthrough . Exciting times ahead Regards Peter
andrew
4/6/2016
Hi Peter, Thanks for the info. In Australia, the mainstream with the specialists is mostly BioOss and membrane. Regarding synthetics, we only have either bTCP Or BondBone by MIS (biphasic CS, but not mixed with anything else). So you can see, we are very limited here in Australia. I have been using purely Bondbone (biphasic CS only) in my implant graft cases in past 5 years when it first came out in Australia, but results not been good. Very quick resorption and minimal bone formation. So the only way I see to proceed here is to mix Bondbone (biphasic CS) with bTCP myself. What proportions would you suggest I mix it, and what size bTCP should I be using?
Peter Fairbairn
4/7/2016
Sheraton Porto ......night lecture after hands on day
Peter Fairbairn
4/7/2016
The Sheraton , evening lecture after hands on day Peter
Peter Fairbairn
4/7/2016
Hi Andrew Mix it at 60 % BTcP and 40% CS and try use smaller particle size of BTcP ...Peter
andrew
5/8/2016
Peter, I have 2 sizes in Australia of bTCP I can get............200-500um OR 500-1000um. Which size bTCP should I choose to mix with the CaSO4?
Dr. John McCullough
4/5/2016
Peter, How about a combination of BondBone, irradiated cancellous and L-PRP? how would you mix and apply this? Dr. John McCullough
Dr. John McCullough
4/5/2016
Peter, I'm thinking specificily of an upper central where potentially you have a fenestration, desiring a screw retained prosthesis.
Gary
4/6/2016
Peter I am using Easy graft, does this need a membrane? Also can this be left exposed? Sorry to go slightly off topic
Peter Fairbairn
4/6/2016
Leal , contact CPM Pharma ( Carlos Ribiero ) in Porto . John , Hi you mean L-PRF , best not to mix with the Bond Bone , just mix the bond bone with the Allograft and then you can place the L-PRF over it if you wish to improve the soft tissue healing.. Bond Apatite from Augma is another nice product well packaged but personally I prefer BTcP as I said and allograft which I used to mix about ten years ago .. Peter
OsseoNews
4/7/2016
Quick editorial update: We spoke to the people at Augma and below is their response for the reason they chose to use HA in their new CS composite graft, Bond Apatite. Regarding long term space maintainers: Actually b-TCP could have been used, however we instead chose to use HA in a controlled particle size distribution with our Biphasic Calcium Sulfate matrix in Bond Apatite®. The HA was chosen because it enables the use of the graft in a large diversity of bone defects without any concerns about whether it will give sufficient space maintenance for wide defects with less bony wall support. If the clinician did not make the right evaluation about what should be the best space maintainer for a specific case, the material will compensate for this and give good three dimensional stabilization due to the HA. The HA was used as an innocuous space maintainer; it has no influence on the bone growth, it just provides space maintenance for the Biphasic Calcium Sulfate, which is more than 60% of the graft, and which resorbs into the patient’s own bone in a large defect. In addition, it is important to note that the Calcium Sulfate itself is different than any other CS used in grafting products. The CS used in the European composite graft you referred to that is mixed with b-TCP, is a CS Hemihydrate, commonly used in dental grafting over the years. However, Bond Apatite’s CS is Biphasic Calcium Sulfate. Biphasic Calcium Sulfate is a patent of Augma Biomaterials and provides improved handling and results over other forms of CS, both in terms of handling and results. On the handling side, CS Hemihydrate does not know how to set and harden in blood and saliva in an amount of time conducive to a surgical procedure. Biphasic Calcium Sulfate, on the other hand, sets and hardens in situ in 3 minutes, providing improved handling and a more comfortable work flow. On the results end, Biphasic Calcium Sulfate’s resorption profile matches the bone growth profile, while CS Hemihydrate’s does not. This means the Biphasic Calcium Sulfate in Bond Apatite® is simultaneously replaced by the patient’s own bone as it resorbs, providing a better quality and quantity of bone in a predictable amount of time.
CRS
4/7/2016
Question is human allograft not available in Europe? That changes the discussion due to availability. In fracture healing bone takes about 6-8 weeks for primary callus then the bone remodels and matures over approximately 4 months. Good calcification shows up on X-ray about four months. The HA which I used thirty years ago is permanent and gets incorporated into bone. Bio OSS stays around forever. In selected cases I have started using easy graft and done a few tunnels. So I am definitely not opposed to synthetics and have not used a pure autograft in years. I think it is very important to try new materials and see how they work in various clinical situations. However bone physiology is the one parameter which is difficult to change. I Ike it when there is actual bone, nascent or regenerated to support the implant. Great discussion.
Peter Fairbairn
4/8/2016
Yes CRS agree ........ more residual material less host bone ......... simple .......habits are hard to change for Dentists. The Systemic review of Hl Chan ,,, and Wang in Jomi suggested that Xenograft had 23 % less host bone and Synthetic had 22 % more .......we are not dealing with a hard substance ( like Wood ) but a living one ... Most research is obsessed with solely quantity of material and Quality is ignored sadly ... Yes Synthetic materials like CS and CaP s have been used in this field for over 100 years ..... there is nothing new , mixing Di and Hemihydrates with CS again was done decades ago .... But the synthetics are much better now and Augma is a great company helping as others are in exploring them..
CRS
4/9/2016
But are human allografts readily available in Europe? Could be different marketing scenario. In US bone banks seem to be marketed more, I like the results I get with human bone but nothing is perfect. I am guardedly optimistic with the Guidor product. I think volume needed and case selection is key. Growth factors are all over the board also. Thanks Peter.
andrew
4/12/2016
Peter Fairbain how does the cs/btcp materials eg. ethoss/vital fortoss compare with Novabone. Does Novabone work just as well as it is also synthetic?
Peter Fairbairn
4/13/2016
Hi CRS , yes they are in some countries and some not strangely (France not , Swtizerland ye etc ) . BUt these new Cap and Cs products seen to be a very exciting area as the bone growth is very impressive although surgical skill is needed and following the protocol is advised , as with everything. Hi Andrew , I have never used Novabone so cannot really comment , I lectured with George Kotsakis of Washington State Uni in Madrid at the end of last year and he showed some interesting cases . It is a Ha Silicate material which has always been interesting but again is said to be fully bio-absorped so great idea .. Regards Peter
andrew yong
4/13/2016
Peter, with EthOss, to what limits can you push it and still get reliable consistent results? I have been onto the EthOss website and you show cases of loss of buccal plate giving great results. However, what about cases where the tooth has been extracted 10 years ago and the ridge has lost a lot of bone width - in this case, it would be considered as a 1 wall defect where you would require a block bone graft. Can you still EthOss here to graft first to bulid out buccal bone width, then 3 months later place implant?
Dr Nehal
4/13/2016
Hi if anybody knows about novabone putty or novabone morsels as i have mixed results with morsels and little better results with putty
Peter Fairbairn
4/14/2016
Hi Andrew , yes you can do it both ways and I show cases in my talks , BUT best to keep it simple and use in easy case that are shown . You can buy the new club that Speith uses ........ but it takes time to get the drive he has consistently. The real future is Tunnel grafting where we are getting amazing results ...in fact can use BTcP Cad/ CAM blocks where you place through a tunnel incision as well if you like blocks . Saw a great talk by Thomas on Saturday on tunnel block approach ... Regards Peter
Gary
5/26/2016
Peter, Do we need to obtain primary closure when using Ethoss with large bone rebuilding cases that utilized a papilla sparing mid-crestal flap? Typical Example: Severely deficient pre-maxilla area due to trauma Maxillary lateral and central incisor were lost years ago Need to grow an additional 5mm vertically and 5mm horzontially. Treatment: papilla sparing mid-crestal flap, degranulate and clean and once the ethoss sets hard, does one need primary closure of the tissue in the crestal area with ethoss? (I like to keep the periostium free of horizontal releasing incisions if at all possible, for comfort, blood supply issues. nerve issues, so I sleep better- and cut less ) Gary
Peter Fairbairn
5/27/2016
Hi Gary , 5 mm is a more challenging case and maybe getting used to the materials and protocols with easier cases first is the best way to go .... as in Golf you do not play Augusta for your first round of golf with no Practice .. The need for primary closure can be patient dependant and for a consistent result is preferred as whilst it will heal over by secondary intention ( over a stable graft , see our research on Pubmed ) it can vary in some patients.. Without seeing this case I would say it is challenging and yes can be done but start easier ... Also read the protocol ( Also Pubmed ) where you will see that early placement of then Implant is another factor that is helpful . Kind Regards Peter
andrew
5/27/2016
Hi Peter, in the above situation where there is a big defect and we are not implanting at the time of grafting, when you say "early placement of the implant is helpful", how early should you put the implant in the Ethoss grafted site - 2 months? 3 months? after grafting?
Peter Fairbairn
5/27/2016
At Three months ( usually from 10 weeks on ) the key with big grafts is the stability of the graft therefore difficult to assess the case without seeing . That is why the Implants are placed at grafting as well to improve stability of the graft and as Ti is semi-conductive it up-regulates the host response as well ( Sasaki et al Jomi 2013 ). Muscle pull on the graft site can effect the outcome so must be checked . Peter
Gary
5/29/2016
Peter, Thankyou for all your help and insight! I was wondering if you could elaborate on the tunneling technique utilizing BTcP Cad/ CAM blocks, because in the USA I do not know anyone who is lecturing/teaching this (perhaps you do?). I am aware Greg Steiner (fom stiener lab) is evaluating/trying a technique by taking cone beam 3-d x-rays and printing (making) a BTcP overlay graft to the desired dimension that fits closely to the underlying bone. Then he utilizes a mid-crestal incision full thickness reflection with vertical releasing incisions. The onlay printed BTCP graft is then fix to the ridge with screws. Greg apparently has had moderate incision line opening in a few cases. Don't know any more than this. Not sure about how the bone needs to be prepared, etc. In the tunneling technique utilizing BTcP Cad/ CAM blocks how is the host bone prepared? Do you use 2 fixation screws? One on each end of the BTcP Cad/ CAM blocks? So you end up with two vertical incisions and tunnel (kind of like the tunnel that connects England and France :) I assume the BTcP Cad/ CAM blocks were printed in a similar manner that Greg Steiner is trying? Please Help enlighten us/me.
John
4/18/2016
Have anybody used Calcium Hydroxide ( not calcium sulfate) mixed with bone graft for socket preservation. Someone told me that and I want to see if anyone use that technique. Thank you

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