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Endodontic Materials in Clinical Practice


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and what might be expected to happen.

      The term ‘hydraulic’ is also applied in another context: so‐called ‘hydraulic condensation’, or the technique of forcing a fluid material to fill the space of a root canal by means of, say, a gutta‐percha cone pushed into it. The relationship of the term to hydraulic machinery is obvious: transmission of pressure using a liquid. In that physical sense, it is legitimate [7] (but then a syringe is also ‘hydraulic’). The difficulty seems to be in prevention of extrusion (v.s.) – simple hydrostatics says that this is likely, and promotional material seems to imply that it is expected. It is for others to decide whether the use of such techniques is appropriate.

      Another weakness is found in the use of irrigants. It is perhaps well known that chlorhexidine reacts with EDTA‐containing products, precipitating material that will clog tubules and canals. But reaction also occurs between chlorhexidine and various other irrigants, producing with NaOCl various chlorinated substances and precipitates, which may be coloured [8]. Hydrolysis to produce 4‐chloroaniline, a toxic substance, has also been suggested [9]. Essentially, the possible chemical interaction between all substances used in any sequential treatment should be considered for adverse effects as a matter of routine. Neither independence, nor complementarity, nor synergy may be assumed. It makes sense to ensure that some rinsing occurs between each irrigant used to minimize risks. Even so, since diffusion into tubules and accessory canals must occur, the efficiency of that rinsing cannot be very great. Reactions in the deeper tissue must be expected. In fact, that is how staining occurs in the first place. Indeed, even a mixture that is advocated (Chapter 5), HEDP‐NaOCl, clearly has an oxidation reaction proceeding fairly rapidly, although the speculated details appear not yet to be verified [10].

      A related issue arises in respect of the formulation of products. It is incumbent on researchers to know what they are working with, the composition of materials, and all setting, mechanical, and physical properties and subsequent degradations. Failure to do so can be considered a lapse. However, it is often singularly difficult to get such information: it does not appear in full in product literature, it does not appear in Material Safety Data Sheets because only known or expected hazardous materials need be declared, and it is often denied to enquirers by the manufacturer on grounds of trade secrets. We are owed full declaration of ingredients in manufactured foodstuffs, even if the wording is obfuscated by industry jargon, so that we can avoid adverse reactions or belief violations. We expect to know what is in cosmetics, perfumes, and anything else we put on our bodies, for similar reasons. Likewise with pharmaceuticals. So why, then, is it permissible to sell products that will be implanted in patients without a full list of ingredients and components? The possibility of direct adverse effects is certainly of great concern (especially because we differ widely in our sensitivities). Given that many materials are used in sequence or are contiguous on completion, that concern is raised to an imperative. It is surely inappropriate, if not arrogant, for a manufacturer tacitly to imply that we do not need to know because they have decided it is safe, and that no regulation is thereby contravened. The regulations must be addressed.

      Whilst on the subject of irrigation, it is often said that a solution is applied specifically to remove the smear layer resulting from instrumentation. That smear layer must, of course, be composed of the same proportions of matrix and mineral as the underlying tissue. It follows that no single solution can achieve such removal: mineral can be dissolved, and matrix oxidized, but not by the same agent. Likewise, there can be no selectivity on the part of the agents: chemically, smeared material is essentially indistinguishable from its source. Diffusion ensures that an acid or chelator, say, will reach underlying material in due course (and, of course, reach more remote areas than the canal being treated via accessory canals and so on). Very often, one sees references to so‐called ‘appropriate concentrations’, which supposedly avoid overextended reaction, without recognizing that both time and concentration – to say nothing of temperature – affect rate, whilst the extent of dissolution depends on the relative amounts of smeared material and reactant (volume × concentration), assuming that factors such as flow and streaming are not involved. Even then, one cannot assume uniformity of thickness or of any of the relevant factors over the entire space, most especially because it is tapered. Always, there is a compromise – in particular because the extent of the smeared material is unknown and progress cannot be monitored. Protocols based on the mean behaviour of a laboratory series cannot inform on the status of the individual case – an example of the fallacy of averages: sample means convey no information on distribution and thus on behaviour in the tails [11].