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<article article-type="research-article" dtd-version="3.0" xml:lang="en"
	xmlns:xlink="http://www.w3.org/1999/xlink">
	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">JORM</journal-id>
			<journal-title-group>
				<journal-title>Journal of Oral &amp; Maxillofacial Research</journal-title>
			</journal-title-group>
			<issn pub-type="epub">2029-283X</issn>
			<publisher>
				<publisher-name>Stilus Optimus</publisher-name>
				<publisher-loc>Kaunas, Lithuania</publisher-loc>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="publisher-id">v1n2e4ht</article-id>
			<article-id pub-id-type="doi">10.5037/jomr.2010.1204</article-id>
			<article-categories>
				<subj-group subj-group-type="article-type">
					<subject>Original Paper</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>Prevention of Cutaneous Tissue Contracture During Removal of Craniofacial Implant Superstructures for CT and MRI Studies</article-title>
			</title-group>
			<contrib-group>
				<contrib contrib-type="author" id="contrib1">
					<name>
						<surname>Sullivan</surname>
						<given-names>Maureen</given-names>
					</name>
					<xref ref-type="aff" rid="aff1">1</xref>
				</contrib>
				<contrib contrib-type="author" id="contrib2">
					<name>
						<surname>Rossitto</surname>
						<given-names>Rachael</given-names>
					</name>
					<xref ref-type="aff" rid="aff1">1</xref>
				</contrib>
				<contrib contrib-type="author" id="contrib3" corresp="yes">
					<name>
						<surname>Casey</surname>
						<given-names>David</given-names>
					</name>
					<xref ref-type="aff" rid="aff1">1</xref>
				</contrib>
			</contrib-group>
            <aff id="aff1" rid="aff1">
			<sup>1</sup>
			<institution>Department of Dentistry and Maxillofacial Prosthetics, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, N.Y.</institution>
			<country>USA.</country></aff>
			<author-notes>
				<corresp>David M. Casey, 
				<institution>Department of Dentistry and Maxillofacial Prosthetics, Roswell Park Cancer Institute</institution>
				<addr-line>Elm and Carlton Streets, NY 14263, Buffalo, New York</addr-line>
				<country>USA</country>
				<phone>716 845 5972</phone>
				Fax: 716 845 3061<email>david.casey@roswellpark.org</email>
				</corresp>
			</author-notes>
			<pub-date pub-type="collection">
			<season>Apr-Jun</season>
			<year>2010</year>
			</pub-date>
			<pub-date pub-type="epub">
				<day>1</day>
				<month>7</month>
				<year>2010</year>
				</pub-date>
			<volume>1</volume>
			<issue>2</issue>
			<elocation-id>e4</elocation-id>
				<history>
				<date date-type="received">
				<day>23</day>
				<month>3</month>
				<year>2010</year>
				</date>
				<date date-type="accepted">
				<day>4</day>
				<month>4</month>
				<year>2010</year>
				</date>
				</history>
			<permissions>
				<copyright-statement> Copyright &#169; Sullivan M, Rossitto R, Casey DM. Published in the JOURNAL OF ORAL &amp; MAXILLOFACIAL RESEARCH
					(http://www.ejomr.org), 1 July 2010.</copyright-statement>
				<copyright-year>2010</copyright-year>
				<license license-type="open-access"
					xlink:href="http://creativecommons.org/licenses/by-nc-nd/3.0/">
					<license-p>This is an open-access article, first published in the JOURNAL OF
						ORAL &amp; MAXILLOFACIAL RESEARCH, distributed under the terms of the
						Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported
						License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted non-commercial use, distribution, and
						reproduction in any medium, provided the original work and is properly
						cited. The copyright, license information and link to the original
						publication on http://www.ejomr.org must be included.</license-p>
				</license>
			</permissions>
			<self-uri xlink:href="http://www.ejomr.org/JOMR/archives/2010/2/e4/e4ht.htm"
				xlink:type="simple"/>
			<abstract>
			<title>ABSTRACT</title>
				<sec sec-type="objectives">
					<title>Objectives</title>
					<p>Head and neck cancer patients who have lost facial parts following 
		surgical intervention frequently require craniofacial implant retained 
		facial prostheses for restoration. Many craniofacial implant patients 
		require computed tomography and magnetic resonance imaging scans as part 
		of their long-term follow-up care. Consequently removal of implant 
		superstructures and peri-abutment tissue management is required for 
		those studies. The purpose of the present paper was to describe a method 
		for eliminating cranial imaging artifacts in patients with craniofacial 
		implants.</p>
				</sec>
				<sec sec-type="material and methods">
					<title>Material and Methods</title>
					<p>Three 
		patients wearing extraoral implant retained facial prostheses needing 
		either computed tomography or magnetic resonance imaging studies were 
		discussed. Peri-implant soft tissues contracture after removal of 
		percutaneous craniofacial implant abutments during computed tomography 
		and magnetic resonance imaging studies was prevented using a method 
		proposed by authors. The procedure involves temporary removal of the 
		supra-implant components prior to imaging and filling of the tissue 
		openings with polyvinyl siloxane dental impression material.</p>
				</sec>
				<sec sec-type="results">
					<title>Results</title>
					<p>Immediately 
		after filling of the tissue openings with polyvinyl siloxane dental 
		impression material patients were sent for the imaging studies, and were 
		asked to return for removal of the silicone plugs and reconnection of 
		all superstructure hardware after imaging procedures were complete. The 
		silicone plugs were easily removed with a dental explorer. The 
		percutaneous abutments were immediately replaced and screwed into the 
		implants which were at the bone level.</p>
				</sec>
				<sec sec-type="conclusions">
					<title>Conclusions</title>
					<p>Presented herein method eliminates the source of artifacts and prevents contracture of 
		percutaneous tissues upon removal of the implant abutments during 
		imaging.</p>
				</sec>
			</abstract>
			<kwd-group>
				<kwd>endosseous implantation</kwd>
				<kwd>X-ray computed tomography</kwd>
				<kwd>magnetic resonance imaging</kwd>
				<kwd>artifacts.</kwd>
			</kwd-group>
		</article-meta>
	</front>
	<body>
		<sec sec-type="intro">
			<title>INTRODUCTION</title>
<p>Imaging techniques such as computed tomography (CT) and magnetic resonance imaging 
(MRI) are routinely used for diagnosis, treatment planning, and monitoring disease 
progression or recurrence in head and neck cancer patients. Many patients who have 
lost facial structures secondary to cancer surgery require craniofacial implant 
retained facial prostheses for restoration of appearance. These include auricular, 
nasal, orbital, or combination prostheses. Facial prosthesis retention by titanium 
craniofacial endosseous implants has become state of the art treatment since first 
reported by Tjellstr&#246;m et al. [<xref ref-type="bibr" rid="B1">1</xref>,<xref ref-type="bibr" rid="B2">2</xref>]. Tjellstr&#246;m and Br&#229;nemark&#39;s 
pioneering work using titanium craniofacial osseointegrated implants was an consequence 
of Br&#229;nemark&#39;s earlier work developing the titanium intraoral osseointegrated implant 
[<xref ref-type="bibr" rid="B3">3</xref>,<xref ref-type="bibr" rid="B4">4</xref>].</p>
<p>Endosseous implants are small (3 - 5 mm in length), made of titanium, and by 
themselves do not cause significant artifacts on CT or MRI. Attached to the implants 
however, are abutments and superstructures of other metals which may include gold 
alloys and ferromagnetic materials (<xref ref-type="fig" rid="fig1">Figure 1</xref>). These abutments 
and superstructures can cause localized artifacts and image distortion in CT and 
MRI scans contributing to difficulties in interpretation and subsequently reducing 
their diagnostic accuracy (<xref ref-type="fig" rid="fig2">Figure 2A</xref>) [<xref ref-type="bibr" rid="B5">5-13</xref>].</p>
				
			<fig id="fig1">
				<label>Figure 1</label>
				<caption>
			<p>A typical 2.5 mm long craniofacial 
		implant (Straumann USA, Inc., Andover, MA), with its percutaneous titanium 
		abutment, and integrated by welding, attached stainless steel keeper on 
		right side (Technovent Ltd., Leeds, England).</p>
				</caption>
				<graphic xlink:href="jomr-01-e4-g001.jpg"/>
			</fig>

			<fig id="fig2">
				<label>Figure 2</label>
				<caption>
		<p>A = axial CT scan of a patient 
		bearing a craniofacial implant without removal of prosthesis and embedded 
		magnets, or abutments with stainless steel keepers, showing &quot;starburst&quot; 
		artifact; B = axial CT scan directly through an extraoral implant, with 
		attached titanium abutment, where all non-titanium supra-implant components 
		were removed and no significant artifact is present.</p>
				</caption>
				<graphic xlink:href="jomr-01-e4-g002.jpg"/>
			</fig>	

<p>The various array of retention systems used to attach the facial prostheses to 
the craniofacial implants can be intimidating to the uninitiated radiologist or 
technician [<xref ref-type="bibr" rid="B14">14</xref>]. The titanium craniofacial implant itself ends 
at bone level. There is always a second part, the abutment that connects to the 
implant and perforated the cutaneous tissue. The abutment also is always titanium. 
Connected to the abutment can be a detachable stainless steel keeper, or a keeper 
welded to the abutment as one unit. These units are often found as freestanding, 
and have magnets embedded in the prosthesis. A second type of retention system consists 
of bars connecting the implant abutments, with mechanical retention provided by 
clips embedded in the prosthesis. A third type of retention system consists of bars 
attached to the implant abutments, with stainless steel keepers attached to the 
bars, and magnets embedded in the prosthesis.</p>
<p>While imaging sequences can be optimized to minimize these artifacts, the development 
of simple alternative procedures to address the problem would be of clinical benefit. 
Removal of all metallic components above the level of the implant results in a considerable 
reduction in the CT artifact when studies of the head are performed (<xref ref-type="fig" rid="fig2">Figure 
2B</xref>). Removal of all ferromagnetic components during MRI of any body part is 
also required due to potentially damaging tensile forces of unknown quantity at 
the implant to bone interface. This has previously been described for intraoral 
implants [<xref ref-type="bibr" rid="B15">15</xref>], and has been recommended by one prominent manufacturer 
of craniofacial implant magnetic components (Package insert, Magna-Cap Magnet Attachment 
System, Technovent Ltd., Leeds, England).</p>
<p>When an abutment is removed from cutaneous and subcutaneous tissue that is 3 
or more millimeters thick, these tissues may contract very rapidly. During the time 
it takes to complete the CT or MRI, there can be significant contracture that would 
make it difficult and painful to replace the abutments. In some cases, a surgical 
procedure might be necessary to relocate the implant and insert the abutment.</p>
<p>The purpose of the present paper was to describe a method proposed by authors 
for eliminating cranial imaging artifacts in patients with craniofacial implants.</p>

		</sec>
	<sec sec-type="materials|methods">
			<title>MATERIAL AND METHODS</title>
<p>Three patients wearing implant retained facial prostheses presented for CT or 
MRI studies. Patient I had an ear prosthesis containing magnets (Midi Lip Magnets, 
Technovent Ltd., Leeds, England), with percutaneous abutments composed of titanium 
with stainless steel keepers integrally attached (Magnabutment, Straumann USA, Inc., 
Andover, MA), and required a CT study of the head (<xref ref-type="fig" rid="fig3">Figure 3A</xref>). 
Patient II was wearing a magnetically retained nose prosthesis (Midi Lip Magnets, 
Technovent Ltd., Leeds, England), with a gold alloy laser-welded superstructure 
(Round Bar, Uni 45<sup>&#176;</sup> OD Cylinder, Astra Tech, Molndal, Sweden) with attached 
stainless steel keepers laser-welded to the bar (Maxi Insert Keeper, Technovent 
Ltd., Leeds, England), attached to three titanium implant abutments (45<sup>&#176;</sup> 
UniAbutments, Astra Tech, Molndal, Sweden) and required an MRI study of the spinal 
column (<xref ref-type="fig" rid="fig3">Figure 3B</xref>). Patient III was wearing a magnetically retained 
ear prosthesis containing four magnets (Midi Lip Magnets, Technovent Ltd., Leeds, 
England), on four implants with titanium abutments (Cochlear Americas, Centennial, 
CO, USA) and attached stainless steel keepers (Maxi Abutment Keeper, Technovent 
Ltd., Leeds, England), and required an MRI study of his shoulder region (<xref ref-type="fig" rid="fig3">Figure 3C</xref>). Using the appropriate wrenches supplied by the implant manufacturer, all 
supra-implant components were removed immediately prior to CT imaging of the head 
(<xref ref-type="fig" rid="fig3">Figure 3C</xref>). Where MRI of the head is to be performed, all supra-implant parts were also removed. Where MRI of other body areas is to be performed only magnetic 
and ferromagnetic parts need to be removed.</p>

			<fig id="fig3">
				<label>Figure 3</label>
				<caption>
		<p>A = patient I has 2 craniofacial 
		implants supporting titanium abutments that have stainless steel keepers 
		attached to their ends; B = patient II has a complete superstructure for 
		attachment of a nose prosthesis. It is supported by 3 implants, and fabricated 
		from gold alloy, with attached stainless steel keepers; C = removing percutaneous 
		abutment in patient III with attached stainless steel keeper, showing 7 
		mm thick cutaneous tissue.</p>
				</caption>
				<graphic xlink:href="jomr-01-e4-g003.jpg"/>
			</fig>

<p>Where the percutaneous tissues were greater then 3 mm thick, the openings were 
immediately filled with fast setting polyvinyl siloxane dental impression
material (Elite Implant Medium Body Fast Set, Zhermack Inc., River Edge, NJ, USA) 
(<xref ref-type="fig" rid="fig4">Figure 4A</xref>). A medium or heavy-bodied consistency is recommended 
to prevent the material from flowing during setting. This material hardens quickly, 
thus preventing contracture of the tissues around it. Because fluids can accumulate 
under the silicone plugs and possibly dislodge them, skin tape was placed over the 
plugs. The patients were then immediately sent for the imaging studies, and were 
asked to return for removal of the silicone plugs and reconnection of all superstructure 
hardware after imaging procedures were complete. The silicone plugs were easily 
removed with a dental explorer (<xref ref-type="fig" rid="fig4">Figure 4B</xref>). The percutaneous abutments 
were immediately replaced and screwed into the implants which are at the bone level. 
If any additional superstructures were present, as in patient II (<xref ref-type="fig" rid="fig3">Figure 
3B</xref>), these were then attached to the percutaneous abutments using the appropriate 
retaining screws.</p>

			<fig id="fig4">
				<label>Figure 4</label>
				<caption>
		<p>A = patient I, filling of 
		the cutaneous openings with dental polyvinyl siloxane impression material; 
		B = removal of silicone plugs immediately after completion of study, patient 
		I.</p>
				</caption>
				<graphic xlink:href="jomr-01-e4-g004.jpg"/>
			</fig>

		</sec>
		<sec sec-type="discussion">
		  <title>DISCUSSION</title>
<p>Non-titanium metallic components attached to titanium craniofacial implants can 
cause localized artifacts and distortion of image quality in CT and MRI scans of 
the head. In addition, the potential damaging effects of tensile forces on bone 
surrounding implants caused by magnetic pull on ferromagnetic stainless steel keepers 
attached to craniofacial implants is unknown, and should be avoided. This latter 
effect is irrespective of what part of the body is receiving the MRI study. Titanium 
dental implants alone without superstructures, or titanium orthodontic brackets, 
have not shown to produce MRI artifact [<xref ref-type="bibr" rid="B15">15</xref>,<xref ref-type="bibr" rid="B16">16</xref>].</p>
<p>It has been our experience that where short titanium percutaneous abutments have 
been left in place during CT of the head, no significant artifact has occurred (<xref ref-type="fig" rid="fig2">Figure 
2B</xref>), so long as no non-titanium components are attached. There is evidence that 
larger titanium prostheses like knee or hip prostheses may cause significant CT 
beam hardening effect [<xref ref-type="bibr" rid="B17">17</xref>], however we have not found that to 
be the case with the small craniofacial implants or their titanium abutments alone 
(<xref ref-type="fig" rid="fig2">Figure 2B</xref>).Thus, the percutaneous abutments themselves 
need only be removed in those cases where a non-titanium stainless steel keeper 
component is an integral and non-removable part of the abutment, such as in the 
Magnabutment shown in <xref ref-type="fig" rid="fig1">Figure 1</xref> (Magnabutment, Straumann USA, Inc., 
Andover, MA).</p>
<p>Imaging sequences can be optimized to minimize these artifacts, by temporary 
removal of the supra-implant components prior to imaging and filling of the tissue 
openings with fast setting polyvinyl siloxane impression material. In addition to 
eliminating the source of artifacts, this method importantly prevents contracture 
of percutaneous tissues upon removal of the implant abutments during imaging.</p>
<p>Removal of percutaneous abutments and superstructures is very technique sensitive. 
Specific wrenches made by the implant manufacturers must be used. Components should 
be reconnected using the torque recommended by their manufacturer. Screws can easily 
be fractured, and the actual implant-bone interface can be damaged if too much torque 
is applied. Internal threads in the implant can be irreversibly damaged by cross-threading 
if the angulation of the abutment is not correct while replacing it. An inventory 
of spare components should be available should any replacements be necessary during 
this procedure. It is for these reasons that these procedures should be performed 
only by the practitioners who placed the abutments and superstructures and fabricated 
the prostheses originally.</p>
<p>The time between removal of the components prescanning, and their reconnection 
should be minimal to eliminate the possibility of loss of the silicone plugs and 
the contracture of the percutaneous tissues. In our Institute, patients are always 
advised to have their scans performed here, even for those living out of town. This 
insures prompt and timely removal and reconnection by expert staff.</p>
<p>It should be mentioned that most dental impression materials are not sterile 
as supplied by the manufacturer. That is the reason for recommending the brand of 
polyvinyl siloxane used in this study [<xref ref-type="bibr" rid="B18">18</xref>]. This is the only 
material available in a unidose with all parts pre-packaged and guaranteed sterile.</p>

	</sec>
		<sec sec-type="conclusions">
			<title>CONCLUSIONS</title>
<p>In conclusion, it was developed by authors a protocol for removal of non-titanium 
components used for the retention of facial prostheses, in those patients who are 
to undergo computed tomography or magnetic resonance imaging scanning of the head, 
and for removal of ferromagnetic components for patients needing to be scanned with 
magnetic resonance imaging for any body part. Peri-abutment tissue contracture is 
prevented using polyvinyl siloxane. The procedure is simple, but must be performed 
by knowledgeable personnel, with appropriate instrumentation, and in a timely fashion.</p>

		</sec>
	</body>
	<back>
		<ack>
			<sec sec-type="acknowledgments and disclosure statements">
				<title>ACKNOWLEDGMENTS AND DISCLOSURE STATEMENTS</title>
<p>The authors report no conflicts of interest related to this study.</p>
		 </sec>
		</ack>
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