<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">SS</journal-id><journal-title-group><journal-title>Surgical Science</journal-title></journal-title-group><issn pub-type="epub">2157-9407</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ss.2016.79055</article-id><article-id pub-id-type="publisher-id">SS-70552</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Comparative Study of Bovine Pericardium and Gore-Tex in Tissual Interaction with Wistar Rats Diaphragm
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Artur</surname><given-names>Fracassi Guerra</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mauro</surname><given-names>Razuk Filho</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Neil</surname><given-names>Ferreira Novo</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Willy</surname><given-names>Marcus França</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Department of Medicine, Catholic University of Sao Paulo, Sao Paulo, Brazil</addr-line></aff><aff id="aff2"><addr-line>Department of Medicine—Service of Statistical Studies, Sao Paulo, Brazil</addr-line></aff><aff id="aff1"><addr-line>Medical Science and Health Faculty, Catholic University of Sao Paulo, Sao Paulo, Brazil</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>willy@drwilly.com.br(WMF)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>01</day><month>09</month><year>2016</year></pub-date><volume>07</volume><issue>09</issue><fpage>381</fpage><lpage>389</lpage><history><date date-type="received"><day>July</day>	<month>15,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>September</month>	<year>9,</year>	</date><date date-type="accepted"><day>September</day>	<month>13,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Introduction
  :
   Simple suture isn’t always possible in large congenital diaphragmatic hernia (cdh) defects. Synthetic materials are used for correction such as Silastic&amp;reg, Gore-Tex&amp;reg (GT), Teflon&amp;reg or biological, such 
  as
   autologous muscle patches.
   
  It was shown that bovine pericardium (bp) was effective to correct those large defects with many positive outcomes when compared with syntactic materials.
   
  Aim: 
  This study aims to establish an experimental model of correction for large diaphragmatic defect with PB and GT patches to compare histologically the tissue interaction between them and diaphragm in young Wistar rats.
   
  Materials &amp; Methods: 15 wistar rats were divided in 3 groups: Rats that used BP was named G1; Rats that used GT was named G2; and rats with only scraping in the diphragm, named G3 (control). Animals were submited to a laparotomy and fixed pathces to diaphragms and harvested 3 weeks later. Area between normal diaphragm and patches were isolated and separated for histological analysis, such 
  as
   
  lymphocytic infiltration (
  inflammation), neovascularization and fibrosis. Results: 
  G1 presented 
  inflammation
   between BP and Diaphragm In 5 Samples. G2 Presented Neovascularization In 5 Samples, But No 
  inflammation
  . Fibrotic tissue overlapping GT patches occurred in 3 samples in G2. Comparing G1 with G2 there was a significant statistical difference concerning 
  inflammation
   (P = 0.0079), in G1. Comparing neovascularization there
   is
   no significant statistical difference (P = 0.4444), despite a slight higher incidence in G2. Fibrosis in both groups presented no significant statistical difference (P = 0.4444), despite a slight higher incidence in G2. There were no alterations in G3. Discussion: Despite 
  the 
  statistical difference in the inflammatory process was more frequent in G1 (P = 0.0079), neovascularization and fibrosis were more frequent in G2. Conclusion: The proposed experimental model was satisfactory to reproduce suture of patches in the diaphragm. These results suggests that inflammation, neovascularization and fibrosis indeed contribute to a benign healing process that reacts
   
  differently in each group but can drive to a more lasting and permanent results when biological patch 
  is 
  consider
  ed
  . Statistical report suggests that this study should be continued with a larger sample of animals and a wider period of time before harvest.
 
</p></abstract><kwd-group><kwd>Diaphragm Hernia</kwd><kwd> Bovine Pericardium</kwd><kwd> Gore-Tex</kwd><kwd> Tissue Interaction and Wistar Rat</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Since Neville et al. (1954) published the correction of large diaphragmatic defects by suturing an hepatic lobe on the endothoracic fascia, other attempts have been suggested to correct these defects by using synthetic materials, as Silastic&#174;, polytetrafluoroethylene, Gore-Tex&#174; (GT) and Teflon&#174; [<xref ref-type="bibr" rid="scirp.70552-ref1">1</xref>] - [<xref ref-type="bibr" rid="scirp.70552-ref3">3</xref>] . However, use of these materials has not always led to the expected outcomes given the recurrent herniation, no-growth of synthetic material and the need for another future definitive surgery [<xref ref-type="bibr" rid="scirp.70552-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref3">3</xref>] .</p><p>Autologous tissues, such as muscles including tissues of the abdominal wall and the large dorsal muscle, were used with good results. Bedini et al. (1997) and Samarakkody et al. (2001) described in two different papers a few cases in which the large dorsal muscle was used. Biological materials, such as lyophilized duramater, were described as methods to correct diaphragmatic defects, but 20% of hernia recurrence occurred. Thus, it was concluded that this is not the ideal material to close these defects [<xref ref-type="bibr" rid="scirp.70552-ref4">4</xref>] .</p><p>Other biological materials were tested in experimental studies aiming the investigation their effectiveness in the correction in large diaphragmatic defects, such as: Small intestine submucosa, acellular dermis both in Sprague-Dowley rats [<xref ref-type="bibr" rid="scirp.70552-ref5">5</xref>] , and also in dog fascia lata [<xref ref-type="bibr" rid="scirp.70552-ref6">6</xref>] .</p><p>Gallo et al. (1982) published an experimental study using bovine pericardium (BP) preserved in 4% glutaraldehyde solution to correct diaphragmatic defects in 15 dogs. According to these authors, there were no adhesion formation between BP and adjacent structures in all dogs but one in which the omentum adhered to BP [<xref ref-type="bibr" rid="scirp.70552-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref8">8</xref>] .</p><p>Another experimental study in rabbits concluded that BP is resorbed and substituted by the host’s resistant fibrous tissue. Moreover, BP is considered a more appropriate biological material to repair hernia with improved tissual incorporation, lower adherence degree and absence of wrinkles as the result of the transplant material when compared to Marlex&#174; [<xref ref-type="bibr" rid="scirp.70552-ref9">9</xref>] .</p><p>Another advantage is BP longevity. Basseto et al. (2011) and Kim et al. (2012) published studies with patients treated with this material more than 20 years and 10 years ago, respectively [<xref ref-type="bibr" rid="scirp.70552-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref11">11</xref>] . A case report published by the authors in 2007 (Pinheiro DFC, 2007; Basseto S. et al., 2011) describes a patient treated with BP to correct a 14 yo gigantic congenital diaphragmatic hernia [<xref ref-type="bibr" rid="scirp.70552-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref12">12</xref>] .</p><p>BP is currently largely used in cardiovascular surgeries due to its moderate elasticity, high resistance to traction, easy manipulation and doesn’t require the use of immune- suppressors [<xref ref-type="bibr" rid="scirp.70552-ref12">12</xref>] .</p><p>Gore-Tex&#174; is among the synthetic fabrics that are frequently utilized to repair defects in human beings by providing greater accumulation of neutrophils [<xref ref-type="bibr" rid="scirp.70552-ref13">13</xref>] . Given its easy handling, flexibility, readily obtainable, good adherence; it is used as support for the growth of fibrous tissue and doesn’t set off infection signs [<xref ref-type="bibr" rid="scirp.70552-ref14">14</xref>] . Notwithstanding, in developing organisms, it might not grow with the children and, consequently, it might result in abnormalities, especially thoracic deformities together with respiratory diseases [<xref ref-type="bibr" rid="scirp.70552-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref16">16</xref>] .</p><p>The present study aims to establish an experimental model of correction for large diaphragm defect and comparing histologically the tissue interaction between BP and GT in the Wistar rat’s diaphragms.</p></sec><sec id="s2"><title>2. Material and Methods</title><p>This study was approved by the Ethics in Research in Animal Experimentation Committee of the Catholic University of S&#227;o Paulo, Medical and Health Science Faculty.</p><p>After 24-hour acclimation in the vivarium, Wistar rats, 30 days up to two months old, average weight 200 g each were submitted to general anesthesia with Ketamine base―50mg/ml (Ketalar&#174;-Crist&#225;lia of Brazil), associated to Xylazine 10 mg/ml (Coopazine&#174;-Coopers Brazil Ltda.). A volume of 0.4 ml of anesthetic per animal was injected intramuscularly in the thigh lateral muscles with insulin syringe and a 20 G needle. This anesthetic composition (175 mg/kg Ketamine and 2.5 mg/kg Xylazine) maintains the animal under profound anesthesia during a period of three hours and painless postoperative period of 6 to 12 hours.</p><p>The rats in all groups were submitted to left subcostal laparotomy to expose the diaphragm. Bowel loops were moved down to lower regions of the abdomen to allow proper visualization of the animal left diaphragm simulating manipulation of the bowel loops to the abdomen as in a real diaphragmatic hernia surgery.</p><p>Small BP or GT patches with approximately 1 cm in diameter were sutured with polypropylene 6 - 0 with simple and separated stiches under the rat’s left diaphragm according to the group. Care was taken to avoid diaphragm lesion in order to prevent pneumothorax (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>The animals were divided in three groups:</p><p>・ Group 1 (BP) composed of 05 animals that had BP patch sutured on the diaphragm with a 6-0 polypropylene cord with simple separated stiches;</p><p>・ Group 2 (GT) composed of 05 animals that had GT patch sutured on the diaphragm with a 6-0 polypropylene cord with simple and separated stiches;</p><p>・ Group 3 (S): or Sham group, composed of 05 animals whose diaphragms were wounded by scraping with anatomical tweezers to their full extent, similar to the length of BP and GT patches sutured in rats of G1 and G2.</p><fig-group id="fig1"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title>(a) shows BP patch&#174; (black arrows) as it is sutured on the diaphragm (*) and (b) shows Gore-Tex&#174; (white arrow) already sutured on the diaphragm. Liver (L).</title></caption><fig id ="fig1_1"><label> (b)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2301056x2.png"/></fig></fig-group><p>Three weeks latter all the animals were sacrificed and the diaphragms with their respective patches were removed and preserved in formalin 10% for histological analysis in Hematoxylin and Eosin.</p><p>Statistical analysis used was the Fischer’s Exact Test (Siegel, 2006), for small sample, once it is an under-graduation research that can explain why sample is limited, despite the important results. Significance was noticed with p &lt; 0.05.</p></sec><sec id="s3"><title>3. Results</title><p>Histologic analysis showed in the rats of G1 the presence of lymphocytic infiltration (inflammation) in the very limit between BP and the diaphragm (<xref ref-type="fig" rid="fig2">Figure 2</xref>), no edema, preserved blood vessels and specifically abundance of small caliber veins, indicating a possible neovascularization, as shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>.</p><p>All data can be seen in <xref ref-type="table" rid="table1">Table 1</xref>, where comparison between G1 and G2 are clearer concerning lymphocytic infiltration (inflammation), neovascularization and fibrosis, (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>In G1 animals can be seen the presence of inflammation right in the edge between BP patch and diaphragm in all 5 samples, but neovascularization was found in only in 3 samples, where one of them had associated fibrosis. G2 presented neovascularization in 5 samples, but no samples with inflammation. Fibrotic tissue overlapping GT patches occurred in 3 samples in G2, such as well-delimited fibrotic capsules.</p><p>When comparing G1 &#215; G2 there was a significant statistical difference concerning inflammation (p = 0.0079), in G1. When comparing neovascularization in G1 &#215; G2 were obtained no significant statistical difference (p = 0.4444), between both groups, despite a slightly higher incidence in G2. When comparing G1 &#215; G2 concerning fibrosis, there no significant statistical difference (p = 0.5238), despite a slightly higher incidence in G2. There were no alterations in G3 (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>It was possible to visualize the formation of fibrotic tissue in the sections on the G2</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Shows BP patch between the diaphragm and the liver (L) of the Wistar rat with lymphocytic infiltrate (Li) between the D and BP, 100&#215;</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2301056x3.png"/></fig><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Lymphocytic infiltration (Li) between the diaphragm (D) and bovine pericardium patch (BP), in G1. White arrows show small caliber veins (neovascularization), 400&#215;</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2301056x4.png"/></fig><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Presents the distribution of histological changings concerning inflammatory infiltration, neovascularization and fibrosis in all groups</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Histology</th><th align="center" valign="middle"  colspan="2"  >G1 (PB)</th><th align="center" valign="middle"  colspan="2"  >G2 (GT)</th><th align="center" valign="middle"  colspan="2"  >G3 (Control)</th><th align="center" valign="middle" >p</th></tr></thead><tr><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >PB &#215; GT</td></tr><tr><td align="center" valign="middle" >Inflammation</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.0079</td></tr><tr><td align="center" valign="middle" >Neovascul.</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >60</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.4444</td></tr><tr><td align="center" valign="middle" >Fibrosis</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >0.5238</td></tr></tbody></table></table-wrap><p>patches (<xref ref-type="fig" rid="fig4">Figure 4</xref>). There are (well delimited) fibrotic capsules and formation of vases showed in <xref ref-type="fig" rid="fig5">Figure 5</xref>.</p><p>In the histological analysis of the rats in G3 (Control), it is possible to visualize a complete diaphragm recovery with no Lymphocytic infiltration (inflammation), neovascularization or fibrotic scars (<xref ref-type="fig" rid="fig6">Figure 6</xref>).</p><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Fibrotic tissue (FT) overlapping GT between the diaphragm (D) and the liver (L), and the presence of new blood vessels (arrows), 200&#215;</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2301056x5.png"/></fig><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> Transition between diaphragm (D) and the fibrotic tissue (FT) overlapping GT patch. Well-delimited fibrotic capsules (FC), small caliber blood vessels (arrows) do exist, and lymphocytic infiltration is absent. 100&#215;</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2301056x6.png"/></fig><fig id="fig6"  position="float"><label><xref ref-type="fig" rid="fig6">Figure 6</xref></label><caption><title> Intact diaphragm after scraping on G3-200&#215;</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/2-2301056x7.png"/></fig></sec><sec id="s4"><title>4. Discussion</title><p>Synthetic materials are relatively easy to suture, have good resistance and can be placed as a dome shape and apparently guarantee an improved diaphragmatic function when compared to what the flat material would guarantee [<xref ref-type="bibr" rid="scirp.70552-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref2">2</xref>] . Despite all these advantages, several complications are described in the literature, such as: material displacement, hernia resurgence and thoracoabdominal deformities [<xref ref-type="bibr" rid="scirp.70552-ref3">3</xref>] .</p><p>Several authors described the advantages of muscle autologous correction in for large CDH defects [<xref ref-type="bibr" rid="scirp.70552-ref4">4</xref>] . Muscles, such as distal latissimo dorsi, were used with good results. However, several newborns with CDH need extra-corporeal membrane oxygenation (ECMO) support which involves systemic anticoagulants and the need for extensive dissection would put these children at a high bleeding risk [<xref ref-type="bibr" rid="scirp.70552-ref3">3</xref>] .</p><p>Bovine pericardium seems to concentrate all the features of muscles and all the features of synthetic materials (resistance, easy manipulation and can be placed as dome shape) [<xref ref-type="bibr" rid="scirp.70552-ref9">9</xref>] - [<xref ref-type="bibr" rid="scirp.70552-ref11">11</xref>] . Furthermore, BP is a biological material that is capable of growing with the child without induce deformities or mutilation such as the autologus muscle patches and without the need for other surgeries for substituition [<xref ref-type="bibr" rid="scirp.70552-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref13">13</xref>] .</p><p>In the present study the inflammatory process in the G1 animals showed significant statistical difference concerning inflammation (p = 0.0079), when compared to G2 that had no inflammation. Inflammation is known as the first step for a normal wound healing and this is presented in 100% of G1 animal and can suggest a better cicatrization process. Despite we had only one animal in G1 that presented fibrosis, suggesting adhesion, Gallo et al. (1982) published that there were no adhesion formation between BP and adjacent structures in all dogs but one in which the omentum adhered to BP [<xref ref-type="bibr" rid="scirp.70552-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.70552-ref8">8</xref>] .</p><p>Neovascularization has not been published yet in the literature about this kind of tissue interaction, but in the present study we had 3 animals in G1 and 5 animals in G2 that presented neovascularization in the edge between patches and diaphragm, but with no significant statistical difference (p = 0.4444). Neovascularization (angiogenesis) is the second phase of a normal healing and would suggest that incorporation of the patch is going well.</p><p>Once fibrosis is the last step for a normal healing the patches of both groups were expected to have a good or even more frequent fibrosis around the patches. This study presented only 1 animal in G1 and 3 animals in G2 that presented fibrosis, but with no significant statistical difference (p = 0.5238). This could be result of a short time for the harvest day (3 weeks), specially in G1 that inflammatory process is more frequent. Maybe G1 would need a little more time to establish a proper fibrosis.</p></sec><sec id="s5"><title>5. Conclusion</title><p>In conclusion, the proposed experimental model was satisfactory to reproduce suture of patches in the diaphragm. These results suggests that inflammation, neovascularization and fibrosis indeed contribute to a benign healing process that respond differently in each group but can drive to a more lasting and permanent results when consider a biological patch. Statistical report suggests that this study should be continued with a larger sample of animals and a wider period of time before harvest.</p></sec><sec id="s6"><title>Acknowledgements</title><p>In appreciation for the Scientific Initiation fellowship granted to the Biologist Luciana Canabarro for her invaluable help with laboratory practices; to Mrs. Elizabeth de Almeida for preparation of tissue slides for microscopy examination and to all the team of the Biomaterial Laboratory at FCMS/PUC-SP.</p></sec><sec id="s7"><title>Cite this paper</title><p>Guerra, A.F., Filho, M.R., Novo, N.F. and Fran&#231;a, W.M. (2016) Comparative Study of Bovine Pericardium and Gore-Tex in Tissual Interaction with Wistar Rats Diaphragm. Surgical Science, 7, 381-389. http://dx.doi.org/10.4236/ss.2016.79055</p></sec></body><back><ref-list><title>References</title><ref id="scirp.70552-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Neville, W.E. and Clowes Jr., G.H.A. 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