Thoracic wall reconstruction with Collamend® in trauma: report of a case and review of the literature
© Coccolini et al.; licensee BioMed Central Ltd. 2012
Received: 26 November 2012
Accepted: 20 December 2012
Published: 23 December 2012
Despite progress in reconstructive techniques, rebuilding portions of the thorax remains challenging, in particular when large resections, contamination or infection are involved. No other cases of thoracic reconstruction in trauma patients with biological prosthesis have been described since now.
We report a case of thoracic reconstruction in highly infected field in a trauma patient. We also performed a literature review about the topic.
Collamend® demonstrated its usefulness in thoracic wall reconstruction even in trauma patients and infected fields.
KeywordsBiological prosthesis Cross-linked Thoracic Reconstruction Infected fields Trauma Collamend
Thoracic wall (TW) reconstruction involves different surgical specialties as oncologic, plastic or trauma surgeon. Despite progress in reconstructive techniques, rebuilding portions of the thorax remains challenging, in particular when large resections, contamination or infection are involved. The successful reconstruction must preserve thoracic wall stability and respiratory function, eliminate dead spaces, avoid or reduce the risk of infection and protect the underlying viscera [1, 2]. Indications for full thickness resection of thoracic wall are primary thoracic tumors, extensive extra-thoracic neoplastic diseases, congenital aplasia or traumatic events [3–5].
Beyond anatomical repair with soft tissue flaps and plastic surgery techniques many different prosthetic materials have been used for TW reconstruction. Polypropylene, polyester, expanded polytetrafluoroethylene (PTFE) and polyethylmethacrylate sandwiched between layers of polypropylene have been used . In the last 15 years innovative materials have been introduced. Biological meshes comprised of several different materials: partially remodeling prosthesis are made of porcine dermal collagen (PDC), human dermal collagen (HDC), and bovine pericardium collagen (BPC). Completely remodeling prostheses are made of swine intestinal sub-mucosa (SIS), HDC and BDC. The partially remodeling prostheses are optimal in TW or abdominal reconstruction because of they resist better to mechanical stress. They are physically modified with cross-linkages between the collagen fibers which strengthen them [7, 8].
In trauma surgery it often happens to stabilize thoracic wall injuries. Different techniques have been reported with different devices. The main challenge in trauma surgery is the potential contamination or the infection of the surgical field. One of the main characteristic of biological materials is the possibility to be used safely in contaminated or infected fields.
Biological prostheses have already demonstrated their usefulness and versatility in many fields [9–15]. However as the main part of literature is composed by case series and case reports, they still require more evidence-based data . Recently a decisional model about the use of these mesh have been proposed by the Italian Biological Prosthesis Work Group . In the last years the Italian Chapter of the European Hernia Society started the Italian Register of Biological Prosthesis (IRBP). Also the European Hernia Society, in the European Register of Biological Prosthesis (ERBP) is recruiting cases of biological meshes implanted all around Europe .
Materials and methods
We report a case of TW reconstruction with Bard CollaMend® (Davol, Cranston, RI) in a patient victim of trauma.
A retrospective review was conducted of all reported cases of use of biological prosthesis in TW reconstruction in trauma published up to September, 2012 on PUBMED (1966–2012), using the key words, “thorax, reconstruction, biological, trauma”.
No other reports exist about the TW reconstruction in trauma with biological prosthesis.
The majority of patients were treated for TW reconstruction after surgical debulking procedure for thoracic malignancies or for extended abdominal tumors which interested the chest wall. TW reconstruction is a real challenge for thoracic surgeons as well. The reconstructive options are reduced under circumstances of potential of demonstrated wound infection. Biologic materials are specially indicated in potentially contaminated or contaminated surgical fields . Their resistance to the proteases activity either bacterial either human is demonstrated. Moreover they have the unique characteristic to promote the early revascularization of the regenerate tissue. This allows to antibiotics to early reach the infected zone and by reducing the bacterial possibilities to create biologic niches as in synthetic prosthesis it favors the infection healing. A mild inflammatory response to these materials encourages active tissue deposition and natural cytokine production with a consequent healing process and tissue repair. As organized tissue deposition occurs, bio-scaffold is gradually remodeled by host, yielding a repaired tissue structure that is entirely host derived [14, 19, 20].
The challenge in TW reconstruction is the complex mechanisms involved in respiration. It implies muscular and elastic forces whom combined work results in the respiratory equilibrium. It briefly consists in a mild intra-thoracic negative pressure. A prosthetic material have to maintain this equilibrium constant to allow the patient to breath. It also has to avoid at the same time the air passage through the prosthesis preventing the subsequent pneumo-thorax. The alteration of the respiratory equilibrium results in either obstructive or restrictive impairment. Thoracic reconstructive materials must have either enough rigidity to allow the thorax to move symmetrically either elasticity to be able to adapt to the thorax movement. When a big portion of TW have to be removed and consequently many ribs lack, the reconstruction process risks to create an additional respiratory death space. Some reconstructive methods insert metal devices to guarantee the necessary rigidity. However if infection is suspected or demonstrated the insertion of a foreign body becomes a risky procedure.
In infected fields two are the possibilities: anatomic reconstruction with flap transposition or the use of biologics. The use of synthetic materials have been widely described with very good results, but in our opinion is very risky in potentially contaminated or infected fields. Reported side effects of synthetic materials include secondary wound infection in up to 6% of cases, seroma formation, insufficient tensile strength with respiratory failure, long-term onset of restrictive lung disease, graft dehiscence, chronic pain, hemorrhage and wall deformities in pediatric patients [3, 21–23]. As counterpart, the experience in TW reconstruction with biologics is limited. Their use is progressively increasing and giving good results . No other cases have been reported in literature of thoracic reconstruction in trauma patients. However in selected cases such a kind of materials could offers a very trustworthy alternative. The present case demonstrated the possibility to treat infections also by multi-resistant bacteria with the contemporary implantation of a biologic mesh. The described case was very challenging for the necessity to repair TW and the impossibility to implant foreign body. The Pseudomonas Aeruginosa MRSA infected wound, in fact reduced the therapeutic options. The patients needed a procedure as shorter and as less invasive as possible. He could hardly tolerate a long TW reconstructive procedure as in elective patients.
If biologics demonstrated to have usefulness properties, as counterpart the main obstacle to their use is the cost. It is absolutely higher than synthetic mesh, and in patients without infected or, at least potentially contaminated field the use of biologics have not a clearly stated rationale.
Collamend® demonstrated its usefulness in thoracic wall reconstruction even in trauma patients and infected fields. Biological prosthesis confirmed to be a good alternative to synthetic materials either in reconstructive thoracic surgery. However dedicated studies from high experienced centers are needed.
- Holton LH, Chung T, Silverman RP, et al: Comparison of acellular dermal matrix and synthetic mesh for lateral chest wall reconstruction in a rabbit model. Plast Reconstr Surg. 2007, 119: 1238-46. 10.1097/01.prs.0000254347.36092.9c.View ArticlePubMed
- Ge PS, Imai TA, Aboulian A, VanNatta TL: The use of acellular dermal matrix for chest wall reconstruction. Ann Thor Surg. 2010, 90: 1799-1804. 10.1016/j.athoracsur.2010.07.080.View Article
- Zardo P, Zhang R, Wiegmann B, Haverich A, Fischer S: Biological Materials for Diaphragmatic Repair: Initial Experiences with the PeriGuard Repair Patch®. Thorac Cardiov Surg. 2011, 59: 40-44. 10.1055/s-0030-1250499.View Article
- Rocco G, Fazioli F, Scognamiglio F, et al: The combination of multiple materials in the creation of an artificial anterior chest cage after extensive demolition for recurrent chondrosarcoma. J Thorac Cardiovasc Surg. 2007, 133: 1112-1114. 10.1016/j.jtcvs.2006.11.045.View ArticlePubMed
- Hanna WC, Ferri LE, Fata P, et al: The current status of traumatic diaphragmatic injury: lessons learned from 105 patients over 13 years. Ann Thorac Surg. 2008, 85: 1044-1048. 10.1016/j.athoracsur.2007.10.084.View ArticlePubMed
- Weyant MJ, Bains MS, Venkatraman E, et al: Results of chest wall resection and reconstruction with and without rigid prosthesis. Ann Thorac Surg. 2006, 81: 279-85. 10.1016/j.athoracsur.2005.07.001.View ArticlePubMed
- Ansaloni L, Catena F, Coccolini F, Fini M, Gazzotti F, Giardino R, Pinna AD: Peritoneal adhesions to prosthetic materials: an experimental comparative study of treated and untreated polypropylene meshes placed in the abdominal cavity. J Laparoendosc Adv Surg Tech A. 2009, 19 (3): 369-74. 10.1089/lap.2008.0366.View ArticlePubMed
- Gaertner WB, Bonsack ME, Delaney JP: Experimental evaluation of four biologic prostheses for abdominal hernia repair. J Gastrointest Surg. 2007, 11: 1275-1285. 10.1007/s11605-007-0242-8.View ArticlePubMed
- Ansaloni L, Catena F, Coccolini F, Gazzotti F, D'Alessandro L, Daniele Pinna A: Inguinal hernia repair with porcine small intestine submucosa: 3-year follow-up results of a randomized controlled trial of Lichtenstein's repair with polypropylene mesh versus Surgisis Inguinal Hernia Matrix. Am J Surg. 2009
- Campanelli G, Catena F, Ansaloni L: Prosthetic abdominal wall hernia repair in emergency surgery: from polypropylene to biological meshes. World J Emerg Surg. 2008, 3: 33-10.1186/1749-7922-3-33.PubMed CentralView ArticlePubMed
- Ansaloni L, Catena F, Gagliardi S, Gazzotti F, D'Alessandro L, Pinna AD: Hernia repair with porcine small-intestinal submucosa. Hernia. 2007, 11 (4): 321-6. 10.1007/s10029-007-0225-4.View ArticlePubMed
- Gagliardi S, Ansaloni L, Catena F, Gazzotti F, D'Alessandro L, Pinna AD: Hernioplasty with Surgisis(R) Inguinal Hernia Matrix (IHM)trade mark. Surg Technol Int. 2007, 16: 128-33.PubMed
- Catena F, Ansaloni L, Gazzotti F, Gagliardi S, Di Saverio S, D'Alessandro L, Pinna AD: Use of porcine dermal collagen graft (Permacol) for hernia repair in contaminated fields. Hernia. 2007, 11 (1): 57-60. 10.1007/s10029-006-0171-6.View ArticlePubMed
- Catena F, Ansaloni L, Leone A, De Cataldis A, Gagliardi S, Gazzotti F, Peruzzi S, et al: Lichtenstein repair of inguinal hernia with Surgisis inguinal hernia matrix soft-tissue graft in immunodepressed patients. Hernia. 2005, 9 (1): 29-31. 10.1007/s10029-004-0273-y.View ArticlePubMed
- Ansaloni L, Catena F, D'Alessandro L: Prospective randomized, double-blind, controlled trial comparing Lichtenstein's repair of inguinal hernia with polypropylene mesh versus Surgisis gold soft tissue graft: preliminary results. Acta Biomed. 2003, 74 (Suppl 2): 10-4.PubMed
- Ansaloni L, Catena F, Coccolini F, Negro P, Campanelli G, Miserez M: New "biological" meshes: the need for a register. The EHS Registry for Biological Prostheses: call for participating European surgeons. Hernia. 2009, 13 (1): 103-8. 10.1007/s10029-008-0440-7.View ArticlePubMed
- Coccolini F, Agresta F, Bassi A, Catena F, Crovella F, Ferrara R, Gossetti F, et al: Italian Biological Prosthesis Work-Group (IBPWG): proposal for a decisional model in using biological prosthesis. World J Emerg Surg. 2012, on line first
- Cavallaro A, LoMenzo E, DiVita M, Zanghì A, Cavallaro V, Veroux PF, Cappellani A: Use of biological meshes for abdominal wall reconstruction in highly contaminated fields. World J Gastroenterol. 2010, 16 (15): 1928-1933. 10.3748/wjg.v16.i15.1928.PubMed CentralView ArticlePubMed
- Record RD, Hillegonds D, Simmons C, Tullius R, Rickey FA, Elmore D, Badylak SF: In vivo degradation of 14-C labelled small intestine submucosa (SIS) when used for urinary bladder repair. Biomaterials. 2001, 22: 2653-2659. 10.1016/S0142-9612(01)00007-2.View ArticlePubMed
- Badylak S, Kokini K, Tuyllius B, Symmons-Byrd A, Morff R: Mosphologic study of small intestinal submucosa as a body wall repair device. J Surg Res. 2002, 103: 190-202. 10.1006/jsre.2001.6349.View ArticlePubMed
- Lee SL, Poulos ND, Greenholz SK: Staged reconstruction of large congenital diaphragmatic defects with synthetic patch followed by reversed latissimus dorsi muscle. J Pediatr Surg. 2002, 37: 367-370. 10.1053/jpsu.2002.30837.View ArticlePubMed
- Arnold PG, Pairolero PC: Chest-wall reconstruction: an account of 500 consecutive patients. Plast Reconstr Surg. 1996, 98: 804-810. 10.1097/00006534-199610000-00008.View ArticlePubMed
- Sugarbaker DJ, Jaklitsch MT, Bueno R, et al: Prevention, early detection, and management of complications after 328 consecutive extrapleural pneumonectomies. J Thorac Cardiovasc Surg. 2004, 128: 138-146. 10.1016/j.jtcvs.2004.02.021.View ArticlePubMed
- Ouellet JF, Ball CG, Kortbeek JB, Mack LA, Kirkpatrick AW: Bioprosthetic mesh use for the problematic thoracoabdominal wall: outcomes in relation to contamination and infection. Am J Surg. 2012, 203: 594-597. 10.1016/j.amjsurg.2012.01.008.View ArticlePubMed
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