Effect on the tensile strength of human acellular dermis (Epiflex®) of in-vitro incubation simulating an open abdomen setting

Acellular dermal products and transplants are starting to play a significant role in reconstructive surgery [1‐3]. Human acellular dermis (hAD) may offer some advantages over xenogeneic material, such as reduced immunogenicity and increased safety with regard to potential prion infections [4]. Although the hAD Alloderm® has been extensively used outside of Europe and in particular in the USA [5‐9], it is not approved for use in Germany where tissue transplants are required to meet the stringent safety requirements of the German drug law. Epiflex® is currently the only hAD approved for use as a medicinal product in Europe [4].

Dermis is rich in collagen of various subtypes [10] and its biomechanical strength is principally a function of the density and degree of hydration [11] and crosslinking [12] of the collagen fibers. These factors will also influence the extent to which a hAD retains its mechanical strength when incubated in aggressive fluids akin to those present in an infected open abdomen.

An open abdomen is defined as an abdominal wall fascial defect persisting after laparotomy. This condition may be induced, or accepted in case of a planned second look, for prevention of abdominal compartment syndrome or during “damage control surgery”, or it may simply be impossible to close the abdomen due to loss of domain, extensive abdominal wall resection or insufficient fascial stability in the case of peritonitis [13]. Due to the success of commercial and non-commercial vacuum therapy regimes in open abdomen management, fascial closure rates of up to 100% in young damage control trauma patients can be achieved [13, 14]. Closure rates in multimorbid septic abdominal populations are approximately only 30%. In cases where fascial closure fails or vacuum therapy is not available the abdomen is traditionally closed with a synthetic mesh [15]. Since the abdominal compartment is usually contaminated in such patients, a resorbable mesh (e.g. Vicryl) is used. These meshes resorb in the time taken for the abdominal defect to be filled by granulation tissue and a planned ventral hernia is developing. This hernia will then be repaired after 6–12 months, when secondary wound healing finished and an aseptic condition is achieved, with non-resorbable, synthetic meshes and/or component separation techniques [16]. Application of a biological mesh such as hAD in the initial phase could be a novel approach in such patients. To function in this setting, a hAD must be sufficiently structurally resistant to the hostile environment of an open abdomen containing blood, urine or stool from fistulas and typical bacteria found in peritonitis patients. If such a treatment regime could obviate planned ventral hernias, this could reduce morbidity, and the requirement for revisions. Manufactures of these biological meshes are heavily advertising these for the closure of a septic open abdomen, claiming their biostability without a proper proof. The intention was the proof of principle and to identify conditions not suitable for a repair with acellular dermis.

All of our research was carried out in compliance to the Helsinki declaration. The blood donation was approved by the local ethics committee ( Ethic Approval 87/04 of the Ethik Kommission II der Medizinischen Fakultät Mannheim).

Results are show in Figure 3. The breaking strength of hAD in Ringer’s Solution decreases over time. At day 21 the hAD has lost approximately 30% of its breaking strength. Although there is a continuous decrease of the mean breaking strength the differences between day 0 (35.28 ± 3.12 N/mm²) and day 7 (34.19 ± 3.50 N/mm²) and between day 14 (29.32 ± 2.67 N/mm²) and day 21 (24.69 ± 3.27 N/mm²) were not significant. In blood the breaking strength declines as well over time about 32%, although only the comparison between day 0 (34.14 ± 5.46 N/mm²) and 21 (23.38 ± 2.97 N/mm²) and between day 7 (30.0 ± 3.3 N/mm²) and day 21 were significant. A 40% decrease in breaking strength was measured for hAD incubated in urine for 21 days. The decrease was not significant between day 0 (34.3 ± 4.48 N/mm²) and day 7 (32.2 ± 4.215 N/mm²) and between day 7 and day 14 (27.29 ± 3.49 N/mm²). Incubation in a bacterial solution decreased the hAD breaking strength by 51% over a period of 21 days. Although the decrease from day 0 (32.42 ± 1.99 N/mm²) to 21 (16.06 ± 6.87 N/mm²) was significant the intervals from day 0 to 7 (29.01 ± 4.77 N/mm²), from day 7 to 14 (21.33 ± 2.54 N/mm²) and from day 14 to 21 were not significant. Breaking strength of hAD incubated in upper GI secretion showed the most distinct decrease of 78% over 21 days. All intervals showed a significant decrease in breaking strength. Mean breaking strength at day 0 was 33.42 ± 4.79 N/mm², at day7: 25.19 ± 2.94 N/mm², at day 14: 12.14 ± 2.045 N/mm² and at day 21: 7.157 ± 2.84 N/mm² (Table 1).

Comparing the breaking strengths of hAD in the different mediums at day 0 there were no significant differences. At day 7 the only significantly different treatment incubation in upper GI secretion. At day 14 both incubation in upper GI secretion and incubation in the bacteria solution resulted in mechanical strength being lower at the same time point than in the other 3 treatment groups. At this time point, hAD incubated in upper GI was significantly weaker than that incubated in the bacteria solution. At day 21 material incubated in upper GI secretion was again mechanically weaker than that in all other treatments. However, there were no longer any significantly differences amongst the samples incubated in Ringer’s solution, blood, urine and bacteria solution (Table 2).

In the non-parametric analysis of the curves over time according to Koziol et al. the curve of the hAD incubated upper GI secretion is significantly (p = 0.0001) lower than the other curves.

The microscopy analysis of the hAD specimens showed disaggregation of the collagen fibers in all groups over time. In the bacterial and upper GI secretion group, disaggregation seems to occur more rapidly and more distinct when compared over time (Figure 4).

Since open abdomen is a therapeutic option in the treatment of traumatized abdomen or severe peritonitis there is a need for minimizing sequelae [17]. The well-established method of closure with a synthetic resorbable mesh prevents evisceration and chronic foreign body infection, although complication such as massive adhesions and small bowel fistulae are well known [18, 19]. The need for major surgery to reconstruct the abdominal wall and for programmed ventral hernia raises the possibility of further morbidity, increased costs and mortality [20]. With introduction of intra-abdominal negative pressure dressings, delayed primary closure became an option in a high percentage of young trauma patients [21]. Delayed primary closure might be the best option in such patients, but in a majority of older patients with severe peritonitis due to septic focuses this is not feasible [22]. Closure with a tissue transplant could be helpful if adequate mechanical stability could be retained in an open abdomen environment.

Hollinsky and co-workers [23] measured the tensile strength of healthy human abdominal wall using specimens excised from fresh cadaver tissue. They were able to show that the linea alba fails in longitudinal and transversal direction at 39 N. This was calculated to be equivalent to a tensile strength of 10 N/mm² and this may be regarded as the maximum strength required in a healthy human under extreme loads. The mean tensile strength of the transplants in the control group was 35 N/mm² at day 0. Even 25 N/mm², which was the mean strength after 21 days of incubation should be sufficient for Epiflex® to be able to withstand the maximum anticipated force, more so since the in-vitro test disregards adhesion and integration phenomena.

The breaking strength of hAD samples incubated in blood was not significantly different to that of transplants incubated in Ringer’s solution. Epiflex® should therefore be strong enough to reconstruct ventral hernias in an uninfected situation.

Epiflex® incubated in urine had similar properties. It should therefore be suitable for ventral reconstruction in the presence of an urinoma or urinary tract leakage.

Incubation in a bacteria solution resulted in no significant loss of strength at day 0 and 7 when compared to incubation in Ringer’s solution, but there was a significant difference at day 14. At day 21 there was no longer a significant difference. Typical intestinal flora may be capable of reducing the mechanical strength of Epiflex® within the time frame under investigation to a greater extent than blood or urine, although the residual mechanical strength of 16 N/mm² still exceeds the calculated requirement.

The study has limitations with regard to the composition of the bacteria solution. Although the solution represents a common mixture of bacteria found in peritonitic patients, different bacteria mixtures could well have significantly different effects on hAD, since different bacteria strains and species excrete different concentrations of active agents such as collagenase.

Upper GI tract secretion had a powerful effect on the mechanical strength of Epiflex®. Loss of mechanical strength was continuous and when compared to the effects of the other incubation fluids, significantly increased at day 7, 14 and 21. The presence of an upper GI leakage, the closure of an open abdomen with Epiflex® might be compromised. At this stage of an open abdomen therapy, a definite closure is rarely indicated. It is unclear whether a pure pancreatic secretion from a pancreas fistula would have the same impact on the mechanical strength of Epiflex®.

The decrease in mechanical strength in the different liquids might be caused by various factors. Upper GI secretion is a mixture of gastric fluid, bile and pancreatic fluid and contains a heterogeneous mixture of digestive enzymes including proteases, lipases and amylases [24, 25]. The upper GI secretion was frozen shortly after collection at −80°C to retard reduction of enzyme activity. Since the extracellular matrix consists of various proteins, glycoproteins and polysaccharides, enzymatic hydrolysis would seem to be a likely contributor to loss of tensile strength [26, 27]. Bacteria also secrete hydrolytic enzymes such as collagenases, whereby the extent and the composition depends on species and strain. Furthermore, microbial organisms can modify the pH of the environment [28‐30]. This may influence the degradation of bioresorbable materials [31‐33]. It is known that superoxide ions from leukocytes and macrophages accelerate the degradation of absorbable materials [34]. The mechanism leading to loss of mechanical strength in Ringer's solution after 21 days is unclear. Temperature may affect biodegradation [35, 36], however the incubation temperature in our study (37°C) seems unlikely to have exacerbated hydrolysis. Numerous studies demonstrated a significant loss in strength of biodegradable materials in aqueous solutions, presumably by cumulative low-level irreversible hydrolysis [33, 36, 37].

Epiflex® exhibits reduced mechanical strength after 3 weeks of incubation in Ringer’s solution, in body fluids (blood, urine, upper GI secretion) and in a bacteria solution. It seems unlikely that the loss of mechanical strength arising from incubation in Ringer’s solution, blood and urine would be clinically significant in the setting of a primary closure of an open abdomen. The loss of mechanical strength arising from incubation in a bacteria solution suggests that this might be clinically significant in an infected open abdomen situation, depending on the concentration, species and strain of the contaminating organisms. Incubation of Epiflex® in upper GI secretion caused a more pronounced loss of mechanical strength. Use of hAD for open abdomen closure in the presence of upper GI leakage or of a pancreatic fistula may be inappropriate. The authors intend to proceed with a phase I clinical study. The superiority of hAD in regards to the development of ventral hernia must be shown in a phase III study.