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Experimental study of sutureless vascular anastomosis with use of glued prosthesis in rabbits

Authors Vokrri L, Qavdarbasha A, Rudari H, Ahmetaj H, Manxhuka-Kërliu S, Hyseni N, Porcu P, Cinquin P, Sessa C

Received 22 August 2014

Accepted for publication 24 September 2014

Published 27 March 2015 Volume 2015:11 Pages 211—217

DOI https://doi.org/10.2147/VHRM.S73104

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr Daniel A. Duprez


Lulzim Vokrri,1–3,5 Arsim Qavdarbasha,1–3 Hajriz Rudari,1–3 Halil Ahmetaj,1–3 Suzana Manxhuka-Kërliu,1–3 Nexhmi Hyseni,1–3 Paolo Porcu,4 Philippe Cinquin,4,5 Carmine Sessa4,6

1Department of Vascular Surgery, University Clinical Center of Kosovo, 2Medical Faculty, University of Pristina, 3Veterinary Institute, Pristina, Republic of Kosovo; 4Department of Vascular Surgery, University Clinical Center of Grenoble, 5University of Grenoble Alpes/CNRS/TIMC-IMAG UMR 5525 (GMCAO team), Grenoble, 38000, 6University of Grenoble Alpes, Grenoble 38000, France

Objective: The objective of this study is to explore the feasibility and efficacy of a new technique for sutureless vascular anastomosis, using glued prosthesis, as a sole anastomosis fixation method in rabbits.
Methods: Ten rabbits were randomly selected to conduct the experiment. Five rabbits underwent direct anastomosis of infrarenal abdominal aorta, with glued prosthesis. In five other rabbits, reconstruction was done by sutured anastomosis. All animals were immediately examined by echo-Doppler for patency of anastomosis. The burst pressure of the glued anastomosis was measured and compared with that of a sutured artery. The animals were euthanized, and tissue samples were taken for histological examination immediately after the experiment.
Results: Compared to conventional anastomoses, sutureless vascular anastomoses required shorter time of creation and significantly reduced blood loss (P<5%). There was no significant difference on the average blood flow through the anastomosis between two groups at the end of surgery. All anastomoses with glued prosthesis, examined by echo-Doppler, were patent at the anastomotic site, except one, which was stenosed immediately after surgery. In the control group, except one with stenosis, all conventional anastomoses were patent. Mean burst pressure at the anastomotic site for sutureless anastomoses was lower than in control group. Macroscopically, the BioGlue did not demonstrate any adhesion to the surrounding tissue as it was covered by the vascular prosthesis. Histological examination showed low-grade inflammatory reaction in glued anastomoses versus no inflammatory reaction at the sutured anastomoses.
Conclusion: This technique may provide a feasible and successful alternative in vascular surgery. However, further long-term studies are necessary to elucidate the break pressure and degree of inflammation at the anastomotic site.

Keywords: sutureless vascular anastomosis, polytetrafluoroethylene prosthesis, BioGlue, rabbit aorta

Introduction

The standard surgical technique to perform end-to-end vascular anastomosis is a hand suture based on the principles described by Carrel in 1902.1

The design of this experiment of sutureless vascular anastomosis with BioGlue was inspired from two experiments of Schiller et al, adapting it for the rabbit infrarenal abdominal aorta.2,3

Most vascular anastomoses are performed with sutures, which are sometimes technically challenging and can lead to failure from intimal hyperplasia and foreign body reaction.

The introduction of medical adhesive provided another anastomotic technique. Several types of medical adhesives have been successfully used as tissue strengtheners and hemostatic agents. Tissue adhesives and bioadhesives act through polymerization between themselves and adjacent tissues. BioGlue surgical adhesive (CryoLife, Inc, Kennesaw, GA, USA) is currently being used to provide hemostasis on cardiovascular anastomoses in adults.47

Schiller et al, in their short-term study, have identified a significant inflammatory response after application of the glue in the glue control and glue anastomosis groups of the carotid arteries of rabbit. Two cases of early calcification were also detected.2

In their second experimental work on rabbits, Schiller et al reported good results with in vivo use of BioGlue for sutureless anastomosis in 34 carotid arteries of rabbits. However, stenosis, thrombosis, and pseudo-aneurysms were also registered.3

Wippermann et al have found severe inflammatory reactions associated with the use of BioGlue in 12 porcine coronary arteries, when they compared three different types of adhesives: in group I gelatin–resorcinol–formaldehyde glue, in group II n-butyl-2-cyanoacrylate glue, and in group III albumin–glutaraldehyde glue.8

Gundry et al have successfully tested in vitro and in vivo coronary artery bypass graft anastomoses, using BioGlue formulated from bovine albumin and glutaraldehyde on 12 bovine hearts.9 Belleghem et al described the procedure of sutureless anastomosis in iliac arteries of eight mongrel dogs using BioGlue, as moderately successful with good permeability (57%) of anastomosis. In contrast to previous reported studies, they have noticed a clear enzymatic breakdown of the glue before total disappearance in the anastomotic site.10

Our study has evaluated the feasibility and efficacy of an anastomotic technique for sutureless vascular anastomosis by glued prosthesis in an experiment with rabbits. Conventional sutured anastomosis was used as a control group.

Materials and methods

Technology

BioGlue is a surgical adhesive that combines two agents with distinct properties, concentrated, 45% bovine albumin, and 10% glutaraldehyde. BioGlue is a transparent liquid. The compound becomes active once the two components are mixed within the applicator gun, by passing through a specially designed delivery tip.

When coming into contact with blood, it polymerizes into a solid substance with the shape of a glue membrane. The glue gets around 60% of its holding power in 20 seconds, increasing to 95% within 2 minutes, ensuring a rapid procedure. The glue is approved for use in North America and Europe for the treatment of acute aortic dissection, for facilitating sutured arterial anastomoses or sealing off the suture lines.46

The Ethical Committee for Animal Experiments of the Medical Faculty of the Pristina University has approved all procedures. The animal experiment was designed under the Animal Protection Act and accepted by the Commission for Animal Protection in Pristina, Kosovo. Twelve randomly selected healthy gray rabbits, of different age, sex, and weight, were used for the study. Two of them were used for testing the feasibility of the experiment. The remaining ten animals were randomly divided into a study group and a control group. The average age was 22.2 weeks (range 20–25 weeks) with an average weight 3.01 kg (range 2.5–3.8 kg). Sutureless anastomoses of infrarenal abdominal aorta, using glued prosthesis, were performed in five animals. All animals were anesthetized with a combination of ketamine hydrochloride (60–100 mg/kg) (Ketavet; Pharmacia GmbH, Erlangen, Germany) and xylazine hydrochloride (Rompun; Vital com, Backrest, Romania).

After the animal was positioned on operating table, a peripheral intravenous line was placed in the rabbit’s ear vein. Then 10 mg/kg cefazolin was injected intramuscularly for antibiotic prophylaxis. Intravenous crystalloid fluids were also given for maintenance during surgery. Heart rate and rhythm were monitored continuously. Anesthesia was maintained by intramuscular xylazine hydrochloride 5–8 mg/kg/h, for muscle relaxation. After the animals were prepared, a 7-cm long incision in the abdomen was made. Infrarenal abdominal aorta was dissected and mobilized for approximately 6–7 cm. Heparin (1 mg/kg) was administered intravenously, and the abdominal aorta was clamped before transection.

After total transection of the infrarenal abdominal aorta, they underwent direct anastomosis (Figure 1A). In the study group initially, at the distal part of aorta (4 cm distally from the site of anastomosis), a percutaneous transluminal angioplasty balloon catheter 3 mm in diameter and 20 mm long (Boston Scientific, Marlborough, MA, USA) was inserted, as a temporary internal stent to create and seal the anastomosis during gluing. Then, both transected ends of aorta were drawn over the angioplasty catheter and aligned (Figure 1B). A longitudinal incision was made on 20-mm long ePTFE prosthesis with a 4 mm diameter. A small amount of BioGlue (0.5 mL) was applied to the inner surface of prosthesis. Subsequently, the endovascular balloon was inflated and glued prosthesis was applied from outside and around the anastomosis (Figure 1C). Glued prosthesis was essential to avoid inhomogeneous distribution of the glue. After allowing the adhesive to polymerize for 2 minutes, the vascular clamps were removed to reestablish the circulation. The surgical field was carefully kept dry. The site of catheter introduction at the aorta was sutured with one suture, after removal of the balloon catheter (Figure 1D).

Figure 1 Schematic representation of sutureless anastomosis with glued prosthesis.
Notes: (A) Positioning of the ends of the aorta. (B) Insertion of balloon catheter. (C) Positioning of glued prosthesis around anastomosis. (D) Completion of anastomosis.

In the control group, end-to-end anastomosis of the infrarenal abdominal aorta was performed on five other animals, using a 6/0 polypropylene (Ethicon) non-absorbable continuous suture. The distal pulsation was routinely examined to verify the patency of anastomosis. The surgical procedure was accomplished without any major technical difficulty in all animals.

During the experiment, the anastomosis creation time, blood loss, blood flow, and burst pressure of each anastomosis were measured. Data on intraoperative variables were collected, and statistically analyzed.

In vivo measurements

Blood loss

Blood oozing out of the anastomosis during a period of 5 minutes after de-clamping was aspirated and its volume measured.

Doppler control

Immediately after surgery, the patency of the anastomoses was assessed in all the animals with a perivascular flow probe (Perivascular Flow probes; Siemens, Munich, Germany). Moreover, in order to identify any thrombosis or stenosis of the anastomoses, all the animals were examined using Doppler (Sonoace, Medison Co., Ltd. Seoul, South Korea) while still under anesthesia.

The echo-Doppler showed the laminar flow and the absence of blood turbulence at the site of anastomosis, with the exception of the first anastomosis, which was stenosed. This was probably due to the bigger doses of BioGlue used in the vascular prosthesis.

Burst pressure measurement in the anastomotic site

The glued anastomosed infrarenal abdominal aorta was cut off and rinsed with heparin and liquid saline. Then, with the vascular anastomotic break pressure-measuring instrument, the anastomotic break pressure was measured (Figure 2). One end of the artery was connected to a plain needle and fixed with thread; the other end was clipped with a hemostat. Then, the needle was introduced to a distal part of anastomosis, and it was connected to a pressure syringe, a blood transfusion catheter, and blood pressure apparatus, through a three-way stopcock. Subsequently, the anastomosed aorta was irrigated continuously with liquid saline. When the liquid saline in the syringe was simultaneously injected into the aorta and the catheter linked to the blood pressure apparatus, the pressure number read from the apparatus reflected the pressure bearing of the anastomosis. The anastomotic burst pressure was measured.

Figure 2 Vascular anastomotic break pressure-measuring instrument.
Notes: 1, blood pressure apparatus (product of Omron, Medical Instrument Factory, Mannheim Germany); 2, connecting tube (20 mm length and 2.0 mm in diameter, Groupe Didactic, Le Mirlibut, Etainhus, France); 3, three-way turn cock (a product of Instrument Co, Samora Correia, Portugal); 4, pressure syringe (20 mL, a product of Medtronic Company, Deggendorf, Germany); and 5, measuring tube and needle 18 G with plain tip (a product of Groupe Didactic).

Macroscopic assessment

BioGlue did not demonstrate adhesions to the surrounding tissue, because it was covered by vascular prosthesis. On macroscopic examination, the surgery sites were assessed for homogeneity and firmness of the glued prosthesis. They looked identical, and there were no signs of thrombosis on the anastomotic site. While still anesthetized, the rabbits were euthanized with an injection of T61 (Hoechst Veterinaer Co, Frankfurt, Germany). The infrarenal abdominal aortas were removed, longitudinally opened, macroscopically assessed, and fixed in a 4% formaldehyde solution (Roti-Histofix; Carl Roth GmbH-Co, Karlsruhe, Germany).

Statistical analysis

Data are expressed as means ± standard deviations. t-Tests have been used to test the statistical significance of the difference between the study and the control group means. The means were deemed as significant only at 5% level of significance (P<0.05). The difference between the study and the control group was significant for all outcome variables, with the exception of the blood flow of anastomosis.

Results

The technical procedure of end-to-end sutureless anastomosis with glued prosthesis in rabbit’s infra-abdominal aorta was successfully realized, without leakage or visible occlusion. No hematoma was detected in either group (Figure 3). In order to test the efficiency of glued prosthesis anastomosis compared to conventional anastomosis, data on four variables have been collected.

Figure 3 Intraoperative view of sutureless vascular anastomosis by glued prosthesis in rabbit (black arrow).

The anastomosis by glued prosthesis was completed with a shorter completion time. The mean anastomosis time was 7.20±0.29 minutes for the study group and 17.44±0.30 minutes for the control group. The high magnitude of the t-statistic value shows that the difference between the study group mean and the control group mean is significantly different. Thus, the anastomosis time using glued prosthesis is significantly lower (Figure 4).

Figure 4 Time of anastomosis (n=10, *significance at 5%, P=1.32×10–11).

The mean blood loss was 0.20±0.14 mL for sutureless anastomoses, versus 8.58±0.26 mL for sutured anastomoses. Our results have shown that there is statistically significant difference between the two groups. The blood loss in anastomosis by glued prosthesis is significantly lower, than sutured anastomosis (Figure 5).

Figure 5 Blood loss of anastomosis (n=10, *significance at 5%, P=4.19×10–12).

The average blood flow through anastomosis with glued prosthesis at the end of operation was 39±2.55 mL/min and 40.4±2.41 mL/min in the sutureless and sutured anastomoses, respectively, in the control group. The color-Doppler shows the laminar flow and the absence of blood turbulences at the anastomotic site of sutureless aortic anastomosis. One anastomosis by the glued prosthesis was found to be stenosed immediately, probably due to exceeded doses of applied BioGlue. In three other anastomoses, a low degree of inflammation was macroscopically visible. In the control group, all conventional sutured anastomoses were patent. One anastomose showed approximately 50% stenosis, which occurred during suturing (Table 1). By the high magnitude of the t-statistic, we can conclude that the difference among groups is statistically insignificant. Our results have shown that there is no statistically significant difference between the two groups in terms of blood flow through the anastomosis (Figure 6).

Table 1 Doppler and macroscopic findings in ten rabbit infrarenal abdominal aorta
Abbreviations: SG, study group; CG, control group.

Figure 6 The average blood flow of anastomosis (n=10, P=0.398).

The average anastomotic break pressure for study group was 284 mmHg (37.86 kPa), whereas the control group did not have a measurable burst pressure despite increasing the pressure to 300 mmHg (40 kPa) (Figure 7).

Figure 7 Burst pressure of anastomosis (n=10, *significance at 5%, P=3.97×10–15).

Microscopic assessment

In the study group, we observed low-grade inflammation of the arterial wall, at the site of anastomoses.

Histological examination of the abdominal aorta showed a low-grade inflammatory reaction on the adventitial wall of the glued anastomosis, whereas no inflammatory reaction was seen in the control group. Acute inflammatory cell infiltrates were present in the glued anastomosis groups, with the invasion of inflammatory cells located predominantly at the junction between the wall and the glued prosthesis. Some foreign body reaction was detected as mild thickening of the intima around the sutures.

Discussion

The concept and idea of using different vascular devices and medical adhesives for sutureless anastomosis has always been attractive and has therefore resulted in a considerable number of experiments and publications. Exploration of new vascular anastomotic methods has become a focus of attention. The development of alternative methods to construct sutureless vascular anastomoses is characterized by a reduction in technical demand.1114 Fürst and Banerjee in their work presented that intact aortic tissue showed only low-grade or medium-grade inflammation after use of BioGlue.11 Other investigators have also reported satisfactory results using a BioGlue for sutureless vascular anastomosis, sutureless microanastomosis, including hemostatic’s effects and repair of cardiac vessel injuries, and closure of arteriotomy by glued patch.1117 Some authors attribute thrombus formation and stenosis to technical failure rather than to cytotoxicity of medical adhesives.18 In 1968, Gottlob and Blümel had realized sleeve anastomosis in small arteries and veins with enhancement of the anastomosis by bio-fibrin glue. This method has minimized vascular wall injury caused by the suture; however, the procedure involved was difficult and time consuming.19 There is evidence that biological adhesives have a positive impact on the results of cardiovascular operations by shortening the operation time, reducing perioperative bleeding, and providing more suitable tissue consistency for successful operative repair.2022 Obviously, the selection of specific medical adhesive depends on several factors, including quantity of adhesive required, its mechanical properties, hemostatic efficacy, effects on wound healing, and the inflammatory response it stimulates. These factors are especially important when performing microanastomoses, as these are usually time consuming and challenging.2325

Anastomosis techniques without suturing can eliminate vascular injury and foreign body injury within the vessel wall. In this study, we have designed a sutureless anastomosis technique, using a glued prosthesis, which combines the advantages of the sutured and the glued anastomotic technique. This technique may be used in small- and medium-sized vessels. Our experiment suggests that the sutureless anastomosis has moderate advantages over the sutured method. The anastomosing time was shorter, and the blood loss was not significant. As the two vascular ends are anastomosed by glued prosthesis, anastomotic bleeding can safely be prevented. The immediate patency rates and average blood flow of anastomosis were similar.

Nevertheless, a question remained on whether the glued anastomosis supports high intraluminal blood pressure. The answer mainly depends on the intraluminal blood pressure and the sustaining pressure of the anastomosis. Normal human blood pressure is 80 mmHg (10.66 kPa) to 120 mmHg (16.0 kPa), and may increase to 280 mmHg (37.33 kPa) or more in some very rare pathological conditions. The mean burst pressure of the sutureless anastomosis obtained in this experiment was 284 mmHg (37.86 kPa), so we can conclude that the glued anastomosis can sustain normal arterial blood pressure. The anastomosis was able to maintain integrity even at high pressures, which we may find in pathological situations. This implies that the sutureless anastomosis using glued prosthesis can effectively be used in patients with well-controlled systolic blood pressure. However, larger experimental studies with long-term follow-up are needed to more accurately determine the burst pressures of these anastomoses. Unfortunately, the excess doses of medical adhesive applied in the inner surface of ePTFE graft prosthesis probably led to anastomotic stenosis seen on the first case of the study group. The macro- and micro-histological results showed that inflammation in the study group was higher than in the control group. Our in vivo study in rabbits, although small in number, suggests that this anastomosis using glued prosthesis can be effective. These results demonstrate that biological glue made from the combination of bovine albumin and glutaraldehyde is effective in vivo in the creation of sutureless anastomosis. However, the inflammatory effect of BioGlue needs to be taken into account, when choosing to use such a method. Further studies are needed to better evaluate the long-term effects of such methods on the vessel wall.

Rabbits are the small animal of choice for conduits of 1–4 mm in diameter, enabling implantation of longer conduits and having a greater similarity than rats to humans in coagulation, endothelialization, and patency.26

Conclusion

Our first experience with glued prosthesis as a method of sutureless vascular anastomosis has shown that vascular anastomosis was feasible, simple, and fast and can be considered reliable, without major signs of complication. Medical adhesives deserve to be reconsidered as an alternative to suturing in surgery. The hybrid sutureless vascular anastomosis technique with medical adhesives in the future may provide a promising alternative to manual suturing. However, further long-term studies are necessary to elucidate the burst pressure and degree of inflammation in the anastomotic site and to investigate the applicability of this technique in human practice.

Acknowledgment

This work was supported by French state funds managed by the ANR within the Investissements d’Avenir programme (Labex CAMI) under reference ANR-11-LABX-0004

Disclosure

The authors report no conflicts of interest in this work.


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