Surgery of Exotic Animals. Группа авторов

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Название Surgery of Exotic Animals
Автор произведения Группа авторов
Жанр Биология
Серия
Издательство Биология
Год выпуска 0
isbn 9781119139607



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major advance in synthetic monofilament absorbable suture. Journal of Long‐Term Eff ects of Medical Implants 14: 359–368.

      42 Postlethwait, R.W. (1970). Long term comparative study of nonabsorbable suture. Annals of Surgery 171: 892.

      43 Postlethwait, R.W. (1979). Five year study of tissue reaction to synthetic sutures. Annals of Surgery 190: 54–57.

      44 Quesada, G., Diago, V., Redondo, L. et al. (1995). Histologic effects of different suture materials in microsurgical anastomosis of the rat uterine horn. The Journal of Reproductive Medicine 40: 579–584.

      45 Ratner, D., Nelson, B., and Johnson, T. (1994). Basic suture materials and suturing techniques. Seminars in Dermatology 13: 20–26.

      46 Riddick, D.H., De Grazia, C.T., and Maenza, R.M. (1977). Comparison of polyglactic and polyglycolic acid sutures in reproductive tissue. Fertility and Sterility 28: 1220–1225.

      47 van Rijssel, E.J.C., Brand, R., Admiraal, C. et al. (1989). Tissue reaction and surgical knots: the effect of suture size, knot configuration, and knot volume. Obstetrics and Gynecology 74: 64–68.

      48 Rothenburger, S., Spangler, D., Bhende, S. et al. (2002). in vitro evaluation of coated VICRYL™ plus antibacterial suture (coated ployglaction 910‐with triclosan) using zone of inhibiton assays. Surgical Infections (Larchmt) 3 (Suppl. 1): S79–S87.

      49 Roush, J.K. (2003). Biomaterials and surgical implants. In: Textbook of Small Animal Surgery, 3e (ed. D. Slatter), 141–148. Philadelphia, PA: W.B. Saunders.

      50 Salgado, M.A., Lewbart, G.A., Christian, L.S. et al. (2014). Evaluation of five different suture materials in the skin of the earthworm (Lumbricus terrestris). Springerplus 3: 423. https://doi.org/10.1186/2193‐1801‐3‐423.

      51 Sanz, L.E., Patterson, J.A., Kamath, R. et al. (1988). Comparison of Maxon suture with Vicryl, chromic catgut, and PDS sutures in fascial closure in rats. Obstetrics and Gynecology 71: 418–422.

      52 Scheidel, P.H., Wallwiener, D.R., Hollander, D. et al. (1986). Absorbable or nonabsorbable suture material for microsurgical tubal anastomosis: Randomized experimental study in rabbits. Gynecolic and Obstetric Investigation 21: 96–102.

      53 Shepherd, A. (2008). Results of the 2007 AVMA survey of US pet‐owning households regarding use of veterinary services and expenditures. Journal of the American Veterinary Medical Association 233: 727–728.

      54 Smit, I.B., Witte, E., Brand, R. et al. (1991). Tissue reaction to suture materials revisited: Is there argument to change our views? European Surgical Research 23: 347–354.

      55 Smith, D.A., Barker, I.K., and Allen, B. (1988). The effect of ambient temperature and type of wound on healing of cutaneous wounds in the common garter snake (Thamnophis sirtalis). Canadian Journal of Veterinary Research 52: 120–128.

      56 Stewart, D.W., Buffington, P.J., and Wacksman, J. (1990). Suture material in bladder surgery: a comparison of polydioxanone, polyglactin, and chromic catgut. Journal of Urology 143: 1261–1263.

      57 Storch, M.L., Rothernburger, S.J., and Jacinto, G. (2004). Experimental efficacy study of coated VICRYL plus antibacterial suture in guinea pigs challenged with Staphylococcus aureus. Surgical Infections (Larchmt) 5: 281–288.

      58 Tan, R., Bell, R., Dowling, B. et al. (2003). Suture materials: composition and applications in veterinary wound repair. Australian Veterinary Journal 81: 140–145.

      59 Tuttle, A.D., Law, J.M., Harms, C.A. et al. (2006). Evaluation of the gross and histologic reactions to five commonly used suture materials in the skin of the African clawed frog (Xenopus laevis). Journal of the American Association for Laboratory Animal Science 45: 22–26.

      60 Wainstein, M., Anderson, J., and Elder, J.S. (1997). Comparison of effects of suture materials on wound healing in a rabbit pyeloplasty model. Urology 49: 261–264.

      61 Yaltirik, M., Dedeoglu, K., Bilgic, B. et al. (2003). Comparison of four different suture materials in soft tissues of rats. Oral Diseases 9: 284–286.

       Heidi Phillips

      Surgery of exotic animals frequently involves small anatomic structures and the need for consistent and reliable exposure, illumination, precision, and clear focus while operating in a confined space. Using some form of magnification is recommended for most surgeries of small exotic animals (Beeber 2000; Bennett 2000b; Bennett and Lock 2000; Jenkins 2000b; Lock 2000; Mullen 2000; Mullen and Beeber 2000; Samour 2010). Technological advances in magnification surgery and refinement of microinstruments and microsuture enable the exotic animal surgeon to successfully perform technically demanding surgical procedures (Jarrett 2004; Bohan et al. 2010; Carr and Castellucci 2010). Magnification surgery enables visualization of detail and differences of anatomy, pathology, and tissue color and character not otherwise discernible (Jarrett 2004; Mungadi 2010; Al‐Benna 2011; Stanbury and Elfar 2011). Small, bleeding vessels are more readily identified for coagulation, minimizing hemorrhage, and improving outcome for many procedures (Bennett 2000b; Mungadi 2010).

      Resolution is the ability of an optical system to discern detail in an object or distinguish two separate objects. The human eye is the limiting factor of many optical systems, its ocular resolution being 0.2 mm (Carr and Castellucci 2010). This means that people who observe two points closer together than 0.2 mm will see only one point.

      Magnification of an image is increased most easily by decreasing the distance between the eye and the object being imaged. The resolution limit of the unaided eye can be increased by close proximity to objects (Chang 2013). This is not always achievable in surgery as decreasing the distance between the surgeon and patient may not permit safe, aseptic manipulation of instruments and tissues or an ergonomic, comfortable, and sustainable posture for the surgeon (Bennett 2000a). Moreover, the healthiest human eye cannot refocus an image at distances closer than 10–12 cm (Carr and Castellucci 2010). Optical aids such as operating microscopes and surgical loupes can improve resolution by many orders of magnitude (Carr and Castellucci 2010). Optical aids permit safe magnification of tissues by increasing the size of the image of the object that is projected to the surgeon's retina.

      Although operating microscopes and surgical loupes utilize similar optical principles, they differ in how magnification is defined. The distance between the objective lens of operating microscopes and the objects to be operated is fixed, and all users achieve the same magnified image. The distance between the objective lens of a surgical loupe and object to be operated varies according to the surgeon's stature and posture; not all users achieve the same magnified image with the same loupe. As the working distance increases, the magnification power decreases. Loupe models are named according to magnification power, but specified magnification power can be achieved only at a specified distance. Users with longer working distances require higher‐power loupes than users with shorter working distances to achieve the same level of magnification (Chang 2014a).