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Ординатура / Офтальмология / Английские материалы / Diabetes and Ocular Disease Past, Present, and Future Therapies 2nd edition_Scott, Flynn, Smiddy_2009

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114 Diabetes and Ocular Disease

Figure 6.20. Vitreous infusion suction cutter (VISC) with surrounding fiber optics inserted through the pars plana into the vitreous cavity.

Dr. Machemer performed the first pars plana vitrectomy in 1970 and soon realized the potential value of removing not only opaque vitreous hemorrhages but also proliferative membranes, and repairing retinal detachments by releasing vitreous traction [57]. This new surgery provided a way to restore sight for people who had become blind from diabetic retinopathy.

At this early stage, the vitrectomy instruments evolved rapidly with a single hand-held instrument named the vitreous infusion suction cutter (VISC) (Fig. 6.20) providing vitreous infusion, suction, and cutting. The advantages of having a second instrument in the vitreous cavity for additional infusion, diathermy, tissue retraction, aspiration, etc. were soon recognized and bimanual surgical techniques and additional instruments were developed [58].

The initial vitrectomies were performed with just coaxial light from the operating microscope, but intraocular visualization was soon improved by the introduction of fiber-optic light sources into the vitreous cavity.

O’Malley [59,60] emphasized the value of decreasing the diameter of the instrument used in the eye by separating the functions and introducing the guillotine type cutter and 3-port system separating the suction-cutter from the infusion and the fiber-optic light source (Fig. 6.21). Aaberg [61–63], Charles (Fig. 6.22) [64,65], Douvas [66], Federman [67], Kloti [68,69], McCuen [70], Michels (Fig. 6.23) [71–79], Peyman [80], Tolentino [81,82], and many others [83–86] expanded and clarified the indications for vitrectomy and made important contributions to instrumentation and surgical techniques. Recently, the size of vitrectomy instruments has been further reduced to 25 gauge [87]; their use decreases postoperative morbidity and recovery time in selected cases.

Improvements in evaluating eyes with opaque media by ultrasound dramatically increased the success of pars plana vitreous surgery. Coleman and coworkers

History of Evolving Treatments for Diabetic Retinopathy

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Figure 6.21. Early version of Ocutome vitrectomy instrument developed by O’Malley and Heintz, which utilized a back and forth guillotine cutting action of formed vitreous and proliferative tissue aspirated into the side of the instrument tip.

[88,89], and others, developed and refined ultrasound procedures to identify areas of vitreoretinal traction, and the presence, location, and extent of retinal detachments, better.

The use of pars plana vitreous surgery spread rapidly because of its potential to dramatically restore functioning vision for patients who had lost their sight most frequently from complications of diabetic retinopathy, and because of a philosophy of openly sharing experiences and ideas by Dr. Machemer and others involved with the development of pars plana vitreous surgery.

Figure 6.22. Steven T. Charles, M.D., Director of Charles Eye Institute of Memphis, Tennessee. Dr. Charles made many contributions to the development of vitreous surgical instruments and developed numerous creative procedures for vitreous surgery.

116 Diabetes and Ocular Disease

Figure 6.23. Ronald G. Michels, M.D., Professor of Ophthalmology at the Johns Hopkins University School of Medicine, former Director of Wilmer Ophthalmological Institute Vitreoretinal Surgery Service, and Co-Director of The Retina Center in Baltimore, Maryland. Dr. Michels made invaluable contributions to the development of pars plana vitreous surgery by developing new vitreous surgery procedures and publishing extensively on vitreous surgery.

Still, questions remained about when to recommend vitreous surgery for dense nonclearing vitreous hemorrhages, and for eyes with functioning vision but very extensive neovascular proliferation beyond what could reasonably be treated with photocoagulation. Once again, the NEI provided funding for a large multicenter clinical trial named the Diabetic Retinopathy Vitrectomy Study (DRVS) [90], with Dr. Matthew Davis as Director. The DRVS confirmed the benefits of pars plana vitrectomy in removing dense vitreous hemorrhages and extensive neovascularization caused by diabetic retinopathy.

CONCLUSION

The history of the treatment for diabetic retinopathy encompasses almost 60 years and continues to evolve with new innovations. It is composed of many important observations, creative new concepts, elaborate laboratory and clinical research projects, development and refi nement of revolutionary instruments and procedures, sophisticated evaluations confirming the benefits of good control of blood sugar levels, and appropriate photocoagulation and vitreous surgery. A very large number of people have made important contributions to the current level of knowledge and treatment abilities, and the future is even more encouraging for additional discoveries that will further enhance the ability to preserve and regain vision for people with diabetes.

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REFERENCES

1.von Jaeger E. Beitrage zur Pathologie des Auges. 2. Lieferung, S. 33, Tafel XII. Wien, K.K. Hofand Staatsdruckerei; 1855.

2.Banting FG, Best CH. The internal secretion of the pancreas. J Lab Clin Med. 1922;7:251–266.

3.Hutton WL, Snyder WB, Vaiser A, Siperstein MD. Retinal microangiopathy without associated glucose intolerance. Trans Amer Acad Ophthalmol Otolaryngol.

1972;76:968–980.

4.Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin dependent diabetes mellitus. N Engl J Med. 1993;329:977–986.

5.Meyer-Schwickerath G. Verh Dtsch Ges Ophthalmol Heidelberg. 1949;55:256.

6.Meyer-Schwickerath G. Licktkoagulation. Buech Augenarzt. 1959;33:1–96.

7.Meyer-Schwickerath G. Light Coagulation. Translated by SM Drance. St. Louis: CV Mosby Co; 1960:114.

8.Moran-Salas J. Arch Soc Oftal Hispano-Am. 1950;10:566–578.

9.Wetzig PC, Worlton JT. Treatment of diabetic retinopathy by light coagulation: a preliminary study. Br J Ophthalmol. 1963;47:539–541.

10.Wetzig PC, Jepson CN. Treatment of diabetic retinopathy by light coagulation. Am J Ophthalmol. 1966;62:459–465.

11.Amalric MP. Essai de traitement de la retinopathie diabetique exsudative. Bulletin des Societes d’Ophtalmologie de France. 1960;5–6:1–4.

12.Amalric P. Nouvelles considerations concernant l’evolution et le traitment de la retinopathie diabetique. Ophthalmologica. 1967;154:151–160.

13.Okun E, Cibis P. The role of photocoagulation in the treatment of proliferative diabetic retinopathy. Arch Ophthalmol. 1966;75:337–352.

14.Okun E. The effectiveness of photocoagulation in the therapy of proliferative diabetic retinopathy (PDR); (controlled study in 50 patients). Trans Am Acad Ophthalmol Otolaryngol. 1968;72:246–252.

15.Okun E, Johnston G, Boniuk I. Management of Diabetic Retinopathy; a Stereoscopic Presentation. St. Louis: The C.V. Mosby Co; 1971.

16.Wessing AK, Meyer-Schwickerath G. Results of photocoagulation in diabetic retinopathy. In: Goldberg MF, Fine SL, eds. Symposium on the Treatment of Diabetic Retinopathy. Airlie House, Warrenton, VA, September 29 to October 1, 1968. Washington, DC, US Government Printing Office (PHS Publ No 1980), 1969: 569–592.

17.Caird FI, Garrett CJ. Prognosis for vision in diabetic retinopathy. Diabetes. 1963;12: 389–397.

18.Beetham WP. Visual prognosis of proliferating diabetic retinopathy. Br J Ophthalmol. 1963;47:611–619.

19.Campbell CJ, Rittler MC, Koester CJ. The optical maser as a retinal coagulator: an evaluation. Trans Am Acad Ophthalmol Otolaryngol. 1963;67:58–67.

20.Campbell CJ, Koester CJ, Curtice V, et al. Clinical studies in laser photocoagulation.

Arch Ophthalmol. 1965;74:57–65.

21.Zweng HC, Flocks M, Kapany NS, et al. Experimental laser photocoagulation. Am J Ophthalmol. 1964;58:353–362.

22.Beetham WP, Aiello LM, Balodimos MC, et al. Ruby laser photocoagulation of early diabetic neovascular retinopathy: preliminary results of a long-term controlled study. Arch Ophthalmol. 1970;83:261–272.

118 Diabetes and Ocular Disease

23.Aiello LM, Beetham WP, Balodimos MC, et al. Ruby laser photocoagulation in treatment of diabetic proliferating retinopathy: preliminary report. In: Goldberg MF, Fine SL, eds. Symposium on the Treatment of Diabetic Retinopathy. Airlie House, Warrenton, VA, September 29–October 1, 1968. Washington, DC, US Government Printing Office (PHS Publ No 1980), 1968:437–463.

24.L’Esperance FA. An ophthalmic argon laser photocoagulation system: design, construction, and laboratory investigations. Trans Am Ophthalmol Soc. 1968;66:827–904.

25.L’Esperance FA. Argon laser photocoagulation of diabetic retinal neovascularization: a five year appraisal. Trans Am Acad Ophthalmol Otolaryngol. 1973;77:OP6–OP24.

26.Little HL, Zweng HC, Peabody RR. Argon laser slit lamp retinal photocoagulation.

Trans Am Acad Ophthalmol Otolaryngol. 1970;74:85–97.

27.Zweng HC, Little HL, Peabody RR. Further observations on argon laser photocoagulation of diabetic retinopathy. Trans Am Acad Ophthalmol Otolaryngol. 1972;76:990–1004.

28.Patz A, Maumanee AE, Ryan SJ. Argon laser photocoagulation: advantages and limitations. Trans Am Acad Ophthalmol Otolaryngol. 1971;75:569–579.

29.Davis MD. Natural course of diabetic retinopathy. In: Kimura SJ, Caygill WM, eds. Vascular Complications of Diabetes Mellitus with Special Emphasis on Microangiopathy of the Eye. St. Louis: C.V. Mosby; 1967:139–169, Chapter 10.

30.Davis MD. The natural course of diabetic retinopathy. Trans Am Acad Ophthalmol Otolaryngol. 1968;72:237–240.

31.Gass JDM. A fluoroscein angriographic study of macular dysfunction secondary to retinal vascular disease. IV Diabetic retinal angiopathy. Arch Ophthalmol. 1968;80:583–591.

32.Kohner EM, Dollery CT. Fluoroscein angiography of the fundus in diabetic retinopathy. Br Med Bull. 1970;26:166–170.

33.Bresnick GH, de Venecia G, Myers FL, et al. Retinal ischemia in diabetic retinopathy. Arch Ophthalmol. 1975;93:1300–1310.

34.Bresnick GH, Engerman R, Davis MD, et al. Patterns of ischemia in diabetic retinopathy. Trans Am Acad Ophthalmol Otolaryngol. 1976;81:OP694.

35.Kohner EM. The evolution and natural history of diabetic retinopathy. Int Ophthalmol Clin. 1978;18:1–16.

36.Patz A. Clinical and experimental studies on retinal neovascularization, Thirty-Ninth Edward Jackson Memorial Lecture. Am J Ophthalmol. 1982;94:715–743.

37.Shimizu K, Kobayashi Y, Muraoka K. Midperipheral fundus involvement in diabetic retinopathy. Ophthalmology. 1981;88:601–612.

38.Patz A, Schatz H, Ryan SJ, et al. Argon laser photocoagulation for treatment of advanced diabetic retinopathy. Trans Am Acad Ophthalmol Otolaryngol. 1972;76:984.

39.Patz A, Schatz H, Berkow JW, et al. Macular edema-an overlooked complication of diabetic retinopathy. Trans Am Acad Ophthalmol Otolaryngol. 1973;77: OP34–OP42.

40.Merin S, Yanko L, Ivry M. Treatment of diabetic maculopathy by argon-laser. Br J Ophthalmol. 1974;58:85–91.

41.Blankenship GW. Diabetic macular edema and argon laser photocoagulation: a pro-

spective randomized study. Ophthalmology. 1979;86:69–75.

42. British Multicentre Study Group. Photocoagulation for diabetic maculopathy: a randomized controlled clinical trial using the xenon arc. Diabetes. 1983;32:1010–1016.

43.Luft R, et al. Hypophysectomy in man. Further experiences in severe diabetes mellitus. Br Med J. 1955;2:752–756.

History of Evolving Treatments for Diabetic Retinopathy

119

44.Bradley RF, Rees SB. Surgical pituitary ablation for diabetic retinopathy. In: Goldberg MF, Fine SL, eds. Symposium on the Treatment of Diabetic Retinopathy. Airlie House, Warrenton, VA, September 29–October 1, 1968. Washington, DC, US Government Printing Office (PHS Publ No 1980), 1968:171–191.

45.Field RA, McMeel JW, Sweet WH, Schepens CL. Hypophyseal stalk section for angiopathic diabetic retinopathy. In: Goldberg MF, Fine SL, eds. Symposium on the Treatment of Diabetic Retinopathy. Airlie House, Warrenton, VA, September 29–October 1, 1968. Washington, DC, US Government Printing Office (PHS Publ No 1980), 1968:213–225.

46.Oakley NW, Joplin GF, Kohner EM, Fraser TR. The treatment of diabetic retinopathy by pituitary implantation of radioactive yttrium. In: Goldberg MF, Fine SL, eds.

Symposium on the Treatment of Diabetic Retinopathy. Airlie House, Warrenton, VA, September 29–October 1, 1968. Washington, DC, US Government Printing Office (PHS Publ No 1980), 1968:317–329.

47.Diabetic Retinopathy Study Research Group. Preliminary report on effects of photocoagulation therapy. Am J Ophthalmol. 1976;81:383–396.

48.Early Treatment Diabetic Retinopathy Study Research Group. Photocoagulation for diabetic macular edema, Early Treatment Diabetic Retinopathy Study (ETDRS) Report No. 1. Arch Ophthalmol. 1985;103:1796–1806.

49.Doft BH, Blankenship GW. Single versus multiple treatment sessions of argon laser panretinal photocoagulation for proliferative diabetic retinopathy. Ophthalmology. 1982;89:772–779.

50.Blankenship GW, Machemer R. Long term diabetic vitrectomy results, report of 10 year follow-up. Ophthalmology. 1985;92:503–506.

51.Blankenship GW. Red krypton and blue-green argon panretinal laser photocoagulation for proliferative diabetic retinopathy: a laboratory and clinical comparison. Trans Am Acad Ophth Soc. 1986;84:967–1003.

52.Blankenship GW. A clinical comparison of central and peripheral argon laser panretinal photocoagulation for proliferative diabetic retinopathy. Ophthalmology. 1988;95:170–177.

53.Blankenship GW. Fifteen-year argon laser and xenon photocoagulation results of Bascom Palmer Eye Institute’s patients participating in the Diabetic Retinopathy Study. Ophthalmology. 1991;98:125–128.

54.Wade EC, Blankenship GW. The effect of short versus long exposure times of argon laser photocoagulation on proliferative diabetic retinopathy. Graefe’s Arch Clin Exp Ophthalmol. 1990;228:226–231.

55.Machemer R, Buettner H, Norton EWD, Parel JM. Vitrectomy: a pars plana approach.

Trans Am Acad Ophthalmol Otolaryngol. 1971;75:813–820.

56.Machemer R, Parel JM, Buettner H. A new concept for vitreous surgery. 1. Instrumentation. Am J Ophthalmol. 1972;73:1–7.

57.Machemer R. Vitrectomy in diabetic retinopathy; removal of preretinal proliferations.

Trans Am Acad Ophthalmol Otolaryngol. 1975;79:OP394–OP395.

58.Machemer R. A new concept for vitreous surgery. 7. Two instrument techniques in pars plana vitrectomy. Arch Ophthalmol. 1974;92:407–412.

59.O’Malley C, Heintz RM. Vitrectomy via the pars plana, a new instrument system.

Trans Pac Coast Otoophthalmol Soc. 1972;50:121–137.

60.O’Malley C, Heintz RM. Vitrectomy with an alternative instrument system. Ann Ophthalmol. 1975;7:585–588.

61.Aaberg TM. Clinical results in vitrectomy for diabetic traction retinal detachment. Am J Ophthalmol. 1979;88:246–253.

120 Diabetes and Ocular Disease

62.Aaberg TM. Pars plana vitrectomy for diabetic traction retinal detachment. Ophthalmology. 1981;88:639–642.

63.Aaberg TM, Abrams GW. Changing indications and techniques for vitrectomy in management of complications of diabetic retinopathy. Ophthalmology. 1987;94:775–779.

64.Charles S. Endophotocoagulation. Retina. 1981;1:117–120.

65.Charles S. Vitreous Microsurgery, 2nd edn. Baltimore: Williams & Wilkins Co; 1987.

66.Douvas NG. Microsurgical roto-extractor instrument for vitrectomy. Mod Probl Ophthalmol. 1975;15:253–260.

67.Federman JL, Cook K, Bross R, et al. Intraocular microsurgery: I. New instrumentation (SITE). Ophthalmic Surg. 1976;7:82–87.

68.Kloti R. Vitrektomie I. Ein neues instrument fur die hintere vitrektomie. Graefe’s Arch Klin Ophthalmol. 1973;187:161–170.

69.Kloti R. Indications for vitrectomy and results in 115 cases. In: McPherson A, ed. New and Controversial Aspects of Vitreoretinal Surgery. St. Louis: The CV Mosby Co.; 1977:237–244.

70.McCuen BW, Rinkoff JS. Silicone oil for progressive anterior ocular neovascularization after failed diabetic vitrectomy. Arch Ophthalmol. 1989;107:677–682.

71.Michels RG, Ryan SJ. Results and complications of 100 consecutive cases of pars plana vitrectomy. Am J Ophthalmol. 1975;80:24–29.

72.Michels RG. Vitrectomy for complications of diabetic retinopathy. Arch Ophthalmol. 1978;96:237–246.

73.Rice TA, Michels RG. Long-term anatomic and functional results of vitrectomy for diabetic retinopathy. Am J Ophthalmol. 1980;90:297–303.

74.Michels RG. Vitreous Surgery. St. Louis: The CV Mosby Co; 1981.

75.Thompson JT, Auer CL, de Bustros S, et al. Prognostic indicators of success and failure in vitrectomy for diabetic retinopathy. Ophthalmology. 1986;93:290–295.

76.Thompson JT, de Bustros S, Michels RG, et al. Results of vitrectomy for proliferative diabetic retinopathy. Ophthalmology. 1986;93:1571–1574.

77.Thompson JT, de Bustros S, Michels RG, Rice TA. Results and prognostic factors in vitrectomy for diabetic vitreous hemorrhage. Arch Ophthalmol. 1987;105:191–195.

78.de Bustros S, Thompson JT, Michels RG, Rice TA. Vitrectomy for progressive proliferative diabetic retinopathy. Arch Ophthalmol. 1987;105:196–199.

79.Thompson JT, de Bustros S, Michels RG, Rice TA. Results and prognostic factors in vitrectomy for diabetic traction retinal detachment of the macula. Arch Ophthalmol. 1987;105:497–502.

80.Peyman GA, Dodich NA. Experimental vitrectomy. Instrumentation and surgical technique. Arch Ophthalmol. 1971;86:548–551.

81.Tolentino FI, Banko A, Schepens CL, et al. Vitreous surgery. XII. New instrumentation for vitrectomy. Arch Ophthalmol. 1975;93:667–672.

82.Tolentino FI, Freeman HM, Tolentino FL. Closed vitrectomy in the management of diabetic traction retinal detachment. Ophthalmology. 1980;87:1078–1089.

83.Mandelcorn MS, Blankenship GW, Machemer R. Pars plana vitrectomy for the management of severe diabetic retinopathy. Am J Ophthalmol. 1976;81:561–570.

84.Blankenship GW, Machemer R. Pars plana vitrectomy for the management of severe diabetic retinopathy and analysis of results five years following surgery. Ophthalmology. 1978;85:553–559.

85.Blankenship GW. Stability of pars plana vitrectomy results for diabetic retinopathy complications, a comparison of five-year and six-month post-vitrectomy findings. Arch Ophthalmol. 1981;99:1009–1012.

History of Evolving Treatments for Diabetic Retinopathy

121

86.Blankenship GW, Machemer R. Long term diabetic vitrectomy results, report of 10 year follow-up. Ophthalmology. 1985;92:503–506.

87.Fujii GY, de Juan E, Humayun MS, et al. A new 25 gauge instrument system for transconjunctival sutureless vitrectomy surgery. Ophthalmology. 2002;109:1807–1813.

88.Coleman DJ. Ultrasound in vitreous surgery. Trans Am Acad Ophthalmol Otolaryngol. 1972;76:467–479.

89.Coleman DJ, Franzen LA. Preoperative evaluation and prognostic value of ultrasonic display of vitreous hemorrhage. Arch Ophthalmol. 1974;92:375–381.

90.Diabetic Retinopathy Vitrectomy Study Research Group. Early vitrectomy for severe proliferative diabetic retinopathy in eyes with useful vision: results of a randomized trial. DRVS Report Number 3. Ophthalmology. 1988;95:1307–1320.

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7

Photography, Angiography, and

Ultrasonography in Diabetic

Retinopathy

ANDREW LAM, MD,

NICHOLAS G. ANDERSON, MD,

CARL D. REGILLO, MD,

AND GARY C. BROWN, MD, MBA

CORE MESSAGES

Fundus photography plays an important role in monitoring progression of diabetic retinopathy.

Fundus photography is becoming a popular method of screening large populations for diabetic retinopathy.

Fluorescein angiography is useful to identify areas of nonperfusion, increased vascular permeability, and neovascularization.

Fluorescein angiography is useful to guide laser treatment of clinically significant macular edema.

Ultrasound is useful when media opacity obscures visualization of the fundus and often helps determine appropriate timing of surgical intervention.

Fundus photography, fluorescein angiography, and ultrasonography are valuable tools in the management of diabetic retinopathy. These modalities enable clinicians to document pathology, monitor progression, and guide treatment of this increasingly prevalent disease. In this chapter, the indications and clinical

utility of these tests in the management of diabetic retinopathy will be reviewed.

FUNDUS PHOTOGRAPHY

Background. In 1886, Jackman and Webster published the first report of a retinal photograph taken of a living human [1]. An albo-carbon light source provided illumination for their 2.5 min exposure. While the quality of this first image was limited, by the early 20th century, Fredrick Dimmer had produced photographs of sufficient quality to be incorporated into the first photographic atlas of

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