Journal List > J Korean Ophthalmol Soc > v.55(7) > 1009725

Moon and Park: Outcomes of Vitrectomy for Severe Vitreous Hemorrhage of Unknown Etiology

Abstract

Purpose

To analyze the clinical course and outcomes of vitrectomy for severe vitreous hemorrhage of unknown etiology and to determine the primary cause of hemorrhage during the surgical process.

Methods

The medical records of patients who showed vitreous hemorrhage of Grade IV at their initial visit with no remarkable ophthalmologic or trauma history were reviewed retrospectively. All included patients underwent vitrectomy for severe vitreous hemorrhage for which a primary cause was not revealed before the surgery. The authors investigated the postoperative visual outcome, complications, and etiology of vitreous hemorrhage that was determined during the surgical process. We also analyzed the detailed intraoperative and postoperative funduscopic findings of patients with poor postoperative visual outcomes (BCVA < 20/200).

Results

Among the 50 eyes of 50 patients, the causes of vitreous hemorrhage included: branch retinal vein occlusion (48%), central retinal vein occlusion (16%), age-related macular degeneration (12%), retinal tear (8%), diabetic retinopathy (4%), rhegmatogenous retinal detachment (4%), Terson's syndrome (2%), Eales’ disease (2%) and unknown causes (4%). The mean best-corrected visual acuity (BCVA) before surgery was 2.17 ± 0.53 (log MAR) and it was recovered to 0.64 ± 0.58 (log MAR) 6 months after the surgery (p < 0.001). The branch retinal vein occlusion showed better visual outcome than other disease entities. On funduscopic examination of the patients with poor visual outcome whose postoperative BCVA was poorer than 20/200, macular ischemia, macular degeneration, macular edema, submacular hemorrhage, tractional retinal detachment (including macular), or optic nerve atrophy were verified.

Conclusions

After the vitrectomy for severe vitreous hemorrhage of unknown origin, pathologic findings of macular or irreversible optic nerve atrophy showed poor postoperative BCVA. Of all the causes of vitreous hemorrhage that were revealed after the surgery, branch retinal vein occlusion was the most common etiology of this condition and showed the most favorable visual outcome, comparatively.

References

1. Butner RW, McPherson AR. Spontaneous vitreous hemorrhage. Ann Ophthalmol. 1982; 14:268–70.
2. Dana MR, Werner MS, Viana MA, Shapiro MJ. Spontaneous and traumatic vitreous hemorrhage. Ophthalmology. 1993; 100:1377–83.
crossref
3. Lean JS, Gregor Z. The acute vitreous haemorrhage. Br J Ophthalmol. 1980; 64:469–71.
crossref
4. Lindgren G, Sjodell L, Lindblom B. A prospective study of dense spontaneous vitreous hemorrhage. Am J Ophthalmol. 1995; 119:458–65.
crossref
5. Spraul CW, Grossniklaus HE. Vitreous Hemorrhage. Surv Ophthalmol. 1997; 42:3–39.
crossref
6. Mason JO 3rd, Colagross CT, Haleman T, et al. Visual outcome and risk factors for light perception and no light perception vision after vitrectomy for diabetic retinopathy. Am J Ophthalmol. 2005; 140:231–5.
crossref
7. Two-year course of visual acuity in severe proliferative diabetic retinopathy with conventional management. Diabetic Retinopathy Vitrectomy Study (DRVS) report #1. Ophthalmology. 1985; 92:492–502.
8. Tolentino FI, Schephens CL, Freeman HM. Vitreoretinal disorders. Philadelphia: Saunders;1976. p. 416–31.
9. Isernhagen RD, Smiddy WE, Michels RG, et al. Vitrectomy for nondiabetic vitreous hemorrhage. Not associated with vascular disease. Retina. 1988; 8:81–7.
10. Verbraeken H, Van Egmond J. Non-diabetic and non-oculo- traumatic vitreous haemorrhage treated by pars plana vitrectomy. Bull Soc Belge Ophtalmol. 1999; 272:83–9.
11. Oyakawa RT, Michels RG, Blase WP. Vitrectomy for nondiabetic vitreous hemorrhage. Am J Ophthalmol. 1983; 96:517–25.
crossref
12. Ziemianski MC, McMeel JW, Franks EP. Natural history of vitreous hemorrhage in diabetic retinopathy. Ophthalmology. 1980; 87:306–12.
crossref
13. Kuppermann BD, Thomas EL, de Smet MD, Grillone LR. Pooled efficacy results from two multinational randomized controlled clinical trials of a single intravitreous injection of highly purified ovine hyaluronidase (Vitrase) for the management of vitreous hemorrhage. Am J Ophthalmol. 2005; 140:573–84.
crossref
14. Avery RL, Pearlman J, Pieramici DJ, et al. Intravitreal bevacizumab (Avastin) in the treatment of proliferative diabetic retinopathy. Ophthalmology. 2006; 1695.e1–15.
crossref
15. Moradian S, Valaee M, Ahmadieh H, et al. Outcomes of vitrectomy for non-traumatic non-diabetic vitreous hemorrhage. Iran J Ophthalmic Res. 2007; 2:46–51.
16. Ratnarajan G, Mellington F, Saldanha M, et al. Long-term visual and retinopathy outcomes in a predominately type 2 diabetic patient population undergoing early vitrectomy and endolaser for severe vitreous haemorrhage. Eye (Lond). 2011; 25:704–8.
crossref
17. Jalkh AE, Avila MP, El-Markabi H, et al. Immersion A- and B-scan ultrasonography. Its use in preoperative evaluation of diabetic vitreous hemorrhage. Arch Ophthalmol. 1984; 102:686–90.
18. Kumar A, Verma L, Jha SN, et al. Ultrasonic errors in analysis of vitreous haemorrhage. Indian J Ophthalmol. 1990; 38:162–3.
19. Rabinowitz R, Yagev R, Shoham A, Lifshitz T. Comparison between clinical and ultrasound findings in patients with vitreous hemorrhage. Eye (Lond). 2004; 18:253–6.
crossref
20. Russell SR, Blodi CF, Folk JC. Vitrectomy for complicated retinal detachments secondary to branch retinal vein occlusions. Am J Ophthalmol. 1989; 108:6–9.
crossref
21. Koh YM, Choi GJ, Na KS. Clinical analysis of vitrectomy efficiency for non-diabetic vitreous hemorrhage. J Korean Ophthalmol Soc. 2002; 43:255–60.
22. Ratnarajan G, Mellington F, Saldanha M, et al. Long-term visual and retinopathy outcomes in a predominately type 2 diabetic patient population undergoing early vitrectomy and endolaser for severe vitreous haemorrhage. Eye (Lond). 2011; 25:704–9.
crossref
23. Tan HS, Mura M, Bijl HM. Early vitrectomy for vitreous hemorrhage associated with retinal tears. Am J Ophthalmol. 2010; 150:529–33.
crossref
24. Lee KH, Park SJ, Lee J, Chung H. Clinical characteristics of branch retinal vein occlusion with vitreous hemorrhage. J Korean Ophthalmol Soc. 1998; 39:336–41.

Table 1.
Baseline characteristic of the patients
Characteristics Values
Number of eyes (patients) 50 (50)
Age (years) 60.2 ± 12.7
Sex (male/female) 31/19
Comorbidity (%)
  Diabetic mellitus 12 (24)
  Cardiovascular disease 4 (8)
  Cerebrovascular disease 6 (12)
Preoperative BCVA (log MAR) 2.17 ± 0.53
Preoperative IOP (mm Hg) 18.2 ± 9.7
Number of eyes with cataract (%) 32 (64)
Number of eyes with RAPD (%) 34 (68)
Duration from diagnosis to surgery (days) 14.7 ± 9.2

Values are presented as mean ± SD.

BCVA = best corrected visual acuity; IOP = intraocular pressure;

RAPD = relative afferent pupillary defect.

Table 2.
Intraoperative diagnosis of severe vitreous hemorrhage and postoperative visual outcome according to etiology
Final diagnosis No. of eyes (%) Postoperative visual outcome (no. of eyes (%))
VA ≥ 20/200 VA < 20/200
BRVO(%) 24 (48) 22 (91.7) 2 (8.3)
CRVO(%) 8 (16) 5 (62.5) 3 (37.5)
ARMD (%) 6 (12) 2 (33.3) 4 (66.7)
Retinal tear (%) 4 (8) 4 (100) 0 (0)
Diabetic retinopathy (%) 2 (4) 0 (0) 2 (100)
RRD (%) 2 (4) 2 (100) 0 (0)
Terson's syndrome (%) 1 (2) 1 (100) 0 (0)
Eale's syndrome (%) 1 (2) 1 (100) 0 (0)
Unknown (%) 2 (4) 2 (100) 0 (0)
Total (%) 50 (100) 39 (78) 11 (22)

VA = visual acuity; BRVO = branch retinal vein occlusion; CRVO = central retinal vein occlusion; ARMD = age-related macular degeneration; RRD = rhegmatogenous retinal detachment.

Table 3.
Findings of patients with poor postoperative visual outcomes (BCVA < 20/200)
No. Sex/Age (years) Initial VA Final VA (postop. 6 months) Major cause of poor VA (postop. 6 months) Final diagnosis
1 M/71 HM CF 70 cm Macular edema BRVO
2 M/62 CF 50 cm CF 70 cm Macular degeneration ARMD
3 F/55 HM CF 50 cm Macular ischemia CRVO
4 M/74 LP (+) CF 50 cm Optic atrophy ARMD
5 F/68 HM HM Macular ischemia BRVO
6 M/79 HM LP (-) Submacular hemorrhage total RD ARMD
7 M/63 HM HM Macular degeneration ARMD
8 M/69 CF 70 cm CF 70 cm Macular edema CRVO
9 M/54 HM HM Macular ischemia CRVO
10 F/44 CF 70 cm 0.02 TRD (including macular) DMR
11 M/60 HM CF 30 cm Submacular hemorrhage DMR

BCVA = best corrected visual acuity; VA = visual acuity; Postop = post operation; HM = hand movement; CF = counting finger; LP = light perception; RD = retinal detachment; TRD = tractional retinal detachment; BRVO = branch retinal vein occlusion; ARMD = age-related macular degeneration; CRVO = central retinal vein occlusion; DMR = diabetic retinopathy.

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