A clinical study of comparison of
pterygium surgery with and without Mitomycin- C on bare sclera technique
Gupta ML 1, Meena RK 2,
Bhardwaj V 3
1Dr. Mohan Lal Gupta, Associate Professor, Dept. Of Ophthalmology,
Jhalawar Medical College, Jhalawar, Rajasthan, 2Dr. Ravindra Kumar
Meena, Assistant Professor, Department Of Ophthalmology, Jhalawar
Medical College, Jhalawar, Rajasthan, 3Dr Veena Bhardwaj, Professor
Department Of Ophthalmology, Jhalawar Medical College, Jhalawar,
Rajasthan, India
Address for
correspondence: Dr. Mohan Lal Gupta, Email:
dr.mohanlalgupta14@gmail.com
Abstract
Introduction:
A pterygium is a triangular wedge of fibro-vascular conjunctival tissue
that appears on the epibulbar conjunctiva, which can be removed by
various methods. Recurrence of Pterygium after exicision is a very
common problem encountered by ophthalmologist. Several methods have
been suggested to avoid these recurrences. We studied the recurrence
rate of pterygium after application of intraoperative mitomycin C
(0.04%). Method:
This is a prospective study of fifty eyes in fifty patients who
underwent pterygium excision by the same surgeon using intraoperative
topical mitomycin C(25 patients) and without using mitomycin c(25
patients) during September 20014—September 2015 in the
ophthalmology department at Jhalawar medical college, Jhalawar( raj.).
0.04% Mitomycin applied to bare sclera after excision for two minutes
by swab sticks. Postoperative follow up period was 6 months. Outcomes
measured in the form of recurrence and complications were analyzed. Results: In Group A
with use of mitomycin C there was no recurrence after 6 months
follow-up while in Group B recurrence was seen in 5 patients within 3-6
months, however in group A, 1 patient had scleral thinning. Conclusion:
Intraoperative administration of mitomycin C 0.04% is safe and
effective to prevent pterygium recurrences.
Keywords:
Bare Sclera, Mitomycin C, Pterygium, Recurrence
Manuscript received: 15th
Nov 2015, Reviewed:
1st Dec 2015
Author Corrected: 4th
Dec 2015, Accepted for
Publication: 10th Dec 2015
Introduction
A pterygium is a wing-shaped growth of fibrovascular subconjunctival
tissue onto the cornea. Several hypotheses have been described to its
etiology. Prevalence rates range from 0.7-31% in various populations
around the world and the condition is more common in warm, dry
climates. Ultraviolet radiation exposure is a major risk factor for its
development [1,2].
Some findings suggest that an immunologic dysfunction plays a role in
the pathogenesis of pterygium, and recent studies have shown that
pterygium have increased levels of proangiogenic growth factors such as
basic fibroblast growth factor (FGF) and vascular endothelial growth
factor (VEGF)[3,4].
Pterygium is a worldwide condition with a
‘‘pterygium belt’’ between the
latitudes 30˚north and south of the equator.[5,6] it is more common in
sub- tropical and tropical areas [7]. Pterygium is prevalent in Hong
Kong, situated 22˚north of the equator [2]. Ultraviolet radiation
exposure is a major risk factor for its development[1,3].
The first line of treatment for primary pterygium is surgical excision
[1]. In pterygium surgery a variety of surgical procedures are in use.
The bare sclera technique is still common because of its simplicity.
There are overwhelming evidences that the sole use of the bare sclera
technique is associated with a high risk of local recurrence.
Adjunctive therapies, as beta-irradiation and antimetabolic drugs, like
mitomycin C (MMC) are used to decrease the recurrence rate [8].
Simple excision carries a high recurrence rate ranging from
24%–89% [2,7]. Recurrent pterygium are more difficult to
treat and various other treatment modalities are usually indicated i.e.
Conjunctival autograft transplantation and triethylene-thiophosphor-
amide (Thio-tepa), an antimitotic, Mitomycin C [7].
To prevent recurrence, two major adjunctive therapies are usually
performed: (1) the application of antimetabolites, and (2) conjunctival
or limbal autograft. Although many other therapeutic modalities have
been proposed, it requires extensive studies of efficiency and safety
before a new procedure can be considered as ideal [6]. Addition of MMC
at various concentrations has been reported to be effective in
preventing recurrence [2]. Mitomycin C is an antibiotic-antineoplastic
agent. It is a metabolic inhibitor extracted from Streptomyces
caespitosus that inhibits DNA synthesis [1] resulting in an inhibition
of the cellular proliferation for a long time [8] which selectively
inhibits the synthesis of DNA, cellular RNA, and protein [7]. The
mechanism of action seems to be inhibition of fibroblast proliferation
at the level of the episclera. However, MMC may cause devastating
complications such as scleral necrosis and microbial infections [2].
Material
and Method
A prospective, comparative clinical study was conducted from September
2014 to September 2015 in the department. Of ophthalmology at Jhalawar
medical college, Jhalawar. Fifty eyes of 50 patients with primary
pterygium were included in the study. Informed consent was obtained
from all patients before recruitment. All patients underwent full
ophthalmologic examination before and after surgery, including visual
acuity, slit-lamp examination, fundoscopy On slit lamp examination
grading of Pterygium was done based on extent of corneal involvement:
Grade I – crossing limbus, Grade II – midway
between limbus and pupil, Grade III – reaching up to
pupillary margin, Grade IV – crossing pupillary margin.
Grades of Pterygium
Exclusion criteria
1. Collagen vascular disease
2. Autoimmune disease
3. Pregnancy
4. Ocular surface pathology or infection
5. Previous limbal surgery
6. Diabetes mellitus
7. Recurrent pterygium, Pseudo Pterygium,
8. Lime injury associated symblephron,
9. History of ocular injuries
10. Corneal opacities and degeneration was excluded .
All 50 patients divided in two groups 25 in each:
Group A in which 0.04% mitomycin c was used.
Group B: without mitomycin c use.
All surgeries were done by single surgeon. Steps of surgery (1) eye was
anesthesised by instillation of proparacaine hydrochloride 0.5%
eyedrops in conjunctival sac 2-3 times every 1-2 minutes (2) eye was
paint by betadiene and draped after that wire speculum was applied.(3)
Pterygium was excised by 11 number bard - parker blade and separated
from underlines sclera. The remaining sub-conjunctival degenerative
part of Pterygium was excised with wescott scissor. The conjuctival and
corneal surfaces were smoothened by scraping with a
bard–parker blade and bleeding vessels were cauterized by
electric cautery. (4) In patients of Group A, 0.04% percent of
mitomycin C applied on bare sclera by cotton swab for two minutes and
after that sclera is irrigated by 50 ml of normal saline.(5) In group
B, sclera was left as such without mitomycin C application. (6) eye was
patched with antibiotic ointment for 24 hours.
On Postoperatively 0.3% tobramycin sulphate eye drop applied six times
a day for 15 days, 1% predinsolone acetate eye drop four times a day
for one week, followed by tapering dose for subsequent three weeks and
0.5% carboxymethylcellulose eye drop four times a day for one month
were given. Patients were asked to follow up on 1-day, 7-day, 1-month,
3-month and every 6-monthly regarded complications and recurrence of
Pterygium.
The main postoperative outcomes were recurrence of Pterygium and
complication of mitomycin C. Recurrence was defined as fibro-vascular
proliferation invading the cornea more than 1.5 mm at the site of
previously excised Pterygium. The complications were in terms of
postoperative corneal complication and complications of mitomycin C
i.e. puncate keratopathy, corneal melting, scleral necrosis, corneal
perforation, cataract and secondary glaucoma.
Results
Fifty eyes of fifty patients were operated for Pterygium surgery in
which 25 patients were included in Group A, in which mitomycin C was
applied and rest 25 patients were included in Group B and they left
with bare sclera. All patients were followed up for 6 months.
In Group A: Mean
Age of surgically managed patients was 46.08± 9.11 (range 30
- 60 yrs) out of which 60% were males (15) and 40% were females (10),
20 Patients had nasal Pterygium and 5 patients had bilateral Pterygium.
5 patients were having Grade IV Pterygium, 15 patients were having
Grade III Pterygium, 3 patients were having Grade II Pterygium and 2
patients were having Grade I Pterygium.
In Group B:
Mean Age of surgically managed patients was 45.52± 9.90
(range 30 - 60 yrs) out of which 60% were males (15) and 40% were
females (10), 15 Patients had nasal Pterygium and 10 patients had
bilateral Pterygium. 7 patients were having Grade IV Pterygium, 10
patients were having Grade III Pterygium, 5 patients were having Grade
II Pterygium and 3 patients were having Grade I Pterygium. In Group A,
1 patient developed thinning of sclera after six months and there was
no recurrence after follow up. In Group B, 5 patients developed
recurrence after six month follow up.
Table No 1: Distribution
of cases according to site of pterygium
Gender
|
Nasal
|
Nasal/temporal
|
Total
|
Male
|
22
|
08
|
30
|
Female
|
13
|
07
|
20
|
Total
|
35
|
15
|
50
|
Table No
2: Comparison of visual acuity before surgery
Visual Acuity
|
Group
A before Surgery
|
Group
B before surgery
|
6/6
|
11
|
11
|
6/9
|
02
|
02
|
6/12
|
12
|
12
|
Total
|
25
|
25
|
Table No. 3: Comparison
of visual acuity after surgery
Visual
acuity
|
Group
A after surgery
|
Group
B after surgery
|
6/6
|
14
|
14
|
6/9
|
11
|
11
|
6/12
|
00
|
00
|
Total
|
25
|
25
|
Table No 4: Distribution
of cases according to recurrence rat
Group
A
|
Group
B
|
Z
value
|
P
value
|
significance
|
00/25
|
05/25
|
2.2704
|
0.0232
|
significant
|
Table 5: Distribution of cases according to complication
Group
A
|
Group
B
|
Z
value
|
P
value
|
significance
|
01/25
|
01/25
|
0.9947
|
0.3199
|
Non
significant
|
Discussion
There were no statistically significant differences observed in age,
gender, laterality and visual acuity among the groups. All patients
completely recovered, and no other abnormal ocular or systemic
complications were observed during the six-month follow-up period
except scleral thinning in one case in group A. our main outcome
measure was recurrence rate Generally, pterygium recurrences occur
during the first 6 months after surgery. A number of factors such as
the type of pterygium, age of the patient, environmental agents, and
surgical technique may be responsible [9] but No recurrence was
observed up to one month after surgery in group A However, at three
months, recurrence was observed in three eyes (12%) and at four months
in two eyes (8%) in the group B. In Group A MMC were used
intraoperatively at a concentration of 0.4 mg/ml over bare sclera for 3
min. The rate of recurrence was 00% in comparison with 38% reported by
Chen et al[10] and 10.5% by Manning et al[11] with the application of
0.4 mg/ml for 3 min. This concurs with previous studies on
intraoperative application of MMC with a rate of recurrence of 25%
[12]. Various concentrations of MMC with different durations of
application have been used, but the minimal safe and effective dosage
and application time are still not certain [13].
Because recurrence rates differed significantly at three months (p =
0.02372) table no. 4 that observation had enough support by various
study A L Young et al[5] Allan BDS et al[14].
One and only complication which was seen in group A was scleral
thinning (p value>0.05) table no.05 which was supported by
Rubinfeld et al[15],Safianik B et al[16] Zhivov A et al [17], Peponis V
et al[18].
The limitations of the study were the short follow-up period and the
small size of the study groups. With a longer follow-up period,
recurrence rates and side effects related to the adjunctive drugs could
be analyzed more accurately. Larger sample sizes could make the
statistical analysis stronger. Overall we can say that 0.04% mitomycin
c is safe and effective to prevent recurrence after pterygium
excision.[19]
Conclusion
0.04% mitomycin c is effective to prevent recurrence after pterygium
surgery.
Funding:
Nil, Conflict of
interest: None initiated
Permission
from IRB:
Yes
References
1. Shinyoung Hwang, Sangkyung Choi A Comparative Study of Topical
Mitomycin C, Cyclosporine, and Bevacizumab after Primary Pterygium
Surgery Korean J Ophthalmol 2015;29(6):375-381
http://dx.doi.org/10.3341/kjo.2015.29.6.375.
2. Mustafa Ozsutcu, Emre Ayintap, Julide C U Akkan, Arif Koytak, and
Cengiz Aras Repeated bevacizumab injections versus mitomycin C in
rotational conjunctival flap for prevention of pterygium recurrence
Indian J Ophthalmol. 2014 Apr; 62(4): 407–411. doi:
10.4103/0301-4738.120220.
3. Kria L, Ohira A, Amemiya T. Immunohistochemical localization of
basic fibroblast growth factor, platelet derived growth factor,
transforming growth factor-beta and tumor necrosis factor-alpha in
pterygium. Acta Histochem. 1996;98:195–201.
4. Aspiotis M, Tsanou E, Gorezis S, Ioachim E, Skyrlas A, Stefaniotou
M, et al. Angiogenesis in pterygium: Study of microvessel density,
vascular endothelial growth factor, and thrombospondin-1. Eye (Lond)
2007;21:1095–101. [PubMed]
5. A L Young, G Y S Leung, A K K Wong, L L Cheng, D S C LamA randomised
trial comparing 0.02% mitomycin C and limbal conjunctival autograft
after excision of primary pterygiumBr J Ophthalmol
2004;88:995–997. doi: 10.1136/bjo.2003.036830.
6. David Hui-Kang Ma, Lai-Chu See, Su-Bin Liau, Ray Jui-Fang Tsai
.Amniotic membrane graft for primary pterygium: comparison with
conjunctival autograft and topical mitomycin C treatment Br J
Ophthalmol 2000;84:973–978.
7. Halit Oguz1, Emel Basar2 and Bulent Gurler1 Intraoperative
application versus postoperative mitomycin C eye drops in pterygium
surger Acta Ophthalmol. Scand. 1999: 77: 147–150.
8. Gabor Koranyi,1 Ditte Artze´ n,2 Stefan Seregard2 and Eva
Dafgard Kopp2 Intraoperative mitomycin C versus autologous conjunctival
autograft in surgery of primary pterygium with four-year follow-up.
Acta Ophthalmol. 2012: 90: 266–270 ª 2010 The
Authors Journal compilation ª 2010 Acta Ophthalmol doi:
10.1111/j.1755-3768.2010.01936.x.
9. Mutlu FM, Sobaci G, Tatar T, Yildirim E. A comparative study of
recurrent pterygium surgery: Limbal conjunctival autograft
transplantation versus mitomycin C with conjunctival flap.
Ophthalmology. 1999;106:817–21.
10. Chen PP, Ariyasu RG, Kaza V, LaBree LD, McDonnell PJ. A randomized
trial comparing mitomycin C and conjunctival autograft after excision
of primary pterygium. Am J Ophthalmol. 1995;120:151–60. [PubMed]
11. Manning CA, Kloess PM, Diaz MD, Yee RW. Intraoperative mitomycin in
primary pterygium excision. A prospective, randomized trial.
Ophthalmology. 1997;104:844–8. [PubMed]
12. Alpay A, Ugurbas SH, Erdogan B. Comparing techniques for pterygium
surgery. Clin Ophthalmol.2009;3:69–74. [PMC free article] [PubMed]
13. Lam DS, Wong AK, Fan DS, Chew S, Kwok PS, Tso MO. Intraoperative
mitomycin C to prevent recurrence of pterygium after excision: A
30-month follow-up study. Ophthalmology. 1998;105:901–4. [PubMed]
14. Allan BDS, Short P, Crawford GJ, et al. Pterygium excision with
conjunctival autografting: an eVective and safe technique. Br J
Ophthalmol 1993;77:698–701. [PubMed]
15. Rubinfeld RS, Pfister RR, Stein RM, Foster CS, Martin NF, Stoleru
S, et al. Serious complications of topical mitomycin-c after pterygium
surgery.Ophthalmology.1992;99:1647-54. [PubMed]
16. Safianik B, Ben-Zion I & Garzozi HJ (2002): Serious
corneoscleral complications after pterygium excision with mitomycin C.
Br J Ophthalmol 3: 357–358. [PubMed]
17. Zhivov A, Beck R & Guthoff RF (2009): Corneal and
conjunctival findings after mitomycin C application in pterygium sur-
gery: an in-vivo confocal microscopy study. Acta Ophthalmol 2:
166–172. [PubMed]
18. Peponis V, Rosenberg P, Chalkiadakis SE, Insler M
& Amariotakis A (2009): Fungal scleral keratitis and
endophthalmitis fol- lowing pterygium excision. Eur J Ophthal- mol 3:
478–480. [PubMed]
19. Rodriguez JA1, Ferrari C, Hernández GA. Intraoperative
application of topical mitomycin C 0.05% for pterygium surgery. Bol
Asoc Med P R. 2004 Mar-Apr;96(2):100-2. [PubMed]
How to cite this article?
Gupta ML, Meena RK, Bhardwaj V. Clinical study of coparision of
pterygium surgery with and without Mitomycin-C on bare sclera
technique. Int J Med Res Rev 2016;4(1):33-37. doi:
10.17511/ijmrr.2016.i01.005.