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0365-6691/$ - see front matter 2010 Sociedad Espaola de Oftalmologa. Published by Elsevier Espaa, S.L. All rights reserved.
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ARCH SOC ESP OFTALMOL. 2011;86(2):5457
Original article
Evaluation of topical vasoconstrictors in pterygium surgery
and their role in reducing intraoperative bleeding
E. Villegas Becerril,a,b,* L. Prula de Torres,cM. Bergillos Arillo,b,dC. Villegas del Cuvilloe
aClnica de Oftalmologa MASER, Crdoba, SpainbEmpresa Pblica de Hospitales del Alto Guadalquivir. Hospital de Alta Resolucin de Puente Genil, Servicio de Oftalmologa,
Crdoba, SpaincUnidad Docente de Medicina de Familia y Comunitaria, Distrito Sanitario de Crdoba, Crdoba, SpaindClnica de Oftalmologa OFTALMOCOR, Crdoba, SpaineClnica de Oftalmologa, Crdoba, Spain
ARTICLE INFORMATION
Article history:
Received on July 20, 2010
Accepted on Oct. 26, 2010
Keywords:Pterygium
Vasoconstrictors
Bleeding
Complications
Phenylephrine
*Corresponding author.
E-mail: [email protected] (E. Villegas Becerril).
A B S T R A C T
Objective: To reduce vascularisation before surgery through the application of topical
vasoconstrictors, decreases the rate of intraoperative bleeding, improves the dynamics of
the surgery and reduces the difficulty in surgical performance.
Methods: Only patients with primary pterygium were included in the study. A prospective
randomized clinical trial was designed to compare intraoperative bleeding, need forcauterization and surgical time a group that was administered phenylephrine. preoperatively
and one which did not receive it. The sample was divided into two groups: 1st (n=27)
received topical phenylephrine (F) 0.1ml (10%), twice in 5minutes before surgery. 2nd (n=30)
did not receive phenylephrine (NoF). The technique was similar in both groups using
conjunctival autograft suturing. In both groups, the subconjunctival aneasthesia was
performed with 0.5% bupivacaine hydrochloride with epinephrine 1:200,000.
Results:A total of 57 patients were included in the study. The mean operation time for
group F was 15.57minutes (SD: 1.8min) and the NoF group 16.51min (SD to 1.82min, P=.057).
In the group F, it was necessary to use diathermy in 2 patients (7.4%) and in the NoF group
cauterisation was used in 14 patients (46.7%, Chi-Square=10.848, P=.001. There is a relative
risk 6.3 (95% CI 1.57 - 25.27) times greater than having to cauterise without phenylephrine
when used phenylephrine.
Conclusions:The use of topical vasconstrictors prior to pterygium surgery reduces the rateof bleeding and the time of surgery.
2010 Sociedad Espaola de Oftalmologa. Published by Elsevier Espaa, S.L.
All rights reserved.
ument downloaded from http://www.elsevier.es, day 14/06/2013. This copy is for personal use. Any transmission of this document by any media or format is strictly prohibited.
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ARCH SOC ESP OFTALMOL. 2011;86(2):5457 55
Introduction
Recent etiological theories affirm that pterygium is not only
a degenerative disease but also a proliferative inflammation.1
Surgical extirpation is the treatment of choice. The literature
suggests that simple excision leaving the sclera free is the
only technique with high recurrence rates of between 30%
and 70%.2 Autogenous conjunctival graft seems to be the
best surgical method as it exhibits a low recurrence rate in
addition to less secondary effects.3
It has recently been demonstrated that the Hispanic race
is a risk factor for increased pterygium recurrence rates,
even if the technique is utilized after the primary excision
and conjunctival autograft (CAG).4 The contribution of UV
radiation to the pathogenesis of pterygium has been supportedby epidemiologic data on ocular solar exposure5. In addition,
immunohistochemical studies demonstrate the mutations of
protein p53 due to the damages caused by UV radiation. This
damage induces the production of cytokines, growth factors
and metaloproteinases of the metrics responsible for the
growth of pterygium.6,7
Existing references demonstrate the difficulties due to
intra-op hemorrhage, occasionally requiring the use of
monopolar coagulation or suspending the intervention due to
excessive bleeding. This gives rise to numerous interruptions
and increased surgery times.8-11
Our hypotheses is that the reduction of previous and
intra-op vascularization through the prior application of
vasoconstrictors before surgery diminishes the rate of
intraoperative bleeding, improves the surgery dynamics andreduces the difficulty of the surgical procedure.
Subjects, material and methods
A prospective randomized clinical trial was designed
to compare intraoperative bleeding and cauterization
requirements and surgery times between a group which was
administered phenylephrine before the operation and a group
which was not. An informed consent was requested from each
patient and the study was carried out between September
2009 and February 2010.
Selection of patients and methods
We selected a group of patients (n=57) with an inclusion
criteria of pterygium diagnostic. Only the patients with
primary pterygium were included in the study. The patients
who underwent previous filtration surgery, corneal transplant
or had a history of ocular trauma and exposure to chemical
products were excluded from the study group. The sample
was divided into groups: the first group (n=27) received
topical phenylephrine 0.1ml (10%) on 2 occasions 5 min. prior
to the surgery. The second group (n=30) was not administered
phenylephrine or any other topical vasoconstrictor. The
administration of phenylephrine to each patient was masked
Palabras clave:
Pterigin
VasoconstrictoresSangrado
Complicacin
Felilefrina
Evaluacin de vasoconstrictores tpicos en la ciruga del pterigin y su papelen la disminucin del sangrado intraoperatorio
R E S U M E N
Objetivo: Reducir la vascularizacin previa a la ciruga mediante la aplicacin de vasocon-
strictores tpicos disminuye la tasa de sangrado intraoperatorio, mejora la dinmica de la
ciruga y reduce la dificultad de la actuacin quirrgicaMtodos: Slo los pacientes con pterigin primario se incluyeron en el estudio. Un ensayo
clnico aleatorizado prospectivo fue diseado para comparar el sangrado intraoperatorio,
necesidad de cauterizacin y tiempo de ciruga entre los grupos a los que se les administr
o no fenilefrina preoperatoriamente. La muestra se dividi en dos grupos: 1 (n = 27) recibi-
eron fenilefrina tpica (F) 0,1ml (10%) por dos veces 5 minutos antes de la ciruga; 2 (n = 30)
no se administr fenilefrina (NoF). La tcnica fue similar en ambos grupos, mediante autoin-
jerto conjuntival y sutura. En ambos, la anestesia subconjuntival se realiza con 0,5% de
clorhidrato de bupivacana con epinefrina 1:200.000.
Resultados:Un total de 57 pacientes se incluyeron en el estudio. La media del tiempo quirr-
gico para el grupo F fue de 15,57 minutos (SD: 1,8 min) y para el grupo de NoF de 16,51 min
(SD; 1,82 min; p = 0,057). En el grupo F, fue necesario usar la diatermia en 2 pacientes (7,4%),
en el NoF se us la cauterizacin en 14 pacientes (46,7%; Chi-cuadrado = 10,848; p = 0,001.
Existe un riesgo relativo 6,3 (IC 95%: 1,57 a 25,27) veces mayor de tener que cauterizar sinfenilefrina que cuando se usa fenilefrina.
Conclusiones:El uso de vasconstrictores tpicos previos a la ciruga de pterigin disminuye la
tasa de sangrado y reduce el tiempo de ciruga.
2010 Sociedad Espaola de Oftalmologa. Publicado por Elsevier Espaa, S.L.
Todos los derechos reservados.
ument downloaded from http://www.elsevier.es, day 14/06/2013. This copy is for personal use. Any transmission of this document by any media or format is strictly prohibited.
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56 ARCH SOC ESP OFTALMOL. 2011;86(2):5457
for the only surgeon who carried out all the surgeries in
order to avoid a bias, and in addition it was randomized.
The surgical technique was similar in both groups, with
conjunctival autograft and stitch described by Harvey et al
(2005)11. According to the description of this author, the need
to utilize diathermia was established for intra-op bleeding.
In both groups, subconjunctival anesthesia was performed
with a combination of anesthesia and vasoconstrictor: 0.5%
bupivacaine chlorhydrate with epinephrine in 1:200.000.
Evaluation and follow-up
After the operation, the subjects of both groups were treated
with tobramycine and dexamethasone eyedrops four times a
day, with a gradually diminishing prescription through a four-
week period. All the subjects were assessed 24 hours after the
surgery and one week, one month and 3 months after the
intervention. In each postop visit a slit lamp biomicroscopy
and applanation tonometry was performed.
Statistical analysis
A descriptive statistical analysis was performed, followedby an analysis of the comparability of both groups according
to age and sex. To verify the existence of differences between
both groups the adjustment of the quantitative variables
to normal distribution was previously verified through
the Shapiro-Wilk or Kolmogorov-Smirnov tests. As these
variables followed a normal distribution, the T for Student
test for independent samples was applied. For comparing
qualitative variables the Chi Square test was utilized,
assuming a value of p
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ARCH SOC ESP OFTALMOL. 2011;86(2):5457 57
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ument downloaded from http://www.elsevier.es, day 14/06/2013. This copy is for personal use. Any transmission of this document by any media or format is strictly prohibited.