Delivered by Ingenta to: Economics Dept IP: 46.161.56.124 On: Tue, 28 Jun 2016 17:04:46
Copyright (c) Oceanside Publications, Inc. All rights reserved.
For permission to copy go to https://www.oceansidepubl.com/permission.htm
The effect of anatomically directed topical steroid drops on
frontal recess patency after endoscopic sinus surgery: A
prospective randomized single blind study
Sang Duk Hong, M.D., Jeon Yeob Jang, M.D., Joon Ho Kim, M.D., Seong Yun Jang, M.D.,
Hyo Yeol Kim, M.D., Ph.D., Hun-Jong Dhong, M.D., Ph.D., and Seung-Kyu Chung, M.D., Ph.D.
ABSTRACT
Background: The failure rate for frontal sinusotomy is higher than that of overall endoscopic sinus surgery (ESS). To prevent frontal sinus obstruction,
systemic or topical steroids are commonly used, but systemic steroid therapy can cause significant morbidity and topical sprays can not be distributed to the
frontal ostium. This study was designed to determine the efficacy of anatomically directed topical steroid drops in reducing frontal ostium stenosis compared
with topical steroid sprays after ESS.
Methods: A prospective, randomized, single-blind study was conducted in 43 patients (77 nasal cavities) who had undergone ESS, including frontal
sinusotomy. Twenty-one patients (39 nasal cavities) used steroid drops applied with the Mygind technique, and 22 patients (38 nasal cavities) used steroid
sprays for 8 weeks postoperatively. The patency of the frontal ostium was evaluated endoscopically 3 months postoperatively.
Results: The study included 29 men and 14 women (mean age, 48.2 years; range, 19 – 62 years). Endoscopic scores in terms of polypoid change, edema,
and scar in the middle meatus and frontal recess were not significantly different between the groups, although the drop group showed a tendency to superior
scores when compared with the spray group (p 0.05). The frontal sinus patency of the drop group was significantly higher than of the spray group (p
0.05).
Conclusion: Topical steroid drops using the Mygind technique led to a 16% improvement in frontal sinus patency rates in 3 month after ESS in this study
compared with postoperative topical steroid use.
(Am J Rhinol Allergy 26, 209 –212, 2012; doi: 10.2500/ajra.2012.26.3758)
E
ndoscopic sinus surgery (ESS) yields excellent results in the treat-
ment of chronic rhinosinusitis, with large series and literature
reviews reporting 90% success rates.
1
However, patients undergoing
frontal sinus surgery, especially those with polypoid mucosa, tend to
have difficulties maintaining adequate sinus ostia patency postoper-
atively, because of the narrow diameter of the frontal sinus and
propensity for circumferential scarring.
Jacobs et al.
2
performed 105 frontal sinusotomies and reported
70.5% of cases had abnormal frontal recess findings. Kennedy et al.,
3
in 1992, reported that the stenosis rate of the maxillary sinus ostia was
2%, but that the stenosis rate of the frontal sinus ostia was 11.9%
(27.3% in patients with polyposis). Treatment options for preventing
frontal ostium stenosis after ESS include systemic and topical ste-
roids, application of mitomycin C, packing absorbable material into
the frontal ostium, prolonged stenting, and steroid eluting stenting (in
an animal model).
4–7
None of these treatment options are considered
definitive. Short-term systemic steroid therapy has played an impor-
tant role in many sinonasal diseases, including allergic rhinitis, nasal
polyposis, and the reduction of postoperative reactive edema. Some
studies found that systemic steroids were effective for mucosal le-
sions of the frontal recess.
8
However, because of the untoward effects
of chronic oral steroid use, topical nasal steroid therapy, which has
minimal systemic effects, is preferred.
Topical nasal steroids are most commonly dispensed as sprays, and
these sprays are widely used postoperatively. However, some studies
reported that particles from topical nasal sprays reach only as far as
the inferior turbinate, anterior surface of middle turbinate, and nasal
floor rather than the middle meatus or frontal recess after ESS.
9,10
Alternatively, significantly larger amounts of particles from topical
nasal drops, with anatomic positioning, such as the Mygind
11
(supine
and head extended) position, reached the middle meatus, including
the frontal recess.
9,10
A retrospective study using topical nasal drops
with Mygind positioning showed benefits in preventing maxillary
and frontal sinus ostia stenosis.
12
Many studies have investigated the
use of topical nasal steroids in the treatment of chronic rhinosinusitis
after ESS. However, the effectiveness of topical nasal steroid drops
compared with sprays for frontal ostium patency after ESS still has
not been determined.
The objective of this study was to determine the effectiveness of
intranasal steroid drops with anatomically directed positioning, com-
pared with spray forms, after endoscopic frontal sinusotomy.
MATERIALS AND METHODS
A prospective, randomized, single-blind case-control study was
conducted. The Institutional Review Board of Samsung Medical Cen-
ter granted approval for this study. The indications for ESS included
(1) symptoms meeting the criteria of the American Academy of Oto-
laryngology Task Force on Rhinosinusitis guideline
13
and (2) radio-
logical confirmation with computed tomography (CT). Among the
candidates for ESS, patients who underwent frontal sinusotomy with
a neofrontal ostium of 4 mm–-confirmed with 4-mm-diameter long
curved suction tips—were offered an opportunity to volunteer for
recruitment into this study. All subjects provided informed consent.
The exclusion criteria of this study included (1) history of using the
systemic steroids within the 4 weeks before the surgery, (2) poor
overall health, (3) fungal sinusitis or the presence of a tumor, and (4)
an age of 18 years.
Preoperative data were collected regarding smoking, allergy status,
asthma status, preoperative Lund-Mackay CT scores, presence of
polyps, and history of previous sinus operations.
A single surgeon (S.K.C.) conducted all operations. During frontal
sinusotomy, meticulous dissection was performed and care was taken
to not detach the mucosa around the neo-ostium. All frontal neo-ostia
were large, as much as 4 mm in diameter, confirmed with 4-mm-long
From the Department of Otorhinolaryngology–Head and Neck Surgery, Samsung
Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
The authors have no conflicts of interest to declare pertaining to this article
Address correspondence and reprint requests to Seung-Kyu Chung, M.D., Ph.D.,
Department of Otorhinolaryngology– Head and Neck Surgery, Samsung Medical
Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Gangnam-gu,
Seoul 135-710, Korea
E-mail address: rhinochung@skku.edu
Copyright © 2012, OceanSide Publications, Inc., U.S.A.
American Journal of Rhinology & Allergy 209
DO NOT COPY