Closure of Oroantral Fistula Comparison Between Buccal
Closure of Oroantral Fistula Comparison Between Buccal
Closure of Oroantral Fistula Comparison Between Buccal
Keywords: Buccal advancement flap, buccal fat pad, oroantral fistula closure, oroantral fistula, Rehrmann flap
fistula requires surgical intervention.[1] OAF of size <5 mm Address for correspondence: Dr. Madan Mishra,
may also require surgical closure if sinus infection is evident.[2] 5C/19, Vrindavan Colony, Lucknow, Uttar Pradesh, India.
E‑mail: [email protected]
OAF causes excruciating pain, escape of fluids from nose, Received: 09 February 2021, Accepted in
escape of air from mouth into nose, epistaxis, change in voice Revised Form: 14 May 2021, Published: 13 December 2021
www.njms.in
For reprints contact: [email protected]
DOI:
How to cite this article: Shukla B, Singh G, Mishra M, Das G, Singh A.
10.4103/njms.njms_323_21 Closure of oroantral fistula: Comparison between buccal fat pad and buccal
advancement flap: A clinical study. Natl J Maxillofac Surg 2021;12:404-9.
404 © 2021 National Journal of Maxillofacial Surgery | Published by Wolters Kluwer - Medknow
Shukla, et al.: Closure of oroantral fistula – Comparison between buccal fat pad and buccal advancement flap: A clinical study
postnasal discharge, popping out of antral polyp into oral with complaints of OAF were included in this prospective,
cavity, and sinusitis. comparative analytic study. All the patients included in
the study were informed about the surgical procedures
The closure of OAF is technique‑sensitive, arduous, and and the associated complications, and written informed
challenging. Various techniques can be utilized for the consent was signed by all of them. Medically compromised
closure; regardless of the technique used, success of the patients, smokers, drug and alcohol abusers, malignancy
surgical procedure depends on effective removal of fistulous cases, patients with history of previous sinus disease or
tract and complete extermination of any sinus pathology previous sinus surgery, patients with previous radiotherapy
and/or infection. The major factors determining the type of to the maxilla, and patient not willing to participate in the
surgery for closure of OAF are dimension and location of the study were excluded from this study. Intraoral periapical,
defect. The other decisive factors could be the adequacy and panoramic, and occipitomental view radiographs were taken;
health of adjoining tissue.[1] computed tomography was kept optional and advised only
for selective cases. Routine blood investigations along with
The most popular and commonly used method for surgical viral markers were done. The patients were randomly divided
closure of OAF is buccal advancement flap, which is known as into two groups. In Group I, OAF was treated with a buccal
Rehrmann flap.[3,4] It is simple, easy to harvest, and versatile advancement flap, and in Group II, BFP was sutured over the
flap. It has an excellent blood supply because of its broad defect. In both groups, local anesthesia (LA) was administered
base, which makes it a reliable and highly successful surgical via posterior and middle superior alveolar nerve blocks and
option for OAF management. Its vicinity to the surgical site greater palatine nerve block using 2% lidocaine and 1:80,000
makes it an ideal choice, thus avoiding second surgical site epinephrine. Fistula lining was excised, and bony defect was
morbidity. As it has adequate bulk of tissue, the closure of exposed. Two divergent incisions were given, and a standard
OAF is tensionless, ensuring adequate blood flow to the trapezoid buccal flap was reflected in both groups. Cleaning
tissue. It has a major disadvantage of subsequent reduction and necessary debridement of the maxillary sinus were done.
of buccal vestibular depth.[5] Furthermore, the tented mucosa All surgeries were done by the same surgeon in this study.
even after healing may get traumatized during chewing, and
it invariably hinders with prosthetic rehabilitation of missing In Group I (control), the bony defect was closed by advancing
tooth/teeth in the same region. the buccal flap over the fistula and suturing the flap to
the undermined palatal mucosa using horizontal mattress
Another relatively less popular technique for closure of OAF is sutures (3.0 polyglactin); buccal and palatal alveolar bone
the use of pedicled buccal fat pad (BFP). It was first described reduction was done as needed before final closure. In
by Egyedi.[6] It has a constant and reliable blood supply Group II (experimental), the BFP was transferred to the
when it is used as a pedicled flap. The size of BFP remains surgical area through the same incision. BFP was gently
constant in an individual, regardless of the body weight and dissected out and delivered over the defect avoiding
fat distribution of an individual. It is present adjacent to the excessive traction and sutured to the surrounding tissue with
surgical site, so it reduces surgical time. It is easy to harvest, 3.0 polyglactin. Then, the buccal mucoperiosteal flap was
is easy to mobilize, has excellent blood supply, and causes sutured to its original position with 3.0 polyglactin suture.
minimal donor‑site morbidity. Complete epithelialization Duration of surgery (from incision till closure) was noted in
takes place over a period of 2–3 weeks. Buccal sulcus depth each group. All the patients were advised not blow through
is also not affected by this procedure; hence, it overcomes nose, avoid sneezing coughing and vigorous mouth rinsing
the disadvantage of reduction in the vestibular depth that for next seven days. Antibiotics, anti‑inflammatory‑analgesics,
occurs if reconstructed with buccal advancement flap.[7] and nasal decongestants were prescribed for 7 days in both
groups.
The aim of this study was to evaluate and compare the clinical
outcomes of the buccal advancement flap and BFP used for All patients were called for follow‑up on the 1st, 7th, 14th,
closure of OAF. and 21st day postoperatively. Pain, mouth opening, edema,
infection, and wound dehiscence were evaluated on each
MATERIALS AND METHODS visit. Pain was assessed on a 10‑mm visual analog scale
and allotted four categories: 0 ‑ No pain, 1–3 ‑ mild pain,
This study was conducted at the department of oral and 3–7 ‑ moderate pain, and 7–10 ‑ severe pain. Edema was
maxillofacial surgery of our institute after taking permission evaluated by preoperative and postoperative extraoral
from the institutional ethical committee. Twenty ASA measurement of tragus‑pogonium and tragus‑subnasale,
Group I and II patients of age ranging from 24 to 64 years by a tape measure laid on the skin.[8] Mouth opening was
National Journal of Maxillofacial Surgery / Volume 12 / Issue 3 / September-December 2021 405
Shukla, et al.: Closure of oroantral fistula – Comparison between buccal fat pad and buccal advancement flap: A clinical study
evaluated by measuring maximum interincisal distance on Pain was absent in both the groups at immediate postoperative
each follow‑up. period because of effect of LA. On intergroup comparison,
pain scores were slightly higher in Group II (3.50 ± 0.97)
The data were analyzed using descriptive statistical on postoperative day 1; the difference was statistically
methods including the Mann–Whitney U‑test, Chi‑square insignificant when compared with Group I. On days 7 and
test, Student’s “t”‑test, and paired “t”‑test, to compare the 14, the pain score was higher in Group II and the difference
independent groups and repeated‑measures ANOVA with was statistically significant (P = 0.040 and P = 0.030). No
SPSS software version 15.0 (SPSS Inc., Chicago Ill., USA). pain was observed on day 21 in both groups [Table 2 and
Statistical significance was defined at P < 0.05. Figure 2]. On intragroup comparison, in Group I, pain was
increased (2.90 ± 0.57) on day 1 as compared to baseline;
RESULTS and it was statistically significant. On day 7, pain was
higher (1.30 ± 0.95) than baseline but not statistically
The mean age of selected patients in both the treatment significant. On days 14 and 21, no pain was reported by any
groups was comparable. The mean age of the patients in patient. However, in Group II, on day 1 (3.50 ± 0.97) and
Group I was 45.00 ± 13.33 years whereas in Group II was day 7 (2.20 ± 0.79), the pain was more than baseline and
44.00 ± 13.13 years [Table 1]. was statistically significant as well. On day 14 (0.60 ± 0.84),
pain was slightly higher than baseline, but it was statistically
Duration of surgery in patients of Group II (29.90 ± 2.88 min) insignificant. On day 21, no patient reported for pain
was slightly higher than that of Group I (27.90 ± 2.28 min), [Table 3 and Figure 3].
and the difference in mean duration of surger y
between the two groups was found to be statistically In both the groups, at baseline (preoperatively), there was no
insignificant (P = 0.103) [Figure 1]. statistically significant (P = 0.638) difference in maximum mouth
opening. At each postoperative follow‑up, we did intergroup
Table 1: Comparison of Age of Study Population Between the evaluation. We found out that maximum mouth opening was
Groups less in Group II. On postoperative days 7 and 14, reduction in
Age Group Group I Group II Total (n=20) maximum mouth opening was statistically significant [Table 4
(years) (n=10) (n=10)
and Figure 4]. On intragroup evaluation, in Group I, maximum
No. % No. % No. %
mouth opening was less than baseline on day 1. On days 7, 14,
21‑30 2 20.00 2 20.00 4 20.00
31‑40 2 20.00 2 20.00 4 20.00
and 21, maximum mouth opening was more than baseline. In
41‑50 2 20.00 2 20.00 4 20.00 Group II, maximum mouth opening was less than baseline on
51‑60 3 30.00 3 30.00 6 30.00 days 1 and 7, whereas on days 14 and 21, it increased up to a
>60 1 10.00 1 10.00 2 10.00 level more than the baseline [Table 5 and Figure 5].
χ2=0.000 (df=4); P=1.000
‘Min.‑Max. (Median) 25‑64 (46.50) 24‑61 (45.50) 24‑64 (45.50) On intergroup comparison, we observed that in both groups,
Mean±SD 45.00+13.33 44.00+13.13 44.50+12.89 postoperative edema was present on day 1. On day 7, two
Table 2: Comparison of Pain Score at different time intervals Between the Groups
Group I (n=10) Group II (n=10) Mann Whitney test
Range Med. Mean SD Range Med. Mean SD ‘Z’ ‘’P’
Baseline 0‑0 0.00 0.00 0.00 0‑0 0.00 0.00 0.00 ‑ ‑
Day 1 2‑4 3.00 2.90 0.57 2‑5 3.00 3.50 0.97 1.500 0.134
Day 7 0‑3 1.00 1.30 0.95 1‑3 2.00 2.20 0.79 2.054 0.040
Day 14 0‑0 0.00 0.00 0.00 0‑2 0.00 0.60 0.84 2.166 0.030
Day 21 0‑0 0.00 0.00 0.00 0‑0 0.00 0.00 0.00 0.000 1.000
Table 3: Intragroup Change in Pain Score (from Baseline) at different time intervals (Wilcoxon Signed Rank Test)
Group I (n=10) Group II (n=10)
Mean ch. SD Z P Mean ch. SD Z P
Day 1 2.90 0.57 2.913 0.004 3.50 0.97 2.844 0.004
Day 7 1.30 0.95 2.565 0.010 2.20 0.79 2.842 0.004
Day 14 0.00 0.00 0.000 1.000 0.60 0.84 1.857 0.063
Day 21 0.00 0.00 0.000 1.000 0.00 0.00 0.000 1.000
patients of Group I and 8 patients of Group II had edema; on Egyedi first described the use of BFP for the reconstruction of
day 14, three patients of Group II had edema. On day 21, no intraoral defects.[6] Since then, many surgeons have advocated
patient had edema in each group [Table 6 and Figure 6]. On
intragroup evaluation, in Group I, edema reduced in 80% of
cases on day 7, and on day 14 and 21, none of the patient
had edema. Thus, changes in edema status at day 7, 14, and
21 were found to be statistically significant. In Group II,
edema reduced in 20% of cases on day 7, 70% of cases on
day 14, and 100% of cases on day 21. Thus, changes in
edema status at day 14 and 21 were found to be statistically
significant [Table 7].
Table 5: Intragroup Change in Mouth Opening (from Baseline) at different time intervals (Paired ‘t’ test)
Group I (n=10) Group II (n=10)
Mean Ch. SD % Ch. Z P Mean Ch. SD % Ch. Z P
Day 1 ‑1.90 1.97 ‑5.44 3.051 0.014 ‑3.40 1.35 ‑9.83 7.965 <0.001
Day 7 1.40 2.17 4.01 ‑2.040 0.072 ‑1.10 0.88 ‑3.18 3.973 0.003
Day 14 3.00 2.21 8.60 ‑4.291 0.002 1.10 1.73 3.18 ‑2.012 0.075
Day 21 4.40 2.41 12.61 ‑5.766 <0.001 3.40 1.43 9.83 ‑7.520 <0.001
the use of BFP for closure of OAF.[7,12‑14] BFP has a central body
and four processes, namely buccal, pterygoid, superficial,
and deep temporal extensions. Buccal and deep temporal
branches of the maxillary artery and transverse facial and
small branches of the facial artery are its blood supply.[5,15]
Baumann et al. had stated that, because of the ease of access
and rich blood supply, BFP is suitable for closure of defects
of the posterior maxilla as far as the region of the hard and
soft palate and the retromolar region of the mandible.[16]
Figure 5: Intragroup change in mouth opening (from baseline) at different
time intervals (paired t‑test)
Utmost care should be employed for BFP removal. The
incidences of complication are very less. Few of the possible
complications include injury to facial nerve, hematoma,
infection, and edema. Tideman et al. stated that BFP should
cover the defect satisfactorily, and it should not be sutured
under tension, as it may impede the blood supply.[15,17] In the
present study, we did not encounter any case of infection or
dehiscence. It may be attributed to the fact that BFP has ample
blood supply.[17] If excess fat is harvested and sutured over the
defect or there is herniation of fat on postoperative follow‑up,
it may be easily trimmed off by a pair of scissors or dissectors.[5]
The occurrence of reduced mouth opening was more evident Financial support and sponsorship
on Group II; it had profound trismus on all follow‑up days. Nil.
However, in Group I, trismus subsided up to 21st follow‑up
day. According to Colella et al. and Chien et al., reduced Conflicts of interest
mouth opening can be due to scar retraction and lack of There are no conflicts of interest.
lamina propria in the submucosa of the resected tissues.[20,21]
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