INTRODUCTION

Functional endoscopic sinus surgery (FESS) is the most physiological and well-accepted treatment for chronic sinus disease that is unresponsive to medical treatment.1 In spite of recent advances in technology, controlling the bleeding during endoscopic sinus surgery (ESS) remains a challenge.

The surgical field in ESS is very narrow and is surrounded by vital structures, such as orbit and brain. Even a small amount of bleed during surgery can soil the tip of the endoscope and obscure the field. Repeated soiling of the tip of the endoscope prolongs the procedure. Operating under such compromised conditions in addition to the narrow and delicate field increases the risk of injury to the adjacent vital structures. Also, if performed under poor visualization, damage to the mucosa may further lead to postoperative synechiae formation. Hence, an optimal bloodless field is crucial for the surgeon.2

Purpose of this study is to devise a method of obtaining bloodless field for the performing surgeon.

Various techniques have been used to secure a dry operating field, which includes Fowler's position, hypotensive agents like beta-adrenergic blockade, and preoperative steroids and topical vasoconstrictors. However, with all these techniques, excessive bleeding still remains a problem during ESS.3,4

As the maxillary artery is the major source of supply to the nose, vasoconstriction of this artery may significantly reduce the blood supply to the nose, thus minimizing bleeding during the procedure.2 This artery can be accessed via greater palatine foramen.

MATERIALS AND METHODS

The study was conducted at a tertiary care hospital after approval by institutional ethical committee.

A detailed clinical history was taken, and complete ear, nose, and throat examination was performed on all the patients. Patients were subjected to diagnostic nasal endoscopy and computed tomography (CT) imaging, and the disease was graded using Lund and Mackay system. Those subjects with bilateral similar grading were included in the study.

Inclusion Criteria

All patients above the age of 18 years with chronic rhinosinusitis or polyposis who are undergoing ESS were included.

Exclusion Criteria

  • Asymmetrical disease

  • Poorly controlled hypertension

  • Bleeding disorders

  • Use of anticoagulants

  • Acute infections

Written informed consent was obtained from all the patients before enrolling them to the study. A total of 32 patients with bilateral disease were enrolled for the study. All the patients were treated preoperatively with topical steroids and an antibiotic course. All relevant investigations required for preanesthetic evaluation were done, and patients were prepared for surgery.

Since all the patients had bilateral disease, one nostril was used as test side and the other side acted as control. The test and the control side for each patient were determined by block randomization technique. Surgeon was given two similar syringes marked left and right filled with either drug or saline for infiltration. Surgeon carried out the procedure on all patients who were blinded to the side of test and control. In addition to the pterygopalatine fossa (PPF) block, both the nostrils were infiltrated with 2 mL of 2% xylocaine with 1:200,000 adrenaline at the beginning of the surgery. Infiltration was done at the axilla of the middle turbinate, along the anterior insertion of the uncinate process and head of the middle turbinate. The surgical procedure was alternated between both the sides every 30 minutes and bleeding was assessed using Boezaart and Vander Merwe scale every 15 minutes. The subjects underwent clearance of disease from all the sinuses on both sides.

Infiltration Technique

The greater palatine foramen is located over the hard palate just anterior to the posterior edge of the hard palate opposite the second molar tooth, halfway between the tooth and the midline of the hard palate. This point is palpated and felt as a depression and that point is marked and identified on monitor. The needle used for infiltration was bent at 25 mm from the tip at an angle of 45° in order to perform an effective infiltration of the PPF. After aspirating to ensure that the needle was not in a blood vessel, the PPF was infiltrated with the test drug (2% xylocaine and 1:80,000 adrenaline) on one side. Same procedure was followed on the other side and saline was infiltrated.

Assessment of Bleeding

Surgical field was assessed by the operating surgeon for bleeding every 15 minutes on both test and control side, using Boezaart and Vander Merwe scale (Table 1). The total of all the grades was taken and compared with the control side (Table 2). The vital parameters like mean arterial pressure (MAP), heart rate (HR), blood pressure (BP), and residual carbon dioxide were documented throughout the procedure.

Statistical Analysis

Data were entered into Microsoft Excel data sheet and were analyzed using Statistical Package for the Social Sciences version 22 software. Categorical data were represented in the form of frequencies and proportions. Chi-square was used as test of significance. Continuous data were represented as mean and standard deviation. Independent t-test or Mann–Whitney U test was used as test of significance to identify the mean difference between two groups; p <0.05 was considered as statistically significant.

RESULTS

A total of 32 patients with bilateral sinonasal disease were enlisted for the study. The mean age of the subjects was 39.1 ± 15.2 years. Majority of the patients were males (59.4%).

Most common diagnosis in the subjects was bilateral ethmoidal polyposis (56.25%) followed by chronic rhinosinusitis (37.5%). Allergic fungal sinusitis with polyposis was found in two patients (6.25%). Mean duration of the illness was 1.47 years.

Table 1:Boezaart and Vander Merwe grading

GradesEndoscopic grading of nasal bleeding
0No bleeding (cadaveric conditions)
ISlight bleeding – no suctioning required
IISlight bleeding – occasional suctioning required
IIISlight bleeding – frequent suctioning required; bleeding threatens surgical field a few seconds after
IVModerate bleeding – frequent suctioning required and bleeding threatens surgical field directly after
VSevere bleeding – constant suctioning required; bleeding appears faster than it can be removed by suction; surgical filed severely threatened and surgery usually is not possible

Table 2: Boezaart scoring of subjects on test and control side

PatientsSurgical grade
Test sideControl side
 11316
 2610
 31010
 477
 5816
 61115
 746
 81010
 91012
101215
11610
121116
13811
141919
1567
16613
17136
1855
191614
20610
211212
22611
2346
2488
251212
26713
27711
2868
29812
30129
31109
3299

The preoperative mean endoscopic grading on test and control side was 2, and CT grading was 4 on the test side and 5 on control side. The endoscopic and CT grading was matched on both the sides so that results could be compared.

Left nostril was the test side in 12 patients and right in the remaining 20 patients. The mean surgical grade on the test side was 9.0 ± 3.5 and on the control side was 10.9 ± 3.5. The difference in mean surgical grade was statistically significant (p = 0.034) (Table 3). A correlation between preoperative endoscopic and CT grade and intraoperative surgical grade was established. Statistically significant positive correlation was found between endoscopic grade and surgical grade (p = 0.007). A positive correlation was found between CT grade and surgical grade, but was not statistically significant (p = 0.464) (Table 4).

Table 3: Comparison of surgical grade between test and control side

     Injection site     Control site     p-value
MeanSDMeanSD
Endoscopic grade1.91.0      1.81.0      0.02
CT grade4.51.34.71.50.347
Blood loss9.03.510.93.50.034

SD: Standard deviation

Table 4: Correlation between surgical grade and endoscopic/CT and vital parameters

     Correlation coefficientp-value
Endoscopic grading0.0410.02
CT scan grade0.1720.347
Heart rate0.0590.001
Systolic BP0.3990.024
Diastolic BP0.0530.047.
Mean arterial pressure0.5300.002

The vital parameters like HR, BP, and MAP were also found to influence the bleeding. There was a positive correlation between these factors and the surgical grade during the procedure.

DISCUSSION

The methods used for achieving a bloodless field for performing safe and clean ESS cannot be overemphasized. There are many methods, both preoperatively and intraoperatively, to control bleeding during FESS described in the literature. The preoperative measures include the use of preoperative corticosteroids, preoperative use of β-blockers, antihypertensive agents, and surgical pledgets with oxymetazoline, phenylephrine, or cocaine, for bleeding control. The intraoperative technique includes both esthetic and surgical methods like controlled hypotension, patient positioning, use of bipolar cautery, intermittent positive pressure ventilation, warm saline irrigation, hemostatic biomaterials, topical vasoconstrictors, topical infiltration of local anesthetic and adrenaline, and the use of laryngeal mask airway.5-8 With all these techniques, obtaining a bloodless field during ESS still remains a challenge.

Pterygopalatine fossa infiltration has been used to control bleeding by many endoscopic sinus surgeons, but there is no universal consensus regarding its efficacy in achieving a bloodless field. There are studies which claim definite decrease in bleeding adopting these techniques as well as those which confront the efficacy of the technique.2

The current study was done on 32 patients with chronic rhinosinusitis and ethmoidal polyposis. The mean surgical grade on test side was 9.0 ± 3.5 and in control side was 10.9 ± 3.5. This difference in mean surgical grade was statistically significant (p = 0.034). Two other studies reflected similar results.2,9 The current study supports their observation. In another study conducted by Valdes et al,10 they found no statistical difference between injected and noninjected site in terms of surgical grade and blood loss. Furthermore, there was no correlation between surgical field improvement, MAP, and HR either. The effect is thought to be due to vasoconstriction effect of adrenaline on maxillary artery situated in the PPF that reduces the mucosal blood flow to the sinuses and turbinates.

The vital parameters like MAP, HR, and BP were documented throughout the procedure. It was observed that these parameters had an independent effect over bleeding. There was a significant positive correlation with vital parameters and bleeding. Another study concluded that MAP had influence on bleeding, and good operating field was achieved by maintaining MAP in the range of 65 to 78 mm Hg.11 In our study, the surgical field on the test side was reasonably bloodless though MAP was at a higher range (89.3 ± 6.4), and this effect could be attributed to PPF infiltration.

Other significant observation of the study is that with increasing preoperative endoscopic grade, there was a concurrent increase in bleeding at the time of surgery (p = 0.007) (Table 2).

Although many complications have been described in literature, we did not encounter any complication related to the infiltration technique in the study subjects. This technique is relatively safe, simple with minimal complications, and also reduces bleeding significantly. Hence, it can be routinely incorporated in all ESS.

CONCLUSION

The result of this study shows that infiltration of PPF with 2% xylocaine with 1:80,000 adrenaline significantly reduces the bleeding, thus improving visualization of the surgical field during FESS. Since the technique is simple with minimal complications, it can be routinely incorporated in all ESS.

CLINICAL SIGNIFICANCE

This study is pivotal in devising an additional method for providing a clear bloodless operative field which, to date, is one of the major challenges faced by the otorhinolaryngologist.

Conflicts of interest

Source of support: Nil

Conflict of interest: None