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<article article-type="other" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML">
  <front>
    <journal-meta>
      <journal-id journal-id-type="pmc">JRMS</journal-id>
      <journal-id journal-id-type="pubmed">J Res Med Sci</journal-id>
      <journal-id journal-id-type="publisher-id">Journal of Research in Medical Sciences</journal-id>
      <journal-title>Journal of Research in Medical Sciences</journal-title>
      <issn pub-type="ppub">1735-1995</issn>
	<issn pub-type="epub">1735-7136</issn>
      <publisher>
        <publisher-name>Medknow Publications Pvt Ltd</publisher-name>
	<publisher-loc>India</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">JRMS-18-400</article-id>
      <article-id pub-id-type="pmid">24174945</article-id>
      <article-categories>
	<subj-group subj-group-type="headings">
		<subject>Original Article</subject>
	</subj-group>
      </article-categories>
      <title-group>
        <article-title>Septal injection in comparison with inferior turbinates injection of botulinum toxin A in patients with allergic rhinitis</article-title>
      </title-group>
	<contrib-group>
<contrib contrib-type="author">
<name><surname>Abtahi</surname>
<given-names>Sayed M</given-names></name>
<xref ref-type="aff" rid="aff1"/></contrib>
<contrib contrib-type="author">
<name><surname>Hashemi</surname>
<given-names>Sayed M</given-names></name>
<xref ref-type="aff" rid="aff1"></xref></contrib>
<contrib contrib-type="author">
<name><surname>Abtahi</surname>
<given-names>Sayed H</given-names></name>
<xref ref-type="aff" rid="aff1"></xref></contrib>
<contrib contrib-type="author">
<name><surname>Bastani</surname>
<given-names>Bagher</given-names></name>
<xref ref-type="aff" rid="aff1"></xref></contrib>
</contrib-group>
<aff id="aff1">Department of Otolaryngology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, </aff>

      <author-notes>
	<corresp id="cor1"><bold>Address for correspondence:</bold>Bagher Bastani, Department of Otolaryngology, School of Medicine, Isfahan University of Medical Sciences, Isfahan,  <email xlink:href="bastan389@gmail.com">bastan389@gmail.com</email></corresp>

      </author-notes>
      <pub-date pub-type="ppub">
        <season>May</season>
        <year>2013</year>
      </pub-date>
      <volume>18</volume>
      <issue>5</issue>
      <fpage>400</fpage>
      <lpage>404</lpage>   
      
<history>
<date date-type="received"><day>27</day><month>1</month><year>2013</year></date>

<date date-type="rev-recd"><day>4</day><month>3</month><year>2013</year></date>
</history>

      <permissions>
        <copyright-statement>Copyright: &#x000a9; Journal of Research in Medical Sciences</copyright-statement>
        <copyright-year>2013</copyright-year>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/3.0"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
</license>
      </permissions>
      <abstract><sec id="st1"><title>Background:</title><p> Botulinum toxin A (BTA) is a promising therapeutic option in the treatment of allergic rhinitis (AR). Although recent studies have introduced BTA septal injection as an alternative method, the conventional localization for the injection of BTA in patients with AR is still the nasal turbinates. This study was designed to compare the effectiveness and safety of septal BTA injection with turbinal BTA injection in patients with AR. <sec id="st1"><title>Materials and Methods:</title><p> This open&#8209;label study was performed on 50 patients with AR who were randomly allocated to septal and turbinal BTA injection groups. All patients received an injection of 40 U of BTA (Dysport&#894;, Ipsen Ltd, Maidenhead, UK) in each side of the nose and were followed for 8 weeks. Prior to the intervention and 8 weeks later, symptom severity and quality of life scores were calculated using the AR symptom severity and Rhinasthma questionnaires respectively. <sec id="st1"><title>Results:</title><p> Comparison of pre&#8209; and post&#8209;treatment symptom severity scores within each group showed a significant reduction of total symptom severity score and severity of sneezing, rhinorrhea, and congestion in both groups (P &lt; 0.05). However, post&# 8209;treatment symptom severity scores were not significantly different between two groups (P &gt; 0.05). Both methods have improved the quality</p>
</sec>
<sec id="st2"><title>Materials and Methods:</title><p> This open&#8209;label study was performed on 50 patients with AR who were randomly allocated to septal and turbinal BTA injection groups. All patients received an injection of 40 U of BTA (Dysport&#894;, Ipsen Ltd, Maidenhead, UK) in each side of the nose and were followed for 8 weeks. Prior to the intervention and 8 weeks later, symptom severity and quality of life scores were calculated using the AR symptom severity and Rhinasthma questionnaires respectively. <sec id="st2"><title>Results:</title><p> Comparison of pre&#8209; and post&#8209;treatment symptom severity scores within each group showed a significant reduction of total symptom severity score and severity of sneezing, rhinorrhea, and congestion in both groups (P &lt; 0.05). However, post&# 8209;treatment symptom severity scores were not significantly different between two groups (P &gt; 0.05). Both methods have improved the quality</p>
</sec>
<sec id="st3"><title>Results:</title><p> Comparison of pre&#8209; and post&#8209;treatment symptom severity scores within each group showed a significant reduction of total symptom severity score and severity of sneezing, rhinorrhea, and congestion in both groups (P &lt; 0.05). However, post&# 8209;treatment symptom severity scores were not significantly different between two groups (P &gt; 0.05). Both methods have improved the quality</p>
</sec>
<sec id="st4"><title>Conclusion:</title><p> Although both septal and turbinal BTA injections are effective on patients with AR, septal administration of BTA could be safer and easier method. However, further investigations are required to achieve more accurate results.</p>
</sec>
</abstract>
      <kwd-group><kwd>Allergic rhinitis</kwd>
<kwd>botulinum toxin A</kwd>
<kwd>quality of life</kwd>
</kwd-group>	
      
    </article-meta>
  </front>
  <body>
	<sec><title/>
</sec><sec><title>Introduction</title><p>Allergic rhinitis (AR) is a common immunoglobulin-E-mediated disease of the nasal mucosa that usually occurs after exposure to various indoor and outdoor allergens including dust mites, insects, animal dander, molds, and pollens. AR is characterized by nasal congestion, paroxysmal repetitive sneezing, watery rhinorrhea, and pruritus. <sup><xref ref-type="bibr" rid="ref1">1</xref></sup>,<sup><xref ref-type="bibr" rid="ref2">2</xref></sup> These bothersome symptoms may have negative effects on daily activities, quality of sleep, and productivity. <sup><xref ref-type="bibr" rid="ref3">3</xref></sup> AR affects up to 40&#x0025; of the general population, <sup><xref ref-type="bibr" rid="ref4">4</xref></sup>,<sup><xref ref-type="bibr" rid="ref5">5</xref></sup>,<sup><xref ref-type="bibr" rid="ref6">6</xref></sup> and imposes a considerable burden both on patients and society. <sup><xref ref-type="bibr" rid="ref7">7</xref></sup> Although the quality of life of patients with AR is significantly impaired, <sup><xref ref-type="bibr" rid="ref8">8</xref></sup>,<sup><xref ref-type="bibr" rid="ref9">9</xref></sup> it can be improved by appropriate treatment. <sup><xref ref-type="bibr" rid="ref10">10</xref></sup></p>

<p> Therefore, depending on the pathogenesis of the particular type of rhinitis and symptoms of the patient, several therapeutic options are available for the treatment of nasal hyperreactivity. <sup><xref ref-type="bibr" rid="ref11">11</xref></sup> Various pharmacologic options including intranasal corticosteroids, oral and topical antihistamines, decongestants, intranasal cromolyn, intranasal anticholinergics, and leukotriene receptor antagonists have been widely used for the treatment of AR. <sup><xref ref-type="bibr" rid="ref12">12</xref></sup>,<sup><xref ref-type="bibr" rid="ref13">13</xref></sup> However, few of these conventional methods lead to significant symptom relief. <sup><xref ref-type="bibr" rid="ref11">11</xref></sup> For this reason, novel therapeutic methods have to be developed.</p>

<p>Botulinum toxin A (BTA) is a neurotoxin with metalloproteinase activity that inhibits the release of acetylcholine from the presynaptic nerve endings at the neuromuscular and neuroglandular junctions. <sup><xref ref-type="bibr" rid="ref11">11</xref></sup>,<sup><xref ref-type="bibr" rid="ref14">14</xref></sup>,<sup><xref ref-type="bibr" rid="ref15">15</xref></sup> Based on the anticholinergics activities of BTA, it has been used in the treatment of patients with idiopathic rhinitis <sup><xref ref-type="bibr" rid="ref16">16</xref></sup>,<sup><xref ref-type="bibr" rid="ref17">17</xref></sup>,<sup><xref ref-type="bibr" rid="ref18">18</xref></sup>,<sup><xref ref-type="bibr" rid="ref19">19</xref></sup> or AR, <sup><xref ref-type="bibr" rid="ref20">20</xref></sup>,<sup><xref ref-type="bibr" rid="ref21">21</xref></sup> and has reduced its symptoms effectively. <sup><xref ref-type="bibr" rid="ref16">16</xref></sup>,<sup><xref ref-type="bibr" rid="ref17">17</xref></sup>,<sup><xref ref-type="bibr" rid="ref18">18</xref></sup>,<sup><xref ref-type="bibr" rid="ref19">19</xref></sup>,<sup><xref ref-type="bibr" rid="ref20">20</xref></sup>,<sup><xref ref-type="bibr" rid="ref21">21</xref></sup> Although initial investigations have described the nasal turbinates as the site of BTA injection, <sup><xref ref-type="bibr" rid="ref16">16</xref></sup>,<sup><xref ref-type="bibr" rid="ref17">17</xref></sup>,<sup><xref ref-type="bibr" rid="ref18">18</xref></sup>,<sup><xref ref-type="bibr" rid="ref19">19</xref></sup>,<sup><xref ref-type="bibr" rid="ref20">20</xref></sup>,<sup><xref ref-type="bibr" rid="ref19">19</xref></sup> recent studies have suggested that the nasal septum could be more suitable alternative site for BTA injection. <sup><xref ref-type="bibr" rid="ref22">22</xref></sup> However, no study has compared the effectiveness and safety of BTA injection into the nasal turbinates with those of BTA injection into the nasal septum.</p>

<p>In light of the above, this comparative study was designed to determine the safer and more suitable site for BTA injection in patients who suffer from AR.</p>


</sec><sec sec-type='materials|methods'><title>Materials and Methods</title><p>Study population and design</p>

<p> After approval of the study by the Ethic Committee of Isfahan University of Medical Sciences and obtaining informed consent, this open-label randomized clinical trial was performed on patients who were referred to the ENT outpatient clinics of "Al-zahra" and "Kashani" hospitals. This investigation was performed in Isfahan, Iran, between March 2011 and April 2012.</p>

<p>A convenience sample of 50 patients of both genders was entered into this study. Participants were included in this study if they fulfilled the criteria of AR according to the allergic rhinitis and its Impact on Asthma (ARIA). <sup><xref ref-type="bibr" rid="ref23">23</xref></sup></p>

<p> Any anatomic abnormality of the nasal cavities such as nasal septal deviation and nasal polyp, previous rhinoplasty or septoplasty, pregnancy, history of persistent asthma, systemic corticosteroid therapy, malignancy, diabetes mellitus or other significant medical diseases were considered as the exclusion criteria. In addition, participants who received any medication for AR over 2 months prior to the study were excluded.</p>

<p>Using simple randomization, patients who met all criteria for enrollment were randomly allocated into 2 treatment groups of inferior turbinate injection and septal injection <xref ref-type="fig" rid="F1">Figure 1</xref>.<fig id="F1"><label>Figure 1</label><caption><p>Consort diagram of participation</p>
</caption><alt-text>Figure 1</alt-text><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="JResMedSci_2013_18_5_400_119450_u4.tif"/></fig></p>

<p> Data collection</p>

<p> In addition to demographic data, patients&#x2032; information was collected using reliable and valid Persian editions of 2 questionnaires including AR symptom severity questionnaire and Rhinasthma questionnaire for quality of life. <sup><xref ref-type="bibr" rid="ref24">24</xref></sup></p>

<p> The AR symptom severity questionnaire consists of 5 items according to ARIA criteria (sneezing, watery runny nose, nasal obstruction, nasal itching, conjunctivitis) and asses the severity of each symptom on a 4 point scale (0: No symptom, 1: Mild, 2: Moderate, 3: Severe).</p>

<p>The Rhinasthma is a 42 item quality of life questionnaire. Patients were asked to indicate items they had directly experienced, and to indicate the importance of each of them on a 4 point scale (1 = not important; 4 = very important). <sup><xref ref-type="bibr" rid="ref25">25</xref></sup></p>

<p> Before and 8 weeks after the intervention (at the last follow-up session), all patients answered the Rhinasthma questionnaire, and the symptom severity questionnaire was filled by the investigator based on the patients&#x2032; history.</p>

<p> Intervention and follow-up</p>

<p> In order to make a BTA solution with a concentration of 100 U/ml, each 500 U BTA vial (Dysport<sup>&#174;</sup> , Ipsen Ltd., Maidenhead, UK) was diluted with 5 ml sterile water. Ten min prior to the injection, local anesthesia was applied using 10&#x0025; lidocaine spray. While patients were in the sitting position, they received an injection of 40 U BTA (0.4 ml) in each side using a 27 G hypodermic needle. In the first group, BTA was injected into the bilateral inferior turbinates (in the anterior tip of turbinate). In the second group, patients underwent bilateral subperichondrial septal injection of BTA (in the anterior 1 cm submucoperichondrial of septum). BTA was injected very slowly. All injections were performed by a single otolaryngologist.</p>

<p>Follow-up visits were arranged on a 2 weekly basis for 8 weeks (4 follow-up visits with a 2 week interval). On each follow-up session, patients were asked about the symptom severity and possible adverse effects.</p>

<p> Statistical analysis</p>

<p> Statistical analysis was performed using the Statistical Package for the Social Sciences (SPSS) 20.0 (SPSS Inc., Chicago, IL, USA). Independent t-test, Mann-Whitney U-test, Wilcoxon test and Chi-square were used when appropriate. P &lt; 0.05 were considered statistically significant.</p>

<p>Sample template for the Consort diagram showing the flow of participants through each stage of a randomized trial</p>


</sec><sec><title>Results</title><p>Baseline and demographic data</p>

<p> There was no significant differences between 2 groups regarding baseline data <xref ref-type="table" rid="T1">Table 1</xref>.{Table 1}</p>

<p> Efficacy</p>

<p> Effects on symptom severity score.</p>

<p>Comparison of pre- and post-treatment total symptom severity score within each group showed that BTA injection into both sites has significantly reduced the symptom severity score (P &lt; 0.0001). However, post-treatment symptom severity score was not significantly different between two groups (P: 0.18) <xref ref-type="table" rid="T2">Table 2</xref>.{Table 2}</p>

<p>Comparison of pre- and post-treatment severity score of each symptom within 2 groups revealed that both methods of BTA injection have significantly improved the severity of sneezing, rhinorrhea and congestion; however, they have not been effective on nasal itching and conjunctivitis. No significant differences were found between the treatment groups in any of post-treatment severity scores <xref ref-type="table" rid="T2">Table 2</xref>.</p>

<p> Effects on quality of life</p>

<p> Participants of both treatment groups have experienced significant improvement in their quality of life. However, there was no statistically significant differences between two groups regarding the post-treatment Rhinasthma score <xref ref-type="table" rid="T3">Table 3</xref>.{Table 3}</p>

<p> Adverse effects</p>

<p> During the follow-up sessions, 4 (16&#x0025;) patients in the inferior turbinate group reported adverse effect (3 subjects had epistaxis, and 1 had nasal mucosa dryness). The number of subjects who developed adverse effect was significantly lower in the nasal septum group and only 1 (4&#x0025;) patient complained of epistaxis (P value: 0.03). All adverse effects were mild-moderate and were treated appropriately.</p>


</sec><sec><title>Discussion</title><p>AR is a common systemic inflammatory condition <sup><xref ref-type="bibr" rid="ref24">24</xref></sup> that was first defined in 1929. <sup><xref ref-type="bibr" rid="ref26">26</xref></sup> Since then, it has been a global health problem that causes major illness and disability world-wide. <sup><xref ref-type="bibr" rid="ref24">24</xref></sup> AR affects various aspects of daily-life of people regardless of their sex, age, ethnicity or country. <sup><xref ref-type="bibr" rid="ref7">7</xref></sup></p>

<p> Because AR usually imposes indirect costs, its economic impact is often underestimated. <sup><xref ref-type="bibr" rid="ref7">7</xref></sup> Given the high prevalence of AR and its substantial effects on quality of life of patients, several therapeutic strategies have been developed to improve the quality of life and reduce the symptom severity.</p>

<p>BTA has recently emerged as a promising new treatment for different types of rhinitis. <sup><xref ref-type="bibr" rid="ref11">11</xref></sup>,<sup><xref ref-type="bibr" rid="ref16">16</xref></sup>,<sup><xref ref-type="bibr" rid="ref17">17</xref></sup>,<sup><xref ref-type="bibr" rid="ref18">18</xref></sup>,<sup><xref ref-type="bibr" rid="ref20">20</xref></sup>,<sup><xref ref-type="bibr" rid="ref21">21</xref></sup>,<sup><xref ref-type="bibr" rid="ref22">22</xref></sup> The role of BTA in the treatment of idiopathic rhinitis was first described by Kim et al. <sup><xref ref-type="bibr" rid="ref16">16</xref></sup> Then, Wen et al. performed a study on rats, and reported that local BTA treatment could be a long lasting method to reduce symptoms of AR. <sup><xref ref-type="bibr" rid="ref27">27</xref></sup></p>

<p> Ozcan et al. <sup><xref ref-type="bibr" rid="ref17">17</xref></sup> and Sapci et al. <sup><xref ref-type="bibr" rid="ref18">18</xref></sup> confirmed the effectiveness of BTA as a therapeutic option for idiopathic rhinitis in human subjects, and Unal et al. reported the same result for patients with AR; <sup><xref ref-type="bibr" rid="ref21">21</xref></sup> however, all these investigations used the technique of injection of BTA into the inferior or middle turbinates.</p>

<p>Recently, Braun et al. described the new technique of BTA injection into the nasal septum in patients with idiopathic rhinitis. They concluded that this new method can achieve good symptom control and patient comfort. In addition, they suggested comparison of nasal septal injection with the conventional turbinal injection technique. <sup><xref ref-type="bibr" rid="ref22">22</xref></sup></p>

<p> To the best of our knowledge, this is the first study that has compared the effectiveness and safety of BTA injection in different sites in patients with AR.</p>

<p>Present study demonstrated that both turbinal and septal injection of BTA can significantly improve the average of symptom severity and quality of life of patients with AR.</p>

<p>When a treatment can improve bothersome symptoms such as rhinorrhea, nasal congestion and sneezing, it would not be surprising to find it effective on the quality of life of patients. Laskawi also demonstrated that intranasal injection of BTA is a helpful option to improve the quality of life in patients with various head and face disorders such as AR. <sup><xref ref-type="bibr" rid="ref28">28</xref></sup></p>

<p> In addition to the total symptom severity score, BTA injection reduced the severity of all symptoms except nasal itching and conjunctivitis.</p>

<p>These findings match with the results that Ozcan et al. have reported. They demonstrated that intranasal BTA injection improves nasal discharge, nasal obstruction and sneezing, whereas it has no effect on itching. <sup><xref ref-type="bibr" rid="ref17">17</xref></sup> Unal et al. also described a significant reduction of sneezing and nasal congestion in patients with AR after treatment with BTA. <sup><xref ref-type="bibr" rid="ref21">21</xref></sup></p>

<p> It is well-known that the nasal secretory activity is under parasympathetic control. <sup><xref ref-type="bibr" rid="ref17">17</xref></sup>,<sup><xref ref-type="bibr" rid="ref22">22</xref></sup> Moreover, it has been suggested that acetylcholine may play an significant role in the sneezing reflex. <sup><xref ref-type="bibr" rid="ref11">11</xref></sup></p>

<p> The effectiveness of intranasal injection of BTA in the treatment of AR symptoms can be attributed to the anticholinergics properties of BTA that affect the large number of serous glands in the nasal cavity, and result in decreased nasal secretory response. <sup><xref ref-type="bibr" rid="ref22">22</xref></sup>,<sup><xref ref-type="bibr" rid="ref29">29</xref></sup> BTA selectively inactivates peripheral cholinergic nerve terminals by blocking the release of acetylcholine from the cholinergic nerve endings in the nasal mucosa or preganglionic cholinergic nerve terminals in sphenopalatine ganglion. These two mechanisms have been considered as the main mechanisms of action of BTA in the nasal cavity. <sup><xref ref-type="bibr" rid="ref16">16</xref></sup>,<sup><xref ref-type="bibr" rid="ref17">17</xref></sup></p>

<p> Furthermore, Rohrbach et al. demonstrated that nasal application of BTA in pigs can lead to a degeneration of nasal glands and ducts and a diffuse glandular apoptosis. However, they did not observe any necrosis or inflammation following the application of BTA. <sup><xref ref-type="bibr" rid="ref30">30</xref></sup></p>

<p> Similar to the previous studies, we have found no complications of intranasal injection of BTA. <sup><xref ref-type="bibr" rid="ref16">16</xref></sup>,<sup><xref ref-type="bibr" rid="ref17">17</xref></sup>,<sup><xref ref-type="bibr" rid="ref18">18</xref></sup>,<sup><xref ref-type="bibr" rid="ref22">22</xref></sup></p>

<p> Our experience demonstrated that septal BTA injection could be an easier technique than the septal injection. The nasal septum can usually be visualized without any difficulty. Similarly, Braun et al. has reported septal injection as an easy and well-tolerated intranasal BTA injection technique. <sup><xref ref-type="bibr" rid="ref22">22</xref></sup></p>

<p> We also observed significantly lower rate of adverse effect in patients treated with septal injection of BTA. The rich vascular supply of the inferior turbinate <sup><xref ref-type="bibr" rid="ref31">31</xref></sup> may increase the risk of adverse effects. When BTA is injected into the nasal septum, the injection is performed by the submucoperichondrial approach. Submucoperichondrial injection could be associated with a lower systemic absorption of BTA, and therefore lead to a lower rate of systemic adverse effects.</p>

<p>Kim et al. has reported that rich blood vessels in the mucosa of the inferior turbinate might lead to more rapid absorption and clearing of the BTA. <sup><xref ref-type="bibr" rid="ref16">16</xref></sup> Hence, submucoperichondrial injection of BTA in the nasal septum may result is more duration of BTA effect. However, long-term follow-up is needed to compare these 2 methods regarding the duration of effects on AR symptoms.</p>

<p>When two treatment methods have similar efficacy, their other characteristics play a more important role in the process of technique selection. Safety and ease of administration are among the most important characteristics that significantly affects the success of a treatment. Injection of BTA into the septum was easier than turbinal injection and caused significantly fewer adverse effects. Given these two important factors and the equal efficacy of septal and turbinal BTA injection, it seems that septal BTA injection could be a more suitable technique.</p>

<p>Since, this study was conducted with an open-label design; re-investigation of this study with a double-blind study design may lead to more accurate results. In addition, we used a subjective method to assess the severity of symptoms; therefore, using rhinomanometry, rhinoresistometry and acoustic rhinometry to objectify the severity of nasal discharge and nasal patency can increase the reliability of findings.</p>


</sec><sec><title>Conclusion</title><p>Although both septal and turbinal BTA injections are effective on symptom severity and quality of life of patients with AR, septal administration of BTA could be safer and easier technique. However, further investigations are required to achieve more accurate results.</p>


</sec><sec><title>Limitations of the study</title><p>The sample size may be not enough to mention definitely about "Adverse Reactions" and Safety of this treatment option.</p>


</sec>
  </body>
  <back>
	<ack><p>We are grateful to the Isfahan University of Medical Sciences for financial support (Grant No. 390564). We also express our gratitude to for statistical consultant.</p>
</ack>
	
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