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The Effectiveness of Botulinum Toxin Type A Injections in the Management of Sialorrhea.

Introduction

Sialorrhea is characterized by excessive drooling or salivation. Whilst normal in the early years, the condition should be regarded as pathological after the age of four (1, 2). Pathologic drooling can occur as an isolated condition associated with hypersalivation, but also as the side effects of amyotrophic lateral sclerosis, cerebral palsy, Parkinson's disease, or of their respective medication. Its most common cause in childhood is cerebral palsy, with a rate of 10 to 38% of the cases (3). In adults, Parkinson's disease is the most common (70 to 80%) cause of sialorrhea (4, 5). It is also seen in about 30 to 80% of adult schizophrenia patients as a result of clozapine treatment (6). While the underlying diseases alone are significant conditions, concomitant presence of sialorrhea can give rise to both social issues and local issues such as aspiration, skin problems or infection (7).

Treatment of sialorrhea is not easy. Therefore, as well as conservative treatment methods, highly invasive methods are also used. Conservative treatment often begins by regulating dietary habits.

Oral-motor exercises, intraoral devices or palatal training devices can be used. While medical treatment modalities include medication and botulinum toxin, invasive methods like surgery or radiotherapy are also among the available options (8, 9).

This study was designed to evaluate the effectiveness of botulinum toxin type A injections in the pediatric patients referred to our clinic because of sialorrhea.

Methods

Incidence of sialorrhea in each pediatric patient was followed with the help of their families and assessed before and in the third month after their botulinum toxin type A injection (Botox[R], Allergan, USA). The study was launched in May 2016 after approval was obtained from the Ethics Committee of Cukurova University, Faculty of Medicine. Consent was obtained from the families of all patients.

Botulinum toxin type A injection (Botox[R], Allergan, USA) was administered to both pairs of the parotid glands and the submandibular glands in each patient. The procedure was performed in the operating room under sterile conditions and injections were administered under sedation in all patients. In each patient, botulinum toxin type A injection was first administered to the two parotid glands, then to the two submandibular glands. Botulinum toxin type A, delivered by cold chain, was diluted with 1cc sterile physiological saline to obtain 100IU botulinum toxin. The syringe was changed after this process and the solution was administered via insulin syringes. After the respective regions of the parotid glands and the submandibular glands were cleansed with antiseptic solution, botulinum toxin injections were administered via an insulin syringe to the parotid gland (10 units each) and the submandibular gland pairs (20 units each) at a maximum of 2mg/kg in total. No additional therapies were given after the procedure and all patients were discharged on the same day. Families of patients were asked to fill out visual analog scales before the procedure and in the third month after the procedure and rate the severity and frequency of their patient's condition on a scale of 0 to 10. The effectiveness of the method was assessed by comparing these results.

Results

Twenty-seven pediatric patients who were referred to and treated for sialorrhea at the Otolaryngology Department, Faculty of Medicine of the Cukurova University were included in the study. Of the 27 patients 17 were female and 10 were male with a mean age of 11.5 (Min: 6, Max: 16 years). All patients had cerebral palsy accompanied by severe sialorrhea. According to the visual analog scale filled out by the families, all patients had profuse sialorrhea to the extent of soiling their clothes and hands. Visual analog scale analysis of patients before the injections showed a mean drooling value of 7.9 (Min: 5, Max: 10) and a mean frequency value of 7.7 (Min: 5, Max: 10). Analysis of the visual analog scales filled out by the families three months after the injection showed a mean drooling value of 4.4 (Min: 3, Max: 9) and a mean frequency value of 4.6 (Min: 3, Max: 9) (Figure 1). The analysis showed significant reduction both in the severity and the frequency of sialorrhea in a majority of the patients after botulinum toxin type A injection. No complications were experienced in any of the patients after the procedure.

Discussion

Efficacy of botulinum toxin, a potent neurotoxin that inhibits acetylcholine release, in sialorrhea was first reported in patients with Parkinson's disease (10). There are many studies that report about the effectiveness of botulinum toxin injections into the parotid and the submandibular glands in the management of sialorrhea. Facial paralysis, however, is the major risk associated with this procedure. While local anesthesia is recommended in some studies, there are others that recommend, as we did in our study, to perform the procedure under general anesthesia or sedation (11, 12).

Many studies indicate that administering botulinum toxin injections in the right doses and at the right intervals are vital for the efficacy of the treatment, and discuss the impact of patient-related factors and the surgeon's experience on the outcome (13-15). Research has shown that the dosage of injection to the salivary glands, and injecting botulinum toxin to the submandibular glands in addition to the parotid glands will increase the effectiveness of the treatment (14, 16). In our cases, the aim was to manage sialorrhea in a single dose, without increasing the dosage and by injecting botulinum toxin into both pairs of the parotid and submandibular glands. Many studies indicate that a need for booster injections arose in the long-term follow-up of patients (7, 11, 12).

Facial paralysis or another kind of complication associated with injection to the parotid glands was not encountered in any of our patients. One study reported effective results and a success rate of up to 89% in the management of sialorrhea with weight-based dosing strategy (17). There are also studies reporting of unsuccessful response in 30 to 50% of the cases when botulinum toxin was administered only to the submandibular glands (16, 18). Booster injections may be needed in some patients since the effect of the toxin is temporary. In our study we aimed to present the early results after a single dose of botulinum toxin.

There are studies that report ultrasound-guided administration of the injections to the submandibular glands could increase the success of the method by up to 80% (19). Another study describing ultrasound-guided administration of botulinum toxin injections in 111 patients reported that the method is safe and effective and could provide reduction in the rates of adverse events. The study reported a 68% success rate with this technique in the management of sialorrhea (20). Lack of ultrasound usage in the procedure and the short follow-up periods are major shortcomings of our study.

Conclusion

Botulinum toxin type A was found to be an effective, safe and less invasive method for the management of sialorrhea in pediatric patients.

Ethics Committee Approval: Ethics committee approval was received for this study from the Ethics Committee of Cukurova University School of Medicine (04/Mayis/2016 No: 4/2016).

Informed Consent: Written informed consent was obtained from the parents of patients who participated in this study.

Peer-review: Externally peer-reviewed.

Conflict of Interest: The authors have no conflicts of interest to declare.

Financial Disclosure: The authors declared that this study has received no financial support.

References

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Ozgur Surmelioglu [iD], Muhammed Dagkiran [iD], Ulku Tuncer [iD], Suleyman Ozdemir [iD], Ozgur Tarkan [iD], Fikret Cetik [iD], Mete Kiroglu [iD]

Department of Otorhinolaryngology, Cukurova University School of Medicine, Adana, Turkey

ORCID IDs of the authors: O.S. 0000-0001-5041-2802; M.D. 0000-0002-1923-3731; U.T. 0000-0003-3738-1751; S.O. 0000-0002-0125-1536; O.T. 0000-0003-1021-5219; F.C. 0000-0002-3722-2542; M.K. 0000-0001-5711-9182.

Cite this article as: Surmelioglu O, Dagkiran M, Tuncer U, Ozdemir S, Tarkan O, Cetik F, Kiroglu M. The Effectiveness of Botulinum Toxin Type A Injections in the Management of Sialorrhea. Turk Arch Otorhinolaryngol 2018; 56(2): 111-3.

This study was presented at the 38th National Otolaryngology head and neck surgery congress, October 26-30, 2016, Antalya, Turkey.

Corresponding Author:

Ozgur Surmelioglu; surmeli2004@yahoo.com

Received Date: 23.02.2017

Accepted Date: 16.03.2018

DOI: 10.5152/tao.2018.2411
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Title Annotation:Original Investigation
Author:Surmelioglu, Ozgur; Dagkiran, Muhammed; Tuncer, Ulku; Ozdemir, Suleyman; Tarkan, Ozgur; Cetik, Fikre
Publication:Turkish Archives of Otorhinolaryngology
Date:Jun 1, 2018
Words:1931
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