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The use of botulinum toxin in head and face medicine: An interdisciplinary field
Head & Face Medicine volume 4, Article number: 5 (2008)
In this review article different interdisciplinary relevant applications of botulinum toxin type A (BTA) in the head and face region are demonstrated.
Patients with head and face disorders of different etiology often suffer from disorders concerning their musculature (example: synkinesis in mimic muscles) or gland-secretion.
This leads to many problems and reduces their quality of life. The application of BTA can improve movement disorders like blepharospasm, hemifacial spasm, synkinesis following defective healing of the facial nerve, palatal tremor, severe bruxism, oromandibular dystonias hypertrophy of the masseter muscle and disorders of the autonomous nerve system like hypersalivation, hyperlacrimation, pathological sweating and intrinsic rhinitis.
The application of botulinum toxin type A is a helpful and minimally invasive treatment option to improve the quality of life in patients with head and face disorders of different quality and etiology. Side effects are rare.
Historical milestones, introduction
Justinus Kerner first described the symptoms of botulism in detail . Pierre van Ermengem isolated the microorganism "bacillus botulinus" . In 1979 A.B. Scott first used botulinum toxin (BTA) therapeutically to correct strabism injecting the toxin into external eye muscles .
The clinical use of BTA expanded during the last years (for review see ). A lot of movement disorders and disorders of the autonomous nerve system can be treated with this option (see Table 1) and the head and neck region is an interdisciplinary focus in this field. BTA prevents the release of acetylcholine (ACHE) in synapses. ACHE acts as a neurotransmitter for the innervation of muscles and different gland tissues. Blocking the release of ACHE leads to a reduction of pathological movement of muscles and secretion of glands in the head and neck area increasing the quality of life for patients. In this connection the following pathological states of high interdisciplinary relevance are focused in this article:
movement disorders of the facial nerve (blepharospasm, hemifacial spasm, facial nerve palsy, synkinesis following defective healing of the facial nerve, aesthetic applications, posttraumatic wound healing preventing excessive scaring),
hypersalivation of different etiologies,
gustatory sweating and
intrinsic or allergic rhinitis.
Facial nerve paralysis, synkinesis following defective healing of the facial nerve, hemifacial spasm, blepharospasm, aesthetic applications, prevention of scar formation
Classical indications to be treated with BTA are the treatment of patients suffering from a blepharospasm or a hemifacial spasm. Patients with a blepharospasm suffer from repetetive cramps of the orbicularis oculi muscles leading to eye closure. Patients suffering from a hemifacial spasm experience repetetive tonic-clonic cramps of one half of the mimic musculature (example see Fig 1). BTA is suited to treat these diseases by injecting the substance into certain muscle depending on the clinical picture. Doses vary from 1.25 to 5 units Botox® per injection point.
BTA is also helpful in other disorders of the mimic musculature. In some cases a facial nerve paralysis leads to an affection of the cornea with severe problems like a "keratitis e lagophthalmo". In such cases an injection into the levator palpebrae muscle can close the eye for some time to protect the cornea . We use dosages of 5–10 units Botox®, the injection is done subcutaneously in the middle of the upper lid. After about 3–4 months the eye "opens" again and that is usually referring to the regeneration time of the paralysis.
In addition the esthetic outcome of a paralysis of the marginal branch of the facial nerve can be improved by injecting 2.5–5 units Botox® into the depressor labii muscle of the normal side .
Synkinesis are a non-avoidable sequelae following reconstruction of the facial nerve in patients suffering from malignant tumors of the parotid gland. Synkinesis are characterized by synchronous but not intended movements of certain areas of mimic muscles becoming mostly evident during spontaneous movements of the face based on emotional expressions. Mass movements can be reduced using BTA. This options has been described first by our group [7–9].
We normally inject BTA using 6 injection-points around the eye to reduce foreign movements of the orbicularis oculi muscle (see Fig 2). The complete injection design and the total dosage depend on the extent of mass movements and may vary from patient to patient. We normally use dosages from 1.25–5 units Botox® on each injection point. Side effects are very rare ; the reason for that could be that lower dosages are necessary to treat synkinesis compared to other facial dyskinesis like hemifacial spasm or blepharospam.
Another interesting indication is the intraoperative application of BTA during the surgical supply of fresh wounds of the face. It has been demonstrated that weakening of face muscles neighbouring facial wounds leads to a better aesthetic outcome. The reason may be that after the immobilization of the treated muscles the borders of fresh wounds better adapt without muscular tension leading to excellent aesthetic results .
For all facial applications the duration of the effect normally begins within 3–5 days and amounts 3–4 months. Then the treatment has to be repeated. Side effects like a ptosis (Fig 4), a "keratitis e lagophthalmo" or tearing are rare.
An important, increasing field of application is the use of BTA in different pain syndromes, especially in patients suffering from tension headache, migraine and chronic daily headache (for review see [14, 15]).
Repetitive dystonic contractions of the muscles of the soft palate (palatoglossus and palatopharyngeus muscles, salpingopharyngeus, tensor and levator veli palatini muscles) lead to a rhythmic elevation of the soft palate . This can cause speech and also swallowing disorders due to a velopharyngeal insufficiency. Most patients suffering from palatal tremor complain of "ear clicking". This rhythmic tinnitus is caused by a repetitive opening and closure of the orifice of the Eustachian tube. A particular sequelae of pathological movements of soft palate muscles is the syndrome of a "patulous Eustachian tube" . These patients suffer from "autophonia" caused by an open Eustachian tube due to the increased muscle tension of the paratubal muscles (salpingopharyngeus, tensor and levator veli palatini muscles).
In a first treatment session, the application of five units of Botox® (uni- or bilaterally) into the soft palate is adequate in most cases. If necessary, this can be increased to two times 15 units of Botox®. The application is normally performed transorally (transpalatinal or via postrhinoscopy) under endoscopic control. To optimise the detection of the target muscle, injection under electromyographic control is recommended. To avoid side effects such as iatrogenic velopharyngeal insufficiency the treatment should be started with low doses as described above.
Hyperactivity of jaw muscles
Oromandibular dystonia (OMD)
In patients with an OMD tongue prostrusions and abnormal movements of the jaw are dominant feature of the clinical picture (Fig 5) . That may result in severe symptoms for the patient like dysarthria and dysphagia. An exact inspection, palpation and electromyographic investigations are suited as diagnostic tools.
Depending of the kind of movement disorder, botulinun toxin injections into the floor of the mouth, the extrinsic tongue muscles and different jaw muscles have to be done to improve the clinical picture. We avoid injections into intinsic tongue muscles because weakening these muscles may result into relevant side effects like swallowing disorders, speech problems and problems of jawing.
Different approaches for injections are described like the external and internal approach of the pterygoideus medialis muscle as an example.
In the treatment of OMD, we use doses up to 50 units Botox®.
Severe Bruxism 
If severe bruxisms does not improve after conventional therapeutic measures, additional injections with botulinum toxin may improve the clinical picture. Injections have to be done into the masseter and temporalis muscles ; doses up to 60 units Botox® per muscle are described. The treatment can be performed using electromyography.
Hypertrophy of the masseter muscle
Hypertrophy of the masseter muscle leads to a difference in the symmetry of the face .
The injection can be performed transoral or from outside.
In the literature, injections up to 50 units Botox® into each masseter muscle are recommended.
BTA also is used in patients with a fracture of the jaw for immobilisation of the jaw, in patients with a jaw luxation caused by a hyperactivity of the lateral pterygoid muscle and in patients with a lockjaw.
Autonomous Nerve System
Hypersalivation is of high relevance for patients suffering from different diseases (see Fig 6) [21, 22]. Some patients of this group are not able to swallow their saliva because of a stenosis of the upper esophagus sphincter region caused by scar formation after a tumor resection. In other patients the sensory control of the entrance of the larynx is reduced and therefore saliva may pass the larynx and reach the trachea and the bronchus. That leads to permanent aspiration and aspiration pneumonia. In a third group of patients problems of the wound healing process after extended surgery exist, like fistulas following laryngectomies. In these cases saliva is a very aggressive agens preventing a normal healing process. In addition, different neurological disorders include hypersalivation as a very serious symptom.
Based on our expanded experiences literature, we prefer in our patients the ultra-sound-guided injection into the parotid and submandibular gland on each side. We inject into the parotid gland 22.5 units Botox® on each side, distributed on 3 points. The submandibular glands are treated by a ultrasound-guided one or 2-point injection of a total of 15 units Botox® per gland. It has been shown by objective datas in a lot of papers that BTA injections are effective in reducing the saliva flow, accompanied by very few side effects.
Gustatory sweating, sweating of the face
Gustatory sweating is a common sequelae following parotid gland surgery [23–28]. The treatment of gustatory sweating with BTA has been described first by our group in 1994 (first treated patient December 1993 [23, 27]) and became the first line treatment option in these patients.
To get an optimal outcome, we recommend marking of the sweating area by Minor's test and then dividing the sweating area in "boxes" using a waterproof pen. The injections are done intracutaneously (see Fig 7).
The effectiveness of BTA treatment in patients with gustatory sweating has been confirmed by a lot of other authors. Some patients report a benefit after BTA-injection already at the same day and interestingly, the positive effect remains much longer than in patients with movement disorders . Some patients reach several years of a symptom free interval.
The treatment of hyperhidrosis of the head and/or the face are based on the same principles as described for patients with gustatory sweating. The doses which are reached for each individual patient depend on the size of the sweating area to be treated.
Hyperlacrimation (example see Fig 8) can be caused by a stenosis of the lacrimal duct, by misdirected secretory fibers following a degenerative paresis of the facial nerve (crocodile tears) or after a mechanical irritation of the cornea (in patients with a lagophthalmus). The application of BTA is a helpful tool to reduce pathological tearing in these patients in order to reach normal levels of tear liquid production [29–31]. We inject 5–10 units Botox® into the pars palpebralis of the lacrimal gland (technique see Fig 9). None of our patients suffered from a "dry eye" after BTA treatment of the lacrimal gland.
In the last few years, the application of Botulinum toxin type A in patients with intrinsic or allergic rhinitis has been described [32–34]. In experimants the existence of apoptosis of nasal glands has been demonstrated . The main symptom in patients suffering from these diseases is extensive rhinorrhea with secretions dripping from the nose.
There are two methods for applying BTA in these patients (Fig 10): it can either be injected into the middle and lower nasal turbinates , or it can be applied with a sponge soaked in a solution of BTA (Fig. 10) .
For the injection we use 10 units of Botox® for each turbinate (middle and lower nasal turbinates).
With the other technique, the sponges are loaded with a solution containing 40 units of Botox® and one is applied on each side.
The positive effect of the injections has been demonstrated in placebo-controlled studies . Nasal secretion is reduced for about 12 weeks (example see Fig 11). Side effects such as epistaxis or nasal crusting were uncommon.
New developments and aspects
Some new developments in the use of BTA in head and face medicine are to mention here (see ). BTA application in patients suffering from tinnitus  or depressions  have been treated with BTA. Further investigations will show whether there is a real hope for clinical use of BTA in these indications.
The application of botulinum toxin type A is a helpful and minimally invasive treatment option in different functional disorders improving the quality of life in patients with head and face disorders of different etiology. Side effects are rare.
It is stated that informed written consent was obtained for publication of the patients images.
Kerner J: Vergiftung durch verdorbene Würste. Tübinger Blätter f Naturwissensch u Arzneykunde. 1817, 3: 1-25.
Van Ermengem E: Über eine neuen anaeroben Bacillus und seine Beziehungen zum Botulismus. Z Hyg Infektionskrankh. 1897, 26: 1-56.
Scott AB: Botulinum toxin injection into extraocular muscles as an alternative to strabismus surgery. Opthalmol. 1980, 87 (10): 1044-1049.
Truong DD, Jost WH: Botulinum toxin: clinical use. Parkinsonism Relat Disord. 2006, 12: 331-55.
Merte RL, Lanzl IM: Botulinum toxin injection for production of ptosis. Ophthalmologe. 2007, 104: 767-770.
Laskawi R, Rohrbach S: Botulinum toxin in Otolaryngology. HNO. 2004, 52: 635-641.
Laskawi R, Damenz W, Roggenkämper P, Baetz A: Botulinum toxin treatment in patients with facial synkinesis. Eur Arch Otorhinolaryngol. 1994, 195-199. Suppl
Roggenkämper P, Laskawi R, Damenz W, Schröder M, Nüßgens Z: Orbicular synkinesis after facial paralysis: treatment with botulinum toxin. Documenta Ophthalmologica. 1994, 86: 395-402.
Laskawi R: Combination of hypoglossal-facial nerve anastomosis and botulinum toxin injections to optimize mimic rehabilitation following removal of acoustic neurinomas. Plast Reconstr Surg. 1997, 99: 1006-1011.
Laskawi R, Rohrbach S, Rödel R: Surgical and nonsurgical treatment options in patients with movement disorders of the platysma. J Oral Maxillofac Surg. 2002, 60: 157-162.
Laskawi R, Rohrbach S: Surgical and conservative methods for restoring impaired motor function: facial nerve, spinal accessory nerve, hypoglossal nerve (not including vagal nerve or swallowing). GMS Curr Top Otorhinolaryngol Head Neck Surg. 2005, 4: Doc 10
Gassner HG, Brissett Ae, Otley CC, Boahene DK, Biggust AJ, Weaver AL, Sherris DA: Botulinum toxin to improve facial wound healing: A prospective, blinded, placebo-controlled study. Mayo Clin Proc. 2006, 81: 1023-1028.
Dastoor SF, Misch CE, Wang HL: Botulinum toxin (Botox) to enhance facial macroesthetics: a literature review. J Oral Implantol. 2007, 33: 164-71.
Samton J, Mauskop A: Treatment of headaches with botulinum toxin. Expert Rev Neurother. 2006, 6: 313-22.
Junghans K, Rohrbach S, Ellies M, Laskawi R: Improvement of chronic facial pain and facial dyskinesia with the help of botulinum toxin application. Head Face Med. 2007, 3: 32-
Penney SE, Bruce IA, Saeed SR: Botulinum toxin is effective and safe for palatal tremor: a report of five cases and a review of the literature. J Neurol. 2006, 253: 857-60.
Olthoff A, Laskawi R, Kruse E: Successful treatment of autophonia with botulinum toxin: case report. Ann Otol Rhinol Laryngol. 2007, 116: 594-8.
Laskawi R, Rohrbach S: Oromandibular dystonia. Clinical forms, diagnosis and examples of therapy with botulinum toxin. Laryngorhinootologie. 2001, 80: 708-13.
Clark GT, Ram S: Four oral motor disorders: bruxism, dystonia, dyskinesia and drug-induced dystonic extrapyramidal reactions. Dent Clin North Am. 2007, 51: 225-43.
Arikan OK, Tan FU, Kendi T, Koc C: Use of botulinum toxin type A for the treatment of masseteric muscle hypertrophy. J Otolaryngol. 2006, 35: 40-3.
Ellies M, Gottstein U, Rohrbach-Volland S, Arglebe C, Laskawi R: Reduction of Salivary Flow with Botulinum Toxin: Extended Report on 33 Patients with Drooling, Salivary Fistulas and Sialadenitis. Laryngoscope. 2004, 114: 1856-1860.
Benson J, Daugherty KK: Botulinum toxin A in the treatment of sialorrhea. Ann Pharmacother. 2007, 41: 79-85.
Drobik C, Laskawi R: Frey Syndrom: Therapie mit Botulinum-Toxin. HNO aktuell. 1994, 2: 142-144.
Laskawi R, Drobik C, Schönebeck C: Up-to-date report of botulinum toxin treatment in patients with gustatory sweating. Laryngoscope. 1998, 108: 381-384.
Laskawi R, Ellies M, Rödel R, Schoenebeck C: Gustatory sweating – Clinical implications and etiologic aspects. J Oral Maxillofac Surg. 1999, 57: 642-648.
Laskawi R, Rohrbach S: Treatment of gustatory sweating with botulinum toxin: Special aspects. ORL. 2001, 63: 294-297.
Laskawi R, Rohrbach S: Frey's syndrome: treatment with botulinum toxin. Hyperhidrosis and botulinum toxin in dermatology. Edited by: Kreyden OP, Böni R, Burg G. 2002, Curr Probl Dermatol, Basel, Karger, 30: 170-177.
Glaser DA: The use of botulinum toxins to treat hyperhidrosis and gustatory sweating syndrome. Neurotox Res. 2006, 9: 173-177.
Meyer M: Störungen der Tränendrüsen. Botulinumtoxintherapie im Kopf-Hals-Bereich. Edited by: Laskawi R, Roggenkämper P. 2004, Urban und Vogel, München, 313-322.
Riemann R, Pfenningsdorf S, Riemann E, Naumann M: Successful treatment of crocodile tears by injection of botulinum toxin into lacrimal gland: a case report. Ophthalmology. 1999, 106: 2322-2324.
Whittaker KW, Matthews BN, Fitt AW, Sandramouli S: The use of botulinum toxin A in the treatment of functional epiphora. Orbit. 2003, 22: 193-198.
Özcan C, Vayisoglu Y, Dogu O, Görür K: The effect of intranasal injection of botulinum toxin A on the symptoms of vasomotor rhinitis. Am J Otolaryngol. 2006, 27: 314-8.
Rohrbach S, Olthoff A, Laskawi R, Giefer B, Götz W: Botulinum toxin type A induces apoptosis in nasal glands of guinea pigs. Ann Otol Rhinol Laryngol. 2001, 110: 1045-50.
Rohrbach S, Laskawi R: Minimally invasive application of botulinum toxin type A in nasal hypersecretion. ORL J Otorhinolaryngol Relat Spec. 2001, 63: 382-4.
Laskawi R: Botulinum toxin treatment in the head and neck region: current aspects, developments, and problems. HNO. 2007, 55: 437-442.
Stidham KR, Solomon PH, Robersson JB: Evaluation of botulinum toxin A treatment of tinnitus. Otolaryngol Head Neck Surg. 2005, 132: 883-889.
Finzi E, Wasserman E: Treatment of depression with botulinum toxin A: a case series. Dermatol Surg. 2006, 32: 645-649.
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Laskawi, R. The use of botulinum toxin in head and face medicine: An interdisciplinary field. Head Face Med 4, 5 (2008). https://doi.org/10.1186/1746-160X-4-5
- Facial Nerve
- Masseter Muscle
- Botulinum Toxin Type
- Hemifacial Spasm