The Impact of Surgical Technique on PDC

Methods of exposing canines are today left to the personal choice of the surgeon and orthodontist. According to an unpublished survey among orthodontists in Sweden 2012, 80% of them use the closed technique only, 9% use the open technique only and 11% use both techniques. This result may be compared to a similar survey performed in the UK, where 29% selected a closed surgical technique only, 40% selected an open surgical technique only and the remainder chose combinations of techniques.

Mentioned reasons for preference of the closed technique are less pain and need for analgesics and faster recovery of pain, postsurgically. Some orthodontists that prefer the open exposure technique have experienced more patient related pain or discomfort in the closed exposure technique, in association with activation in orthodontically forced eruption, because the palatally impacted canine is moved beyond the mucoperiosteal flap. There are no previous studies in this aspect, though.

Factors as operation time, total treatment time and periodontal health measurements after surgical exposure and orthodontic forced eruption of impacted canines, have shown heterogeneity in different retrospective studies.

The management of the palatally impacted canines is a multidisciplinary, time consuming treatment, contributing to relatively high society costs, why this study is taking place, trying to clarify some issues in the choice of method and treatment.

Subjects Patients with diagnosis of uni- or bilateral palatally impacted canine/-s planned for surgical exposure are included consecutively at three orthodontic centers of the Public Dental Health Service in the towns of Orebro, Eskilstuna and Jönköping, Sweden.

Procedure At the appointment for treatment information, the orthodontist gives potential study participants and their parents verbal and written information about the trial. The potential study participants and their parents will be allowed at least one week to decide whether to participate in the trial and if they agree to participate, the written consent will be submitted to the orthodontic centre.

After informed consent is obtained, the participants are randomly allocated to 1 of 2 interventions.

A computer generated randomization is undertaken to ensure that there are equal numbers allocated to each intervention. Allocation concealment is held by one individual per centre, not involved with the trial, who will be contacted by the consenting clinician when the patient is going to be referred for surgical exposure. There will be no stratification for age or gender into the two different groups.

If maxillary deciduous canine are present; they are removed at the time of surgical exposure. The two different surgical exposure techniques are described under "Intervention arms".

The patients are given verbal and written postsurgical information.

Verbal pre-/postsurgical information consists of the recommendation of:

• Analgetic (paracetamol first choice) 1 hour before surgery and there after every 6 to 8th hour 2 days post surgically, according to the dosage recommended
• Tooth paste without sodium is recommended when used directly in association with chlorhexidine rinse

Together with the written postsurgical information, a questionnaire is handed out at the surgical clinic to the patients, for assessment of their experience of pain and discomfort in the evening of the day of surgical exposure and one week there after. The postsurgical questionnaire contains questions that are validated. This questionnaire is submitted to the orthodontic centre at the first postsurgical control.

After surgical exposure orthodontic force is applied; in the closed technique group no later than 2 weeks post surgically and in the open technique group when bonding attachment is possible. In both surgical exposure groups orthodontic force is applied to the palatally impacted canine via the chain attached to the bonded attachment on the canine, to a fixed orthodontic appliance.

Questionnaires are handed out to the patients every 3rd month at the orthodontic clinic, to evaluate the patients´ perceptions of pain and discomfort, until the impacted canine is orthodontically positioned in the dental arch. These questionnaires are submitted at the orthodontic clinic the same day, in association with orthodontic appointment. Questionnaire to assess patients´ perceptions of dental anxiety is handed out to the patient before treatment, when the impacted canine has erupted and when active treatment is finished in each surgical exposure group, at the orthodontic centre. Dental anxiety will be evaluated and described according to Cuthbert MI and Melamed BG. The patients are followed until the active orthodontic treatment is finished and an orthodontic retainer is fitted.

Observation schedule and material/registrations:

Before surgical treatment (T0):

• Impression for study cast/ Registrations: sagittal, transversal and vertical relation, crowding and spacing of teeth (measured according to the current clinical routine), maxillary dental development stage according to Björk
• Panoramic radiograph/ Registrations: mesial position of the impacted canine crown, mesial inclination of the canine to the midline, distance to the occlusal line according to Ericson and Kurol
• CBCT (cone beam computed tomography) examination/ Registrations: exact position and follicle size of the impacted canine; crestal bone height in the lateral incisor in the impacted and nonimpacted contra lateral side in the same patient; root resorption in the impacted canine, the incisors and the eventual first premolar in the impacted and nonimpacted contra lateral side in the same patient
• Clinical examination (according to clinical routine)/ Registrations: periodontal pocket depth, gingival bleeding on probing, gingival recession; in the lateral incisor in the impacted and nonimpacted contra lateral side in the same patient
• CFSS-DS (dental anxiety) questionnaire/ Assessment of dental anxiety
• Registration of age, gender, presence of deciduous canine and date of eventual extraction of deciduous canine

The day of surgical exposure (T1):

• A questionnaire (for the first evening and one week after surgical exposure)/ Assessment of experience of pain, discomfort (measured in VAS-scales) and consumption of analgesics one week after surgical exposure
• Measurement and registration of operation duration

Palatally impacted canine erupted; here: when bonding attachment is possible/ approximately ⅓-½ of the clinical crown of the impacted canine is exposed intraorally (T2):

• Measurement and registration of the duration for the canine to erupt into the oral cavity; time between T1 and T2
• Registration of presence, type and number of complications/failures associated with surgical technique
• CFSS-DS questionnaire/ Assessment of dental anxiety

Previously impacted canine positioned in the dental arch; here: canine ligated to .016x.022 nickel titanium/standard steel arch-wire in the .018-appliance system and .019x.025 nickel-titanium/ standard steel arch-wire in the .022-appliance system (T3):

• Registration of presence, type and number of complications/failures associated with orthodontic treatment
• Measurement and registration of duration between T2 and T3

Orthodontic retainer is fitted/ Active treatment finished (T4):

• Impression for study cast/ Registration of sagittal, transversal/ vertical relation, crowding/spacing of teeth (measured according to the current clinical routine)
• Clinical examination(according to clinical routine/ Registration of pocket depth, gingival bleeding on probing, gingival recession in the canine, the lateral incisor and the first premolar in the impacted and nonimpacted contra lateral side in the same patient
• CFSS-DS questionnaire/ Assessment of dental anxiety
• Measurement and registration of duration between T3 and T4

Within 2 months after active treatment is finished (retainer fitted):

• CBCT examination/ Registration of crestal bone height in the canine, the lateral incisor and the first premolar in the impacted and nonimpacted contra lateral side in the same patient; root resorption in the canine, the incisors and the first premolar in the impacted and nonimpacted contra lateral side in the same patient

Between the day of surgical exposure (T1) and the day when the previously impacted canine is positioned in the dental arch; here: canine inligated to .016x.022 nickel titanium/ standard steel arch-wire in the .018-appliance system and .019x.025 nickel-titanium/ standard steel arch-wire in the .022-appliance system (T3):

• A questionnaire is handed out to the patient every 3rd month at orthodontic appointments between T1 and T3/ Assessment of patients´ perceptions of pain and discomfort (measured in VAS-scales) and consumption of analgesics

Ethical aspects The Regional Ethic Board of Uppsala University, Uppsala, Sweden, which follows the guidelines of the Declaration of Helsinki has approved the study. The Radiation Protection Boards of the County Councils of Örebro, Eskilstuna and Jönköping have approved the planned radiographic examinations in the study. Patientdata are processed according to the laws Personuppgiftslagen, PUL, (1998:204) and Patientdatalagen (2008:355). The examinations and treatments used in this trial are the current examinations and treatments of palatally impacted canines in Sweden, which have been practiced during several years. All surgical exposures and orthodontic treatments are performed by specialists in dental pediatrics/ clinicians and specialists in orthodontics, respectively, with many years of surgical experience.