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Ultracain ds forte

Manufactured by Sanofi
Sourced in France, United States, Germany

Ultracain DS Forte is a local anesthetic solution containing articaine hydrochloride and epinephrine. It is designed for use in dental procedures requiring local anesthesia.

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10 protocols using ultracain ds forte

1

Single-Stage Implant Placement with Bone Biopsy

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All interventions were performed by the same surgeon (B.T.) under local anesthesia (Ultracain DS Forte, Sanofi-Aventis, Paris, France). A midcrestal incision was made to raise a full-thickness flap. A modular trephine drill (Full-Tech Kft, Szigetszentmiklós, Hungary) designed for the study (internal 2 mm, outer 2.7 mm in diameter and 10 mm in length) was used as an initial drill to collect bone core biopsy samples, as shown in Figure 2. The implant site preparation was continued with the manufacturer’s drills according to their protocol. Directly after implant placement (Straumann SP RN implants with Ti-SLA surface, Straumann GmBH, Basel, Switzerland), resonance frequency analysis (RFA) was carried out to measure implant stability. A one-stage healing protocol was applied, and interrupted nonresorbable sutures were used to close the flap around the gingiva formers. Antibiotics (1 g amoxicillin-clavulanic acid twice a day for 7 days), anti-inflammatory drugs (275 mg naproxen 3 times a day for 3 days) and chlorhexidine mouthwash (twice a day for 7 days) were prescribed, and the sutures were removed 7 days after implant placement.
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2

Low-Level Laser Therapy for Oral Surgery

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Surgery was performed under local anesthesia with 2 ml of 4% articaine with 1:100,000 epinephrine (Ultracain® D-S Forte; Sanofi Aventis, Topkapı, Istanbul, Turkey). A single surgeon performed all the surgical procedures in order to avoid variations due to the different surgeon skills, which may influence the results. Following surgery, all patients received 500 mg paracetamol (Parol; Atabay Pharmaceuticals and Fine Chemicals, Inc., Istanbul, Turkey) and benzydamine hydrochloride + chlorhexidine gluconate gargle antiseptic solution (Farhex; Santa Farma, Istanbul, Turkey) two times per day for 7 days.
In the present experimental study, LLLT was performed using a gallium-aluminum-arsenide (GaAlAs) diode laser device (Cheese Dental Laser System; Wuhan Gigaa Optronics Technology Co., Ltd., Wuhan, China) was used. Parameters of the LLLT are given in Table I.
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3

Local Anesthetic Tooth Isolation

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One specialist performed all the treatments in a single visit. All the teeth were anesthetized using a local anesthetic solution containing 4% articaine with 1:100,000 epinephrine (Ultracain DS Forte; Sanofi-Aventis, Bridgewater, NJ, USA) by inferior alveolar nerve block. After anesthesia, the relevant tooth was isolated with a rubber dam, and a standard access cavity was prepared using diamond burs.
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4

Dental Implant Placement Protocol

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Before surgery, all patients were advised to rinse with 0.2% chlorhexidine for 1 min. Local anesthesia was performed by the infiltration of articaine containing 1:100,000 adrenaline (Ultracain D-S forte, Sanofi, Vienna, Austria) at the implant site. Midcrestal and intrasulcular incisions were conducted to enable raising a minimal full-thickness flap and exposing the alveolar ridge. Implant bed preparation was performed using spiral drills of increasing diameter under copious irrigation. All bone-level tapered implants (SLActive®, Institut Straumann AG, Basel, Switzerland) were placed according to the standard protocol of the manufacturer. Two-thirds of the implants (n = 21) had a regular platform, while one-third (n = 9) had a narrow platform. Implants revealing an insertion torque of <35 Ncm were destined for a two-stage procedure with uncovering after 3 months. Implants demonstrating a higher insertion torque were provided with a healing abutment. Sutures (Neosorb Rapid, medipac®, Kilkis, Greece) were removed after 7–10 days. Postoperative pain was controlled by administering 400 mg ibuprofen every 6 h. After a healing period of at least 3 months, all patients were scheduled for digital and conventional impression taking.
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5

Dental Implant Placement: Surgical Technique

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All surgeries were performed under local
anesthesia (Ultracain DS Forte, Sanofi Aventis,
Istanbul, Turkey). Following the placement of a
midcrestal incision, full-thickness flaps were raised.
Implants were placed using a customized surgical
guide according to standard surgical protocols; the
same surgical kit was used for both groups. All
implants were placed according to the manufacturers’
instructions. The mesial–distal aspect of the alveolar
ridge was used as a reference. Healing abutments were
attached to the implants for transmucosal healing
(Figure 2)and (Figure 3).
The mucoperiosteal flaps were sutured with silk
sutures (Dogsan Medical Supplies Industry, Trabzon,
Turkey) after implant placement. Postoperative
prescriptions included antibiotics (1000 mg
amoxicillin and clavulanic acid, twice daily for 7
days, starting from the day of surgery), analgesics
(600 mg ibuprofen as required, every 6 h), and 0.2%
chlorhexidine mouthwash (twice daily for 2 weeks,
starting from the day after surgery). Sutures were
removed 7 days after surgery.
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6

Implant Rehabilitation with Zirconia Crowns

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Patients were rehabilitated with bone level tapered implants (Institute Straumann AG, Basel, Switzerland) following the standard surgical protocol of the manufacturer under local anesthesia (Ultracain D-S forte, Sanofi, Vienna, Austria). Suture removal was scheduled after 7–10 days. Postoperative analgesia was controlled by ibuprofen 400 mg every 6 h. After a healing period of ≥3 months, impression-taking was performed to fabricate screw-retained zirconia crowns.
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7

Diagnosing Temporomandibular Joint Arthralgia

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The study patients were recruited from the outpatient clinic of the Department of Oral and Maxillofacial Surgery of UMCG. A sample size calculation was performed for the primary outcome measure for the initial follow-up period of the study, as described previously. 8 (link) The inclusion criteria were age ≥ 16 years, pain in the TMJ region aggravated by mandibular movement (i.e., protrusion, maximal mouth opening, and/or lateral excursions) and/ or during function, the presence of TMJ arthralgia after 2 weeks of 600 mg ibuprofen three times daily (to exclude acute inflammatory pain), and the disappearance of TMJ arthralgia after a diagnostic intra-articular injection with a local anaesthetic in the TMJ (Ultracain D-S Forte; Sanofi, Amsterdam, the Netherlands; to exclude myogenous pain). 13 (link) The exclusion criteria were systemic rheumatic disease, bony ankylosis of the TMJ, prior open TMJ surgery, pregnancy, concurrent use of anti-inflammatory drugs, muscle relaxants, anti-depressants, and/or steroids, other medical contraindications, unwillingness to receive either study treatment, and the inability to speak Dutch or English.
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8

Zygomatic Implant Placement Procedure

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All four patients were operated by the same surgeon which performed by using 4% articaine and 1:100000 epinephrine as local anesthetic agent (Ultracain DS forte, Sanofi-Aventis, Germany). We designed a horizontal crestal incision in the area of upper maxilla in which zygomatic implants were going to be placed and a full-thickness mucoperiosteal flap was raised to the infraorbitary foramen in order to visualize hard tissue. Implant drilling sequence was performed, and implants were placed following the previous digital planification. Finally, the healing abutment was placed and after repositioning of the flaps, the wound was closed with 4–0 nylon sutures (Supramid, Serag-Wiessner, Germany). Cuadro de los pacientes con las posiciones de los implantes.
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9

Endodontic Root Canal Treatment Procedure

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As in the similar studies carried out before, local anesthetic solution containing 1:100,000 epinephrine (Ultracain DS Forte; Sanofi-Aventis) and 4% articaine was used for the inferior alveolar nerve block.6 (link),15 (link) After anesthesia, a standard access cavity was prepared in the mandibular teeth and the root canal orifices were found using #10 manual K-files (VDW). The teeth were isolated by using a rubber dam. The working length was set to 1 mm shorter than the apical foramen by using #10 K-file and an apex locator (J. Morita Co., Tustin, CA) and then confirmed with periapical radiography. The working length was repeatedly checked throughout the treatment procedure. One of the three file systems was used for shaping and cleaning the root canals in a single visit. Each file was used only in a single tooth.
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10

Maxillary Sinus Lift Procedure

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All necessary dental treatments were applied before the sinus lifting procedure. The sinus lifting operation was carried out under local anesthesia (Ultracain DS Forte, Sanofi Aventis, Istanbul, Turkey) in a staged surgical approach. The maxillary sinus was grafted utilizing a lateral window technique, as described by Kent and Block [20 (link)]. Chlorhexidine digluconate solution 0.12% was used to rinse patients’ mouths for 2 min prior to surgery.
Briefly, via crestal and vertical incisions and muco-periosteal flap elevation, a lateral window was prepared with a dental carbide bur, followed by a wide-diameter diamond bur, to avoid sinus membrane perforation. The lateral window was dissected and reflected inward after the sinus mucosa was detached completely from the maxillary sinus walls (Figure 1).
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