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Title: Determine the Effect of Tramadol Injection as Adjuvant Anesthetic and Analgesia Following Surgical Removal of Mandibular Third Molar
Authors: Kaleem Ullah Khan, Adnan Babar, Syed Yasir, Wajid Meraj
Journal: Pakistan Armed Forces Medical Journal (PAFMJ)
Publisher: Army Medical College, Rawalpindi.
Country: Pakistan
Year: 2022
Volume: 72
Issue: 4
Language: English
DOI: 10.51253/pafmj.v72i4.3183
Keywords: TramadolImpacted third molar extractionLocal anesthesiaSubmucosal injectionPost-extraction pain
Objective: To establish the efficacy of mean pain control after submucosal tramadol injection compared to placebo after surgical removal of the impacted third molar.
Study Design: Quasi-Experimental Study.
Place and Duration of Study: Department of Maxillofacial Surgery, Armed Forces Institute of Dentistry, Rawalpindi Pakistan, from Feb to Aug 2018.
Methodology: All the patients had symmetrical bilateral impactions of the third molar on an orthopantomogram. The surgical site was randomly selected, and those in Group-T received Tramadol injection submucosally adjacent to the extraction socket immediately after the first tooth extraction, and Group-P received Saline. After the second extraction, Group-T received a Saline injection, and Group-P received Tramadol in the same manner. Patients were followed 24 hours post-operative for pain grading at 2, 4 and 24 hours, frequency and concentration of analgesic intake and duration of anaesthesia.
Results: Mean age of participants was 23.80±2.80 years. Means of pain intensity of Group without Tramadol after 2, 4 and 24 hours of extraction are 8.40±0.90, 6.30±0.40 and 2.10 ± 0.40, respectively, and those with Tramadol are 5.90±0.50, 4.50±0.30 and 1.60±0.40 respectively.
Conclusion: Our study concluded that Tramadol was more effective in providing analgesia after third molar surgery than local anaesthesia alone.
To establish the efficacy of mean pain control after submucosal tramadol injection compared to placebo after surgical removal of the impacted third molar.
Quasi-experimental study involving 100 patients undergoing surgical removal of impacted third molars. Patients were divided into two groups: Group-T received submucosal tramadol injection adjacent to the extraction socket after the first extraction, and Group-P received saline. After the second extraction, the groups were switched. Pain intensity was assessed using a 10-mm Visual Analogue Scale (VAS) at 2, 4, and 24 hours post-operatively. Frequency and concentration of analgesic intake and duration of anesthesia were also recorded. Data was analyzed using SPSS version 20.0 with a paired sample t-test.
graph TD
A["Patient Selection & Consent"] --> B["Surgical Removal of Third Molar"];
B --> C["Random Assignment to Groups"Tramadol/Placebo""];
C --> D["First Extraction & Submucosal Injection"];
D --> E["Second Extraction & Submucosal Injection"Cross-over""];
E --> F["Post-operative Pain Assessment VAS"];
F --> G["Record Analgesic Intake & Anesthesia Duration"];
G --> H["Data Analysis SPSS, t-test"];
H --> I["Conclusion"];
The study suggests that submucosal tramadol is effective in controlling post-operative pain following third molar surgery, likely due to localized higher drug concentration at the surgical site. This localized administration may offer analgesic benefits with fewer systemic side effects compared to systemic administration. The findings support tramadol's role as an adjuvant anesthetic and analgesic.
Patients receiving submucosal tramadol experienced significantly less pain compared to the placebo group at 2, 4, and 24 hours post-operatively. Mean pain intensity at 2, 4, and 24 hours for the group without Tramadol was 8.40±0.90, 6.30±0.40, and 2.10±0.40, respectively. For the group with Tramadol, the mean pain intensities were 5.90±0.50, 4.50±0.30, and 1.60±0.40, respectively.
Submucosal administration of tramadol along with local anesthesia is more effective in providing effective and prolonged analgesia following impacted third molar extraction surgery compared to local anesthesia alone.
- The study was conducted from February 2018 to August 2018.
- A sample size of 50 was calculated using G power 3.1.9.2 software, but 100 patients were included in the research.
- Mean age of participants was 23.80±2.80 years.
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