Tooth Extraction Status Nos Clinical Trial
Official title:
Acutely Infected Teeth: To Extract Or Not To Extract?
This prospective study was performed on 82 participants. Severe pain on percussion of the relevant tooth was considered as basic criteria when deciding on acute infection phase. The acutely infected teeth were labeled as the study group (n=35) and the asymptomatic ones as the control group (n=47). The extractions were done in the usual way. Amount of anesthetic solution used and durations of extractions were recorded.
This research designed as a prospective study between February 2017 and June 2017. An ethical
committee approval was obtained (document number 2017/01). The patients were selected among
medically healthy volunteers, who referred to us for extraction only one mandibular molar
tooth. The informed consents were obtained. Exclusion criteria were smoking, oral
contraceptive use, any conditions affecting the immune system, usage of antibiotics in last
two weeks and the teeth needed surgical extractions.
A total of 82 patients aged between 15 and 79 years (mean 40.52 ± 15.46) met the study
criteria. When deciding on acute infection phase, percussion sensitivity was accepted as the
basic criteria. It was defined as severe pain when a dental mirror was dropped about 1 cm
above the tooth.
Patients with acutely infected teeth were labeled as "study group" (n = 35) and the
asymptomatic patients as "control group" (n = 47). The null hypothesis of the study was
"there is no significant difference between the acutely infected and asymptomatic lower molar
teeth in terms of the complications that may occur during and after tooth extraction". The
level of statistical significance was accepted as 0.05 and SigmaPlot 11.0 (Systat Software,
Inc., San Jose, Calif.) program was used for statistical analyses.
Surgical Method All the extractions were performed by the same operator. The investigators
used 4% Articaine and 1:100,000 epinephrine HCL as the anesthetic solution. Inferior alveolar
nerve (IAN) and buccal nerve (BN) blockages were performed by using 1.5 mL. and 0.5 mL of
solution, respectively. If the anesthesia had failed, the same procedure was repeated. The
amount of anesthetic solution used for each patient was recorded.
Numbness on the half of the lower lip, and feeling no pain when probing the periodontal space
of the target tooth was accepted a successful IAN blockage. Then the BN blockage was
performed and the routine extraction was completed. Unless there was a radiographically
confirmed granulation tissue, the investigators did not curette the extraction sockets. The
investigators also did not package any medications into the wounds or did not suture. A
sterile damp gauze was placed tightly on the extraction area and the patients were asked to
bite it for 20 minutes. Extraction durations were noted for each patient.
All patients were given postoperative instructions. In the presence of a possible
complication, they were asked to apply to our clinic and not to use antibiotics on their own.
Postoperative Evaluation of Systemic Condition The investigators called all the patients on
first and second post-extraction days for assessing the systemic signs of fever, fatigue, and
shivering.
Postoperative Evaluation of The Extraction Wound If the patients applied with severe pain,
The investigators recorded onset time and characteristic of the pain. In the intraoral
examination, no granulation tissue as a sign of healing and exposed bare alveolar bone was
accepted as alveolar osteitis.
The investigators use SigmaPlot 11.0 (Systat Software, Inc., San Jose, CA) package software
programme for statistical analysis. To compare the rates of AO, chi-square test with Yates
correction was employed. Shapiro-Wilk normality test was performed on the data for the amount
of anesthetic solution used and the duration of extractions. Since the data did not fit the
normal distribution, nonparametric Mann Whitney U test was used.
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