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Identification of an effective and safe bolus dose and lockout time for patient-controlled sedation (PCS) using dexmedetomidine in dental treatments: a randomized clinical trial.
Rhee, Seung-Hyun; Kweon, Young-Seok; Won, Dong-Ok; Lee, Seong-Whan; Seo, Kwang-Suk.
Afiliação
  • Rhee SH; Department of Dental Anesthesiology, School of Dentistry, Seoul National University, Seoul, Republic of Korea.
  • Kweon YS; Department of Brain and Cognitive Engineering, Korea University, Seoul, Republic of Korea.
  • Won DO; Department of Artificial Intelligence Convergence, Hallym University, Chuncheon, Republic of Korea.
  • Lee SW; Department of Artificial Intelligence, Korea University, Seoul, Republic of Korea.
  • Seo KS; Department of Dental Anesthesiology, School of Dentistry, Seoul National University, Seoul, Republic of Korea.
J Dent Anesth Pain Med ; 24(1): 19-35, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38362260
ABSTRACT

Background:

This study investigated a safe and effective bolus dose and lockout time for patient-controlled sedation (PCS) with dexmedetomidine for dental treatments. The depth of sedation, vital signs, and patient satisfaction were investigated to demonstrate safety.

Methods:

Thirty patients requiring dental scaling were enrolled and randomly divided into three groups based on bolus doses and lockout times group 1 (low dose group, bolus dose 0.05 µg/kg, 1-minute lockout time), group 2 (middle dose group, 0.1 µg/kg, 1-minute), and group 3 (high dose group, 0.2 µg/kg, 3-minute) (n = 10 each). ECG, pulse, oxygen saturation, blood pressure, end-tidal CO2, respiratory rate, and bispectral index scores (BIS) were measured and recorded. The study was conducted in two stages the first involved sedation without dental treatment and the second included sedation with dental scaling. Patients were instructed to press the drug demand button every 10 s, and the process of falling asleep and waking up was repeated 1-5 times. In the second stage, during dental scaling, patients were instructed to press the drug demand button. Loss of responsiveness (LOR) was defined as failure to respond to auditory stimuli six times, determining sleep onset. Patient and dentist satisfaction were assessed before and after experimentation.

Results:

Thirty patients (22 males) participated in the study. Scaling was performed in 29 patients after excluding one who experienced dizziness during the first stage. The average number of drug administrations until first LOR was significantly lower in group 3 (2.8 times) than groups 1 and 2 (8.0 and 6.5 times, respectively). The time taken to reach the LOR showed no difference between groups. During the second stage, the average time required to reach the LOR during scaling was 583.4 seconds. The effect site concentrations (Ce) was significantly lower in group 1 than groups 2 and 3. In the participant survey on PCS, 8/10 in group 3 reported partial memory loss, whereas 17/20 in groups 1 and 2 recalled the procedure fully or partially.

Conclusion:

PCS with dexmedetomidine can provide a rapid onset of sedation, safe vital sign management, and minimal side effects, thus facilitating smooth dental sedation.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Dent Anesth Pain Med Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Dent Anesth Pain Med Ano de publicação: 2024 Tipo de documento: Article