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- Publisher Website: 10.1016/j.jdent.2024.105082
- Scopus: eid_2-s2.0-85194293896
- PMID: 38762080
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Article: Satisfaction with government recommended pre-procedural mouth rinses in the mitigation of Covid-19 in Hong Kong SAR: A triple blind randomized controlled clinical trial
Title | Satisfaction with government recommended pre-procedural mouth rinses in the mitigation of Covid-19 in Hong Kong SAR: A triple blind randomized controlled clinical trial |
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Authors | |
Keywords | COVID-19 Pandemics Pre-procedural mouthrinses Satisfaction ratings |
Issue Date | 1-Jul-2024 |
Publisher | Elsevier |
Citation | Journal of Dentistry, 2024, v. 146 How to Cite? |
Abstract | Objective: To evaluate satisfaction and acceptability with three pre-procedural mouthrinses recommended by the Government of Hong Kong Special Administrative Region (HKSAR) during the COVID-19 pandemic. Material and methods: A triple-blind parallel-arm randomised controlled clinical trial was conducted. Following eligibility assessment, participants were block-randomised to the three intervention pre-procedural mouthrinses groups: Povidone-iodine, Hydrogen Peroxide and Chlorhexidine Digluconate. Participants rinsed with one of the mouthrinses assigned prior to any dental treatment. Participants, operators and assessors were blind to the assigned mouthrinses (triple blind). Satisfaction ratings were assessed on a 10 cm visual analogue scale (VAS) and acceptability of the mouthrinses were determined. Results: Following clinical screening, 228 participants were involved in the trial. The mean overall VAS satisfaction was 7.35 (SD 1.68). There was no significant difference in VAS satisfaction ratings among the three groups (p>0.05) nor in between groups. Acceptability of the mouthrinses was high with the vast majority (89.5 %, 204) willing to use the mouthrinses again if pre-procedural mouthrinsing is required. There was no significant difference in acceptability ratings (p>0.05). There were some aspects such as taste and smell that participants commented on (on average, 24.6 %, 56), although no significant difference in prevalence of reports among groups (p>0.05). Conclusions: There were high rates of satisfaction and acceptability of the HKSAR Government recommended pre-procedural mouthrinses for the mitigation of COVID-19 transmission in the dental setting. There was no significant difference in satisfaction and acceptability rates among the three recommended pre-procedural mouthrinses. Clinical relevance: The high satisfaction and acceptability rates of the HKSAR Government recommended pre-procedural mouthrinses in the mitigation of COVID-19 in this clinical trial lends support for the HKSAR's policy on pre-procedural mouthrinses in the dental setting and this has implications for practice and policy during pandemics. |
Persistent Identifier | http://hdl.handle.net/10722/353626 |
ISSN | 2023 Impact Factor: 4.8 2023 SCImago Journal Rankings: 1.313 |
DC Field | Value | Language |
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dc.contributor.author | Huang, Shan | - |
dc.contributor.author | Leung, Yiu Yan | - |
dc.contributor.author | Neelakantan, Prasanna | - |
dc.contributor.author | Chan, Kwok Hung | - |
dc.contributor.author | Leung, Joy Ka Yi | - |
dc.contributor.author | Hung, Fan Ngai | - |
dc.contributor.author | McGrath, Colman | - |
dc.date.accessioned | 2025-01-22T00:35:20Z | - |
dc.date.available | 2025-01-22T00:35:20Z | - |
dc.date.issued | 2024-07-01 | - |
dc.identifier.citation | Journal of Dentistry, 2024, v. 146 | - |
dc.identifier.issn | 0300-5712 | - |
dc.identifier.uri | http://hdl.handle.net/10722/353626 | - |
dc.description.abstract | Objective: To evaluate satisfaction and acceptability with three pre-procedural mouthrinses recommended by the Government of Hong Kong Special Administrative Region (HKSAR) during the COVID-19 pandemic. Material and methods: A triple-blind parallel-arm randomised controlled clinical trial was conducted. Following eligibility assessment, participants were block-randomised to the three intervention pre-procedural mouthrinses groups: Povidone-iodine, Hydrogen Peroxide and Chlorhexidine Digluconate. Participants rinsed with one of the mouthrinses assigned prior to any dental treatment. Participants, operators and assessors were blind to the assigned mouthrinses (triple blind). Satisfaction ratings were assessed on a 10 cm visual analogue scale (VAS) and acceptability of the mouthrinses were determined. Results: Following clinical screening, 228 participants were involved in the trial. The mean overall VAS satisfaction was 7.35 (SD 1.68). There was no significant difference in VAS satisfaction ratings among the three groups (p>0.05) nor in between groups. Acceptability of the mouthrinses was high with the vast majority (89.5 %, 204) willing to use the mouthrinses again if pre-procedural mouthrinsing is required. There was no significant difference in acceptability ratings (p>0.05). There were some aspects such as taste and smell that participants commented on (on average, 24.6 %, 56), although no significant difference in prevalence of reports among groups (p>0.05). Conclusions: There were high rates of satisfaction and acceptability of the HKSAR Government recommended pre-procedural mouthrinses for the mitigation of COVID-19 transmission in the dental setting. There was no significant difference in satisfaction and acceptability rates among the three recommended pre-procedural mouthrinses. Clinical relevance: The high satisfaction and acceptability rates of the HKSAR Government recommended pre-procedural mouthrinses in the mitigation of COVID-19 in this clinical trial lends support for the HKSAR's policy on pre-procedural mouthrinses in the dental setting and this has implications for practice and policy during pandemics. | - |
dc.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Journal of Dentistry | - |
dc.subject | COVID-19 | - |
dc.subject | Pandemics | - |
dc.subject | Pre-procedural mouthrinses | - |
dc.subject | Satisfaction ratings | - |
dc.title | Satisfaction with government recommended pre-procedural mouth rinses in the mitigation of Covid-19 in Hong Kong SAR: A triple blind randomized controlled clinical trial | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.jdent.2024.105082 | - |
dc.identifier.pmid | 38762080 | - |
dc.identifier.scopus | eid_2-s2.0-85194293896 | - |
dc.identifier.volume | 146 | - |
dc.identifier.eissn | 1879-176X | - |
dc.identifier.issnl | 0300-5712 | - |