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Erschienen in: Clinical Oral Investigations 3/2021

10.07.2020 | Original Article

Comparison between isolated and associated with codeine acetaminophen in pain control of acute apical abscess: a randomized clinical trial

verfasst von: Paula Barcellos da Silva, Aline Teixeira Mendes, Maria Beatriz Ferreira Cardoso, Ricardo Abreu da Rosa, Angela Longo do Nascimento, Jefferson Ricardo Pereira, Marcus Vinícius Reis Só

Erschienen in: Clinical Oral Investigations | Ausgabe 3/2021

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Abstract

Objectives

The study aimed to compare the acetaminophen administration efficacy or its combination with codeine for pain control in acute apical abscesses cases.

Materials and Methods

Thirty-nine patients who sought emergency treatment in the Faculty of Dentistry of the Federal University of Rio Grande do Sul were included, all of them with acute apical abscess diagnosis. These patients were divided into two groups: acetaminophen group—prescription of acetaminophen (1000 mg) and acetaminophen–codeine group—prescription of acetaminophen (1000 mg) + codeine (30 mg), both with oral intake every 6 h for 3 days. The pain scores were recorded by the patients on their own at 6, 12, 24, 48, and 72 h after finishing clinical assistance, by filling a pain evolution journal, containing a visual analogue scale (VAS). Student t test was conducted to investigate different mean ages between groups 1 and 2. A comparison of weight and means of initial pain scores between groups was carried out using the Mann–Whitney U test. Chi-square test was performed to compare gender, affected tooth, education, initial swelling, and frequency of adverse effect between test and control groups. Mann–Whitney U test was applied to compare groups in the same period. Friedman’s test was used to compare results from the same group over time.

Results

Both groups showed score reduction over time (P < 0.05). Paracetamol-codeine group showed significant pain score reduction at 48 h registers when compared to baseline and at 6 h scores (P < 0.05). Further, pain scores at 72 h were significantly lower, when compared to the baseline, at 6 h, and at 12 h scores (P < 0.05). Acetaminophen group showed significant pain score reduction observed at 72 h, when compared to the baseline and at 6 h scores (P < 0.05). There were no significant differences in pain score reduction over time between groups (P > 0.05). There was no difference between the groups regarding the frequency of adverse reactions (P > 0.05).

Conclusion

Both medications were effective for pain control in acute apical abscess cases. The findings might have inferred in pain control of acute apical abscess associated pain in patients who used an antibiotic drug. External validity of the findings for acute apical abscess cases with no need for an antibiotic prescription is uncertain.

Clinical relevance

This paper suggests acetaminophen 1000 mg can be used for pain control in the treatment of acute apical abscess associated with systemic manifestation.
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Metadaten
Titel
Comparison between isolated and associated with codeine acetaminophen in pain control of acute apical abscess: a randomized clinical trial
verfasst von
Paula Barcellos da Silva
Aline Teixeira Mendes
Maria Beatriz Ferreira Cardoso
Ricardo Abreu da Rosa
Angela Longo do Nascimento
Jefferson Ricardo Pereira
Marcus Vinícius Reis Só
Publikationsdatum
10.07.2020
Verlag
Springer Berlin Heidelberg
Erschienen in
Clinical Oral Investigations / Ausgabe 3/2021
Print ISSN: 1432-6981
Elektronische ISSN: 1436-3771
DOI
https://doi.org/10.1007/s00784-020-03374-6

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