Microorganisms in closed periapical lesions

The purpose of this study was to investigate the microorganisms of strictly selected closed periapical lesions associated with both refractory endodontic therapy and pulpal calcification. Definitive criteria were established that assured complete clinical isolation of the periapical lesion from the...

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Bibliographic Details
Published inInternational endodontic journal Vol. 31; no. 1; pp. 39 - 47
Main Authors Abou-Rass, M., Bogen, G.
Format Journal Article
LanguageEnglish
Published Oxford BSL Blackwell Science Ltd 01.01.1998
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Summary:The purpose of this study was to investigate the microorganisms of strictly selected closed periapical lesions associated with both refractory endodontic therapy and pulpal calcification. Definitive criteria were established that assured complete clinical isolation of the periapical lesion from the oral and periodontal environment. A total of 13 criteria‐referenced lesions were selected from 70 patients with endodontic surgical indications. A well controlled culturing method was used in all cases and samples were taken by one clinician at three separate sites during each surgery. Samples taken at the surgical window and within the body of the lesion served as controls, whilst a third sample was taken at the apex. In all 13 cases, samples taken from the apex yielded microorganisms comprising 63.6% obligate anaerobes and 36.4% facultative anaerobes. Prevalence of the isolated species was 31.8% for Actinomyces sp., 22.7%, Propionibacterium sp., 18.2%Streptococcus sp., 13.6%Staphlyococcus sp., 4.6%Porphyromonas gingivalis, 4.6%Peptostreptococcus micros and 4.6% Gram‐negative enterics. The results of this investigation indicate that closed periapical lesions associated with calcified teeth or those resistant to root canal treatment harbour bacteria. The inability to eradicate all root canal microorganisms during root canal treatment, along with anatomical factors, may allow further bacterial colonization of the root apex and surrounding periapical tissues, and consequently prevent healing.
Bibliography:ark:/67375/WNG-N82G87BH-8
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ArticleID:IEJ88
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0143-2885
1365-2591
DOI:10.1046/j.1365-2591.1998.t01-1-00088.x