Periodontal disease prevalence and oral hygiene status of adults with cystic fibrosis: A case–control study

Author:

Coffey Niamh1ORCID,O'Leary Fiona1,Burke Francis1,Kirwan Laura2,O'Regan Paul2,Plant Barry3,Roberts Anthony1,Hayes Martina4

Affiliation:

1. Department of Restorative Dentistry University College Cork Cork Ireland

2. Cystic Fibrosis Registry of Ireland University College Dublin Dublin Ireland

3. Adult Cystic Fibrosis Unit Cork University Hospital Cork Ireland

4. Department of Restorative Dentistry Dublin Dental University Hospital Dublin Ireland

Abstract

AbstractAimTo investigate the prevalence of gingivitis and periodontitis, and the oral hygiene status of adults with cystic fibrosis (CF) in the Republic of Ireland.Materials and MethodsA case–control study in the form of a clinical examination of 92 adults with a diagnosis of CF was carried out in the adult CF unit in Cork University Hospital. A 40‐item questionnaire was used to capture socio‐demographic variables and medical and dental information. Two calibrated examiners carried out a periodontal assessment on participants, using the WHO‐recommended CPI‐modified index, and oral hygiene status was measured using the Greene–Vermillion index. The results were compared with a population‐based control group of similar socio‐demographic profile.ResultsOral hygiene levels (plaque and calculus) were significantly worse in people with CF, with a median plaque index of 0.83 (interquartile range [IQR] 0.333–1.542) in the CF group compared with 0.5 (IQR 0.167–0.667) in the non‐CF group. Calculus index in the CF group was 0.33 (IQR 0.17–0.83) compared with 0.33 (IQR 0.125–0.33) in the non‐CF group. However, periodontal disease levels were significantly lower in the CF group. Gingivitis (bleeding on probing ≥ 10% sites) was seen in 67.4% of the CF group, compared with 83.7% of the non‐CF group, OR 0.365 (95% confidence interval [CI] 0.181–0.736), relative risk (RR) 0.779 (95% CI 0.655–0.928). Mild periodontitis (periodontal probing depth [PPD] < 5 mm) was seen in 15.2% of the CF group, compared with 31.5% of the non‐CF group, OR 0.390 (CI 0.190–0.800), RR 0.483 (95% CI 0.273–0.852). Severe periodontitis (PPD ≥ 6 mm) was seen in 0% of the CF group, compared with 9.8% of the non‐CF group. There was a tendency, albeit non‐significant, towards reduced periodontitis in PWCF who regularly took antibiotics, particularly azithromycin.ConclusionsIn this study, adults with CF had poor oral hygiene practices, with high levels of plaque and calculus. Despite this finding, adults with CF had lower levels of clinical gingivitis and periodontitis than seen in a non‐CF control group. Further study is required to examine the causes of this phenomenon.

Funder

Cystic Fibrosis Ireland

Health Research Board

College of International Security Affairs

Publisher

Wiley

Subject

Periodontics

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