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RESEARCH REPORT |
1 Centers for Disease Control and Prevention/Division of Oral Health/Surveillance, Investigations, and Research Branch, 4770 Buford Highway, MSF10, Chamblee, GA 30341, USA; and
2 School of Industrial & Systems Engineering, Georgia Institute of Technology, Atlanta, GA 30332-0205, USA;
* corresponding author, sig1{at}cdc.gov
| ABSTRACT |
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KEY WORDS: coronal caries incidence increment attack rate adults
| INTRODUCTION |
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Currently, water fluoridation is the main caries-prevention program that affects older adults. Other common primary prevention programs delivered at the community levelschool-based/-linked sealant programs and delivery of fluoride via mouthrinse, supplement, or topical applicationsprimarily target children (ASTDD, 2002). Medicaid (a Federally funded, state-operated and -administered program that provides medical benefits to indigent or low-income persons) frequently covers only emergency dental care for adults (Oral Health America, 2003), and Medicare (a Federal health insurance program for the elderly) does not cover routine dental services.
These interventions may be able to prevent significant amounts of dental caries in older adults. While national surveys provide cross-sectional data to estimate the prevalence and severity of caries, at present, we have no longitudinal estimates of new caries at the national level. However, at the state and community levels, longitudinal data for older adults suggest that they may have more new caries than children (Hand et al., 1988a). Two previous articles estimated new dental caries among older adults by averaging the findings from some of these studies (Garcia, 1989; Leake, 2001). Neither article, however, took study variance into account in deriving summary measures, or examined if outcome measures were homogenous across studies.
Finally, demographic trends suggest that the number of older adults will continue to increase relative to the general population (Administration on Aging, 2000), and that these older adults are more likely to retain their teeth than were previous generations (US Department of Health and Human Services, 2000).
| METHODS |
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Inclusion Criteria
We included studies with populations whose mean age was greater than 60 yrs, conducted among populations with characteristics similar to those of the aggregate US population (i.e., we excluded findings from studies conducted exclusively among populations with other diseases such as cancer, who were institutionalized, or were treatment groups in caries-prevention trials). Included studies had to be of sufficient design qualityprospective, cohort studies that used probability sampling of a general population. Examiner reliability had to be reported, and diagnostic criteria had to be specified. We excluded studies that did not report sufficient information for a variance to be calculated. Six studies consisting of 3113 older adults (mean age = 66.5 yrs) met our inclusion criteria (Table
).
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To estimate annual incidence, we assumed that the probability of experiencing caries was the same for each study year. We first calculated the probability that no disease was incurred over the study interval, and then took the nth root of this value (where n represents number of yrs in study) to calculate the probability that no disease was incurred in a given year. We then subtracted this value from 1 to obtain the annual incidence.
Some studies reported separate measures for specific groups. For these studies, we estimated the outcome measure (standard error) for the population by taking the weighted average (standard error =
na*sea2 + nb*seb2/na + nb) of the reported groups.
We excluded studies that reported increment or attack rate but did not report a variance, standard deviation, or standard error. For studies reporting incidence but not a standard error, we calculated the standard error with the following formula: (standard error =
incidence*(1 incidence)/n).
Most studies did not include crowns in their outcome measures for disease. For studies that reported increment or attack rate including and excluding crowns, we used the outcome measure, which excluded crowns.
To make the findings of studies that adjusted for examiner reversals more comparable with the results of studies that did not, we reported, when possible, crude estimates of new disease that did not net out negative reversals. Netting out negative reversals may underestimate new disease (Burt and Eklund, 1999). Two studies comparing the two methods found that the net method resulted in more biased estimates of new caries in older adults than did the crude method. One study found that using the crude instead of the net estimation method increased estimates of incidence, increment, and attack rate by 44%, 119%, and 124%, respectively (Slade and Caplan, 2000), while, similarly, the other found that crude increment estimates were 121% higher (Beck et al., 1995). We also calculated estimates of new disease adjusted for analytic convention by inflating net measures by the above percentages.
Analysis
We calculated the 95% confidence intervals for each outcome measure reported in each study. To estimate summary measures across studies, we used a random-effects model, which assumes that each study was randomly selected from a hypothetical population of studies [DerSimonian and Laird method (Normand, 1999)]. We calculated summary measures (unadjusted and adjusted for netting out examiner reversals) for all studies and for North American studies.
To determine if the dental health status of the study populations was similar to that of the US population as a whole, we compared the mean number of teeth present and mean number of decayed and filled coronal surfaces among the study populations at baseline (1981 to 1997) against the national estimates from the National Health and Nutrition Examination Survey (NHANES) III (19881991) (Winn et al., 1996) for similar age groups. Using a chi-square test (QW) (Normand, 1999), we tested for homogeneity of effect size (new disease) among studies. For effect sizes failing the heterogeneity test, we estimated the quantity I2, which describes the percentage of total variation, across studies, due to heterogeneity vs. chance (Higgins et al., 2003). Thus, if study populations at baseline had dental health status similar to that of the US population, and if new disease outcomes are homogenous across studies, our findings may be applicable to the US population.
Finally, to identify potential sources of heterogeneity, we examined the correlation coefficients between each outcome measure and: (1) population baseline risk factors [measured by age and number of decayed, missing, and filled tooth surfaces (DMFS)] and (2) study design factors (measured by study length, whether the examination included 3rd molars, and whether it netted out examiner reversals) (Appendix Table 3).
| RESULTS |
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| DISCUSSION |
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Caries among the elderly is also more likely to remain untreated; their mean number of untreated decayed surfaces (1.6) (Winn et al., 1996) is about four times that among US schoolchildren (0.4) (Kaste et al., 1996). This may be partly attributable to the limited safety net available to provide routine dental care to adultslower-income adults are about 6 times more likely to have untreated decay than their higher-income counterparts (Drury et al., 1999). Untreated decay reflects a need not only for treatment services, but also for preventive interventions.
We found that study design characteristics were more likely to contribute to heterogeneity than were differences in baseline risk. None of the outcome measures was correlated with baseline risk variables, suggesting that risk differences did not contribute to heterogeneity among outcomes. This may be because neither baseline age nor DMFS differed greatly by study; the respective coefficients of variation were 0.07 and 0.09. Only two study design variables were correlated with outcome measures and thus may have contributed to heterogeneitywhether the study netted out examiner reversals, and the study duration (time to first follow-up).
We adjusted the data to control for netting out examiner reversals; however, we could not do so completely for study duration. Study duration influences the outcome measure in at least two ways. First, subjects with higher levels of baseline disease may be more likely to drop out as study duration increases. To control for this effect, we used the shortest reported study interval. Second, the probability of recurrent caries should increase as duration increases; thus, the probability that the outcome measure is truly cumulative decreases. Incidence would be especially sensitive to increased study duration, since it is measured at the person, not the tooth, level. This may be why Sweden, where the study lasted two years longer than any of the other studies, accounted for 60% of the variation in mean incidence when the Q statistic was calculated for all adjusted studies. Our hypothesisthat confounding due to study duration will be greater for incidence than for incrementis also supported by the higher Q statistic for the adjusted summary measure for all incidence studies than for all increment studies (2.5 times higher).
Our findings suggest that older adults experience caries at rates equal to or greater than those in children, the primary recipients of caries-prevention services. For quantification of the benefit of prevention among older adults, further research is needed on the effectiveness of preventiontwo recent reviews found few studies conducted among adult populations (Rozier, 2001; Truman et al., 2002)and treatment costs, which may be substantially higher if adults with more affected surfaces require procedures such as crowns to treat new decay.
| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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Received June 6, 2004; Last revision February 18, 2005; Accepted April 25, 2005
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