Multivariate associations between predictors of accurate dementia diagnoses by family physicians and the reference standard memory clinic team diagnosis
Adjusted odds ratio (95% CI) | P | |
---|---|---|
ADL dependency, score1–4 | 5.35 (2.00–13.9) | .0212 |
Years since symptoms started | 1.84 (1.08–3.14) | .026 |
Somatic comorbidity present | 0.48 (0.25–0.89) | .006 |
n = 93. | ||
ADL, activities of daily living (1 = independent to 4 = fully dependent); CI = confidence interval. |
Predictors of presence/absence of dementia
The univariate analyses revealed that informant availability, years of education, sex of the family physician, number of cognitive symptoms, ADL dependency, somatic comorbidity, blood abnormality, behavioral changes, and duration and severity of the symptoms were associated with the presence or absence of dementia (Table 3). Neither the number of applied recommendations nor the use of the MMSE was related to the presence or absence of dementia.
The multivariate logistic regression model (Table 5) revealed that ADL dependency (OR = 5.28, P = .001) and time since the first symptoms started (OR per year =1.84, P = .026) independently predicted the presence of dementia, whereas somatic comorbidity predicted the absence of dementia (OR = 0.48, P = .021).
The ROC area of the model with all 9 significant univariate variables from Table 4 was 0.86 (95% confidence interval [CI], 0.77–0.94). Reduction of the model to the 3 significant multivariate variables (ADL, time since the first symptoms were noticed, and somatic comorbidity) resulted in an ROC area of 0.79 (95% CI, 0.70–0.88). The family physicians’ global diagnosis had an ROC area of 0.74 (95% CI, 0.63–0.85). Finally, the ROC area of the expected DSM-III-R diagnosis was only 0.50 (95% CI, 0.37–0.62).
Discussion
The family physicians’ diagnosis based on their assessment of all available information was reasonably accurate. Formal DSM-III-R diagnoses, derived by integrating the recorded symptoms, resulted in poor accuracy. Degree of ADL functioning, the duration of symptoms, and the presence of somatic comorbidity independently contributed to the prediction of presence or absence of dementia. Neither the number of diagnostic recommendations made nor the use of the MMSE added to the family physicians’ accuracy. The latter is rather disappointing news for makers of all 3 dementia guidelines. Many of the current diagnostic recommendations in the dementia guidelines are based at best on lower quality evidence from observational studies. Trials are lacking in which diagnostic interventions by family physicians are tested against usual diagnostics.
It was remarkable that neither the core symptoms of dementia (cognitive impairment) nor the DSM criteria added to the diagnostic accuracy. Our findings raise the question of how family physicians made their diagnoses. In this respect, the concept of illness scripts (also called pattern recognition) may be helpful to understand how clinicians make diagnostic decisions.35 According to this concept, clinicians base their decisions more on accumulated clinical patient pictures during their medical career or so-called illness scripts than on medical-deductive reasoning, which is taught in medical schools and offered in evidence-based guidelines.36 The illness scripts family physicians have of suspected dementia patients may be triggered more by ADL malfunctioning than by cognitive dysfunction.
When the time effort per patient of the family physicians and the memory clinic is compared, the family physicians performed well. The family physicians invested on average 3.5 consultations per patient. Multiplied by the average consultation time of 10 minutes in Dutch family practices, this yields a total consultation time of 35 minutes per patient to arrive at a diagnosis. This time should be compared with the 4.5 hours needed per patient for high-tech diagnostic assessment at the memory clinic. Taking the limited time and low-tech approach into account, it must be concluded that the family physicians did a fair job in diagnosing suspected patients.
We did not confirm the hypothesis that continuity of care enhanced diagnostic accuracy. In contrast to the finding of Eefsting and colleagues,1 the number of contacts with a patient showed a trend toward a negative association with diagnostic accuracy. A possible explanation is that only contacts related to the evaluation of dementia were recorded in our study; a larger number of contacts may therefore reflect a family physicians’ diagnostic difficulty or uncertainty rather than better continuity of care.
Strengths of our study include the detailed information from the family physician assessments, the primary care setting, and the use of a memory clinic as the reference standard. A limitation was that the diagnostic criteria of the family physicians’ guideline were based on the DSM-III-R, whereas the memory clinic used the DSM-IV criteria.20,24 Nevertheless, this difference may have accounted for the diagnostic variation only to a small degree.37 Second, the finding that additional value was not found for use of the MMSE or for a more frequent use of recommendations might be explained by the fact that the family physicians in this study already applied the recommendations on a large scale. Higher use, therefore, did not add much to the diagnostic accuracy of the family physicians. Third, concerning the importance of the availability of an informant, the kind of information the family physicians received from these informants remains unclear, as the content of the informant interview was neither standardized nor registered. Fourth, few patients per family physician were included. The numbers of included patients per family physician, however, are only a little below the incidence figures for dementia in the Netherlands.38 Anecdotal reactions from the participating family physicians revealed that some patients were not included because they did not want medical interference and some were unable to travel to the memory clinic. Finally, we modeled various predictors to estimate the presence or absence of dementia and derived a reduced model. In this modeling we did not adjust for overfitting and did not prospectively validate the model. This tactic was necessary given the relatively small number of subjects in the study.28 Therefore, before our reduced prediction model can be used in medical practice it should first be validated on new patients.