Original article
Detecting HIV Associated Neurocognitive Disorders in Adolescents: What Is the Best Screening Tool?

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Abstract

Purpose

To examine the ability of the HIV-Dementia Scale (HDS) and Mini Mental State Exam (MMSE) to detect encephalopathy in adolescents living with human immunodeficiency virus (HIV) and/or acquired immunodeficency syndrome (AIDS).

Method

The study was based on chart review (N = 71) from 1999 to 2006, extracting data from psychological testing, disease classification, and demographic variables. HDS and MMSE scores were independent. Diagnosis of encephalopathy used American Academy of Neurology Criteria. Receiver Operating Characteristic Curves were plotted.

Results

Six patients had encephalopathy. The HDS identified five of these cases (83% sensitivity, 76% specificity). The MMSE identified three cases (50% sensitivity, 92% specificity).

Conclusion

Based on the study results, the HDS appears to be clinically useful.

Section snippets

Methods

Psychological and medical charts of 71 patients, who completed psychological assessments between April 1999 and July 2006, were reviewed independently. Neurology consultation was based on psychological testing results (not HDS scores) or clinical symptoms upon exam in a hospital-based Adolescent Clinic. The neurologist, blinded to the results of the HIV dementia scale, MMSE and IQ results, determined the presence of encephalopathy using AAN criteria [6].

Data were de-identified and coded in

Results

All patients were African-American. Patients with CDC classifications B and C were prescribed antiretroviral medications. Adherence data were not available. Six patients (Table 1), 8% of sample (all male, all six perinatally infected) had a diagnosis of encephalopathy (three patients, encephalopathy, NOS; one patient, herpes encephalitis; one patient, encephalitis history and toxoplasmosis of brain; and one patient, HIV encephalopathy). One patient had lymphoma of the brain and was excluded. No

Discussion

The HDS correctly classified five of six adolescents with encephalopathy, in comparison to the MMSE identifying three of the six; nonetheless the HDS was not found to be statistically significantly superior to the MMSE. Small sample size, lack of a base rate for encephalopathy in ALWHA, as well as earlier studies suggesting that the HDS is lacking in sensitivity but is highly specific [14] may account for this finding. Consistent with findings by Morgan et al [14], in our sample, which was

Acknowledgments

The authors thank Lucy Civitello, M.D. who provided guidance with the initial study design and who was the neurologist to whom we referred our patients for assessment. We also express our appreciation to Jennifer Marsh, J.D., Ph.D. who conducted the initial data analysis and was responsible for the integrity of the data. We thank Constance L. Trexler, B.S.N., R.N., C.P.N., and Stephanie Crane, B.A., Ph.D., who were responsible for the chart review and administrative support.

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