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Departments of 1 Neurology and 2 Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.
Departments of 3 Medicine and 5 Neurology, Yale University School of Medicine, New Haven, Connecticut.
4 Teleradiology Solutions, Bangalore, India.
6 Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York.
7 Department of Statistics, Ohio State University, Columbus.
8 Institute for Neurodegenerative Disorders, New Haven, Connecticut.
9Aging Brain Center, Institue for Aging Research, Hebrew SeniorLife, Boston, Massachusetts.
Address correspondence to Tamara G. Fong, MD, PhD, 330 Brookline Avenue, Boston, MA 02215. E-mail: tfong{at}bidmc.harvard.edu
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Methods. Participants included hospitalized general medical patients aged 65 years and older with documented delirium and no relevant medical conditions or preexisting abnormalities on neuroimaging prospectively studied using 99mTc HMPAO single photon emission computed tomography (SPECT) scans obtained during and after resolution of delirium. Twenty-two patients enrolled in the study, of whom six completed both scans. All participants underwent neuropsychological assessment immediately prior to SPECT scanning. SPECT images were compared across all participants during delirium; for patients completing paired scans, within-patient comparisons were made.
Results. Visual assessment of SPECT scans revealed perfusion abnormalities in frontal (5 participants) or parietal regions (6 participants); scans were normal in 11 participants (50%). Region-of-interest analysis identified reduced blood flow (p <.01) in the left inferior frontal, right temporal, right occipital, and pontine regions. Analysis of paired scans revealed reversible abnormalities in three participants (p <.001), with decreased right parietal perfusion in two participants and increased left parietal perfusion in one participant.
Conclusions. The results of this study of a small group of general medical patients are suggestive that frontal or parietal cerebral perfusion abnormalities occur in delirium, and these findings need to be confirmed by future, larger studies. These results may help to improve basic understanding of delirium pathophysiology, to identify long-term changes, and to evaluate response to treatment over time.
The aim of the present study is to use SPECT to determine patterns of regional cerebral perfusion among hospitalized general medical patients both during and after resolution of delirium. Determining distinct anatomic patterns in delirium might help to identify pathways underlying the clinical phenomena of delirium and clarify whether there are common neuroanatomic patterns among the diverse etiologies for delirium, findings which may in turn lead to more effective preventive and treatment strategies.
| METHODS |
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65 years, presence of delirium as documented by the Confusion Assessment Method (CAM) (14), and absence of relevant medical conditions (epilepsy, drug and/or alcohol abuse, moderate to severe dementia, coma, severe illness, or respiratory isolation). Patients were excluded if computed tomography and/or magnetic resonance imaging (MRI) demonstrated any preexisting abnormalities, including tumors, large strokes, or focal atrophy. Of 103 consecutive patients meeting study eligibility criteria, 81 patients were excluded because of refusal to participate (n = 58), early hospital discharge (n = 10), illness, agitation or dementia (n = 7), poor quality scans (n = 3), inability to consent (n = 2), or incomplete neuropsychological testing (n = 1). Twenty-two patients met eligibility criteria and completed SPECT scanning and neuropsychological testing during delirium. Six of these patients were retested after resolution of delirium. The remaining 16 patients did not have complete clinical improvement of delirium prior to hospital discharge. A single patient who had paired SPECT scans but incomplete neuropsychological testing was included only in the analysis of paired scans. Written informed consent was obtained using a dual consent procedure from each patient and a surrogate according to procedures approved by the Yale Institutional Review Board.
Cognitive Assessments and Variables
The Mini-Mental State Examination (MMSE) was used as an overall measure of cognitive function (15). Attention, which is invariably impaired in delirium, was measured with the Digit Span Test (16) and vigilance subtest from the Cognitive Test for Delirium (CTD) (17). The presence and severity of delirium were documented using the CAM (14), a validated and widely used instrument for the diagnosis of delirium, and additional measures of delirium severity included the Delirium Rating Scale-98 (DRS) (18) and the CTD (17). Preexisting dementia was assessed using the Modified Blessed Dementia Rating Scale (19), and functional status was determined using the Index of Activities of Daily Living (20). Admitting diagnoses, severity of illness, laboratory results, vital signs, and medications were obtained from a brief nurse interview and review of the medical records.
SPECT Imaging
Immediately following cognitive testing, participants were taken to the SPECT scanner, placed in a darkened, quiet environment, and after 5 minutes injected with 962 MBq (26 mCi) of 99 mTc HMPAO. Fifteen minutes after injection, participants were placed in a two- or three-headed SPECT camera (Axis 3000 or Prism 2000; Phillips Medical Systems, Best, The Netherlands) outfitted with high-resolution parallel hole collimators. To minimize anticipated head movement, a series of seven serial 5-minute images were obtained into a symmetric photopeak window centered at 140 keV. The serial SPECT scans were summed, transverse reconstructed, and filtered using a 3-D low-pass ramp filter with order 4.0 and cutoff 0.26. Homogeneous attenuation correction was performed by using the Chang method (21) with an attenuation of 0.11/cm.
SPECT Analysis
Analysis of SPECT blood flow images was performed in three ways: (i) visual analysis of scans; (ii) semiquantitative region of interest (ROI) analysis; and (iii) statistical parametric mapping (SPM99; Wellcome Department of Imaging Neuroscience, London, U.K.; http://www.fil.ion.ucl.ac.uk/spm/) of paired scan data sets.
Images were reviewed independently and by consensus by two board-certified nuclear medicine physicians (J.S., A.D.) and a neurologist (H.B.) with extensive clinical expertise in SPECT perfusion studies and qualitative interpretation of perfusion abnormalities. Reviewers were blinded to specific clinical information about individual participants. All scans were compared with the participant's baseline computed tomography and/or MRI to ensure that the perfusion changes did not correlate with an existing anatomic lesion.
For the semiquantitative ROI analysis, initial normalization of the participant scans was performed using SPM99 with MedX 3.4 (Sensor Systems, Sterling, VA), implemented on a Linux platform (7.0; Red Hat Software, Inc., Raleigh, NC) by a protocol published previously (22,23). Briefly, the SPM realign function was used to create a mean image and reslice the reconstructed images. Images were then spatially normalized to the SPM SPECT template in the SPM standard anatomical space (MNI space). Smoothing was performed using a 10 x 10 x 12 mm Gaussian kernel. Proportional scaling to the global mean was performed using an analysis threshold of 0.8.
Following established methods (24), circular ROI measuring 6024 mm3 were defined for the cerebellum, inferior frontal, superior frontal, parietal, temporal, and occipital lobes. A circular ROI measuring 3528 mm3 was defined for the pons and midbrain. The regions were placed over representative areas on a normal MRI template in standard anatomical space (see http://www.mrc-cbu.cam.ac.uk/Imaging/mnispace.html) by two separate observers (J.S. and A.D.). The SPECT scans were coregistered to the MRI, and the same regions were pasted over the normalized SPECT images. The numbers of counts in each ROI were calculated and normalized to the mean counts in the two cerebellar regions for each participant to create a blood flow ratio. The cerebellum was used as the reference region because it has not been found to be significantly involved in delirium and because of low variation of counts in this region. Comparisons of blood flow ratios were made against age- and handedness-matched controls (n = 11) from a standard SPECT databank.
The data from six participants with paired scans were compared using a paired-sample t test for areas of relative hyper- and hypoperfusion on SPECT images obtained during active and then resolved delirium. The extent threshold (k) below which clusters were rejected was 125 voxels, which is equivalent to a volume of 1 cm3 and corresponds to the approximate resolution of brain SPECT imaging. The voxel level threshold was set at 0.01.
| RESULTS |
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80 years old, with 12 years of education. Most were women, and all were right-handed. Over half had impairment in activities of daily living, and most had preexisting cognitive impairment. During hospitalizations, 89% of participants were rated as moderately ill, and 11% as mildly ill. All participants had delirium according the CAM criteria, with the delirium rated as mild in 50% and moderate in 44% by clinical judgment and delirium severity scores on the CAM (4) and DRS. However, mean scores on the CTD and DRS were slightly above cutoffs for delirium, suggesting that the average delirium severity was mild. During delirium, an average score of 19.1 (±5.2) on the MMSE indicates significant cognitive impairment. Mean scores on the forward and backward digit span and vigilance tests indicate substantial impairments in attention. The cause of delirium on medical record review was felt to be multifactorial in the majority of cases, with the most common contributing factors being medications (77%), preexisting dementia or cognitive impairment (59%), infection (50%), dehydration (36%), metabolic (36%), hypoxia (14%), and immobility (14%).
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| DISCUSSION |
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The neuroanatomical localization of delirium pathology has implications for understanding both symptoms and underlying mechanisms. Some of the key features of delirium, including inattention, disorientation, and comprehension deficits, have been associated with regional pathology. For example, attention is associated with the nondominant posterior parietal and bifrontal areas, the thalamus, and the pons (25,26); orientation is associated with nondominant parietal, medial orbitofrontal and temporal cortex (27,28); and comprehension is associated with frontal and temporal regions (29,30). Thus, the predominance of findings in the frontal and parietal regions and pons (by ROI analyses) is an important result in this study, and is consistent with what is known of the neuroanatomical localization of important delirium symptoms.
There are a number of limitations to this study. Because participants must lie still for the SPECT scan, only those persons with hypoactive delirium could be included. Inclusion of participants with more prominent delirium symptoms, where changes may be more evident, or use of other functional imaging techniques, might allow for detection of subtle perfusion changes. In addition, changes in global blood flow could not be determined, and such changes in perfusion might play a critical role in delirium. In contrast to the visual assessment and SPM analysis of the paired scans, the ROI analysis identified trends, but not statistically significant differences in the parietal lobe. This discrepancy may be related to the small sample size (i.e., inadequate power) or to methodological errors (i.e., positioning of the ROI in the parietal lobe), or could reflect variability of perfusion changes in this region, as observed in the paired scan analysis with increased perfusion in one participant and decreased perfusion in others. A reduction in blood flow in the pons, an area critical for attention, was detected only in the ROI analysis, and further confirmation of this finding is needed.
Delirium is a heterogeneous, global process resulting in fluctuating mental status that likely involves widespread electrophysiological and neurochemical abnormalities. For these reasons, delirium is inherently challenging to study. Furthermore, patients most likely to suffer from delirium are older patients who commonly have preexisting brain abnormalities, such as atrophy, vascular insults, tumors, or dementia, which could contribute to changes in blood flow independent of delirium, and making comparisons across individuals is difficult. To minimize effects of multiple variables, within-individual comparisons of paired scans obtained in delirious and nondelirious states were intended to address this methodological challenge. Unfortunately, logistical difficulties (such as early discharge or persistence of delirium) made it possible to obtain paired scans in only 6 of the 22 participants, and limited the conclusions that can be drawn from this study. Furthermore, although on average the paired participants had a 41% reduction in severity of delirium score, they may not have fully recovered by the time of the second scan. Controls from a normal SPECT database were used, rather than controls chosen from the same hospitalized cohort who did not develop delirium, and it is possible that changes seen on the paired scans may have been the result of treatment, underlying medical illness, or other aspects of the hospitalization. Although there were no baseline differences between participants who were able to have paired scans compared to those who had only a single scan, the findings from these six individuals cannot be generalized across all participants. Future studies will benefit from strong efforts to obtain serial scans on individuals with delirium, to more fully characterize longitudinal changes, and to better understand the variability in severity and recovery from delirium.
Despite the considerable challenge of enrolling actively delirious and ill patients, this study was able to obtain SPECT scans in a sizable number of general medical patients and provides important preliminary data in the study of functional brain changes in delirium. The results suggest potential involvement of the frontal and parietal lobes in the neuropathology of delirium. Because delirium is such an important clinical syndrome, and because little is known about the fundamental pathophysiology of delirium, efforts to unravel the underpinnings of delirium represent a crucial step along the path toward providing necessary and appropriately targeted improvements in treatment and preventive strategies. Moreover, these results may provide a basis to identify long-term changes and to evaluate response to treatment over time.
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We acknowledge with much gratitude the following people for their invaluable help: Sandra Ginter for project coordination; Kelly McNally for assistance with SPECT analysis and interpretation; and Joseph Agostini, MD, for assistance with medical record abstraction.
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Received July 6, 2006
Accepted September 28, 2006
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