Correction of partial volume effects in myocardial SPECT

BACKGROUND: Marked partial volume effects occur in myocardial single photon emission computed tomographic (SPECT) studies because of limited resolution in imaging the myocardial wall and contractile motion of the heart. Little work has been undertaken to develop correction techniques for SPECT except for efforts to improve the reconstructed resolution. Our purpose was to examine the extent of the problem and propose a correction method. METHODS AND RESULTS: A potential correction method, developed initially for positron emission tomography, involved estimation of extravascular density by means of subtracting vascular density derived in a blood pool study from total density derived from a transmission study. Provided partial volume errors are the same for transmission and emission data, activity per gram of extravascular tissue can be obtained by means of dividing the perfusion regional data by extravascular density for the same region. Simulations were designed to assess the importance of partial volume errors and the use of extravascular density to correct the errors. Recovery coefficients for the myocardium were estimated by means of simulation of the beating heart on the basis of published values for ventricular dimensions. Resolution for transmission with a scanning line source system was compared with emission resolution. The effect of spillover on measured partial volume losses was assessed, and a method for matching spillover for emission and extravascular density was demonstrated. Correction for partial volume effects was demonstrated for a phantom with variable wall thickness. Significant variation in recovery coefficient was demonstrated between posterior and septal walls for individual patients independent of heart size. Filtering was necessary to account for the difference in transmission resolution measured in the axial direction. Spillover effects had a significant influence on the measured recovery for small objects; however, for a specific reconstruction algorithm and defined region size, correction was implemented to match the spillover effects for emission and extravascular density. Use of extravascular density for correction of partial volume loss, for ordered subsets expectation maximization reconstruction with compensation for resolution, was demonstrated to be accurate to within 10%. CONCLUSIONS: The feasibility of correcting partial volume effects with extravascular density was demonstrated. Correction is effective provided care is taken to match both resolution and spillover for emission and extravascular density.     

A nonlinear spatially variant object-dependent system model for prediction of partial volume effects and scatter in PET

Accurate quantitation of small lesions with positron emission tomography (PET) requires correction for the partial volume effect. Traditional methods that use Gaussian models of the PET system were found to be insufficient. A new approach that models the non-Gaussian object-dependent scatter was developed. The model consists of eight simple functions with a total of 24 parameters. Images of line and disk sources in circular and elliptical cylinders, and an anthropomorphic chest phantom were used to determine the parameter values. Empirical rules to determine these parameter values for various objects based on those for a reference object, a 21.5-cm circular cylinder, were also proposed. For seven spheroids and a 3.4-cm cylinder, pixel values predicted by the model were compared with the measured values. The model-to-measurement-ratio was 1.03+/-0.07 near the center of the spheroids and 0.99+/-0.03 near the center of the 3.4-cm cylinder. In comparison, the standard single Gaussian model had corresponding ratios of 1.27+/-0.09 and 1.24+/-0.03, respectively, and the corresponding ratios for a double Gaussian model were 1.13+/-0.09 and 1.05+/-0.01. Scatter fraction (28.5%) for a line source in the 21.5-cm cylinder was correctly estimated by our model. Because of scatter, we found that errors in the measurement of activity in spheroids with diameters from 0.6 to 3.4 cm were more significant than previously appreciated.     

A method to correct for scatter, spillover, and partial volume effects in region of interest analysis in PET

Scatter and spatial resolution effects degrade the accuracy of radioactivity concentration estimates obtained from positron emission tomography (PET) data. We present and evaluate a methodology for region quantification which accounts for these degradations. The method is based on analysis of sinogram data and does not require dynamic data sequences to be reconstructed. Moreover, estimates of region variance are also produced which may be used to define weights for model analyses that use weighted least squares minimization in order to obtain unbiased parameter estimates. We evaluate the method using both simulation and measured data and find that, with an appropriate model of scatter and spatial resolution effects, it is unbiased and capable of quantifying myocardial concentration with no more than a 5% error in accuracy for myocardium as thin as 10 mm.     

Morphologic image processing operators: reduction of partial volume effects for improved 3D visualization of CT data

AIM: The quality of segmentation and three-dimensional reconstruction of anatomical structures in tomographic slices is often impaired by disturbances due to partial volume effects (PVE). The potential for artefact reduction by use of the morphological image processing operators (MO) erosion and dilation is investigated. DESIGN: The CT examinations of 31 patients with pathological alterations in lung or brain were segmented using automatic region growing and the MO were applied in a different number of iterations. The processed regions were 3D-reconstructed (shaded surface display, MIP, volume rendering) and the occurrence of PVE-related artefacts using the signal-to-background ratio (SBR) prior to and after MO application was compared. RESULTS: For all patients under review, the artefacts caused by PVE were significantly reduced by erosion (lung: mean SBRpre = 1.67, SBRpost = 4.83; brain: SBRpre = 1.06, SBRpost = 1.29) even with only a small number of iterations. Region dilation was applied to integrate further structures (e.g. at tumor borders) into a configurable neighbourhood for segmentation and quantitative analysis. CONCLUSIONS: The MO represent an efficient approach for the reduction of PVE artefacts in 3D-CT reconstructions and allow optimized visualization of individual objects.     

The Index of Drug Involvement: a partial validation

Social workers often need a wider range of assessment scales that can be used in education, research, and practice. The Index of Drug Involvement (IDI) is a short-form assessment scale that may be of use to social work educators, researchers, and practitioners who work with clients with drug abuse or chemical dependency problems. This article describes the IDI; provides information about its administration, scoring, and interpretation; and describes the initial research conducted to validate the instrument. This article provides information about the reliability of the IDI; reports the standard error of measurement; and presents findings concerning the content, construct, and criterion validity of the instrument. Also presented is initial information about the development and use of a clinical cutting score that will help practitioners evaluate the clinical significance of a drug abuse problem and that can be a guide for establishing initial and final treatment goals.     

PET validation of a novel prefrontal task: Delayed response alteration.

Deficits in working memory have been proposed to explain the performance failures of frontally lesioned primates on delayed alternation (DA) and delayed response (DR) tasks. The authors examined a computerized test of delayed response alternation (DRA), which combines elements of DR and DA in a sample of 18 normal volunteers who underwent oxygen-15 PET regional cerebral blood flow scans during the DRA and a sensorimotor control task. Significant activations were observed in a network of frontal, parietal, occipital, and temporal regions during initial task performance. A qualitatively similar but somewhat reduced set of activations was observed in a subset of participants who repeated the task after practice and instruction. These results are consistent with distributed models of working memory derived from studies of nonhuman primates and suggest that the frontal lobes contribute to human working memory function. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

A new integrated system for three-dimensional echocardiographic reconstruction: development and validation for ventricular volume with application in human subjects

OBJECTIVES: The purpose of this study was to improve three-dimensional echocardiographic reconstruction by developing an automated mechanism for integrating spark gap locating data with corresponding images in real time and to validate use of this mechanism for the measurement of left ventricular volume. BACKGROUND: Initial approaches to three-dimensional echocardiographic reconstruction were often limited by inefficient reconstructive processes requiring manual coordination of two-dimensional images and corresponding spatial locating data. METHODS: In this system, a single computer overlays the binary-encoded positional data on the two-dimensional echocardiographic image, which is then recorded on videotape. The same system allows images to be digitized, traced, analyzed and displayed in three dimensions. This system was validated by using it to reconstruct 11 ventricular phantoms (19 to 271 ml) and 11 gel-filled excised ventricles (21 to 236 ml) imaged in intersecting long- and short-axis views and by apical rotation. To measure cavity volume, a surface was generated by an algorithm that takes advantage of the full three-dimensional data set. RESULTS: Reconstructed cavity volumes agreed well with actual values: y = 0.96x + 2.2 for the ventricular phantoms in long- and short-axis views (r = 0.99, SEE = 2.7 ml); y = 0.95x + 2.9 for the phantoms, reconstructed by apical rotation (r = 0.99, SEE = 2.7 ml); and y = 0.99x + 0.11 ml for the excised ventricles (reconstructed in long- and short-axis views; r = 0.99, SEE = 5.9 ml). The mean difference between three-dimensional and actual volumes was 3% of the mean (3.0 ml) for the phantoms and 6% (4.6 ml) for the excised ventricles. Observer variability was 2.3% for the phantoms and 5.6% for the excised ventricles. Application to 14 normal subjects demonstrated feasibility of left ventricular reconstruction, which provided values for stroke volume that agreed well with an independent Doppler measure (y = 0.97x + 0.94; r = 0.95, SEE = 3.2 ml), with an observer variability of 4.9% (2.4 ml). CONCLUSIONS: A system has therefore been developed that automatically integrates locating and imaging data in no more time than the component two-dimensional echocardiographic scans. This system can accurately reconstruct ventricular volumes in vitro over a wide range and is feasible in vivo, thus laying the foundation for further applications. It has increased the efficiency of three-dimensional reconstruction and enhanced our ability to address clinical and research questions with this technique.     

Butorphanol-mediated antinociception in mice: partial agonist effects and mu receptor involvement

In the present experiments, we characterized the agonist and antagonist effects of butorphanol in mice. In the mouse radiant-heat tail-flick test, the mu agonists morphine and fentanyl and the kappa agonist U50,488H were fully effective as analgesics, whereas butorphanol was partially effective (producing 82% of maximal possible analgesic effect). Naltrexone was approximately equipotent in antagonizing the effects of morphine, fentanyl and butorphanol; in vivo apparent pA2 values for these naltrexone/agonist interactions were 7.5 (unconstrained). Naltrexone was approximately 10 times less potent in antagonizing the effect of U50,488H (average apparent pK(B) = 6.7). The selective mu antagonist beta-funaltrexamine (0.1-1.0 mg/kg) antagonized the effects of butorphanol in a dose-dependent insurmountable manner. Pretreatment with nor-binaltorphimine (32 mg/kg), a kappa-selective antagonist, did not reliably antagonize butorphanol, and naltrindole (20 and 32 mg/kg), a delta-selective antagonist, failed to antagonize the effects of butorphanol. Low doses of butorphanol (1.0, 1.8 or 3.2 mg/kg) caused parallel, rightward shifts in the dose-effect curve for morphine and parallel leftward shifts in the dose-effect curve for U50,488H. Taken together, the results of the present study suggest that butorphanol is a partial agonist in the mouse radiant-heat tail-flick test and that activity at mu receptors accounts for the majority of its antinociceptive effects.     

Blood letting for BSL: the effects of timing and sites on blood volume

The purpose of this study was to establish the most appropriate timing and site for obtaining an adequate volume of blood for accurate measurement of blood sugar levels by blood glucose monitors. The 248 samples of blood used in the study were collected from 18 men and 16 women recruited from a group of people with type II diabetes mellitus who were attending an outpatient Diabetes Centre. Neither the timing between lancing and collecting the blood nor the sites from which blood was obtained significantly affected the volume of blood samples. Sufficient blood to give an accurate measure of blood sugar levels from monitors requiring 30, 15-18 and five microlitres of blood was obtained from 37%, 65% and 98% of the procedures respectively.     

Neural effects of visualizing and perceiving aversive stimuli: a PET investigation

Cerebral blood flow was recorded (using positron emission tomography) while middle-aged subjects viewed or visualized pictures of neutral or aversive stimuli, and then determined whether auditorily presented statements correctly described the stimuli. Visualizing aversive stimuli enhanced cerebral blood flow, relative to visualizing neutral stimuli, in areas 17 (right) and 18 (bilateral), as well as the anterior insula (bilateral) and middle frontal cortex (left). Areas 17 and 18 have been identified as supporting the representations that underlie the experience of imagery, and the anterior insula is a major cortical recipient of input from the autonomic nervous system. Perceiving aversive stimuli enhanced cerebral blood flow, relative to neutral stimuli, in area 46, the angular gyrus and area 19, area 47, and the middle temporal gyrus (all in the left hemisphere). All of these areas have previously been implicated in visual object identification. It is striking that negative emotion did not modulate activation in any areas in the same way during imagery and perception.     

Inverse duration effects in partial report.

In partial-report experiments, an array of stimuli is displayed briefly, followed by a probe indicating the items to be reported. When exposure duration of the array is increased, 2 contrasting outcomes have been found: Some experiments find that performance improves (direct-duration effect); others find that it deteriorates (inverse-duration effect). The objective here was to identify the reasons for the discrepant results. This was done by investigating the roles played by 5 factors that differed between the 2 sets of contrasting studies. An inverse-duration effect was obtained in each of 6 experiments; its magnitude was affected by retinal eccentricity and by the number of items denoted by the probe. The effect was independent of array configuration and of number of items in the array. The direct-duration effect was shown to arise from a confounding of exposure duration and brightness. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Post-exercise rehydration in man: effects of volume consumed and drink sodium content

The interaction between the volume and composition of fluids ingested was investigated in terms of rehydration effectiveness. Twelve male volunteers, dehydrated by 2.06 +/- 0.02% (mean +/- SE) of body mass by intermittent cycle exercise, consumed a different drink volume on four separate weeks; six subjects received drink L (23 mmol.l-1 Na+) in each trial and six were given drink H (61 mmol.l-1 Na+). Volumes consumed were equivalent to 50%, 100%, 150%, and 200% of body mass loss (trials A, B, C, and D, respectively). Blood and urine samples were obtained before exercise and for 7.5 h after exercise. Less urine was excreted following rehydration in trial A than in all other trials. Cumulative urine output (median ml) was less in trial B (493, range 181-731) than D (1361, range 1014-1984), which was not different from trial C (867, range 263-1191) in group L. In group H, the volume excreted in trial B (260, range 137-376) was less than trials C (602, range 350-994) and D (1001, range 714-1425), and the volume in trial C was less than in trial D. These results suggest that both sodium concentration and fluid volume consumed interact to affect the rehydration process. A drink volume greater than sweat loss during exercise must be ingested to restore fluid balance, but unless the sodium content of the beverage is sufficiently high this will merely result in an increased urinary output.     

"The Gambling Craving Scale: Psychometric validation and behavioral outcomes": Correction to Young and Wohl (2009).

Reports an error in "The Gambling Craving Scale: Psychometric validation and behavioral outcomes" by Matthew M. Young and Michael J. A. Wohl (Psychology of Addictive Behaviors, 2009[Sep], Vol 23[3], 512-522). Some data in Table 4 was inadvertently omitted. The complete Table 4 is presented in the erratum. (The following abstract of the original article appeared in record 2009-14441-012.) Although craving is an important feature of problem gambling, there is a paucity of research investigating craving to gamble. A major stumbling block for craving research in gambling has been the lack of a methodologically sound, multidimensional measure of gambling-related craving. This article reports the development of the Gambling Craving Scale (GACS). In Study 1 (N = 220), a factor analysis revealed the emergence of a 9-item scale with 3 factors: Anticipation, Desire, and Relief. An important finding was that the GACS predicted problem gambling severity, depression, and positive and negative affect. In Study 2 (N = 145), the factor structure of the GACS was confirmed using a community sample of gamblers. In Study 3 (N = 46), GACS scores significantly predicted persistence at play on a virtual slot machine in the face of continued loss. Specifically, the more participants craved to gamble, the longer they engaged in play. The implications of craving for the development and maintenance of problem gambling severity are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

A clinical laboratory model for direct assessment of medication-induced antihyperalgesia and subjective effects: Initial validation study.

Analgesic medications are often tested in clinical laboratory studies by observing their ability to reduce the pain produced by noxious stimuli presented to healthy skin. These medications may then be used clinically to reduce disease-related hyperalgesia. This article describes a clinical laboratory model useful for testing a medication's ability to reduce hyperalgesia in humans. Results demonstrate that ultraviolet (UV) light induces hyperalgesia, commonly prescribed analgesic medications reduce UV-induced hyperalgesia, and this UV-induced hyperalgesia model can be used to assess the time course of a medication's antihyperalgesia effects. Coupled with participant-rated measures of drug liking and mood, this model may prove useful for predicting the clinical efficacy and side-effect profile of novel analgesic medications in cost-efficient and statistically powerful laboratory studies. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effect of pindolol on hormone secretion and body temperature: partial agonist effects

Pindolol has been shown to be a partial agonist at 5-HT1A receptors in preclinical studies. It has also been reported to inhibit the effects of other 5-HT1A partial agonists such as ipsapirone and buspirone on hormone secretion and body temperature in man, indicating its antagonist action at 5-HT1A receptors in man. To determine if pindolol has 5-HT1A agonist as well as antagonist effects in man, pindolol, 30 mg, p.o. and placebo, were given single blind in random order to 23 normal men with indwelling venous catheters and its effects on hormone secretion and body temperature noted. Pindolol significantly increased basal plasma cortisol concentrations, whereas it decreased plasma prolactin (PRL) concentrations and body temperature. The increase in plasma cortisol due to pindolol suggests a 5-HT1A agonist action and is consistent with a 5-HT1A partial agonist mechanism in man whereas the PRL effects are consistent with an antagonist action at 5-HT1A receptors. The effects of pindolol on plasma cortisol concentration and body temperature were significantly negatively correlated. Furthermore, these results indicate significant differences in the 5-HT1A-dependent regulation of PRL and the hypothalamo-pituitary-adrenal (HPA) axis and body temperature, and suggest that human basal PRL secretion is tonically stimulated by 5-HT1A mechanism whereas the HPA axis and body temperature are not. Since rodent studies suggest differences in 5-HT1A receptor sensitivity between males and females, the results reported here need to be replicated in females. These differences in the effect of pindolol are discussed in terms of receptor reserve theory.     

"Specificity of treatment effects: Cognitive therapy and relaxation for generalized anxiety and panic disorders": Correction.

Reports an error in "Specificity of treatment effects: Cognitive therapy and relaxation for generalized anxiety and panic disorders" by Jedidiah Siev and Dianne L. Chambless (Journal of Consulting and Clinical Psychology, 2007[Aug], Vol 75[4], 513-522). The individual measures were not listed in the domains labeled "Panic" and "Cognitive" for the ?st and Westling (1995) citation in Table 3. The corrected table is included, with the added text appearing in bold font. (The following abstract of the original article appeared in record 2007-11558-001.) The aim of this study was to address claims that among bona fide treatments no one is more efficacious than another by comparing the relative efficacy of cognitive therapy (CT) and relaxation therapy (RT) in the treatment of generalized anxiety disorder (GAD) and panic disorder without agoraphobia (PD). Two fixed-effects meta-analyses were conducted, for GAD and PD separately, to review the treatment outcome literature directly comparing CT with RT in the treatment of those disorders. For GAD, CT and RT were equivalent. For PD, CT, which included interoceptive exposure, outperformed RT on all panic-related measures, as well as on indices of clinically significant change. There is ample evidence that both CT and RT qualify as bona fide treatments for GAD and PD, for which they are efficacious and intended to be so. Therefore, the finding that CT and RT do not differ in the treatment of GAD, but do for PD, is evidence for the specificity of treatment to disorder, even for 2 treatments within a CBT class, and 2 disorders within an anxiety class. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Reward magnitude and partial reinforcement effects in a single runway.

The partial reinforcement acquisition effect (PRAE) in running speeds and the frustration effect (activity following nonreward compared with reward) were measured simultaneously in an alley whose goal-box floor was a stabilimeter. Experimental groups of 9 male Charles River albino rats each received 50 or 100% reinforcement combined factorially with 3 magnitudes of reward (1, 3, or 9 pellets). A control group of 18 Ss was never rewarded. The size of the PRAE was a direct function of reward magnitude, and crossing of 50 and 100% curves was found for all alley segments, including the goal segment. The frustration effect (FE) was present by the 2nd day of training for the 3- and 9-pellet groups, and the size of the FE was directly related to reward magnitude. The present study is unique in that (a) the findings were free from the effects of reward contrast, (b) behavior antecedent to the goal indicated that incentive was effectively manipulated, and (c) an unrewarded control group was used. (31 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)