Problems in developing an instrument for the rapid assessment of personality status

2000 ◽  
Vol 15 (S1) ◽  
pp. 29-33 ◽  
Author(s):  
E. Van Horn ◽  
C. Manley ◽  
D. Leddy ◽  
D. Cicchetti ◽  
P. Tyrer

SummaryPurposeTo assess the validity of a quick assessment instrument (10 minutes) for assessing personality status, the Rapid Personality Assessment Schedule (PAS-R).Subjects and methodsThe PAS-R was evaluated in psychotic patients recruited in one of the centres involved in a multicentre randomised controlled trial of intensive vs standard case management (the UK700 case management trial). Patients were assessed using both a full version of the PAS (PAS-I – ICD version) and the PAS-R. The weighted kappa statistic was used to gauge the (criterion-related) validity of the PAS-R using the PAS-I as the gold standard. Both measure code personality status using a four-point rating of severity in addition to recording individual categories of personality disorder.ResultsOne hundred fifty-five (77%) of 201 patients recruited were assessed with both instruments. The weighted kappa statistic was 0.31, suggesting only moderate agreement between the PAS-I and PAS-R instruments under the four-point rating format, and 0.39 for the dichotomous personality disorder/no disorder separation. The sensitivity (64%) and specificity (82%) of the PAS-R in predicting PAS-I personality disorder were as satisfactory as for other screening instruments but still somewhat disappointing, and the PAS-R had an overall diagnostic accuracy of 78%.ConclusionThe PAS-R is a quick and rough method of detecting personality abnormality but is not a substitute for a fuller assessment.

2000 ◽  
Vol 15 (S1) ◽  
pp. 7-10 ◽  
Author(s):  
P. Tyrer ◽  
C. Manley ◽  
E. Van Horn ◽  
D. Leddy ◽  
O.C. Ukoumunne

SummaryOne hundred fifty-five (77%) of 201 participants recruited in a trial of intensive vs standard case management of patients with recurrent psychotic illness had their personality status measured before treatment and were followed up for two years. The primary outcome was the total number of days spent in psychiatric hospitalisation in the two years following randomisation. Thirty-three (21%) of the patients had a personality disorder and their duration of hospital stay (105 days) was greater than in those without personality disorder (56 days). There was weak evidence that intensive case management more effective in reducing the duration of care in those with personality disorder than in those without personality disorder.


2017 ◽  
Vol 33 (3) ◽  
pp. 158-165
Author(s):  
Natalia Calvo ◽  
Naia Sáez-Francàs ◽  
Sergi Valero ◽  
Jesús Castro-Marrero ◽  
José Alegre Martín ◽  
...  

Abstract. The study examines the relationship between a categorical and a dimensional personality assessment instrument in patients with Chronic Fatigue Syndrome (CFS). A total of 162 CFS patients were included in the study (91.4% women; mean age 47.5 years). All subjects completed the Spanish versions of the Personality Diagnostic Questionnaire-4+ (PDQ-4+) and the Temperament and Character Inventory-Revised (TCI-R). Results: 78 (48.1%) of the patients presented a Personality Disorder (PD), the most frequent being Cluster C, specifically Obsessive-compulsive disorder, followed by Avoidant disorder. PDs showed a specific pattern of correlation with temperament scales. All PD clusters correlated positively with Harm Avoidance and Self-Transcendence, and negatively with Reward Dependence, Self-Directedness, and Cooperativeness. In a logistic regression analysis, Self-Directedness and Cooperativeness predicted PD presence. The findings are consistent with previous studies in non-CFS samples and suggest that the combination of the Temperament and Character dimensions (low Self-Directedness and Cooperativeness and high Harm Avoidance and Self-Transcendence) correlates with PD severity, and that Self-Directedness and Cooperativeness are associated with PD presence in CFS patients. The integration of these two perspectives expands the current comprehension of personality pathology in CFS patients.


Healthcare ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 810
Author(s):  
Areej Y. Bayahya ◽  
Wadee Alhalabi ◽  
Sultan H. AlAmri

Smart health technology includes physical sensors, intelligent sensors, and output advice to help monitor patients’ health and adjust their behavior. Virtual reality (VR) plays an increasingly larger role to improve health outcomes, being used in a variety of medical specialties including robotic surgery, diagnosis of some difficult diseases, and virtual reality pain distraction for severe burn patients. Smart VR health technology acts as a decision support system in the diseases diagnostic test of patients as they perform real world tasks in virtual reality (e.g., navigation). In this study, a non-invasive, cognitive computerized test based on 3D virtual environments for detecting the main symptoms of dementia (memory loss, visuospatial defects, and spatial navigation) is proposed. In a recent study, the system was tested on 115 real patients of which thirty had a dementia, sixty-five were cognitively healthy, and twenty had a mild cognitive impairment (MCI). The performance of the VR system was compared with Mini-Cog test, where the latter is used to measure cognitive impaired patients in the traditional diagnosis system at the clinic. It was observed that visuospatial and memory recall scores in both clinical diagnosis and VR system of dementia patients were less than those of MCI patients, and the scores of MCI patients were less than those of the control group. Furthermore, there is a perfect agreement between the standard methods in functional evaluation and navigational ability in our system where P-value in weighted Kappa statistic= 100% and between Mini-Cog-clinical diagnosis vs. VR scores where P-value in weighted Kappa statistic= 93%.


2003 ◽  
Vol 1860 (1) ◽  
pp. 103-108 ◽  
Author(s):  
Shawn Landers ◽  
Wael Bekheet ◽  
Lynne Falls

Like many provincial and municipal agencies, the British Columbia Ministry of Transportation (BCMoT) contracts out the collection of pavement surface condition data. Because BCMoT is committed to contracts with multiple private contractors, quality assurance (QA) plays a critical role in ensuring that the data are collected accurately and repeatably from year to year. Comprehensive QA testing procedures for surface distress data have been developed and implemented since the data collection has been based on visual ratings with event boards. Control sites that are manually surveyed are used to evaluate whether the contractor is correctly applying the BCMoT pavement surface distress rating system. To date, the QA testing has been based on a composite-index–based criterion for assessing the level of agreement and supplemented with the detailed severity and density rating data. However, the use of a composite index presents some limitations related to the model formulation and weightings assigned to particular distress types. Although the detailed ratings are useful as a diagnostic tool to pinpoint discrepancies, in the disaggregated format, they are not conducive as acceptance criteria for QA testing. Not widely used in the field of engineering, Cohen’s weighted kappa statistic has been applied since the 1960s in other areas to assess the level of agreement beyond chance among raters. The statistic was therefore identified as a possible solution for improving the ministry’s QA surface distress testing process by providing an overall measure of the level of agreement between the detailed manual benchmark survey and the contractor severity and density ratings. The application is described of Cohen’s weighted kappa statistic for visual surface distress survey QA testing using the BCMoT survey and testing procedures as a case study.


1999 ◽  
Vol 174 (1) ◽  
pp. 74-78 ◽  
Author(s):  
Francis Creed ◽  
Tom Burns ◽  
Tom Butler ◽  
Sarah Byford ◽  
Robin Murray ◽  
...  

BackgroundCase management, particularly in intensive form, has been widely introduced for the treatment of severe mental illness. However, the optimal intensity of case management has not been determined.AimsWe aimed to assess whether intensive case management (small case load) reduces hospitalisation and costs compared with standard case management.MethodDevelopment and rationale of a large randomised controlled trial comparing intensive case management (case load per worker? 15 patients) with standard case management (case load 30–35 patients)ResultsTwo-year outcome data will be obtained on patients representative of the seriously mentally ill in inner-city mental health services.ConclusionsThe study planned with 700 patients should be sufficient to detect small differences in the readmission of patients to hospital (10%), the number of days spent in hospital over a two-year period (10 days) and the average weekly cost of care per patient. The sample is large enough to compare the cost-effectiveness of intensive and standard case management in mild and severe disability and in people of African–Caribbean origin and White Caucasians.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 1108-1108
Author(s):  
Abigail T. Lang ◽  
Linda P. Grooms ◽  
Mollie Sturm ◽  
Michelle Walsh ◽  
Terah Koch ◽  
...  

Abstract Background The introduction of bleeding assessment tools (BATs) to quantify the presence and severity of commonly reported bleeding symptoms has received increased interest over the past decade. Bleeding scores, along with laboratory data and family history, can assist the clinician in the assessment of a suspected mild bleeding disorder (MBD). While clinician-administered BATs have been utilized frequently, implementation and validation of the accuracy of a self-report or parent-proxy BAT have yet to be investigated. The primary objective of this study was to determine the accuracy of a parent-administered BAT by measuring the level of agreement between parent and clinician responses to the Condensed MCMDM-1VWD Bleeding Questionnaire. Methods Our study population included children aged 0-19 years presenting to the hematology clinic at Nationwide Children's Hospital (Columbus, OH) for initial evaluation of a suspected MBD or for follow-up evaluation of a previously diagnosed MBD. At the time of the visit, the parent/caregiver completed a short demographic survey and a modified version (targeted for a 6th grade comprehension level) of the Condensed MCMDM-1VWD Bleeding Questionnaire. The treating provider also completed the BAT by interviewing the patient and his/her caregiver; clinicians were blinded to the results of the parent BAT. Both the parent and clinician versions of the BAT were scored and analyzed in the same manner for ease of comparison. We calculated the percentage of agreement and weighted kappa statistic for individual bleeding symptoms as well as the mean across all questionnaire items. We also examined the agreement between caregiver and clinician responses in regards to patient age, gender, diagnosis (new versus follow-up patient), and parent education level. Results To date, we have enrolled 55 eligible patients. The overall mean bleeding score (BS) as calculated from the parent-report BAT was 5.98 (range: -1-25), while the mean BS for the clinician-report BAT was 3.87 (range: 0-16). The mean percentage of agreement between parents and clinicians across all items was 76% (range: 58-98%). The mean weighted kappa statistic was 0.31 (range: -0.04-0.79), representing fair agreement (based on Landis and Koch criteria); the mean Gwet's AC1 (an alternative kappa statistic) was 0.72 (range: 0.48-0.98), representing substantial agreement. Overall, 20% of parent and clinician total bleeding scores matched exactly, and an additional 42% of parent and clinician scores varied by only one to two points. 82% of the study population had an abnormal total bleeding score (defined as ≥2) when rated by parents and 78% had an abnormal total score when rated by clinicians (82% agreement, kappa = 0.43, Gwet's AC1 = 0.73). Tests for equal kappa coefficients did not show significant differences in agreement between parents and clinicians when compared by patient gender, age, diagnosis, or parent education level. Discussion To our knowledge, the results of a patient and/or parent-administered BAT score have not been studied to determine their accuracy and feasibility of use as a screening method for patients with a suspected MBD. While parents tended to over-report bleeding as compared to clinicians, overall, parent and clinician bleeding scores were similar in our study, and these results lend support for the potential use of a modified proxy-report BAT in a clinic setting. Additional research into the construct of the parent-administered BAT is needed to further improve the accuracy of parent-reported bleeding symptoms. Disclosures: Lang: OSUCOM Bennett Medical Student Research Scholarship: Research Funding; ASH HONORS Award: Research Funding.


1989 ◽  
Vol 9 (1) ◽  
pp. 67-74 ◽  
Author(s):  
Donald W. Stewart ◽  
David Koulack

Retrospective dream reports from 179 undergraduate students were scored by two independent raters in an attempt to assess the reliability of a newly-developed rating system for lucid dream content. The weighted Kappa statistic, which provides an index of chance-corrected interrater agreement for qualitative data, was used to assess the reliability of the ratings. The results indicated that the lucid dream rating system could be reliably used to identify different types of lucid dream content in dream reports, but some categories were less efficacious than others. Suggested revisions to the rating system are discussed.


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