• 정신신체의학
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• 제3권2호
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• pp.139-146
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• 1995

공황장애 환자에서 동반되는 인격장애의 양상을 조사하고, 인격장애 특성의 과다(過多)에 따른 공황증상의 심각도, 만성도, 전반적인 정신병리의 차이를 알아보고자 자기보고형 측정도구인 Personality Disorder Questionnaire-Revised(PDQ-R)와 간이 정신상태검사(SCL-90-R)를 이용하여 조사하였다. 대상은 전형적인 공황장애 환자 45명과 성별. 나이, 교육정도를 조합한 건강대조군 45명이었으며 이들에게 PDQ-R을 실시하여 공황장애 환자군과 대조군의 인격장애 양상을 비교 조사하였다. 또한 공황장애 환자만을 대상으로 공황증상의 심각도와 함께 SCL-90-R로 인격장애 동반여부에 따른 증상의 차이를 조사하여 다음과 같은 결과를 얻었다. 1) 공황장애 환자들은 대조군에 비하여 전체 PDQ-R점수가 유의하게 높게 나타나 차이가 있었다. 공황장애군은 대조군에 비하여 편집성, 의존성, 회피성 인격의 특징과 함께 반사회성, 경계성 경향을 나타내었다. 2) PDQ-R총점이 높은 집단과 낮은 집단 사이에 광장공포증상과 불안증상이 유의한 차이가 있었으나, 공황발작 빈도, 공황증상의 최근 심각도, 공포증상으로 인한 사회적 기능장애, 만성도 여부, 광장공포증 때 회피 및 공포증상의 정도에는 차이가 없었다. 3) SCL-90-R을 이용하여 동반증상을 알아본 결과 PDQ-R총점이 높은 군은 낮은 군에 비하여 모든 증상 항목이 의미 있게 높게 나타났다. 이러한 본 연구의 결과는 PDQ-R을 이용한 인격장애 측정시 동반증상이 영향을 미쳐 혼합되어 나타났을 가능성을 고려해야 하겠으며 앞으로 더욱 체계적인 조사방법과 함께 추적조사를 통하여 치료에 따른 인격장애의 변화를 관찰해야 하겠다.

• 기본간호학회지
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• 제12권2호
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• pp.231-239
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• 2005

Purpose: Investigation of the quality of life (QoL), family support and associated variables in patients with Parkinson's disease. Methods: The data were collected from 102 patients registered in the neurology department of C University Hospital. QoL was assessed using the Parkinson's Disease Questionnaire (PDQ-39) and Family Support Scale. Modified Hoehn and Yahr (H & Y) stages were obtained from an interview and clinical examination by a neurologist. Collected data were analyzed using the SAS program. Results: The participants' PDQ-39 average score was 34.34. The scores were significantly higher for participants who were older, who had a job and who were over 2.5 on the H & Y stage. The average for Family support scores was 41.6. Participants who had a living spouse, religion and a job scored higher than those who did not. PDQ-39 score had a positive correlation with age, job, and H & Y stage. Family support and PDQ-39 score were also positively correlated. Conclusion: It is recommended a program involving family that improves family support and be developed and that it be varied according to different H & Y stages, in order to improve QoL.

• The Korean Journal of Pain
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• 제30권1호
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• pp.51-58
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• 2017

Background: Recently symptoms-based screening questionnaires have gained attention for screening for a neuropathic pain component (NePC) in various chronic pain conditions. The present study assessed the usefulness of four commonly used NePC screening questionnaires including the Self-completed douleur neuropathique 4 (S-DN4), the ID Pain, the painDETECT questionnaire (PDQ), and the Self-completed Leeds Assessment of neuropathic Symptoms and Signs (S-LANSS) questionnaire in patients with chronic low back pain (CLBP) to assess the presence of NePC. Methods: This is a single-center cross-sectional study where patients with CLBP, with or without leg pain, were included. Participants were initially screened for NePC presence by a physician according to the regular practice, and later assessed using screening questionnaires. The diagnostic accuracy of these questionnaires was compared assuming the physician-made diagnosis as the gold standard. Results: A total of 215 patients with CLBP of which 164 (76.3%, 95% CI, 70.2-81.5) had a NePC were included. S-DN4, ID Pain, and PDQ have an area under the curve (AUC) > 0.8 indicating excellent discrimination. However, S-LANSS has an AUC of 0.69 (0.62-0.75), indicating low discrimination. S-DN4 has a significantly higher AUC as compared to ID Pain (d(AUC) = 0.063, P < 0.01) and S-LANSS (d(AUC) = 0.197, P < 0.01). But the AUC of S-DN4 does not significantly differ from that of PDQ (d(AUC) = 0.013, P = 0.62). Conclusions: S-DN4, ID Pain, and PDQ, but not S-LANSS, have good discriminant validity to screen for NePCs in patients with CLBP. Despite using all the tests, 20-30% of patients with an NePC were missed. Thus, these questionnaires can only be used as an initial clue in screening for NePCs, but do not replace clinical judgment.

• 한국CDE학회논문집
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• 제10권4호
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• pp.274-283
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• 2005

Product data quality (PDQ) is a real and significant issue in today's manufacturing environment. In the Korean automotive industry, much of the design work takes place with the support of software tools, such as CAD systems. Although many designers frequently encounter quality problems regarding product data, there is no investigation into the present state of CAD usage and PDQ activities before. The Korean automotive industry is responsible for about 11.1 percent of the total value of manufactured goods in Korea and 7.9 percent of employment in manufacturing. A study performed by the Research Triangle Institute showed that imperfect interoperability imposes at least $\$1$ billion per year on the members of the U.S. automotive supply chain. The trends toward concurrent engineering and out-sourcing have elevated the importance of high-quality product data and efficient product data exchange. This paper shows the results from a survey of PDQ conducted on seven 1st tiers among members of the Korean automotive supply chain.

• 한국자동차공학회논문집
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• 제13권1호
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• pp.184-193
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• 2005

Digital representations of products and parts have largely replaced physical drawings as the form in which product data are stored, analyzed, and communicated among the people contributing to the design of an automobile. Many individuals and companies participate in the design of an increasingly complex automobile; hence, the design process depends critically on team members' ability to share information about essential design elements. These trends have elevated the importance of the quality of product data and its efficient exchange. In this paper, we show state-of-the-art on Product Data Quality(PDQ), and activities of PDQ assurance. And we propose a novel design history-based approach for diagnosis and healing of a CAD model.

• 재활치료과학
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• 제8권1호
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• pp.73-84
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• 2019

목적: 파킨슨병 환자를 위해 개발된 표준화된 운동프로그램과 작업기반의 활동으로 구성된 Lee Silverman Voice Treatment (LSVT) BIG 치료 프로그램을 지역사회에 거주하는 파킨슨병 환자에게 제공한 후 파킨슨병 환자의 운동기능과 삶의 질에 어떠한 영향을 미치는 지를 알아보고자 하였다. 연구방법: 본 연구는 단일군 전후실험설계(one-group pretest and post test design)를 사용하였다. 치료 전 후에는 통합형 파킨슨병 평가척도(Unified Parkinson's Disease Rating Scale-III: UPDRS-III), Time up and go(TUG), 파킨슨 질병 검사지(Parkinson's Disease Questionnaire-39: PDQ-39)을 사용하여 운동기능 및 삶의 질의 변화를 측정하였다. LSVT-BIG치료는 프로토콜에 의거하여 매일 1회 주4일 60분간 실시하여 대상자별로 총 16회기를 실시하였다. 결과분석은 그래프를 통한 시각적 분석과 치료 전 후 측정값의 변화를 비교하였다. 결과: 치료 전 후로 UPDRS, TUG에서 모든 대상자들의 수행능력이 향상되었다. 또한, PDQ-39의 감소로 치료 후 모든 대상자들의 삶의 질 또한 긍정적으로 향상되었다. 결론: 지역사회 내에서 거주하는 파킨슨병 환자에게 LSVT-BIG 치료의 적용은 파킨슨환자의 운동기능 증진 및 삶의 질 증진에 긍정적인 영향을 주었다.

• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2009년도 춘계학술대회 논문집
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• pp.23-24
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• 2009

• 한국정밀공학회:학술대회논문집
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• 한국정밀공학회 2008년도 춘계학술대회 논문집
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• pp.901-902
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• 2008

• Clinical Psychopharmacology and Neuroscience
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• 제16권4호
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• pp.461-468
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• 2018

Objective: Cognitive disturbance is one of the major symptoms of depression and may be improved by treatment with antidepressants. This study aimed to investigate the predictors of cognitive improvement in patients with major depressive disorder (MDD) who were taking antidepressants. Methods: This study included 86 patients with MDD who completed 12 weeks of antidepressant monotherapy. Cognitive symptoms were assessed using the Perceived Deficits Questionnaire-Korean version (PDQ-K), which addresses four domains of cognitive functioning (attention/concentration, retrospective memory, prospective memory, and organization/planning) and was administered at study entry and at the 12-week end point. A variety of demographic, clinical, and treatment-related variables were evaluated as predictors of changes in total and domain scores. Results: All PDQ-K domains showed significant improvement after 12 weeks of antidepressant treatment. More severe initial depressive symptoms, fewer sick-leave days at study entry, and reduced use of concomitant anxiolytics/hypnotics during treatment were significantly associated with greater cognitive improvement. Conclusion: Cognitive symptoms are more responsive to antidepressant treatment in patients with severe MDD. Reduced use of anxiolytics and hypnotics could improve the cognitive functioning of patients with MDD taking antidepressants.

• 지역사회간호학회지
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• 제33권1호
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• pp.105-113
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• 2022

Purpose: The purpose of this study is to explore the roles and function of family in mediating the relationship between depression and quality of life of patients with Parkinson's disease (PD). Most studies have found that depression is particularly common in patients with PD and further associated with poor quality of life. Family function, as a mediator, is based on a strength orientation perspective that emphasizes not only their responsibilities and risks but also recuperative powers and growth potential. Methods: Overall 157 adults with idiopathic Parkinson's disease were enrolled in this study via outpatient clinic and completed a set of assessment to measure depression using BDI, family APGAR questionnaire, and patients' quality of life using PDQ-8. Hierarchical multiple regression analysis was conducted to examine the mediating role of family APGAR score in the relationship between BDI and PDQ-8. Results: Patients' depression, gait disturbance, duration of illness, and family function were statistically significant on quality of life. These factors accounted for 60% of the variance in quality of life. Family function has a partial mediating effect on the relationship between depression and quality of life. Conclusion: Findings from the study suggest that although PD patients' depression impacts their quality of life, by having strong family function, the extent to which depression impacts the quality of life can be favorably mitigated. Additionally, these outcomes have important implications for future model development regarding PD patients.