• Asian Pacific Journal of Cancer Prevention
• /
• 제15권14호
• /
• pp.5927-5936
• /
• 2014

Introduction: Breast cancer is the most common cancer among Jordanians. Breast cancer patients suffer from several negative consequences after treatment and these include pain, fatigue, sexual problems, appearance and body image concerns, with psychological dysfunction. This could affect the patient quality of life and psychological well-being. To the best of our knowledge, there is no published quantitative data on the quality of life and psychological well-being of breast cancer patients in Jordan. The objective of this study was to obtain such data and assess predictors with calculated scores. Methods: In this cross-sectional study conducted among breast cancer patients in Jordan diagnosed in 2009 and 2010, assessment was performed using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30), the Breast Module (QLQ-BR23) and the Hospital Anxiety and Depression Scale (HADS). Clinical, demographic and psychosocial indicators that could predict patient quality of life scores were collected. Results: The number of patients interviewed was 236 (mean age=$50.7{\pm}10.7$ years). The mean Global Health score for the QLQ-C30 was $63.7{\pm}20.2$ SD. Among functional scales, "social functioning" scored the highest ($mean=78.1{\pm}28.6$ SD), whereas "emotional functioning" scored the lowest ($mean=59.0{\pm}SD\;33.5$). For the QLQ-BR23, the worst scores within the functional scales were for "body image" ($mean=52.1{\pm}36.8$ SD) and "future perspective" ($mean=52.9{\pm}38.5$ SD). The worst symptom was "upset by hair loss" ($mean=69.8{\pm}43.0$). The mean HADS scores was $18.{\pm}9.0$ SD. Out of study participants, 53% scored abnormal on the anxiety scale and 45% on the depression scale. Severe depression and severe anxiety were detected among 8% and 14% of study participants, respectively. Statistically significant predictors for individual scores were similar to those reported in published studies, such as the presence of recurrence since baseline, family history of cancer, low educational status, current social problems, extent of the disease, presence of financial difficulties, and employment status. Conclusions and Recommendations: Breast cancer survivors in Jordan have overall good quality of life scores when compared with patients from Western countries. However, their psychological wellbeing is more impaired. There is an urgent need for psychosocial support programs and psychological screening and consultation for breast cancer patients at hospitals of the Ministry of Health in Jordan.

• Journal of the Korean Academy of Child and Adolescent Psychiatry
• /
• 제16권2호
• /
• pp.160-172
• /
• 2005

ADHD는 소아정신질환 가운데 가장 흔한 신경발달학적 질환으로 간주되고 있다. ADHD의 원인은 아직 명확하게 밝혀지지는 않았지만 다양한 유전적 및 신경학적 요인들이 관여하는 것은 틀림없고, 이들이 신경계의 특정 부위와 경로에 이상을 초래하는 것으로 알려져 있다. 이 논문에서는 최근의 연구들을 중심으로 ADHD의 원인과 관련한 신경발달학적 측면을 고찰하고자 한다. 방법은 Medline검색을 통해 최근 발표된 논문들, ADHD관련 단행본, ADHD를 특집으로 한 몇 개의 잡지에 실린 종설 논문들 및 연관 참고문헌 등을 토대로 조사하였다. 결과는 ADHD의 신경발달학적 측면에서 일부 유전적인 요인과 임신 및 출생전후의 환경적 요인 등이 복합적으로 작용하여 발달하는 뇌를 변형시킴으로서 주로 대뇌의 prefrontal cortex-striatal network를 구조적으로 혹은 기능적으로 저하되어 발생하는 것으로 생각할 수 있다. 임신 2기에 ADHD의 발생과 관련한 대뇌 및 소뇌 이상을 초래한다는 주장을 하기도 하였으며, 이들 이상은 더 이상 진행하지 않고 고정된 것이라는 주장도 있지만, ADHD의 원인과 관련하여 신경발달학적으로 어떤 시기에, 어떤 손상이나 영향에 의해, 어떤 이상이 초래하여 발생하는지에 대해서는 아직 연구가 매우 부족하다. 결론적으로 주의력 체계와 관련한 신경전달회로의 차이, 도파민계와 노에피네프린계의 기능이나 증상과 관련한 차이 등 을 포함하여 신경발달학적인 면에 대한 보다 심도 있는 연구들이 시행되어야 할 것이다.

• 정신신체의학
• /
• 제2권1호
• /
• pp.3-9
• /
• 1994

암의 원인, 과정 및 예후와 심리적 특성 또는 행동변인들(behavioral variables) 사이에 연관성이 있는지, 있다면 어떻게 영향을 미치는지 아직 결정적인 증거는 제시되지 않고 있다. 이에 대해서는 동질(homogeneous)집단을 대상으로 치밀하게 고안된 전향적 (well-designed, prospective) 연구계획을 통하여 장기간의 추적조사가 필요할 것으로 생각된다. 또한 암환자에서 나타나는 정신과적 문제에 신속하게 대처하기 위하여 종양전문의와 정신과 의사간의 긴밀한 자문체계가 수립되어야 할 것이다. 정신종양학 분야에서 정신과 의사의 역할과 연구의 촛점은 다음과 같이 될 수 있다. 1. 암 예방: 원인적 측면에서 암의 발생과 연관되는 것으로 알려진 정신사회적, 요인들을 감소 또는 제거시키는 역할(예를 들면 스트레스, 흡연, 주정중독 등). 2. 암 치료: 1) 암의 각종 치료에서 환자의 순응(compliance)을 강화시켜 주는 역할. 2) 암환자에서 병발한 정신장애의 치료. 3) 암환자의 동통이나 오심 등의 치료. 4) 암환자의 삶의 질(quality of life)에 대한 지각을 향상시키도록 도와주는 역할. 3. 암 연구: 1) 암의 발생 또는 암환자의 생존에 영향을 미치는 정신사회적 요인들의 조사. 2) 심리반응 또는 정신사회적 요인들과 면역반응사이의 연관성 조사. 3) 암환자에서의 정신치료와 인지-행동치료의 효과규명. 4) 화학요법제 또는 방사선치료가 정신병리와 인지기능에 미치는 영향 조사 등.

• 대한한의학회지
• /
• 제41권2호
• /
• pp.80-95
• /
• 2020

Objectives: The purpose of this study is to assess the quality of the Journal of Korean medicine case reports. Methods: Case reports published in the Journal of Korean Medicine from January 2015 to March 2020 were selected by using Oriental Medicine Advanced Searching Integrated System (OASIS) and the journal search system of the Korean Medical Association (https://www.jkom.org). The quality of the case reports was assessed using the Consensus-based Clinical Case Reporting Guideline Development (CARE) guidelines. Results: 33 case reports were selected for the assessment. Based on the CARE guidelines, 61.54% of the case reports included necessary information, but the quality level was uneven. More than 60% of the reports were missing data regarding 'Discussion of the strengths and limitations in your approach to this case', 'Intervention adherence and tolerability', 'Timeline', 'Medical, family, and psychosocial history including relevant genetic information', 'Patient perspective or experience', 'Adverse and unanticipated events', 'Administration of intervention', and 'De-identified demographic information and other patient specific information'. In most reports of over 90%, data regarding 'Diagnostic challenges', 'Intervention adherence and tolerability', and 'Key word' were not included. Conclusions: Efforts are needed to improve the quality of case reports in the Journal of Korean Medicine, and it is necessary to develop appropriate guidelines for case reporting for the Journal of Korean Medicine. In addition, all articles submitted to the Journal of Korean Medicine are to be complied with submission instructions and CARE guidelines.

• 사상체질의학회지
• /
• 제30권2호
• /
• pp.28-41
• /
• 2018

Objectives The purpose of this study is to evaluate the quality of case reports about Sasang Constitutional Medicine(SCM). Methods Case reports published from March, 2015 to March, 2018 in Journal of SCM were identified by searching from Oriental Medicine Advanced Searching Integrated System(OASIS). We assessed the quality of reporting of them based on CAse REport (CARE) guideline. Results A total of 39 case reports were finally included for the assessment. Overall quality of reporting was acceptable because case report even less reporting items mentioned 70.4% of them. However, the quality level was uneven because the maximum report rate was 77.8 %, the minimum 44.4 %, and the median 66.7 % when rigorously assessed. More than 50% of 39 case reports did not report 6 items about intervention adherence and tolerability, Diagnostic challenges, patient's perspective on interventions, informed consent, timeline, and adverse events, and did not sufficiently report 4 items about inclusion of terms such as case reports or SCM in keyword, symptoms of patient in abstract, information such as occupation relevant with psychosocial history, and the rationale for conclusions. Conclusions Efforts to improve the quality of reporting in SCM, and to develop case reporting guidelines appropriate for SCM are required.

• 대한간호학회지
• /
• 제47권1호
• /
• pp.14-24
• /
• 2017

Purpose: The purpose of this study was to construct and test a hypothetical model of self-management in patients with hemodialysis based on the Self-Regulation Model and resource-coping perspective. Methods: Data were collected from 215 adults receiving hemodialysis in 17 local clinics and one tertiary hospital in 2016. The Hemodialysis Self-management Instrument, the Revised Illness Perception Questionnaire, Herth Hope Index and Multidimensional Scale of Perceived Social Support were used. The exogenous variable was social context; the endogenous variables were cognitive illness representation, hope, self-management behavior, and illness outcome. For data analysis, descriptive statistics, Pearson correlation analysis, factor analysis, and structural equation modeling were performed. Results: The hypothetical model with six paths showed a good fitness to the empirical data: GFI=.96, AGFI=.90, CFI=.95, RMSEA=.08, SRMR=.04. The factors that had an influence on self-management behavior were social context (${\beta}=.84$), hope and cognitive illness representation (${\beta}=.37$ and ${\beta}=.27$) explaining 92.4% of the variance. Self-management behavior mediated the relationship between psychosocial coping resources and illness outcome. Conclusion: This research specifies a more complete spectrum of the self-management process. It is important to recognize the array of clinical resources available to support patients' self-management. Healthcare providers can facilitate self-management through collaborative care and understanding the ideas and emotions that each patient has about the illness, and ultimately improve the health outcomes. This framework can be used to guide self-management intervention development and assure effective clinical assessment.

• Archives of Plastic Surgery
• /
• 제49권4호
• /
• pp.488-493
• /
• 2022

Background Currently, the BREAST-Q can effectively measure patient's satisfaction on the quality of life from the patient's perspective in relation to different type of breast reconstruction. However, evaluation of patient satisfaction and cosmetic outcomes in breast reconstruction may have potential to led bias. Methods To maximize the benefits of using BREAST-Q to evaluate clinical outcome, we performed comparative study focused on the correlation between postoperative BREAST-Q and cosmetic outcomes assessed by medical professionals. For the current analysis, we used three postoperative BREAST-Q scales (satisfaction with breast, psychosocial well-being, and sexual well-being). The Ten-Point Scale by Visser et al was applied to provide reproducible grading of the postoperative cosmetic outcomes of the breast. The system includes six subscales that measured overall aesthetic outcome, volume, shape, symmetry, scarring, and nipple-areolar complex. The photographic assessments were made by five medical professionals who were shown photographs on a computer screen in a random order. Obtained data were stored in Excel and evaluated by Spearman's correlations using SPSS Statistics. Results We enrolled 92 women in this study, 10 did not respond to all scales of postoperative BREAST-Q, the remaining 82 women had undergone breast reconstruction. The correlation between BREAST-Q score and aesthetic score measured by Ten-Point Scale for the three BREAST-Q scales all show positive values in Spearman's correlation coefficient. Conclusion A significant correlation without any bias observed was found between the patient's satisfaction measured by BREAST-Q after breast reconstruction and the medical expert's aesthetic evaluation.

• 사회복지연구
• /
• 제49권4호
• /
• pp.159-193
• /
• 2018

본 연구는 한부모 가족 발생 유형, 즉 사별, 이혼, 미혼 한부모의 삶의 어려움과 이를 극복하고 자립하는 과정, 자립의 과정에서 작용하는 강점을 비교 탐색하는 데 목적이 있다. 강점은 강점관점의 틀을 중심으로 개인, 환경적, 삶의 요소 차원으로 분석하였다. 세 유형의 한부모 가족의 자립 경험, 강점 자원의 공통점과 차이점을 살펴봄으로써, 자립에 도움이 될 수 있는 보편적 제반 조건들을 파악함과 동시에 각 유형의 독특성을 확인하는데 의의가 있다. 이를 위해 사별 4사례, 이혼 8사례, 미혼모 8사례로 총 20사례를 심층 면접하였다. 연구 결과, 세 유형 모두에게 자립은 하나의 완결된 사건이 아니며, 엄마로서 주어진 책임을 다하기 위하여 그 힘을 갖추어나가는 과정으로서의 자립을 의미하였다. 힘을 갖추는 것은 경제적 자립을 위한 힘을 갖는 것뿐 아니라 자신의 삶에 대한 수용, 통제감 갖기, 자기 개발을 통해 역량강화되며 심리사회적 힘을 갖는 것을 의미하였다. 이들의 자립 경험과 강점 분석을 통해 자립 과정에 중요한 공통 자원과 경험의 독특성, 차이점 등을 확인 할 수 있었다. 연구결과를 토대로 한부모 가족을 위한 서비스 전달체계의 기능과 제도적 지원에 대한 실천적 정책적 함의를 제시하였다.

• 사회복지연구
• /
• 제49권4호
• /
• pp.221-249
• /
• 2018

본 연구는 국가아동학대정보시스템 내 아동보호서비스에 연루된 학대발생가정 정보를 분석하여 아동보호서비스 관점에서 아동학대와 가정폭력의 중복발생을 살펴보았다. 국외연구들은 학대발생가정에서 가정폭력과 중복발생 비율이 상당히 높으며 학대발생 예방이나 서비스 제공에 있어 이 중복발생이 매우 중요한 지점이라고 지적하나 국내에 관련연구는 아직 많지 않고, 더욱이 아동보호서비스의 관점에서 중복발생을 논의한 연구는 거의 없다. 본 연구는 학대발생가정 내 가정 폭력 중복발생 실태와 중복발생가정의 특성을 분석하였고, 기존 이론과 실증연구에 기반하여 설정한 가정폭력과 아동학대 발생의 관계에 관한 가설들을 검증하였다. 분석결과, 아동보호서비스에 연루된 학대발생가정의 21.4%에서 가정폭력과의 중복발생이 관찰되었고, 중복발생 가정은 아동학대만 발생한 가정과 여러 측면에서 다른 특성을 보였다. 또한, 가정폭력과 아동학대 발생은 관련이 있었으나, 구체적인 관계의 양상은 학대 하위유형에 따라 차이를 보였다. 연구결과에 기반하여 아동학대 발생의 이론적 함의와 가정폭력 피해자 지원서비스와 아동보호서비스의 서비스 통합과 협력에 관한 정책적, 실천적 방안들을 논하였다.

• 모자간호학회지
• /
• 제2권1호
• /
• pp.70-86
• /
• 1992

What is the meaning of menopause experienced by urban Korean women? Nurses need an under standing of menopause as it is experienced by women themselves. Nursing needs to build knowledge of womens' health experiences. This phenomenological study examined what menopause means to modern Korean woman to build a structure of knowledge useful for practice to enhance the quality of life of women throughout this experience. Traditional definition of menopause according to physiological changes, as illness and more recently as psychosociocultural phenomena were examined along with the folk lore information generally available in the society A review of the research and scientific literature was done from the perspectives of four models including the medical model of menopause as disease, the psychosocial model as positive and negative behavioral responses to menopause, a feminist model of menopause as a time of rebirth and a nursing model of the changing patterns of meaning, rythms and transformation women experience through menopause. Van Kaam's method was used to analyse data audio-recorded during interviews by the investigator with 65 women, 40 to 60 years of agey whose confidentility was assured. Interpretation of the data was enhanced luther by consultation with professional colleugues and with informants. Four rhythmical patterns of process emerged : from suffering to comfort, from oppression to freedom from being a good wife and wise mother to becoming a woman and from a hard life to an abundant life. The detailed common elements making up each of the four patterns and definitions of each pattern were presented. Each pattern was discussed critically from the point of view of medical, psychosociocultural, womens' and nursing models. The structural definition of the synthesis of the four process patterns was stated as : in spite of suffering the middle-aged urban Korean woman find she is able to help herself to feel comfortable and to realize release as she moves from oppression to liberation and freedom from being a good wife and wise mother she experiences rebirth as a woman : she begins to live a profitable and valuable life : her life becomes one of transformed abundant living. The definition transcends the medical and phychosociocultural model to embody a nursing model. The analysis was critiqued by using Parse' Human Becomming theory of nursing because the emerging themes were process patterns. Parse' theory provides and explanation of the experience of menopause consistant with the data which enhances nursing understanding of womens' experience of menopause. Parse' practice methodology provide guidance for promoting womens' quality of life throughout the experience of menopause. Feminist analysis contributes valuable critique to nursing research, richly expanding the perspective from traditional approaches to promote understanding of the meaning of womens' health experiences.