• 제목/요약/키워드: Physically ill patients

검색결과 9건 처리시간 0.026초

내외과계 환자의 정신과 약물치료에서 약물-약물 상호작용 - 고려대학교 부속병원의 자문조정의 경험을 통하여 - (Drug-drug Interactions between Psychotropic Agents and Other Drugs in Physically Ill Patients - Experience of Consultation-liason in Korea University Hospital -)

  • 이민수;이헌정
    • 생물정신의학
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    • 제6권1호
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    • pp.49-66
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    • 1999
  • Polypharmacotherapy, both psychotropic and nonpsychotropic, is widespread in various situations including psychiatric hospitals and general hospitals. As the clinical practice of using more than one drug at a time increase, the clinician is faced with ever-increasing number of potential drug interactions. Although many interactions have little clinical significances, some may interfere with treatment or even be life-threatening. The objective of this review is evaluation for drug-drug interactions often encountered in psychiatric consultation. Drug interactions can be grouped into two principal subdivisions : pharmacokinetic and pharmacodynamic. These subgroups serve to focus attention on possible sites of interaction as a drug moves from the site of administration and absorption to its site of action. Pharmacokinetic processes are those that include transport to and from the receptor site and consist of absorption, distribution on body tissue, plasma protein binding, metabolism, and excretion. Pharmacodynamic interactions occur at biologically active sites. In psychiatric consultation, these two subdivisions of drug interactions between psychotropic drugs and other drugs are likely to happen. We gathered informations of the drugs used in physically ill patients who are consulted to psychiatric department in Korea University Hospital. And we reviewed the related literatures about the drug-drug interactions between psychotropic drugs and other drugs.

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Finding Meaning in Life Threatening Illness

  • Kim, Mira
    • Journal of Hospice and Palliative Care
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    • 제23권2호
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    • pp.39-43
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    • 2020
  • This paper aims to explore how to help terminally ill patients and their families find meaning in their suffering from the logotherapeutic perspective, which is the essence of palliative care. For this purpose, this paper examines the main concepts and principles of logotherapy, and specific approaches based on the logotherapeutic perspective to help terminally ill patients and their families find meaning in life are presented. Emphasizing the will to meaning as the primary motive to explain human behaviors and based on its unique perspective of the human being, which is called the dimensional ontology, logotherapy considers the human being to consist of the body, the mind, and the spirit. The dimensional ontology implies that the human being "has" the body and the mind, but the human being "is" the spirit itself. Therefore, even though a human being can be sick physically or psychologically, Accordingly, it is essential to help these patients realize that they are not their illnesses, but just have them, and to rise above themselves to reach out toward something meaningful or someone to love; despite their suffering, they can still do something meaningful, even in a small way. Above all, the most important thing for these patients is to acknowledge that they have already lived a meaningful life and to believe that their meaningful work has been safely preserved in the past and nothing can take it from them, for as spiritual beings, their lives have been meaningful unconditionally.

호스피스 병동에 입원한 말기 암환자의 통증에 영향을 미치는 요인 : 입원 경과 시점에 따른 분석 (Factors Influencing Pain with Terminally Ill Cancer Patients in Hospice Units)

  • 노유자;김남초;홍영선;용진선
    • 대한간호학회지
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    • 제31권2호
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    • pp.206-220
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    • 2001
  • The purpose of this study was to investigate the impact of depression, discomfort, spirituality, physical care, and opioid use on pain with terminally ill cancer patients residing in hospice units. The convenient sample of this study consisted of 41 terminally ill cancer patients at three hospice units in university affiliated hospitals. Patients were interviewed with structured questionnaires three times at predetermined intervals: admission to the hospice unit (Time 1), one week later (Time 2), and two weeks later (Time 3). The data was collected from January 1998 to January 1999 and was analyzed using ANOVA, Pearson correlation coefficient, and multivariate multiple regression. 1. The mean age of the participants was approximately 55 years old. In terms of diagnosis, lung cancer showed the highest frequency (19.5%), followed by stomach cancer and rectal cancer (17.1%). The motive of seeking hospice unit admission was control (72. 2%), followed by spiritual care (50%), and symptom relief (38.9%). 2. Regarding the type of pain felt, the highest pain frequency the participants experienced was deep pain (55%), followed by multiple pain (25%), intestinal pain (10%), then superficial (5%) and neurogenic pain (5%). For the level of pain measured by VAS, there was no significant difference among the three time points; Time 1 (5.04$\pm$2.21), Time 2 (4.82$\pm$2.58) and Time 3(4.73$\pm$2.51). 3. There was significant change seen in spirituality and physical care in each time interval. Namely, the longer the length of admission at the hospice unit, the higher the importance of spirituality (p=0.0001) and the more the physical care the participants received (p=0.01). The opioid use at the three time points showed the following frequencies : Time 1 (75.6%), Time 2 (85.4%) and Time 3 (75.6%). 4. Regarding factors influencing pain, the pain level was significantly affected by the depression level (p〈0.01) and the opioid use (p〈0.1). These results were the most significant at the two time points (Time 1 and Time 2). At Time 3 (two weeks later), the pain level was significantly affected by the depression level (p〈0.05) and the amount of physical care the participants received (p〈0.1). In conclusion, the terminally ill cancer patients had moderate pain, were generally depressed, and were treated with opioid analgesics. As approaching death, the patients received more physical care due to increased physical symptoms experienced and they had a higher perception of the importance of spirituality. Thus, health care professionals need to provide continuous care for each of them to die comfortably physically, psycho- logically, and spiritually.

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수면 무호흡증이 있는 양극성 장애 환자에서 급속 정온요법으로 인해 발생한 급성 호흡 장애 (Acute Respiratory Distress due to Rapid Tranquilization in a Bipolar Patient with Sleep Apnea)

  • 함병주;서용진;김린
    • 수면정신생리
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    • 제8권2호
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    • pp.144-147
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    • 2001
  • Chemical restraint or "rapid tranquilization" is another option in treating patients who are a danger to themselves or others and struggle violently once physically restrained. The most commonly used drugs are benzodiazepines and antipsychotics. The use of benzodiazepines, either alone or in combination with high potency neuroleptics, has increased in recent years. Benzodiazepines are extremely safe but may cause respiratory depression and hypotension. Respiratory depression is more likely with intravenous administration, therefore these medications should be given slowly and titrated to the desired effect. Special care should be taken when sedating patients who are under the influence of alcohol or narcotics and are sleep apneic patients. This report deals with a case of respiratory distress in a patient with sleep apnea syndrome after the rapid tranqulization. All patients receiving chemical restraint must be carefully monitored. For critically ill patients who require sedation or chemical restraint, the constant attendance of a physician may be warranted.

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신체질환이 있는 소아청소년의 정신신체의학적 관리-총론 (Psychosomatic Management of Medically Ill Children and Adolescents)

  • 이문수;조숙행
    • 정신신체의학
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    • 제16권1호
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    • pp.17-24
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    • 2008
  • 소아청소년에서의 정신신체의학은 자문조정 정신의학이라고도 불리며 신체적 질환이 있는 소아청소년에서의 정신건강 서비스를 제공하는 것으로, 정신과에서는 정신사회학적 질병모델에 익숙한 반면 타과 의료진의 경우 생의학적 질병모델에 입각하여 접근하기 때문에 원활한 의사소통을 통한 타과 의료진과의 협업 체계 구축이 중요하다. 신체질환이 있는 소아청소년의 정신과적 문제에 대해서는 개별 질환에 초점을 맞추고 의학적 심리적 정신과적 인자들의 상호작용과 그 영향을 밝히는 범주적 접근법과 질병에 걸렸다는 사실로 인하여 스트레스를 경험하는 아동 자체에 대한 접근에 주안점을 두는 비범주적 접근법으로 나눌 수 있다. 이러한 신체질환이 있는 소아청소년의 치료에 그들의 발달단계에 맞는 고유한 치료기법의 적용이 필요하다. 비약물학적인 치료의 경우 경험적으로 입증된 치료(empirically supportive therapy)들을 구분하려는 시도도 이루어지고 있다.

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정신장애인에 대한 사회편견 연구 (Social Stigma on People with Mental Disorder)

  • 양옥경
    • 한국사회복지학
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    • 제35권
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    • pp.231-261
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    • 1998
  • 본 연구는 일반인들의 정신장애인에 대한 편견적 태도 및 생각이 어느정도인가를 살펴보고자 하는데 목적을 둔 것으로 크게 3개 차원에서의 비교연구에 초점을 두었다. 하나는 인구사회학적 및 지역별 차이에 따른 일반인의 정신장애인에 대한 편견비교이며, 다른 하나는 지체장애인아 대한 편견과의 비교이며, 마지막 하나는 정신장애인, 그 가족, 그리고 전문가들의 편견과의 비교분석이다. 연구대상은 18세 이상의 성인으로, 일반인 300명, 정신장애인, 그 가족, 전문가 각 100명씩 총 600명이다. 표본은 우선 지역을 선점한 후 지역내 조사답변자를 선점하였다. 지역으로는 서울, 경산, 홍성이 선정되었고, 일반인은 무작위표집하였으며, 나머지는 각 지역의 병 의원을 통해 표집하였다. 자료수집에는 정신장애인 편견척도, 장애인 편견척도를 포함한 설문지를 활용하였다. 분석결과, 우리나라 일반인의 정신장애인에 대한 편견은 그다지 심하지 않은 것으로 나타났다. 한 인간으로서 이들을 수용하는 정도는 높았으나, 이들에게 '사회적응하여 사는 사람'으로 '사회인'으로서의 역할을 부여하는데 있어서는 아직까지 낮은 수용도를 보이고 있었다. 특히 병원에 입원한 정신장애인에 대한 부정적 인식이 컷으며, 사회봉사의 경험이 편견의 정도를 낮추는데 지대한 공헌을 하였다. 장애인에 대한 편견과의 비교에서는 격리치료에서는 정신장애인에게, 불임수술에서는 장애인에게 높은 편견적 태도를 보였다. 대도시에서의 편견은 낮은 반면, 중소도시와 군/읍단위에서의 편견은 항목별로 뚜렷한 차이를 보였다. 나이, 교육적도, 월수입에 따른 차이도 크게 보였다. 정신장애인들의 자기편견의 경우도 항목별 차이를 보이는 가운데 타인과의 관계속에서 이해되는 부분에 대한 편견이 높았다. 가족과 전문가에게서도 대체로 낮은 편견을 보이는 가운데 항목별 차이를 나타냈다. 이같은 결과는 특정편견에 긍정적, 부정적 영향을 미치는 요소들에 대해 전분가의 개입이 필요함을 드러내 준 것이다. 정신보건정책의 수립에 있어서도 입원치료중심의 정책이 아니라 지역사회에서 사회전체가 정신장애인들의 인권을 인정해주는 사회통합의 정책을 마련하여야 함도 시사해주고 있다고 하겠다.

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일 대학병원 내과계열 및 외과계열 외래 환자들의 항우울제에 대한 태도 및 인식에 대한 연구 (Comparison of Attitude Toward Antidepressants Between Medical and Surgical Group Outpatients in a Korean University Hospital)

  • 이상수;서정석;문석우;남범우
    • 정신신체의학
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    • 제16권1호
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    • pp.52-58
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    • 2008
  • 연구목적 : 항우울제는 정신과 의사뿐만 아니라 많은 비정신과 의사들에 의해 처방 되어지는 정신과 약물이다. 하지만 항우울제에 대해 부정적인 인식이 높은 게 현실이다. 따라서 본 연구는 대학병원 외래를 방문한 일반 환자군들을 대상으로 항우울제에 대한 전반적인 인식과 태도를 알아봄으로써, 항우울제 및 정신과 약물에 대한 사회적 편견 및 오해를 줄여 나가고, 지역사회 정신건강 발전에 도움이 되는 기초 자료로 삼고자 연구를 시행하였다. 방법 : 일 지역 대학병원에 내원한 내과계열 및 외과계열 외래 환자들 200명을 대상으로 정신과 전공의 2인 및 수련의가 외래 대기실에서 환자들을 면담하여 연구 목적을 설명하고, 항우울제에 대한 인식과 태도에 대해 평가하기 위하여 12문항으로 고안한 자가 보고형 설문지를 사용하였다. 결과 : 1) 내과 및 외과 계열 환자들 모두에서 항우울제에 대한 부정적인 인식이 매우 높았다. 2) 외과계열 외래 환자들이 내과 계열 환자들보다 항우울제 약물이 몸에 해롭다고 생각하는 비율이 더 높았다. 3) 항우울제 복용 경험이 없는 환자들이 항우울제에 대해서 부정적인 인식과 태도를 갖고 있었다. 4) 항우울제 복용 거부 이유로는 약물 부작용에 대한 두려움이 높았다. 결론 : 항우울제의 처방시 일반인들의 항우울제에 대한 부정적인 인식을 이해하고, 항우울제에 대해 근거있고 객관적인 사실을 설명하는 적극적인 노력이 더욱 필요하다.

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만성통증 환자의 통증 조절 (Chronic pain control in patients with rheumatoid arthritis)

  • 은영
    • 근관절건강학회지
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    • 제2권1호
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    • pp.17-40
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    • 1995
  • Rheumatoid arthritis is the one of the chronic diseases, one of its major symptoms is a chronic pain. Despite developing medical treatment and surgical techniques, it is suggested that to control the pain is the goal of the treatment. But pain is an inner experience and even those closest to the patient cannot truly observe its progress or share in its suffering. The National Academy of Sciences Institute of Medicine's report on Pain and Disability concluded that there is no objective measure of pain-(exactly) no pain thermometer-nor can there ever be one, because the experience of pain is inseparable from personal perception and social influence such as culture. To explore chronic pain experience is to understand the process and property of the patient's perception of pain through the response to pain, the coping with pain, and the adaptation to pain. Therefore a qualitative study was conducted in order to gain an understanding of pain experience of patients with RA in korea. I used naturalistic inquiry as a research methodology, which had 5 axioms, the first is that realities are multiple, constructed, and holistic, the second is that knower and known are interactive, inseparable, the third is only time and context bound working hypotheses(idiographic statements) are possible, the forth is all entities are in a state of mutual simultaneous shaping, so that it is impossible to distinguish causes from effects and the last is that inquiry is value-bound. Purposive sampling was conducted as a sampling. 20 subjects who experienced pain over 10 years, lived in middle-sized city and big city in Korea, and 17 women and 3 men. The subject's age was from 32 to 62 (average 48.8), all were married, living with their spouse and children, except two-one divorced and the other widow before they became ill. I collected data using In depth structured interview. I had interviews two or three times with each subject, and the interviews were conducted at each subject's home. Each interview lasted about two hours an average. A recording was taken with the consent of the subject. I used inductive data analysis-such as unitizing and categorizing. unitizing is a process of coding, whereby raw data are systematically transformed and aggregated into units. Categorizing is a process wherby previously unitized data are organized into categories that provide descriptive or inferential information about the context or setting from which the units were derived. This process is used constant comparative method. The pain controlling process is composed of behavior of pain control. The behaviors of pain control are rearranging of ADL, hiddening role conflict, balancing treatment, and changing social relation. Rearranging of ADL includes diet management, sleep management, and the adjustment of daily life activities. The subjects try to rearrange their daily activities by modified style of motions, rearranging time span & range of activities, using auxillary facilities, and getting help in order to keep on the pace of daily life. Hiddening role conflict means to reduce conflicts between sick role and their role as a family member. In this process, the subjects use two modes, one is to control the pain complaints, and the other is to internalize the value which is to stay home is good for caring her children and being a good mother. To control pain complaints is done by 'enduring', 'understanding' the other family members, or making them undersood in order to reduce pain. Balancing treatment is composed of two aspects. One is to keep the pain within the endurable level, the other is to keep in touch with medical personnel in order to get the information of treatment and emotional support. Changing social relation is made by information seeking and sharing, formation of mutual support relation, and finally simplification of social relationships. The subjects simplify their social relationships by refraining from relations with someone who makes them physically and psychologically strained. In particular the subjects are apt to avoid contact with in-laws, and the change of relation to in-laws results in lessening the family boundary. In the course of this process, they confront the crisis of family confict result in family dissolution. This crisis is related to the threat of self-existence. Findings from this study contribute to understanding the chronic pain experience. To advance this study, we should compare this result with other cases in different cultural contexts. I think to interpret these results, korean cultural background should be considered. Especially the different family concept, more broader family members and kinship network, and the traditional medical knowledge influences patients' behavior.

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광주시(光州市) 의료시설(醫療施設)의 입지(立地)와 주민(住民)의 효율적(效率的) 이용(利用) (The Location of Medical Facilities and Its Inhabitants' Efficient Utilization in Kwangju City)

  • 전경숙
    • 한국지역지리학회지
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    • 제3권2호
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    • pp.163-193
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    • 1997
  • 복지사회를 지향하는 오늘날, 건강 중진에 직접 관계되는 의료시설의 접근성 문제는 주요 과제이다. 특히 삶의 질이라는 측면에서 질병의 치료 외에 건강진단, 예방과 회복, 요양 및 응급서비스의 비중이 커지고, 인구의 노령화 현상이 진전되면서 의료시설의 효율적인 입지가 주 관심사로 대두되고 있다. 의료시설은 주민의 생존과 직접 관계되는 기본적이고도 필수적인 중심시설로, 지역 주민은 균등한 혜택을 받을 수 있어야 한다. 이를 실현시키기 위해서는 기본적으로는 효율성과 평등성을 기반으로 1차 진료기관이 균등 분포해야 한다. 이에 본 연구에서는, 광주시를 사례지역으로 선정하여 의료시설의 입지와 그에 대한 주민의 효율적 이용에 관하여 분석하였다. 분석에 있어서는 통계자료와 기존의 연구 성과 외에 설문 및 현지조사 자료를 기반으로 시설 측면과 이용자 측면을 동시에 고찰하였다. 우선 의료 환경의 변화 및 의료시설의 변화 과정을 고찰하고, 이어서 의료시설의 유형별 입지 특성과 주민의 분포 특성을 고려한 지역별 의료수준을 분석하였다. 그리고 유형별 의료시설의 이용행태와 그 요인을 구명한 후, 마지막으로 장래 이용 유형의 예측과 문제지역의 추출, 나아가서는 시설의 합리적인 입지와 경영 방향을 제시하였다. 본 연구 결과는, 앞으로 신설될 의료시설의 적정 입지에 관한 기본 자료로서는 물론 지역 주민의 불평등성 해소라는 응용적 측면에서 의의를 지닌다.

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