1.Duodenoduodenal Intussusception due to a Migrated Percutaneous Radiologic Gastrostomy Tube: A Case Report.
Ji Won HONG ; Sang Hun KIM ; Jin A YOON ; Myung Jun SHIN ; Yong Beom SHIN
Journal of the Korean Dysphagia Society 2019;9(1):50-53
Patients with dysphagia often have difficulty in supplying adequate nutrition orally, and thus they often use gastrostomy for nutrition support. If the nutrition affects the deterioration of the disease, as in amyotrophic lateral sclerosis, the majority of patients will have a gastrostomy tube for proper nutrition. To prevent complications from gastrostomy tubes, it is important to educate the caregiver or patient about how to properly manage it. If these patients opt for home care because of financial or cultural reasons, it will be difficult for their healthcare team to observe them closely, leading to complications due to lax tube management. In this case, appropriate management education becomes more important. This paper reports an extremely rare case of duodenal intussusception caused by a migrated percutaneous radiologic gastrostomy (PRG) tube in a patient with amyotrophic lateral sclerosis (ALS) using simultaneous oral and enteral nutrition. The patient was treated successfully with urgent tube removal using the air reduction maneuver. This case highlights the importance of gastrostomy management.
Amyotrophic Lateral Sclerosis
;
Caregivers
;
Deglutition Disorders
;
Education
;
Enteral Nutrition
;
Gastrostomy*
;
Home Care Services
;
Humans
;
Intussusception*
;
Motor Neuron Disease
;
Patient Care Team
2.Perceptions of Contraception and Patterns of Switching Contraceptive Methods Among Family-planning Acceptors in West Nusa Tenggara, Indonesia
Yuli AMRAN ; Narila Mutia NASIR ; Dini DACHLIA ; Fitra YELDA ; Budi UTOMO ; Iwan ARIAWAN ; Rita DAMAYANTI
Korean Journal of Preventive Medicine 2019;52(4):258-264
OBJECTIVES: The perceptions of family-planning (FP) acceptors regarding contraception influence the reasons for which they choose to switch their method of contraception. The objective of this study was to analyze the perceptions of contraception and rationales for switching contraceptive methods among female FP acceptors in West Nusa Tenggara, Indonesia. METHODS: This study involved the analysis of secondary data from the Improve Contraceptive Method Mix study, which was conducted in 2013 by the Center for Health Research, University of Indonesia. The design of the study was cross-sectional. We performed 3 stages of sampling using the cluster technique and selected 4819 women who were FP acceptors in West Nusa Tenggara Province, Indonesia as the subjects of this study. The data were analyzed using multiple logistic regression. RESULTS: The predominant pattern of switching contraceptive methods was switching from one non-long-term method of contraception to another. Only 31.0% of the acceptors reported a rational pattern of switching contraceptive methods given their age, number of children, and FP motivations. Perceptions of the side effects of contraceptive methods, the ease of contraceptive use, and the cost of the contraceptives were significantly associated (at the level of α=0.05) with rational patterns of switching contraceptive methods. CONCLUSIONS: Perceptions among FP-accepting women were found to play an important role in their patterns of switching contraceptive methods. Hence, fostering a better understanding of contraception through high-quality counseling is needed to improve perceptions and thereby to encourage rational, effective, and efficient contraceptive use.
Child
;
Contraception
;
Contraceptive Agents
;
Counseling
;
Family Planning Services
;
Female
;
Foster Home Care
;
Humans
;
Indonesia
;
Logistic Models
;
Methods
;
Patient Acceptance of Health Care
3.Health care perspectives on community care
Journal of the Korean Medical Association 2018;61(10):586-589
The Ministry of Health and Welfare announced a plan for community care in March 2018. Community care is a concept of social services that includes residential, welfare, and health care services, as well as direct care. It is a policy to actively prepare for an aged society. Various services must be developed for comprehensive community care. It is especially necessary to ensure that adequate resources are provided for home care and visiting care. To achieve this goal, the benefit policies of health insurance and long-term care insurance must be changed. Community service providers and infrastructure must be expanded, and a diverse professional workforce should be trained. Doctors need training and experience as team leaders, as they will be able to work with nurses, nutritionists, and social workers. It will be particularly important to operate clinics as group practices rather than as solo practices. Change is also needed in community hospitals, which must receive orientations regarding early patient discharge plans and community-centered collaboration. Hospitals should serve as health care safety nets, including short-term stays and same-day care. Regional governance is important for community care. Doctors must work with a variety of institutions, including community health centers, welfare centers, and elderly facilities. Medical professionals should prepare for and lead future social changes.
Aged
;
Community Health Centers
;
Community Health Services
;
Cooperative Behavior
;
Delivery of Health Care
;
Group Practice
;
Health Services for the Aged
;
Home Care Services
;
Hospitals, Community
;
Humans
;
Insurance, Health
;
Insurance, Long-Term Care
;
Nutritionists
;
Patient Discharge
;
Private Practice
;
Social Change
;
Social Welfare
;
Social Work
;
Social Workers
4.Nurses' Opinions of Patient Involvement in Relation to Patient-centered Care During Bedside Handovers.
Lee KHUAN ; Muhamad HANAFIAH JUNI
Asian Nursing Research 2017;11(3):216-222
PURPOSE: Advocates for societal change and consumerism have been instrumental in popularizing patient involvement in various aspects of health care. Patient involvement in bedside handovers during shift changes should facilitate patient-centered care. This study's purpose was to explore Malaysian nurses' opinions about patient involvement during bedside handovers, and whether patient involvement during bedside handovers reflected patient-centered care. METHODS: A qualitative study with four focus-group discussions was conducted with 20 registered nurses from general wards in a Malaysian public hospital. Semi-structured interviews were used to elicit participants' opinions. NVivo 10 software was used for data management and content analysis was used to analyze the data. RESULTS: Several participants used inconsistent methods to involve patients in bedside handovers and others did not involve the patients at all. The participants' interpretations of the concept of patient-centered care were ambiguous; they claimed that patient involvement during bedside handovers was impractical and, therefore, not reflective of patient-centered care. Some nurses' subjective views of patient involvement as impractical during bedside handovers were manifested in their deliberate exclusion of patients from the handover process. CONCLUSIONS: Changes in patient involvement and nursing practices congruent with patient-centered care require that nurse educators in hospital settings reform nursing education to focus on fostering of communication skills needed to function in nurse-patient partnerships. Guidelines for patient involvement consistent with patient-centered values should be developed using ward nurses' subjective views and introduced to all registered nurses in practice.
Delivery of Health Care
;
Education, Nursing
;
Focus Groups
;
Foster Home Care
;
Hospitals, Public
;
Humans
;
Nurses
;
Nursing
;
Patient Handoff
;
Patient Participation*
;
Patient-Centered Care*
;
Patients' Rooms
5.An Integrative Review of Home Care Service for Pregnant Women, Mothers, Infants, and Toddlers in Vulnerable Group.
Journal of Korean Academy of Nursing 2017;47(5):577-588
PURPOSE: This study was intended to integrate the evidence of home care service intervention for mothers and children in vulnerable groups through an integrative literature review. METHODS: We searched the MEDLINE (PubMED), EMBASE, Cochrane Central Register of Controlled Trials, CINAHL, DBpia databases. The quality of the articles was assessed by one doctoral researcher and verified by one professor of community health nursing who had participated in the systematic review of literature. A framework was developed to identify the intervention patterns in the selected papers and categorize various elements. The extracted intervention elements were grouped into potential themes, which were verified by assessors on whether they clearly reflected the interventions in the papers. RESULTS: Among 878 searched papers, we selected 16 papers after excluding literature that does not satisfy the selection criteria and quality evaluation. The intervention elements of 16 selected papers were categorized into six themes. The extracted intervention elements were divided into the themes of Patient-specific/Situation-specific care planning and intervention, Emphasis on self care competency, Intense home visit by developmental milestone, Reinforcing and modeling mother-child attachment, Communication and interaction across the intervention, Linkage with community resource and multidisciplinary approach. CONCLUSION: As a result of the analysis of proper interventions of home care services for mothers and children in vulnerable groups, it was found that it is necessary to consider indispensable intervention elements that can standardize the quality of home care services, and conduct studies on developing intervention programs based on the elements.
Child
;
Child, Preschool
;
Community Health Nursing
;
Female
;
Home Care Services*
;
House Calls
;
Humans
;
Infant*
;
Mothers*
;
Patient Selection
;
Pregnant Women*
;
Self Care
;
Vulnerable Populations
7.Analysis of Symptoms and Provided Services in Home-Based Cancer Patients.
Woo Jeong KIM ; Min Young KIM ; Weon Young CHANG
Asian Oncology Nursing 2013;13(2):67-75
PURPOSE: This study was to identify symptoms and provided services of home-based cancer patients in J province. METHODS: 1,350 data poins for 167 home-based cancer patients were analyzed retrospectively. 13 symptoms and 39 service items were measured by tools for home-based cancer patients suggested by the Ministry for Health, Welfare and Family Affairs. RESULTS: The mean number of provided services was 7.4+/-9.1. The most common symptoms were fatigue, anorexia, and pain. Patients whose duration after diagnosis was over 6 years, who had metastasis, or who underwent terminal care had more symptoms. Patient education, emotional and spiritual support, and basic assessment and services were provided most often. Frequency of provided services in patients whose duration after diagnosis was over 6 years or who had metastasis was higher. Services such as symptom and pain control, or death of the patient/the bereaved were provided with more support with patients who underwent terminal care. CONCLUSION: There were some differences in provided services according to medical characteristics. Patients experienced diverse symptoms, but services regarding these symptoms seemed to be insufficient. For more effective services, cooperation between organizations for home-based cancer patients is needed to form a better management model based on the merit of each facility or patient characteristics.
Anorexia
;
Fatigue
;
Home Care Services
;
Humans
;
Neoplasm Metastasis
;
Nursing Services
;
Patient Education as Topic
;
Retrospective Studies
;
Terminal Care
8.Clinical Features of Patients on Home Oxygen Therapy Due to Chronic Respiratory Failure at One University Hospital.
Kyoung Hee KIM ; Tae Yun PARK ; Eun Sun KIM ; Keun Bum CHUNG ; Sang Min LEE ; Jae Joon YIM ; Chul Gyu YOO ; Young Whan KIM ; Sung Koo HAN ; Seok Chul YANG
The Korean Journal of Internal Medicine 2012;27(3):311-316
BACKGROUND/AIMS: Home oxygen therapy (HOT) costs a great deal every year and demand for the service is growing. In Korea, health insurance has covered HOT since November 1, 2006. The objective of this study was to evaluate clinical features of patients who used long-term HOT due to chronic respiratory failure and to determine the appropriateness of oxygen prescriptions. METHODS: Between November 2006 and April 2010, patients prescribed long-term HOT were enrolled in the study at a tertiary university referral hospital and their medical records and telephone survey information were evaluated. In total, 340 patients were evaluated retrospectively. RESULTS: Regarding the initial indications for HOT, their mean PaO2 was 49.8 mmHg and mean SpO2 was 82.2%. Underlying diseases included chronic obstructive pulmonary disease (COPD, 19.8%), lung cancer (12.6%), and interstitial lung disease (11.2%). The admission rate within 1 year was 53.4% and the average number of admissions was 1.64/patient. Other underlying diseases for which oxygen was prescribed, despite not meeting the insurance coverage criteria, were lung cancer (36.6%) and interstitial pneumonia (16.6%). CONCLUSIONS: Home oxygen prescriptions have increased since health insurance coverage was extended. However, cases of oxygen prescriptions frequently do not meet the coverage criteria. It is important to discuss extending the coverage criteria to other disease groups, such as interstitial lung disease and lung cancer, in terms of cost-effectiveness. Further, physicians prescribing oxygen therapy should be educated regarding the criteria.
Adult
;
Aged
;
Aged, 80 and over
;
Cause of Death
;
Chronic Disease
;
Eligibility Determination
;
Emergency Service, Hospital
;
Female
;
*Home Care Services, Hospital-Based
;
Hospitalization
;
*Hospitals, University
;
Humans
;
Insurance Coverage
;
Insurance, Health
;
Kaplan-Meier Estimate
;
Male
;
Middle Aged
;
*Oxygen Inhalation Therapy
;
Patient Compliance
;
Program Evaluation
;
Republic of Korea
;
Respiratory Insufficiency/diagnosis/etiology/mortality/*therapy
;
Retrospective Studies
;
Time Factors
;
Treatment Outcome
;
Young Adult
9.Needs Assessment for the Beneficiaries of Home-Based Cancer Patients Management Project.
Ju Hyung LEE ; Jung Im PARK ; Ji Hoon KANG ; Jung Ho YOUM ; Dai Ha KOH ; Keun Sang KWON
Journal of Agricultural Medicine & Community Health 2011;36(4):238-250
OBJECTIVES: This study was performed to investigate the service needs of the beneficiaries who had enrolled in home-based management programs for cancer patients. METHODS: From March to May 2009, 676 cancer patients who were registered in home-based cancer patient management programs were selected as subjects for this study. The data were collected using a questionnaire along with a face-to-face interview performed by officers in charge of the home-based care programs of 47 regional health centers. Fifteen patients were excluded due to incomplete data, leaving 661 subjects who were ultimately enrolled in the study. RESULTS: The mean age of subjects was 64.0 +/- 12.5 years, and males comprised 45.1% (298/661) of the sample. The results of factor analysis for service needs showed that there were five main categories and Cronbach's alpha ranged from 0.593 to 0.890 for each factor. The service needs categories in order of importance were social support, information and education, psychological problems, physical symptoms and household chores. The service needs scores were significantly different when subjects were stratified by age, habitation, religion and disease classification. When we divided the subjects into complete remission, under treatment and terminally ill groups, the needs scores of the terminally ill patient group were significantly higher than those of the other groups (p<0.001). CONCLUSIONS: Service provision based on patient and beneficiary needs could be an effective intervention to reduce the economic burden of cancer management and to improve the quality of life of cancer patients receiving home-based care. Therefore, it is recommended that individual cancer patient care programs be developed and administered according to patient age, habitation and disease severity.
Family Characteristics
;
Fees and Charges
;
Home Care Services
;
Humans
;
Male
;
Needs Assessment
;
Patient Care
;
Quality of Life
;
Terminally Ill
;
Surveys and Questionnaires
10.An Analysis of the Meaning of Respite for Family Caregivers of Elderly with Dementia.
Mi Ryeong SONG ; Yong Mi LEE ; Suk Hee CHEON
Journal of Korean Academy of Nursing 2010;40(4):482-492
PURPOSE: This study was a qualitative research study in which focus group interviews were used to collect data on the meaning of respite for family caregivers who are taking care of elders with dementia. METHODS: The focus group interviews and participants consisted of 2 family caregiver groups, for a total of 8 people taking care of their elders and 5 professional caregivers working in a geriatrics hospital or social welfare institutions. Content analysis was used and debriefing notes were referred in order to analyze the data. RESULTS: The meaning of respite in this research was measured using 4 main categories: 'Temporary break from routine', 'direct help', 'psychological comfort', 'valuables which cannot be taken easily' and 9 subcategories: 'Temporary diversion of attention', 'temporarily free from my duty', 'taking care of oneself', 'receiving economic help', 'empathize with others', 'comfort based on trust', 'resting together with the elder', 'no time to rest', 'cannot get out of one's obligatory duty'. CONCLUSION: The findings of the study show that rest means not only a temporary relief from caretaking, but also a real respite based on the patients' stable state and comfort. These results indicate a new meaning for respite, that the first step of respite program has to begin even when the caregivers do not recognize the need for respite.
Adult
;
Aged
;
Caregivers/*psychology
;
Dementia/*nursing
;
Family
;
Female
;
Geriatric Nursing
;
Home Nursing
;
Humans
;
Interviews as Topic
;
Male
;
Middle Aged
;
Nurse-Patient Relations
;
*Respite Care

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