1.Mental Health Conditions of Nurses in Acute Care Hospitals
Junna KUNII ; Tomomi NOMURA ; Yuko TAKAYAMA ; Yoshiko SERA
Journal of the Japanese Association of Rural Medicine 2017;66(1):27-37
This study sought to analyze the conditions of nurses in acute care hospitals struggling with mental health issues. We administered a questionnaire survey to 204 nurses and analyzed 163 valid responses. A total of 81 conditions related to the working environment and 35 conditions related to interpersonal relations were identified. Conditions related to the working environment included working overtime beyond regular workhours, feelings of stress due to assignments, frequency of night shifts, stress in new environments, mistakes made on the job, worries about assigned positions, worries about work procedures, inability to take public and paid holidays, balance between work and raising children, heavy burden of responsibility, loss of confidence, flashbacks to occasions of past stress, trauma, and poor quality of nursing care. Conditions related to interpersonal relations included stress due to pressure from superiors and co-workers, attitude of senior colleagues, stress from senior colleagues, verbal abuse from superiors, behavior of doctors, negative feelings toward patients, changes in department assignments after maternity leave, verbal abuse from co-workers, verbal abuse from senior colleagues, neglect of duties by chief nurses, attitude of juniors, cooperation with other departments, and training of juniors. There were more statements about conditions related to the working environment than to interpersonal relations.
2.End of life care of persons with amyotrophic lateral sclerosis in hospice
Shuichi Kato ; Eisuke Ozawa ; Munehiro Shimada ; Jun Kurokawa ; Takahito Nishida ; Yoshiko Kasahara ; Keiko Takahashi ; Tomoko Ashiya ; Yoshiko Sugasawa ; Mayuko Nomura
Palliative Care Research 2010;5(2):137-144
This article describes the end of life of seven people with amyotrophic lateral sclerosis (ALS) under the care of a hospice. The reasons for admission to hospice were for the management of distressing symptoms and the support of families who were unable to continue care at home because of the increased burden of care and/or illness of families. The sufferings experienced by the patients with ALS included disability due to muscle weakness(100%), pain(100%), discomfort (100%), dyspnea (71%), difficulties in communication (71%), drooling (43%), insomnia (43%), loneliness (43%), swallowing difficulties (28%), clenching the mucosa inside the cheek (28%), anxiety (28%), the perception of being a burden to the family (28%), and concerns as to why they had developed ALS (28%). Opioid medication was effective in the management of dyspnea, pain and discomfort. The results showed that special attention should be paid to frequent changing of the patient's position during nursing care, including the passive movement of joints and massage. The use of communication aids was essential to allow people with ALS to communicate effectively and, together with support of joy of the patients and family, the quality of life could be improved. End of life care within a hospice is a useful alternative option for persons with ALS, extending hospice care in Japan from people with advanced cancer to other disease groups. Palliat Care Res 2010; 5(2): 137-143
3.Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
Priya JAGOTA ; Yoshikazu UGAWA ; Zakiyah ALDAAJANI ; Norlinah Mohamed IBRAHIM ; Hiroyuki ISHIURA ; Yoshiko NOMURA ; Shoji TSUJI ; Cid DIESTA ; Nobutaka HATTORI ; Osamu ONODERA ; Saeed BOHLEGA ; Amir AL-DIN ; Shen-Yang LIM ; Jee-Young LEE ; Beomseok JEON ; Pramod Kumar PAL ; Huifang SHANG ; Shinsuke FUJIOKA ; Prashanth Lingappa KUKKLE ; Onanong PHOKAEWVARANGKUL ; Chin-Hsien LIN ; Cholpon SHAMBETOVA ; Roongroj BHIDAYASIRI
Journal of Movement Disorders 2023;16(3):231-247
Clinical case studies and reporting are important to the discovery of new disorders and the advancement of medical sciences. Both clinicians and basic scientists play equally important roles leading to treatment discoveries for both cures and symptoms. In the field of movement disorders, exceptional observation of patients from clinicians is imperative, not just for phenomenology but also for the variable occurrences of these disorders, along with other signs and symptoms, throughout the day and the disease course. The Movement Disorders in Asia Task Force (TF) was formed to help enhance and promote collaboration and research on movement disorders within the region. As a start, the TF has reviewed the original studies of the movement disorders that were preliminarily described in the region. These include nine disorders that were first described in Asia: Segawa disease, PARK-Parkin, X-linked dystonia-parkinsonism, dentatorubral-pallidoluysian atrophy, Woodhouse-Sakati syndrome, benign adult familial myoclonic epilepsy, Kufor-Rakeb disease, tremulous dystonia associated with mutation of the calmodulin-binding transcription activator 2 gene, and paroxysmal kinesigenic dyskinesia. We hope that the information provided will honor the original researchers and help us learn and understand how earlier neurologists and basic scientists together discovered new disorders and made advances in the field, which impact us all to this day.