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1.
Journal of Korean Academy of Fundamental Nursing ; : 345-358, 2013.
Artigo em Coreano | WPRIM | ID: wpr-646113

RESUMO

PURPOSE: The purpose of this study was to develop a protocol that would help prevent accidents, apply physical restraints properly, and reduce the use of physical restraints in nursing homes. METHOD: A review of the literature and analysis of existing statutes and regulations were used to develop the preliminary protocol. To test the validity of this preliminary protocol, ten experts were selected from academia and clinical practice to review the protocol. The initial protocol was finalized after it had been reviewed by experts and tested for clinical validity in five different nursing homes. RESULT: The protocol consists of objectives, definitions and accident probability assessment, principle of using physical restraints, monitoring and documentation of physical restraints. CONCLUSION: The findings of this study can be used as guidelines to focus on preventing accidents arising out of use of physical restraints, assessing the probability of accidents, and reducing the use of physical restraints through preventive interventions. This will be helpful to prevent ethical, physical, or psychological problems arising from use of physical restraints and to protect the rights of elderly people in nursing homes.


Assuntos
Idoso , Humanos , Direitos Humanos , Casas de Saúde , Enfermagem , Restrição Física , Controle Social Formal
2.
The Korean Journal of Critical Care Medicine ; : 47-50, 2009.
Artigo em Coreano | WPRIM | ID: wpr-650242

RESUMO

Cerebral venous sinus thrombosis (CVT) is a rare disease that's associated with a wide variety of clinical signs and symptoms, and CVT is a potentially lethal condition. Iron deficiency anemia (IDA) as the cause of an adult case of CVT is very rare. We report here on a patient with CVT with intracerebral hemorrhage that was caused by IDA, and the patient was treated with hemodilution. We suggest that hemodilution should be considered as another therapeutic option for CVT with cerebral hemorrhage in a patient suffering with IDA.


Assuntos
Adulto , Humanos , Anemia Ferropriva , Hemorragia Cerebral , Hemodiluição , Ferro , Doenças Raras , Trombose dos Seios Intracranianos , Estresse Psicológico , Trombose Venosa
3.
Journal of the Korean Neurological Association ; : 264-267, 2009.
Artigo em Coreano | WPRIM | ID: wpr-185556

RESUMO

Central pontine myelinolysis (CPM) is a neurologic disorder that is usually related to rapid correction of hyponatremia and chronic alcoholism. CPM involves concentrated, symmetric, noninflammatory demyelination within the central pons; this pathology also occurs in extrapontine regions. Frequently observed clinical manifestations are sudden weakness, dysphagia, dysarthria, loss of consciousness, and locked-in syndrome. We describe herein a case of CPM predominated by cerebellar signs without typical symptoms, but with involvement of the cerebellum or cerebellar peduncle.


Assuntos
Alcoolismo , Ataxia Cerebelar , Cerebelo , Transtornos de Deglutição , Doenças Desmielinizantes , Disartria , Hiponatremia , Mielinólise Central da Ponte , Doenças do Sistema Nervoso , Quadriplegia , Inconsciência
4.
Journal of the Korean Neurological Association ; : 282-285, 2009.
Artigo em Coreano | WPRIM | ID: wpr-185551

RESUMO

Dural carotid-cavernous fistula (CCF) is characterized by arteriovenous communications between the meningeal branches of the internal or external carotid arteries and the cavernous sinus. Although the triad of chemosis, proptosis, and ocular bruit has been regarded as a classic sign of CCF, dural CCF often lacks these features. Dural CCF is a rare cause of ophthalmoplegia, and so it may be overlooked when the classic symptoms are absent. We report herein a case of bilateral dural CCF that presented as unilateral isolated abducens nerve palsy.


Assuntos
Nervo Abducente , Doenças do Nervo Abducente , Artéria Carótida Externa , Seio Cavernoso , Cavernas , Diplopia , Exoftalmia , Fístula , Oftalmoplegia
5.
Journal of the Korean Balance Society ; : 234-236, 2007.
Artigo em Coreano | WPRIM | ID: wpr-128480

RESUMO

The idiopathic hypereosinophilic syndrome (IHES) is a heterogenous spectrum of disorders, characterized by a long lasting hypereosinophilia without identifiable underlying cause and by the presence of various end-organ dysfunction. The neurologic manifestations of IHES can be encephalopathy, organic psycho syndrome and polyneuropathy and in rare cases polymyositis. Central nervous system involvement is the second mostclinically important complication of the hypereosinophilic syndrome as it is associated with chronic disability and a poor prognosis. In this report, we describe two patients of IHES who presented anisolated third nerve palsy with pupillary involvement and were improved by corticosteroid therapy. They satisfied the criteria of IHES and the third cranial nerve was the only site of neurologic involvement. Early recognition of neurologic involvement in IHES and prompt treatment could lead to good outcome


Assuntos
Humanos , Sistema Nervoso Central , Síndrome Hipereosinofílica , Manifestações Neurológicas , Nervo Oculomotor , Doenças do Nervo Oculomotor , Polimiosite , Polineuropatias , Prognóstico
6.
Korean Journal of Aerospace and Environmental Medicine ; : 369-378, 1998.
Artigo em Coreano | WPRIM | ID: wpr-75236

RESUMO

No abstract available.


Assuntos
Dípteros
7.
Korean Journal of Aerospace and Environmental Medicine ; : 255-261, 1998.
Artigo em Coreano | WPRIM | ID: wpr-23168

RESUMO

No abstract available.


Assuntos
Suporte Vital Cardíaco Avançado
8.
Annals of Dermatology ; : 215-218, 1997.
Artigo em Inglês | WPRIM | ID: wpr-70671

RESUMO

Blueberry muffin rashes occur in various diseases including TORCH syndrome, transfusion reactions, leukemia, hereditary spherocytosis and neonatal sepsis. We report a case of congenital CMV(cytomegalovirus) infection showing blueberry muffin skin lesions which revealed dermal erythropoiesis. Even though these cutaneous findings were nonspecific, they could provide a valuable clue in approach the congenital viral infection in the perinatal period.


Assuntos
Mirtilos Azuis (Planta) , Eritropoese , Exantema , Leucemia , Sepse , Pele , Reação Transfusional
9.
Annals of Dermatology ; : 188-190, 1997.
Artigo em Inglês | WPRIM | ID: wpr-87319

RESUMO

Congenital absence of nails usually occur as a rare isolated anomaly or combined with other ectodermal defects. This anomaly is regarded as an inherited disorder either dominantly or recessively but quite a few cases were reported as sporadically developed. The patient was a 2-month-old girl who had no nails on both her 2nd, 3rd toes but had rudimentary nails on her left big toe and both 4th toes at birth. We could not find any other congenital deformity, any family history of inherited diseases related to anonychia. Radiological findings revealed no visualization of both 4th distal phalanges, only. We report this case as congenital anonychia of a sporadic type which may have developed independently from an underlying bone abnormality. We also review other reported cases in the literature.


Assuntos
Feminino , Humanos , Lactente , Anormalidades Congênitas , Ectoderma , Hallux , Parto , Dedos do Pé
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