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1.
Eur J Oncol Nurs ; 48: 101802, 2020 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-32942231

RESUMO

PURPOSE: Extravasation incidence is exceptionally low; however, ulceration or necrosis occurs in severe cases, possibly requiring surgical treatment. Early extravasation signs and symptoms are not always evident on treatment day, and inflammation, which leads to ulceration or necrosis, may appear several days later. Therefore, to minimize damage, identification of high-risk groups is required. This study aims to investigate the relationship between subcutaneous edema which is an early extravasation sign, and skin surface temperature using a thermosensitive liquid crystal film. METHODS: Patients receiving chemotherapy through a peripheral intravenous catheter were recruited. Subcutaneous tissue around the catheterization site was observed for the presence of subcutaneous edema by ultrasonography. During chemotherapy initiation, a thermosensitive liquid crystal film was placed on the catheterization site. Color changes of the film were observed, and each case was classified according to low-temperature distribution patterns. To investigate the factors associated with temperature distribution pattern, logistic regression analysis was performed using clinically selected independent variables. RESULTS: Data from 63 patients were analyzed. No obvious extravasation was observed. Film analysis revealed 34 cases of broadening low-temperature area from the vein and 23 cases of non-broadening low-temperature area from the vein. Subcutaneous edema was observed in 18 patients: 17 with broadening low-temperature area from the vein and 1 with non-broadening low-temperature area from the vein. Subcutaneous edema was positively correlated with broadening low-temperature area from the vein. CONCLUSION: Catheter site skin temperature distribution pattern during chemotherapy was associated with subcutaneous edema which is the early extravasation sign immediately after chemotherapy.


Assuntos
Cateterismo Periférico/efeitos adversos , Edema/diagnóstico , Reação no Local da Injeção/etiologia , Cristais Líquidos , Neoplasias/tratamento farmacológico , Medição de Risco/métodos , Temperatura Cutânea , Administração Cutânea , Idoso , Antineoplásicos/administração & dosagem , Feminino , Humanos , Reação no Local da Injeção/diagnóstico por imagem , Japão , Masculino , Pessoa de Meia-Idade , Termografia/métodos , Ultrassonografia/métodos
2.
Vet Radiol Ultrasound ; 60(6): 668-679, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31515897

RESUMO

Computed tomographic angiography (CTA) and magnetic resonance imaging (MRI) have been described as methods for preoperative surgical planning in cats with feline injection site sarcomas (FISS), however, few published studies have compared these modalities. The objective of this retrospective, secondary analysis study was to determine if imaging features of FISS on CTA and MRI are predictive of neoplastic peritumoral projections. Archived data from a previous prospective study were retrieved for 10 cats with FISS. All cats had been evaluated in a single anesthetic episode with MRI and dual phase CT (CTA) imaging followed by surgical removal. Histopathological grading and targeted histopathology of imaging-identified peritumoral projections were performed. Two observers evaluated the CTA and MRI studies for FISS shape, margination, size, enhancement pattern, postcontrast uniformity, pre- and postcontrast margination, the number of muscles involved, mass mineralization, and bone lysis. Metal was present in the imaging field of three of 10 cats, resulting in one nondiagnostic MRI. Peritumoral projections were detected in all cats with both imaging modalities, and most were benign. At least one neoplastic peritumoral projection was detected in six cats using MRI, five cats using CTA, and three cats with both modalities. Higher grade FISS were larger than low grade using MRI, and FISS were larger using MRI. Other FISS imaging features using MRI and CTA were similar. Findings supported use of either MRI or CTA for detecting neoplastic peritumoral projections in cats with FISS. Authors recommend CTA for cats with known metallic objects in the scan field.


Assuntos
Doenças do Gato/diagnóstico por imagem , Reação no Local da Injeção/veterinária , Sarcoma/veterinária , Neoplasias de Tecidos Moles/veterinária , Animais , Doenças do Gato/patologia , Doenças do Gato/terapia , Gatos , Terapia Combinada/veterinária , Angiografia por Tomografia Computadorizada/veterinária , Feminino , Reação no Local da Injeção/diagnóstico por imagem , Injeções/veterinária , Imageamento por Ressonância Magnética/veterinária , Masculino , Gradação de Tumores/veterinária , Valor Preditivo dos Testes , Estudos Prospectivos , Estudos Retrospectivos , Sarcoma/diagnóstico por imagem , Neoplasias de Tecidos Moles/diagnóstico por imagem
3.
J Xray Sci Technol ; 27(1): 73-81, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30373997

RESUMO

BACKGROUND: During the MRI examination, pediatric patients sleep under the sedation so that the image artifacts caused by the patient motion could be minimized. However, the sedative injection at the buttocks might cause a difficulty in the diagnosis of the buttock diseases using the MRI manifestations. OBJECTIVE: This study aims to explore the imaging characteristics of MR for the pediatric patients with the sedative injected at the buttocks in order to correctly diagnose the diseases. METHODS: MR imaging data of 64 pediatric patients injected with the sedative at the buttocks were retrospectively collected, including 8 cases of buttock disease. The imaging manifestations were analyzed and compared. RESULTS: Out of 64 patients, 8 were diagnosed as the buttock diseases. MR imaging manifestations of the sedatives injected at the buttocks were the locally patchy and streaky long T1 and long T2 signals and were different from what were shown for the normal tissues and diseases. CONCLUSION: The sedative injected at the buttocks has the MRI manifestations different from the normal tissues and diseases. Correctly understanding the MRI manifestations for the pediatric patients with the injection of sedative at the buttocks would reduce the chances of the misdiagnosis on the diseases.


Assuntos
Nádegas/diagnóstico por imagem , Hipnóticos e Sedativos/efeitos adversos , Reação no Local da Injeção/diagnóstico por imagem , Pré-Escolar , Diagnóstico Diferencial , Feminino , Humanos , Hipnóticos e Sedativos/administração & dosagem , Lactente , Recém-Nascido , Reação no Local da Injeção/patologia , Injeções Intramusculares , Imageamento por Ressonância Magnética , Masculino
4.
Vaccine ; 36(20): 2783-2787, 2018 05 11.
Artigo em Inglês | MEDLINE | ID: mdl-29653847

RESUMO

BACKGROUND: Extensive clinical investigations are mandatory to evaluate the safety and reactogenicity of vaccines. The recording of common adverse events like injection site soreness or general discomfort derives from individual subjective perceptions. Thermal imaging at the injection site possibly provides a non-subjective and a non-invasive approach to supplement this evaluation. RESULTS: A protocol for quantified injection-site infrared imaging included 86 participants during a flu vaccine campaign, 40% of whom had a thermal reaction of 1 °C; 25-30% had no thermal response. There was little subjective pain reporting and no clinical correlations were observed except with post-vaccination erythema. Higher responses were linked with advanced age and multiple previous vaccinations. CONCLUSION: Evan if influenza vaccine was only moderately reactogenic, a thermal response was detectable in about 70% of vaccinees, though no relationship to reactogenicity was seen. Infrared imaging might however be a prospective tool for individual studies of vaccine-induced vascular responses.


Assuntos
Vacinas contra Influenza/efeitos adversos , Influenza Humana/prevenção & controle , Reação no Local da Injeção/diagnóstico por imagem , Vacinação/efeitos adversos , Adulto , Fatores Etários , Idoso , Análise de Variância , Identificação Biométrica , Eritema/diagnóstico por imagem , Eritema/etiologia , Feminino , Humanos , Vacinas contra Influenza/uso terapêutico , Raios Infravermelhos , Reação no Local da Injeção/etiologia , Masculino , Pessoa de Meia-Idade , Temperatura Cutânea , Termografia/métodos
6.
Toxicol Pathol ; 45(4): 472-480, 2017 06.
Artigo em Inglês | MEDLINE | ID: mdl-28443458

RESUMO

Infusion site reactions are common following subcutaneous infusion of drugs. Such reactions can lead to discontinuation of the treatment. Therefore, assessment of such reactions is essential during preclinical safety studies, and magnetic resonance imaging (MRI) can assist in evaluation. Here, in vivo and ex vivo MRI evaluations were used in addition to classical histopathology to assess the infusion site reaction to ND0701, a novel formulation of apomorphine base developed for the treatment of Parkinson's disease, in comparison to the commercial apomorphine hydrochloride (HCl) formulation. Both formulations, each at two concentrations, were continuously administered subcutaneously for 20 hr to each of 3 male and 3 female domestic pigs. Based on MRI evaluations, there was a gradual decrease in the volume of the subcutaneous lesions over 4 weeks, with smaller lesions and quicker resolution with ND0701 at concentrations 2.5- to 5-fold higher when compared to the commercial apomorphine HCl formulation. Histopathological evaluation of ND0701 revealed only minimal inflammation at the sites of infusion, whereas the commercial apomorphine HCl caused persistent inflammatory reactions and necrosis. This study provides support to the use of MRI in preclinical testing of subcutaneous drugs when evaluating local site reactions.


Assuntos
Antiparkinsonianos/efeitos adversos , Apomorfina/efeitos adversos , Reação no Local da Injeção/diagnóstico por imagem , Injeções Subcutâneas/efeitos adversos , Imageamento por Ressonância Magnética , Animais , Antiparkinsonianos/administração & dosagem , Apomorfina/administração & dosagem , Biomarcadores/sangue , Modelos Animais de Doenças , Avaliação Pré-Clínica de Medicamentos , Feminino , Masculino , Doença de Parkinson/tratamento farmacológico , Suínos
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