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1.
Acad Emerg Med ; 4(12): 1147-52, 1997 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9408431

RESUMO

OBJECTIVES: To determine whether an effective telephone callback system can be successfully implemented in a busy ED and to quantify the benefits that can be obtained related to the follow-up care of elder patients. METHODS: This was a prospective, cohort study conducted at a community teaching hospital during a 6-month period. Consecutive patients > or = 60 years old and released from the ED were selected for telephone follow-up. Calls were made by a research nurse within 72 hours after the patient's ED visit. Follow-up information included current medical status, problems encountered during the ED visit, compliance, and impact of the illness on self-care capabilities. RESULTS: Seventy-nine percent (831/1,048) of the patients selected for telephone follow-up were successfully contacted. The calls lasted an average of 4 +/- 2.5 minutes. Although 94% (778/831) of these patients had a regular physician, 14% failed to make their recommended follow-up arrangements. Compliance was significantly improved when a follow-up physician was contacted during the patient's ED visit. Approximately 96% of the patients were either satisfied or very satisfied with their ED care. However, 13% (109/831) had moderate deterioration in their ability to care for themselves. Of the patients contacted, 333 (40%) required further clarification of their home care instructions, 31 were advised to return to the ED for reevaluation, and 26 were referred to a medical social worker for psychosocial concerns. CONCLUSION: A telephone callback system is a feasible and effective method to improve follow-up care of elder patients released from the ED.


Assuntos
Assistência ao Convalescente/organização & administração , Continuidade da Assistência ao Paciente/organização & administração , Serviço Hospitalar de Emergência/organização & administração , Telefone , Atividades Cotidianas , Idoso , Estudos de Viabilidade , Feminino , Pesquisa sobre Serviços de Saúde , Hospitais Comunitários , Hospitais de Ensino , Humanos , Masculino , Michigan , Pessoa de Meia-Idade , Educação de Pacientes como Assunto , Satisfação do Paciente , Avaliação de Programas e Projetos de Saúde , Estudos Prospectivos , Fatores de Tempo
2.
Vaccine ; 30(13): 2320-8, 2012 Mar 16.
Artigo em Inglês | MEDLINE | ID: mdl-22306859

RESUMO

Bovine respiratory disease causes significant economic losses in both beef and dairy calf industries. Although multi-factorial in nature, the disease is characterized by an acute fibrinous lobar pneumonia typically associated with the isolation of Mannheimia haemolytica. M. haemolytica A1 and A6 are the two most commonly isolated serotypes from cattle, however, the majority of vaccines have not demonstrated cross-serotype protection. In the current study, the efficacy of a novel, attenuated live vaccine, containing both M. haemolytica serotype A1 and Pasteurella multocida, was evaluated in calves challenged with M. haemolytica serotype A6. Although the challenge was more severe than expected, vaccinated calves had reduced clinical scores, lower mortality, and significantly lower lung lesion scores compared to the placebo-vaccinated control group. The results demonstrate that vaccination with an attenuated live vaccine containing M. haemolytica serotype A1 can protect calves against clinical disease following challenge with M. haemolytica serotype A6.


Assuntos
Vacinas Bacterianas/imunologia , Doenças dos Bovinos/prevenção & controle , Proteção Cruzada/imunologia , Mannheimia haemolytica/imunologia , Pasteurella multocida/imunologia , Pasteurelose Pneumônica/prevenção & controle , Animais , Proteínas de Bactérias/genética , Proteínas de Bactérias/imunologia , Proteínas de Bactérias/metabolismo , Vacinas Bacterianas/administração & dosagem , Sequência de Bases , Bovinos , Doenças dos Bovinos/imunologia , Doenças dos Bovinos/microbiologia , Exotoxinas/genética , Exotoxinas/imunologia , Exotoxinas/metabolismo , Mannheimia haemolytica/classificação , Mannheimia haemolytica/genética , Mannheimia haemolytica/patogenicidade , Dados de Sequência Molecular , Pasteurella multocida/genética , Pasteurelose Pneumônica/imunologia , Pasteurelose Pneumônica/microbiologia , Pasteurelose Pneumônica/mortalidade , Sorotipagem , Resultado do Tratamento , Vacinação/veterinária , Vacinas Atenuadas/administração & dosagem , Vacinas Atenuadas/imunologia
3.
Can Fam Physician ; 30: 332-8, 1984 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21279012

RESUMO

The demographic and medical characteristics of patients using the emergency department of the Gatineau Memorial Hospital in Wakefield, Quebec were studied. These characteristics are compared with those reported in the medical literature. A youthful, predominantly male population presented to the emergency department, usually because of trauma or respiratory illness. Seventy-five percent of the patients were seen within 20 minutes of their arrival. Medications were prescribed slightly over 50% of the time, but laboratory and radiology services were infrequently used. Of the patients seen, 6.4% were transferred to larger city hospitals. These transferred patients most frequently were trauma victims needing complicated surgery or specialized services.

4.
Infect Immun ; 66(9): 4087-92, 1998 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9712752

RESUMO

Pasteurella haemolytica serotype 1 is the bacterial agent responsible for the pathophysiological events associated with bovine pneumonic pasteurellosis. Our previous studies support a role for the lipopolysaccharide (LPS) from P. haemolytica in the induction of proinflammatory cytokines. One of the pathological hallmarks of bovine pneumonic pasteurellosis is an influx of neutrophils into the alveolar spaces. This pronounced influx suggests the local production of a chemotactic factor(s) such as interleukin-8 (IL-8). In the context of the lung, the alveolar macrophage appears to be the major producer of IL-8, a proinflammatory cytokine with potent neutrophil chemotactic activity. By using Northern blot analysis, we have examined the kinetics of IL-8 mRNA expression in P. haemolytica LPS-stimulated bovine alveolar macrophages and found that 1 ng of LPS per ml induces maximal expression of IL-8 mRNA. The results also indicate a biphasic time course expression pattern in which IL-8 mRNA levels peak between 1 and 2 h in the first phase and between 16 and 24 h in the second phase (P < 0.01). In addition, monospecific polyclonal antibodies were used to demonstrate the role of tumor necrosis factor alpha (TNF-alpha) in the second phase of IL-8 mRNA expression. Our findings support a role for P. haemolytica LPS and TNF-alpha in the induction of IL-8 from bovine alveolar macrophages.


Assuntos
Regulação da Expressão Gênica , Interleucina-8/genética , Lipopolissacarídeos/imunologia , Macrófagos Alveolares/imunologia , Mannheimia haemolytica/imunologia , Fator de Necrose Tumoral alfa/imunologia , Animais , Anticorpos/metabolismo , Bovinos , Clonagem Molecular , DNA Complementar , Regulação da Expressão Gênica/efeitos dos fármacos , Humanos , Cinética , Lipopolissacarídeos/farmacologia , Macrófagos Alveolares/efeitos dos fármacos , RNA Mensageiro , Proteínas Recombinantes/farmacologia , Fator de Necrose Tumoral alfa/genética , Fator de Necrose Tumoral alfa/metabolismo , Fator de Necrose Tumoral alfa/farmacologia
5.
Immunology ; 37(2): 419-28, 1979 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-468307

RESUMO

The sera of four sisters were found to lack the sixth component of complement (C6) and the serum of one was also partially deficient in the second component (C2). Two other blood relatives were found to be heterozygous for both deficiencies, while only one sibling had normal values. The father of these eight siblings was heterozygous for C2D and C6D and in the third generation, six children were heterozygous for C6 deficiency was treated for chronic active brucel-transmitted; the C6 deficiency was not linked to the HLA system, while the C2-deficiency segregated with the haplotype A10,B18. The proband, homozygous for C6 deficiency was treated for chronic active Brucellosis and in another sibling with C6 deficiency, toxoplasmosis was diagnosed. Neither bleeding disorders nor a tendency to collagen diseases have been observed and the opsonic activity was normal in the sera of all family members.


Assuntos
Complemento C2/deficiência , Complemento C6/deficiência , Adulto , Feminino , Doenças Genéticas Inatas/genética , Genótipo , Antígenos HLA , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem
6.
Microb Pathog ; 30(6): 347-57, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11399141

RESUMO

Pasteurella (Mannheimia) haemolytica leukotoxin (Lkt) and lipopolysaccharide (LPS) are the primary virulence factors contributing to the pathogenesis of lung injury in bovine pneumonic pasteurellosis. Previous studies have characterized in vitro responses of bovine alveolar macrophages (AMs) to Lkt and LPS. Activation of AMs with Lkt or LPS causes induction of proinflammatory cytokines, and Lkt causes cytolysis of AMs at higher concentrations. Since AMs are exposed to both of these bacterial virulence factors during disease, previous studies may have underestimated the possibility of functional interactions between Lkt and LPS. The purpose of this study was to characterize the effect of simultaneous exposure to both Lkt and LPS on AM cytolysis and proinflammatory cytokine expression. Using cellular leakage of lactate dehydrogenase as an indirect measure of cytolysis, we studied AM responses to Lkt alone, LPS alone and Lkt+LPS. We found that 80-200 pg/ml LPS, which does not itself cause cytolysis, synergistically enhanced the cytolysis induced by 2-5 Lkt units (LU)/ml Lkt. Northern blot analysis demonstrated that synergism between Lkt and LPS resulted in increased levels of IL-8 mRNA, and that the kinetic patterns of TNF-alpha and IL-8 mRNA expression induced by Lkt+LPS differed from those induced by each agent separately. Finally, the WEHI 164 (clone 13) bioassay was used to show that Lkt/LPS synergism resulted in enhanced secretion of biologically active TNF-alpha. These results provide direct evidence of synergism between Lkt and LPS in AM cytolysis and inflammatory cytokine expression. Additional studies to characterize the molecular basis of this phenomenon are indicated.


Assuntos
Toxinas Bacterianas/farmacologia , Citocinas/metabolismo , Citotoxinas/farmacologia , Exotoxinas/farmacologia , Lipopolissacarídeos/farmacologia , Macrófagos Alveolares/efeitos dos fármacos , Mannheimia haemolytica/patogenicidade , Animais , Bovinos , Sinergismo Farmacológico , Interleucina-8/metabolismo , Pasteurelose Pneumônica/etiologia , Fator de Necrose Tumoral alfa/metabolismo
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