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1.
BMJ ; 322(7288): 704-8, 2001 Mar 24.
Artigo em Inglês | MEDLINE | ID: mdl-11264208

RESUMO

OBJECTIVE: To determine whether benzodiazepines are associated with an increased risk of hip fracture. DESIGN: Case-control study. PARTICIPANTS: All incident cases of hip fracture not related to traffic accidents or cancer in patients over 65 years of age. 245 cases were matched to 817 controls. SETTING: Emergency department of a university hospital. MAIN OUTCOME MEASURES: Exposure to benzodiazepines and other potential risk or protective factors or lifestyle items. RESULTS: The use of benzodiazepines as determined from questionnaires, medical records, or plasma samples at admission to hospital was not associated with an increased risk of hip fracture (odds ratio 0.9, 95% confidence interval 0.5 to 1.5). Hip fracture was, however, associated with the use of two or more benzodiazepines, as determined from questionnaires or medical records but not from plasma samples. Of the individual drugs, only lorazepam was significantly associated with an increased risk of hip fracture (1.8, 1.1 to 3.1). CONCLUSION: Except for lorazepam, the presence of benzodiazepines in plasma was not associated with an increased risk of hip fracture. The method used to ascertain exposure could influence the results of case-control studies.


Assuntos
Acidentes por Quedas , Benzodiazepinas/efeitos adversos , Fraturas do Quadril/etiologia , Lorazepam/efeitos adversos , Idoso , Benzodiazepinas/sangue , Estudos de Casos e Controles , Intervalos de Confiança , Humanos , Estilo de Vida , Lorazepam/sangue , Razão de Chances , Risco
2.
Ann Fr Anesth Reanim ; 6(4): 301-5, 1987.
Artigo em Francês | MEDLINE | ID: mdl-3307549

RESUMO

The aim of this study was to compare the quality of postanaesthetic recovery after anaesthesia with methohexitone (M) or with propofol (P). Thirty patients undergoing spinal surgery were randomly assigned to either group. The induction dose was 2 mg . kg-1 for both M and P. Anaesthesia was maintained by continuous infusion. The rate was 0.15 mg . kg-1 . min-1 for P and 0.07 mg . kg-1 . min-1 for M. Analgesia was obtained with fentanyl with the same doses in both groups. The maintenance doses were subsequently decreased by 50 and 75% of the initial values. This work compared the quality induction and the criteria of recovery (Aldrete score, Newman test). In two patients in each group, sensory evoked potentials (SEP) were recorded to monitor neurological integrity. The quality of induction was similar in both groups. Awakening was significantly more rapid in group P. The SEP were much decreased in group P, whilst there were few changes in group M. Monitoring of medullar integrity is mandatory in spinal surgery, requiring a rapid recovery. This objective was obtained with shorter delays in patients anaesthetized with propofol than in those who had received methohexitone. However, the former, at the doses used, seemed to depress the SEP.


Assuntos
Período de Recuperação da Anestesia , Anestésicos , Metoexital , Fenóis , Período Pós-Operatório , Canal Medular/cirurgia , Adulto , Ensaios Clínicos como Assunto , Potenciais Evocados/efeitos dos fármacos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Propofol
7.
Eur Spine J ; 12(1): 84-90, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12592551

RESUMO

Cervical spinal surgery through anterior approaches can lead to ear, nose and throat (ENT) complications, some of which, such as obstruction of upper airways by edema, are potentially life threatening. The purpose of this study was to evaluate the incidence of various categories of ENT lesions and to determine whether preventive treatment with methylprednisolone (Mp) is useful in this indication. In a prospective trial, 236 patients who were undergoing anterior cervical spine surgery were separated into two groups, a control group (group I: 158 patients) and a group receiving 1 mg/kg of Mp intravenously at the end of the operation and 12 and 24 h later (group II: 78 patients). All 236 patients underwent nasofibroscopic examination by an ENT specialist the day before the operation and 24 and 36 h after the operation. The lesions observed during these examinations and reported symptoms such as uncomfortable sensation, odynophagia, or dysphagia were compared between the two groups (chi(2) or Mann-Whitney test) in terms of relative risk, with a confidence interval of 95%. Quantitative findings were compared using Student's t-test ( P<0.05). Demographic characteristics and duration of endotracheal intubation were comparable in the two groups. The ENT examination was considered abnormal in 30 patients of group I and 15 patients of group II preoperatively (NS). It was abnormal in 146 patients of group I (92%) and 46 patients of group II (59%) postoperatively. Altered vocal cord motility was noted in six patients of group I and two patients of group II. The relative risk was 1.6 (CI: 1.3-1.9). Postoperatively, 130 patients in group I and 56 of group II (NS) reported unwanted symptoms. The observed lesions were significantly more severe in group I ( P<0.001), involving primarily the pharyngeal wall, the arytenoids, and the vocal cords. The results of this study indicate that ENT complications of anterior cervical spinal surgery are diminished by administration of Mp. Systematic ENT examination is warranted before this type of operation.


Assuntos
Vértebras Cervicais/cirurgia , Edema Laríngeo/prevenção & controle , Metilprednisolona/uso terapêutico , Procedimentos Neurocirúrgicos/efeitos adversos , Doenças Faríngeas/prevenção & controle , Complicações Pós-Operatórias/prevenção & controle , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Transtornos de Deglutição/etiologia , Transtornos de Deglutição/prevenção & controle , Feminino , Humanos , Fixadores Internos/efeitos adversos , Intubação Intratraqueal/efeitos adversos , Edema Laríngeo/etiologia , Laringe/efeitos dos fármacos , Laringe/lesões , Laringe/fisiopatologia , Masculino , Pessoa de Meia-Idade , Procedimentos Neurocirúrgicos/métodos , Doenças Faríngeas/etiologia , Faringe/efeitos dos fármacos , Faringe/lesões , Faringe/fisiopatologia , Complicações Pós-Operatórias/etiologia , Estudos Prospectivos , Resultado do Tratamento , Paralisia das Pregas Vocais/etiologia , Paralisia das Pregas Vocais/prevenção & controle
8.
Anaesthesia ; 43 Suppl: 44-5, 1988 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-3259096

RESUMO

This study evaluated the effects of propofol on somatosensory evoked cortical potentials in 20 ASA grade 1 or 2 patients who underwent spinal surgery. Anaesthesia consisted of propofol, dextromoramide, 50% nitrous oxide and oxygen mixture. The induction dose of propofol was 2 mg/kg and was followed by an infusion of 6 mg/kg for the first hour and 3 mg/kg subsequently. Somatosensory evoked cortical potentials were recorded on the scalp and compared to pre-operative values using Student's paired t-test. We observed a significant depression of evoked potential 10 minutes after induction, which continued until the early phase of recovery. Because of its short and quickly reversible action, propofol is an acceptable agent when clinical monitoring of the spinal cord is indicated but is not satisfactory when monitoring has to be based on somatosensory cortical evoked potentials.


Assuntos
Anestésicos/farmacologia , Córtex Cerebral/fisiologia , Potenciais Somatossensoriais Evocados/efeitos dos fármacos , Fenóis/farmacologia , Adulto , Anestesia Geral , Avaliação de Medicamentos , Humanos , Propofol , Coluna Vertebral/cirurgia , Fatores de Tempo
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