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1.
Spine J ; 6(4): 364-9, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16825040

RESUMO

BACKGROUND CONTEXT: Substantial variation exists regarding the use of sedation before interventional spine techniques. Patient preference should play an important role in decision making regarding the need for sedation. However, little is known about patients' anxiety levels before spinal injections and their perceptions about the necessity of sedation. PURPOSE: To determine patient perception for need for sedation before epidural steroid injections and zygapophyseal joint injections. STUDY DESIGN/SETTING: Survey of consecutive spinal injection patients in an outpatient spine center. PATIENT SAMPLE: 500 consecutive lumbar, thoracic, and cervical patients receiving spinal injections. OUTCOME MEASURES: A 12-item questionnaire assessing patients' perceived anxiety before to a spinal injection. METHODS: Subjects were given the questionnaire after their spinal injection. Percentages requesting sedation for a first and potential second procedure were assessed. Additionally, anxiety level and pain rating, location of injection, age, sex, and other medication use were analyzed to determine the effect on the request for sedation. RESULTS: 17% of patients questioned requested sedation before an injection, and 28% would request sedation if they were to have a second injection. CONCLUSIONS: Routine sedation before diagnostic and therapeutic injections is not necessary as the majority of patients would not request sedation before the procedure when given the option. However, in some patients sedation is indicated, and all patients would benefit from educational material on sedation before the injection.


Assuntos
Hipnóticos e Sedativos/uso terapêutico , Injeções Epidurais/estatística & dados numéricos , Injeções Espinhais/estatística & dados numéricos , Injeções/estatística & dados numéricos , Articulação Zigapofisária , Ansiedade , Comportamento de Escolha , Tomada de Decisões , Feminino , Humanos , Masculino , Dor/prevenção & controle , Medição da Dor , Defesa do Paciente , Inquéritos e Questionários
2.
Pain Physician ; 9(1): 53-6, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16700281

RESUMO

BACKGROUND: Great variability exists in the reported frequency of transitional vertebra in the general population as well as in symptomatic lumbar spine patients. OBJECTIVE: To determine the occurrence rate of transitional vertebra in consecutive lumbar spine patients in our practice. DESIGN: A prospective, observational study METHODS: Plain films were viewed and the presence or absence of a lumbar transitional vertebra was documented. Transitional vertebrae were classified as incomplete or complete. RESULTS: Of the 300 consecutive patients, 30% had a transitional vertebra. CONCLUSION: Our percentage of patients with a transitional vertebra was higher than the percentages reported for the general population. This supports our belief that the alteration in mechanics caused by a transitional vertebra may at times contribute to pain generation. Additionally, as a transitional segment may not always be visualized on MRI, obtaining plain films prior to an injection or surgery will help prevent confusion over the appropriate level for the procedure.


Assuntos
Dor Lombar/epidemiologia , Vértebras Lombares/patologia , Região Lombossacral/patologia , Doenças da Coluna Vertebral/epidemiologia , Humanos , Incidência , Dor Lombar/complicações , Vértebras Lombares/anormalidades , Região Lombossacral/anormalidades , Estudos Prospectivos , Estudos Retrospectivos , Sacro/patologia , Doenças da Coluna Vertebral/classificação , Doenças da Coluna Vertebral/etiologia , Doenças da Coluna Vertebral/patologia
3.
Arch Phys Med Rehabil ; 85(3): 479-84, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15031837

RESUMO

OBJECTIVE: To determine patient satisfaction, relief of pain, frequency of injections, change of function, and subsequent surgical rate in patients who received epidural steroid injections (ESIs) for the diagnosis of lumbar spinal stenosis (LSS). DESIGN: Retrospective review conducted using a standard set of questions asked over the telephone, 6 to 36 months after the patient received an ESI. SETTING: An outpatient spine center. PARTICIPANTS: One hundred forty patients at or over the age of 55 years diagnosed with LSS who received ESI(s). INTERVENTION: Transforaminal or caudal fluoroscopically guided ESIs with 60 to 100mg of triamcinalone in combination with local anesthetic or normal saline. Main outcome measures Duration and amount of pain relief, change in functional status, patient satisfaction, and surgical rate, assessed by a 5-item questionnaire. RESULTS: Of the 140 participants, 32% reported more than 2 months of pain relief, 39% reported less than 2 months of pain relief, and 29% reported no relief from the injection(s). Twenty percent subsequently had surgery. Fifty-three percent reported improvement in their functional abilities. Seventy-four percent where at least somewhat satisfied with ESI as a form of treatment. CONCLUSIONS: ESI is a reasonable treatment for LSS, providing one third of our patient population with sustained relief and more than half with sustained improvement in function.


Assuntos
Glucocorticoides/administração & dosagem , Satisfação do Paciente , Estenose Espinal/tratamento farmacológico , Estenose Espinal/fisiopatologia , Triancinolona/administração & dosagem , Idoso , Feminino , Fluoroscopia , Humanos , Injeções Epidurais/métodos , Masculino , Medição da Dor , Recuperação de Função Fisiológica/fisiologia , Estudos Retrospectivos , Estenose Espinal/diagnóstico por imagem , Fatores de Tempo , Resultado do Tratamento
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