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1.
Rheumatology (Oxford) ; 51(8): 1447-54, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22467087

RESUMO

OBJECTIVE: To compare the efficacy of surgical decompression vs local steroid injection in the treatment of idiopathic CTS. METHODS: This is an open, prospective, randomized clinical trial. We studied the effects of surgical decompression vs local steroid injection in 163 wrists with a clinical diagnosis and neurophysiological confirmation of CTS, with an extended follow-up of 2 years. The primary end point was the percentage of wrists that reached a ≥ 20% improvement in the visual analogue scale score for nocturnal paraesthesias. Statistical analysis was done by Student's t-test for continuous variables and by chi-square test for categorical variables. Analyses were performed on an intent-to-treat basis. P < 0.05 were considered statistically significant. RESULTS: Both treatment groups had comparable severity of CTS at baseline. Eighty wrists were randomly assigned to surgical decompression and 83 wrists to local steroid injection. Fifty-five wrists in the surgery group and 48 wrists in the injection group completed the 2-year follow-up. In the intent-to-treat analysis, at 2-year follow-up, 60% of the wrists in the injection group vs 69% in the surgery group reached a 20% response for nocturnal paraesthesias (P < 0.001). CONCLUSION: Our findings suggest that both local steroid injection and surgical decompression are effective treatments in alleviating symptoms in primary CTS at 2-year follow-up. Surgery has an additional benefit in the 2-year follow-up, although clinical relevance of those differences remains to be defined. TRIAL REGISTRATION: Current Controlled Trials, www.controlled-trials.com, ISRCTN26264638.


Assuntos
Síndrome do Túnel Carpal/tratamento farmacológico , Síndrome do Túnel Carpal/cirurgia , Descompressão Cirúrgica , Glucocorticoides/administração & dosagem , Parametasona/administração & dosagem , Adulto , Idoso , Terapia Combinada , Feminino , Seguimentos , Humanos , Injeções Intra-Articulares , Masculino , Pessoa de Meia-Idade , Medição da Dor , Estudos Prospectivos , Resultado do Tratamento
2.
Can J Anaesth ; 53(6): 591-4, 2006 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16738294

RESUMO

PURPOSE: This report describes treatment with epidural dextran-40 and paramethasone injection of postural headache resulting from spontaneous intracranial hypotension in a pregnant patient. CLINICAL FEATURES: A 39-yr-old pregnant woman consulted the pain clinic for the assessment of a debilitating postural headache which was non-responsive to conventional analgesic treatment. Clinical findings and cranial magnetic resonance imaging indicated the diagnosis of spontaneous intracranial hypotension syndrome. Treatment with an epidural blood patch was not undertaken for several reasons. A lumbar epidural injection with dextran-40 and paramethasone led to a significant improvement in the symptoms and allowed a progressive discontinuation of adjuvant treatment with oral steroids, with complete resolution of symptoms. CONCLUSION: We report a case of spontaneous intracranial hypotension in a pregnant patient successfully treated by epidural injection of dextran-40 and paramethasone, with adjuvant oral steroid therapy. Clinical trials are warranted to establish the efficacy of this treatment as an alternative to the epidural blood patch administration.


Assuntos
Analgesia Epidural , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/uso terapêutico , Dextranos/administração & dosagem , Dextranos/uso terapêutico , Cefaleia/tratamento farmacológico , Hipotensão Intracraniana/tratamento farmacológico , Parametasona/administração & dosagem , Parametasona/uso terapêutico , Substitutos do Plasma/administração & dosagem , Substitutos do Plasma/uso terapêutico , Adulto , Feminino , Cefaleia/etiologia , Cefaleia/patologia , Humanos , Hipotensão Intracraniana/complicações , Hipotensão Intracraniana/patologia , Imageamento por Ressonância Magnética , Gravidez
5.
Arthritis Rheum ; 52(2): 612-9, 2005 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15692981

RESUMO

OBJECTIVE: Optimal treatment of carpal tunnel syndrome (CTS) has not been established. This study compared the effects of local steroid injection versus surgical decompression in new-onset CTS of at least 3 months' duration. METHODS: In a 1-year, prospective, randomized, open, controlled clinical trial, we studied the effects of surgical decompression versus local steroid injection in 163 wrists with a clinical and neurophysiologic diagnosis of CTS. Clinical assessments were done at baseline and at 3, 6, and 12 months after treatment. The primary end point was the percentage of wrists that reached a >or=20% improvement in the visual analog scale score for nocturnal paresthesias at 3 months of followup. Statistical analysis was done by Student's t-test for continuous variables and by chi-square test for categorical variables. Analyses were performed on an intent-to-treat basis. P values less than 0.05 were considered statistically significant. RESULTS: Both treatment groups had comparable severity of CTS at baseline. Eighty wrists were randomly assigned to the surgery group and 83 wrists to the local steroid injection group. In the intent-to-treat analysis, at 3 months of followup, 94.0% of the wrists in the steroid injection group versus 75.0% in the surgery group reached a 20% response for nocturnal paresthesias (P = 0.001). At 6 and 12 months, the percentages of responders were 85.5% versus 76.3% (P = 0.163) and 69.9% versus 75.0% (P = 0.488), for local steroid injection and surgical decompression, respectively. CONCLUSION: Over the short term, local steroid injection is better than surgical decompression for the symptomatic relief of CTS. At 1 year, local steroid injection is as effective as surgical decompression for the symptomatic relief of CTS.


Assuntos
Síndrome do Túnel Carpal/terapia , Descompressão Cirúrgica , Esteroides/administração & dosagem , Síndrome do Túnel Carpal/fisiopatologia , Feminino , Humanos , Injeções Intra-Articulares , Masculino , Pessoa de Meia-Idade , Parametasona/administração & dosagem , Estudos Prospectivos , Resultado do Tratamento
6.
Int J Fertil Womens Med ; 45(4): 273-8, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-10997483

RESUMO

OBJECTIVE: The aim of this study was to investigate the oral effects of tibolone and mestranol plus paramethasone on the skin of postmenopausal women. A second purpose was to determine endometrial thickness with transvaginal ultrasound. MATERIALS AND METHODS: This randomized study was carried out in 39 healthy postmenopausal women. Skin biopsies were obtained from the thigh area by a single punch, before and after treatment, and the sections were evaluated. Current characteristics of both groups were measured at follow-up. RESULTS: No gross differences were observed in size, distribution or imaging of collagen, elastic or reticular fibers. Statistically significant changes were found in the papillar dermis thickness. There were no statistically significant differences in the sonographic measurements. CONCLUSION: The estrogen/glucocorticoid combination provides a way to evaluate in parallel the cellular metabolism effects on the irreversible aging process. The current results encourage widening these observations of the possible advantage of this combination, in order to alleviate the cellular degenerative process.


Assuntos
Anabolizantes/farmacologia , Congêneres do Estradiol/farmacologia , Glucocorticoides/farmacologia , Mestranol/farmacologia , Norpregnenos/farmacologia , Parametasona/farmacologia , Pele/efeitos dos fármacos , Idoso , Envelhecimento/efeitos dos fármacos , Envelhecimento/patologia , Anabolizantes/administração & dosagem , Endométrio/diagnóstico por imagem , Endométrio/efeitos dos fármacos , Congêneres do Estradiol/administração & dosagem , Terapia de Reposição de Estrogênios , Feminino , Glucocorticoides/administração & dosagem , Humanos , Mestranol/administração & dosagem , Pessoa de Meia-Idade , Norpregnenos/administração & dosagem , Pós-Menopausa , Pele/patologia , Ultrassonografia
9.
J Radiol ; 81(2): 141-6, 2000 Feb.
Artigo em Francês | MEDLINE | ID: mdl-10705144

RESUMO

PURPOSE: To evaluate the contribution of principal imaging techniques in diagnosis and treatment in adhesive capsulitis of the shoulder. MATERIALS AND METHODS: In 20 patients presenting adhesive capsulitis of shoulder since mean of 6,7 months, the following examinations were performed: radiographies, angioscintigraphy, MRI as well as an opaque arthrography and a bursography associated with corticosteroid injection. Patients were followed during one year. RESULTS: The opaque arthrography was to affirm the adhesive capsulitis for the inclusion of the patients. Radiographies (patchy demineralization) and scintigraphy (hyperfixation) were often pathological. In MRI, T1 fat-saturated sequences after contrast injection almost always showed enhancement of the articular capsula, the synovia, the miscellaneous bone or the sub-acromial bursa. The latter was often modified and retracted at bursography. In 19 of 20 cases, a functional improvement was observed after the opacifications. CONCLUSION: Therapeutic effect of both arthrography and bursography is almost proved. Post contrast MRI confirms presence of vascular troubles in all the shoulder structures even at this advanced stage.


Assuntos
Bursite/diagnóstico , Diagnóstico por Imagem , Articulação do Ombro/patologia , Adulto , Idoso , Anti-Inflamatórios/administração & dosagem , Anti-Inflamatórios/uso terapêutico , Artrografia , Bursite/diagnóstico por imagem , Bursite/tratamento farmacológico , Meios de Contraste , Feminino , Seguimentos , Glucocorticoides/administração & dosagem , Glucocorticoides/uso terapêutico , Humanos , Cápsula Articular/patologia , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Parametasona/administração & dosagem , Parametasona/uso terapêutico , Estudos Prospectivos , Cintilografia , Compostos Radiofarmacêuticos , Articulação do Ombro/efeitos dos fármacos , Membrana Sinovial/patologia
11.
Rev Rhum Engl Ed ; 65(12): 771-7, 1998 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9923046

RESUMO

OBJECTIVE: To demonstrate the therapeutic value of subacromial bursography (with a steroid injection) in adhesive capsulitis of the shoulder inadequately improved by arthrographic glenohumeral distension with steroid injection. METHOD: Twenty cases of adhesive capsulitis documented by glenohumeral arthrography were studied prospectively. A steroid was injected during distension arthrography, which was followed by physical therapy. Subacromial bursography without steroid injection was done routinely for diagnostic purposes. Constant's simplified score and range of motion were determined in each patient at baseline and after one, three, six and 12 months. Patients who were inadequately improved after one to three months underwent repeat subacromial bursography with steroid injection, followed by physical therapy. RESULTS: Of the 20 patients, 13 were noticeably improved 1.7 months on average after the distension arthrography. Of the remaining seven patients, six were improved 0.7 months on average after the bursography with steroid injection. CONCLUSION: Glenohumeral distension arthrography with steroid injection followed by physical therapy is effective in expediting the spontaneously favorable outcome of adhesive capsulitis and also allows to confirm the diagnosis. However, the subacromial bursa is almost consistently involved. Subacromial bursography with steroid injection can be useful in cases that fail to respond to conventional therapy.


Assuntos
Artrografia , Bolsa Sinovial/diagnóstico por imagem , Bursite/tratamento farmacológico , Bursite/radioterapia , Articulação do Ombro/diagnóstico por imagem , Adulto , Idoso , Bolsa Sinovial/efeitos dos fármacos , Terapia Combinada , Feminino , Glucocorticoides/uso terapêutico , Humanos , Masculino , Manipulação Ortopédica , Pessoa de Meia-Idade , Parametasona/uso terapêutico , Amplitude de Movimento Articular/efeitos dos fármacos , Ruptura , Articulação do Ombro/efeitos dos fármacos , Sinovectomia , Resultado do Tratamento
13.
Artigo em Inglês | MEDLINE | ID: mdl-8959545

RESUMO

Although true allergic reactions due to systemic corticosteroid therapy are not frequent, they should be kept in mind since allergic reactions to this kind of therapy are possible. We report two cases of specific adverse reactions resulting from systemic corticosteroid therapy which were diagnosed by provocation tests. The corticosteroids involved in each case were paramethasone and betamethasone, and methyl-prednisolone in both of them. Additives and other corticosteroids were studied by skin tests and challenges, with negative results. The structures of paramethasone and betamethasone are similar, with a 16 carbon methyl group in both, and with a fluoride in the alpha position of the 6 carbon in paramethasone, and a fluoride in the beta position of the 9 carbon and a 6 carbon methyl group in betamethasone. Methyl-prednisolone differs from that of other corticosteroids in its 6 carbon methyl group. We report two cases of specific adverse reactions caused by corticosteroids. Positive challenge tests showed a possible immunologic hypersensitivity mechanism in both cases. The patients' reactions demonstrated cross-reactivity between methyl-prednisolone and the corticosteroids having a 16 carbon methyl group, and fluoride or methyl radicals on the 6 carbon.


Assuntos
Corticosteroides/administração & dosagem , Corticosteroides/efeitos adversos , Corticosteroides/imunologia , Adulto , Anafilaxia/induzido quimicamente , Angioedema/induzido quimicamente , Betametasona/administração & dosagem , Betametasona/efeitos adversos , Reações Cruzadas/imunologia , Vias de Administração de Medicamentos , Feminino , Humanos , Masculino , Metilprednisolona/administração & dosagem , Metilprednisolona/efeitos adversos , Pessoa de Meia-Idade , Parametasona/administração & dosagem , Parametasona/efeitos adversos
14.
Gynecol Endocrinol ; 10(2): 125-8, 1996 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8701786

RESUMO

To evaluate hormone replacement therapy effects at the peripheral level, the present trial explored the oral effects of mestranol (80 micrograms/day for 10 days) and mestranol plus paramethasone (80 micrograms + 6 mg/day for 10 days) on the skin of postmenopausal women. This double-blind study included 13 patients. Skin biopsies were obtained from the thigh area by a single punch, 5 mm in diameter, before and after treatment, and the sections, six per sample, were micrometrically evaluated. Various features of the epidermis and dermis layers were stained using the hematoxylin and eosin, Masson, Verhoeff's and Gomori techniques. Statistically significant changes were found in the papillar dermis thickness; mestranol reduced it and mestranol plus paramethasone increased it. The current results encourage widening these observations of the possible advantage of this estrogen/glucocorticoid combination, in order to alleviate the cellular degenerative process.


Assuntos
Anti-Inflamatórios/uso terapêutico , Congêneres do Estradiol/uso terapêutico , Terapia de Reposição de Estrogênios , Mestranol/uso terapêutico , Parametasona/uso terapêutico , Pele/efeitos dos fármacos , Administração Oral , Idoso , Envelhecimento/efeitos dos fármacos , Envelhecimento/patologia , Anti-Inflamatórios/farmacologia , Método Duplo-Cego , Congêneres do Estradiol/farmacologia , Feminino , Humanos , Mestranol/farmacologia , Pessoa de Meia-Idade , Parametasona/farmacologia , Pele/patologia
15.
Ann Pharmacother ; 30(1): 37-40, 1996 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-8773164

RESUMO

OBJECTIVE: To report a patient with an anaphylactic reaction related to povidone administration. CASE SUMMARY: A 37-year-old man with a history of allergic rhinitis presented with urticaria, dyspnea, wheezing, rhinorrhea, and dysphonia 20 minutes after the intraarticular administration of mepivacaine hydrochloride and paramethasone acetate in his right knee. Two months after this episode, he was admitted for controlled provocation tests. Tests on mepivacaine were negative. The preparation of paramethasone contained the excipients benzalkonium chloride, polysorbate 80, and povidone. In vitro tests and provocation were negative with polysorbate 80 and benzalkonium chloride, but positive with povidone. DISCUSSION: Povidone, a mixture of synthetic polymers, is commonly used as an excipient in pharmaceutical products, an additive in food products, and a dispersant and stabilizer in hairsprays. Although it is well tolerated when used topically or parenterally, local and systemic effects have been reported. Furthermore, multiorgan involvement resulting from accumulation of the drug in the reticuloendothelial system has been described. The immunologic properties of povidone have not been explored in humans, but have been in animals. In fact, the capacity of povidone to release histamine and its immunogenicity are proportional to its molecular weight. An immunoglobulin (Ig) E-mediated hypersensitivity reaction in asthma has been reported. In our case, povidone was responsible for the syndrome. However, we cannot determine the exact mechanism. An unspecific histamine release and/or an IgE-mediated hypersensitivity could be involved. CONCLUSIONS: Povidone was responsible for a severe anaphylactic reaction in our patient. The possibility of an iatrogenic adverse effect caused by the excipient but not by the active ingredient should be considered in patients exhibiting similar symptoms. We believe that the excipients used in the preparation of all medicines should be disclosed.


Assuntos
Anafilaxia/induzido quimicamente , Excipientes Farmacêuticos/efeitos adversos , Povidona/efeitos adversos , Adulto , Anestésicos Locais/administração & dosagem , Anestésicos Locais/uso terapêutico , Anti-Inflamatórios/administração & dosagem , Anti-Inflamatórios/uso terapêutico , Humanos , Testes Intradérmicos , Masculino , Mepivacaína/administração & dosagem , Mepivacaína/uso terapêutico , Parametasona/administração & dosagem , Parametasona/uso terapêutico , Rinite Alérgica Perene/complicações
16.
Artigo em Inglês | MEDLINE | ID: mdl-7582165

RESUMO

Two patients treated with parenteral paramethasone (Triniol) and dexamethasone (Sedionbel) are described. A few minutes after administration of the drugs, they presented urticaria (patients 1 and 2) and conjunctivitis (patient 1). The purpose of our study was to determine the cause of the patients' reactions, the immunological mechanisms involved and whether these patients would be able to tolerate any kind of corticoid. Clinical examinations and skin, oral and parenteral challenges with different corticosteroids and ELISA tests were performed. In the two patients, skin and ELISA tests with paramethasone were negative, as was the prick test with each of its excipients. A single-blind parenteral challenge with Triniol was positive in both patients after the administration of 1 ml of the drug, and negative with its excipients. We also carried out oral and parenteral challenges with other corticosteroids and found intolerance to some of them. These results suggest that paramethasone caused pseudoallergic reactions in our patients. Corticosteroids different from paramethasone also produced hypersensitivity reactions in these patients; however, a few of them were tolerated. The basic mechanisms of those reactions are not yet fully understood. To our knowledge, this is the first report of a pseudo-allergy caused by paramethasone.


Assuntos
Angioedema/induzido quimicamente , Conjuntivite Alérgica/diagnóstico , Dexametasona/efeitos adversos , Parametasona/efeitos adversos , Urticária/induzido quimicamente , Adulto , Angioedema/diagnóstico , Angioedema/terapia , Conjuntivite Alérgica/induzido quimicamente , Conjuntivite Alérgica/terapia , Dexametasona/administração & dosagem , Dexametasona/imunologia , Feminino , Humanos , Imunoglobulina E/sangue , Injeções Intramusculares , Masculino , Parametasona/administração & dosagem , Parametasona/imunologia , Testes Cutâneos , Urticária/diagnóstico , Urticária/terapia
17.
Educ. méd. contin ; (47): 5-9, mar. 1995. tab
Artigo em Espanhol | LILACS | ID: lil-178303

RESUMO

Presentamos el caso de dos sujetos sometidos a tratamiento parenteral con los corticoides dexametasona y parametasona (Triniol). A los pocoso minutos de su administración desarrollaron un cuadro urticariforme y uno de ellos ademas una inyeccion conjuntival en el ojo derecho. Fueron sometidos a pruebas cutáneas con todos los componentes del Triniol. Por separado, siendo esta positiva tras la administración intramuscular de 1 ml de la sustancia y negativa con cada uno de los excipientes del preparado. las pruebas "in vitro" destinadas a detectar IgE especifica frente a la parametasona, fueron negativas. Adicionalmente realizamos provocaciones orales y parenterales con otros corticoides encontrando intolerancia a varios de ellos


Assuntos
Humanos , Masculino , Corticosteroides/administração & dosagem , Corticosteroides/efeitos adversos , Conjuntivite Alérgica , Parametasona/administração & dosagem , Urticária
18.
Artigo em Francês | MEDLINE | ID: mdl-7638397

RESUMO

INTRODUCTION: The authors report a prospective study on the treatment of radicular compression using epidural infiltrations. MATERIAL AND METHODS: An open study was performed on 200 patients suffering from radicular compression due to either herniated lumbar discs (124 cases), lumbar stenosis (32 cases) or segmental lumbar stenosis (44 cases) and treated by epidural infiltrations. RESULTS: Of the 200 patients studied, 74 per cent did not need subsequent surgical treatment. Therapeutic effect was influenced by several parameters: etiology of radicular compression: 65 per cent favorable results in herniated discs; 69 per cent in lumbar stenosis; and 91 per cent favorable results in segmental lumbar stenosis; age of patients: 100 per cent favorable in patients > 70 years, while only very few favorable results in patients < 20 years of age. Chronic or acute radicular pain: among the patients who had herniated discs requiring subsequent surgery, 65 per cent presented with acute lesions (pain for < 4 months). In patients with lumbar stenosis requiring surgery, 80 per cent had acute lesion and in patients with segmental lumbar stenosis, no patients complained of acute pain. DISCUSSION: Avoiding surgical treatment is not the only parameter which should be studied in evaluating the effectiveness of treatment. Lassale's pre and postoperative evaluation with a minimum 1 year follow up showed improvement in all non surgical cases. When compared to the literature, this study shows favorable long term results.


Assuntos
Injeções Epidurais/métodos , Deslocamento do Disco Intervertebral/complicações , Vértebras Lombares , Radiculopatia/tratamento farmacológico , Estenose Espinal/complicações , Adolescente , Adulto , Idoso , Bupivacaína/administração & dosagem , Interpretação Estatística de Dados , Feminino , Seguimentos , Humanos , Injeções Epidurais/efeitos adversos , Deslocamento do Disco Intervertebral/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Parametasona/administração & dosagem , Estudos Prospectivos , Radiculopatia/etiologia , Estenose Espinal/tratamento farmacológico
19.
J Dermatol ; 20(5): 304-7, 1993 May.
Artigo em Inglês | MEDLINE | ID: mdl-8340536

RESUMO

A 43-year-old woman had asymptomatic eruptions on the anterior sides of both legs for 5 years. Biopsy specimens revealed the typical findings of necrobiosis lipoidica. An immunofluorescence study demonstrated no deposits of immunoglobulins, complement, or fibrinogen in vessel walls. Immunohistochemical staining revealed CD4 positive lymphocytes dominating in the lesion and strong expression of ICAM-1 on the endothelial cells, giant cells, lymphocytes and dermal fibroblasts in the lesion. The eruptions resolved remarkably with oral corticosteroid therapy.


Assuntos
Necrobiose Lipoídica/tratamento farmacológico , Parametasona/análogos & derivados , Administração Oral , Adulto , Complemento C3/análise , Feminino , Humanos , Imunoglobulinas/análise , Imuno-Histoquímica , Necrobiose Lipoídica/imunologia , Necrobiose Lipoídica/patologia , Parametasona/administração & dosagem
20.
An Otorrinolaringol Ibero Am ; 18(4): 361-74, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1716859

RESUMO

The presence of sensitive symptoms, symptoms of parasympathetic ganglion's affection, as well as signs of affection of other cranial nerves accompanying to Bell's palsy, led us to consider and treat this disorder as a symptom of motor lesion of a possible primary neuron inflammation. Although we have not found valid statistical correlations between the lesion and location patterns, we have found, however, that continues electromyographic studies, and the early treatment carried out, may be of great interest to avoid sequels. The treatment was focussed to eliminate both the possible cause and the inflammatory process, as to improve neuron regeneration. From 60 patients selected to enter this study, 91,66 percent recovered the motor function.


Assuntos
Paralisia Facial/terapia , Adolescente , Adulto , Idoso , Goma de Mascar , Criança , Protocolos Clínicos , Paralisia Facial/diagnóstico , Paralisia Facial/tratamento farmacológico , Feminino , Humanos , Derivados da Hipromelose , Masculino , Massagem , Metilcelulose/administração & dosagem , Metilcelulose/análogos & derivados , Pessoa de Meia-Idade , Parametasona/análogos & derivados , Parametasona/uso terapêutico , Vitaminas/uso terapêutico , gama-Globulinas/uso terapêutico
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