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1.
Eur J Appl Physiol ; 104(1): 79-86, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18542987

RESUMO

The purpose was to study the effect of endoscopic thoracic sympathectomy (ETS) for palmar and/or axillary hyperhidrosis on physiological responses at rest, and during sub-maximal and maximal exercise in ten healthy patients (7 females and 3 males 18-40 years old) with idiopathic palmar and/or axillary hyperhidrosis. T2-T3 thoracoscopic sympathectomy was performed using a simplified one stage bilateral procedure. Physiological variables were recorded at rest and during sub-maximal (steady-state) and maximal treadmill exercise immediately prior to and 70 days (+/-7.5, SD) after bilateral ETS. Exercise performance capacity and peak VO(2) were not found to be different following bilateral ETS than prior to the ETS. However, heart rate was significantly reduced at rest (14%), at sub-maximal exercise (12.3%), and at peak exercise (5.7%), together with a significant increase in oxygen pulse (11.8, 12.7, and 7.8%, respectively). The rate pressure product (RPP) was also significantly reduced following the surgical procedure at all three study stages, while all other physiological variables measured remained unchanged. It is suggested that thoracic-sympathetic denervation affects the heart, sweating, and circulation of the respective denervated region but does not affect exercise performance or mechanical/physiologic efficiency, despite a significant reduction in heart rate (both at rest and during exercise). The latter was, most likely, fully compensated by an increase in stroke volume and less likely by an improved muscle O(2) extraction due to more efficient blood distribution, keeping the work-rate and oxygen uptake unaffected.


Assuntos
Sistema Cardiovascular/inervação , Exercício Físico , Hiperidrose/cirurgia , Sistema Respiratório/inervação , Simpatectomia/métodos , Toracoscopia , Tórax/inervação , Adaptação Fisiológica , Adulto , Pressão Sanguínea , Tolerância ao Exercício , Feminino , Frequência Cardíaca , Humanos , Hiperidrose/fisiopatologia , Masculino , Consumo de Oxigênio , Volume Sistólico , Simpatectomia/efeitos adversos , Toracoscopia/efeitos adversos , Resultado do Tratamento
3.
J Am Coll Surg ; 190(3): 315-8, 2000 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10703857

RESUMO

BACKGROUND: Colonic pseudo-obstruction is a poorly understood syndrome, described by Ogilvie, and characterized by signs of large-bowel obstruction, without a mechanical cause. An imbalance in the autonomic nerve supply to the colon has been suggested as the pathophysiology. Recently, promising results with pharmacologic manipulation with neostigmine have been described. STUDY DESIGN: A prospective study was undertaken with 11 consecutive patients with clinical and radiologic signs of colonic pseudo-obstruction, in one general hospital, over a 1-year period. Patients were treated primarily with 2.5 mg of neostigmine in 100 mL of saline for 1 hour, under cardiac monitoring. Results were assessed by the clinical and radiologic responses. RESULTS: Rapid and effective spontaneous decompression of the colon was achieved in 8 patients after a single dose of neostigmine, within a mean of 90 minutes from the beginning of treatment. In another two patients decompression occurred only after a second dose was administered 3 hours after the first dose. In one patient, no changes were observed and colonoscopic decompression was performed. No significant bradycardia was observed in any of the patients. CONCLUSIONS: Neostigmine is a simple, safe, and effective therapy for treatment of colonic pseudo-obstruction.


Assuntos
Pseudo-Obstrução do Colo/tratamento farmacológico , Neostigmina/uso terapêutico , Parassimpatomiméticos/uso terapêutico , Doença Aguda , Adulto , Idoso , Idoso de 80 Anos ou mais , Pseudo-Obstrução do Colo/diagnóstico por imagem , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Estudos Prospectivos , Radiografia , Resultado do Tratamento
5.
Dig Dis Sci ; 45(11): 2247-51, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11215748

RESUMO

We investigated the effect of octreotide in the treatment of severe acute pancreatitis in a case-control study. Experimental and clinical studies on the effect of octreotide in the treatment of acute pancreatitis have shown controversial results. Since January 1992, we have been conducting a prospective randomized study on the effect of octreotide in severe acute pancreatitis, in three hospitals in Israel. The entering criteria included three or more of the Ranson prognostic signs and CT findings of severe pancreatitis. Patients were randomly assigned to conservative treatment either with or without octreotide (0.1 mg subcutaneously three times a day). The end points of the study included: complication rate (ARDS, sepsis, renal failure, pseudocyst, fistula, and abscess), length of hospital stay, and mortality. From January 1992 to December 1996, 60 patients entered the study. After evaluating the files, 10 patients were excluded due to failure to meet the entering criteria, incomplete data, or incorrect diagnosis. Of the remaining 50 patients, 25 were assigned to octreotide (treatment group) and 25 to conservative treatment only (control group). The two groups matched with regard to age, sex, etiology, and severity of the disease. The complication rate was lower in the treatment group with regard to sepsis (24% vs 76%, P = 0.0002) and ARDS (28% vs 56%, P = 0.04). The hospital stay was shorter in the treatment group (20.6 vs 33.1 days, P = 0.04). Two patients died in the treatment group and eight in the control group (P < 0.019). These results suggest that octreotide may have a beneficial effect in the treatment of severe acute pancreatitis.


Assuntos
Octreotida/uso terapêutico , Pancreatite Necrosante Aguda/tratamento farmacológico , Adulto , Idoso , Estudos de Casos e Controles , Feminino , Humanos , Injeções Subcutâneas , Tempo de Internação , Masculino , Pessoa de Meia-Idade , Octreotida/efeitos adversos , Pancreatite Necrosante Aguda/mortalidade , Taxa de Sobrevida , Resultado do Tratamento
7.
J Trauma ; 40(3): 472-5, 1996 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-8601873

RESUMO

Blast injuries are rare, and although blast-induced perforations of the bowel have been described in the past, the entity of a delayed perforation caused by an evolving injury has not been reported. We report three men injured by the explosion of a terrorist bombing in open air. They suffered primary blast injuries, which resulted in isolated perforations of the terminal ileum. They were operated at different times after the blast event. The resected specimens were examined under light microscopy. One patient was operated immediately, and had three perforations in the terminal ileum. In the other two patients, abdominal complaints appeared only 24 and 48 hours later. These two patients were found to have hematomas in the wall of the terminal ileum, and small perforations therein, with almost no contamination of the peritoneal cavity. On histological examination, there were small perforations with disruption of all intestinal layers. In the vicinity of the perforations, the mucosa was necrotic and disorganized. The submucosa showed edema and vascular thrombi, and at several points mucus was shown dissecting through the muscularis propria, thus creating minute microperforations. Because of the findings in these patients, we suggest a mechanism of evolving damage to the bowel wall and delayed perforation rather than delayed diagnosis, after blast injuries. We suggest that patients exposed to a significant blast should be watched carefully for at least 48 hours.


Assuntos
Traumatismos por Explosões/complicações , Doenças do Íleo/etiologia , Íleo/lesões , Perfuração Intestinal/etiologia , Adolescente , Adulto , Diagnóstico Diferencial , Humanos , Doenças do Íleo/patologia , Doenças do Íleo/cirurgia , Perfuração Intestinal/patologia , Perfuração Intestinal/cirurgia , Masculino , Fatores de Tempo
8.
J Am Coll Surg ; 181(2): 121-4, 1995 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-7627383

RESUMO

BACKGROUND: Experimental and clinical studies on the effect of octreotide in the treatment of patients with acute pancreatitis have presented controversial results. Since January 1992, we have been conducting a prospective randomized study on the clinical effect of octreotide in severe acute pancreatitis, at three hospitals in Israel. STUDY DESIGN: The entering criteria included three or more of the Ranson's prognostic signs and computed tomographic findings of severe pancreatitis. Patients were randomly assigned to conservative treatment either with or without octreotide (0.1 mg injected subcutaneously three times a day). The end points of the study included: complication rate (adult respiratory distress syndrome [ARDS], sepsis, renal failure, pseudocyst, fistula, and abscess), length of hospital stay, and mortality. RESULTS: During the first two years (from January 1992 to December 1993), 51 patients entered the study. After evaluation, 13 patients were excluded due to failure to meet the entering criteria, incomplete data, or incorrect diagnosis. Of the remaining 38 patients, 19 were assigned to octreotide (treatment group) and 19 to conservative treatment alone (control group). The two groups were matched with regard to age, sex, etiology, and severity of disease. The complication rate was lower in the treatment group compared with the control group with regard to sepsis (26 compared with 74 percent, p = 0.004) and ARDS (37 compared with 63 percent, p = 0.1). The hospital stay was shorter in the treatment group compared with the control group (17.9 compared with 34.1 days, p = 0.02). Death occurred in two patients in the treatment group and six patients in the control group. CONCLUSIONS: Although some of the parameters did not reach statistical significance, these preliminary results suggest that octreotide may have a beneficial effect in the treatment of patients with severe acute pancreatitis. This study is scheduled to continue for two more years.


Assuntos
Octreotida/uso terapêutico , Pancreatite/tratamento farmacológico , Abscesso/etiologia , Abscesso/prevenção & controle , Doença Aguda , Infecções Bacterianas/prevenção & controle , Feminino , Humanos , Injeções Subcutâneas , Tempo de Internação , Masculino , Pessoa de Meia-Idade , Octreotida/administração & dosagem , Fístula Pancreática/etiologia , Fístula Pancreática/prevenção & controle , Pseudocisto Pancreático/etiologia , Pseudocisto Pancreático/prevenção & controle , Pancreatite/complicações , Estudos Prospectivos , Insuficiência Renal/etiologia , Insuficiência Renal/prevenção & controle , Síndrome do Desconforto Respiratório/etiologia , Síndrome do Desconforto Respiratório/prevenção & controle , Método Simples-Cego , Taxa de Sobrevida
9.
Hum Reprod ; 10(5): 1065-9, 1995 May.
Artigo em Inglês | MEDLINE | ID: mdl-7657742

RESUMO

This study was undertaken to investigate a possible relationship between endogenous secretion of growth hormone (GH) during ovarian stimulation and treatment outcome in patients undergoing in-vitro fertilization (IVF) and embryo transfer. Plasma samples obtained from 19 women who had successfully completed all stages of IVF/embryo transfer were analysed retrospectively. Based on the increase in GH during treatment, 11 GH responders and eight GH non-responders were identified. Mean daily GH concentrations for the GH responders and GH non-responders were 3.5 +/- 1.8 and 1.8 +/- 0.8, 5.4 +/- 2.3 and 0.5 +/- 0.2, and 9.0 +/- 1.9 and 0.7 +/- 0.1 ng/ml (P < 0.05) for days 10, 11 and 12 respectively. Plasma insulin-like growth factor-I slightly increased with treatment in both groups. No significant difference between these groups was found in relation to treatment duration, number of human menopausal gonadotrophin ampoules used, oestradiol peak values, and number of oocytes retrieved or fertilization rate. Seven of the 11 GH responder women conceived in comparison with one pregnancy among eight GH non-responder patients (P < 0.05). In view of the absence of differences in the clinical and laboratory parameters, we suggest that the occurrence of pregnancies among GH responder patients might be related to a positive local effect of GH or its mediators on uterine receptivity at the time of nidation.


Assuntos
Hormônio do Crescimento/sangue , Técnicas Reprodutivas , Adulto , Implantação do Embrião/fisiologia , Transferência Embrionária , Estradiol/sangue , Feminino , Fertilização in vitro , Humanos , Infertilidade Feminina/sangue , Infertilidade Feminina/terapia , Fator de Crescimento Insulin-Like I/metabolismo , Menotropinas/administração & dosagem , Indução da Ovulação , Gravidez , Estudos Retrospectivos
10.
Can J Neurol Sci ; 3(3): 205-10, 1976 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-963639

RESUMO

A case of congenital, intraspinal, extradural cyst is reported with pain as the only presenting feature. In the past, the lack of pain has been considered one of the characteristics of these rare lesions. In other reported cases, when pain has been present, it was minimal and never the presenting feature. The clinical and radiographic features and the surgical treatment are described. The pathogenesis is discussed and the literature reviewed. An addition to the surgical technique is given whereby one of the post operative complications may be obviated.


Assuntos
Cistos/congênito , Doenças da Medula Espinal/congênito , Adolescente , Cistos/diagnóstico por imagem , Cistos/patologia , Humanos , Masculino , Radiografia , Doenças da Medula Espinal/diagnóstico por imagem , Doenças da Medula Espinal/patologia
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