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1.
Eur Spine J ; 20 Suppl 2: S278-83, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21274730

RESUMO

We report a case of type 1 complex regional pain syndrome (CRPS I) of the left leg following the implantation of an artificial disc type in the L4/5 segment of the lumbar spine using a midline left-sided retroperitoneal approach. This approach included the mobilisation of the sympathetic trunk with incision and resection of the intervertebral disc. The perioperative and immediate postoperative periods were uneventful, but on the second postoperative day the patient complained of a progressive allodynia of the whole left leg in combination with weakness of the limb. Neurological examination did not reveal any radicular deficit or paresis. A sympathetic reaction following the mobilisation of the sympathetic trunk during the ventral preparation of the spine was suspected and investigated further. A diagnosis of CRPS I was proposed, and the patient was treated with analgesia, co-analgesics for pain alienation, and systemic corticosteroid therapy. A computed tomography-guided sympathetic block and lymphatic drainage were performed. Following conservative orthopaedic rehabilitation therapy, the degree of pain, allodynia, weakness, and swelling were reduced and the condition of the patient was ameliorated. The cost-benefit ratio of spinal arthroplasty is still controversial. The utility of this paper is to debate a possible cause of a painful complication, which can invalidate the results of a successful operation.


Assuntos
Artroplastia/efeitos adversos , Vértebras Lombares/cirurgia , Implantação de Prótese/efeitos adversos , Distrofia Simpática Reflexa/etiologia , Analgésicos/uso terapêutico , Drenagem , Humanos , Disco Intervertebral/cirurgia , Bloqueio Nervoso , Distrofia Simpática Reflexa/tratamento farmacológico , Distrofia Simpática Reflexa/cirurgia , Resultado do Tratamento
2.
Schmerz ; 21(6): 545-52, 2007 Nov.
Artigo em Alemão | MEDLINE | ID: mdl-17899213

RESUMO

BACKGROUND: In a non-interventional study the efficacy and tolerability of oral transmucosal fentanyl citrate (OTFC) was studied in patients with opioid-treated cancer pain suffering from breakthrough pain. PATIENTS AND METHODS: The prospective multicenter observational trial included 406 patients. For 3-4 months, efficacy of OTFC treatment for breakthrough pain was documented using a numerical analog pain intensity scale (NAS). Further, OTFC therapy was rated and adverse events were recorded. RESULTS: With application of oral transmucosal fentanyl citrate median pain intensity fell from NAS 8 points at the beginning to NAS 2 points at the end of the study. The median effective dosage was 400 g. Tolerability was rated as good or very good by 87.5% of the patients. CONCLUSION: Oral transmucosal fentanyl citrate is a safe and effective treatment for breakthrough pain in chronic cancer-related pain.


Assuntos
Fentanila/administração & dosagem , Fentanila/uso terapêutico , Administração Oral , Adulto , Idoso , Idoso de 80 Anos ou mais , Analgésicos Opioides/administração & dosagem , Analgésicos Opioides/uso terapêutico , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos
3.
Zentralbl Gynakol ; 125(9): 338-45, 2003 Sep.
Artigo em Alemão | MEDLINE | ID: mdl-14569515

RESUMO

The prevention of breast cancer is increasingly of focus in health-politics policies and has gained a valid position in the area of medical intervention. Data from a current meta-analysis of all four randomised Tamoxifen prevention studies illustrate a reduction of 38 % (Odds ratio 0.62; 95 % CI 0.42-0.89) in the incidence of breast cancer. This observation lead to registration of this drug in the USA for the prevention of breast cancer in women with a calculated 5-year risk of > 1.66 %. In addition to Tamoxifen, further substances are currently being tested with the aim of improving the therapeutic index whilst reducing incidence and mortality rates. These are primarily substances which have proven efficacy in the treatment of breast cancer (other antioestrogens, aromatase inhibitors and GnRH-analogues) or those whose mechanism of action predict a preventative effect (retinoids, phytooestrogens, substitution preparations e. g. Tibolone). In Germany, chemoprevention is currently only to be recommended within study protocols, as to date no substance is approved in the indication 'prevention of breast cancer'. A essential contribution to the accrual of valid data is the conduct of breast cancer prevention trials. The participation of women with high risk of breast cancer in Germany is, in contrast to comparable international studies, problematic. Data on the current knowledge and attitude of the female population towards such trials (gathered via a questionnaire of the DACH in 7 000 women) show that only 19.5 % of the women questioned during a consultation with a gynaecologist were aware of the possibility of active chemoprevention. However, 55.3 % stated that they would be prepared to take such a substance, were chemoprevention possible. Studies for both pre- and post-menopausal women with increased risk of breast cancer are currently active in Germany (GISS and IBIS-II of the study group GABG - German Adjuvant Breast cancer Group). An intensive information campaign to raise public awareness of breast cancer risk amongst women and their physicians is planned in conjunction with the IBIS-II study (www.brustkrebsvorbeugen.de). Latest literature recommendations for prevention of breast cancer (Chlebowski et al.) have been assessed.


Assuntos
Anticarcinógenos/uso terapêutico , Neoplasias da Mama/prevenção & controle , Neoplasias da Mama/tratamento farmacológico , Feminino , Alemanha , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Educação de Pacientes como Assunto , Reprodutibilidade dos Testes
4.
Rofo ; 164(1): 47-54, 1996 Jan.
Artigo em Alemão | MEDLINE | ID: mdl-8630360

RESUMO

PURPOSE: With a series of 31 transluminal stent-graft procedures, we assessed the feasibility and clinical effectiveness of a new stent-graft for the treatment of infrarenal abdominal aortic aneurysms (AAAs). METHODS: We treated the patients (male; mean age 71 years) with straight or bifurcated nitinol stents covered with woven dacron graft material for infrarenal eccentric saccular AAA (n = 4) or AAA involving the bifurcation and the common iliac arteries (n = 27). The 18-F delivery system was advanced via a surgical arteriotomy and the stent-graft was placed under fluoroscopic control. Follow-up period ranged from 8 days to 9 months. RESULTS: The implantation of the stent-grafts was technically successful in 30/31 cases. Procedure-related complications were acute hepatic failure due to gastric bleeding in a patient with liver cirrhosis, graft occlusion due to emboli originating from the left atrium (n = 1), macro-embolisation (n = 3), local haematoma (n = 1) and av-fistula (n = 1) requiring surgery. A post-implantation syndrome with leukocytosis and elevated C-reactive protein was observed in all patients. CONCLUSIONS: Endoluminal repair of infrarenal AAA with use of dacron covered nitinol stent-grafts is feasible, safe and clinically effective. However, careful long-term evaluation is necessary.


Assuntos
Aneurisma da Aorta Abdominal/cirurgia , Prótese Vascular , Stents , Idoso , Ligas , Angiografia Digital , Aneurisma da Aorta Abdominal/diagnóstico por imagem , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Polietilenotereftalatos , Complicações Pós-Operatórias , Fatores de Tempo , Tomografia Computadorizada por Raios X
5.
J Clin Psychol ; 42(6): 887-90, 1986 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-3805302

RESUMO

The Mini-Mult and MMPI were administered in random order to 60 blind male veterans admitted to a residential rehabilitation program. Mini-Mult scores predicted the presence or absence of MMPI pathology in 81.7% of the cases. Correlations between the individual Mini-Mult and MMPI scales were significant at the p less than .01 level, but not of sufficient magnitude to permit their interchangeability or to allow for profile diagnosis on the basis of Mini-Mult scores. Analysis of the false negatives raises questions about the clinical significance of an abnormal MMPI in the population studied. The results support the value of the Mini-Mult as a screening device, but not as a substitute for a detailed psychological assessment of the blind.


Assuntos
Cegueira/complicações , MMPI , Transtornos Mentais/prevenção & controle , Cegueira/psicologia , Humanos , Masculino , Programas de Rastreamento , Transtornos Mentais/diagnóstico , Pessoa de Meia-Idade
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