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1.
Transplant Proc ; 35(5): 1691-3, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12962760

RESUMO

OBJECTIVE: The objective of this study is to assess a Simulect (basiliximab) regimen in routine clinical practice in the Spanish kidney transplantation units to evaluate efficacy and safety. METHODS: In this prospective, observational study, data on demographics, parameters of efficacy, and safety in patients who under with kidney transplantation treated with Simulect (basiliximab) were collected through an on-line collection system. RESULTS: One hundred sixty three patients at 18 kidney transplant units included 12 months follow-up. The patient mean age was 52 years (DS 13,67) including 96 (58.90%) men and 67 (41.10%) women. Cold ischemia time was 19 hours (DS 6,79). Only 2 patients presented with PRA >50%. For prophylactic immunosuppression, 67.13% of patients received triple therapy with CNI (cyclosporine 49.65% or tacrolimus 17.48%), MMF (66.43%) or AZA (10.49%), and steroids. Incidence of acute rejection (AR) at 12 months was 12.27% (1.84% steroid-resistant). In subgroup analysis, AR was 13.5% in nondiabetics and 4.5% in diabetics, including 3 steroid-resistant episodes (1.84%) in nondiabetics and none in diabetics. In relation to donor age, AR was incidence 10.3% in patients with kidneys from donors aged 50 years or younger and 10.6% when donors were older than 50 years, including 1 (1.73%) and 2 (1.93%) steroid-resistant episodes, respectively. The graft and patient survival rates at 12 months were 90% and 98%, respectively. CONCLUSIONS: Simulect (basiliximab) used in routine clinical practice provided good prophylaxis against acute rejection in several kidney transplant patient populations, similar to that observed in randomized clinical studies with excellent tolerability and safety.


Assuntos
Anticorpos Monoclonais/uso terapêutico , Transplante de Rim/imunologia , Proteínas Recombinantes de Fusão , Corticosteroides/uso terapêutico , Fatores Etários , Basiliximab , Resistência a Medicamentos , Quimioterapia Combinada , Feminino , Seguimentos , Rejeição de Enxerto/epidemiologia , Humanos , Imunossupressores/uso terapêutico , Transplante de Rim/mortalidade , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Espanha , Análise de Sobrevida , Fatores de Tempo
2.
Transplant Proc ; 35(5): 1704-5, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12962765

RESUMO

To evaluate the efficacy and safety of conversion from cyclosporine to tacrolimus, we analyzed 55 kidney transplant patients who were converted due to cosmetic reasons in 42 patients, acute rejection in 2 patients, and other causes in 11 patients. At the doses and levels used, the development of diabetes mellitus was minimized. Disappearance of cosmetic side-effects and improvement of cardiovascular risk factors, together with conservation of renal function, encourage us to use tacrolimus as an efficacious and safe immunosuppressive therapy.


Assuntos
Ciclosporina/efeitos adversos , Transplante de Rim/imunologia , Tacrolimo/uso terapêutico , Adulto , Glicemia/metabolismo , Pressão Sanguínea , Colesterol/sangue , Feminino , Seguimentos , Humanos , Imunossupressores/efeitos adversos , Imunossupressores/uso terapêutico , Masculino , Estudos Retrospectivos , Segurança , Fatores de Tempo , Ácido Úrico/sangue
7.
Nefrologia ; 21(6): 528-37, 2001.
Artigo em Espanhol | MEDLINE | ID: mdl-11881422
11.
Transplantation ; 65(5): 653-61, 1998 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-9521199

RESUMO

BACKGROUND: In renal transplantation, triple-drug therapy (low-dose cyclosporine [CsA] combined with azathioprine plus steroids) has been replacing double-drug therapy (CsA plus steroids) in clinical practice without much evidence in favor of either therapy. Previous trials comparing the two immunosuppressive regimens gave conflicting results. We attempted to determine whether triple therapy is at least equivalent to double therapy. METHODS: A randomized trial was performed in 250 adult cadaveric renal transplant recipients, comparing double therapy (CsA [10 mg/kg/day] plus prednisone) with triple therapy (CsA [6 mg/kg/day] plus azathioprine plus prednisone). The median follow-up time was 930 days. RESULTS: The incidence of acute rejection episodes refractory to treatment was 11% in double therapy and 4% in triple therapy (relative risk reduction: 64%; 95% confidence interval: 5-100%; P=0.035). Patients in the double therapy group required more intensive antirejection treatment, and their pathologic lesions were more severe. The proportion of patients with acute rejection was similar (double therapy: 45% vs. triple therapy: 40%) as was the incidence of chronic renal dysfunction (double therapy: 17% vs. triple therapy: 15.5%), the 4-year graft survival (double therapy: 71% vs. triple therapy: 83%, P=0.089), and patient survival (double therapy: 94% vs. triple therapy: 93%). In 29 patients (23%), 35 episodes of azathioprine-induced leukopenia were recorded, and in 9 of them azathioprine had to be discontinued. The incidence of other adverse events did not differ between the groups. CONCLUSIONS: Triple therapy caused fewer episodes of refractory acute rejection episodes and was as efficacious and safe as double therapy.


Assuntos
Azatioprina/administração & dosagem , Ciclosporina/administração & dosagem , Imunossupressores/administração & dosagem , Transplante de Rim/métodos , Prednisona/administração & dosagem , Doença Aguda , Adolescente , Adulto , Ciclosporina/sangue , Intervalo Livre de Doença , Combinação de Medicamentos , Feminino , Seguimentos , Rejeição de Enxerto/prevenção & controle , Humanos , Imunossupressores/efeitos adversos , Rim/fisiologia , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Análise de Regressão , Fatores de Tempo
13.
An Med Interna ; 12(2): 65-8, 1995 Feb.
Artigo em Espanhol | MEDLINE | ID: mdl-7749011

RESUMO

UNLABELLED: Renal tubular acidosis is a syndrome of disordered renal acidification, we have studied a group of patients transplanted. Their cases clinic patients have been analyzed with no-present infectious disease, or tubulointerstitial diseases or urinary infection, immunosuppression with prednisone and azatioprine only, no have to ingest cyclosporine and period graft superior 3 months. We haven't neither patient with proximal renal tubular acidosis. We have been reported 7 cases of distal renal tubular acidosis. All the patients have make the furosemide test. Only one case hyperkalemia renal tubular acidosis. Histologic kidney had been chronic rejection. CONCLUSION: renal tubular acidosis is not infrequent of kidney transplantation and this syndrome connect with chronic rejection.


Assuntos
Acidose Tubular Renal/diagnóstico , Transplante de Rim/efeitos adversos , Complicações Pós-Operatórias/diagnóstico , Acidose Tubular Renal/fisiopatologia , Biópsia , Cadáver , Rejeição de Enxerto/diagnóstico , Rejeição de Enxerto/fisiopatologia , Humanos , Rim/patologia , Transplante de Rim/fisiologia , Complicações Pós-Operatórias/fisiopatologia
15.
An Esp Pediatr ; 26(3): 179-83, 1987 Mar.
Artigo em Espanhol | MEDLINE | ID: mdl-3579057

RESUMO

Problems found in the development of a program for individual supplementation of fluoride to infants and pre-school children in a primary pediatric outpatient unit are commented. Problems included knowledge of the level of fluoride in public water supply, in infant formulas and in mineral water used in their preparation and selection of a practical and regular method for supplying fluoride in the first year (having in mind other sources of fluoride) and in older children, and taking into account economic problems. Practical tables with the amount of fluoride in Spanish drinkable water, in commonly available infant formulas and mineral bottled waters, are shown.


Assuntos
Cárie Dentária/prevenção & controle , Fluoretos/administração & dosagem , Administração Oral , Fatores Etários , Criança , Pré-Escolar , Fluoretação , Fluorose Dentária/prevenção & controle , Humanos , Lactente , Alimentos Infantis
16.
An Esp Pediatr ; 26(1): 27-9, 1987 Jan.
Artigo em Espanhol | MEDLINE | ID: mdl-3826939

RESUMO

A prospective study is made of the tuberculin test sensitivity at 3 and 12 months after neonatal vaccination with BCG. From the results obtained in 419 tests the conclusion is that the percentage of positive tests is 3.8% and 1.6% at 3 and 12 months respectively, considering the threshold of positivity equal or superior to 10 mm (or 18.9 y 5.6% respectively with the threshold at 5 mm). These results are lower than the ones described previously, and therefore the conclusion is that in Cantabria the tuberculin tests should be valued without taken in consideration the antecedent of previous vaccination with BCG.


Assuntos
Vacina BCG , Teste Tuberculínico , Tuberculose/prevenção & controle , Humanos , Recém-Nascido , Estudos Prospectivos , Espanha , Fatores de Tempo
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